Javascript doit fonctionner ! Activez-le et rechargez cette page.
Le Rézo de JeuxDeMots
• Types de relations
• Types de noeuds
• Consolider
le terme
  Options  
             

  Filtrage type relations : +   - (ex: 4, 12, 18, 36, 444, 555, 777)
  Filtrage valeur :          min   max
  Filtrage type noeuds :   +   - (ex: 4, 6, 8, 9, 10, 12, 18, 36, 444, 555, 777)

  Présentation de sortie :   (ex: -rien-, cloud, nicecloud)
 

'en:microcephaly-capillary malformation syndrome'
(id=6818475 ; fe=en:microcephaly-capillary malformation syndrome ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=48596.54998779297 creation date=2017-06-25 touchdate=2025-08-13 23:53:07.000)
≈ 847 relations sortantes

  1. en:microcephaly-capillary malformation syndrome -- r_associated #0: 43 / 1 -> en:behavioral variant of frontotemporal dementia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:behavioral variant of frontotemporal dementia | rel=r_associated | relid=0 | w=43
  2. en:microcephaly-capillary malformation syndrome -- r_associated #0: 43 / 1 -> en:hypophosphatemic rickets with hypercalciuria, hereditary
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hypophosphatemic rickets with hypercalciuria, hereditary | rel=r_associated | relid=0 | w=43
  3. en:microcephaly-capillary malformation syndrome -- r_associated #0: 43 / 1 -> en:myopathy with exercise intolerance, swedish type
    n1=en:microcephaly-capillary malformation syndrome | n2=en:myopathy with exercise intolerance, swedish type | rel=r_associated | relid=0 | w=43
  4. en:microcephaly-capillary malformation syndrome -- r_associated #0: 43 / 1 -> en:osteogenesis imperfecta, recessive perinatal lethal, with microcephaly and cataracts
    n1=en:microcephaly-capillary malformation syndrome | n2=en:osteogenesis imperfecta, recessive perinatal lethal, with microcephaly and cataracts | rel=r_associated | relid=0 | w=43
  5. en:microcephaly-capillary malformation syndrome -- r_associated #0: 43 / 1 -> en:progressive microcephaly
    n1=en:microcephaly-capillary malformation syndrome | n2=en:progressive microcephaly | rel=r_associated | relid=0 | w=43
  6. en:microcephaly-capillary malformation syndrome -- r_associated #0: 43 / 1 -> en:urocanase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:urocanase deficiency | rel=r_associated | relid=0 | w=43
  7. en:microcephaly-capillary malformation syndrome -- r_associated #0: 43 / 1 -> en:waisman syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:waisman syndrome | rel=r_associated | relid=0 | w=43
  8. en:microcephaly-capillary malformation syndrome -- r_associated #0: 43 / 1 -> en:wells jankovic syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:wells jankovic syndrome | rel=r_associated | relid=0 | w=43
  9. en:microcephaly-capillary malformation syndrome -- r_associated #0: 42 / 0.977 -> en:alkaptonuria
    n1=en:microcephaly-capillary malformation syndrome | n2=en:alkaptonuria | rel=r_associated | relid=0 | w=42
  10. en:microcephaly-capillary malformation syndrome -- r_associated #0: 42 / 0.977 -> en:cerebral cavernous malformation
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cerebral cavernous malformation | rel=r_associated | relid=0 | w=42
  11. en:microcephaly-capillary malformation syndrome -- r_associated #0: 42 / 0.977 -> en:congenital dyserythropoietic anemia, type i
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital dyserythropoietic anemia, type i | rel=r_associated | relid=0 | w=42
  12. en:microcephaly-capillary malformation syndrome -- r_associated #0: 41 / 0.953 -> en:arthrogryposis multiplex congenita, neurogenic type (disorder)
    n1=en:microcephaly-capillary malformation syndrome | n2=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | rel=r_associated | relid=0 | w=41
  13. en:microcephaly-capillary malformation syndrome -- r_associated #0: 41 / 0.953 -> en:glucose transporter protein type 1 deficiency syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:glucose transporter protein type 1 deficiency syndrome | rel=r_associated | relid=0 | w=41
  14. en:microcephaly-capillary malformation syndrome -- r_associated #0: 41 / 0.953 -> en:gracile syndrome (disorder)
    n1=en:microcephaly-capillary malformation syndrome | n2=en:gracile syndrome (disorder) | rel=r_associated | relid=0 | w=41
  15. en:microcephaly-capillary malformation syndrome -- r_associated #0: 41 / 0.953 -> en:muscle-eye-brain disease, congenital muscular dystrophy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:muscle-eye-brain disease, congenital muscular dystrophy | rel=r_associated | relid=0 | w=41
  16. en:microcephaly-capillary malformation syndrome -- r_associated #0: 41 / 0.953 -> en:sly syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:sly syndrome | rel=r_associated | relid=0 | w=41
  17. en:microcephaly-capillary malformation syndrome -- r_associated #0: 41 / 0.953 -> en:thyroid dyshormonogenesis 4
    n1=en:microcephaly-capillary malformation syndrome | n2=en:thyroid dyshormonogenesis 4 | rel=r_associated | relid=0 | w=41
  18. en:microcephaly-capillary malformation syndrome -- r_associated #0: 41 / 0.953 -> en:vesicoureteral reflux (1 patient)
    n1=en:microcephaly-capillary malformation syndrome | n2=en:vesicoureteral reflux (1 patient) | rel=r_associated | relid=0 | w=41
  19. en:microcephaly-capillary malformation syndrome -- r_associated #0: 40 / 0.93 -> en:aspartylglycosaminuria
    n1=en:microcephaly-capillary malformation syndrome | n2=en:aspartylglycosaminuria | rel=r_associated | relid=0 | w=40
  20. en:microcephaly-capillary malformation syndrome -- r_associated #0: 40 / 0.93 -> en:bothnia retinal dystrophy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:bothnia retinal dystrophy | rel=r_associated | relid=0 | w=40
  21. en:microcephaly-capillary malformation syndrome -- r_associated #0: 40 / 0.93 -> en:congenital capillary hemangioma
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital capillary hemangioma | rel=r_associated | relid=0 | w=40
  22. en:microcephaly-capillary malformation syndrome -- r_associated #0: 40 / 0.93 -> en:isovaleric acidemia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:isovaleric acidemia | rel=r_associated | relid=0 | w=40
  23. en:microcephaly-capillary malformation syndrome -- r_associated #0: 40 / 0.93 -> en:microgyria
    n1=en:microcephaly-capillary malformation syndrome | n2=en:microgyria | rel=r_associated | relid=0 | w=40
  24. en:microcephaly-capillary malformation syndrome -- r_associated #0: 40 / 0.93 -> en:variable cardiac defects
    n1=en:microcephaly-capillary malformation syndrome | n2=en:variable cardiac defects | rel=r_associated | relid=0 | w=40
  25. en:microcephaly-capillary malformation syndrome -- r_associated #0: 40 / 0.93 -> en:xeroderma pigmentosum
    n1=en:microcephaly-capillary malformation syndrome | n2=en:xeroderma pigmentosum | rel=r_associated | relid=0 | w=40
  26. en:microcephaly-capillary malformation syndrome -- r_associated #0: 39 / 0.907 -> en:3-methylglutaconic aciduria type 1
    n1=en:microcephaly-capillary malformation syndrome | n2=en:3-methylglutaconic aciduria type 1 | rel=r_associated | relid=0 | w=39
  27. en:microcephaly-capillary malformation syndrome -- r_associated #0: 39 / 0.907 -> en:bietti crystalline corneoretinal dystrophy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:bietti crystalline corneoretinal dystrophy | rel=r_associated | relid=0 | w=39
  28. en:microcephaly-capillary malformation syndrome -- r_associated #0: 39 / 0.907 -> en:congenital leptin deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital leptin deficiency | rel=r_associated | relid=0 | w=39
  29. en:microcephaly-capillary malformation syndrome -- r_associated #0: 39 / 0.907 -> en:deficiency of glucosyltransferase 1
    n1=en:microcephaly-capillary malformation syndrome | n2=en:deficiency of glucosyltransferase 1 | rel=r_associated | relid=0 | w=39
  30. en:microcephaly-capillary malformation syndrome -- r_associated #0: 39 / 0.907 -> en:delayed myelination
    n1=en:microcephaly-capillary malformation syndrome | n2=en:delayed myelination | rel=r_associated | relid=0 | w=39
  31. en:microcephaly-capillary malformation syndrome -- r_associated #0: 39 / 0.907 -> en:familial benign neonatal epilepsy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:familial benign neonatal epilepsy | rel=r_associated | relid=0 | w=39
  32. en:microcephaly-capillary malformation syndrome -- r_associated #0: 39 / 0.907 -> en:marles greenberg persaud syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:marles greenberg persaud syndrome | rel=r_associated | relid=0 | w=39
  33. en:microcephaly-capillary malformation syndrome -- r_associated #0: 39 / 0.907 -> en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency | rel=r_associated | relid=0 | w=39
  34. en:microcephaly-capillary malformation syndrome -- r_associated #0: 38 / 0.884 -> en:brody myopathy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:brody myopathy | rel=r_associated | relid=0 | w=38
  35. en:microcephaly-capillary malformation syndrome -- r_associated #0: 38 / 0.884 -> en:congenital disorder of glycosylation type ig
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital disorder of glycosylation type ig | rel=r_associated | relid=0 | w=38
  36. en:microcephaly-capillary malformation syndrome -- r_associated #0: 38 / 0.884 -> en:menkes disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:menkes disease | rel=r_associated | relid=0 | w=38
  37. en:microcephaly-capillary malformation syndrome -- r_associated #0: 38 / 0.884 -> en:syndrome of apparent mineralocorticoid excess
    n1=en:microcephaly-capillary malformation syndrome | n2=en:syndrome of apparent mineralocorticoid excess | rel=r_associated | relid=0 | w=38
  38. en:microcephaly-capillary malformation syndrome -- r_associated #0: 37 / 0.86 -> en:autosomal recessive muscular dystrophy with limb girdle distribution
    n1=en:microcephaly-capillary malformation syndrome | n2=en:autosomal recessive muscular dystrophy with limb girdle distribution | rel=r_associated | relid=0 | w=37
  39. en:microcephaly-capillary malformation syndrome -- r_associated #0: 37 / 0.86 -> en:autosomal recessive primary microcephaly
    n1=en:microcephaly-capillary malformation syndrome | n2=en:autosomal recessive primary microcephaly | rel=r_associated | relid=0 | w=37
  40. en:microcephaly-capillary malformation syndrome -- r_associated #0: 37 / 0.86 -> en:hnsha due to aldolase a deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hnsha due to aldolase a deficiency | rel=r_associated | relid=0 | w=37
  41. en:microcephaly-capillary malformation syndrome -- r_associated #0: 37 / 0.86 -> en:hypotonia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hypotonia | rel=r_associated | relid=0 | w=37
  42. en:microcephaly-capillary malformation syndrome -- r_associated #0: 37 / 0.86 -> en:insulin autoimmune syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:insulin autoimmune syndrome | rel=r_associated | relid=0 | w=37
  43. en:microcephaly-capillary malformation syndrome -- r_associated #0: 37 / 0.86 -> en:jankovic rivera syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:jankovic rivera syndrome | rel=r_associated | relid=0 | w=37
  44. en:microcephaly-capillary malformation syndrome -- r_associated #0: 36 / 0.837 -> en:argininemia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:argininemia | rel=r_associated | relid=0 | w=36
  45. en:microcephaly-capillary malformation syndrome -- r_associated #0: 36 / 0.837 -> en:cerebral atrophy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cerebral atrophy | rel=r_associated | relid=0 | w=36
  46. en:microcephaly-capillary malformation syndrome -- r_associated #0: 36 / 0.837 -> en:fronto-facio-nasal dysplasia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:fronto-facio-nasal dysplasia | rel=r_associated | relid=0 | w=36
  47. en:microcephaly-capillary malformation syndrome -- r_associated #0: 36 / 0.837 -> en:hereditary factor xi deficiency disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary factor xi deficiency disease | rel=r_associated | relid=0 | w=36
  48. en:microcephaly-capillary malformation syndrome -- r_associated #0: 36 / 0.837 -> en:knobloch syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:knobloch syndrome | rel=r_associated | relid=0 | w=36
  49. en:microcephaly-capillary malformation syndrome -- r_associated #0: 36 / 0.837 -> en:megalencephaly cutis marmorata telangiectatica congenita
    n1=en:microcephaly-capillary malformation syndrome | n2=en:megalencephaly cutis marmorata telangiectatica congenita | rel=r_associated | relid=0 | w=36
  50. en:microcephaly-capillary malformation syndrome -- r_associated #0: 36 / 0.837 -> en:moderate steroid 21-hydroxylase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:moderate steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=36
  51. en:microcephaly-capillary malformation syndrome -- r_associated #0: 36 / 0.837 -> en:morm syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:morm syndrome | rel=r_associated | relid=0 | w=36
  52. en:microcephaly-capillary malformation syndrome -- r_associated #0: 36 / 0.837 -> en:paroxysmal extreme pain disorder
    n1=en:microcephaly-capillary malformation syndrome | n2=en:paroxysmal extreme pain disorder | rel=r_associated | relid=0 | w=36
  53. en:microcephaly-capillary malformation syndrome -- r_associated #0: 36 / 0.837 -> en:presentey anomaly
    n1=en:microcephaly-capillary malformation syndrome | n2=en:presentey anomaly | rel=r_associated | relid=0 | w=36
  54. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:5 alpha steroid reductase 2 deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:5 alpha steroid reductase 2 deficiency | rel=r_associated | relid=0 | w=35
  55. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:5' 10' methylenetetrahydrofolate reductase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:5' 10' methylenetetrahydrofolate reductase deficiency | rel=r_associated | relid=0 | w=35
  56. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:allgrove syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:allgrove syndrome | rel=r_associated | relid=0 | w=35
  57. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:arginine:glycine amidinotransferase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:arginine:glycine amidinotransferase deficiency | rel=r_associated | relid=0 | w=35
  58. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:atrophoderma vermiculatum
    n1=en:microcephaly-capillary malformation syndrome | n2=en:atrophoderma vermiculatum | rel=r_associated | relid=0 | w=35
  59. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:autosomal recessive asexual dwarfism
    n1=en:microcephaly-capillary malformation syndrome | n2=en:autosomal recessive asexual dwarfism | rel=r_associated | relid=0 | w=35
  60. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:bardet-biedl syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:bardet-biedl syndrome | rel=r_associated | relid=0 | w=35
  61. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:beckwith-wiedemann syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:beckwith-wiedemann syndrome | rel=r_associated | relid=0 | w=35
  62. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism
    n1=en:microcephaly-capillary malformation syndrome | n2=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=35
  63. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:chylomicron retention disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:chylomicron retention disease | rel=r_associated | relid=0 | w=35
  64. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:citrin deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:citrin deficiency | rel=r_associated | relid=0 | w=35
  65. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:classical phenylketonuria
    n1=en:microcephaly-capillary malformation syndrome | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=35
  66. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration | rel=r_associated | relid=0 | w=35
  67. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:congenital onset
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital onset | rel=r_associated | relid=0 | w=35
  68. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:deafness, sensorineural, and male infertility
    n1=en:microcephaly-capillary malformation syndrome | n2=en:deafness, sensorineural, and male infertility | rel=r_associated | relid=0 | w=35
  69. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:dentatorubral-pallidoluysian atrophy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:dentatorubral-pallidoluysian atrophy | rel=r_associated | relid=0 | w=35
  70. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:disorder of central nervous system due to xeroderma pigmentosum
    n1=en:microcephaly-capillary malformation syndrome | n2=en:disorder of central nervous system due to xeroderma pigmentosum | rel=r_associated | relid=0 | w=35
  71. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:enterokinase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:enterokinase deficiency | rel=r_associated | relid=0 | w=35
  72. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:epilepsy, myoclonic, benign adult familial, type 2
    n1=en:microcephaly-capillary malformation syndrome | n2=en:epilepsy, myoclonic, benign adult familial, type 2 | rel=r_associated | relid=0 | w=35
  73. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:familial hypoaldosteronism
    n1=en:microcephaly-capillary malformation syndrome | n2=en:familial hypoaldosteronism | rel=r_associated | relid=0 | w=35
  74. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:female restricted epilepsy with intellectual disability syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:female restricted epilepsy with intellectual disability syndrome | rel=r_associated | relid=0 | w=35
  75. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:game friedman paradice syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:game friedman paradice syndrome | rel=r_associated | relid=0 | w=35
  76. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:gamma-glutamyltransferase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:gamma-glutamyltransferase deficiency | rel=r_associated | relid=0 | w=35
  77. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:geroderma osteodysplastica
    n1=en:microcephaly-capillary malformation syndrome | n2=en:geroderma osteodysplastica | rel=r_associated | relid=0 | w=35
  78. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:hemolytic anemia due to pyruvate kinase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hemolytic anemia due to pyruvate kinase deficiency | rel=r_associated | relid=0 | w=35
  79. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:hereditary factor xii deficiency disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary factor xii deficiency disease | rel=r_associated | relid=0 | w=35
  80. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:hereditary neuraxial edema
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary neuraxial edema | rel=r_associated | relid=0 | w=35
  81. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:hereditary palmoplantar keratoderma gamborg nielsen type
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary palmoplantar keratoderma gamborg nielsen type | rel=r_associated | relid=0 | w=35
  82. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:hnsha due to glutathione synthetase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hnsha due to glutathione synthetase deficiency | rel=r_associated | relid=0 | w=35
  83. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:hyperprolinemia type 2
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hyperprolinemia type 2 | rel=r_associated | relid=0 | w=35
  84. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:hypertelorism
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hypertelorism | rel=r_associated | relid=0 | w=35
  85. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:hypokalemia, familial
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hypokalemia, familial | rel=r_associated | relid=0 | w=35
  86. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:lipoid proteinosis of urbach and wiethe
    n1=en:microcephaly-capillary malformation syndrome | n2=en:lipoid proteinosis of urbach and wiethe | rel=r_associated | relid=0 | w=35
  87. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:lipoprotein glomerulopathy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:lipoprotein glomerulopathy | rel=r_associated | relid=0 | w=35
  88. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:maple syrup urine disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:maple syrup urine disease | rel=r_associated | relid=0 | w=35
  89. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:melanoma astrocytoma syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:melanoma astrocytoma syndrome | rel=r_associated | relid=0 | w=35
  90. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency | rel=r_associated | relid=0 | w=35
  91. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:microcephalic osteodysplastic dysplasia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:microcephalic osteodysplastic dysplasia | rel=r_associated | relid=0 | w=35
  92. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:microcephalic primordial dwarfism toriello type
    n1=en:microcephaly-capillary malformation syndrome | n2=en:microcephalic primordial dwarfism toriello type | rel=r_associated | relid=0 | w=35
  93. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:microcephaly, progressive (3 to 8 sd below the mean)
    n1=en:microcephaly-capillary malformation syndrome | n2=en:microcephaly, progressive (3 to 8 sd below the mean) | rel=r_associated | relid=0 | w=35
  94. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:muscle amp deaminase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:muscle amp deaminase deficiency | rel=r_associated | relid=0 | w=35
  95. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:pancreatic triacylglycerol lipase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:pancreatic triacylglycerol lipase deficiency | rel=r_associated | relid=0 | w=35
  96. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:prickle1-related progressive myoclonus epilepsy with ataxia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:prickle1-related progressive myoclonus epilepsy with ataxia | rel=r_associated | relid=0 | w=35
  97. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:short nose
    n1=en:microcephaly-capillary malformation syndrome | n2=en:short nose | rel=r_associated | relid=0 | w=35
  98. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:short stature
    n1=en:microcephaly-capillary malformation syndrome | n2=en:short stature | rel=r_associated | relid=0 | w=35
  99. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:spinocerebellar ataxia, autosomal recessive 2
    n1=en:microcephaly-capillary malformation syndrome | n2=en:spinocerebellar ataxia, autosomal recessive 2 | rel=r_associated | relid=0 | w=35
  100. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:spondylo-ocular syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:spondylo-ocular syndrome | rel=r_associated | relid=0 | w=35
  101. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:stambp, 1-bp del, 411c
    n1=en:microcephaly-capillary malformation syndrome | n2=en:stambp, 1-bp del, 411c | rel=r_associated | relid=0 | w=35
  102. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:walker-warburg syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:walker-warburg syndrome | rel=r_associated | relid=0 | w=35
  103. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:werdnig-hoffmann disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:werdnig-hoffmann disease | rel=r_associated | relid=0 | w=35
  104. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:wolman disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:wolman disease | rel=r_associated | relid=0 | w=35
  105. en:microcephaly-capillary malformation syndrome -- r_associated #0: 35 / 0.814 -> en:x-linked lissencephaly
    n1=en:microcephaly-capillary malformation syndrome | n2=en:x-linked lissencephaly | rel=r_associated | relid=0 | w=35
  106. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:3-methylglutaconic aciduria type 3
    n1=en:microcephaly-capillary malformation syndrome | n2=en:3-methylglutaconic aciduria type 3 | rel=r_associated | relid=0 | w=34
  107. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:acrocallosal syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:acrocallosal syndrome | rel=r_associated | relid=0 | w=34
  108. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:adrenal gland hyperplasia ii
    n1=en:microcephaly-capillary malformation syndrome | n2=en:adrenal gland hyperplasia ii | rel=r_associated | relid=0 | w=34
  109. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:allanson pantzar mcleod syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:allanson pantzar mcleod syndrome | rel=r_associated | relid=0 | w=34
  110. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:arterial tortuosity syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:arterial tortuosity syndrome | rel=r_associated | relid=0 | w=34
  111. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:autosomal dominant idiopathic familial dystonia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:autosomal dominant idiopathic familial dystonia | rel=r_associated | relid=0 | w=34
  112. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:autosomal recessive distal osteolysis syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:autosomal recessive distal osteolysis syndrome | rel=r_associated | relid=0 | w=34
  113. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:autosomal recessive idiopathic familial dystonia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:autosomal recessive idiopathic familial dystonia | rel=r_associated | relid=0 | w=34
  114. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:cardiac glycogen phosphorylase kinase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cardiac glycogen phosphorylase kinase deficiency | rel=r_associated | relid=0 | w=34
  115. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:cerebrotendinous xanthomatosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cerebrotendinous xanthomatosis | rel=r_associated | relid=0 | w=34
  116. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:cockayne syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cockayne syndrome | rel=r_associated | relid=0 | w=34
  117. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:cohen syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cohen syndrome | rel=r_associated | relid=0 | w=34
  118. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:congenital
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital | rel=r_associated | relid=0 | w=34
  119. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:congenital adrenal hyperplasia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital adrenal hyperplasia | rel=r_associated | relid=0 | w=34
  120. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:congenital amegakaryocytic thrombocytopenia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital amegakaryocytic thrombocytopenia | rel=r_associated | relid=0 | w=34
  121. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:congenital porencephaly
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital porencephaly | rel=r_associated | relid=0 | w=34
  122. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:cryptophthalmos syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cryptophthalmos syndrome | rel=r_associated | relid=0 | w=34
  123. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:cutaneous capillary malformation
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cutaneous capillary malformation | rel=r_associated | relid=0 | w=34
  124. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:dopa-responsive dystonia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:dopa-responsive dystonia | rel=r_associated | relid=0 | w=34
  125. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:ectodermal dysplasia/ skin fragility syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:ectodermal dysplasia/ skin fragility syndrome | rel=r_associated | relid=0 | w=34
  126. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:fatal congenital nonlysosomal heart glycogenosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:fatal congenital nonlysosomal heart glycogenosis | rel=r_associated | relid=0 | w=34
  127. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:fatal infantile lactic acidosis with methylmalonic aciduria
    n1=en:microcephaly-capillary malformation syndrome | n2=en:fatal infantile lactic acidosis with methylmalonic aciduria | rel=r_associated | relid=0 | w=34
  128. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:frontotemporal dementia, chromosome 3-linked
    n1=en:microcephaly-capillary malformation syndrome | n2=en:frontotemporal dementia, chromosome 3-linked | rel=r_associated | relid=0 | w=34
  129. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:hearing impairment
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hearing impairment | rel=r_associated | relid=0 | w=34
  130. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:hereditary cerebellar atrophy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary cerebellar atrophy | rel=r_associated | relid=0 | w=34
  131. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:hereditary peripheral neuropathy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary peripheral neuropathy | rel=r_associated | relid=0 | w=34
  132. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:hmg-coa lyase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hmg-coa lyase deficiency | rel=r_associated | relid=0 | w=34
  133. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:hypoplasia of corpus callosum
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hypoplasia of corpus callosum | rel=r_associated | relid=0 | w=34
  134. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:kohlschutter tonz syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:kohlschutter tonz syndrome | rel=r_associated | relid=0 | w=34
  135. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:leigh disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:leigh disease | rel=r_associated | relid=0 | w=34
  136. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:leukotriene c4 synthase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:leukotriene c4 synthase deficiency | rel=r_associated | relid=0 | w=34
  137. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:lissencephaly syndrome, norman-roberts type
    n1=en:microcephaly-capillary malformation syndrome | n2=en:lissencephaly syndrome, norman-roberts type | rel=r_associated | relid=0 | w=34
  138. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:low set ears
    n1=en:microcephaly-capillary malformation syndrome | n2=en:low set ears | rel=r_associated | relid=0 | w=34
  139. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:maroteaux-lamy syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:maroteaux-lamy syndrome | rel=r_associated | relid=0 | w=34
  140. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:masa syndrome (disorder)
    n1=en:microcephaly-capillary malformation syndrome | n2=en:masa syndrome (disorder) | rel=r_associated | relid=0 | w=34
  141. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:microcephaly cervical spine fusion anomalies
    n1=en:microcephaly-capillary malformation syndrome | n2=en:microcephaly cervical spine fusion anomalies | rel=r_associated | relid=0 | w=34
  142. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:mitochondrial neurogastrointestinal encephalomyopathy syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | rel=r_associated | relid=0 | w=34
  143. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:neuroacanthocytosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:neuroacanthocytosis | rel=r_associated | relid=0 | w=34
  144. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:nonaka myopathy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:nonaka myopathy | rel=r_associated | relid=0 | w=34
  145. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:north american indian childhood cirrhosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:north american indian childhood cirrhosis | rel=r_associated | relid=0 | w=34
  146. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:okihiro syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:okihiro syndrome | rel=r_associated | relid=0 | w=34
  147. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:ptosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:ptosis | rel=r_associated | relid=0 | w=34
  148. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:reardon hall slaney syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:reardon hall slaney syndrome | rel=r_associated | relid=0 | w=34
  149. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:rud syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:rud syndrome | rel=r_associated | relid=0 | w=34
  150. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:saito kuba tsuruta syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:saito kuba tsuruta syndrome | rel=r_associated | relid=0 | w=34
  151. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:schulman upshaw syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:schulman upshaw syndrome | rel=r_associated | relid=0 | w=34
  152. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | rel=r_associated | relid=0 | w=34
  153. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:spondyloenchondromatosis with basal ganglia calcification
    n1=en:microcephaly-capillary malformation syndrome | n2=en:spondyloenchondromatosis with basal ganglia calcification | rel=r_associated | relid=0 | w=34
  154. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:stambp, arg178ter
    n1=en:microcephaly-capillary malformation syndrome | n2=en:stambp, arg178ter | rel=r_associated | relid=0 | w=34
  155. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:tetra-amelia autosomal recessive
    n1=en:microcephaly-capillary malformation syndrome | n2=en:tetra-amelia autosomal recessive | rel=r_associated | relid=0 | w=34
  156. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:tmem70 related mitochondrial encephalo-cardio-myopathy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:tmem70 related mitochondrial encephalo-cardio-myopathy | rel=r_associated | relid=0 | w=34
  157. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:trichohepatoenteric syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:trichohepatoenteric syndrome | rel=r_associated | relid=0 | w=34
  158. en:microcephaly-capillary malformation syndrome -- r_associated #0: 34 / 0.791 -> en:ventricular septal defect
    n1=en:microcephaly-capillary malformation syndrome | n2=en:ventricular septal defect | rel=r_associated | relid=0 | w=34
  159. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:2-hydroxyglutaric aciduria
    n1=en:microcephaly-capillary malformation syndrome | n2=en:2-hydroxyglutaric aciduria | rel=r_associated | relid=0 | w=32
  160. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:abnormal toe positioning
    n1=en:microcephaly-capillary malformation syndrome | n2=en:abnormal toe positioning | rel=r_associated | relid=0 | w=32
  161. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:allan-herndon-dudley syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:allan-herndon-dudley syndrome | rel=r_associated | relid=0 | w=32
  162. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:arrhythmogenic right ventricular dysplasia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:arrhythmogenic right ventricular dysplasia | rel=r_associated | relid=0 | w=32
  163. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:ateliotic dwarfism without insulinopenia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:ateliotic dwarfism without insulinopenia | rel=r_associated | relid=0 | w=32
  164. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:autosomal recessive ocular albinism
    n1=en:microcephaly-capillary malformation syndrome | n2=en:autosomal recessive ocular albinism | rel=r_associated | relid=0 | w=32
  165. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:beta-aminoisobutyricaciduria
    n1=en:microcephaly-capillary malformation syndrome | n2=en:beta-aminoisobutyricaciduria | rel=r_associated | relid=0 | w=32
  166. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:capillary malformation are apparent at birth
    n1=en:microcephaly-capillary malformation syndrome | n2=en:capillary malformation are apparent at birth | rel=r_associated | relid=0 | w=32
  167. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:cerebellar ataxia, cayman type
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cerebellar ataxia, cayman type | rel=r_associated | relid=0 | w=32
  168. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:charcot-marie-tooth disease type 4
    n1=en:microcephaly-capillary malformation syndrome | n2=en:charcot-marie-tooth disease type 4 | rel=r_associated | relid=0 | w=32
  169. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:congenital cataracts, facial dysmorphism, and neuropathy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital cataracts, facial dysmorphism, and neuropathy | rel=r_associated | relid=0 | w=32
  170. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:congenital microcephaly
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital microcephaly | rel=r_associated | relid=0 | w=32
  171. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | rel=r_associated | relid=0 | w=32
  172. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:congenital nephrogenic diabetes insipidus
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital nephrogenic diabetes insipidus | rel=r_associated | relid=0 | w=32
  173. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:cutis laxa, autosomal recessive
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cutis laxa, autosomal recessive | rel=r_associated | relid=0 | w=32
  174. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:cytochrome-c oxidase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cytochrome-c oxidase deficiency | rel=r_associated | relid=0 | w=32
  175. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:deafness, congenital, with inner ear agenesis, microtia, and microdontia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:deafness, congenital, with inner ear agenesis, microtia, and microdontia | rel=r_associated | relid=0 | w=32
  176. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:ear, patella, short stature syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:ear, patella, short stature syndrome | rel=r_associated | relid=0 | w=32
  177. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:enlarged extraaxial space on brain imaging
    n1=en:microcephaly-capillary malformation syndrome | n2=en:enlarged extraaxial space on brain imaging | rel=r_associated | relid=0 | w=32
  178. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:familial erythrocytosis due to diphosphoglycerate mutase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:familial erythrocytosis due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32
  179. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:heritable pulmonary arterial hypertension due to bmpr2 mutation
    n1=en:microcephaly-capillary malformation syndrome | n2=en:heritable pulmonary arterial hypertension due to bmpr2 mutation | rel=r_associated | relid=0 | w=32
  180. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:hnsha due to diphosphoglycerate mutase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hnsha due to diphosphoglycerate mutase deficiency | rel=r_associated | relid=0 | w=32
  181. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:holoprosencephaly with fetal akinesia-hypokinesia sequence
    n1=en:microcephaly-capillary malformation syndrome | n2=en:holoprosencephaly with fetal akinesia-hypokinesia sequence | rel=r_associated | relid=0 | w=32
  182. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:hypoplasia of the maxilla
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hypoplasia of the maxilla | rel=r_associated | relid=0 | w=32
  183. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:intestinal epithelial dysplasia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:intestinal epithelial dysplasia | rel=r_associated | relid=0 | w=32
  184. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:isaacs syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:isaacs syndrome | rel=r_associated | relid=0 | w=32
  185. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:lecithin acyltransferase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:lecithin acyltransferase deficiency | rel=r_associated | relid=0 | w=32
  186. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:mandibuloacral dysplasia with type a lipodystrophy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:mandibuloacral dysplasia with type a lipodystrophy | rel=r_associated | relid=0 | w=32
  187. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:megalencephalic leukoencephalopathy with subcortical cysts
    n1=en:microcephaly-capillary malformation syndrome | n2=en:megalencephalic leukoencephalopathy with subcortical cysts | rel=r_associated | relid=0 | w=32
  188. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:moloney syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:moloney syndrome | rel=r_associated | relid=0 | w=32
  189. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:multiple endocrine neoplasia type 1
    n1=en:microcephaly-capillary malformation syndrome | n2=en:multiple endocrine neoplasia type 1 | rel=r_associated | relid=0 | w=32
  190. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:neonatal progeroid syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:neonatal progeroid syndrome | rel=r_associated | relid=0 | w=32
  191. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:orotic aciduria
    n1=en:microcephaly-capillary malformation syndrome | n2=en:orotic aciduria | rel=r_associated | relid=0 | w=32
  192. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:periventricular heterotopia, x-linked
    n1=en:microcephaly-capillary malformation syndrome | n2=en:periventricular heterotopia, x-linked | rel=r_associated | relid=0 | w=32
  193. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:pseudocholinesterase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:pseudocholinesterase deficiency | rel=r_associated | relid=0 | w=32
  194. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:right ventricular hypertrophy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:right ventricular hypertrophy | rel=r_associated | relid=0 | w=32
  195. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:sanfilippo syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:sanfilippo syndrome | rel=r_associated | relid=0 | w=32
  196. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:sellars beighton syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:sellars beighton syndrome | rel=r_associated | relid=0 | w=32
  197. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:short stature with valvular heart disease and characteristic facies syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:short stature with valvular heart disease and characteristic facies syndrome | rel=r_associated | relid=0 | w=32
  198. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:simpson golabi behmel syndrome type 1
    n1=en:microcephaly-capillary malformation syndrome | n2=en:simpson golabi behmel syndrome type 1 | rel=r_associated | relid=0 | w=32
  199. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:skull hypoplasia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:skull hypoplasia | rel=r_associated | relid=0 | w=32
  200. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:sloping forehead
    n1=en:microcephaly-capillary malformation syndrome | n2=en:sloping forehead | rel=r_associated | relid=0 | w=32
  201. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:tay-sachs disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:tay-sachs disease | rel=r_associated | relid=0 | w=32
  202. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:tuberous sclerosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:tuberous sclerosis | rel=r_associated | relid=0 | w=32
  203. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:tyrosinemia, type iii
    n1=en:microcephaly-capillary malformation syndrome | n2=en:tyrosinemia, type iii | rel=r_associated | relid=0 | w=32
  204. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:uv-sensitive syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:uv-sensitive syndrome | rel=r_associated | relid=0 | w=32
  205. en:microcephaly-capillary malformation syndrome -- r_associated #0: 32 / 0.744 -> en:valinemia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:valinemia | rel=r_associated | relid=0 | w=32
  206. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:3-methylglutaconic aciduria type 5
    n1=en:microcephaly-capillary malformation syndrome | n2=en:3-methylglutaconic aciduria type 5 | rel=r_associated | relid=0 | w=31
  207. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:5-oxoprolinase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:5-oxoprolinase deficiency | rel=r_associated | relid=0 | w=31
  208. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:amelogenesis imperfecta and gingival hyperplasia syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:amelogenesis imperfecta and gingival hyperplasia syndrome | rel=r_associated | relid=0 | w=31
  209. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:autosomal recessive spastic paraplegia type 11
    n1=en:microcephaly-capillary malformation syndrome | n2=en:autosomal recessive spastic paraplegia type 11 | rel=r_associated | relid=0 | w=31
  210. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:basal ganglia disease, biotin-responsive
    n1=en:microcephaly-capillary malformation syndrome | n2=en:basal ganglia disease, biotin-responsive | rel=r_associated | relid=0 | w=31
  211. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:benign autosomal dominant microcephaly
    n1=en:microcephaly-capillary malformation syndrome | n2=en:benign autosomal dominant microcephaly | rel=r_associated | relid=0 | w=31
  212. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | rel=r_associated | relid=0 | w=31
  213. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:childhood myocerebrohepatopathy spectrum
    n1=en:microcephaly-capillary malformation syndrome | n2=en:childhood myocerebrohepatopathy spectrum | rel=r_associated | relid=0 | w=31
  214. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:congenital pancreatic enterokinase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital pancreatic enterokinase deficiency | rel=r_associated | relid=0 | w=31
  215. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:congenital smallness
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital smallness | rel=r_associated | relid=0 | w=31
  216. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:craniodiaphyseal dysplasia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:craniodiaphyseal dysplasia | rel=r_associated | relid=0 | w=31
  217. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:familial c3b inhibitor deficiency syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:familial c3b inhibitor deficiency syndrome | rel=r_associated | relid=0 | w=31
  218. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:familial hemiplegic migraine
    n1=en:microcephaly-capillary malformation syndrome | n2=en:familial hemiplegic migraine | rel=r_associated | relid=0 | w=31
  219. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:familial renal iminoglycinuria
    n1=en:microcephaly-capillary malformation syndrome | n2=en:familial renal iminoglycinuria | rel=r_associated | relid=0 | w=31
  220. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:fetal microcephaly
    n1=en:microcephaly-capillary malformation syndrome | n2=en:fetal microcephaly | rel=r_associated | relid=0 | w=31
  221. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related
    n1=en:microcephaly-capillary malformation syndrome | n2=en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related | rel=r_associated | relid=0 | w=31
  222. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:fructose-1,6-bisphosphatase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:fructose-1,6-bisphosphatase deficiency | rel=r_associated | relid=0 | w=31
  223. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:fucosidosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:fucosidosis | rel=r_associated | relid=0 | w=31
  224. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:giacci familial neurogenic acroosteolysis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:giacci familial neurogenic acroosteolysis | rel=r_associated | relid=0 | w=31
  225. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:glutamate formiminotransferase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:glutamate formiminotransferase deficiency | rel=r_associated | relid=0 | w=31
  226. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:glycine dehydrogenase (decarboxylating) deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:glycine dehydrogenase (decarboxylating) deficiency | rel=r_associated | relid=0 | w=31
  227. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:gurrieri sammito bellussi syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:gurrieri sammito bellussi syndrome | rel=r_associated | relid=0 | w=31
  228. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:hereditary adrenal unresponsiveness to corticotropin
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary adrenal unresponsiveness to corticotropin | rel=r_associated | relid=0 | w=31
  229. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:hereditary fructose intolerance
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary fructose intolerance | rel=r_associated | relid=0 | w=31
  230. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:hereditary motor neuron disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary motor neuron disease | rel=r_associated | relid=0 | w=31
  231. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:hereditary optic atrophy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary optic atrophy | rel=r_associated | relid=0 | w=31
  232. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:hypomagnesemia 1, intestinal
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hypomagnesemia 1, intestinal | rel=r_associated | relid=0 | w=31
  233. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:interleukin-1 receptor-associated kinase 4 deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:interleukin-1 receptor-associated kinase 4 deficiency | rel=r_associated | relid=0 | w=31
  234. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:kaufman-mckusick syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:kaufman-mckusick syndrome | rel=r_associated | relid=0 | w=31
  235. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:lethal congenital contracture syndrome 1
    n1=en:microcephaly-capillary malformation syndrome | n2=en:lethal congenital contracture syndrome 1 | rel=r_associated | relid=0 | w=31
  236. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation
    n1=en:microcephaly-capillary malformation syndrome | n2=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | rel=r_associated | relid=0 | w=31
  237. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:macdermot winter syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:macdermot winter syndrome | rel=r_associated | relid=0 | w=31
  238. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:majeed syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:majeed syndrome | rel=r_associated | relid=0 | w=31
  239. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:neuraminidase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:neuraminidase deficiency | rel=r_associated | relid=0 | w=31
  240. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:ohdo syndrome, maat-kievit-brunner type
    n1=en:microcephaly-capillary malformation syndrome | n2=en:ohdo syndrome, maat-kievit-brunner type | rel=r_associated | relid=0 | w=31
  241. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:pediatric failure to thrive
    n1=en:microcephaly-capillary malformation syndrome | n2=en:pediatric failure to thrive | rel=r_associated | relid=0 | w=31
  242. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:peeling skin syndrome, acral type
    n1=en:microcephaly-capillary malformation syndrome | n2=en:peeling skin syndrome, acral type | rel=r_associated | relid=0 | w=31
  243. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:peutz-jeghers syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=31
  244. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | rel=r_associated | relid=0 | w=31
  245. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:porphobilinogen synthase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:porphobilinogen synthase deficiency | rel=r_associated | relid=0 | w=31
  246. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:propionic acidemia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:propionic acidemia | rel=r_associated | relid=0 | w=31
  247. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:pulmonary hypertension in neurofibromatosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:pulmonary hypertension in neurofibromatosis | rel=r_associated | relid=0 | w=31
  248. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:pyle metaphyseal dysplasia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:pyle metaphyseal dysplasia | rel=r_associated | relid=0 | w=31
  249. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:sinus histiocytosis with massive lymphadenopathy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:sinus histiocytosis with massive lymphadenopathy | rel=r_associated | relid=0 | w=31
  250. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:small for gestational age
    n1=en:microcephaly-capillary malformation syndrome | n2=en:small for gestational age | rel=r_associated | relid=0 | w=31
  251. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:stambp, arg424ter
    n1=en:microcephaly-capillary malformation syndrome | n2=en:stambp, arg424ter | rel=r_associated | relid=0 | w=31
  252. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:sting-associated vasculopathy with onset in infancy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:sting-associated vasculopathy with onset in infancy | rel=r_associated | relid=0 | w=31
  253. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:sudden infant death with dysgenesis of the testes syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:sudden infant death with dysgenesis of the testes syndrome | rel=r_associated | relid=0 | w=31
  254. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:x-linked dystonia parkinsonism
    n1=en:microcephaly-capillary malformation syndrome | n2=en:x-linked dystonia parkinsonism | rel=r_associated | relid=0 | w=31
  255. en:microcephaly-capillary malformation syndrome -- r_associated #0: 31 / 0.721 -> en:x-linked epilepsy with learning disability and behavior disorder syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:x-linked epilepsy with learning disability and behavior disorder syndrome | rel=r_associated | relid=0 | w=31
  256. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:abnormal hair whorl
    n1=en:microcephaly-capillary malformation syndrome | n2=en:abnormal hair whorl | rel=r_associated | relid=0 | w=30
  257. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:adenine phosphoribosyltransferase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:adenine phosphoribosyltransferase deficiency | rel=r_associated | relid=0 | w=30
  258. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | rel=r_associated | relid=0 | w=30
  259. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:alstrom syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:alstrom syndrome | rel=r_associated | relid=0 | w=30
  260. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:atrial septal defect
    n1=en:microcephaly-capillary malformation syndrome | n2=en:atrial septal defect | rel=r_associated | relid=0 | w=30
  261. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:autosomal dominant late onset basal ganglia degeneration
    n1=en:microcephaly-capillary malformation syndrome | n2=en:autosomal dominant late onset basal ganglia degeneration | rel=r_associated | relid=0 | w=30
  262. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:autosomal recessive ichthyosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:autosomal recessive ichthyosis | rel=r_associated | relid=0 | w=30
  263. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:autosomal recessive scid
    n1=en:microcephaly-capillary malformation syndrome | n2=en:autosomal recessive scid | rel=r_associated | relid=0 | w=30
  264. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:behr syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:behr syndrome | rel=r_associated | relid=0 | w=30
  265. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:borjeson-forssman-lehmann syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:borjeson-forssman-lehmann syndrome | rel=r_associated | relid=0 | w=30
  266. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:capillary fragility abnormality
    n1=en:microcephaly-capillary malformation syndrome | n2=en:capillary fragility abnormality | rel=r_associated | relid=0 | w=30
  267. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:capillary malformations, small, multiple, diffuse
    n1=en:microcephaly-capillary malformation syndrome | n2=en:capillary malformations, small, multiple, diffuse | rel=r_associated | relid=0 | w=30
  268. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:cerebellar ataxia ectodermal dysplasia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cerebellar ataxia ectodermal dysplasia | rel=r_associated | relid=0 | w=30
  269. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:congenital clinodactyly
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital clinodactyly | rel=r_associated | relid=0 | w=30
  270. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:cystinosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cystinosis | rel=r_associated | relid=0 | w=30
  271. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:dicarboxylicaminoaciduria
    n1=en:microcephaly-capillary malformation syndrome | n2=en:dicarboxylicaminoaciduria | rel=r_associated | relid=0 | w=30
  272. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:dyskeratosis congenita, autosomal recessive
    n1=en:microcephaly-capillary malformation syndrome | n2=en:dyskeratosis congenita, autosomal recessive | rel=r_associated | relid=0 | w=30
  273. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:ehlers-danlos syndrome, arthrochalasia type
    n1=en:microcephaly-capillary malformation syndrome | n2=en:ehlers-danlos syndrome, arthrochalasia type | rel=r_associated | relid=0 | w=30
  274. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:encephalopathy due to sulfite oxidase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:encephalopathy due to sulfite oxidase deficiency | rel=r_associated | relid=0 | w=30
  275. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:ethanolaminosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:ethanolaminosis | rel=r_associated | relid=0 | w=30
  276. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:familial encephalopathy with neuroserpin inclusion bodies
    n1=en:microcephaly-capillary malformation syndrome | n2=en:familial encephalopathy with neuroserpin inclusion bodies | rel=r_associated | relid=0 | w=30
  277. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:fatal familial insomnia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:fatal familial insomnia | rel=r_associated | relid=0 | w=30
  278. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:foxg1 syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:foxg1 syndrome | rel=r_associated | relid=0 | w=30
  279. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:frontotemporal dementia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:frontotemporal dementia | rel=r_associated | relid=0 | w=30
  280. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:fryns macrocephaly
    n1=en:microcephaly-capillary malformation syndrome | n2=en:fryns macrocephaly | rel=r_associated | relid=0 | w=30
  281. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:gaze palsy, familial horizontal, with progressive scoliosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:gaze palsy, familial horizontal, with progressive scoliosis | rel=r_associated | relid=0 | w=30
  282. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:generalized epilepsy and paroxysmal dyskinesia syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:generalized epilepsy and paroxysmal dyskinesia syndrome | rel=r_associated | relid=0 | w=30
  283. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:hippocampal hypoplasia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hippocampal hypoplasia | rel=r_associated | relid=0 | w=30
  284. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:hnsha due to glucose phosphate isomerase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hnsha due to glucose phosphate isomerase deficiency | rel=r_associated | relid=0 | w=30
  285. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:hypermanganesemia with dystonia polycythemia and cirrhosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hypermanganesemia with dystonia polycythemia and cirrhosis | rel=r_associated | relid=0 | w=30
  286. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:infantile globoid cell leukodystrophy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:infantile globoid cell leukodystrophy | rel=r_associated | relid=0 | w=30
  287. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:infantile hypophosphatasia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:infantile hypophosphatasia | rel=r_associated | relid=0 | w=30
  288. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:joubert syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:joubert syndrome | rel=r_associated | relid=0 | w=30
  289. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:maternally inherited mitochondrial dystonia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:maternally inherited mitochondrial dystonia | rel=r_associated | relid=0 | w=30
  290. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:methylmalonyl-coenzyme a mutase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:methylmalonyl-coenzyme a mutase deficiency | rel=r_associated | relid=0 | w=30
  291. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:microcephaly microcornea syndrome seemanova type
    n1=en:microcephaly-capillary malformation syndrome | n2=en:microcephaly microcornea syndrome seemanova type | rel=r_associated | relid=0 | w=30
  292. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:mitochondrial dna depletion syndrome 2 (myopathic type)
    n1=en:microcephaly-capillary malformation syndrome | n2=en:mitochondrial dna depletion syndrome 2 (myopathic type) | rel=r_associated | relid=0 | w=30
  293. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:mohr-tranebjaerg syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:mohr-tranebjaerg syndrome | rel=r_associated | relid=0 | w=30
  294. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:nathalie syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:nathalie syndrome | rel=r_associated | relid=0 | w=30
  295. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:nevus anemicus
    n1=en:microcephaly-capillary malformation syndrome | n2=en:nevus anemicus | rel=r_associated | relid=0 | w=30
  296. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:oculocutaneous albinism type 4
    n1=en:microcephaly-capillary malformation syndrome | n2=en:oculocutaneous albinism type 4 | rel=r_associated | relid=0 | w=30
  297. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:otoonychoperoneal syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:otoonychoperoneal syndrome | rel=r_associated | relid=0 | w=30
  298. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:patent foramen ovale
    n1=en:microcephaly-capillary malformation syndrome | n2=en:patent foramen ovale | rel=r_associated | relid=0 | w=30
  299. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:pelizaeus merzbacher like disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:pelizaeus merzbacher like disease | rel=r_associated | relid=0 | w=30
  300. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:persistent mullerian duct syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:persistent mullerian duct syndrome | rel=r_associated | relid=0 | w=30
  301. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:phenylketonuria ii
    n1=en:microcephaly-capillary malformation syndrome | n2=en:phenylketonuria ii | rel=r_associated | relid=0 | w=30
  302. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:pontocerebellar hypoplasia type 2
    n1=en:microcephaly-capillary malformation syndrome | n2=en:pontocerebellar hypoplasia type 2 | rel=r_associated | relid=0 | w=30
  303. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:prolonged electroretinal response suppression
    n1=en:microcephaly-capillary malformation syndrome | n2=en:prolonged electroretinal response suppression | rel=r_associated | relid=0 | w=30
  304. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:rna polymerase iii-related leukodystrophy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:rna polymerase iii-related leukodystrophy | rel=r_associated | relid=0 | w=30
  305. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:sarcosinemia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:sarcosinemia | rel=r_associated | relid=0 | w=30
  306. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:sotos syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:sotos syndrome | rel=r_associated | relid=0 | w=30
  307. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:spinal muscular atrophy with respiratory distress 1
    n1=en:microcephaly-capillary malformation syndrome | n2=en:spinal muscular atrophy with respiratory distress 1 | rel=r_associated | relid=0 | w=30
  308. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:sulfite oxidase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:sulfite oxidase deficiency | rel=r_associated | relid=0 | w=30
  309. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:thomas syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:thomas syndrome | rel=r_associated | relid=0 | w=30
  310. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:von hippel-lindau syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:von hippel-lindau syndrome | rel=r_associated | relid=0 | w=30
  311. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:warsaw breakage syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:warsaw breakage syndrome | rel=r_associated | relid=0 | w=30
  312. en:microcephaly-capillary malformation syndrome -- r_associated #0: 30 / 0.698 -> en:wide nose
    n1=en:microcephaly-capillary malformation syndrome | n2=en:wide nose | rel=r_associated | relid=0 | w=30
  313. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:alpha-1 antitrypsin deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:alpha-1 antitrypsin deficiency | rel=r_associated | relid=0 | w=29
  314. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:alpha, alpha-trehalase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:alpha, alpha-trehalase deficiency | rel=r_associated | relid=0 | w=29
  315. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:aminomethyltransferase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:aminomethyltransferase deficiency | rel=r_associated | relid=0 | w=29
  316. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:andersen syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:andersen syndrome | rel=r_associated | relid=0 | w=29
  317. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:angioma hereditary neurocutaneous
    n1=en:microcephaly-capillary malformation syndrome | n2=en:angioma hereditary neurocutaneous | rel=r_associated | relid=0 | w=29
  318. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:argininosuccinic aciduria
    n1=en:microcephaly-capillary malformation syndrome | n2=en:argininosuccinic aciduria | rel=r_associated | relid=0 | w=29
  319. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:autosomal recessive inheritance
    n1=en:microcephaly-capillary malformation syndrome | n2=en:autosomal recessive inheritance | rel=r_associated | relid=0 | w=29
  320. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:becker generalized myotonia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:becker generalized myotonia | rel=r_associated | relid=0 | w=29
  321. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:bowen-conradi syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:bowen-conradi syndrome | rel=r_associated | relid=0 | w=29
  322. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:chondrodysplasia punctata syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:chondrodysplasia punctata syndrome | rel=r_associated | relid=0 | w=29
  323. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:cleft palate
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cleft palate | rel=r_associated | relid=0 | w=29
  324. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:congenital dyserythropoietic anemia, type ii
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital dyserythropoietic anemia, type ii | rel=r_associated | relid=0 | w=29
  325. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:crigler-najjar syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:crigler-najjar syndrome | rel=r_associated | relid=0 | w=29
  326. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:delayed psychomotor development, profound
    n1=en:microcephaly-capillary malformation syndrome | n2=en:delayed psychomotor development, profound | rel=r_associated | relid=0 | w=29
  327. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:dmd-associated dilated cardiomyopathy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:dmd-associated dilated cardiomyopathy | rel=r_associated | relid=0 | w=29
  328. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:donnai-barrow syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:donnai-barrow syndrome | rel=r_associated | relid=0 | w=29
  329. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:epiphyseal dysplasia, multiple, 4
    n1=en:microcephaly-capillary malformation syndrome | n2=en:epiphyseal dysplasia, multiple, 4 | rel=r_associated | relid=0 | w=29
  330. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:fatty acid hydroxylase-associated neurodegeneration
    n1=en:microcephaly-capillary malformation syndrome | n2=en:fatty acid hydroxylase-associated neurodegeneration | rel=r_associated | relid=0 | w=29
  331. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:gerstmann-straussler-scheinker disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:gerstmann-straussler-scheinker disease | rel=r_associated | relid=0 | w=29
  332. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:glycogen storage disease type i
    n1=en:microcephaly-capillary malformation syndrome | n2=en:glycogen storage disease type i | rel=r_associated | relid=0 | w=29
  333. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:hyperimmunoglobulin e syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hyperimmunoglobulin e syndrome | rel=r_associated | relid=0 | w=29
  334. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:i-cell disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:i-cell disease | rel=r_associated | relid=0 | w=29
  335. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:isolated hypoplasia of the right ventricle
    n1=en:microcephaly-capillary malformation syndrome | n2=en:isolated hypoplasia of the right ventricle | rel=r_associated | relid=0 | w=29
  336. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:lethal congenital contracture syndrome 2
    n1=en:microcephaly-capillary malformation syndrome | n2=en:lethal congenital contracture syndrome 2 | rel=r_associated | relid=0 | w=29
  337. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:lissencephaly, x-linked, 2
    n1=en:microcephaly-capillary malformation syndrome | n2=en:lissencephaly, x-linked, 2 | rel=r_associated | relid=0 | w=29
  338. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:microcephaly deafness syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:microcephaly deafness syndrome | rel=r_associated | relid=0 | w=29
  339. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:multicentric osteolysis nodulosis arthropathy spectrum
    n1=en:microcephaly-capillary malformation syndrome | n2=en:multicentric osteolysis nodulosis arthropathy spectrum | rel=r_associated | relid=0 | w=29
  340. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:neu-laxova syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:neu-laxova syndrome | rel=r_associated | relid=0 | w=29
  341. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:neurofibromatosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:neurofibromatosis | rel=r_associated | relid=0 | w=29
  342. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:papillon-lefevre syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:papillon-lefevre syndrome | rel=r_associated | relid=0 | w=29
  343. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:pseudohypoaldosteronism, type 1, recessive form
    n1=en:microcephaly-capillary malformation syndrome | n2=en:pseudohypoaldosteronism, type 1, recessive form | rel=r_associated | relid=0 | w=29
  344. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:secondary microcephaly
    n1=en:microcephaly-capillary malformation syndrome | n2=en:secondary microcephaly | rel=r_associated | relid=0 | w=29
  345. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:severe early childhood onset retinal dystrophy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:severe early childhood onset retinal dystrophy | rel=r_associated | relid=0 | w=29
  346. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:severe steroid 21-hydroxylase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:severe steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=29
  347. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:sonoda syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:sonoda syndrome | rel=r_associated | relid=0 | w=29
  348. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:spastic tetraparesis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:spastic tetraparesis | rel=r_associated | relid=0 | w=29
  349. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:spondyloepiphyseal dysplasia tarda, toledo type
    n1=en:microcephaly-capillary malformation syndrome | n2=en:spondyloepiphyseal dysplasia tarda, toledo type | rel=r_associated | relid=0 | w=29
  350. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:stambp, glu42gly
    n1=en:microcephaly-capillary malformation syndrome | n2=en:stambp, glu42gly | rel=r_associated | relid=0 | w=29
  351. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:transthyretin related familial amyloid cardiomyopathy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:transthyretin related familial amyloid cardiomyopathy | rel=r_associated | relid=0 | w=29
  352. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:type ii acrocephalopolysyndactyly
    n1=en:microcephaly-capillary malformation syndrome | n2=en:type ii acrocephalopolysyndactyly | rel=r_associated | relid=0 | w=29
  353. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:tyrosinemia type ii
    n1=en:microcephaly-capillary malformation syndrome | n2=en:tyrosinemia type ii | rel=r_associated | relid=0 | w=29
  354. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:variable facial dysmorphic features
    n1=en:microcephaly-capillary malformation syndrome | n2=en:variable facial dysmorphic features | rel=r_associated | relid=0 | w=29
  355. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:waardenburg anophthalmia syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:waardenburg anophthalmia syndrome | rel=r_associated | relid=0 | w=29
  356. en:microcephaly-capillary malformation syndrome -- r_associated #0: 29 / 0.674 -> en:zellweger syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:zellweger syndrome | rel=r_associated | relid=0 | w=29
  357. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:21-hydroxylase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:21-hydroxylase deficiency | rel=r_associated | relid=0 | w=28
  358. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:acid phosphatase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:acid phosphatase deficiency | rel=r_associated | relid=0 | w=28
  359. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:acrodermatitis enteropathica
    n1=en:microcephaly-capillary malformation syndrome | n2=en:acrodermatitis enteropathica | rel=r_associated | relid=0 | w=28
  360. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:adenylosuccinate lyase deficiency (disorder)
    n1=en:microcephaly-capillary malformation syndrome | n2=en:adenylosuccinate lyase deficiency (disorder) | rel=r_associated | relid=0 | w=28
  361. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:amelogenesis imperfecta - recessive - rough
    n1=en:microcephaly-capillary malformation syndrome | n2=en:amelogenesis imperfecta - recessive - rough | rel=r_associated | relid=0 | w=28
  362. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:aminoacylase 1 deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:aminoacylase 1 deficiency | rel=r_associated | relid=0 | w=28
  363. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:ataxia with vitamin e deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:ataxia with vitamin e deficiency | rel=r_associated | relid=0 | w=28
  364. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:autoinflammation, lipodystrophy and dermatosis syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:autoinflammation, lipodystrophy and dermatosis syndrome | rel=r_associated | relid=0 | w=28
  365. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:autosomal recessive sideroblastic anemia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:autosomal recessive sideroblastic anemia | rel=r_associated | relid=0 | w=28
  366. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:brachydactyly
    n1=en:microcephaly-capillary malformation syndrome | n2=en:brachydactyly | rel=r_associated | relid=0 | w=28
  367. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:caused by mutation in the stam-binding protein gene (stambp, 606247.0001)
    n1=en:microcephaly-capillary malformation syndrome | n2=en:caused by mutation in the stam-binding protein gene (stambp, 606247.0001) | rel=r_associated | relid=0 | w=28
  368. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:cerebral hemorrhage with amyloidosis, hereditary, dutch type
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cerebral hemorrhage with amyloidosis, hereditary, dutch type | rel=r_associated | relid=0 | w=28
  369. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:chitty hall baraitser syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:chitty hall baraitser syndrome | rel=r_associated | relid=0 | w=28
  370. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:congenital alpha-2-antiplasmin deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital alpha-2-antiplasmin deficiency | rel=r_associated | relid=0 | w=28
  371. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:congenital disorder of glycosylation type ic
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital disorder of glycosylation type ic | rel=r_associated | relid=0 | w=28
  372. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:congenital sucrase-isomaltase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital sucrase-isomaltase deficiency | rel=r_associated | relid=0 | w=28
  373. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:congenital transferrin deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital transferrin deficiency | rel=r_associated | relid=0 | w=28
  374. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:cystathionine beta-synthase deficiency disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cystathionine beta-synthase deficiency disease | rel=r_associated | relid=0 | w=28
  375. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:deafness, progressive, with stapes fixation
    n1=en:microcephaly-capillary malformation syndrome | n2=en:deafness, progressive, with stapes fixation | rel=r_associated | relid=0 | w=28
  376. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:dubin-johnson syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:dubin-johnson syndrome | rel=r_associated | relid=0 | w=28
  377. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:ehlers-danlos syndrome, type vi
    n1=en:microcephaly-capillary malformation syndrome | n2=en:ehlers-danlos syndrome, type vi | rel=r_associated | relid=0 | w=28
  378. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:epidermolysis bullosa simplex with pyloric atresia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:epidermolysis bullosa simplex with pyloric atresia | rel=r_associated | relid=0 | w=28
  379. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:factor v and factor viii, combined deficiency of
    n1=en:microcephaly-capillary malformation syndrome | n2=en:factor v and factor viii, combined deficiency of | rel=r_associated | relid=0 | w=28
  380. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:fibular hypoplasia and complex brachydactyly
    n1=en:microcephaly-capillary malformation syndrome | n2=en:fibular hypoplasia and complex brachydactyly | rel=r_associated | relid=0 | w=28
  381. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:glycogen storage disease type iib
    n1=en:microcephaly-capillary malformation syndrome | n2=en:glycogen storage disease type iib | rel=r_associated | relid=0 | w=28
  382. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:glycogen storage disease type x
    n1=en:microcephaly-capillary malformation syndrome | n2=en:glycogen storage disease type x | rel=r_associated | relid=0 | w=28
  383. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:hereditary factor x deficiency disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary factor x deficiency disease | rel=r_associated | relid=0 | w=28
  384. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:hereditary methemoglobinemia, enzymatic type
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary methemoglobinemia, enzymatic type | rel=r_associated | relid=0 | w=28
  385. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:hydrocephalus with cerebellar agenesis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hydrocephalus with cerebellar agenesis | rel=r_associated | relid=0 | w=28
  386. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:hydromicrocephaly
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hydromicrocephaly | rel=r_associated | relid=0 | w=28
  387. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:isolated hyperchlorhidrosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:isolated hyperchlorhidrosis | rel=r_associated | relid=0 | w=28
  388. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:kuskokwim disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:kuskokwim disease | rel=r_associated | relid=0 | w=28
  389. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:lethal congenital contracture syndrome type 3
    n1=en:microcephaly-capillary malformation syndrome | n2=en:lethal congenital contracture syndrome type 3 | rel=r_associated | relid=0 | w=28
  390. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:leukodystrophy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:leukodystrophy | rel=r_associated | relid=0 | w=28
  391. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:merrf syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:merrf syndrome | rel=r_associated | relid=0 | w=28
  392. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:methylene thf reductase deficiency and homocystinuria
    n1=en:microcephaly-capillary malformation syndrome | n2=en:methylene thf reductase deficiency and homocystinuria | rel=r_associated | relid=0 | w=28
  393. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:mucopolysaccharidosis type i
    n1=en:microcephaly-capillary malformation syndrome | n2=en:mucopolysaccharidosis type i | rel=r_associated | relid=0 | w=28
  394. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:neurodegeneration due to cerebral folate transport deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:neurodegeneration due to cerebral folate transport deficiency | rel=r_associated | relid=0 | w=28
  395. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:neurodegeneration with brain iron accumulation 4
    n1=en:microcephaly-capillary malformation syndrome | n2=en:neurodegeneration with brain iron accumulation 4 | rel=r_associated | relid=0 | w=28
  396. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:neutral lipid storage disease with myopathy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:neutral lipid storage disease with myopathy | rel=r_associated | relid=0 | w=28
  397. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:one patient was less severely affected
    n1=en:microcephaly-capillary malformation syndrome | n2=en:one patient was less severely affected | rel=r_associated | relid=0 | w=28
  398. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:optic atrophy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:optic atrophy | rel=r_associated | relid=0 | w=28
  399. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:port wine stain
    n1=en:microcephaly-capillary malformation syndrome | n2=en:port wine stain | rel=r_associated | relid=0 | w=28
  400. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:port-wine stain in proteus syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:port-wine stain in proteus syndrome | rel=r_associated | relid=0 | w=28
  401. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:port-wine stain in rubinstein-taybi syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:port-wine stain in rubinstein-taybi syndrome | rel=r_associated | relid=0 | w=28
  402. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:prader-willi habitus, osteopenia, and camptodactyly
    n1=en:microcephaly-capillary malformation syndrome | n2=en:prader-willi habitus, osteopenia, and camptodactyly | rel=r_associated | relid=0 | w=28
  403. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:prolidase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:prolidase deficiency | rel=r_associated | relid=0 | w=28
  404. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:purine-nucleoside phosphorylase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:purine-nucleoside phosphorylase deficiency | rel=r_associated | relid=0 | w=28
  405. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:rapadilino syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:rapadilino syndrome | rel=r_associated | relid=0 | w=28
  406. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:renal tubulopathy with encephalopathy and liver failure syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:renal tubulopathy with encephalopathy and liver failure syndrome | rel=r_associated | relid=0 | w=28
  407. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:richards-rundle syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:richards-rundle syndrome | rel=r_associated | relid=0 | w=28
  408. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:schindler disease, type i
    n1=en:microcephaly-capillary malformation syndrome | n2=en:schindler disease, type i | rel=r_associated | relid=0 | w=28
  409. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:short distal phalanx of finger
    n1=en:microcephaly-capillary malformation syndrome | n2=en:short distal phalanx of finger | rel=r_associated | relid=0 | w=28
  410. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:simplified cortical gyral pattern
    n1=en:microcephaly-capillary malformation syndrome | n2=en:simplified cortical gyral pattern | rel=r_associated | relid=0 | w=28
  411. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:spondylocarpotarsal synostosis syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:spondylocarpotarsal synostosis syndrome | rel=r_associated | relid=0 | w=28
  412. en:microcephaly-capillary malformation syndrome -- r_associated #0: 28 / 0.651 -> en:waardenburg syndrome type 4
    n1=en:microcephaly-capillary malformation syndrome | n2=en:waardenburg syndrome type 4 | rel=r_associated | relid=0 | w=28
  413. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:3-methylglutaconic aciduria type iv
    n1=en:microcephaly-capillary malformation syndrome | n2=en:3-methylglutaconic aciduria type iv | rel=r_associated | relid=0 | w=27
  414. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:alpha-fetoprotein deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:alpha-fetoprotein deficiency | rel=r_associated | relid=0 | w=27
  415. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:anemia, hypochromic microcytic, with iron overload
    n1=en:microcephaly-capillary malformation syndrome | n2=en:anemia, hypochromic microcytic, with iron overload | rel=r_associated | relid=0 | w=27
  416. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:antley-bixler syndrome, autosomal dominant
    n1=en:microcephaly-capillary malformation syndrome | n2=en:antley-bixler syndrome, autosomal dominant | rel=r_associated | relid=0 | w=27
  417. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:ataxia telangiectasia syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:ataxia telangiectasia syndrome | rel=r_associated | relid=0 | w=27
  418. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:brachydactyly syndrome type b
    n1=en:microcephaly-capillary malformation syndrome | n2=en:brachydactyly syndrome type b | rel=r_associated | relid=0 | w=27
  419. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:brown-vialetto-van laere syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:brown-vialetto-van laere syndrome | rel=r_associated | relid=0 | w=27
  420. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:capillary malformation-arteriovenous malformation (disorder)
    n1=en:microcephaly-capillary malformation syndrome | n2=en:capillary malformation-arteriovenous malformation (disorder) | rel=r_associated | relid=0 | w=27
  421. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:capillary-venous malformation
    n1=en:microcephaly-capillary malformation syndrome | n2=en:capillary-venous malformation | rel=r_associated | relid=0 | w=27
  422. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:carbamoyl-phosphate synthetase i deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:carbamoyl-phosphate synthetase i deficiency | rel=r_associated | relid=0 | w=27
  423. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:cerebral lipidosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cerebral lipidosis | rel=r_associated | relid=0 | w=27
  424. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:cerebroretinal microangiopathy with calcifications and cysts (disorder)
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | rel=r_associated | relid=0 | w=27
  425. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:cleft lip/palate-ectodermal dysplasia syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cleft lip/palate-ectodermal dysplasia syndrome | rel=r_associated | relid=0 | w=27
  426. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:combined pituitary hormone deficiency genetic form
    n1=en:microcephaly-capillary malformation syndrome | n2=en:combined pituitary hormone deficiency genetic form | rel=r_associated | relid=0 | w=27
  427. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:corpus callosum agenesis neuronopathy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:corpus callosum agenesis neuronopathy | rel=r_associated | relid=0 | w=27
  428. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:desmosterolosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:desmosterolosis | rel=r_associated | relid=0 | w=27
  429. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:dihydrouracil dehydrogenase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:dihydrouracil dehydrogenase deficiency | rel=r_associated | relid=0 | w=27
  430. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:dystonia 12
    n1=en:microcephaly-capillary malformation syndrome | n2=en:dystonia 12 | rel=r_associated | relid=0 | w=27
  431. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | rel=r_associated | relid=0 | w=27
  432. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:episodic ataxia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:episodic ataxia | rel=r_associated | relid=0 | w=27
  433. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:familial acantholysis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:familial acantholysis | rel=r_associated | relid=0 | w=27
  434. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:familial creutzfeldt-jakob
    n1=en:microcephaly-capillary malformation syndrome | n2=en:familial creutzfeldt-jakob | rel=r_associated | relid=0 | w=27
  435. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:folinic acid responsive seizure syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:folinic acid responsive seizure syndrome | rel=r_associated | relid=0 | w=27
  436. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:geniospasm 1
    n1=en:microcephaly-capillary malformation syndrome | n2=en:geniospasm 1 | rel=r_associated | relid=0 | w=27
  437. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:glomuvenous malformations
    n1=en:microcephaly-capillary malformation syndrome | n2=en:glomuvenous malformations | rel=r_associated | relid=0 | w=27
  438. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:glutathione synthetase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:glutathione synthetase deficiency | rel=r_associated | relid=0 | w=27
  439. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:hepatolenticular degeneration
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hepatolenticular degeneration | rel=r_associated | relid=0 | w=27
  440. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:hereditary cerebellar degeneration
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary cerebellar degeneration | rel=r_associated | relid=0 | w=27
  441. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:hereditary cerebral amyloid angiopathy, icelandic type
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary cerebral amyloid angiopathy, icelandic type | rel=r_associated | relid=0 | w=27
  442. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:hereditary cutaneous vascular syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary cutaneous vascular syndrome | rel=r_associated | relid=0 | w=27
  443. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=27
  444. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:histidinemia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:histidinemia | rel=r_associated | relid=0 | w=27
  445. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:hnsha due to pyrimidine-5'-nucleotidase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hnsha due to pyrimidine-5'-nucleotidase deficiency | rel=r_associated | relid=0 | w=27
  446. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:hyperphosphatasia with mental retardation
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hyperphosphatasia with mental retardation | rel=r_associated | relid=0 | w=27
  447. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:hyperprolinemia type 1
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hyperprolinemia type 1 | rel=r_associated | relid=0 | w=27
  448. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:hypomyelination and congenital cataract
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hypomyelination and congenital cataract | rel=r_associated | relid=0 | w=27
  449. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:inherited metabolic disorder of nervous system
    n1=en:microcephaly-capillary malformation syndrome | n2=en:inherited metabolic disorder of nervous system | rel=r_associated | relid=0 | w=27
  450. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:jervell and lange nielsen syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:jervell and lange nielsen syndrome | rel=r_associated | relid=0 | w=27
  451. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:laron syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:laron syndrome | rel=r_associated | relid=0 | w=27
  452. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:laurence-moon syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:laurence-moon syndrome | rel=r_associated | relid=0 | w=27
  453. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:mannosidosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:mannosidosis | rel=r_associated | relid=0 | w=27
  454. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:medium-chain acyl-coa dehydrogenase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:medium-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=27
  455. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:morquio syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:morquio syndrome | rel=r_associated | relid=0 | w=27
  456. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:mowat-wilson syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:mowat-wilson syndrome | rel=r_associated | relid=0 | w=27
  457. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:multiple sulfatase deficiency disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:multiple sulfatase deficiency disease | rel=r_associated | relid=0 | w=27
  458. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:n-acetylglutamate synthase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:n-acetylglutamate synthase deficiency | rel=r_associated | relid=0 | w=27
  459. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:naxos disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:naxos disease | rel=r_associated | relid=0 | w=27
  460. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:netherton syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:netherton syndrome | rel=r_associated | relid=0 | w=27
  461. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:niemann-pick disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:niemann-pick disease | rel=r_associated | relid=0 | w=27
  462. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:non-polyposis turcot syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:non-polyposis turcot syndrome | rel=r_associated | relid=0 | w=27
  463. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:northern epilepsy syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:northern epilepsy syndrome | rel=r_associated | relid=0 | w=27
  464. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:oculocerebral hypopigmentation syndrome type preus
    n1=en:microcephaly-capillary malformation syndrome | n2=en:oculocerebral hypopigmentation syndrome type preus | rel=r_associated | relid=0 | w=27
  465. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:odontohypophosphatasia (disorder)
    n1=en:microcephaly-capillary malformation syndrome | n2=en:odontohypophosphatasia (disorder) | rel=r_associated | relid=0 | w=27
  466. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:pentosuria
    n1=en:microcephaly-capillary malformation syndrome | n2=en:pentosuria | rel=r_associated | relid=0 | w=27
  467. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:pituitary adenoma, familial isolated (disorder)
    n1=en:microcephaly-capillary malformation syndrome | n2=en:pituitary adenoma, familial isolated (disorder) | rel=r_associated | relid=0 | w=27
  468. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:port-wine stain associated with spinal dysraphism
    n1=en:microcephaly-capillary malformation syndrome | n2=en:port-wine stain associated with spinal dysraphism | rel=r_associated | relid=0 | w=27
  469. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:retinitis punctata albescens (disorder)
    n1=en:microcephaly-capillary malformation syndrome | n2=en:retinitis punctata albescens (disorder) | rel=r_associated | relid=0 | w=27
  470. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:seizures usually occur in the first months of life
    n1=en:microcephaly-capillary malformation syndrome | n2=en:seizures usually occur in the first months of life | rel=r_associated | relid=0 | w=27
  471. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:smith-mccort dysplasia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:smith-mccort dysplasia | rel=r_associated | relid=0 | w=27
  472. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:spinocerebellar ataxia with epilepsy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:spinocerebellar ataxia with epilepsy | rel=r_associated | relid=0 | w=27
  473. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:spondyloenchondrodysplasia with immune dysregulation
    n1=en:microcephaly-capillary malformation syndrome | n2=en:spondyloenchondrodysplasia with immune dysregulation | rel=r_associated | relid=0 | w=27
  474. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:stambp, ivs4ds, g-t, +5
    n1=en:microcephaly-capillary malformation syndrome | n2=en:stambp, ivs4ds, g-t, +5 | rel=r_associated | relid=0 | w=27
  475. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:succinic semialdehyde dehydrogenase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:succinic semialdehyde dehydrogenase deficiency | rel=r_associated | relid=0 | w=27
  476. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:upper limb defect with eye and ear abnormalities syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:upper limb defect with eye and ear abnormalities syndrome | rel=r_associated | relid=0 | w=27
  477. en:microcephaly-capillary malformation syndrome -- r_associated #0: 27 / 0.628 -> en:verloes bourguignon syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:verloes bourguignon syndrome | rel=r_associated | relid=0 | w=27
  478. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:aicardi syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:aicardi syndrome | rel=r_associated | relid=0 | w=26
  479. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:al awadi syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:al awadi syndrome | rel=r_associated | relid=0 | w=26
  480. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:albinotic fundus
    n1=en:microcephaly-capillary malformation syndrome | n2=en:albinotic fundus | rel=r_associated | relid=0 | w=26
  481. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:alpha-methylacyl-coa racemase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:alpha-methylacyl-coa racemase deficiency | rel=r_associated | relid=0 | w=26
  482. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps
    n1=en:microcephaly-capillary malformation syndrome | n2=en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps | rel=r_associated | relid=0 | w=26
  483. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | rel=r_associated | relid=0 | w=26
  484. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:baller-gerold syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:baller-gerold syndrome | rel=r_associated | relid=0 | w=26
  485. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:behrens baumann dust syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:behrens baumann dust syndrome | rel=r_associated | relid=0 | w=26
  486. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:biotinidase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:biotinidase deficiency | rel=r_associated | relid=0 | w=26
  487. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:childhood hypophosphatasia (disorder)
    n1=en:microcephaly-capillary malformation syndrome | n2=en:childhood hypophosphatasia (disorder) | rel=r_associated | relid=0 | w=26
  488. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:choreoathetosis/spasticity, episodic
    n1=en:microcephaly-capillary malformation syndrome | n2=en:choreoathetosis/spasticity, episodic | rel=r_associated | relid=0 | w=26
  489. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:combined malonic and methylmalonic aciduria
    n1=en:microcephaly-capillary malformation syndrome | n2=en:combined malonic and methylmalonic aciduria | rel=r_associated | relid=0 | w=26
  490. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:congenital abnormality
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital abnormality | rel=r_associated | relid=0 | w=26
  491. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:congenital bowing of long bone
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital bowing of long bone | rel=r_associated | relid=0 | w=26
  492. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:congenital disorder of glycosylation type ia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital disorder of glycosylation type ia | rel=r_associated | relid=0 | w=26
  493. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:congenital plasminogen activator inhibitor deficiency type 1
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital plasminogen activator inhibitor deficiency type 1 | rel=r_associated | relid=0 | w=26
  494. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:crisponi syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:crisponi syndrome | rel=r_associated | relid=0 | w=26
  495. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:deficiency of fructokinase
    n1=en:microcephaly-capillary malformation syndrome | n2=en:deficiency of fructokinase | rel=r_associated | relid=0 | w=26
  496. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:development of small head that was not present at birth
    n1=en:microcephaly-capillary malformation syndrome | n2=en:development of small head that was not present at birth | rel=r_associated | relid=0 | w=26
  497. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:glutamate-cysteine ligase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:glutamate-cysteine ligase deficiency | rel=r_associated | relid=0 | w=26
  498. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:hereditary cystatin c amyloid angiopathy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary cystatin c amyloid angiopathy | rel=r_associated | relid=0 | w=26
  499. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:hereditary dysplasia of blood vessel
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary dysplasia of blood vessel | rel=r_associated | relid=0 | w=26
  500. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:hereditary spastic paralysis, infantile onset ascending
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary spastic paralysis, infantile onset ascending | rel=r_associated | relid=0 | w=26
  501. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:hereditary vascular fragility
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary vascular fragility | rel=r_associated | relid=0 | w=26
  502. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:hnsha due to glutathione reductase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hnsha due to glutathione reductase deficiency | rel=r_associated | relid=0 | w=26
  503. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:hypospadias-mental retardation syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hypospadias-mental retardation syndrome | rel=r_associated | relid=0 | w=26
  504. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:lactase deficiency, congenital
    n1=en:microcephaly-capillary malformation syndrome | n2=en:lactase deficiency, congenital | rel=r_associated | relid=0 | w=26
  505. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:macular corneal dystrophy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:macular corneal dystrophy | rel=r_associated | relid=0 | w=26
  506. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:methylcrotonyl-coa carboxylase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:methylcrotonyl-coa carboxylase deficiency | rel=r_associated | relid=0 | w=26
  507. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:microcephaly, amish type (disorder)
    n1=en:microcephaly-capillary malformation syndrome | n2=en:microcephaly, amish type (disorder) | rel=r_associated | relid=0 | w=26
  508. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:micronychia (disorder)
    n1=en:microcephaly-capillary malformation syndrome | n2=en:micronychia (disorder) | rel=r_associated | relid=0 | w=26
  509. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:microphthalmia, syndromic 8
    n1=en:microcephaly-capillary malformation syndrome | n2=en:microphthalmia, syndromic 8 | rel=r_associated | relid=0 | w=26
  510. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:miller-mckusick-malvaux-syndrome (3m syndrome)
    n1=en:microcephaly-capillary malformation syndrome | n2=en:miller-mckusick-malvaux-syndrome (3m syndrome) | rel=r_associated | relid=0 | w=26
  511. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:mousa al din al nassar syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:mousa al din al nassar syndrome | rel=r_associated | relid=0 | w=26
  512. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:myoclonic jerk
    n1=en:microcephaly-capillary malformation syndrome | n2=en:myoclonic jerk | rel=r_associated | relid=0 | w=26
  513. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:myopathy, early-onset, with fatal cardiomyopathy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:myopathy, early-onset, with fatal cardiomyopathy | rel=r_associated | relid=0 | w=26
  514. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:peters-plus syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:peters-plus syndrome | rel=r_associated | relid=0 | w=26
  515. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:pituitary thyroid hormone resistance
    n1=en:microcephaly-capillary malformation syndrome | n2=en:pituitary thyroid hormone resistance | rel=r_associated | relid=0 | w=26
  516. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:port-wine stain with associated anomalies
    n1=en:microcephaly-capillary malformation syndrome | n2=en:port-wine stain with associated anomalies | rel=r_associated | relid=0 | w=26
  517. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:primary hyperoxaluria
    n1=en:microcephaly-capillary malformation syndrome | n2=en:primary hyperoxaluria | rel=r_associated | relid=0 | w=26
  518. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:pseudotrisomy 13 syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=26
  519. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88
    n1=en:microcephaly-capillary malformation syndrome | n2=en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 | rel=r_associated | relid=0 | w=26
  520. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:pyruvate carboxylase deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:pyruvate carboxylase deficiency | rel=r_associated | relid=0 | w=26
  521. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:seizures, refractory
    n1=en:microcephaly-capillary malformation syndrome | n2=en:seizures, refractory | rel=r_associated | relid=0 | w=26
  522. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:sitosterolemia with xanthomatosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:sitosterolemia with xanthomatosis | rel=r_associated | relid=0 | w=26
  523. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:spastic ataxia, charlevoix-saguenay type
    n1=en:microcephaly-capillary malformation syndrome | n2=en:spastic ataxia, charlevoix-saguenay type | rel=r_associated | relid=0 | w=26
  524. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:spastic paraplegia 15, autosomal recessive
    n1=en:microcephaly-capillary malformation syndrome | n2=en:spastic paraplegia 15, autosomal recessive | rel=r_associated | relid=0 | w=26
  525. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:spondyloenchondrodysplasia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:spondyloenchondrodysplasia | rel=r_associated | relid=0 | w=26
  526. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:spondyloepiphyseal dysplasia, omani type
    n1=en:microcephaly-capillary malformation syndrome | n2=en:spondyloepiphyseal dysplasia, omani type | rel=r_associated | relid=0 | w=26
  527. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:stambp, arg38cys
    n1=en:microcephaly-capillary malformation syndrome | n2=en:stambp, arg38cys | rel=r_associated | relid=0 | w=26
  528. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:stambp, phe100tyr
    n1=en:microcephaly-capillary malformation syndrome | n2=en:stambp, phe100tyr | rel=r_associated | relid=0 | w=26
  529. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:transcobalamin ii deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:transcobalamin ii deficiency | rel=r_associated | relid=0 | w=26
  530. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:tungland bellman syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:tungland bellman syndrome | rel=r_associated | relid=0 | w=26
  531. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> en:xanthinuria, type i
    n1=en:microcephaly-capillary malformation syndrome | n2=en:xanthinuria, type i | rel=r_associated | relid=0 | w=26
  532. en:microcephaly-capillary malformation syndrome -- r_associated #0: 26 / 0.605 -> syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=syndrome | rel=r_associated | relid=0 | w=26
  533. en:microcephaly-capillary malformation syndrome -- r_associated #0: 25 / 0.581 -> anomalie congénitale
    n1=en:microcephaly-capillary malformation syndrome | n2=anomalie congénitale | rel=r_associated | relid=0 | w=25
  534. en:microcephaly-capillary malformation syndrome -- r_associated #0: 24 / 0.558 -> syndrome de Walker-Warburg
    n1=en:microcephaly-capillary malformation syndrome | n2=syndrome de Walker-Warburg | rel=r_associated | relid=0 | w=24
  535. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> absence de croissance
    n1=en:microcephaly-capillary malformation syndrome | n2=absence de croissance | rel=r_associated | relid=0 | w=20
  536. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> acrodermatite entéropathique
    n1=en:microcephaly-capillary malformation syndrome | n2=acrodermatite entéropathique | rel=r_associated | relid=0 | w=20
  537. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> anomalie du développement
    n1=en:microcephaly-capillary malformation syndrome | n2=anomalie du développement | rel=r_associated | relid=0 | w=20
  538. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> anomalie du septum auriculaire
    n1=en:microcephaly-capillary malformation syndrome | n2=anomalie du septum auriculaire | rel=r_associated | relid=0 | w=20
  539. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> asthénie sénile
    n1=en:microcephaly-capillary malformation syndrome | n2=asthénie sénile | rel=r_associated | relid=0 | w=20
  540. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> atrophie optique
    n1=en:microcephaly-capillary malformation syndrome | n2=atrophie optique | rel=r_associated | relid=0 | w=20
  541. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> atrophie optique infantile avec chorée et paraplégie spastique
    n1=en:microcephaly-capillary malformation syndrome | n2=atrophie optique infantile avec chorée et paraplégie spastique | rel=r_associated | relid=0 | w=20
  542. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> atrophie optique infantile héréditaire compliquée de Behr
    n1=en:microcephaly-capillary malformation syndrome | n2=atrophie optique infantile héréditaire compliquée de Behr | rel=r_associated | relid=0 | w=20
  543. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> atrophie optique liée au sexe
    n1=en:microcephaly-capillary malformation syndrome | n2=atrophie optique liée au sexe | rel=r_associated | relid=0 | w=20
  544. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> atrophie optique liée au sexe de Völker-Dieben
    n1=en:microcephaly-capillary malformation syndrome | n2=atrophie optique liée au sexe de Völker-Dieben | rel=r_associated | relid=0 | w=20
  545. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> atrophie optique polyneuropathie et surdité
    n1=en:microcephaly-capillary malformation syndrome | n2=atrophie optique polyneuropathie et surdité | rel=r_associated | relid=0 | w=20
  546. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> atrophie optique tardive liée au sexe
    n1=en:microcephaly-capillary malformation syndrome | n2=atrophie optique tardive liée au sexe | rel=r_associated | relid=0 | w=20
  547. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> atrophie optique-paraplégie spastique
    n1=en:microcephaly-capillary malformation syndrome | n2=atrophie optique-paraplégie spastique | rel=r_associated | relid=0 | w=20
  548. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> atrophie optique, surdité, épilepsie, spasticité et décès précoce
    n1=en:microcephaly-capillary malformation syndrome | n2=atrophie optique, surdité, épilepsie, spasticité et décès précoce | rel=r_associated | relid=0 | w=20
  549. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> atrophie optique, surdité, ophtalmoplégie et myopathie
    n1=en:microcephaly-capillary malformation syndrome | n2=atrophie optique, surdité, ophtalmoplégie et myopathie | rel=r_associated | relid=0 | w=20
  550. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> bébé bronzé (syndrome du)
    n1=en:microcephaly-capillary malformation syndrome | n2=bébé bronzé (syndrome du) | rel=r_associated | relid=0 | w=20
  551. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> Bec de lièvre
    n1=en:microcephaly-capillary malformation syndrome | n2=Bec de lièvre | rel=r_associated | relid=0 | w=20
  552. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> bec de lièvre
    n1=en:microcephaly-capillary malformation syndrome | n2=bec de lièvre | rel=r_associated | relid=0 | w=20
  553. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> blépharophimosis-ptosis-épicanthus inversus (syndrome)
    n1=en:microcephaly-capillary malformation syndrome | n2=blépharophimosis-ptosis-épicanthus inversus (syndrome) | rel=r_associated | relid=0 | w=20
  554. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> brachydactylie
    n1=en:microcephaly-capillary malformation syndrome | n2=brachydactylie | rel=r_associated | relid=0 | w=20
  555. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> cataracte liée au sexe avec dent de Hutchinson
    n1=en:microcephaly-capillary malformation syndrome | n2=cataracte liée au sexe avec dent de Hutchinson | rel=r_associated | relid=0 | w=20
  556. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> communication inter-auriculaire
    n1=en:microcephaly-capillary malformation syndrome | n2=communication inter-auriculaire | rel=r_associated | relid=0 | w=20
  557. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> communication interauriculaire
    n1=en:microcephaly-capillary malformation syndrome | n2=communication interauriculaire | rel=r_associated | relid=0 | w=20
  558. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> communication interventriculaire
    n1=en:microcephaly-capillary malformation syndrome | n2=communication interventriculaire | rel=r_associated | relid=0 | w=20
  559. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> congénital
    n1=en:microcephaly-capillary malformation syndrome | n2=congénital | rel=r_associated | relid=0 | w=20
  560. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> congenital
    n1=en:microcephaly-capillary malformation syndrome | n2=congenital | rel=r_associated | relid=0 | w=20
  561. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> congénitale
    n1=en:microcephaly-capillary malformation syndrome | n2=congénitale | rel=r_associated | relid=0 | w=20
  562. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> débilité sénile
    n1=en:microcephaly-capillary malformation syndrome | n2=débilité sénile | rel=r_associated | relid=0 | w=20
  563. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> déficience auditive
    n1=en:microcephaly-capillary malformation syndrome | n2=déficience auditive | rel=r_associated | relid=0 | w=20
  564. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> déficience congénitale
    n1=en:microcephaly-capillary malformation syndrome | n2=déficience congénitale | rel=r_associated | relid=0 | w=20
  565. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> déficit congénital en mégacaryocytes
    n1=en:microcephaly-capillary malformation syndrome | n2=déficit congénital en mégacaryocytes | rel=r_associated | relid=0 | w=20
  566. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> déficit en biotinidase
    n1=en:microcephaly-capillary malformation syndrome | n2=déficit en biotinidase | rel=r_associated | relid=0 | w=20
  567. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> déficit en céto-acide décarboxylase
    n1=en:microcephaly-capillary malformation syndrome | n2=déficit en céto-acide décarboxylase | rel=r_associated | relid=0 | w=20
  568. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> déficit en cytochrome oxydase
    n1=en:microcephaly-capillary malformation syndrome | n2=déficit en cytochrome oxydase | rel=r_associated | relid=0 | w=20
  569. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> déficit en cytochrome-c oxydase
    n1=en:microcephaly-capillary malformation syndrome | n2=déficit en cytochrome-c oxydase | rel=r_associated | relid=0 | w=20
  570. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> déficit en neuraminidase
    n1=en:microcephaly-capillary malformation syndrome | n2=déficit en neuraminidase | rel=r_associated | relid=0 | w=20
  571. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> déficit en prolidase
    n1=en:microcephaly-capillary malformation syndrome | n2=déficit en prolidase | rel=r_associated | relid=0 | w=20
  572. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> déficit en pyruvate carboxylase
    n1=en:microcephaly-capillary malformation syndrome | n2=déficit en pyruvate carboxylase | rel=r_associated | relid=0 | w=20
  573. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> déficit en semialdéhyde succinique-déshydrogénase
    n1=en:microcephaly-capillary malformation syndrome | n2=déficit en semialdéhyde succinique-déshydrogénase | rel=r_associated | relid=0 | w=20
  574. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> déficit en sulfite-oxydase
    n1=en:microcephaly-capillary malformation syndrome | n2=déficit en sulfite-oxydase | rel=r_associated | relid=0 | w=20
  575. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> déformation congénitale
    n1=en:microcephaly-capillary malformation syndrome | n2=déformation congénitale | rel=r_associated | relid=0 | w=20
  576. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> déliquescence
    n1=en:microcephaly-capillary malformation syndrome | n2=déliquescence | rel=r_associated | relid=0 | w=20
  577. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> démence (sémiologie)
    n1=en:microcephaly-capillary malformation syndrome | n2=démence (sémiologie) | rel=r_associated | relid=0 | w=20
  578. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> démence dégénérative primaire
    n1=en:microcephaly-capillary malformation syndrome | n2=démence dégénérative primaire | rel=r_associated | relid=0 | w=20
  579. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> démence forme dépressive ou délirante
    n1=en:microcephaly-capillary malformation syndrome | n2=démence forme dépressive ou délirante | rel=r_associated | relid=0 | w=20
  580. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> démence fronto-temporale
    n1=en:microcephaly-capillary malformation syndrome | n2=démence fronto-temporale | rel=r_associated | relid=0 | w=20
  581. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> démence frontotemporale
    n1=en:microcephaly-capillary malformation syndrome | n2=démence frontotemporale | rel=r_associated | relid=0 | w=20
  582. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> démence présénile
    n1=en:microcephaly-capillary malformation syndrome | n2=démence présénile | rel=r_associated | relid=0 | w=20
  583. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> démence sénile
    n1=en:microcephaly-capillary malformation syndrome | n2=démence sénile | rel=r_associated | relid=0 | w=20
  584. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> démence sénile avec delirium ou état confusionnel aigu
    n1=en:microcephaly-capillary malformation syndrome | n2=démence sénile avec delirium ou état confusionnel aigu | rel=r_associated | relid=0 | w=20
  585. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> difformité congénitale
    n1=en:microcephaly-capillary malformation syndrome | n2=difformité congénitale | rel=r_associated | relid=0 | w=20
  586. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> dysplasie craniodiaphysaire
    n1=en:microcephaly-capillary malformation syndrome | n2=dysplasie craniodiaphysaire | rel=r_associated | relid=0 | w=20
  587. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> dystonie dopasensible
    n1=en:microcephaly-capillary malformation syndrome | n2=dystonie dopasensible | rel=r_associated | relid=0 | w=20
  588. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> dystrophie des cônes liée au sexe
    n1=en:microcephaly-capillary malformation syndrome | n2=dystrophie des cônes liée au sexe | rel=r_associated | relid=0 | w=20
  589. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> dystrophie des cônes liée au sexe avec reflet rétinien jaune-vert
    n1=en:microcephaly-capillary malformation syndrome | n2=dystrophie des cônes liée au sexe avec reflet rétinien jaune-vert | rel=r_associated | relid=0 | w=20
  590. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:acrorenal mandibular syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:acrorenal mandibular syndrome | rel=r_associated | relid=0 | w=20
  591. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein
    n1=en:microcephaly-capillary malformation syndrome | n2=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | rel=r_associated | relid=0 | w=20
  592. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:adducted thumbs and arthrogryposis syndrome christian type
    n1=en:microcephaly-capillary malformation syndrome | n2=en:adducted thumbs and arthrogryposis syndrome christian type | rel=r_associated | relid=0 | w=20
  593. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:age-related physical debility
    n1=en:microcephaly-capillary malformation syndrome | n2=en:age-related physical debility | rel=r_associated | relid=0 | w=20
  594. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:anauxetic dysplasia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:anauxetic dysplasia | rel=r_associated | relid=0 | w=20
  595. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:and hypogonadotropic hypogonadism
    n1=en:microcephaly-capillary malformation syndrome | n2=en:and hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=20
  596. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:and myopathy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:and myopathy | rel=r_associated | relid=0 | w=20
  597. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:and proeminent incisors
    n1=en:microcephaly-capillary malformation syndrome | n2=en:and proeminent incisors | rel=r_associated | relid=0 | w=20
  598. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:aphalangy and syndactyly with microcephaly syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:aphalangy and syndactyly with microcephaly syndrome | rel=r_associated | relid=0 | w=20
  599. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:arterial dissection and lentiginosis syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:arterial dissection and lentiginosis syndrome | rel=r_associated | relid=0 | w=20
  600. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:autosomal dominant focal dystonia dyt25 type
    n1=en:microcephaly-capillary malformation syndrome | n2=en:autosomal dominant focal dystonia dyt25 type | rel=r_associated | relid=0 | w=20
  601. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:autosomal recessive spastic paraplegia type 39
    n1=en:microcephaly-capillary malformation syndrome | n2=en:autosomal recessive spastic paraplegia type 39 | rel=r_associated | relid=0 | w=20
  602. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:bamforth syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:bamforth syndrome | rel=r_associated | relid=0 | w=20
  603. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:bestrophinopathy, autosomal recessive
    n1=en:microcephaly-capillary malformation syndrome | n2=en:bestrophinopathy, autosomal recessive | rel=r_associated | relid=0 | w=20
  604. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:birth defect
    n1=en:microcephaly-capillary malformation syndrome | n2=en:birth defect | rel=r_associated | relid=0 | w=20
  605. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:braddock syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:braddock syndrome | rel=r_associated | relid=0 | w=20
  606. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:brain calcification rajab type
    n1=en:microcephaly-capillary malformation syndrome | n2=en:brain calcification rajab type | rel=r_associated | relid=0 | w=20
  607. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:branched-chain ketoaciduria
    n1=en:microcephaly-capillary malformation syndrome | n2=en:branched-chain ketoaciduria | rel=r_associated | relid=0 | w=20
  608. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:cardiac anomaly and heterotaxy syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cardiac anomaly and heterotaxy syndrome | rel=r_associated | relid=0 | w=20
  609. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:cardiomyopathy and renal anomaly syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cardiomyopathy and renal anomaly syndrome | rel=r_associated | relid=0 | w=20
  610. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:cerebral gigantism
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cerebral gigantism | rel=r_associated | relid=0 | w=20
  611. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:cervical hypertrichosis and peripheral neuropathy syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cervical hypertrichosis and peripheral neuropathy syndrome | rel=r_associated | relid=0 | w=20
  612. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:classical maple syrup urine disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:classical maple syrup urine disease | rel=r_associated | relid=0 | w=20
  613. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:cleft lip
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cleft lip | rel=r_associated | relid=0 | w=20
  614. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:cone-dystrophy
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cone-dystrophy | rel=r_associated | relid=0 | w=20
  615. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:congenital analbuminemia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital analbuminemia | rel=r_associated | relid=0 | w=20
  616. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:congenital anomaly
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital anomaly | rel=r_associated | relid=0 | w=20
  617. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:congenital cataract with ataxia and deafness syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital cataract with ataxia and deafness syndrome | rel=r_associated | relid=0 | w=20
  618. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:congenital defect
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital defect | rel=r_associated | relid=0 | w=20
  619. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type 1h
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital disorder of glycosylation type 1h | rel=r_associated | relid=0 | w=20
  620. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type 2e
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital disorder of glycosylation type 2e | rel=r_associated | relid=0 | w=20
  621. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type id
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital disorder of glycosylation type id | rel=r_associated | relid=0 | w=20
  622. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type ie
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital disorder of glycosylation type ie | rel=r_associated | relid=0 | w=20
  623. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation, type if
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital disorder of glycosylation, type if | rel=r_associated | relid=0 | w=20
  624. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:congenital malformation
    n1=en:microcephaly-capillary malformation syndrome | n2=en:congenital malformation | rel=r_associated | relid=0 | w=20
  625. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:cooper jabs syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cooper jabs syndrome | rel=r_associated | relid=0 | w=20
  626. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:craniofacial ulnar renal syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:craniofacial ulnar renal syndrome | rel=r_associated | relid=0 | w=20
  627. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:cutaneous photosensitivity and lethal colitis syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:cutaneous photosensitivity and lethal colitis syndrome | rel=r_associated | relid=0 | w=20
  628. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:deafness
    n1=en:microcephaly-capillary malformation syndrome | n2=en:deafness | rel=r_associated | relid=0 | w=20
  629. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:deafness and myopia syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:deafness and myopia syndrome | rel=r_associated | relid=0 | w=20
  630. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | rel=r_associated | relid=0 | w=20
  631. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:developmental anomaly
    n1=en:microcephaly-capillary malformation syndrome | n2=en:developmental anomaly | rel=r_associated | relid=0 | w=20
  632. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:developmental fault
    n1=en:microcephaly-capillary malformation syndrome | n2=en:developmental fault | rel=r_associated | relid=0 | w=20
  633. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:diaphanospondylodysostosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:diaphanospondylodysostosis | rel=r_associated | relid=0 | w=20
  634. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:diaphragmatic hernia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:diaphragmatic hernia | rel=r_associated | relid=0 | w=20
  635. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:Dubin-Johnson's syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:Dubin-Johnson's syndrome | rel=r_associated | relid=0 | w=20
  636. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:Dubin-Sprinz disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:Dubin-Sprinz disease | rel=r_associated | relid=0 | w=20
  637. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:ectodermal dysplasia with blindness syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:ectodermal dysplasia with blindness syndrome | rel=r_associated | relid=0 | w=20
  638. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:ehlers-danlos syndrome kyphoscoliotic and deafness type
    n1=en:microcephaly-capillary malformation syndrome | n2=en:ehlers-danlos syndrome kyphoscoliotic and deafness type | rel=r_associated | relid=0 | w=20
  639. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:ehlers-danlos syndrome vascular-like type
    n1=en:microcephaly-capillary malformation syndrome | n2=en:ehlers-danlos syndrome vascular-like type | rel=r_associated | relid=0 | w=20
  640. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:exomphalos
    n1=en:microcephaly-capillary malformation syndrome | n2=en:exomphalos | rel=r_associated | relid=0 | w=20
  641. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:familial median cleft of upper and lower lip
    n1=en:microcephaly-capillary malformation syndrome | n2=en:familial median cleft of upper and lower lip | rel=r_associated | relid=0 | w=20
  642. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:fountain syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:fountain syndrome | rel=r_associated | relid=0 | w=20
  643. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:generalized peeling skin syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:generalized peeling skin syndrome | rel=r_associated | relid=0 | w=20
  644. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | rel=r_associated | relid=0 | w=20
  645. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:halal syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:halal syndrome | rel=r_associated | relid=0 | w=20
  646. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:hall riggs syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hall riggs syndrome | rel=r_associated | relid=0 | w=20
  647. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:harelip
    n1=en:microcephaly-capillary malformation syndrome | n2=en:harelip | rel=r_associated | relid=0 | w=20
  648. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:heart defects limb shortening
    n1=en:microcephaly-capillary malformation syndrome | n2=en:heart defects limb shortening | rel=r_associated | relid=0 | w=20
  649. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20
  650. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:hypomandibular faciocranial dysostosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hypomandibular faciocranial dysostosis | rel=r_associated | relid=0 | w=20
  651. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:hypophosphatasia infantile
    n1=en:microcephaly-capillary malformation syndrome | n2=en:hypophosphatasia infantile | rel=r_associated | relid=0 | w=20
  652. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:I-cell disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:I-cell disease | rel=r_associated | relid=0 | w=20
  653. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:insulin growth factor i deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:insulin growth factor i deficiency | rel=r_associated | relid=0 | w=20
  654. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:juvenile amyotrophic lateral sclerosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:juvenile amyotrophic lateral sclerosis | rel=r_associated | relid=0 | w=20
  655. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:kallman syndrome with heart disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:kallman syndrome with heart disease | rel=r_associated | relid=0 | w=20
  656. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:keratoconus posticus
    n1=en:microcephaly-capillary malformation syndrome | n2=en:keratoconus posticus | rel=r_associated | relid=0 | w=20
  657. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:late-onset junctional epidermolysis bullosa
    n1=en:microcephaly-capillary malformation syndrome | n2=en:late-onset junctional epidermolysis bullosa | rel=r_associated | relid=0 | w=20
  658. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:Leroy's i-cell disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:Leroy's i-cell disease | rel=r_associated | relid=0 | w=20
  659. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:lethal larsen-like syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:lethal larsen-like syndrome | rel=r_associated | relid=0 | w=20
  660. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:leucinosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
  661. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome | rel=r_associated | relid=0 | w=20
  662. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:lissencephaly type 3 familial fetal akinesia sequence syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | rel=r_associated | relid=0 | w=20
  663. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:major physical defect
    n1=en:microcephaly-capillary malformation syndrome | n2=en:major physical defect | rel=r_associated | relid=0 | w=20
  664. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:manouvrier syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:manouvrier syndrome | rel=r_associated | relid=0 | w=20
  665. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:maple-tree syrup disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:maple-tree syrup disease | rel=r_associated | relid=0 | w=20
  666. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency | rel=r_associated | relid=0 | w=20
  667. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | rel=r_associated | relid=0 | w=20
  668. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:microcephaly albinism digital anomalies syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:microcephaly albinism digital anomalies syndrome | rel=r_associated | relid=0 | w=20
  669. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:Mohr-Tranebjaerg syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:Mohr-Tranebjaerg syndrome | rel=r_associated | relid=0 | w=20
  670. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:moyamoya disease with early onset achalasia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:moyamoya disease with early onset achalasia | rel=r_associated | relid=0 | w=20
  671. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:mucopolysaccharidosis i
    n1=en:microcephaly-capillary malformation syndrome | n2=en:mucopolysaccharidosis i | rel=r_associated | relid=0 | w=20
  672. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:multicore disease with mental retardation
    n1=en:microcephaly-capillary malformation syndrome | n2=en:multicore disease with mental retardation | rel=r_associated | relid=0 | w=20
  673. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:najjar syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:najjar syndrome | rel=r_associated | relid=0 | w=20
  674. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:Nathalie syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:Nathalie syndrome | rel=r_associated | relid=0 | w=20
  675. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:Niemann-Pick disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:Niemann-Pick disease | rel=r_associated | relid=0 | w=20
  676. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:nystagmus
    n1=en:microcephaly-capillary malformation syndrome | n2=en:nystagmus | rel=r_associated | relid=0 | w=20
  677. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:oculocutaneous albinism type 6
    n1=en:microcephaly-capillary malformation syndrome | n2=en:oculocutaneous albinism type 6 | rel=r_associated | relid=0 | w=20
  678. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:ophthalmoplegia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:ophthalmoplegia | rel=r_associated | relid=0 | w=20
  679. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:palate-blepharophimosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:palate-blepharophimosis | rel=r_associated | relid=0 | w=20
  680. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | rel=r_associated | relid=0 | w=20
  681. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:pelviscapular dysplasia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:pelviscapular dysplasia | rel=r_associated | relid=0 | w=20
  682. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:physical defect
    n1=en:microcephaly-capillary malformation syndrome | n2=en:physical defect | rel=r_associated | relid=0 | w=20
  683. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:pili torti onychodysplasia syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:pili torti onychodysplasia syndrome | rel=r_associated | relid=0 | w=20
  684. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome | rel=r_associated | relid=0 | w=20
  685. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:porencephaly
    n1=en:microcephaly-capillary malformation syndrome | n2=en:porencephaly | rel=r_associated | relid=0 | w=20
  686. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:presenile dementia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:presenile dementia | rel=r_associated | relid=0 | w=20
  687. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:primary immunodeficiency syndrome due to p14 deficiency
    n1=en:microcephaly-capillary malformation syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20
  688. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:renal dysplasia - limb defects syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:renal dysplasia - limb defects syndrome | rel=r_associated | relid=0 | w=20
  689. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:robinow-like syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:robinow-like syndrome | rel=r_associated | relid=0 | w=20
  690. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:sagging
    n1=en:microcephaly-capillary malformation syndrome | n2=en:sagging | rel=r_associated | relid=0 | w=20
  691. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome | rel=r_associated | relid=0 | w=20
  692. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:senile asthenia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:senile asthenia | rel=r_associated | relid=0 | w=20
  693. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:senile dementia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:senile dementia | rel=r_associated | relid=0 | w=20
  694. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:senility
    n1=en:microcephaly-capillary malformation syndrome | n2=en:senility | rel=r_associated | relid=0 | w=20
  695. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:Soto's syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:Soto's syndrome | rel=r_associated | relid=0 | w=20
  696. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:sotos' syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:sotos' syndrome | rel=r_associated | relid=0 | w=20
  697. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:Sotos' syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:Sotos' syndrome | rel=r_associated | relid=0 | w=20
  698. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:spastic paraplegia
    n1=en:microcephaly-capillary malformation syndrome | n2=en:spastic paraplegia | rel=r_associated | relid=0 | w=20
  699. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:split-hand/foot malformation 3
    n1=en:microcephaly-capillary malformation syndrome | n2=en:split-hand/foot malformation 3 | rel=r_associated | relid=0 | w=20
  700. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:spondyloepiphyseal dysplasia tarda kohn type
    n1=en:microcephaly-capillary malformation syndrome | n2=en:spondyloepiphyseal dysplasia tarda kohn type | rel=r_associated | relid=0 | w=20
  701. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome | rel=r_associated | relid=0 | w=20
  702. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:strabismus syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:strabismus syndrome | rel=r_associated | relid=0 | w=20
  703. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:Tay-Sachs disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:Tay-Sachs disease | rel=r_associated | relid=0 | w=20
  704. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:telecanthus
    n1=en:microcephaly-capillary malformation syndrome | n2=en:telecanthus | rel=r_associated | relid=0 | w=20
  705. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:teratosis
    n1=en:microcephaly-capillary malformation syndrome | n2=en:teratosis | rel=r_associated | relid=0 | w=20
  706. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:thiamin-responsive maple syrup urine disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:thiamin-responsive maple syrup urine disease | rel=r_associated | relid=0 | w=20
  707. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:timothy syndrome type 2
    n1=en:microcephaly-capillary malformation syndrome | n2=en:timothy syndrome type 2 | rel=r_associated | relid=0 | w=20
  708. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:tubular renal disease with cardiomyopathy syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:tubular renal disease with cardiomyopathy syndrome | rel=r_associated | relid=0 | w=20
  709. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:type a 14
    n1=en:microcephaly-capillary malformation syndrome | n2=en:type a 14 | rel=r_associated | relid=0 | w=20
  710. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:type Völker-Dieben
    n1=en:microcephaly-capillary malformation syndrome | n2=en:type Völker-Dieben | rel=r_associated | relid=0 | w=20
  711. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:type Went
    n1=en:microcephaly-capillary malformation syndrome | n2=en:type Went | rel=r_associated | relid=0 | w=20
  712. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:unspecified senile psychotic condition
    n1=en:microcephaly-capillary malformation syndrome | n2=en:unspecified senile psychotic condition | rel=r_associated | relid=0 | w=20
  713. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:von Recklinghausen's disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:von Recklinghausen's disease | rel=r_associated | relid=0 | w=20
  714. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:Wolman's disease
    n1=en:microcephaly-capillary malformation syndrome | n2=en:Wolman's disease | rel=r_associated | relid=0 | w=20
  715. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:X-linked
    n1=en:microcephaly-capillary malformation syndrome | n2=en:X-linked | rel=r_associated | relid=0 | w=20
  716. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability with acromegaly and hyperactivity syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | rel=r_associated | relid=0 | w=20
  717. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability with ataxia and apraxia syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:x-linked intellectual disability with ataxia and apraxia syndrome | rel=r_associated | relid=0 | w=20
  718. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome | rel=r_associated | relid=0 | w=20
  719. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:yemenite deaf-blind hypopigmentation syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:yemenite deaf-blind hypopigmentation syndrome | rel=r_associated | relid=0 | w=20
  720. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:Zellweger syndrome
    n1=en:microcephaly-capillary malformation syndrome | n2=en:Zellweger syndrome | rel=r_associated | relid=0 | w=20
  721. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:zellweger-like syndrome without peroxisomal anomaly
    n1=en:microcephaly-capillary malformation syndrome | n2=en:zellweger-like syndrome without peroxisomal anomaly | rel=r_associated | relid=0 | w=20
  722. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> en:zinc-deficiency type
    n1=en:microcephaly-capillary malformation syndrome | n2=en:zinc-deficiency type | rel=r_associated | relid=0 | w=20
  723. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> Fenn (diagramme de)
    n1=en:microcephaly-capillary malformation syndrome | n2=Fenn (diagramme de) | rel=r_associated | relid=0 | w=20
  724. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> fente labiale
    n1=en:microcephaly-capillary malformation syndrome | n2=fente labiale | rel=r_associated | relid=0 | w=20
  725. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> fente labiopalatine et blépharophimosis
    n1=en:microcephaly-capillary malformation syndrome | n2=fente labiopalatine et blépharophimosis | rel=r_associated | relid=0 | w=20
  726. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> foramen ovale perméable
    n1=en:microcephaly-capillary malformation syndrome | n2=foramen ovale perméable | rel=r_associated | relid=0 | w=20
  727. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> fucosidose
    n1=en:microcephaly-capillary malformation syndrome | n2=fucosidose | rel=r_associated | relid=0 | w=20
  728. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> gigantisme cérébral
    n1=en:microcephaly-capillary malformation syndrome | n2=gigantisme cérébral | rel=r_associated | relid=0 | w=20
  729. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> hérédité autosomale récessive
    n1=en:microcephaly-capillary malformation syndrome | n2=hérédité autosomale récessive | rel=r_associated | relid=0 | w=20
  730. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle
    n1=en:microcephaly-capillary malformation syndrome | n2=hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle | rel=r_associated | relid=0 | w=20
  731. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> histidinémie
    n1=en:microcephaly-capillary malformation syndrome | n2=histidinémie | rel=r_associated | relid=0 | w=20
  732. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> histiocytose sinusale hémophagocytaire
    n1=en:microcephaly-capillary malformation syndrome | n2=histiocytose sinusale hémophagocytaire | rel=r_associated | relid=0 | w=20
  733. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> hvd
    n1=en:microcephaly-capillary malformation syndrome | n2=hvd | rel=r_associated | relid=0 | w=20
  734. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> hyperoxalurie primaire
    n1=en:microcephaly-capillary malformation syndrome | n2=hyperoxalurie primaire | rel=r_associated | relid=0 | w=20
  735. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> hyperoxalurie primitive
    n1=en:microcephaly-capillary malformation syndrome | n2=hyperoxalurie primitive | rel=r_associated | relid=0 | w=20
  736. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> hyperplasie congénitale des surrénales
    n1=en:microcephaly-capillary malformation syndrome | n2=hyperplasie congénitale des surrénales | rel=r_associated | relid=0 | w=20
  737. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> hypertélorisme
    n1=en:microcephaly-capillary malformation syndrome | n2=hypertélorisme | rel=r_associated | relid=0 | w=20
  738. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> hypertélorisme-microtie-fente faciale
    n1=en:microcephaly-capillary malformation syndrome | n2=hypertélorisme-microtie-fente faciale | rel=r_associated | relid=0 | w=20
  739. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> hypertélorisme, hypospadias, polysyndactylie (syndrome)
    n1=en:microcephaly-capillary malformation syndrome | n2=hypertélorisme, hypospadias, polysyndactylie (syndrome) | rel=r_associated | relid=0 | w=20
  740. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> hypertrophie du ventricule droit
    n1=en:microcephaly-capillary malformation syndrome | n2=hypertrophie du ventricule droit | rel=r_associated | relid=0 | w=20
  741. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> hypertrophie ventriculaire droite
    n1=en:microcephaly-capillary malformation syndrome | n2=hypertrophie ventriculaire droite | rel=r_associated | relid=0 | w=20
  742. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> hypertrophie ventricule droit
    n1=en:microcephaly-capillary malformation syndrome | n2=hypertrophie ventricule droit | rel=r_associated | relid=0 | w=20
  743. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> hypertrophies du ventricule droit
    n1=en:microcephaly-capillary malformation syndrome | n2=hypertrophies du ventricule droit | rel=r_associated | relid=0 | w=20
  744. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> hypophosphatasie foetale
    n1=en:microcephaly-capillary malformation syndrome | n2=hypophosphatasie foetale | rel=r_associated | relid=0 | w=20
  745. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> hypophosphatasie infantile
    n1=en:microcephaly-capillary malformation syndrome | n2=hypophosphatasie infantile | rel=r_associated | relid=0 | w=20
  746. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> hypoplasie crânienne
    n1=en:microcephaly-capillary malformation syndrome | n2=hypoplasie crânienne | rel=r_associated | relid=0 | w=20
  747. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> hypothyroïdie (manifestations neuromusculaires dans l')
    n1=en:microcephaly-capillary malformation syndrome | n2=hypothyroïdie (manifestations neuromusculaires dans l') | rel=r_associated | relid=0 | w=20
  748. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> hypotonie
    n1=en:microcephaly-capillary malformation syndrome | n2=hypotonie | rel=r_associated | relid=0 | w=20
  749. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> hypotonie musculaire
    n1=en:microcephaly-capillary malformation syndrome | n2=hypotonie musculaire | rel=r_associated | relid=0 | w=20
  750. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> Hypotonie musculaire
    n1=en:microcephaly-capillary malformation syndrome | n2=Hypotonie musculaire | rel=r_associated | relid=0 | w=20
  751. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> hypotonie, obésité et incisives proéminentes
    n1=en:microcephaly-capillary malformation syndrome | n2=hypotonie, obésité et incisives proéminentes | rel=r_associated | relid=0 | w=20
  752. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> insuffisance staturale
    n1=en:microcephaly-capillary malformation syndrome | n2=insuffisance staturale | rel=r_associated | relid=0 | w=20
  753. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> intolérance au fructose
    n1=en:microcephaly-capillary malformation syndrome | n2=intolérance au fructose | rel=r_associated | relid=0 | w=20
  754. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> kératocône postérieur-fente labiale-petite taille
    n1=en:microcephaly-capillary malformation syndrome | n2=kératocône postérieur-fente labiale-petite taille | rel=r_associated | relid=0 | w=20
  755. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> Kjer (atrophie optique de type)
    n1=en:microcephaly-capillary malformation syndrome | n2=Kjer (atrophie optique de type) | rel=r_associated | relid=0 | w=20
  756. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> leucinose
    n1=en:microcephaly-capillary malformation syndrome | n2=leucinose | rel=r_associated | relid=0 | w=20
  757. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> maladie congénitale
    n1=en:microcephaly-capillary malformation syndrome | n2=maladie congénitale | rel=r_associated | relid=0 | w=20
  758. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> Maladie congénitale
    n1=en:microcephaly-capillary malformation syndrome | n2=Maladie congénitale | rel=r_associated | relid=0 | w=20
  759. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> maladie de dubin-johnson
    n1=en:microcephaly-capillary malformation syndrome | n2=maladie de dubin-johnson | rel=r_associated | relid=0 | w=20
  760. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> maladie de Niemann-Pick
    n1=en:microcephaly-capillary malformation syndrome | n2=maladie de Niemann-Pick | rel=r_associated | relid=0 | w=20
  761. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> maladie de Roger
    n1=en:microcephaly-capillary malformation syndrome | n2=maladie de Roger | rel=r_associated | relid=0 | w=20
  762. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> maladie de Tay-Sachs
    n1=en:microcephaly-capillary malformation syndrome | n2=maladie de Tay-Sachs | rel=r_associated | relid=0 | w=20
  763. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> maladie de tay-sachs
    n1=en:microcephaly-capillary malformation syndrome | n2=maladie de tay-sachs | rel=r_associated | relid=0 | w=20
  764. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> maladie de Tay-sachs
    n1=en:microcephaly-capillary malformation syndrome | n2=maladie de Tay-sachs | rel=r_associated | relid=0 | w=20
  765. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> maladie de wolman
    n1=en:microcephaly-capillary malformation syndrome | n2=maladie de wolman | rel=r_associated | relid=0 | w=20
  766. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> Maladie de Wolman
    n1=en:microcephaly-capillary malformation syndrome | n2=Maladie de Wolman | rel=r_associated | relid=0 | w=20
  767. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> maladie de Wolman
    n1=en:microcephaly-capillary malformation syndrome | n2=maladie de Wolman | rel=r_associated | relid=0 | w=20
  768. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> maladie des urines à l'odeur de sirop d'érable
    n1=en:microcephaly-capillary malformation syndrome | n2=maladie des urines à l'odeur de sirop d'érable | rel=r_associated | relid=0 | w=20
  769. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> maladie des urines avec odeur de sirop erable
    n1=en:microcephaly-capillary malformation syndrome | n2=maladie des urines avec odeur de sirop erable | rel=r_associated | relid=0 | w=20
  770. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> maladie du sirop d'érable
    n1=en:microcephaly-capillary malformation syndrome | n2=maladie du sirop d'érable | rel=r_associated | relid=0 | w=20
  771. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> malformation
    n1=en:microcephaly-capillary malformation syndrome | n2=malformation | rel=r_associated | relid=0 | w=20
  772. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> malformation congénitale
    n1=en:microcephaly-capillary malformation syndrome | n2=malformation congénitale | rel=r_associated | relid=0 | w=20
  773. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> microdélétion 5q35
    n1=en:microcephaly-capillary malformation syndrome | n2=microdélétion 5q35 | rel=r_associated | relid=0 | w=20
  774. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> migraine hémiplégique familiale
    n1=en:microcephaly-capillary malformation syndrome | n2=migraine hémiplégique familiale | rel=r_associated | relid=0 | w=20
  775. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> mucolipidose II
    n1=en:microcephaly-capillary malformation syndrome | n2=mucolipidose II | rel=r_associated | relid=0 | w=20
  776. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> mucolipidose type ii
    n1=en:microcephaly-capillary malformation syndrome | n2=mucolipidose type ii | rel=r_associated | relid=0 | w=20
  777. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> mucolipidose type II
    n1=en:microcephaly-capillary malformation syndrome | n2=mucolipidose type II | rel=r_associated | relid=0 | w=20
  778. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> mucopolysaccharidose de type I
    n1=en:microcephaly-capillary malformation syndrome | n2=mucopolysaccharidose de type I | rel=r_associated | relid=0 | w=20
  779. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> myopathie multicore avec retard mental, petite taille et hypogonadisme hypogonadotrophique
    n1=en:microcephaly-capillary malformation syndrome | n2=myopathie multicore avec retard mental, petite taille et hypogonadisme hypogonadotrophique | rel=r_associated | relid=0 | w=20
  780. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> neuro-acanthocytose
    n1=en:microcephaly-capillary malformation syndrome | n2=neuro-acanthocytose | rel=r_associated | relid=0 | w=20
  781. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> neurofibromatose
    n1=en:microcephaly-capillary malformation syndrome | n2=neurofibromatose | rel=r_associated | relid=0 | w=20
  782. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> neurofibromatose de Recklinghausen
    n1=en:microcephaly-capillary malformation syndrome | n2=neurofibromatose de Recklinghausen | rel=r_associated | relid=0 | w=20
  783. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> neurofibromatose de recklinghausen
    n1=en:microcephaly-capillary malformation syndrome | n2=neurofibromatose de recklinghausen | rel=r_associated | relid=0 | w=20
  784. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> neurofibromatose de type périphérique
    n1=en:microcephaly-capillary malformation syndrome | n2=neurofibromatose de type périphérique | rel=r_associated | relid=0 | w=20
  785. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> neurofibromatose de type VI
    n1=en:microcephaly-capillary malformation syndrome | n2=neurofibromatose de type VI | rel=r_associated | relid=0 | w=20
  786. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> nystagmus
    n1=en:microcephaly-capillary malformation syndrome | n2=nystagmus | rel=r_associated | relid=0 | w=20
  787. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> nystagmus congénital isolé
    n1=en:microcephaly-capillary malformation syndrome | n2=nystagmus congénital isolé | rel=r_associated | relid=0 | w=20
  788. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> nystagmus lié au sexe
    n1=en:microcephaly-capillary malformation syndrome | n2=nystagmus lié au sexe | rel=r_associated | relid=0 | w=20
  789. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> ophtalmoplégie, hypotonie, ataxie, hypoacousie et athétose
    n1=en:microcephaly-capillary malformation syndrome | n2=ophtalmoplégie, hypotonie, ataxie, hypoacousie et athétose | rel=r_associated | relid=0 | w=20
  790. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> oxalose
    n1=en:microcephaly-capillary malformation syndrome | n2=oxalose | rel=r_associated | relid=0 | w=20
  791. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> oxalose primitive
    n1=en:microcephaly-capillary malformation syndrome | n2=oxalose primitive | rel=r_associated | relid=0 | w=20
  792. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> oxaloses
    n1=en:microcephaly-capillary malformation syndrome | n2=oxaloses | rel=r_associated | relid=0 | w=20
  793. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> paraplégie spastique avec atrophie optique et démence
    n1=en:microcephaly-capillary malformation syndrome | n2=paraplégie spastique avec atrophie optique et démence | rel=r_associated | relid=0 | w=20
  794. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> pathologie congénitale
    n1=en:microcephaly-capillary malformation syndrome | n2=pathologie congénitale | rel=r_associated | relid=0 | w=20
  795. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> persistance du foramen ovale
    n1=en:microcephaly-capillary malformation syndrome | n2=persistance du foramen ovale | rel=r_associated | relid=0 | w=20
  796. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> petite taille, hyperextensibilité, hernie et dépression oculaire
    n1=en:microcephaly-capillary malformation syndrome | n2=petite taille, hyperextensibilité, hernie et dépression oculaire | rel=r_associated | relid=0 | w=20
  797. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> psychose présénile
    n1=en:microcephaly-capillary malformation syndrome | n2=psychose présénile | rel=r_associated | relid=0 | w=20
  798. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> psychose sénile
    n1=en:microcephaly-capillary malformation syndrome | n2=psychose sénile | rel=r_associated | relid=0 | w=20
  799. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> ptose
    n1=en:microcephaly-capillary malformation syndrome | n2=ptose | rel=r_associated | relid=0 | w=20
  800. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> ptôse
    n1=en:microcephaly-capillary malformation syndrome | n2=ptôse | rel=r_associated | relid=0 | w=20
  801. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> ptosis
    n1=en:microcephaly-capillary malformation syndrome | n2=ptosis | rel=r_associated | relid=0 | w=20
  802. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> Recklinghausen (maladie de von)
    n1=en:microcephaly-capillary malformation syndrome | n2=Recklinghausen (maladie de von) | rel=r_associated | relid=0 | w=20
  803. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> Recklinghausen (neurofibromatose de)
    n1=en:microcephaly-capillary malformation syndrome | n2=Recklinghausen (neurofibromatose de) | rel=r_associated | relid=0 | w=20
  804. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> retard de croissance
    n1=en:microcephaly-capillary malformation syndrome | n2=retard de croissance | rel=r_associated | relid=0 | w=20
  805. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> retard de croissance staturo-pondérale
    n1=en:microcephaly-capillary malformation syndrome | n2=retard de croissance staturo-pondérale | rel=r_associated | relid=0 | w=20
  806. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> Retard de croissance staturo-pondérale
    n1=en:microcephaly-capillary malformation syndrome | n2=Retard de croissance staturo-pondérale | rel=r_associated | relid=0 | w=20
  807. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> retard mental, retard de croissance, surdité, microgénitalisme lié au sexe
    n1=en:microcephaly-capillary malformation syndrome | n2=retard mental, retard de croissance, surdité, microgénitalisme lié au sexe | rel=r_associated | relid=0 | w=20
  808. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> rétention des chylomicrons (maladie de la)
    n1=en:microcephaly-capillary malformation syndrome | n2=rétention des chylomicrons (maladie de la) | rel=r_associated | relid=0 | w=20
  809. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> sclérodermie tubéreuse de bourneville
    n1=en:microcephaly-capillary malformation syndrome | n2=sclérodermie tubéreuse de bourneville | rel=r_associated | relid=0 | w=20
  810. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> sclérose tubéreuse du cerveau
    n1=en:microcephaly-capillary malformation syndrome | n2=sclérose tubéreuse du cerveau | rel=r_associated | relid=0 | w=20
  811. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> semialdéhyde succinique-déshydrogénase (déficit en)
    n1=en:microcephaly-capillary malformation syndrome | n2=semialdéhyde succinique-déshydrogénase (déficit en) | rel=r_associated | relid=0 | w=20
  812. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> sénescence sans mention de psychose
    n1=en:microcephaly-capillary malformation syndrome | n2=sénescence sans mention de psychose | rel=r_associated | relid=0 | w=20
  813. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> sénilité
    n1=en:microcephaly-capillary malformation syndrome | n2=sénilité | rel=r_associated | relid=0 | w=20
  814. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> sirop d'érable (urine à odeur de)
    n1=en:microcephaly-capillary malformation syndrome | n2=sirop d'érable (urine à odeur de) | rel=r_associated | relid=0 | w=20
  815. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> Sotos (syndrome de)
    n1=en:microcephaly-capillary malformation syndrome | n2=Sotos (syndrome de) | rel=r_associated | relid=0 | w=20
  816. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> syndrome de douleur extrême paroxystique
    n1=en:microcephaly-capillary malformation syndrome | n2=syndrome de douleur extrême paroxystique | rel=r_associated | relid=0 | w=20
  817. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> syndrome de dubin-johnson
    n1=en:microcephaly-capillary malformation syndrome | n2=syndrome de dubin-johnson | rel=r_associated | relid=0 | w=20
  818. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Dubin-Johnson
    n1=en:microcephaly-capillary malformation syndrome | n2=syndrome de Dubin-Johnson | rel=r_associated | relid=0 | w=20
  819. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> syndrome de glissement
    n1=en:microcephaly-capillary malformation syndrome | n2=syndrome de glissement | rel=r_associated | relid=0 | w=20
  820. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Laurence-Moon
    n1=en:microcephaly-capillary malformation syndrome | n2=syndrome de Laurence-Moon | rel=r_associated | relid=0 | w=20
  821. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> syndrome de soto
    n1=en:microcephaly-capillary malformation syndrome | n2=syndrome de soto | rel=r_associated | relid=0 | w=20
  822. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Sotos
    n1=en:microcephaly-capillary malformation syndrome | n2=syndrome de Sotos | rel=r_associated | relid=0 | w=20
  823. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> syndrome de sotos
    n1=en:microcephaly-capillary malformation syndrome | n2=syndrome de sotos | rel=r_associated | relid=0 | w=20
  824. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> syndrome de synostose spondylo-carpo-tarsale
    n1=en:microcephaly-capillary malformation syndrome | n2=syndrome de synostose spondylo-carpo-tarsale | rel=r_associated | relid=0 | w=20
  825. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Treft-Sanborn-Carey
    n1=en:microcephaly-capillary malformation syndrome | n2=syndrome de Treft-Sanborn-Carey | rel=r_associated | relid=0 | w=20
  826. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Zellweger
    n1=en:microcephaly-capillary malformation syndrome | n2=syndrome de Zellweger | rel=r_associated | relid=0 | w=20
  827. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> syndrome du retard de développement
    n1=en:microcephaly-capillary malformation syndrome | n2=syndrome du retard de développement | rel=r_associated | relid=0 | w=20
  828. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> tare congénitale
    n1=en:microcephaly-capillary malformation syndrome | n2=tare congénitale | rel=r_associated | relid=0 | w=20
  829. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> télécanthus
    n1=en:microcephaly-capillary malformation syndrome | n2=télécanthus | rel=r_associated | relid=0 | w=20
  830. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> télécanthus-hypertélorisme-strabisme (syndrome)
    n1=en:microcephaly-capillary malformation syndrome | n2=télécanthus-hypertélorisme-strabisme (syndrome) | rel=r_associated | relid=0 | w=20
  831. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> trouble psychotique sénile non précisé
    n1=en:microcephaly-capillary malformation syndrome | n2=trouble psychotique sénile non précisé | rel=r_associated | relid=0 | w=20
  832. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> une anomalie congénitale
    n1=en:microcephaly-capillary malformation syndrome | n2=une anomalie congénitale | rel=r_associated | relid=0 | w=20
  833. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> van Bogaert (xanthomatose cérébrotendineuse de)
    n1=en:microcephaly-capillary malformation syndrome | n2=van Bogaert (xanthomatose cérébrotendineuse de) | rel=r_associated | relid=0 | w=20
  834. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> vice de conformation
    n1=en:microcephaly-capillary malformation syndrome | n2=vice de conformation | rel=r_associated | relid=0 | w=20
  835. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> vieillesse sans mention de psychose
    n1=en:microcephaly-capillary malformation syndrome | n2=vieillesse sans mention de psychose | rel=r_associated | relid=0 | w=20
  836. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> Völker-Dieben (atrophie optique liée au sexe de)
    n1=en:microcephaly-capillary malformation syndrome | n2=Völker-Dieben (atrophie optique liée au sexe de) | rel=r_associated | relid=0 | w=20
  837. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> Walker-Warburg (syndrome de)
    n1=en:microcephaly-capillary malformation syndrome | n2=Walker-Warburg (syndrome de) | rel=r_associated | relid=0 | w=20
  838. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> Warburg
    n1=en:microcephaly-capillary malformation syndrome | n2=Warburg | rel=r_associated | relid=0 | w=20
  839. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> Went (atrophie optique liée au sexe de)
    n1=en:microcephaly-capillary malformation syndrome | n2=Went (atrophie optique liée au sexe de) | rel=r_associated | relid=0 | w=20
  840. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> Wolman (maladie de)
    n1=en:microcephaly-capillary malformation syndrome | n2=Wolman (maladie de) | rel=r_associated | relid=0 | w=20
  841. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> xanthique (lithiase)
    n1=en:microcephaly-capillary malformation syndrome | n2=xanthique (lithiase) | rel=r_associated | relid=0 | w=20
  842. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> xanthomatose cérébro-tendineuse
    n1=en:microcephaly-capillary malformation syndrome | n2=xanthomatose cérébro-tendineuse | rel=r_associated | relid=0 | w=20
  843. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> xanthomatose cérébrotendineuse
    n1=en:microcephaly-capillary malformation syndrome | n2=xanthomatose cérébrotendineuse | rel=r_associated | relid=0 | w=20
  844. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> xanthomatose cérébrotendineuse de Van Bogaert
    n1=en:microcephaly-capillary malformation syndrome | n2=xanthomatose cérébrotendineuse de Van Bogaert | rel=r_associated | relid=0 | w=20
  845. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> xeroderma pigmentosum
    n1=en:microcephaly-capillary malformation syndrome | n2=xeroderma pigmentosum | rel=r_associated | relid=0 | w=20
  846. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> Xeroderma pigmentosum
    n1=en:microcephaly-capillary malformation syndrome | n2=Xeroderma pigmentosum | rel=r_associated | relid=0 | w=20
  847. en:microcephaly-capillary malformation syndrome -- r_associated #0: 20 / 0.465 -> xérodermite pigmentaire
    n1=en:microcephaly-capillary malformation syndrome | n2=xérodermite pigmentaire | rel=r_associated | relid=0 | w=20
≈ 1196 relations entrantes

  1. en:maple syrup urine disease --- r_associated #0: 698 --> en:microcephaly-capillary malformation syndrome
    n1=en:maple syrup urine disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=698
  2. maladie du sirop d'érable --- r_associated #0: 604.37 --> en:microcephaly-capillary malformation syndrome
    n1=maladie du sirop d'érable | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=604.37
  3. leucinose --- r_associated #0: 599.18 --> en:microcephaly-capillary malformation syndrome
    n1=leucinose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=599.18
  4. en:branched-chain ketoaciduria --- r_associated #0: 520 --> en:microcephaly-capillary malformation syndrome
    n1=en:branched-chain ketoaciduria | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=520
  5. trouble psychotique sénile non précisé --- r_associated #0: 405 --> en:microcephaly-capillary malformation syndrome
    n1=trouble psychotique sénile non précisé | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=405
  6. asthénie sénile --- r_associated #0: 400 --> en:microcephaly-capillary malformation syndrome
    n1=asthénie sénile | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=400
  7. démence forme dépressive ou délirante --- r_associated #0: 400 --> en:microcephaly-capillary malformation syndrome
    n1=démence forme dépressive ou délirante | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=400
  8. démence sénile avec delirium ou état confusionnel aigu --- r_associated #0: 400 --> en:microcephaly-capillary malformation syndrome
    n1=démence sénile avec delirium ou état confusionnel aigu | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=400
  9. sénescence sans mention de psychose --- r_associated #0: 400 --> en:microcephaly-capillary malformation syndrome
    n1=sénescence sans mention de psychose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=400
  10. débilité sénile --- r_associated #0: 395 --> en:microcephaly-capillary malformation syndrome
    n1=débilité sénile | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=395
  11. psychose présénile --- r_associated #0: 395 --> en:microcephaly-capillary malformation syndrome
    n1=psychose présénile | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=395
  12. démence dégénérative primaire --- r_associated #0: 385 --> en:microcephaly-capillary malformation syndrome
    n1=démence dégénérative primaire | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=385
  13. psychose sénile --- r_associated #0: 373 --> en:microcephaly-capillary malformation syndrome
    n1=psychose sénile | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=373
  14. en:senile asthenia --- r_associated #0: 360 --> en:microcephaly-capillary malformation syndrome
    n1=en:senile asthenia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=360
  15. en:senility --- r_associated #0: 360 --> en:microcephaly-capillary malformation syndrome
    n1=en:senility | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=360
  16. en:unspecified senile psychotic condition --- r_associated #0: 360 --> en:microcephaly-capillary malformation syndrome
    n1=en:unspecified senile psychotic condition | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=360
  17. vieillesse sans mention de psychose --- r_associated #0: 360 --> en:microcephaly-capillary malformation syndrome
    n1=vieillesse sans mention de psychose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=360
  18. démence présénile --- r_associated #0: 351 --> en:microcephaly-capillary malformation syndrome
    n1=démence présénile | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=351
  19. en:age-related physical debility --- r_associated #0: 345 --> en:microcephaly-capillary malformation syndrome
    n1=en:age-related physical debility | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=345
  20. syndrome de glissement --- r_associated #0: 340 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome de glissement | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=340
  21. anomalie congénitale --- r_associated #0: 334 --> en:microcephaly-capillary malformation syndrome
    n1=anomalie congénitale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=334
  22. en:congenital abnormality --- r_associated #0: 333 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital abnormality | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=333
  23. démence sénile --- r_associated #0: 330 --> en:microcephaly-capillary malformation syndrome
    n1=démence sénile | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=330
  24. en:presenile dementia --- r_associated #0: 330 --> en:microcephaly-capillary malformation syndrome
    n1=en:presenile dementia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=330
  25. sénilité --- r_associated #0: 321 --> en:microcephaly-capillary malformation syndrome
    n1=sénilité | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=321
  26. malformation congénitale --- r_associated #0: 311 --> en:microcephaly-capillary malformation syndrome
    n1=malformation congénitale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=311
  27. en:congenital defect --- r_associated #0: 310 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital defect | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=310
  28. en:congenital anomaly --- r_associated #0: 309 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital anomaly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=309
  29. déformation congénitale --- r_associated #0: 286 --> en:microcephaly-capillary malformation syndrome
    n1=déformation congénitale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=286
  30. déficience congénitale --- r_associated #0: 275 --> en:microcephaly-capillary malformation syndrome
    n1=déficience congénitale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=275
  31. maladie des urines à l'odeur de sirop d'érable --- r_associated #0: 265 --> en:microcephaly-capillary malformation syndrome
    n1=maladie des urines à l'odeur de sirop d'érable | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=265
  32. en:classical maple syrup urine disease --- r_associated #0: 260 --> en:microcephaly-capillary malformation syndrome
    n1=en:classical maple syrup urine disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=260
  33. en:thiamin-responsive maple syrup urine disease --- r_associated #0: 260 --> en:microcephaly-capillary malformation syndrome
    n1=en:thiamin-responsive maple syrup urine disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=260
  34. maladie des urines avec odeur de sirop erable --- r_associated #0: 260 --> en:microcephaly-capillary malformation syndrome
    n1=maladie des urines avec odeur de sirop erable | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=260
  35. déficit en céto-acide décarboxylase --- r_associated #0: 255 --> en:microcephaly-capillary malformation syndrome
    n1=déficit en céto-acide décarboxylase | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=255
  36. en:sotos syndrome --- r_associated #0: 202 --> en:microcephaly-capillary malformation syndrome
    n1=en:sotos syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=202
  37. maladie congénitale --- r_associated #0: 202 --> en:microcephaly-capillary malformation syndrome
    n1=maladie congénitale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=202
  38. gigantisme cérébral --- r_associated #0: 201 --> en:microcephaly-capillary malformation syndrome
    n1=gigantisme cérébral | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=201
  39. en:infantile hypophosphatasia --- r_associated #0: 200 --> en:microcephaly-capillary malformation syndrome
    n1=en:infantile hypophosphatasia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=200
  40. syndrome de soto --- r_associated #0: 200 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome de soto | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=200
  41. hypophosphatasie foetale --- r_associated #0: 199 --> en:microcephaly-capillary malformation syndrome
    n1=hypophosphatasie foetale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=199
  42. hypophosphatasie infantile --- r_associated #0: 199 --> en:microcephaly-capillary malformation syndrome
    n1=hypophosphatasie infantile | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=199
  43. difformité congénitale --- r_associated #0: 195 --> en:microcephaly-capillary malformation syndrome
    n1=difformité congénitale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=195
  44. pathologie congénitale --- r_associated #0: 195 --> en:microcephaly-capillary malformation syndrome
    n1=pathologie congénitale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=195
  45. syndrome de Sotos --- r_associated #0: 195 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome de Sotos | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=195
  46. en:sotos' syndrome --- r_associated #0: 190 --> en:microcephaly-capillary malformation syndrome
    n1=en:sotos' syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=190
  47. Warburg --- r_associated #0: 181 --> en:microcephaly-capillary malformation syndrome
    n1=Warburg | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=181
  48. en:pyruvate carboxylase deficiency --- r_associated #0: 180 --> en:microcephaly-capillary malformation syndrome
    n1=en:pyruvate carboxylase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=180
  49. en:walker-warburg syndrome --- r_associated #0: 180 --> en:microcephaly-capillary malformation syndrome
    n1=en:walker-warburg syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=180
  50. déficit en pyruvate carboxylase --- r_associated #0: 178 --> en:microcephaly-capillary malformation syndrome
    n1=déficit en pyruvate carboxylase | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=178
  51. syndrome de Walker-Warburg --- r_associated #0: 178 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome de Walker-Warburg | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=178
  52. en:xeroderma pigmentosum --- r_associated #0: 177 --> en:microcephaly-capillary malformation syndrome
    n1=en:xeroderma pigmentosum | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=177
  53. xeroderma pigmentosum --- r_associated #0: 173 --> en:microcephaly-capillary malformation syndrome
    n1=xeroderma pigmentosum | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=173
  54. en:zellweger syndrome --- r_associated #0: 172 --> en:microcephaly-capillary malformation syndrome
    n1=en:zellweger syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=172
  55. en:Zellweger syndrome --- r_associated #0: 170 --> en:microcephaly-capillary malformation syndrome
    n1=en:Zellweger syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=170
  56. en:wolman disease --- r_associated #0: 155 --> en:microcephaly-capillary malformation syndrome
    n1=en:wolman disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=155
  57. hyperoxalurie primaire --- r_associated #0: 151 --> en:microcephaly-capillary malformation syndrome
    n1=hyperoxalurie primaire | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=151
  58. maladie de Wolman --- r_associated #0: 151 --> en:microcephaly-capillary malformation syndrome
    n1=maladie de Wolman | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=151
  59. oxaloses --- r_associated #0: 151 --> en:microcephaly-capillary malformation syndrome
    n1=oxaloses | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=151
  60. hyperoxalurie primitive --- r_associated #0: 150 --> en:microcephaly-capillary malformation syndrome
    n1=hyperoxalurie primitive | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=150
  61. en:primary hyperoxaluria --- r_associated #0: 149 --> en:microcephaly-capillary malformation syndrome
    n1=en:primary hyperoxaluria | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=149
  62. oxalose primitive --- r_associated #0: 146 --> en:microcephaly-capillary malformation syndrome
    n1=oxalose primitive | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=146
  63. retard de croissance staturo-pondérale --- r_associated #0: 141 --> en:microcephaly-capillary malformation syndrome
    n1=retard de croissance staturo-pondérale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=141
  64. en:pediatric failure to thrive --- r_associated #0: 140 --> en:microcephaly-capillary malformation syndrome
    n1=en:pediatric failure to thrive | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=140
  65. oxalose --- r_associated #0: 140 --> en:microcephaly-capillary malformation syndrome
    n1=oxalose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=140
  66. Retard de croissance staturo-pondérale --- r_associated #0: 135 --> en:microcephaly-capillary malformation syndrome
    n1=Retard de croissance staturo-pondérale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=135
  67. absence de croissance --- r_associated #0: 135 --> en:microcephaly-capillary malformation syndrome
    n1=absence de croissance | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=135
  68. syndrome du retard de développement --- r_associated #0: 135 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome du retard de développement | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=135
  69. en:congenital malformation --- r_associated #0: 130 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital malformation | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=130
  70. en:birth defect --- r_associated #0: 120 --> en:microcephaly-capillary malformation syndrome
    n1=en:birth defect | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=120
  71. en:cytochrome-c oxidase deficiency --- r_associated #0: 120 --> en:microcephaly-capillary malformation syndrome
    n1=en:cytochrome-c oxidase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=120
  72. déficit en cytochrome oxydase --- r_associated #0: 116 --> en:microcephaly-capillary malformation syndrome
    n1=déficit en cytochrome oxydase | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=116
  73. démence frontotemporale --- r_associated #0: 115 --> en:microcephaly-capillary malformation syndrome
    n1=démence frontotemporale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=115
  74. démence fronto-temporale --- r_associated #0: 113 --> en:microcephaly-capillary malformation syndrome
    n1=démence fronto-temporale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=113
  75. ptosis --- r_associated #0: 110 --> en:microcephaly-capillary malformation syndrome
    n1=ptosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=110
  76. en:ptosis --- r_associated #0: 109 --> en:microcephaly-capillary malformation syndrome
    n1=en:ptosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=109
  77. en:frontotemporal dementia --- r_associated #0: 100 --> en:microcephaly-capillary malformation syndrome
    n1=en:frontotemporal dementia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=100
  78. hypertélorisme --- r_associated #0: 96 --> en:microcephaly-capillary malformation syndrome
    n1=hypertélorisme | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=96
  79. déficit en cytochrome-c oxydase --- r_associated #0: 95 --> en:microcephaly-capillary malformation syndrome
    n1=déficit en cytochrome-c oxydase | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=95
  80. hyperplasie congénitale des surrénales --- r_associated #0: 95 --> en:microcephaly-capillary malformation syndrome
    n1=hyperplasie congénitale des surrénales | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=95
  81. en:congenital adrenal hyperplasia --- r_associated #0: 94 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital adrenal hyperplasia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=94
  82. en:hypertelorism --- r_associated #0: 92 --> en:microcephaly-capillary malformation syndrome
    n1=en:hypertelorism | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=92
  83. en:hypotonia --- r_associated #0: 86 --> en:microcephaly-capillary malformation syndrome
    n1=en:hypotonia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=86
  84. hypotonie --- r_associated #0: 85 --> en:microcephaly-capillary malformation syndrome
    n1=hypotonie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=85
  85. tare congénitale --- r_associated #0: 85 --> en:microcephaly-capillary malformation syndrome
    n1=tare congénitale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=85
  86. ptose --- r_associated #0: 70 --> en:microcephaly-capillary malformation syndrome
    n1=ptose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=70
  87. retard de croissance --- r_associated #0: 70 --> en:microcephaly-capillary malformation syndrome
    n1=retard de croissance | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=70
  88. congénitale --- r_associated #0: 64 --> en:microcephaly-capillary malformation syndrome
    n1=congénitale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=64
  89. en:congenital --- r_associated #0: 64 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=64
  90. en:dubin-johnson syndrome --- r_associated #0: 64 --> en:microcephaly-capillary malformation syndrome
    n1=en:dubin-johnson syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=64
  91. en:niemann-pick disease --- r_associated #0: 63 --> en:microcephaly-capillary malformation syndrome
    n1=en:niemann-pick disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=63
  92. en:i-cell disease --- r_associated #0: 62 --> en:microcephaly-capillary malformation syndrome
    n1=en:i-cell disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=62
  93. congenital --- r_associated #0: 61 --> en:microcephaly-capillary malformation syndrome
    n1=congenital | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=61
  94. en:I-cell disease --- r_associated #0: 61 --> en:microcephaly-capillary malformation syndrome
    n1=en:I-cell disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=61
  95. en:Niemann-Pick disease --- r_associated #0: 61 --> en:microcephaly-capillary malformation syndrome
    n1=en:Niemann-Pick disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=61
  96. persistance du foramen ovale --- r_associated #0: 61 --> en:microcephaly-capillary malformation syndrome
    n1=persistance du foramen ovale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=61
  97. Went (atrophie optique liée au sexe de) --- r_associated #0: 60 --> en:microcephaly-capillary malformation syndrome
    n1=Went (atrophie optique liée au sexe de) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=60
  98. en:Sotos' syndrome --- r_associated #0: 60 --> en:microcephaly-capillary malformation syndrome
    n1=en:Sotos' syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=60
  99. syndrome de dubin-johnson --- r_associated #0: 60 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome de dubin-johnson | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=60
  100. en:patent foramen ovale --- r_associated #0: 58 --> en:microcephaly-capillary malformation syndrome
    n1=en:patent foramen ovale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=58
  101. ptôse --- r_associated #0: 58 --> en:microcephaly-capillary malformation syndrome
    n1=ptôse | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=58
  102. en:mucopolysaccharidosis type i --- r_associated #0: 57 --> en:microcephaly-capillary malformation syndrome
    n1=en:mucopolysaccharidosis type i | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=57
  103. en:optic atrophy --- r_associated #0: 56 --> en:microcephaly-capillary malformation syndrome
    n1=en:optic atrophy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=56
  104. Völker-Dieben (atrophie optique liée au sexe de) --- r_associated #0: 55 --> en:microcephaly-capillary malformation syndrome
    n1=Völker-Dieben (atrophie optique liée au sexe de) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=55
  105. Xeroderma pigmentosum --- r_associated #0: 55 --> en:microcephaly-capillary malformation syndrome
    n1=Xeroderma pigmentosum | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=55
  106. congénital --- r_associated #0: 55 --> en:microcephaly-capillary malformation syndrome
    n1=congénital | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=55
  107. en:mucopolysaccharidosis i --- r_associated #0: 55 --> en:microcephaly-capillary malformation syndrome
    n1=en:mucopolysaccharidosis i | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=55
  108. vice de conformation --- r_associated #0: 55 --> en:microcephaly-capillary malformation syndrome
    n1=vice de conformation | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=55
  109. en:X-linked --- r_associated #0: 54 --> en:microcephaly-capillary malformation syndrome
    n1=en:X-linked | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=54
  110. anomalie du septum auriculaire --- r_associated #0: 53 --> en:microcephaly-capillary malformation syndrome
    n1=anomalie du septum auriculaire | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=53
  111. en:atrial septal defect --- r_associated #0: 53 --> en:microcephaly-capillary malformation syndrome
    n1=en:atrial septal defect | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=53
  112. xanthomatose cérébro-tendineuse --- r_associated #0: 51 --> en:microcephaly-capillary malformation syndrome
    n1=xanthomatose cérébro-tendineuse | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=51
  113. xanthomatose cérébrotendineuse --- r_associated #0: 51 --> en:microcephaly-capillary malformation syndrome
    n1=xanthomatose cérébrotendineuse | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=51
  114. en:Wolman's disease --- r_associated #0: 50 --> en:microcephaly-capillary malformation syndrome
    n1=en:Wolman's disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=50
  115. kératocône postérieur-fente labiale-petite taille --- r_associated #0: 50 --> en:microcephaly-capillary malformation syndrome
    n1=kératocône postérieur-fente labiale-petite taille | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=50
  116. xanthomatose cérébrotendineuse de Van Bogaert --- r_associated #0: 50 --> en:microcephaly-capillary malformation syndrome
    n1=xanthomatose cérébrotendineuse de Van Bogaert | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=50
  117. xérodermite pigmentaire --- r_associated #0: 50 --> en:microcephaly-capillary malformation syndrome
    n1=xérodermite pigmentaire | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=50
  118. atrophie optique liée au sexe --- r_associated #0: 49 --> en:microcephaly-capillary malformation syndrome
    n1=atrophie optique liée au sexe | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=49
  119. fente labiopalatine et blépharophimosis --- r_associated #0: 49 --> en:microcephaly-capillary malformation syndrome
    n1=fente labiopalatine et blépharophimosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=49
  120. syndrome de sotos --- r_associated #0: 49 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome de sotos | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=49
  121. atrophie optique liée au sexe de Völker-Dieben --- r_associated #0: 48 --> en:microcephaly-capillary malformation syndrome
    n1=atrophie optique liée au sexe de Völker-Dieben | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=48
  122. en:cerebrotendinous xanthomatosis --- r_associated #0: 48 --> en:microcephaly-capillary malformation syndrome
    n1=en:cerebrotendinous xanthomatosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=48
  123. en:keratoconus posticus --- r_associated #0: 48 --> en:microcephaly-capillary malformation syndrome
    n1=en:keratoconus posticus | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=48
  124. syndrome de Treft-Sanborn-Carey --- r_associated #0: 48 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome de Treft-Sanborn-Carey | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=48
  125. hypotonie, obésité et incisives proéminentes --- r_associated #0: 47 --> en:microcephaly-capillary malformation syndrome
    n1=hypotonie, obésité et incisives proéminentes | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=47
  126. maladie de wolman --- r_associated #0: 47 --> en:microcephaly-capillary malformation syndrome
    n1=maladie de wolman | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=47
  127. Recklinghausen (neurofibromatose de) --- r_associated #0: 46 --> en:microcephaly-capillary malformation syndrome
    n1=Recklinghausen (neurofibromatose de) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=46
  128. en:major physical defect --- r_associated #0: 46 --> en:microcephaly-capillary malformation syndrome
    n1=en:major physical defect | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=46
  129. foramen ovale perméable --- r_associated #0: 46 --> en:microcephaly-capillary malformation syndrome
    n1=foramen ovale perméable | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=46
  130. hypotonie musculaire --- r_associated #0: 46 --> en:microcephaly-capillary malformation syndrome
    n1=hypotonie musculaire | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=46
  131. hérédité autosomale récessive --- r_associated #0: 46 --> en:microcephaly-capillary malformation syndrome
    n1=hérédité autosomale récessive | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=46
  132. syndrome de Dubin-Johnson --- r_associated #0: 46 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome de Dubin-Johnson | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=46
  133. démence (sémiologie) --- r_associated #0: 45 --> en:microcephaly-capillary malformation syndrome
    n1=démence (sémiologie) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=45
  134. en:cleft lip --- r_associated #0: 45 --> en:microcephaly-capillary malformation syndrome
    n1=en:cleft lip | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=45
  135. en:neurofibromatosis --- r_associated #0: 45 --> en:microcephaly-capillary malformation syndrome
    n1=en:neurofibromatosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=45
  136. hypertélorisme-microtie-fente faciale --- r_associated #0: 45 --> en:microcephaly-capillary malformation syndrome
    n1=hypertélorisme-microtie-fente faciale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=45
  137. intolérance au fructose --- r_associated #0: 45 --> en:microcephaly-capillary malformation syndrome
    n1=intolérance au fructose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=45
  138. mucolipidose type II --- r_associated #0: 45 --> en:microcephaly-capillary malformation syndrome
    n1=mucolipidose type II | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=45
  139. mucolipidose type ii --- r_associated #0: 45 --> en:microcephaly-capillary malformation syndrome
    n1=mucolipidose type ii | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=45
  140. myopathie multicore avec retard mental, petite taille et hypogonadisme hypogonadotrophique --- r_associated #0: 45 --> en:microcephaly-capillary malformation syndrome
    n1=myopathie multicore avec retard mental, petite taille et hypogonadisme hypogonadotrophique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=45
  141. en:autosomal recessive inheritance --- r_associated #0: 44 --> en:microcephaly-capillary malformation syndrome
    n1=en:autosomal recessive inheritance | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=44
  142. en:hereditary fructose intolerance --- r_associated #0: 44 --> en:microcephaly-capillary malformation syndrome
    n1=en:hereditary fructose intolerance | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=44
  143. en:physical defect --- r_associated #0: 44 --> en:microcephaly-capillary malformation syndrome
    n1=en:physical defect | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=44
  144. sirop d'érable (urine à odeur de) --- r_associated #0: 44 --> en:microcephaly-capillary malformation syndrome
    n1=sirop d'érable (urine à odeur de) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=44
  145. syndrome de synostose spondylo-carpo-tarsale --- r_associated #0: 44 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome de synostose spondylo-carpo-tarsale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=44
  146. télécanthus-hypertélorisme-strabisme (syndrome) --- r_associated #0: 44 --> en:microcephaly-capillary malformation syndrome
    n1=télécanthus-hypertélorisme-strabisme (syndrome) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=44
  147. van Bogaert (xanthomatose cérébrotendineuse de) --- r_associated #0: 44 --> en:microcephaly-capillary malformation syndrome
    n1=van Bogaert (xanthomatose cérébrotendineuse de) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=44
  148. déficit en semialdéhyde succinique-déshydrogénase --- r_associated #0: 43 --> en:microcephaly-capillary malformation syndrome
    n1=déficit en semialdéhyde succinique-déshydrogénase | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=43
  149. en:acrocallosal syndrome --- r_associated #0: 43 --> en:microcephaly-capillary malformation syndrome
    n1=en:acrocallosal syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=43
  150. en:cooper jabs syndrome --- r_associated #0: 43 --> en:microcephaly-capillary malformation syndrome
    n1=en:cooper jabs syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=43
  151. en:familial encephalopathy with neuroserpin inclusion bodies --- r_associated #0: 43 --> en:microcephaly-capillary malformation syndrome
    n1=en:familial encephalopathy with neuroserpin inclusion bodies | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=43
  152. en:insulin growth factor i deficiency --- r_associated #0: 43 --> en:microcephaly-capillary malformation syndrome
    n1=en:insulin growth factor i deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=43
  153. en:lethal larsen-like syndrome --- r_associated #0: 43 --> en:microcephaly-capillary malformation syndrome
    n1=en:lethal larsen-like syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=43
  154. en:waisman syndrome --- r_associated #0: 43 --> en:microcephaly-capillary malformation syndrome
    n1=en:waisman syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=43
  155. fente labiale --- r_associated #0: 43 --> en:microcephaly-capillary malformation syndrome
    n1=fente labiale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=43
  156. maladie de Roger --- r_associated #0: 43 --> en:microcephaly-capillary malformation syndrome
    n1=maladie de Roger | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=43
  157. déliquescence --- r_associated #0: 42 --> en:microcephaly-capillary malformation syndrome
    n1=déliquescence | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=42
  158. en:craniofacial ulnar renal syndrome --- r_associated #0: 42 --> en:microcephaly-capillary malformation syndrome
    n1=en:craniofacial ulnar renal syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=42
  159. en:deafness and myopia syndrome --- r_associated #0: 42 --> en:microcephaly-capillary malformation syndrome
    n1=en:deafness and myopia syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=42
  160. en:fatty acid hydroxylase-associated neurodegeneration --- r_associated #0: 42 --> en:microcephaly-capillary malformation syndrome
    n1=en:fatty acid hydroxylase-associated neurodegeneration | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=42
  161. en:type Völker-Dieben --- r_associated #0: 42 --> en:microcephaly-capillary malformation syndrome
    n1=en:type Völker-Dieben | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=42
  162. hypertélorisme, hypospadias, polysyndactylie (syndrome) --- r_associated #0: 42 --> en:microcephaly-capillary malformation syndrome
    n1=hypertélorisme, hypospadias, polysyndactylie (syndrome) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=42
  163. nystagmus lié au sexe --- r_associated #0: 42 --> en:microcephaly-capillary malformation syndrome
    n1=nystagmus lié au sexe | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=42
  164. syndrome de douleur extrême paroxystique --- r_associated #0: 42 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome de douleur extrême paroxystique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=42
  165. anomalie du développement --- r_associated #0: 41 --> en:microcephaly-capillary malformation syndrome
    n1=anomalie du développement | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=41
  166. déficience auditive --- r_associated #0: 41 --> en:microcephaly-capillary malformation syndrome
    n1=déficience auditive | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=41
  167. déficit en prolidase --- r_associated #0: 41 --> en:microcephaly-capillary malformation syndrome
    n1=déficit en prolidase | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=41
  168. en:autosomal recessive ocular albinism --- r_associated #0: 41 --> en:microcephaly-capillary malformation syndrome
    n1=en:autosomal recessive ocular albinism | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=41
  169. en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy --- r_associated #0: 41 --> en:microcephaly-capillary malformation syndrome
    n1=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=41
  170. en:chylomicron retention disease --- r_associated #0: 41 --> en:microcephaly-capillary malformation syndrome
    n1=en:chylomicron retention disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=41
  171. en:short stature --- r_associated #0: 41 --> en:microcephaly-capillary malformation syndrome
    n1=en:short stature | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=41
  172. en:sinus histiocytosis with massive lymphadenopathy --- r_associated #0: 41 --> en:microcephaly-capillary malformation syndrome
    n1=en:sinus histiocytosis with massive lymphadenopathy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=41
  173. en:succinic semialdehyde dehydrogenase deficiency --- r_associated #0: 41 --> en:microcephaly-capillary malformation syndrome
    n1=en:succinic semialdehyde dehydrogenase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=41
  174. en:teratosis --- r_associated #0: 41 --> en:microcephaly-capillary malformation syndrome
    n1=en:teratosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=41
  175. rétention des chylomicrons (maladie de la) --- r_associated #0: 41 --> en:microcephaly-capillary malformation syndrome
    n1=rétention des chylomicrons (maladie de la) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=41
  176. Walker-Warburg (syndrome de) --- r_associated #0: 40 --> en:microcephaly-capillary malformation syndrome
    n1=Walker-Warburg (syndrome de) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=40
  177. bec de lièvre --- r_associated #0: 40 --> en:microcephaly-capillary malformation syndrome
    n1=bec de lièvre | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=40
  178. en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia --- r_associated #0: 40 --> en:microcephaly-capillary malformation syndrome
    n1=en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=40
  179. en:autosomal recessive asexual dwarfism --- r_associated #0: 40 --> en:microcephaly-capillary malformation syndrome
    n1=en:autosomal recessive asexual dwarfism | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=40
  180. en:behrens baumann dust syndrome --- r_associated #0: 40 --> en:microcephaly-capillary malformation syndrome
    n1=en:behrens baumann dust syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=40
  181. en:deafness, congenital, with inner ear agenesis, microtia, and microdontia --- r_associated #0: 40 --> en:microcephaly-capillary malformation syndrome
    n1=en:deafness, congenital, with inner ear agenesis, microtia, and microdontia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=40
  182. en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related --- r_associated #0: 40 --> en:microcephaly-capillary malformation syndrome
    n1=en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=40
  183. en:generalized epilepsy and paroxysmal dyskinesia syndrome --- r_associated #0: 40 --> en:microcephaly-capillary malformation syndrome
    n1=en:generalized epilepsy and paroxysmal dyskinesia syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=40
  184. en:hereditary cerebral amyloid angiopathy, icelandic type --- r_associated #0: 40 --> en:microcephaly-capillary malformation syndrome
    n1=en:hereditary cerebral amyloid angiopathy, icelandic type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=40
  185. en:spondylocarpotarsal synostosis syndrome --- r_associated #0: 40 --> en:microcephaly-capillary malformation syndrome
    n1=en:spondylocarpotarsal synostosis syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=40
  186. en:type Went --- r_associated #0: 40 --> en:microcephaly-capillary malformation syndrome
    n1=en:type Went | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=40
  187. en:warsaw breakage syndrome --- r_associated #0: 40 --> en:microcephaly-capillary malformation syndrome
    n1=en:warsaw breakage syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=40
  188. hypertrophie du ventricule droit --- r_associated #0: 40 --> en:microcephaly-capillary malformation syndrome
    n1=hypertrophie du ventricule droit | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=40
  189. hypertrophie ventriculaire droite --- r_associated #0: 40 --> en:microcephaly-capillary malformation syndrome
    n1=hypertrophie ventriculaire droite | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=40
  190. hypertrophie ventricule droit --- r_associated #0: 40 --> en:microcephaly-capillary malformation syndrome
    n1=hypertrophie ventricule droit | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=40
  191. hypertrophies du ventricule droit --- r_associated #0: 40 --> en:microcephaly-capillary malformation syndrome
    n1=hypertrophies du ventricule droit | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=40
  192. hypothyroïdie (manifestations neuromusculaires dans l') --- r_associated #0: 40 --> en:microcephaly-capillary malformation syndrome
    n1=hypothyroïdie (manifestations neuromusculaires dans l') | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=40
  193. en:Soto's syndrome --- r_associated #0: 39 --> en:microcephaly-capillary malformation syndrome
    n1=en:Soto's syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=39
  194. en:development of small head that was not present at birth --- r_associated #0: 39 --> en:microcephaly-capillary malformation syndrome
    n1=en:development of small head that was not present at birth | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=39
  195. en:microcephalic primordial dwarfism toriello type --- r_associated #0: 39 --> en:microcephaly-capillary malformation syndrome
    n1=en:microcephalic primordial dwarfism toriello type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=39
  196. en:paroxysmal extreme pain disorder --- r_associated #0: 39 --> en:microcephaly-capillary malformation syndrome
    n1=en:paroxysmal extreme pain disorder | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=39
  197. en:pelizaeus merzbacher like disease --- r_associated #0: 39 --> en:microcephaly-capillary malformation syndrome
    n1=en:pelizaeus merzbacher like disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=39
  198. en:ventricular septal defect --- r_associated #0: 39 --> en:microcephaly-capillary malformation syndrome
    n1=en:ventricular septal defect | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=39
  199. neurofibromatose de Recklinghausen --- r_associated #0: 39 --> en:microcephaly-capillary malformation syndrome
    n1=neurofibromatose de Recklinghausen | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=39
  200. retard mental, retard de croissance, surdité, microgénitalisme lié au sexe --- r_associated #0: 39 --> en:microcephaly-capillary malformation syndrome
    n1=retard mental, retard de croissance, surdité, microgénitalisme lié au sexe | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=39
  201. en:microcephalic osteodysplastic dysplasia --- r_associated #0: 38 --> en:microcephaly-capillary malformation syndrome
    n1=en:microcephalic osteodysplastic dysplasia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=38
  202. en:muscle amp deaminase deficiency --- r_associated #0: 38 --> en:microcephaly-capillary malformation syndrome
    n1=en:muscle amp deaminase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=38
  203. en:nystagmus --- r_associated #0: 38 --> en:microcephaly-capillary malformation syndrome
    n1=en:nystagmus | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=38
  204. en:ophthalmoplegia --- r_associated #0: 38 --> en:microcephaly-capillary malformation syndrome
    n1=en:ophthalmoplegia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=38
  205. en:yemenite deaf-blind hypopigmentation syndrome --- r_associated #0: 38 --> en:microcephaly-capillary malformation syndrome
    n1=en:yemenite deaf-blind hypopigmentation syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=38
  206. paraplégie spastique avec atrophie optique et démence --- r_associated #0: 38 --> en:microcephaly-capillary malformation syndrome
    n1=paraplégie spastique avec atrophie optique et démence | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=38
  207. Kjer (atrophie optique de type) --- r_associated #0: 37 --> en:microcephaly-capillary malformation syndrome
    n1=Kjer (atrophie optique de type) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=37
  208. communication inter-auriculaire --- r_associated #0: 37 --> en:microcephaly-capillary malformation syndrome
    n1=communication inter-auriculaire | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=37
  209. dystrophie des cônes liée au sexe avec reflet rétinien jaune-vert --- r_associated #0: 37 --> en:microcephaly-capillary malformation syndrome
    n1=dystrophie des cônes liée au sexe avec reflet rétinien jaune-vert | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=37
  210. en:3-methylglutaconic aciduria type iv --- r_associated #0: 37 --> en:microcephaly-capillary malformation syndrome
    n1=en:3-methylglutaconic aciduria type iv | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=37
  211. en:cleft lip/palate-ectodermal dysplasia syndrome --- r_associated #0: 37 --> en:microcephaly-capillary malformation syndrome
    n1=en:cleft lip/palate-ectodermal dysplasia syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=37
  212. en:congenital disorder of glycosylation type 2e --- r_associated #0: 37 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital disorder of glycosylation type 2e | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=37
  213. en:hearing impairment --- r_associated #0: 37 --> en:microcephaly-capillary malformation syndrome
    n1=en:hearing impairment | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=37
  214. en:mousa al din al nassar syndrome --- r_associated #0: 37 --> en:microcephaly-capillary malformation syndrome
    n1=en:mousa al din al nassar syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=37
  215. en:prolidase deficiency --- r_associated #0: 37 --> en:microcephaly-capillary malformation syndrome
    n1=en:prolidase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=37
  216. en:senile dementia --- r_associated #0: 37 --> en:microcephaly-capillary malformation syndrome
    n1=en:senile dementia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=37
  217. en:von Recklinghausen's disease --- r_associated #0: 37 --> en:microcephaly-capillary malformation syndrome
    n1=en:von Recklinghausen's disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=37
  218. neuro-acanthocytose --- r_associated #0: 37 --> en:microcephaly-capillary malformation syndrome
    n1=neuro-acanthocytose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=37
  219. neurofibromatose de type périphérique --- r_associated #0: 37 --> en:microcephaly-capillary malformation syndrome
    n1=neurofibromatose de type périphérique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=37
  220. ophtalmoplégie, hypotonie, ataxie, hypoacousie et athétose --- r_associated #0: 37 --> en:microcephaly-capillary malformation syndrome
    n1=ophtalmoplégie, hypotonie, ataxie, hypoacousie et athétose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=37
  221. petite taille, hyperextensibilité, hernie et dépression oculaire --- r_associated #0: 37 --> en:microcephaly-capillary malformation syndrome
    n1=petite taille, hyperextensibilité, hernie et dépression oculaire | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=37
  222. Hypotonie musculaire --- r_associated #0: 36 --> en:microcephaly-capillary malformation syndrome
    n1=Hypotonie musculaire | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=36
  223. Sotos (syndrome de) --- r_associated #0: 36 --> en:microcephaly-capillary malformation syndrome
    n1=Sotos (syndrome de) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=36
  224. communication interauriculaire --- r_associated #0: 36 --> en:microcephaly-capillary malformation syndrome
    n1=communication interauriculaire | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=36
  225. en:familial renal iminoglycinuria --- r_associated #0: 36 --> en:microcephaly-capillary malformation syndrome
    n1=en:familial renal iminoglycinuria | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=36
  226. en:glycogen storage disease type x --- r_associated #0: 36 --> en:microcephaly-capillary malformation syndrome
    n1=en:glycogen storage disease type x | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=36
  227. en:harelip --- r_associated #0: 36 --> en:microcephaly-capillary malformation syndrome
    n1=en:harelip | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=36
  228. en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency --- r_associated #0: 36 --> en:microcephaly-capillary malformation syndrome
    n1=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=36
  229. en:neurodegeneration due to cerebral folate transport deficiency --- r_associated #0: 36 --> en:microcephaly-capillary malformation syndrome
    n1=en:neurodegeneration due to cerebral folate transport deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=36
  230. hvd --- r_associated #0: 36 --> en:microcephaly-capillary malformation syndrome
    n1=hvd | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=36
  231. Wolman (maladie de) --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=Wolman (maladie de) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  232. en:21-hydroxylase deficiency --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:21-hydroxylase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  233. en:beckwith-wiedemann syndrome --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:beckwith-wiedemann syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  234. en:behavioral variant of frontotemporal dementia --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:behavioral variant of frontotemporal dementia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  235. en:bestrophinopathy, autosomal recessive --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:bestrophinopathy, autosomal recessive | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  236. en:braddock syndrome --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:braddock syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  237. en:brain calcification rajab type --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:brain calcification rajab type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  238. en:brown-vialetto-van laere syndrome --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:brown-vialetto-van laere syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  239. en:capillary fragility abnormality --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:capillary fragility abnormality | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  240. en:cockayne syndrome --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:cockayne syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  241. en:cohen syndrome --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:cohen syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  242. en:combined malonic and methylmalonic aciduria --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:combined malonic and methylmalonic aciduria | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  243. en:congenital leptin deficiency --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital leptin deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  244. en:congenital microcephaly --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital microcephaly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  245. en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  246. en:crisponi syndrome --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:crisponi syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  247. en:cutis laxa, autosomal recessive --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:cutis laxa, autosomal recessive | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  248. en:deafness --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:deafness | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  249. en:ehlers-danlos syndrome, type vi --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:ehlers-danlos syndrome, type vi | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  250. en:fatal infantile lactic acidosis with methylmalonic aciduria --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:fatal infantile lactic acidosis with methylmalonic aciduria | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  251. en:glutathione synthetase deficiency --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:glutathione synthetase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  252. en:hereditary cerebellar atrophy --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:hereditary cerebellar atrophy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  253. en:holoprosencephaly with fetal akinesia-hypokinesia sequence --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:holoprosencephaly with fetal akinesia-hypokinesia sequence | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  254. en:hyperprolinemia type 2 --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:hyperprolinemia type 2 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  255. en:hypomagnesemia 1, intestinal --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:hypomagnesemia 1, intestinal | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  256. en:isolated hypoplasia of the right ventricle --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:isolated hypoplasia of the right ventricle | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  257. en:jankovic rivera syndrome --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:jankovic rivera syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  258. en:kuskokwim disease --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:kuskokwim disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  259. en:laurence-moon syndrome --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:laurence-moon syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  260. en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  261. en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  262. en:macdermot winter syndrome --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:macdermot winter syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  263. en:mannosidosis --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:mannosidosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  264. en:masa syndrome (disorder) --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:masa syndrome (disorder) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  265. en:microcephaly microcornea syndrome seemanova type --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:microcephaly microcornea syndrome seemanova type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  266. en:myopathy, early-onset, with fatal cardiomyopathy --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:myopathy, early-onset, with fatal cardiomyopathy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  267. en:najjar syndrome --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:najjar syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  268. en:neutral lipid storage disease with myopathy --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:neutral lipid storage disease with myopathy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  269. en:oculocerebral hypopigmentation syndrome type preus --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:oculocerebral hypopigmentation syndrome type preus | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  270. en:oculocutaneous albinism type 4 --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:oculocutaneous albinism type 4 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  271. en:ohdo syndrome, maat-kievit-brunner type --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:ohdo syndrome, maat-kievit-brunner type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  272. en:pituitary thyroid hormone resistance --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:pituitary thyroid hormone resistance | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  273. en:progressive microcephaly --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:progressive microcephaly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  274. en:right ventricular hypertrophy --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:right ventricular hypertrophy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  275. en:smith-mccort dysplasia --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:smith-mccort dysplasia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  276. en:spinocerebellar ataxia with epilepsy --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:spinocerebellar ataxia with epilepsy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  277. en:spinocerebellar ataxia, autosomal recessive 2 --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:spinocerebellar ataxia, autosomal recessive 2 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  278. en:spondyloepiphyseal dysplasia, omani type --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:spondyloepiphyseal dysplasia, omani type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  279. en:syndrome of apparent mineralocorticoid excess --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:syndrome of apparent mineralocorticoid excess | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  280. en:tyrosinemia type ii --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:tyrosinemia type ii | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  281. en:tyrosinemia, type iii --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:tyrosinemia, type iii | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  282. en:verloes bourguignon syndrome --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:verloes bourguignon syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  283. en:wide nose --- r_associated #0: 35 --> en:microcephaly-capillary malformation syndrome
    n1=en:wide nose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=35
  284. Bec de lièvre --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=Bec de lièvre | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  285. Maladie congénitale --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=Maladie congénitale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  286. dystonie dopasensible --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=dystonie dopasensible | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  287. en:2-hydroxyglutaric aciduria --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:2-hydroxyglutaric aciduria | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  288. en:allan-herndon-dudley syndrome --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:allan-herndon-dudley syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  289. en:arrhythmogenic right ventricular dysplasia --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:arrhythmogenic right ventricular dysplasia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  290. en:arterial tortuosity syndrome --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:arterial tortuosity syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  291. en:autosomal recessive spastic paraplegia type 39 --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:autosomal recessive spastic paraplegia type 39 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  292. en:benign autosomal dominant microcephaly --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:benign autosomal dominant microcephaly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  293. en:carbamoyl-phosphate synthetase i deficiency --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:carbamoyl-phosphate synthetase i deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  294. en:cerebellar ataxia, cayman type --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:cerebellar ataxia, cayman type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  295. en:cerebral gigantism --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:cerebral gigantism | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  296. en:childhood hypophosphatasia (disorder) --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:childhood hypophosphatasia (disorder) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  297. en:congenital cataract with ataxia and deafness syndrome --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital cataract with ataxia and deafness syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  298. en:congenital disorder of glycosylation type 1h --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital disorder of glycosylation type 1h | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  299. en:congenital disorder of glycosylation type id --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital disorder of glycosylation type id | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  300. en:congenital transferrin deficiency --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital transferrin deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  301. en:deficiency of glucosyltransferase 1 --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:deficiency of glucosyltransferase 1 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  302. en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  303. en:dicarboxylicaminoaciduria --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:dicarboxylicaminoaciduria | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  304. en:ectodermal dysplasia with blindness syndrome --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:ectodermal dysplasia with blindness syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  305. en:ehlers-danlos syndrome kyphoscoliotic and deafness type --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:ehlers-danlos syndrome kyphoscoliotic and deafness type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  306. en:familial hypoaldosteronism --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:familial hypoaldosteronism | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  307. en:fryns macrocephaly --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:fryns macrocephaly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  308. en:hereditary dysplasia of blood vessel --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:hereditary dysplasia of blood vessel | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  309. en:histidinemia --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:histidinemia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  310. en:hypomandibular faciocranial dysostosis --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:hypomandibular faciocranial dysostosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  311. en:isolated hyperchlorhidrosis --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:isolated hyperchlorhidrosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  312. en:laron syndrome --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:laron syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  313. en:late-onset junctional epidermolysis bullosa --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:late-onset junctional epidermolysis bullosa | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  314. en:lethal congenital contracture syndrome 2 --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:lethal congenital contracture syndrome 2 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  315. en:lissencephaly type 3 familial fetal akinesia sequence syndrome --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  316. en:mitochondrial neurogastrointestinal encephalomyopathy syndrome --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  317. en:mowat-wilson syndrome --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:mowat-wilson syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  318. en:n-acetylglutamate synthase deficiency --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:n-acetylglutamate synthase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  319. en:nonaka myopathy --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:nonaka myopathy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  320. en:north american indian childhood cirrhosis --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:north american indian childhood cirrhosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  321. en:periventricular heterotopia, x-linked --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:periventricular heterotopia, x-linked | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  322. en:port-wine stain in rubinstein-taybi syndrome --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:port-wine stain in rubinstein-taybi syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  323. en:propionic acidemia --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:propionic acidemia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  324. en:skull hypoplasia --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:skull hypoplasia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  325. en:small for gestational age --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:small for gestational age | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  326. en:spondylo-ocular syndrome --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:spondylo-ocular syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  327. en:stambp, 1-bp del, 411c --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:stambp, 1-bp del, 411c | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  328. en:thomas syndrome --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:thomas syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  329. en:thyroid dyshormonogenesis 4 --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:thyroid dyshormonogenesis 4 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  330. en:waardenburg syndrome type 4 --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:waardenburg syndrome type 4 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  331. en:x-linked dystonia parkinsonism --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:x-linked dystonia parkinsonism | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  332. en:x-linked lissencephaly --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=en:x-linked lissencephaly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  333. nystagmus congénital isolé --- r_associated #0: 34 --> en:microcephaly-capillary malformation syndrome
    n1=nystagmus congénital isolé | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=34
  334. en:maple-tree syrup disease --- r_associated #0: 33 --> en:microcephaly-capillary malformation syndrome
    n1=en:maple-tree syrup disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=33
  335. en:neuroacanthocytosis --- r_associated #0: 33 --> en:microcephaly-capillary malformation syndrome
    n1=en:neuroacanthocytosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=33
  336. hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle --- r_associated #0: 33 --> en:microcephaly-capillary malformation syndrome
    n1=hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=33
  337. neurofibromatose de type VI --- r_associated #0: 33 --> en:microcephaly-capillary malformation syndrome
    n1=neurofibromatose de type VI | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=33
  338. Fenn (diagramme de) --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=Fenn (diagramme de) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  339. dysplasie craniodiaphysaire --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=dysplasie craniodiaphysaire | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  340. en:3-methylglutaconic aciduria type 3 --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:3-methylglutaconic aciduria type 3 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  341. en:aminomethyltransferase deficiency --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:aminomethyltransferase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  342. en:anemia, hypochromic microcytic, with iron overload --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:anemia, hypochromic microcytic, with iron overload | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  343. en:argininosuccinic aciduria --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:argininosuccinic aciduria | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  344. en:ataxia telangiectasia syndrome --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:ataxia telangiectasia syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  345. en:ataxia with vitamin e deficiency --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:ataxia with vitamin e deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  346. en:autosomal recessive primary microcephaly --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:autosomal recessive primary microcephaly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  347. en:cerebral lipidosis --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:cerebral lipidosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  348. en:congenital amegakaryocytic thrombocytopenia --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital amegakaryocytic thrombocytopenia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  349. en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  350. en:congenital disorder of glycosylation type ig --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital disorder of glycosylation type ig | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  351. en:congenital smallness --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital smallness | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  352. en:craniodiaphyseal dysplasia --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:craniodiaphyseal dysplasia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  353. en:cutaneous capillary malformation --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:cutaneous capillary malformation | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  354. en:cutaneous photosensitivity and lethal colitis syndrome --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:cutaneous photosensitivity and lethal colitis syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  355. en:familial acantholysis --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:familial acantholysis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  356. en:fucosidosis --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:fucosidosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  357. en:geniospasm 1 --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:geniospasm 1 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  358. en:glycine dehydrogenase (decarboxylating) deficiency --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:glycine dehydrogenase (decarboxylating) deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  359. en:glycogen storage disease type iib --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:glycogen storage disease type iib | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  360. en:gracile syndrome (disorder) --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:gracile syndrome (disorder) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  361. en:hereditary cystatin c amyloid angiopathy --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:hereditary cystatin c amyloid angiopathy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  362. en:hyperimmunoglobulin e syndrome --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:hyperimmunoglobulin e syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  363. en:lethal congenital contracture syndrome type 3 --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:lethal congenital contracture syndrome type 3 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  364. en:macular corneal dystrophy --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:macular corneal dystrophy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  365. en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  366. en:miller-mckusick-malvaux-syndrome (3m syndrome) --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:miller-mckusick-malvaux-syndrome (3m syndrome) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  367. en:myopathy with exercise intolerance, swedish type --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:myopathy with exercise intolerance, swedish type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  368. en:neonatal progeroid syndrome --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:neonatal progeroid syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  369. en:neurodegeneration with brain iron accumulation 4 --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:neurodegeneration with brain iron accumulation 4 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  370. en:port-wine stain associated with spinal dysraphism --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:port-wine stain associated with spinal dysraphism | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  371. en:segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  372. en:severe early childhood onset retinal dystrophy --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:severe early childhood onset retinal dystrophy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  373. en:sitosterolemia with xanthomatosis --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:sitosterolemia with xanthomatosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  374. en:sly syndrome --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:sly syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  375. en:stambp, ivs4ds, g-t, +5 --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:stambp, ivs4ds, g-t, +5 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  376. en:tubular renal disease with cardiomyopathy syndrome --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:tubular renal disease with cardiomyopathy syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  377. en:werdnig-hoffmann disease --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=en:werdnig-hoffmann disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  378. syndrome de Laurence-Moon --- r_associated #0: 32 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome de Laurence-Moon | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=32
  379. dystrophie des cônes liée au sexe --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=dystrophie des cônes liée au sexe | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  380. en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  381. en:al awadi syndrome --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:al awadi syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  382. en:arginine:glycine amidinotransferase deficiency --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:arginine:glycine amidinotransferase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  383. en:arterial dissection and lentiginosis syndrome --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:arterial dissection and lentiginosis syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  384. en:baller-gerold syndrome --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:baller-gerold syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  385. en:bowen-conradi syndrome --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:bowen-conradi syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  386. en:capillary malformation-arteriovenous malformation (disorder) --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:capillary malformation-arteriovenous malformation (disorder) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  387. en:cervical hypertrichosis and peripheral neuropathy syndrome --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:cervical hypertrichosis and peripheral neuropathy syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  388. en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  389. en:congenital analbuminemia --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital analbuminemia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  390. en:disorder of central nervous system due to xeroderma pigmentosum --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:disorder of central nervous system due to xeroderma pigmentosum | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  391. en:dopa-responsive dystonia --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:dopa-responsive dystonia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  392. en:ehlers-danlos syndrome vascular-like type --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:ehlers-danlos syndrome vascular-like type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  393. en:encephalopathy due to sulfite oxidase deficiency --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:encephalopathy due to sulfite oxidase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  394. en:epilepsy, myoclonic, benign adult familial, type 2 --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:epilepsy, myoclonic, benign adult familial, type 2 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  395. en:epiphyseal dysplasia, multiple, 4 --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:epiphyseal dysplasia, multiple, 4 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  396. en:frontotemporal dementia, chromosome 3-linked --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:frontotemporal dementia, chromosome 3-linked | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  397. en:gaze palsy, familial horizontal, with progressive scoliosis --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:gaze palsy, familial horizontal, with progressive scoliosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  398. en:geroderma osteodysplastica --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:geroderma osteodysplastica | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  399. en:hall riggs syndrome --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:hall riggs syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  400. en:heart defects limb shortening --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:heart defects limb shortening | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  401. en:hypophosphatasia infantile --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:hypophosphatasia infantile | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  402. en:infantile globoid cell leukodystrophy --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:infantile globoid cell leukodystrophy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  403. en:leucinosis --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:leucinosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  404. en:microcephaly deafness syndrome --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:microcephaly deafness syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  405. en:morquio syndrome --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:morquio syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  406. en:nathalie syndrome --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:nathalie syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  407. en:naxos disease --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:naxos disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  408. en:pancreatic triacylglycerol lipase deficiency --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:pancreatic triacylglycerol lipase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  409. en:peeling skin syndrome, acral type --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:peeling skin syndrome, acral type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  410. en:persistent mullerian duct syndrome --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:persistent mullerian duct syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  411. en:pili torti onychodysplasia syndrome --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:pili torti onychodysplasia syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  412. en:porencephaly --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:porencephaly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  413. en:port-wine stain with associated anomalies --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:port-wine stain with associated anomalies | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  414. en:presentey anomaly --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:presentey anomaly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  415. en:saito kuba tsuruta syndrome --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:saito kuba tsuruta syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  416. en:sonoda syndrome --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:sonoda syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  417. en:spastic ataxia, charlevoix-saguenay type --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:spastic ataxia, charlevoix-saguenay type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  418. en:telecanthus --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=en:telecanthus | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  419. fucosidose --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=fucosidose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  420. histidinémie --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=histidinémie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  421. histiocytose sinusale hémophagocytaire --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=histiocytose sinusale hémophagocytaire | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  422. maladie de Niemann-Pick --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=maladie de Niemann-Pick | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  423. migraine hémiplégique familiale --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=migraine hémiplégique familiale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  424. mucolipidose II --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=mucolipidose II | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  425. neurofibromatose --- r_associated #0: 31 --> en:microcephaly-capillary malformation syndrome
    n1=neurofibromatose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=31
  426. Maladie de Wolman --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=Maladie de Wolman | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  427. acrodermatite entéropathique --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=acrodermatite entéropathique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  428. atrophie optique polyneuropathie et surdité --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=atrophie optique polyneuropathie et surdité | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  429. atrophie optique, surdité, ophtalmoplégie et myopathie --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=atrophie optique, surdité, ophtalmoplégie et myopathie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  430. atrophie optique, surdité, épilepsie, spasticité et décès précoce --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=atrophie optique, surdité, épilepsie, spasticité et décès précoce | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  431. brachydactylie --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=brachydactylie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  432. bébé bronzé (syndrome du) --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=bébé bronzé (syndrome du) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  433. déficit congénital en mégacaryocytes --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=déficit congénital en mégacaryocytes | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  434. déficit en biotinidase --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=déficit en biotinidase | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  435. en:5 alpha steroid reductase 2 deficiency --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:5 alpha steroid reductase 2 deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  436. en:Dubin-Sprinz disease --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:Dubin-Sprinz disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  437. en:Tay-Sachs disease --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:Tay-Sachs disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  438. en:acrodermatitis enteropathica --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:acrodermatitis enteropathica | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  439. en:adducted thumbs and arthrogryposis syndrome christian type --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:adducted thumbs and arthrogryposis syndrome christian type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  440. en:alkaptonuria --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:alkaptonuria | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  441. en:allgrove syndrome --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:allgrove syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  442. en:alpha-1 antitrypsin deficiency --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:alpha-1 antitrypsin deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  443. en:anauxetic dysplasia --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:anauxetic dysplasia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  444. en:autosomal recessive scid --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:autosomal recessive scid | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  445. en:brachydactyly --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:brachydactyly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  446. en:capillary malformation are apparent at birth --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:capillary malformation are apparent at birth | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  447. en:capillary-venous malformation --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:capillary-venous malformation | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  448. en:cardiac anomaly and heterotaxy syndrome --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:cardiac anomaly and heterotaxy syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  449. en:cardiac glycogen phosphorylase kinase deficiency --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:cardiac glycogen phosphorylase kinase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  450. en:cardiomyopathy and renal anomaly syndrome --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:cardiomyopathy and renal anomaly syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  451. en:cerebellar ataxia ectodermal dysplasia --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:cerebellar ataxia ectodermal dysplasia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  452. en:cerebral cavernous malformation --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:cerebral cavernous malformation | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  453. en:childhood myocerebrohepatopathy spectrum --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:childhood myocerebrohepatopathy spectrum | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  454. en:chitty hall baraitser syndrome --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:chitty hall baraitser syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  455. en:choreoathetosis/spasticity, episodic --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:choreoathetosis/spasticity, episodic | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  456. en:cone-dystrophy --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:cone-dystrophy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  457. en:congenital disorder of glycosylation type ic --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital disorder of glycosylation type ic | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  458. en:congenital disorder of glycosylation type ie --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital disorder of glycosylation type ie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  459. en:congenital dyserythropoietic anemia, type ii --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital dyserythropoietic anemia, type ii | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  460. en:congenital porencephaly --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital porencephaly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  461. en:deafness, progressive, with stapes fixation --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:deafness, progressive, with stapes fixation | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  462. en:developmental fault --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:developmental fault | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  463. en:diaphragmatic hernia --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:diaphragmatic hernia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  464. en:dmd-associated dilated cardiomyopathy --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:dmd-associated dilated cardiomyopathy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  465. en:familial median cleft of upper and lower lip --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:familial median cleft of upper and lower lip | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  466. en:fatal familial insomnia --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:fatal familial insomnia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  467. en:fronto-facio-nasal dysplasia --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:fronto-facio-nasal dysplasia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  468. en:hereditary adrenal unresponsiveness to corticotropin --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:hereditary adrenal unresponsiveness to corticotropin | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  469. en:hereditary cutaneous vascular syndrome --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:hereditary cutaneous vascular syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  470. en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  471. en:hnsha due to diphosphoglycerate mutase deficiency --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:hnsha due to diphosphoglycerate mutase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  472. en:hnsha due to glucose phosphate isomerase deficiency --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:hnsha due to glucose phosphate isomerase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  473. en:hypermanganesemia with dystonia polycythemia and cirrhosis --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:hypermanganesemia with dystonia polycythemia and cirrhosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  474. en:hyperphosphatasia with mental retardation --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:hyperphosphatasia with mental retardation | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  475. en:hypomyelination and congenital cataract --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:hypomyelination and congenital cataract | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  476. en:insulin autoimmune syndrome --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:insulin autoimmune syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  477. en:isovaleric acidemia --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:isovaleric acidemia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  478. en:kallman syndrome with heart disease --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:kallman syndrome with heart disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  479. en:megalencephaly cutis marmorata telangiectatica congenita --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:megalencephaly cutis marmorata telangiectatica congenita | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  480. en:menkes disease --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:menkes disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  481. en:microcephaly, progressive (3 to 8 sd below the mean) --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:microcephaly, progressive (3 to 8 sd below the mean) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  482. en:microphthalmia, syndromic 8 --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:microphthalmia, syndromic 8 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  483. en:mitochondrial dna depletion syndrome 2 (myopathic type) --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:mitochondrial dna depletion syndrome 2 (myopathic type) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  484. en:non-polyposis turcot syndrome --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:non-polyposis turcot syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  485. en:odontohypophosphatasia (disorder) --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:odontohypophosphatasia (disorder) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  486. en:port wine stain --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:port wine stain | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  487. en:port-wine stain in proteus syndrome --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:port-wine stain in proteus syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  488. en:prader-willi habitus, osteopenia, and camptodactyly --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:prader-willi habitus, osteopenia, and camptodactyly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  489. en:primary immunodeficiency syndrome due to p14 deficiency --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  490. en:pyle metaphyseal dysplasia --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:pyle metaphyseal dysplasia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  491. en:reardon hall slaney syndrome --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:reardon hall slaney syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  492. en:retinitis punctata albescens (disorder) --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:retinitis punctata albescens (disorder) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  493. en:short nose --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:short nose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  494. en:short stature with valvular heart disease and characteristic facies syndrome --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:short stature with valvular heart disease and characteristic facies syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  495. en:simplified cortical gyral pattern --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:simplified cortical gyral pattern | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  496. en:spastic paraplegia 15, autosomal recessive --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:spastic paraplegia 15, autosomal recessive | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  497. en:spondyloenchondrodysplasia --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:spondyloenchondrodysplasia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  498. en:spondyloenchondrodysplasia with immune dysregulation --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:spondyloenchondrodysplasia with immune dysregulation | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  499. en:spondyloepiphyseal dysplasia tarda kohn type --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:spondyloepiphyseal dysplasia tarda kohn type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  500. en:stambp, phe100tyr --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:stambp, phe100tyr | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  501. en:sudden infant death with dysgenesis of the testes syndrome --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:sudden infant death with dysgenesis of the testes syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  502. en:tay-sachs disease --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:tay-sachs disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  503. en:tuberous sclerosis --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:tuberous sclerosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  504. en:von hippel-lindau syndrome --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=en:von hippel-lindau syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  505. maladie de Tay-Sachs --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=maladie de Tay-Sachs | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  506. maladie de Tay-sachs --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=maladie de Tay-sachs | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  507. maladie de dubin-johnson --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=maladie de dubin-johnson | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  508. maladie de tay-sachs --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=maladie de tay-sachs | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  509. neurofibromatose de recklinghausen --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=neurofibromatose de recklinghausen | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  510. nystagmus --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=nystagmus | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  511. sclérodermie tubéreuse de bourneville --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=sclérodermie tubéreuse de bourneville | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  512. sclérose tubéreuse du cerveau --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=sclérose tubéreuse du cerveau | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  513. tonus musculaire diminué --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=tonus musculaire diminué | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  514. télécanthus --- r_associated #0: 30 --> en:microcephaly-capillary malformation syndrome
    n1=télécanthus | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30
  515. atrophie optique --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=atrophie optique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  516. atrophie optique-paraplégie spastique --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=atrophie optique-paraplégie spastique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  517. cataracte liée au sexe avec dent de Hutchinson --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=cataracte liée au sexe avec dent de Hutchinson | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  518. en:3-methylglutaconic aciduria type 1 --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:3-methylglutaconic aciduria type 1 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  519. en:Leroy's i-cell disease --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:Leroy's i-cell disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  520. en:acid phosphatase deficiency --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:acid phosphatase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  521. en:albinotic fundus --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:albinotic fundus | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  522. en:amelogenesis imperfecta - recessive - rough --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:amelogenesis imperfecta - recessive - rough | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  523. en:argininemia --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:argininemia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  524. en:atrophoderma vermiculatum --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:atrophoderma vermiculatum | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  525. en:autosomal dominant idiopathic familial dystonia --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:autosomal dominant idiopathic familial dystonia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  526. en:autosomal recessive distal osteolysis syndrome --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:autosomal recessive distal osteolysis syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  527. en:autosomal recessive ichthyosis --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:autosomal recessive ichthyosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  528. en:bamforth syndrome --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:bamforth syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  529. en:brody myopathy --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:brody myopathy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  530. en:capillary malformations, small, multiple, diffuse --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:capillary malformations, small, multiple, diffuse | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  531. en:cerebral atrophy --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:cerebral atrophy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  532. en:congenital bowing of long bone --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital bowing of long bone | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  533. en:congenital dyserythropoietic anemia, type i --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital dyserythropoietic anemia, type i | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  534. en:congenital onset --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital onset | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  535. en:congenital pancreatic enterokinase deficiency --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital pancreatic enterokinase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  536. en:crigler-najjar syndrome --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:crigler-najjar syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  537. en:deafness, sensorineural, and male infertility --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:deafness, sensorineural, and male infertility | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  538. en:dentatorubral-pallidoluysian atrophy --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:dentatorubral-pallidoluysian atrophy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  539. en:dystonia 12 --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:dystonia 12 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  540. en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:east (epilepsy, ataxia, sensorineural deafness, and tubulopathy) syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  541. en:enterokinase deficiency --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:enterokinase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  542. en:epidermolysis bullosa simplex with pyloric atresia --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:epidermolysis bullosa simplex with pyloric atresia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  543. en:factor v and factor viii, combined deficiency of --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:factor v and factor viii, combined deficiency of | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  544. en:familial hemiplegic migraine --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:familial hemiplegic migraine | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  545. en:fibular hypoplasia and complex brachydactyly --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:fibular hypoplasia and complex brachydactyly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  546. en:fructose-1,6-bisphosphatase deficiency --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:fructose-1,6-bisphosphatase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  547. en:halal syndrome --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:halal syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  548. en:hereditary oculoleptomeningeal amyloid angiopathy --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  549. en:hereditary optic atrophy --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:hereditary optic atrophy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  550. en:hypokalemia, familial --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:hypokalemia, familial | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  551. en:hypophosphatemic rickets with hypercalciuria, hereditary --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:hypophosphatemic rickets with hypercalciuria, hereditary | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  552. en:isaacs syndrome --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:isaacs syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  553. en:jervell and lange nielsen syndrome --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:jervell and lange nielsen syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  554. en:lissencephaly, x-linked, 2 --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:lissencephaly, x-linked, 2 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  555. en:methylene thf reductase deficiency and homocystinuria --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:methylene thf reductase deficiency and homocystinuria | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  556. en:methylmalonyl-coenzyme a mutase deficiency --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:methylmalonyl-coenzyme a mutase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  557. en:microcephaly albinism digital anomalies syndrome --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:microcephaly albinism digital anomalies syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  558. en:microcephaly cervical spine fusion anomalies --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:microcephaly cervical spine fusion anomalies | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  559. en:multicentric osteolysis nodulosis arthropathy spectrum --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:multicentric osteolysis nodulosis arthropathy spectrum | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  560. en:netherton syndrome --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:netherton syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  561. en:northern epilepsy syndrome --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:northern epilepsy syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  562. en:oculocutaneous albinism type 6 --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:oculocutaneous albinism type 6 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  563. en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  564. en:papillon-lefevre syndrome --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:papillon-lefevre syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  565. en:pentosuria --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:pentosuria | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  566. en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  567. en:prickle1-related progressive myoclonus epilepsy with ataxia --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:prickle1-related progressive myoclonus epilepsy with ataxia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  568. en:pseudocholinesterase deficiency --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:pseudocholinesterase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  569. en:rna polymerase iii-related leukodystrophy --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:rna polymerase iii-related leukodystrophy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  570. en:schindler disease, type i --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:schindler disease, type i | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  571. en:secondary microcephaly --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:secondary microcephaly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  572. en:sloping forehead --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:sloping forehead | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  573. en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  574. en:stambp, arg424ter --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:stambp, arg424ter | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  575. en:stambp, glu42gly --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:stambp, glu42gly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  576. en:transthyretin related familial amyloid cardiomyopathy --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:transthyretin related familial amyloid cardiomyopathy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  577. en:trichohepatoenteric syndrome --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:trichohepatoenteric syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  578. en:wells jankovic syndrome --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:wells jankovic syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  579. en:xanthinuria, type i --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=en:xanthinuria, type i | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  580. hypoplasie crânienne --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=hypoplasie crânienne | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  581. insuffisance staturale --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=insuffisance staturale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  582. mucopolysaccharidose de type I --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=mucopolysaccharidose de type I | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  583. xanthique (lithiase) --- r_associated #0: 29 --> en:microcephaly-capillary malformation syndrome
    n1=xanthique (lithiase) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=29
  584. atrophie optique infantile avec chorée et paraplégie spastique --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=atrophie optique infantile avec chorée et paraplégie spastique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  585. blépharophimosis-ptosis-épicanthus inversus (syndrome) --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=blépharophimosis-ptosis-épicanthus inversus (syndrome) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  586. communication interventriculaire --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=communication interventriculaire | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  587. déficit en sulfite-oxydase --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=déficit en sulfite-oxydase | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  588. en:Mohr-Tranebjaerg syndrome --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:Mohr-Tranebjaerg syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  589. en:Nathalie syndrome --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:Nathalie syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  590. en:abnormal hair whorl --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:abnormal hair whorl | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  591. en:acrorenal mandibular syndrome --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:acrorenal mandibular syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  592. en:adenylosuccinate lyase deficiency (disorder) --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:adenylosuccinate lyase deficiency (disorder) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  593. en:amelogenesis imperfecta and gingival hyperplasia syndrome --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:amelogenesis imperfecta and gingival hyperplasia syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  594. en:aminoacylase 1 deficiency --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:aminoacylase 1 deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  595. en:and hypogonadotropic hypogonadism --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:and hypogonadotropic hypogonadism | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  596. en:and proeminent incisors --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:and proeminent incisors | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  597. en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  598. en:autoinflammation, lipodystrophy and dermatosis syndrome --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:autoinflammation, lipodystrophy and dermatosis syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  599. en:autosomal recessive idiopathic familial dystonia --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:autosomal recessive idiopathic familial dystonia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  600. en:autosomal recessive muscular dystrophy with limb girdle distribution --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:autosomal recessive muscular dystrophy with limb girdle distribution | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  601. en:autosomal recessive spastic paraplegia type 11 --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:autosomal recessive spastic paraplegia type 11 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  602. en:bardet-biedl syndrome --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:bardet-biedl syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  603. en:basal ganglia disease, biotin-responsive --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:basal ganglia disease, biotin-responsive | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  604. en:behr syndrome --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:behr syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  605. en:bothnia retinal dystrophy --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:bothnia retinal dystrophy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  606. en:chondrodysplasia punctata syndrome --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:chondrodysplasia punctata syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  607. en:desmosterolosis --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:desmosterolosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  608. en:episodic ataxia --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:episodic ataxia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  609. en:familial creutzfeldt-jakob --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:familial creutzfeldt-jakob | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  610. en:familial erythrocytosis due to diphosphoglycerate mutase deficiency --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:familial erythrocytosis due to diphosphoglycerate mutase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  611. en:foxg1 syndrome --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:foxg1 syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  612. en:hemolytic anemia due to pyruvate kinase deficiency --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:hemolytic anemia due to pyruvate kinase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  613. en:hereditary cerebellar degeneration --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:hereditary cerebellar degeneration | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  614. en:hereditary factor xii deficiency disease --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:hereditary factor xii deficiency disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  615. en:hereditary motor neuron disease --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:hereditary motor neuron disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  616. en:hereditary neuraxial edema --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:hereditary neuraxial edema | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  617. en:hmg-coa lyase deficiency --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:hmg-coa lyase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  618. en:hnsha due to aldolase a deficiency --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:hnsha due to aldolase a deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  619. en:hypoplasia of corpus callosum --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:hypoplasia of corpus callosum | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  620. en:interleukin-1 receptor-associated kinase 4 deficiency --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:interleukin-1 receptor-associated kinase 4 deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  621. en:kaufman-mckusick syndrome --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:kaufman-mckusick syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  622. en:leigh disease --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:leigh disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  623. en:manouvrier syndrome --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:manouvrier syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  624. en:megalencephalic leukoencephalopathy with subcortical cysts --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:megalencephalic leukoencephalopathy with subcortical cysts | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  625. en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  626. en:moderate steroid 21-hydroxylase deficiency --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:moderate steroid 21-hydroxylase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  627. en:moyamoya disease with early onset achalasia --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:moyamoya disease with early onset achalasia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  628. en:multiple sulfatase deficiency disease --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:multiple sulfatase deficiency disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  629. en:neu-laxova syndrome --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:neu-laxova syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  630. en:porphobilinogen synthase deficiency --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:porphobilinogen synthase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  631. en:prolonged electroretinal response suppression --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:prolonged electroretinal response suppression | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  632. en:renal dysplasia - limb defects syndrome --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:renal dysplasia - limb defects syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  633. en:robinow-like syndrome --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:robinow-like syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  634. en:sagging --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:sagging | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  635. en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  636. en:spastic tetraparesis --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:spastic tetraparesis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  637. en:stambp, arg178ter --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:stambp, arg178ter | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  638. en:tungland bellman syndrome --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:tungland bellman syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  639. en:type ii acrocephalopolysyndactyly --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:type ii acrocephalopolysyndactyly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  640. en:upper limb defect with eye and ear abnormalities syndrome --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:upper limb defect with eye and ear abnormalities syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  641. en:x-linked intellectual disability with ataxia and apraxia syndrome --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:x-linked intellectual disability with ataxia and apraxia syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  642. en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  643. malformation --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=malformation | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  644. syndrome de Zellweger --- r_associated #0: 28 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome de Zellweger | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=28
  645. atrophie optique infantile héréditaire compliquée de Behr --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=atrophie optique infantile héréditaire compliquée de Behr | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  646. en:3-methylglutaconic aciduria type 5 --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:3-methylglutaconic aciduria type 5 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  647. en:adenine phosphoribosyltransferase deficiency --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:adenine phosphoribosyltransferase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  648. en:alstrom syndrome --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:alstrom syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  649. en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  650. en:autosomal dominant focal dystonia dyt25 type --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:autosomal dominant focal dystonia dyt25 type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  651. en:biotinidase deficiency --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:biotinidase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  652. en:cerebral hemorrhage with amyloidosis, hereditary, dutch type --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:cerebral hemorrhage with amyloidosis, hereditary, dutch type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  653. en:citrin deficiency --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:citrin deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  654. en:congenital alpha-2-antiplasmin deficiency --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital alpha-2-antiplasmin deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  655. en:congenital nephrogenic diabetes insipidus --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital nephrogenic diabetes insipidus | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  656. en:congenital sucrase-isomaltase deficiency --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital sucrase-isomaltase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  657. en:cystathionine beta-synthase deficiency disease --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:cystathionine beta-synthase deficiency disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  658. en:cystinosis --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:cystinosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  659. en:developmental anomaly --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:developmental anomaly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  660. en:drooping eyelid --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:drooping eyelid | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  661. en:dyskeratosis congenita, autosomal recessive --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:dyskeratosis congenita, autosomal recessive | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  662. en:ectodermal dysplasia/ skin fragility syndrome --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:ectodermal dysplasia/ skin fragility syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  663. en:ethanolaminosis --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:ethanolaminosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  664. en:exomphalos --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:exomphalos | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  665. en:familial c3b inhibitor deficiency syndrome --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:familial c3b inhibitor deficiency syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  666. en:fatal congenital nonlysosomal heart glycogenosis --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:fatal congenital nonlysosomal heart glycogenosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  667. en:fountain syndrome --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:fountain syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  668. en:game friedman paradice syndrome --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:game friedman paradice syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  669. en:gamma-glutamyltransferase deficiency --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:gamma-glutamyltransferase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  670. en:gerstmann-straussler-scheinker disease --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:gerstmann-straussler-scheinker disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  671. en:glomuvenous malformations --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:glomuvenous malformations | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  672. en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  673. en:gurrieri sammito bellussi syndrome --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:gurrieri sammito bellussi syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  674. en:hereditary factor xi deficiency disease --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:hereditary factor xi deficiency disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  675. en:hereditary peripheral neuropathy --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:hereditary peripheral neuropathy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  676. en:hereditary spastic paralysis, infantile onset ascending --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:hereditary spastic paralysis, infantile onset ascending | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  677. en:hnsha due to glutathione reductase deficiency --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:hnsha due to glutathione reductase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  678. en:hnsha due to glutathione synthetase deficiency --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:hnsha due to glutathione synthetase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  679. en:hydrocephalus with cerebellar agenesis --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:hydrocephalus with cerebellar agenesis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  680. en:inherited metabolic disorder of nervous system --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:inherited metabolic disorder of nervous system | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  681. en:knobloch syndrome --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:knobloch syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  682. en:lactase deficiency, congenital --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:lactase deficiency, congenital | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  683. en:lethal congenital contracture syndrome 1 --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:lethal congenital contracture syndrome 1 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  684. en:lipoid proteinosis of urbach and wiethe --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:lipoid proteinosis of urbach and wiethe | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  685. en:lissencephaly syndrome, norman-roberts type --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:lissencephaly syndrome, norman-roberts type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  686. en:majeed syndrome --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:majeed syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  687. en:mandibuloacral dysplasia with type a lipodystrophy --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:mandibuloacral dysplasia with type a lipodystrophy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  688. en:melanoma astrocytoma syndrome --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:melanoma astrocytoma syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  689. en:methylcrotonyl-coa carboxylase deficiency --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:methylcrotonyl-coa carboxylase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  690. en:microcephaly, amish type (disorder) --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:microcephaly, amish type (disorder) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  691. en:mohr-tranebjaerg syndrome --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:mohr-tranebjaerg syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  692. en:moloney syndrome --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:moloney syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  693. en:multicore disease with mental retardation --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:multicore disease with mental retardation | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  694. en:multiple endocrine neoplasia type 1 --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:multiple endocrine neoplasia type 1 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  695. en:one patient was less severely affected --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:one patient was less severely affected | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  696. en:otoonychoperoneal syndrome --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:otoonychoperoneal syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  697. en:pituitary adenoma, familial isolated (disorder) --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:pituitary adenoma, familial isolated (disorder) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  698. en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  699. en:pontocerebellar hypoplasia type 2 --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:pontocerebellar hypoplasia type 2 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  700. en:pulmonary hypertension in neurofibromatosis --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:pulmonary hypertension in neurofibromatosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  701. en:rud syndrome --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:rud syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  702. en:sanfilippo syndrome --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:sanfilippo syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  703. en:sarcosinemia --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:sarcosinemia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  704. en:simpson golabi behmel syndrome type 1 --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:simpson golabi behmel syndrome type 1 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  705. en:spastic paraplegia --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:spastic paraplegia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  706. en:stambp, arg38cys --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:stambp, arg38cys | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  707. en:sting-associated vasculopathy with onset in infancy --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:sting-associated vasculopathy with onset in infancy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  708. en:type a 14 --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:type a 14 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  709. en:variable facial dysmorphic features --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:variable facial dysmorphic features | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  710. en:waardenburg anophthalmia syndrome --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:waardenburg anophthalmia syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  711. en:zellweger-like syndrome without peroxisomal anomaly --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=en:zellweger-like syndrome without peroxisomal anomaly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  712. microdélétion 5q35 --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=microdélétion 5q35 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  713. semialdéhyde succinique-déshydrogénase (déficit en) --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=semialdéhyde succinique-déshydrogénase (déficit en) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  714. une anomalie congénitale --- r_associated #0: 27 --> en:microcephaly-capillary malformation syndrome
    n1=une anomalie congénitale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=27
  715. Recklinghausen (maladie de von) --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=Recklinghausen (maladie de von) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  716. atrophie optique tardive liée au sexe --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=atrophie optique tardive liée au sexe | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  717. déficit en neuraminidase --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=déficit en neuraminidase | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  718. en:Dubin-Johnson's syndrome --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:Dubin-Johnson's syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  719. en:aicardi syndrome --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:aicardi syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  720. en:alpha, alpha-trehalase deficiency --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:alpha, alpha-trehalase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  721. en:alpha-methylacyl-coa racemase deficiency --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:alpha-methylacyl-coa racemase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  722. en:and myopathy --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:and myopathy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  723. en:aphalangy and syndactyly with microcephaly syndrome --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:aphalangy and syndactyly with microcephaly syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  724. en:arthrogryposis multiplex congenita, neurogenic type (disorder) --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:arthrogryposis multiplex congenita, neurogenic type (disorder) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  725. en:ateliotic dwarfism without insulinopenia --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:ateliotic dwarfism without insulinopenia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  726. en:autosomal recessive sideroblastic anemia --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:autosomal recessive sideroblastic anemia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  727. en:bietti crystalline corneoretinal dystrophy --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:bietti crystalline corneoretinal dystrophy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  728. en:cerebroretinal microangiopathy with calcifications and cysts (disorder) --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  729. en:charcot-marie-tooth disease type 4 --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:charcot-marie-tooth disease type 4 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  730. en:congenital cataracts, facial dysmorphism, and neuropathy --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital cataracts, facial dysmorphism, and neuropathy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  731. en:congenital disorder of glycosylation type ia --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital disorder of glycosylation type ia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  732. en:congenital disorder of glycosylation, type if --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital disorder of glycosylation, type if | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  733. en:congenital plasminogen activator inhibitor deficiency type 1 --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital plasminogen activator inhibitor deficiency type 1 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  734. en:corpus callosum agenesis neuronopathy --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:corpus callosum agenesis neuronopathy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  735. en:cryptophthalmos syndrome --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:cryptophthalmos syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  736. en:diaphanospondylodysostosis --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:diaphanospondylodysostosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  737. en:donnai-barrow syndrome --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:donnai-barrow syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  738. en:familial benign neonatal epilepsy --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:familial benign neonatal epilepsy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  739. en:folinic acid responsive seizure syndrome --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:folinic acid responsive seizure syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  740. en:generalized peeling skin syndrome --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:generalized peeling skin syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  741. en:giacci familial neurogenic acroosteolysis --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:giacci familial neurogenic acroosteolysis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  742. en:glucose transporter protein type 1 deficiency syndrome --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:glucose transporter protein type 1 deficiency syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  743. en:glutamate formiminotransferase deficiency --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:glutamate formiminotransferase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  744. en:glutamate-cysteine ligase deficiency --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:glutamate-cysteine ligase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  745. en:hereditary factor x deficiency disease --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:hereditary factor x deficiency disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  746. en:hereditary methemoglobinemia, enzymatic type --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:hereditary methemoglobinemia, enzymatic type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  747. en:hereditary palmoplantar keratoderma gamborg nielsen type --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:hereditary palmoplantar keratoderma gamborg nielsen type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  748. en:hereditary vascular fragility --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:hereditary vascular fragility | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  749. en:heritable pulmonary arterial hypertension due to bmpr2 mutation --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:heritable pulmonary arterial hypertension due to bmpr2 mutation | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  750. en:hyperprolinemia type 1 --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:hyperprolinemia type 1 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  751. en:hypoplasia of the maxilla --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:hypoplasia of the maxilla | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  752. en:hypospadias-mental retardation syndrome --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:hypospadias-mental retardation syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  753. en:juvenile amyotrophic lateral sclerosis --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:juvenile amyotrophic lateral sclerosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  754. en:leukotriene c4 synthase deficiency --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:leukotriene c4 synthase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  755. en:low set ears --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:low set ears | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  756. en:marles greenberg persaud syndrome --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:marles greenberg persaud syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  757. en:maroteaux-lamy syndrome --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:maroteaux-lamy syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  758. en:maternally inherited mitochondrial dystonia --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:maternally inherited mitochondrial dystonia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  759. en:medium-chain acyl-coa dehydrogenase deficiency --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:medium-chain acyl-coa dehydrogenase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  760. en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  761. en:microgyria --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:microgyria | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  762. en:morm syndrome --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:morm syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  763. en:neuraminidase deficiency --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:neuraminidase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  764. en:okihiro syndrome --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:okihiro syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  765. en:palate-blepharophimosis --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:palate-blepharophimosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  766. en:pelviscapular dysplasia --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:pelviscapular dysplasia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  767. en:phenylketonuria ii --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:phenylketonuria ii | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  768. en:pseudohypoaldosteronism, type 1, recessive form --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:pseudohypoaldosteronism, type 1, recessive form | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  769. en:pseudotrisomy 13 syndrome --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:pseudotrisomy 13 syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  770. en:purine-nucleoside phosphorylase deficiency --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:purine-nucleoside phosphorylase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  771. en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  772. en:rapadilino syndrome --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:rapadilino syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  773. en:renal tubulopathy with encephalopathy and liver failure syndrome --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:renal tubulopathy with encephalopathy and liver failure syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  774. en:richards-rundle syndrome --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:richards-rundle syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  775. en:schulman upshaw syndrome --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:schulman upshaw syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  776. en:spinal muscular atrophy with respiratory distress 1 --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:spinal muscular atrophy with respiratory distress 1 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  777. en:split-hand/foot malformation 3 --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:split-hand/foot malformation 3 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  778. en:spondyloepiphyseal dysplasia tarda, toledo type --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:spondyloepiphyseal dysplasia tarda, toledo type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  779. en:strabismus syndrome --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:strabismus syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  780. en:sulfite oxidase deficiency --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:sulfite oxidase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  781. en:timothy syndrome type 2 --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:timothy syndrome type 2 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  782. en:tmem70 related mitochondrial encephalo-cardio-myopathy --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:tmem70 related mitochondrial encephalo-cardio-myopathy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  783. en:transcobalamin ii deficiency --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:transcobalamin ii deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  784. en:urocanase deficiency --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:urocanase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  785. en:valinemia --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:valinemia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  786. en:variable cardiac defects --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:variable cardiac defects | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  787. en:x-linked intellectual disability with acromegaly and hyperactivity syndrome --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  788. en:zinc-deficiency type --- r_associated #0: 26 --> en:microcephaly-capillary malformation syndrome
    n1=en:zinc-deficiency type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=26
  789. Maladie de Tay-Sachs --- r_associated #0: 25 --> en:microcephaly-capillary malformation syndrome
    n1=Maladie de Tay-Sachs | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=25
  790. en:Laron syndrome --- r_associated #0: 25 --> en:microcephaly-capillary malformation syndrome
    n1=en:Laron syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=25
  791. en:Laurence-Moon's syndrome --- r_associated #0: 25 --> en:microcephaly-capillary malformation syndrome
    n1=en:Laurence-Moon's syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=25
  792. en:Rieger anomaly --- r_associated #0: 25 --> en:microcephaly-capillary malformation syndrome
    n1=en:Rieger anomaly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=25
  793. en:allanson pantzar mcleod syndrome --- r_associated #0: 25 --> en:microcephaly-capillary malformation syndrome
    n1=en:allanson pantzar mcleod syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=25
  794. en:deficiency of fructokinase --- r_associated #0: 25 --> en:microcephaly-capillary malformation syndrome
    n1=en:deficiency of fructokinase | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=25
  795. en:delayed myelination --- r_associated #0: 25 --> en:microcephaly-capillary malformation syndrome
    n1=en:delayed myelination | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=25
  796. en:ehlers-danlos syndrome, arthrochalasia type --- r_associated #0: 25 --> en:microcephaly-capillary malformation syndrome
    n1=en:ehlers-danlos syndrome, arthrochalasia type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=25
  797. en:fetal microcephaly --- r_associated #0: 25 --> en:microcephaly-capillary malformation syndrome
    n1=en:fetal microcephaly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=25
  798. en:hepatolenticular degeneration --- r_associated #0: 25 --> en:microcephaly-capillary malformation syndrome
    n1=en:hepatolenticular degeneration | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=25
  799. en:hnsha due to pyrimidine-5'-nucleotidase deficiency --- r_associated #0: 25 --> en:microcephaly-capillary malformation syndrome
    n1=en:hnsha due to pyrimidine-5'-nucleotidase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=25
  800. en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) --- r_associated #0: 25 --> en:microcephaly-capillary malformation syndrome
    n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=25
  801. kératocône posticus --- r_associated #0: 25 --> en:microcephaly-capillary malformation syndrome
    n1=kératocône posticus | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=25
  802. nystagmus héréditaire vertical --- r_associated #0: 25 --> en:microcephaly-capillary malformation syndrome
    n1=nystagmus héréditaire vertical | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=25
  803. acrodermatitis enteropathica --- r_associated #0: 24 --> en:microcephaly-capillary malformation syndrome
    n1=acrodermatitis enteropathica | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=24
  804. colobome de l'iris avec ptosis, hypertélorisme et retard mental --- r_associated #0: 24 --> en:microcephaly-capillary malformation syndrome
    n1=colobome de l'iris avec ptosis, hypertélorisme et retard mental | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=24
  805. cétoacidurie à chaînes ramifiées --- r_associated #0: 24 --> en:microcephaly-capillary malformation syndrome
    n1=cétoacidurie à chaînes ramifiées | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=24
  806. en:5-oxoprolinase deficiency --- r_associated #0: 24 --> en:microcephaly-capillary malformation syndrome
    n1=en:5-oxoprolinase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=24
  807. en:alpha-fetoprotein deficiency --- r_associated #0: 24 --> en:microcephaly-capillary malformation syndrome
    n1=en:alpha-fetoprotein deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=24
  808. en:andersen syndrome --- r_associated #0: 24 --> en:microcephaly-capillary malformation syndrome
    n1=en:andersen syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=24
  809. en:aspartylglycosaminuria --- r_associated #0: 24 --> en:microcephaly-capillary malformation syndrome
    n1=en:aspartylglycosaminuria | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=24
  810. en:dihydrouracil dehydrogenase deficiency --- r_associated #0: 24 --> en:microcephaly-capillary malformation syndrome
    n1=en:dihydrouracil dehydrogenase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=24
  811. en:ear, patella, short stature syndrome --- r_associated #0: 24 --> en:microcephaly-capillary malformation syndrome
    n1=en:ear, patella, short stature syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=24
  812. en:female restricted epilepsy with intellectual disability syndrome --- r_associated #0: 24 --> en:microcephaly-capillary malformation syndrome
    n1=en:female restricted epilepsy with intellectual disability syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=24
  813. en:hernia --- r_associated #0: 24 --> en:microcephaly-capillary malformation syndrome
    n1=en:hernia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=24
  814. en:histidinaemia --- r_associated #0: 24 --> en:microcephaly-capillary malformation syndrome
    n1=en:histidinaemia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=24
  815. en:hydromicrocephaly --- r_associated #0: 24 --> en:microcephaly-capillary malformation syndrome
    n1=en:hydromicrocephaly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=24
  816. en:intestinal epithelial dysplasia --- r_associated #0: 24 --> en:microcephaly-capillary malformation syndrome
    n1=en:intestinal epithelial dysplasia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=24
  817. en:kohlschutter tonz syndrome --- r_associated #0: 24 --> en:microcephaly-capillary malformation syndrome
    n1=en:kohlschutter tonz syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=24
  818. en:lipoprotein glomerulopathy --- r_associated #0: 24 --> en:microcephaly-capillary malformation syndrome
    n1=en:lipoprotein glomerulopathy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=24
  819. en:obesity --- r_associated #0: 24 --> en:microcephaly-capillary malformation syndrome
    n1=en:obesity | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=24
  820. en:tetra-amelia autosomal recessive --- r_associated #0: 24 --> en:microcephaly-capillary malformation syndrome
    n1=en:tetra-amelia autosomal recessive | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=24
  821. maladie de Recklinghausen --- r_associated #0: 24 --> en:microcephaly-capillary malformation syndrome
    n1=maladie de Recklinghausen | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=24
  822. atrophie optique congénitale ou infantile précoce --- r_associated #0: 23 --> en:microcephaly-capillary malformation syndrome
    n1=atrophie optique congénitale ou infantile précoce | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=23
  823. atrophie optique, cataracte, et troubles neurologiques --- r_associated #0: 23 --> en:microcephaly-capillary malformation syndrome
    n1=atrophie optique, cataracte, et troubles neurologiques | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=23
  824. en:angioma hereditary neurocutaneous --- r_associated #0: 23 --> en:microcephaly-capillary malformation syndrome
    n1=en:angioma hereditary neurocutaneous | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=23
  825. en:antley-bixler syndrome, autosomal dominant --- r_associated #0: 23 --> en:microcephaly-capillary malformation syndrome
    n1=en:antley-bixler syndrome, autosomal dominant | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=23
  826. en:beta-aminoisobutyricaciduria --- r_associated #0: 23 --> en:microcephaly-capillary malformation syndrome
    n1=en:beta-aminoisobutyricaciduria | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=23
  827. en:brachydactyly syndrome type b --- r_associated #0: 23 --> en:microcephaly-capillary malformation syndrome
    n1=en:brachydactyly syndrome type b | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=23
  828. en:cleft palate --- r_associated #0: 23 --> en:microcephaly-capillary malformation syndrome
    n1=en:cleft palate | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=23
  829. en:enlarged extraaxial space on brain imaging --- r_associated #0: 23 --> en:microcephaly-capillary malformation syndrome
    n1=en:enlarged extraaxial space on brain imaging | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=23
  830. en:joubert syndrome --- r_associated #0: 23 --> en:microcephaly-capillary malformation syndrome
    n1=en:joubert syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=23
  831. en:lecithin acyltransferase deficiency --- r_associated #0: 23 --> en:microcephaly-capillary malformation syndrome
    n1=en:lecithin acyltransferase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=23
  832. en:merrf syndrome --- r_associated #0: 23 --> en:microcephaly-capillary malformation syndrome
    n1=en:merrf syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=23
  833. en:muscle-eye-brain disease, congenital muscular dystrophy --- r_associated #0: 23 --> en:microcephaly-capillary malformation syndrome
    n1=en:muscle-eye-brain disease, congenital muscular dystrophy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=23
  834. en:ocular depression --- r_associated #0: 23 --> en:microcephaly-capillary malformation syndrome
    n1=en:ocular depression | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=23
  835. en:spondyloenchondromatosis with basal ganglia calcification --- r_associated #0: 23 --> en:microcephaly-capillary malformation syndrome
    n1=en:spondyloenchondromatosis with basal ganglia calcification | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=23
  836. en:tyrosinemia type II --- r_associated #0: 23 --> en:microcephaly-capillary malformation syndrome
    n1=en:tyrosinemia type II | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=23
  837. en:uv-sensitive syndrome --- r_associated #0: 23 --> en:microcephaly-capillary malformation syndrome
    n1=en:uv-sensitive syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=23
  838. contractures congénitales et arachnodactylie --- r_associated #0: 22 --> en:microcephaly-capillary malformation syndrome
    n1=contractures congénitales et arachnodactylie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=22
  839. en:5' 10' methylenetetrahydrofolate reductase deficiency --- r_associated #0: 22 --> en:microcephaly-capillary malformation syndrome
    n1=en:5' 10' methylenetetrahydrofolate reductase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=22
  840. en:and teething delay --- r_associated #0: 22 --> en:microcephaly-capillary malformation syndrome
    n1=en:and teething delay | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=22
  841. en:borjeson-forssman-lehmann syndrome --- r_associated #0: 22 --> en:microcephaly-capillary malformation syndrome
    n1=en:borjeson-forssman-lehmann syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=22
  842. en:congenital clinodactyly --- r_associated #0: 22 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital clinodactyly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=22
  843. en:delayed psychomotor development, profound --- r_associated #0: 22 --> en:microcephaly-capillary malformation syndrome
    n1=en:delayed psychomotor development, profound | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=22
  844. en:glycogen storage disease type i --- r_associated #0: 22 --> en:microcephaly-capillary malformation syndrome
    n1=en:glycogen storage disease type i | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=22
  845. en:hippocampal hypoplasia --- r_associated #0: 22 --> en:microcephaly-capillary malformation syndrome
    n1=en:hippocampal hypoplasia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=22
  846. en:mental retardation --- r_associated #0: 22 --> en:microcephaly-capillary malformation syndrome
    n1=en:mental retardation | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=22
  847. en:micronychia (disorder) --- r_associated #0: 22 --> en:microcephaly-capillary malformation syndrome
    n1=en:micronychia (disorder) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=22
  848. en:orotic aciduria --- r_associated #0: 22 --> en:microcephaly-capillary malformation syndrome
    n1=en:orotic aciduria | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=22
  849. en:osteogenesis imperfecta, recessive perinatal lethal, with microcephaly and cataracts --- r_associated #0: 22 --> en:microcephaly-capillary malformation syndrome
    n1=en:osteogenesis imperfecta, recessive perinatal lethal, with microcephaly and cataracts | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=22
  850. en:peutz-jeghers syndrome --- r_associated #0: 22 --> en:microcephaly-capillary malformation syndrome
    n1=en:peutz-jeghers syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=22
  851. en:sellars beighton syndrome --- r_associated #0: 22 --> en:microcephaly-capillary malformation syndrome
    n1=en:sellars beighton syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=22
  852. en:vesicoureteral reflux (1 patient) --- r_associated #0: 22 --> en:microcephaly-capillary malformation syndrome
    n1=en:vesicoureteral reflux (1 patient) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=22
  853. en:wolman's disease --- r_associated #0: 22 --> en:microcephaly-capillary malformation syndrome
    n1=en:wolman's disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=22
  854. acidurie argininosuccinique --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=acidurie argininosuccinique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  855. acidémie isovalérique --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=acidémie isovalérique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  856. adénite sinusale cytophagique --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=adénite sinusale cytophagique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  857. alcaptonurie --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=alcaptonurie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  858. angiome plan --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=angiome plan | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  859. argininémie --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=argininémie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  860. déficit enzymatique partiel de la surrénale --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=déficit enzymatique partiel de la surrénale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  861. en:abnormal toe positioning --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=en:abnormal toe positioning | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  862. en:absent corpus callosum --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=en:absent corpus callosum | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  863. en:adrenal gland hyperplasia ii --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=en:adrenal gland hyperplasia ii | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  864. en:autosomal dominant late onset basal ganglia degeneration --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=en:autosomal dominant late onset basal ganglia degeneration | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  865. en:becker generalized myotonia --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=en:becker generalized myotonia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  866. en:caused by mutation in the stam-binding protein gene (stambp, 606247.0001) --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=en:caused by mutation in the stam-binding protein gene (stambp, 606247.0001) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  867. en:classical phenylketonuria --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=en:classical phenylketonuria | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  868. en:combined pituitary hormone deficiency genetic form --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=en:combined pituitary hormone deficiency genetic form | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  869. en:congenital capillary hemangioma --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital capillary hemangioma | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  870. en:hyperextensibility --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=en:hyperextensibility | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  871. en:labial fissure --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=en:labial fissure | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  872. en:leukodystrophy --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=en:leukodystrophy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  873. en:muscular hypotonia --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=en:muscular hypotonia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  874. en:myoclonic jerk --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=en:myoclonic jerk | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  875. en:nevus anemicus --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=en:nevus anemicus | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  876. en:oxalosis --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=en:oxalosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  877. en:peters-plus syndrome --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=en:peters-plus syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  878. en:seizures usually occur in the first months of life --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=en:seizures usually occur in the first months of life | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  879. en:seizures, refractory --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=en:seizures, refractory | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  880. en:severe steroid 21-hydroxylase deficiency --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=en:severe steroid 21-hydroxylase deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  881. en:short distal phalanx of finger --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=en:short distal phalanx of finger | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  882. en:x-linked epilepsy with learning disability and behavior disorder syndrome --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=en:x-linked epilepsy with learning disability and behavior disorder syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  883. idiosyncrasie au fructose --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=idiosyncrasie au fructose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  884. maladie de roger --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=maladie de roger | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  885. maladie de von Recklinghausen --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=maladie de von Recklinghausen | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  886. mannosidose --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=mannosidose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  887. mucopolysaccharidose de type 1 --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=mucopolysaccharidose de type 1 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  888. neurofibromatose de type 1 --- r_associated #0: 21 --> en:microcephaly-capillary malformation syndrome
    n1=neurofibromatose de type 1 | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=21
  889. Malformation congénitale --- r_associated #0: 20 --> en:microcephaly-capillary malformation syndrome
    n1=Malformation congénitale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=20
  890. Sénilité --- r_associated #0: 20 --> en:microcephaly-capillary malformation syndrome
    n1=Sénilité | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=20
  891. syndrome --- r_associated #0: 20 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=20
  892. syndrome de Warburg --- r_associated #0: 16 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome de Warburg | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=16
  893. Bracht (manoeuvre de) --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=Bracht (manoeuvre de) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  894. Fuchs (syndrome de) --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=Fuchs (syndrome de) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  895. Giessen (test de) --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=Giessen (test de) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  896. His (faisceau de) --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=His (faisceau de) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  897. Hyperplasie congénitale des surrénales --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=Hyperplasie congénitale des surrénales | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  898. Intolérance au fructose --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=Intolérance au fructose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  899. Maladie de Niemann-Pick --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=Maladie de Niemann-Pick | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  900. Syndrome de Walker-Warburg --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=Syndrome de Walker-Warburg | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  901. démence d'Alzheimer --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=démence d'Alzheimer | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  902. en:congenital atrophy of thyroid --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital atrophy of thyroid | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  903. en:congenital hypothyroidism --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital hypothyroidism | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  904. en:neonatal hypothyroidism --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=en:neonatal hypothyroidism | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  905. fente labio-palatine --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=fente labio-palatine | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  906. fente labiopalatine --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=fente labiopalatine | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  907. hyperornithinémie, hyperammoniémie, homocitrullinurie (syndrome) --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=hyperornithinémie, hyperammoniémie, homocitrullinurie (syndrome) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  908. hypothyroïdie congénitale --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=hypothyroïdie congénitale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  909. hypothyroïdie et psychisme --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=hypothyroïdie et psychisme | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  910. hypothyroïdie néonatale --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=hypothyroïdie néonatale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  911. hypotonie plasmatique --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=hypotonie plasmatique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  912. hypotonie sphinctérienne anale --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=hypotonie sphinctérienne anale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  913. hypotonie sphinctérienne uréthrale --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=hypotonie sphinctérienne uréthrale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  914. hypotonie utérine --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=hypotonie utérine | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  915. hypotonie vésicale --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=hypotonie vésicale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  916. hypotonique --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=hypotonique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  917. hypotrichose --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=hypotrichose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  918. hypotrichose avec anodontie et anhidrose de Touraine --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=hypotrichose avec anodontie et anhidrose de Touraine | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  919. hypotrichose congénitale des cils --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=hypotrichose congénitale des cils | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  920. hypotrichose congénitale simple --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=hypotrichose congénitale simple | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  921. hypotrichose héréditaire de Marie Unna --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=hypotrichose héréditaire de Marie Unna | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  922. hypotrichose, atrophodermie folliculaire et épithéliomatose --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=hypotrichose, atrophodermie folliculaire et épithéliomatose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  923. malentendant (enfant) --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=malentendant (enfant) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  924. obésité --- r_associated #0: 15 --> en:microcephaly-capillary malformation syndrome
    n1=obésité | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=15
  925. insomnie familiale fatale --- r_associated #0: 11 --> en:microcephaly-capillary malformation syndrome
    n1=insomnie familiale fatale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=11
  926. BEC DE LIEVRE --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=BEC DE LIEVRE | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  927. Brachydactylie --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=Brachydactylie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  928. CONGÉNITALE --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=CONGÉNITALE | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  929. Communication interauriculaire --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=Communication interauriculaire | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  930. Dubin-Johnson (syndrome de) --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=Dubin-Johnson (syndrome de) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  931. Fucosidose --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=Fucosidose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  932. Histidinémie --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=Histidinémie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  933. Hypertélorisme --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=Hypertélorisme | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  934. Hypotonie --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=Hypotonie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  935. Insler et Bernstein (score cervical d') --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=Insler et Bernstein (score cervical d') | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  936. Laurence-Moon (syndrome de) --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=Laurence-Moon (syndrome de) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  937. MIGP (orientation) --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=MIGP (orientation) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  938. MOMO (syndrome) --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=MOMO (syndrome) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  939. Malformation --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=Malformation | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  940. Manning (score de) --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=Manning (score de) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  941. Mannosidose --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=Mannosidose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  942. Neurofibromatose --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=Neurofibromatose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  943. Niemann-Pick (maladie de) --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=Niemann-Pick (maladie de) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  944. Ptose --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=Ptose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  945. Ptôse --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=Ptôse | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  946. Retard de croissance --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=Retard de croissance | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  947. Roger (maladie de) --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=Roger (maladie de) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  948. Sengstaken-Blakemore (sonde de) --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=Sengstaken-Blakemore (sonde de) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  949. Syndrome de Sotos --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=Syndrome de Sotos | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  950. Treft-Sanborn-Carey (syndrome de) --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=Treft-Sanborn-Carey (syndrome de) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  951. alcalose métabolique (classification) --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=alcalose métabolique (classification) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  952. arriération --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=arriération | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  953. atonie de l'utérus --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=atonie de l'utérus | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  954. atrophie optique, surdité neurogène, amyotrophie distale neurogénique --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=atrophie optique, surdité neurogène, amyotrophie distale neurogénique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  955. bec de corbin --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=bec de corbin | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  956. bec de cuiller --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=bec de cuiller | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  957. bec de la prostate --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=bec de la prostate | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  958. bec de la rotule --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=bec de la rotule | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  959. bébé collodion --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=bébé collodion | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  960. cataracte-ataxie-surdité et retard mental (syndrome) --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=cataracte-ataxie-surdité et retard mental (syndrome) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  961. cophose --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=cophose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  962. cornée et tyrosinose de type II --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=cornée et tyrosinose de type II | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  963. diabète, photomyoclonies, surdité, néphropathie et dysfonction cérébrale --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=diabète, photomyoclonies, surdité, néphropathie et dysfonction cérébrale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  964. division palatine --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=division palatine | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  965. débilité mentale --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=débilité mentale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  966. démence alcoolique --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=démence alcoolique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  967. démence aluminique --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=démence aluminique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  968. démence héréditaire et infarctus multiples cérébraux --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=démence héréditaire et infarctus multiples cérébraux | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  969. démence myoclonique --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=démence myoclonique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  970. démence parkinsonienne avec dégénérescence pallidopontonigrée --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=démence parkinsonienne avec dégénérescence pallidopontonigrée | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  971. démence précoce --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=démence précoce | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  972. démence pugilistique --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=démence pugilistique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  973. démence régressive --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=démence régressive | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  974. démence sous-corticale --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=démence sous-corticale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  975. démence sémantique --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=démence sémantique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  976. démence sénile de type Alzheimer --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=démence sénile de type Alzheimer | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  977. démence sénile mixte --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=démence sénile mixte | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  978. démence traumatique --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=démence traumatique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  979. démence vasculaire --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=démence vasculaire | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  980. démence vésanique --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=démence vésanique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  981. démence à corps de Lewy --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=démence à corps de Lewy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  982. démences et prions --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=démences et prions | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  983. en:5q microdeletion --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:5q microdeletion | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  984. en:Alzheimer's dementia --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:Alzheimer's dementia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  985. en:Bracht's manoeuvre --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:Bracht's manoeuvre | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  986. en:Fenn's diagram --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:Fenn's diagram | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  987. en:HHH syndrome --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:HHH syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  988. en:Kjer type optic atrophy --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:Kjer type optic atrophy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  989. en:Kjer's type --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:Kjer's type | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  990. en:Recklinghausen's disease --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:Recklinghausen's disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  991. en:Sotos's syndrome --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:Sotos's syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  992. en:Tay Sachs' disease --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:Tay Sachs' disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  993. en:alcaptonuria --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:alcaptonuria | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  994. en:anal sphincter hypotonia --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:anal sphincter hypotonia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  995. en:and dementia --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:and dementia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  996. en:and microgenitalism --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:and microgenitalism | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  997. en:and sensorineural deafness --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:and sensorineural deafness | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  998. en:ataxia --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:ataxia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  999. en:bladder hypotonia --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:bladder hypotonia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1000. en:blepharophimosis --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:blepharophimosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1001. en:brachydactylia --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:brachydactylia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1002. en:bronze baby syndrome --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:bronze baby syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1003. en:cacomorphosis --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:cacomorphosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1004. en:calvarial hypoplasia --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:calvarial hypoplasia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1005. en:capillary haemangiomata --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:capillary haemangiomata | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1006. en:capillary nevus --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:capillary nevus | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1007. en:cataract --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:cataract | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1008. en:congenital eyelashes hypotrichosis --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital eyelashes hypotrichosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1009. en:contractural arachnodactyly --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:contractural arachnodactyly | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1010. en:facial clefting syndrome --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:facial clefting syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1011. en:hearing defect --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:hearing defect | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1012. en:hearing deficiency --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:hearing deficiency | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1013. en:hemangioma simplex --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:hemangioma simplex | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1014. en:homogentisuria --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:homogentisuria | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1015. en:hypacusis and athetosis --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:hypacusis and athetosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1016. en:hyperornithinemia hyperammoniemia homocitrullinuria --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:hyperornithinemia hyperammoniemia homocitrullinuria | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1017. en:hypoacousic child --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:hypoacousic child | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1018. en:hypospadias --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:hypospadias | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1019. en:hypothyreosis --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:hypothyreosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1020. en:hypothyroidism and psychism --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:hypothyroidism and psychism | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1021. en:hypotonic --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:hypotonic | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1022. en:hypotrichosis --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:hypotrichosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1023. en:hypotrichosis congenita simplex --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:hypotrichosis congenita simplex | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1024. en:hypotrichosis-anodontic syndrome --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:hypotrichosis-anodontic syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1025. en:interatrial septal defect --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:interatrial septal defect | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1026. en:interventricular septal defect --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:interventricular septal defect | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1027. en:iris coloboma with ptosis --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:iris coloboma with ptosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1028. en:labiopalatine cleft --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:labiopalatine cleft | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1029. en:late optic atrophy --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:late optic atrophy | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1030. en:microtia --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:microtia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1031. en:myopia --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:myopia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1032. en:nystagmuses --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:nystagmuses | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1033. en:nystaxis --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:nystaxis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1034. en:phosphatide thesaurismosis --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:phosphatide thesaurismosis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1035. en:plasma hypotonia --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:plasma hypotonia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1036. en:polysyndactyly syndrome --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:polysyndactyly syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1037. en:secundum defect --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:secundum defect | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1038. en:sinus venosus defect --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:sinus venosus defect | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1039. en:sphincteric hypotony --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:sphincteric hypotony | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1040. en:talantropia --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:talantropia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1041. en:telangiectoma --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:telangiectoma | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1042. en:type I --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:type I | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1043. en:type VI --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:type VI | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1044. en:uterine hypotonia --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:uterine hypotonia | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1045. en:von recklinghausen's disease --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:von recklinghausen's disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1046. en:with growth retardation --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:with growth retardation | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1047. en:with tapetal-like sheen --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:with tapetal-like sheen | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1048. en:xanthine lithiasis --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=en:xanthine lithiasis | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1049. fente cérébrale de Bichat --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=fente cérébrale de Bichat | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1050. fente de Larrey --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=fente de Larrey | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1051. fente de la glotte --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=fente de la glotte | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1052. fente foetale --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=fente foetale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1053. fente hypophysaire --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=fente hypophysaire | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1054. fente interaryténoïdienne --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=fente interaryténoïdienne | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1055. fente interfessière --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=fente interfessière | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1056. fente labiopalatine et kystes muqueux de la lèvre inférieure --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=fente labiopalatine et kystes muqueux de la lèvre inférieure | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1057. fente labiopalatine, ectropion et dents coniques --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=fente labiopalatine, ectropion et dents coniques | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1058. fente labiopalatine, kyste paramédian muqueux de la lèvre inférieure, ptérygium poplité et anomalies digitogénitales --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=fente labiopalatine, kyste paramédian muqueux de la lèvre inférieure, ptérygium poplité et anomalies digitogénitales | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1059. fente palatine --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=fente palatine | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1060. fissure palatine --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=fissure palatine | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1061. fénotérol --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=fénotérol | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1062. hernie diaphragmatique --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=hernie diaphragmatique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1063. hypertensinase --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=hypertensinase | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1064. hypertensine --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=hypertensine | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1065. hypertensinogène --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=hypertensinogène | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1066. hypertension --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=hypertension | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1067. hypertension abdominale --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=hypertension abdominale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1068. hypertension artérielle --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=hypertension artérielle | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1069. inertie utérine --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=inertie utérine | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1070. macrosomie, obésité, macrocéphalie et anomalies oculaires --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=macrosomie, obésité, macrocéphalie et anomalies oculaires | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1071. maladie d'Alzheimer --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=maladie d'Alzheimer | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1072. maladie de niemann-pick --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=maladie de niemann-pick | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1073. nanisme de type Laron --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=nanisme de type Laron | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1074. neuraminidase (déficit en) --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=neuraminidase (déficit en) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1075. nystagmus myoclonies --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=nystagmus myoclonies | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1076. omphalocèle --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=omphalocèle | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1077. ophtalmoplégie dégénérescence pigmentée de la rétine et cardiomyopathie --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=ophtalmoplégie dégénérescence pigmentée de la rétine et cardiomyopathie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1078. paraplégie spastique familiale --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=paraplégie spastique familiale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1079. polyneuropathie, ophtalmoplégie, leucoencéphalopathie et pseudo-obstruction intestinale --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=polyneuropathie, ophtalmoplégie, leucoencéphalopathie et pseudo-obstruction intestinale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1080. prolidase (déficit en) --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=prolidase (déficit en) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1081. reclassement professionnel --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=reclassement professionnel | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1082. retard mental avec atrophie optique, surdité et épilepsie --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=retard mental avec atrophie optique, surdité et épilepsie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1083. rétention hydrochlorurée sodique --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=rétention hydrochlorurée sodique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1084. rétention membraneuse --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=rétention membraneuse | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1085. rétention placentaire --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=rétention placentaire | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1086. rétention placentaire du postabortum --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=rétention placentaire du postabortum | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1087. rétention sudorale --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=rétention sudorale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1088. rétentionniste --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=rétentionniste | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1089. rétinite pigmentaire, surdité, retard mental, et hypogonadisme --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=rétinite pigmentaire, surdité, retard mental, et hypogonadisme | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1090. sirtuine --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=sirtuine | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1091. sisi-test --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=sisi-test | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1092. sismothérapie --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=sismothérapie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1093. souche de référence --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=souche de référence | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1094. souche transduite --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=souche transduite | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1095. surdité --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=surdité | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1096. syndrome cataracte-ataxie-surdité et retard mental --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome cataracte-ataxie-surdité et retard mental | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1097. syndrome d'Apert --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome d'Apert | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1098. syndrome de Mohr-Tranebjaerg --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome de Mohr-Tranebjaerg | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1099. syndrome de Nathalie --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome de Nathalie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1100. syndrome de warburg --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome de warburg | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1101. syndrome de zellweger --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome de zellweger | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1102. télécardiographie --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=télécardiographie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1103. télécardiophone --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=télécardiophone | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1104. téléclitoridie --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=téléclitoridie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1105. télécobalt --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=télécobalt | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1106. télécobalt-thérapie --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=télécobalt-thérapie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1107. téléconsultation --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=téléconsultation | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1108. télécrâne --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=télécrâne | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1109. télécæsiothérapie --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=télécæsiothérapie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1110. télédermatologie --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=télédermatologie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1111. télédiastole --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=télédiastole | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1112. télédétection --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=télédétection | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1113. urticaire-surdité-amylose rénale --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=urticaire-surdité-amylose rénale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1114. xanthomatose familiale primitive --- r_associated #0: 10 --> en:microcephaly-capillary malformation syndrome
    n1=xanthomatose familiale primitive | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
  1115. Fente labiale --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=Fente labiale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1116. Hypotonique --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=Hypotonique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1117. Nyssen-van Bogaert (syndrome de) --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=Nyssen-van Bogaert (syndrome de) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1118. Tay-Sachs (maladie de) --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=Tay-Sachs (maladie de) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1119. atrophie congénitale de la thyroïde --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=atrophie congénitale de la thyroïde | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1120. bec de perroquet --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=bec de perroquet | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1121. bec du cuboïde --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=bec du cuboïde | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1122. bec du sphénoïde --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=bec du sphénoïde | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1123. bec scléral --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=bec scléral | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1124. brachy-oesophage --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=brachy-oesophage | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1125. brachyclinodactylie --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=brachyclinodactylie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1126. brachycères --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=brachycères | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1127. brachycéphalie --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=brachycéphalie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1128. bécégite --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=bécégite | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1129. crétinismes --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=crétinismes | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1130. en:Sachs' disease --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=en:Sachs' disease | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1131. en:congenital goiter --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=en:congenital goiter | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1132. faisceau de His --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=faisceau de His | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1133. forme génétique de déficience combinée en hormones hypophysaires --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=forme génétique de déficience combinée en hormones hypophysaires | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1134. fuchsine --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=fuchsine | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1135. fucose --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=fucose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1136. fucosidase --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=fucosidase | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1137. fucoside --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=fucoside | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1138. goitre congénital --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=goitre congénital | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1139. histaminergie --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=histaminergie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1140. histaminergique --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=histaminergique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1141. histaminique --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=histaminique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1142. histaminolibération --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=histaminolibération | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1143. histaminolytique --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=histaminolytique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1144. histaminopexie --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=histaminopexie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1145. histaminurie --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=histaminurie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1146. histaminémie --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=histaminémie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1147. histidase --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=histidase | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1148. histidinase --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=histidinase | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1149. histidine --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=histidine | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1150. histidine-ammoniac-lyase --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=histidine-ammoniac-lyase | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1151. histidine-décarboxylase --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=histidine-décarboxylase | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1152. histidine-désaminase --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=histidine-désaminase | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1153. hyperostose vertébrale ankylosante --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=hyperostose vertébrale ankylosante | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1154. hyperoxalurie --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=hyperoxalurie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1155. hyperoxalémie --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=hyperoxalémie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1156. hypothyroïdisme congénital --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=hypothyroïdisme congénital | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1157. infantilisme type brissaud --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=infantilisme type brissaud | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1158. maladie clinique de recklinghausen --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=maladie clinique de recklinghausen | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1159. malf ormation dysraphique --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=malf ormation dysraphique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1160. malformation kystique adénomatoïde du poumon --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=malformation kystique adénomatoïde du poumon | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1161. malformation luxante de la hanche --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=malformation luxante de la hanche | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1162. malformation mamelonnaire --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=malformation mamelonnaire | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1163. malformation mammaire --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=malformation mammaire | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1164. malformation ombilicale --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=malformation ombilicale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1165. malformation utérine --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=malformation utérine | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1166. malformation vaginale --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=malformation vaginale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1167. malformation vasculaire cérébrale du nourrisson --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=malformation vasculaire cérébrale du nourrisson | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1168. malformations de la charnière occipitocervicale --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=malformations de la charnière occipitocervicale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1169. nanisme hypothyroïdien --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=nanisme hypothyroïdien | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1170. neurinome bilatéral du nerf cochléaire (VIII) --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=neurinome bilatéral du nerf cochléaire (VIII) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1171. nystagmus (zone de moindre) --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=nystagmus (zone de moindre) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1172. paraphimosis (réduction d'un) --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=paraphimosis (réduction d'un) | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1173. retardation mentale --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=retardation mentale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1174. semidominance --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=semidominance | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1175. semiquinone --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=semiquinone | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1176. syndrome d'insuffisance thyroïdienne congénitale --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome d'insuffisance thyroïdienne congénitale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1177. syndrome de Fuchs --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=syndrome de Fuchs | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1178. séminal --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=séminal | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1179. séminifère --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=séminifère | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1180. séminomateux --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=séminomateux | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1181. séminome --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=séminome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1182. séminome de l'ovaire --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=séminome de l'ovaire | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1183. séminome du médiastin --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=séminome du médiastin | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1184. séminome spermatocytaire --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=séminome spermatocytaire | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1185. sémiochimique --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=sémiochimique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1186. sémiologie extrapyramidale --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=sémiologie extrapyramidale | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1187. xanthoastrocytome pléomorphe --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=xanthoastrocytome pléomorphe | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1188. xanthochromie --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=xanthochromie | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1189. xanthochromie caroténique --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=xanthochromie caroténique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1190. xanthoerythrodermia perstans --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=xanthoerythrodermia perstans | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1191. xanthogranulome juvénile --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=xanthogranulome juvénile | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1192. xanthogranulome nécrobiotique --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=xanthogranulome nécrobiotique | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1193. xanthogranulome palpébral --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=xanthogranulome palpébral | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1194. xanthohistiocytome --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=xanthohistiocytome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1195. xanthoma disseminatum --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=xanthoma disseminatum | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
  1196. xanthomatose --- r_associated #0: 5 --> en:microcephaly-capillary malformation syndrome
    n1=xanthomatose | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=5
Le service Rézo permet d'énumérer les relations existant pour un terme. Ce service est interrogeable par programme.
Projet JeuxDeMots - url: http://www.jeuxdemots.org
contact: mathieu.lafourcade@lirmm.fr