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'en:hyperinsulinism due to uncoupling protein 2 deficiency'
(id=9102922 ; fe=en:hyperinsulinism due to uncoupling protein 2 deficiency ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=13456 creation date=2017-10-29 touchdate=2025-12-02 07:02:02.000)
≈ 619 relations sortantes

  1. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 43 / 1 -> en:charcot-marie-tooth disease type 2d
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:charcot-marie-tooth disease type 2d | rel=r_associated | relid=0 | w=43
  2. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 43 / 1 -> en:corneal dystrophy, posterior amorphous
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:corneal dystrophy, posterior amorphous | rel=r_associated | relid=0 | w=43
  3. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 43 / 1 -> en:hyperinsulinism due to deficiency of glucokinase
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hyperinsulinism due to deficiency of glucokinase | rel=r_associated | relid=0 | w=43
  4. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 43 / 1 -> en:isolated cryptophthalmos
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:isolated cryptophthalmos | rel=r_associated | relid=0 | w=43
  5. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 43 / 1 -> en:progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome | rel=r_associated | relid=0 | w=43
  6. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 43 / 1 -> en:spinocerebellar ataxia type 37
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia type 37 | rel=r_associated | relid=0 | w=43
  7. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 43 / 1 -> en:timothy syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:timothy syndrome | rel=r_associated | relid=0 | w=43
  8. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 42 / 0.977 -> en:bamforth syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:bamforth syndrome | rel=r_associated | relid=0 | w=42
  9. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 42 / 0.977 -> en:combined d-2- and l-2-hydroxyglutaric aciduria
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:combined d-2- and l-2-hydroxyglutaric aciduria | rel=r_associated | relid=0 | w=42
  10. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 42 / 0.977 -> en:congenital bile acid synthesis defect type 3
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:congenital bile acid synthesis defect type 3 | rel=r_associated | relid=0 | w=42
  11. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 42 / 0.977 -> en:familial alzheimer-like prion disease
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:familial alzheimer-like prion disease | rel=r_associated | relid=0 | w=42
  12. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 42 / 0.977 -> en:hereditary motor and sensory neuropathy type i
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary motor and sensory neuropathy type i | rel=r_associated | relid=0 | w=42
  13. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 42 / 0.977 -> en:hereditary vitamin d dependency syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary vitamin d dependency syndrome | rel=r_associated | relid=0 | w=42
  14. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 42 / 0.977 -> en:sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome | rel=r_associated | relid=0 | w=42
  15. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 41 / 0.953 -> en:dopa-responsive dystonia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:dopa-responsive dystonia | rel=r_associated | relid=0 | w=41
  16. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 41 / 0.953 -> en:insulin autoimmune syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:insulin autoimmune syndrome | rel=r_associated | relid=0 | w=41
  17. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 41 / 0.953 -> en:radial hypoplasia, triphalangeal thumbs and hypospadias
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:radial hypoplasia, triphalangeal thumbs and hypospadias | rel=r_associated | relid=0 | w=41
  18. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 41 / 0.953 -> en:severe steroid 21-hydroxylase deficiency
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:severe steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=41
  19. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 40 / 0.93 -> en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | rel=r_associated | relid=0 | w=40
  20. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 40 / 0.93 -> en:autosomal dominant excess of transthyretin
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant excess of transthyretin | rel=r_associated | relid=0 | w=40
  21. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 40 / 0.93 -> en:autosomal dominant muscular dystrophy with limb girdle distribution
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant muscular dystrophy with limb girdle distribution | rel=r_associated | relid=0 | w=40
  22. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 40 / 0.93 -> en:craniofacial conodysplasia syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:craniofacial conodysplasia syndrome | rel=r_associated | relid=0 | w=40
  23. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 40 / 0.93 -> en:spinocerebellar ataxia 27
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia 27 | rel=r_associated | relid=0 | w=40
  24. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 39 / 0.907 -> en:lowry maclean syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:lowry maclean syndrome | rel=r_associated | relid=0 | w=39
  25. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 39 / 0.907 -> en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis | rel=r_associated | relid=0 | w=39
  26. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 39 / 0.907 -> en:spinocerebellar ataxia 12
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia 12 | rel=r_associated | relid=0 | w=39
  27. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 39 / 0.907 -> en:spinocerebellar ataxia 14
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia 14 | rel=r_associated | relid=0 | w=39
  28. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 39 / 0.907 -> en:spinocerebellar ataxia 18
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia 18 | rel=r_associated | relid=0 | w=39
  29. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 38 / 0.884 -> en:familial adenomatous polyposis
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:familial adenomatous polyposis | rel=r_associated | relid=0 | w=38
  30. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 38 / 0.884 -> en:hnsha due to triosephosphate isomerase deficiency
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hnsha due to triosephosphate isomerase deficiency | rel=r_associated | relid=0 | w=38
  31. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 38 / 0.884 -> en:neuropathy, hereditary motor and sensory, okinawa type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:neuropathy, hereditary motor and sensory, okinawa type | rel=r_associated | relid=0 | w=38
  32. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 37 / 0.86 -> en:alpha 1-antitrypsin deficiency
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:alpha 1-antitrypsin deficiency | rel=r_associated | relid=0 | w=37
  33. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 37 / 0.86 -> en:cleidorhizomelic syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:cleidorhizomelic syndrome | rel=r_associated | relid=0 | w=37
  34. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 37 / 0.86 -> en:dominant beta-thalassemia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:dominant beta-thalassemia | rel=r_associated | relid=0 | w=37
  35. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 37 / 0.86 -> en:drug-induced hyperinsulinemia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:drug-induced hyperinsulinemia | rel=r_associated | relid=0 | w=37
  36. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 37 / 0.86 -> en:hereditary benign intraepithelial dyskeratosis
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary benign intraepithelial dyskeratosis | rel=r_associated | relid=0 | w=37
  37. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 37 / 0.86 -> en:hereditary glucocorticoid resistance
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary glucocorticoid resistance | rel=r_associated | relid=0 | w=37
  38. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 37 / 0.86 -> en:oculootoradial syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:oculootoradial syndrome | rel=r_associated | relid=0 | w=37
  39. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 36 / 0.837 -> en:sohval soffer syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:sohval soffer syndrome | rel=r_associated | relid=0 | w=36
  40. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 36 / 0.837 -> en:spinocerebellar ataxia type 19
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia type 19 | rel=r_associated | relid=0 | w=36
  41. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:abruzzo erickson syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:abruzzo erickson syndrome | rel=r_associated | relid=0 | w=35
  42. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:acromicric dysplasia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:acromicric dysplasia | rel=r_associated | relid=0 | w=35
  43. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:adrenoleukodystrophy
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:adrenoleukodystrophy | rel=r_associated | relid=0 | w=35
  44. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome | rel=r_associated | relid=0 | w=35
  45. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges | rel=r_associated | relid=0 | w=35
  46. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:auriculo-condylar syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:auriculo-condylar syndrome | rel=r_associated | relid=0 | w=35
  47. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:autosomal dominant hypophosphatemic bone disease
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant hypophosphatemic bone disease | rel=r_associated | relid=0 | w=35
  48. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:autosomal dominant idiopathic familial dystonia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant idiopathic familial dystonia | rel=r_associated | relid=0 | w=35
  49. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:autosomal dominant retinitis pigmentosa
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant retinitis pigmentosa | rel=r_associated | relid=0 | w=35
  50. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:avascular necrosis of femur head
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:avascular necrosis of femur head | rel=r_associated | relid=0 | w=35
  51. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:beare-stevenson cutis gyrata syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:beare-stevenson cutis gyrata syndrome | rel=r_associated | relid=0 | w=35
  52. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:blau syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:blau syndrome | rel=r_associated | relid=0 | w=35
  53. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:blepharo-cheilo-dontic syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:blepharo-cheilo-dontic syndrome | rel=r_associated | relid=0 | w=35
  54. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:blindness, scoliosis, arachnodactyly syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:blindness, scoliosis, arachnodactyly syndrome | rel=r_associated | relid=0 | w=35
  55. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:bork stender schmidt syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:bork stender schmidt syndrome | rel=r_associated | relid=0 | w=35
  56. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:brachydactyly type a5 nail dysplasia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:brachydactyly type a5 nail dysplasia | rel=r_associated | relid=0 | w=35
  57. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:brachydactyly type a6
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:brachydactyly type a6 | rel=r_associated | relid=0 | w=35
  58. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:brachymesophalangy 2 and 5
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:brachymesophalangy 2 and 5 | rel=r_associated | relid=0 | w=35
  59. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:cap myopathy
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:cap myopathy | rel=r_associated | relid=0 | w=35
  60. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:carnevale hernandez castillo syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:carnevale hernandez castillo syndrome | rel=r_associated | relid=0 | w=35
  61. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:choreoathetosis, hypothyroidism, and neonatal respiratory distress
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:choreoathetosis, hypothyroidism, and neonatal respiratory distress | rel=r_associated | relid=0 | w=35
  62. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:cleidocranial dysplasia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:cleidocranial dysplasia | rel=r_associated | relid=0 | w=35
  63. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:coloboma of macula with type b brachydactyly
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:coloboma of macula with type b brachydactyly | rel=r_associated | relid=0 | w=35
  64. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:congenital dyserythropoietic anemia type iv
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:congenital dyserythropoietic anemia type iv | rel=r_associated | relid=0 | w=35
  65. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:currarino triad
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:currarino triad | rel=r_associated | relid=0 | w=35
  66. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:dentin dyspalsia, shields type 2
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:dentin dyspalsia, shields type 2 | rel=r_associated | relid=0 | w=35
  67. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:dermoodontodysplasia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:dermoodontodysplasia | rel=r_associated | relid=0 | w=35
  68. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:dominant autosomal hereditary disorder, complete penetrance
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:dominant autosomal hereditary disorder, complete penetrance | rel=r_associated | relid=0 | w=35
  69. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:dominant autosomal hereditary disorder, incomplete penetrance
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:dominant autosomal hereditary disorder, incomplete penetrance | rel=r_associated | relid=0 | w=35
  70. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:dyskeratosis congenita, autosomal dominant
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:dyskeratosis congenita, autosomal dominant | rel=r_associated | relid=0 | w=35
  71. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:dysplasia, saddan
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:dysplasia, saddan | rel=r_associated | relid=0 | w=35
  72. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:ectodermal dysplasia with natal teeth, turnpenny type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:ectodermal dysplasia with natal teeth, turnpenny type | rel=r_associated | relid=0 | w=35
  73. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:epidermolysis bullosa simplex with pyloric atresia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:epidermolysis bullosa simplex with pyloric atresia | rel=r_associated | relid=0 | w=35
  74. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:episodic ataxia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:episodic ataxia | rel=r_associated | relid=0 | w=35
  75. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:familial creutzfeldt-jakob
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:familial creutzfeldt-jakob | rel=r_associated | relid=0 | w=35
  76. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:familial non-autoimmune autosomal dominant hyperthyroidism
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:familial non-autoimmune autosomal dominant hyperthyroidism | rel=r_associated | relid=0 | w=35
  77. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:gemss syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:gemss syndrome | rel=r_associated | relid=0 | w=35
  78. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:glycogen storage disease, hepatic form
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:glycogen storage disease, hepatic form | rel=r_associated | relid=0 | w=35
  79. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:goniodysgenesis-mental retardation-short stature syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:goniodysgenesis-mental retardation-short stature syndrome | rel=r_associated | relid=0 | w=35
  80. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:gracile bone dysplasia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:gracile bone dysplasia | rel=r_associated | relid=0 | w=35
  81. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:haim-munk syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:haim-munk syndrome | rel=r_associated | relid=0 | w=35
  82. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:hereditary pancreatitis
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary pancreatitis | rel=r_associated | relid=0 | w=35
  83. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:hirschsprung disease with type d brachydactyly syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hirschsprung disease with type d brachydactyly syndrome | rel=r_associated | relid=0 | w=35
  84. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:hyaline dystrophy of bruch's membrane
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hyaline dystrophy of bruch's membrane | rel=r_associated | relid=0 | w=35
  85. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:hyperinsulinemia due to insulinoma
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hyperinsulinemia due to insulinoma | rel=r_associated | relid=0 | w=35
  86. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:hyperinsulinism due to focal adenomatous hyperplasia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hyperinsulinism due to focal adenomatous hyperplasia | rel=r_associated | relid=0 | w=35
  87. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia | rel=r_associated | relid=0 | w=35
  88. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:insulin-dependent diabetes mellitus secretory diarrhea syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:insulin-dependent diabetes mellitus secretory diarrhea syndrome | rel=r_associated | relid=0 | w=35
  89. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:intestinal lipofuscinosis
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:intestinal lipofuscinosis | rel=r_associated | relid=0 | w=35
  90. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:late-onset retinal degeneration (disorder)
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:late-onset retinal degeneration (disorder) | rel=r_associated | relid=0 | w=35
  91. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:leukodystrophy, dysmyelinating, with oligodontia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:leukodystrophy, dysmyelinating, with oligodontia | rel=r_associated | relid=0 | w=35
  92. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:mesomelic dysplasia, kantaputra type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:mesomelic dysplasia, kantaputra type | rel=r_associated | relid=0 | w=35
  93. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:microcornea with glaucoma and absent frontal sinus syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:microcornea with glaucoma and absent frontal sinus syndrome | rel=r_associated | relid=0 | w=35
  94. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:microphthalmia, syndromic 3
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:microphthalmia, syndromic 3 | rel=r_associated | relid=0 | w=35
  95. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:moderate steroid 21-hydroxylase deficiency
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:moderate steroid 21-hydroxylase deficiency | rel=r_associated | relid=0 | w=35
  96. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:multiple endocrine neoplasia type 1
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:multiple endocrine neoplasia type 1 | rel=r_associated | relid=0 | w=35
  97. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:multiple epiphyseal dysplasia type 5
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:multiple epiphyseal dysplasia type 5 | rel=r_associated | relid=0 | w=35
  98. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:noonan syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:noonan syndrome | rel=r_associated | relid=0 | w=35
  99. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:ohdo syndrome, maat-kievit-brunner type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:ohdo syndrome, maat-kievit-brunner type | rel=r_associated | relid=0 | w=35
  100. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:paroxysmal extreme pain disorder
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:paroxysmal extreme pain disorder | rel=r_associated | relid=0 | w=35
  101. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:peutz-jeghers syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35
  102. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:pituitary adenoma, familial isolated (disorder)
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:pituitary adenoma, familial isolated (disorder) | rel=r_associated | relid=0 | w=35
  103. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:pseudohypoaldosteronism, type 1, dominant form
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:pseudohypoaldosteronism, type 1, dominant form | rel=r_associated | relid=0 | w=35
  104. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:rudd klimek syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:rudd klimek syndrome | rel=r_associated | relid=0 | w=35
  105. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:shwachman-diamond syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:shwachman-diamond syndrome | rel=r_associated | relid=0 | w=35
  106. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:spinocerebellar ataxia 13
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia 13 | rel=r_associated | relid=0 | w=35
  107. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:spinocerebellar ataxia 25
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia 25 | rel=r_associated | relid=0 | w=35
  108. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:spinocerebellar ataxia 26
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia 26 | rel=r_associated | relid=0 | w=35
  109. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:spinocerebellar ataxia 28
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia 28 | rel=r_associated | relid=0 | w=35
  110. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:spinocerebellar ataxia 29
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia 29 | rel=r_associated | relid=0 | w=35
  111. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:spondyloepiphyseal dysplasia macdermot type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spondyloepiphyseal dysplasia macdermot type | rel=r_associated | relid=0 | w=35
  112. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome | rel=r_associated | relid=0 | w=35
  113. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:strudwick syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:strudwick syndrome | rel=r_associated | relid=0 | w=35
  114. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:teebi naguib al awadi syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:teebi naguib al awadi syndrome | rel=r_associated | relid=0 | w=35
  115. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:timothy syndrome type 2
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:timothy syndrome type 2 | rel=r_associated | relid=0 | w=35
  116. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:vasculopathy, retinal, with cerebral leukodystrophy
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:vasculopathy, retinal, with cerebral leukodystrophy | rel=r_associated | relid=0 | w=35
  117. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:visceral myopathy familial external ophthalmoplegia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:visceral myopathy familial external ophthalmoplegia | rel=r_associated | relid=0 | w=35
  118. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 35 / 0.814 -> en:x-linked intellectual disability with acromegaly and hyperactivity syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | rel=r_associated | relid=0 | w=35
  119. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:acro-dermato-ungual-lacrimal-tooth syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:acro-dermato-ungual-lacrimal-tooth syndrome | rel=r_associated | relid=0 | w=34
  120. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:alagille syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:alagille syndrome | rel=r_associated | relid=0 | w=34
  121. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:alimentary hyperinsulinemia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:alimentary hyperinsulinemia | rel=r_associated | relid=0 | w=34
  122. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth | rel=r_associated | relid=0 | w=34
  123. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:aplasia of lacrimal and salivary glands
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:aplasia of lacrimal and salivary glands | rel=r_associated | relid=0 | w=34
  124. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:autosomal dominant beta2-microglobulinic amyloidosis
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant beta2-microglobulinic amyloidosis | rel=r_associated | relid=0 | w=34
  125. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:autosomal dominant intermediate charcot-marie-tooth disease type e
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant intermediate charcot-marie-tooth disease type e | rel=r_associated | relid=0 | w=34
  126. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:autosomal dominant late onset basal ganglia degeneration
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant late onset basal ganglia degeneration | rel=r_associated | relid=0 | w=34
  127. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:autosomal dominant macrothrombocytopenia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant macrothrombocytopenia | rel=r_associated | relid=0 | w=34
  128. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:autosomal dominant polycystic kidney disease
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant polycystic kidney disease | rel=r_associated | relid=0 | w=34
  129. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:autosomal dominant progressive nephropathy with hypertension
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant progressive nephropathy with hypertension | rel=r_associated | relid=0 | w=34
  130. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:beckwith-wiedemann syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:beckwith-wiedemann syndrome | rel=r_associated | relid=0 | w=34
  131. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:benign autosomal dominant osteopetrosis
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:benign autosomal dominant osteopetrosis | rel=r_associated | relid=0 | w=34
  132. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:bethlem myopathy 1
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:bethlem myopathy 1 | rel=r_associated | relid=0 | w=34
  133. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:book syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:book syndrome | rel=r_associated | relid=0 | w=34
  134. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:burn-mckeown syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:burn-mckeown syndrome | rel=r_associated | relid=0 | w=34
  135. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:cole disease
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:cole disease | rel=r_associated | relid=0 | w=34
  136. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:congenital adrenal hyperplasia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:congenital adrenal hyperplasia | rel=r_associated | relid=0 | w=34
  137. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:congenital pancreatic enterokinase deficiency
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:congenital pancreatic enterokinase deficiency | rel=r_associated | relid=0 | w=34
  138. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:craniofacial deafness hand syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:craniofacial deafness hand syndrome | rel=r_associated | relid=0 | w=34
  139. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:craniosynostosis with dandy-walker malformation and hydrocephalus syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:craniosynostosis with dandy-walker malformation and hydrocephalus syndrome | rel=r_associated | relid=0 | w=34
  140. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:crouzon syndrome with acanthosis nigricans (disorder)
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=34
  141. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:deafness-hypogonadism syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:deafness-hypogonadism syndrome | rel=r_associated | relid=0 | w=34
  142. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:familial benign neonatal epilepsy
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:familial benign neonatal epilepsy | rel=r_associated | relid=0 | w=34
  143. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:familial hypodontia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:familial hypodontia | rel=r_associated | relid=0 | w=34
  144. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:familial isolated arrhythmogenic right ventricular dysplasia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:familial isolated arrhythmogenic right ventricular dysplasia | rel=r_associated | relid=0 | w=34
  145. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:feigenbaum bergeron richardson syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:feigenbaum bergeron richardson syndrome | rel=r_associated | relid=0 | w=34
  146. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:geniospasm 1
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:geniospasm 1 | rel=r_associated | relid=0 | w=34
  147. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:goldberg-shprintzen megacolon syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:goldberg-shprintzen megacolon syndrome | rel=r_associated | relid=0 | w=34
  148. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:hand foot uterus syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hand foot uterus syndrome | rel=r_associated | relid=0 | w=34
  149. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:hereditary elliptocytosis due to alpha spectrin defect
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary elliptocytosis due to alpha spectrin defect | rel=r_associated | relid=0 | w=34
  150. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:hyperparathyroidism-jaw tumor syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hyperparathyroidism-jaw tumor syndrome | rel=r_associated | relid=0 | w=34
  151. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:hypoplastic tibia and postaxial polydactyly syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hypoplastic tibia and postaxial polydactyly syndrome | rel=r_associated | relid=0 | w=34
  152. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:ichthyosis, cyclic, with epidermolytic hyperkeratosis
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:ichthyosis, cyclic, with epidermolytic hyperkeratosis | rel=r_associated | relid=0 | w=34
  153. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:impaired glucose tolerance with hyperinsulism
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:impaired glucose tolerance with hyperinsulism | rel=r_associated | relid=0 | w=34
  154. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:intestinal epithelial dysplasia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:intestinal epithelial dysplasia | rel=r_associated | relid=0 | w=34
  155. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:iris coloboma with ptosis, hypertelorism, and mental retardation
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:iris coloboma with ptosis, hypertelorism, and mental retardation | rel=r_associated | relid=0 | w=34
  156. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:jones syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:jones syndrome | rel=r_associated | relid=0 | w=34
  157. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:lactase deficiency, congenital
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:lactase deficiency, congenital | rel=r_associated | relid=0 | w=34
  158. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:lamellar ichthyosis, autosomal dominant form
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:lamellar ichthyosis, autosomal dominant form | rel=r_associated | relid=0 | w=34
  159. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:li-fraumeni syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:li-fraumeni syndrome | rel=r_associated | relid=0 | w=34
  160. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:mental retardation, x-linked, syndromic 7
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:mental retardation, x-linked, syndromic 7 | rel=r_associated | relid=0 | w=34
  161. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:metaphyseal dysplasia, braun-tinschert type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:metaphyseal dysplasia, braun-tinschert type | rel=r_associated | relid=0 | w=34
  162. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:multiple endocrine neoplasia type 2b
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:multiple endocrine neoplasia type 2b | rel=r_associated | relid=0 | w=34
  163. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:neuronal intestinal pseudoobstruction
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:neuronal intestinal pseudoobstruction | rel=r_associated | relid=0 | w=34
  164. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:pfeiffer syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:pfeiffer syndrome | rel=r_associated | relid=0 | w=34
  165. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:polydactyly, preaxial ii (disorder)
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:polydactyly, preaxial ii (disorder) | rel=r_associated | relid=0 | w=34
  166. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:preaxial deficiency, postaxial polydactyly and hypospadias
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:preaxial deficiency, postaxial polydactyly and hypospadias | rel=r_associated | relid=0 | w=34
  167. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome | rel=r_associated | relid=0 | w=34
  168. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:rombo syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:rombo syndrome | rel=r_associated | relid=0 | w=34
  169. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:small patella syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:small patella syndrome | rel=r_associated | relid=0 | w=34
  170. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:sotos' syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:sotos' syndrome | rel=r_associated | relid=0 | w=34
  171. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:syndactyly, type i
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:syndactyly, type i | rel=r_associated | relid=0 | w=34
  172. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:syndrome, branchio-oculo-facial
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:syndrome, branchio-oculo-facial | rel=r_associated | relid=0 | w=34
  173. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:thickened earlobe with conductive deafness syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:thickened earlobe with conductive deafness syndrome | rel=r_associated | relid=0 | w=34
  174. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:urban schosser spohn syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:urban schosser spohn syndrome | rel=r_associated | relid=0 | w=34
  175. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:visceral myopathy, familial
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:visceral myopathy, familial | rel=r_associated | relid=0 | w=34
  176. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 34 / 0.791 -> en:vitreoretinochoroidopathy (disorder)
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:vitreoretinochoroidopathy (disorder) | rel=r_associated | relid=0 | w=34
  177. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:acromegaloid facial appearance syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:acromegaloid facial appearance syndrome | rel=r_associated | relid=0 | w=32
  178. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:alpha-methylacyl-coa racemase deficiency
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:alpha-methylacyl-coa racemase deficiency | rel=r_associated | relid=0 | w=32
  179. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:angel shaped phalangoepiphyseal dysplasia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:angel shaped phalangoepiphyseal dysplasia | rel=r_associated | relid=0 | w=32
  180. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:autosomal dominant cystoid macular edema
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant cystoid macular edema | rel=r_associated | relid=0 | w=32
  181. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:autosomal dominant epidermolysis bullosa simplex
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant epidermolysis bullosa simplex | rel=r_associated | relid=0 | w=32
  182. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:autosomal dominant muscular dystrophy not predominantly limb girdle
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant muscular dystrophy not predominantly limb girdle | rel=r_associated | relid=0 | w=32
  183. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:autosomal dominant mutilating keratoderma
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant mutilating keratoderma | rel=r_associated | relid=0 | w=32
  184. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:behavioral variant of frontotemporal dementia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:behavioral variant of frontotemporal dementia | rel=r_associated | relid=0 | w=32
  185. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:brachydactyly with syndactyly zhao type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:brachydactyly with syndactyly zhao type | rel=r_associated | relid=0 | w=32
  186. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:brachymorphism-onychodysplasia-dysphalangism syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:brachymorphism-onychodysplasia-dysphalangism syndrome | rel=r_associated | relid=0 | w=32
  187. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:brachytelephalangy, facial dysmorphism, kallmann syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:brachytelephalangy, facial dysmorphism, kallmann syndrome | rel=r_associated | relid=0 | w=32
  188. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:cataract glaucoma syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:cataract glaucoma syndrome | rel=r_associated | relid=0 | w=32
  189. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:charcot-marie-tooth disease, axonal, type 2b (disorder)
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:charcot-marie-tooth disease, axonal, type 2b (disorder) | rel=r_associated | relid=0 | w=32
  190. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:charcot-marie-tooth disease, axonal, type 2f
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:charcot-marie-tooth disease, axonal, type 2f | rel=r_associated | relid=0 | w=32
  191. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:chromosome 11p11.2 deletion syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:chromosome 11p11.2 deletion syndrome | rel=r_associated | relid=0 | w=32
  192. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:chromosome 17q21.31 deletion syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:chromosome 17q21.31 deletion syndrome | rel=r_associated | relid=0 | w=32
  193. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:chromosome 22q11.2 microduplication syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:chromosome 22q11.2 microduplication syndrome | rel=r_associated | relid=0 | w=32
  194. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:coach syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:coach syndrome | rel=r_associated | relid=0 | w=32
  195. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | rel=r_associated | relid=0 | w=32
  196. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:craniosynostosis with facial dysmorphism and brachydactyly syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:craniosynostosis with facial dysmorphism and brachydactyly syndrome | rel=r_associated | relid=0 | w=32
  197. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:de toni-debre-fanconi syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:de toni-debre-fanconi syndrome | rel=r_associated | relid=0 | w=32
  198. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:developmental malformation, deafness, dystonia syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:developmental malformation, deafness, dystonia syndrome | rel=r_associated | relid=0 | w=32
  199. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:edict syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:edict syndrome | rel=r_associated | relid=0 | w=32
  200. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:familial hemiplegic migraine
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:familial hemiplegic migraine | rel=r_associated | relid=0 | w=32
  201. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:familial hypoaldosteronism
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:familial hypoaldosteronism | rel=r_associated | relid=0 | w=32
  202. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:familial spontaneous pneumothorax
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:familial spontaneous pneumothorax | rel=r_associated | relid=0 | w=32
  203. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related | rel=r_associated | relid=0 | w=32
  204. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:generalized epilepsy and paroxysmal dyskinesia syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:generalized epilepsy and paroxysmal dyskinesia syndrome | rel=r_associated | relid=0 | w=32
  205. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:glucocorticoid deficiency with achalasia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:glucocorticoid deficiency with achalasia | rel=r_associated | relid=0 | w=32
  206. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:grayson wilbrandt corneal dystrophy
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:grayson wilbrandt corneal dystrophy | rel=r_associated | relid=0 | w=32
  207. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:halal syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:halal syndrome | rel=r_associated | relid=0 | w=32
  208. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:hereditary cystatin c amyloid angiopathy
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary cystatin c amyloid angiopathy | rel=r_associated | relid=0 | w=32
  209. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:hereditary diffuse gastric adenocarcinoma
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary diffuse gastric adenocarcinoma | rel=r_associated | relid=0 | w=32
  210. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:hereditary isolated hypoparathyroidism due to impaired parathormone secretion
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary isolated hypoparathyroidism due to impaired parathormone secretion | rel=r_associated | relid=0 | w=32
  211. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:huntington disease-like 2
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:huntington disease-like 2 | rel=r_associated | relid=0 | w=32
  212. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:hyperferritinemia, hereditary, with congenital cataracts
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hyperferritinemia, hereditary, with congenital cataracts | rel=r_associated | relid=0 | w=32
  213. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:hyperinsulinism due to hnf4a deficiency
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hyperinsulinism due to hnf4a deficiency | rel=r_associated | relid=0 | w=32
  214. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:hypomagnesemia 1, intestinal
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hypomagnesemia 1, intestinal | rel=r_associated | relid=0 | w=32
  215. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:hypothyroidism due to mutation in transcription factor of pituitary development
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hypothyroidism due to mutation in transcription factor of pituitary development | rel=r_associated | relid=0 | w=32
  216. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:image syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:image syndrome | rel=r_associated | relid=0 | w=32
  217. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:insulin resistance
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:insulin resistance | rel=r_associated | relid=0 | w=32
  218. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:isolated autosomal dominant hypomagnesemia glaudemans type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:isolated autosomal dominant hypomagnesemia glaudemans type | rel=r_associated | relid=0 | w=32
  219. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:ladda zonana ramer syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:ladda zonana ramer syndrome | rel=r_associated | relid=0 | w=32
  220. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:laurin-sandrow syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:laurin-sandrow syndrome | rel=r_associated | relid=0 | w=32
  221. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:leukokeratosis, hereditary mucosal
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=32
  222. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:limb-mammary syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:limb-mammary syndrome | rel=r_associated | relid=0 | w=32
  223. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:lowry yong syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:lowry yong syndrome | rel=r_associated | relid=0 | w=32
  224. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:macular coloboma, cleft palate, hallux valgus syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:macular coloboma, cleft palate, hallux valgus syndrome | rel=r_associated | relid=0 | w=32
  225. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:microphthalmia, syndromic 6 (disorder)
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:microphthalmia, syndromic 6 (disorder) | rel=r_associated | relid=0 | w=32
  226. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:mowat-wilson syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:mowat-wilson syndrome | rel=r_associated | relid=0 | w=32
  227. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:mucopolysaccharidosis ii
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:mucopolysaccharidosis ii | rel=r_associated | relid=0 | w=32
  228. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:multiple gastrointestinal atresias (disorder)
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:multiple gastrointestinal atresias (disorder) | rel=r_associated | relid=0 | w=32
  229. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:neurofibromatosis, type 1-like syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:neurofibromatosis, type 1-like syndrome | rel=r_associated | relid=0 | w=32
  230. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:okihiro syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:okihiro syndrome | rel=r_associated | relid=0 | w=32
  231. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:osteopoikilosis and dacryocystitis
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:osteopoikilosis and dacryocystitis | rel=r_associated | relid=0 | w=32
  232. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:palmoplantar keratoderma with deafness
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:palmoplantar keratoderma with deafness | rel=r_associated | relid=0 | w=32
  233. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:phosphoserine aminotransferase deficiency
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:phosphoserine aminotransferase deficiency | rel=r_associated | relid=0 | w=32
  234. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:piebaldism
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:piebaldism | rel=r_associated | relid=0 | w=32
  235. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:spinocerebellar ataxia 23
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia 23 | rel=r_associated | relid=0 | w=32
  236. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:spinocerebellar ataxia type 2
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia type 2 | rel=r_associated | relid=0 | w=32
  237. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:split-hand-foot malformation with long bone deficiency 1
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:split-hand-foot malformation with long bone deficiency 1 | rel=r_associated | relid=0 | w=32
  238. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:stapes ankylosis with broad thumb and toes (disorder)
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:stapes ankylosis with broad thumb and toes (disorder) | rel=r_associated | relid=0 | w=32
  239. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:thiel-behnke corneal dystrophy
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:thiel-behnke corneal dystrophy | rel=r_associated | relid=0 | w=32
  240. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:transthyretin related familial amyloid cardiomyopathy
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:transthyretin related familial amyloid cardiomyopathy | rel=r_associated | relid=0 | w=32
  241. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:tubular renal disease with cardiomyopathy syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:tubular renal disease with cardiomyopathy syndrome | rel=r_associated | relid=0 | w=32
  242. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:upington disease
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:upington disease | rel=r_associated | relid=0 | w=32
  243. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 32 / 0.744 -> en:wnt4 mullerian aplasia and ovarian dysfunction
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:wnt4 mullerian aplasia and ovarian dysfunction | rel=r_associated | relid=0 | w=32
  244. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:3-hydroxyacyl-coa dehydrogenase deficiency
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:3-hydroxyacyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=31
  245. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:absence of fingerprints with congenital milia syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:absence of fingerprints with congenital milia syndrome | rel=r_associated | relid=0 | w=31
  246. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:achalasia microcephaly
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:achalasia microcephaly | rel=r_associated | relid=0 | w=31
  247. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:ackerman syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:ackerman syndrome | rel=r_associated | relid=0 | w=31
  248. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:acropectorovertebral dysplasia, f-form
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:acropectorovertebral dysplasia, f-form | rel=r_associated | relid=0 | w=31
  249. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:adult onset autosomal dominant leukodystrophy
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:adult onset autosomal dominant leukodystrophy | rel=r_associated | relid=0 | w=31
  250. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:al gazali hirschsprung syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:al gazali hirschsprung syndrome | rel=r_associated | relid=0 | w=31
  251. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough | rel=r_associated | relid=0 | w=31
  252. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=31
  253. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:autosomal dominant focal dystonia dyt25 type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant focal dystonia dyt25 type | rel=r_associated | relid=0 | w=31
  254. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:autosomal dominant ichthyosis
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant ichthyosis | rel=r_associated | relid=0 | w=31
  255. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:branchio-oto-renal syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:branchio-oto-renal syndrome | rel=r_associated | relid=0 | w=31
  256. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:capillary malformation-arteriovenous malformation (disorder)
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:capillary malformation-arteriovenous malformation (disorder) | rel=r_associated | relid=0 | w=31
  257. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:centronuclear myopathy 1
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:centronuclear myopathy 1 | rel=r_associated | relid=0 | w=31
  258. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:charcot-marie-tooth disease, type 2j
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:charcot-marie-tooth disease, type 2j | rel=r_associated | relid=0 | w=31
  259. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:chromosome 3q29 deletion syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:chromosome 3q29 deletion syndrome | rel=r_associated | relid=0 | w=31
  260. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:congenital reticular ichthyosiform erythroderma
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:congenital reticular ichthyosiform erythroderma | rel=r_associated | relid=0 | w=31
  261. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:craniosynostosis, type 2
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:craniosynostosis, type 2 | rel=r_associated | relid=0 | w=31
  262. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:diarrhea 4, malabsorptive, congenital
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:diarrhea 4, malabsorptive, congenital | rel=r_associated | relid=0 | w=31
  263. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:dicer1 syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:dicer1 syndrome | rel=r_associated | relid=0 | w=31
  264. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:ectopic hyperinsulinism
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:ectopic hyperinsulinism | rel=r_associated | relid=0 | w=31
  265. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:ehlers-danlos syndrome vascular-like type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:ehlers-danlos syndrome vascular-like type | rel=r_associated | relid=0 | w=31
  266. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:familial median cleft of upper and lower lip
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:familial median cleft of upper and lower lip | rel=r_associated | relid=0 | w=31
  267. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:fibular aplasia and ectrodactyly syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:fibular aplasia and ectrodactyly syndrome | rel=r_associated | relid=0 | w=31
  268. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:functional hyperinsulinism
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:functional hyperinsulinism | rel=r_associated | relid=0 | w=31
  269. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:glutamate dehydrogenase 1 hyperinsulinism
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:glutamate dehydrogenase 1 hyperinsulinism | rel=r_associated | relid=0 | w=31
  270. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:haspeslagh fryns muelenaere syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:haspeslagh fryns muelenaere syndrome | rel=r_associated | relid=0 | w=31
  271. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:hepatolenticular degeneration
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hepatolenticular degeneration | rel=r_associated | relid=0 | w=31
  272. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:hereditary adrenal unresponsiveness to corticotropin
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary adrenal unresponsiveness to corticotropin | rel=r_associated | relid=0 | w=31
  273. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:hereditary nonpolyposis colorectal cancer
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary nonpolyposis colorectal cancer | rel=r_associated | relid=0 | w=31
  274. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:hereditary oculoleptomeningeal amyloid angiopathy
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=31
  275. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:hereditary stomatocytosis
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary stomatocytosis | rel=r_associated | relid=0 | w=31
  276. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:hereditary systemic amyloidosis
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary systemic amyloidosis | rel=r_associated | relid=0 | w=31
  277. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:hypogonadism-cataract syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hypogonadism-cataract syndrome | rel=r_associated | relid=0 | w=31
  278. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:iatrogenic hyperinsulinism
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:iatrogenic hyperinsulinism | rel=r_associated | relid=0 | w=31
  279. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:inherited disorder of thyroid metabolism
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:inherited disorder of thyroid metabolism | rel=r_associated | relid=0 | w=31
  280. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:jaundice, chronic idiopathic
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:jaundice, chronic idiopathic | rel=r_associated | relid=0 | w=31
  281. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:keratoderma, palmoplantar, diffuse
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:keratoderma, palmoplantar, diffuse | rel=r_associated | relid=0 | w=31
  282. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:leukodystrophy, hypomyelinating, with hypodontia and hypogonadotropic hypogonadism
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:leukodystrophy, hypomyelinating, with hypodontia and hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=31
  283. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:liddle syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:liddle syndrome | rel=r_associated | relid=0 | w=31
  284. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:lissencephaly due to tuba1a (tubulin alpha 1a) mutation
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:lissencephaly due to tuba1a (tubulin alpha 1a) mutation | rel=r_associated | relid=0 | w=31
  285. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:mammary-digital-nail syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:mammary-digital-nail syndrome | rel=r_associated | relid=0 | w=31
  286. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:median nodule of upper lip
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:median nodule of upper lip | rel=r_associated | relid=0 | w=31
  287. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:nemaline myopathy 3
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:nemaline myopathy 3 | rel=r_associated | relid=0 | w=31
  288. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:neuropathy, hereditary thermosensitive
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:neuropathy, hereditary thermosensitive | rel=r_associated | relid=0 | w=31
  289. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:oculocerebral syndrome with hypopigmentation
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:oculocerebral syndrome with hypopigmentation | rel=r_associated | relid=0 | w=31
  290. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:odontoma dysphagia syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:odontoma dysphagia syndrome | rel=r_associated | relid=0 | w=31
  291. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:osteosclerosis, developmental delay, craniosynostosis syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:osteosclerosis, developmental delay, craniosynostosis syndrome | rel=r_associated | relid=0 | w=31
  292. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:roch leri mesosomatous lipomatosis
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:roch leri mesosomatous lipomatosis | rel=r_associated | relid=0 | w=31
  293. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:sting-associated vasculopathy with onset in infancy
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:sting-associated vasculopathy with onset in infancy | rel=r_associated | relid=0 | w=31
  294. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:trigonocephaly with broad thumb syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:trigonocephaly with broad thumb syndrome | rel=r_associated | relid=0 | w=31
  295. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:tungland bellman syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:tungland bellman syndrome | rel=r_associated | relid=0 | w=31
  296. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:vitelliform macular dystrophy
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:vitelliform macular dystrophy | rel=r_associated | relid=0 | w=31
  297. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:waardenburg syndrome, type 4a
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:waardenburg syndrome, type 4a | rel=r_associated | relid=0 | w=31
  298. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 31 / 0.721 -> en:wt limb blood syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:wt limb blood syndrome | rel=r_associated | relid=0 | w=31
  299. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:17q11.2 microduplication syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:17q11.2 microduplication syndrome | rel=r_associated | relid=0 | w=30
  300. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:acrodysostosis
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:acrodysostosis | rel=r_associated | relid=0 | w=30
  301. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:alopecia, epilepsy, pyorrhea, mental subnormality
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:alopecia, epilepsy, pyorrhea, mental subnormality | rel=r_associated | relid=0 | w=30
  302. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps | rel=r_associated | relid=0 | w=30
  303. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:aphalangy and syndactyly with microcephaly syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:aphalangy and syndactyly with microcephaly syndrome | rel=r_associated | relid=0 | w=30
  304. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:autosomal dominant charcot-marie-tooth disease type 2c
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant charcot-marie-tooth disease type 2c | rel=r_associated | relid=0 | w=30
  305. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:autosomal dominant deficiency of plasminogen
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant deficiency of plasminogen | rel=r_associated | relid=0 | w=30
  306. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:bixler christian gorlin syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:bixler christian gorlin syndrome | rel=r_associated | relid=0 | w=30
  307. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:brachydactyly types b and e combined
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:brachydactyly types b and e combined | rel=r_associated | relid=0 | w=30
  308. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:branchiogenic-deafness syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:branchiogenic-deafness syndrome | rel=r_associated | relid=0 | w=30
  309. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:brooke-spiegler syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:brooke-spiegler syndrome | rel=r_associated | relid=0 | w=30
  310. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | rel=r_associated | relid=0 | w=30
  311. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:crigler najjar syndrome, type 1
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:crigler najjar syndrome, type 1 | rel=r_associated | relid=0 | w=30
  312. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:dystonia 12
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:dystonia 12 | rel=r_associated | relid=0 | w=30
  313. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:dystrophia myotonica 2
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:dystrophia myotonica 2 | rel=r_associated | relid=0 | w=30
  314. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:epithelial recurrent erosion dystrophy
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:epithelial recurrent erosion dystrophy | rel=r_associated | relid=0 | w=30
  315. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:familial arthrogryposis-cholestatic hepatorenal syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:familial arthrogryposis-cholestatic hepatorenal syndrome | rel=r_associated | relid=0 | w=30
  316. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:familial encephalopathy with neuroserpin inclusion bodies
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:familial encephalopathy with neuroserpin inclusion bodies | rel=r_associated | relid=0 | w=30
  317. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:familial osteochondritis dissecans
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:familial osteochondritis dissecans | rel=r_associated | relid=0 | w=30
  318. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:familial thyroid dyshormonogenesis
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:familial thyroid dyshormonogenesis | rel=r_associated | relid=0 | w=30
  319. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:fasting hyperinsulinemia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:fasting hyperinsulinemia | rel=r_associated | relid=0 | w=30
  320. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:fibrodysplasia ossificans progressiva
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:fibrodysplasia ossificans progressiva | rel=r_associated | relid=0 | w=30
  321. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:hereditary gastrogenic lactose intolerance
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary gastrogenic lactose intolerance | rel=r_associated | relid=0 | w=30
  322. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:hereditary isolated hypoparathyroidism due to agenesis of parathyroid gland
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary isolated hypoparathyroidism due to agenesis of parathyroid gland | rel=r_associated | relid=0 | w=30
  323. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:hereditary vascular retinopathy
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary vascular retinopathy | rel=r_associated | relid=0 | w=30
  324. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:holt-oram syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:holt-oram syndrome | rel=r_associated | relid=0 | w=30
  325. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:hydrocephalus with obesity and hypogonadism syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hydrocephalus with obesity and hypogonadism syndrome | rel=r_associated | relid=0 | w=30
  326. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:hyperinsulinism due to insulin receptor deficiency
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hyperinsulinism due to insulin receptor deficiency | rel=r_associated | relid=0 | w=30
  327. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:hypoparathyroidism - autosomal dominant
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hypoparathyroidism - autosomal dominant | rel=r_associated | relid=0 | w=30
  328. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:hypotrichosis simplex of scalp
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hypotrichosis simplex of scalp | rel=r_associated | relid=0 | w=30
  329. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:idiopathic transient neonatal hyperinsulinemia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:idiopathic transient neonatal hyperinsulinemia | rel=r_associated | relid=0 | w=30
  330. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:johnson neuroectodermal syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:johnson neuroectodermal syndrome | rel=r_associated | relid=0 | w=30
  331. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:keratitis, hereditary
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:keratitis, hereditary | rel=r_associated | relid=0 | w=30
  332. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:leopard syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:leopard syndrome | rel=r_associated | relid=0 | w=30
  333. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:leukotriene c4 synthase deficiency
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:leukotriene c4 synthase deficiency | rel=r_associated | relid=0 | w=30
  334. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:lubani al saleh teebi syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:lubani al saleh teebi syndrome | rel=r_associated | relid=0 | w=30
  335. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:lung fibrosis, immunodeficiency, 46,xx gonadal dysgenesis syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:lung fibrosis, immunodeficiency, 46,xx gonadal dysgenesis syndrome | rel=r_associated | relid=0 | w=30
  336. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:mandibulofacial dysostosis
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:mandibulofacial dysostosis | rel=r_associated | relid=0 | w=30
  337. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:marfan syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:marfan syndrome | rel=r_associated | relid=0 | w=30
  338. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:mcpherson clemens syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:mcpherson clemens syndrome | rel=r_associated | relid=0 | w=30
  339. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:microphthalmia, syndromic 5
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:microphthalmia, syndromic 5 | rel=r_associated | relid=0 | w=30
  340. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:mitochondrial neurogastrointestinal encephalomyopathy syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | rel=r_associated | relid=0 | w=30
  341. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones | rel=r_associated | relid=0 | w=30
  342. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:morava mehes syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:morava mehes syndrome | rel=r_associated | relid=0 | w=30
  343. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:multiple epiphyseal dysplasia beighton type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:multiple epiphyseal dysplasia beighton type | rel=r_associated | relid=0 | w=30
  344. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:myopathy, distal, tateyama type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:myopathy, distal, tateyama type | rel=r_associated | relid=0 | w=30
  345. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:north american indian childhood cirrhosis
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:north american indian childhood cirrhosis | rel=r_associated | relid=0 | w=30
  346. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:other hyperinsulinism
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:other hyperinsulinism | rel=r_associated | relid=0 | w=30
  347. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:pancreatic colipase deficiency
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:pancreatic colipase deficiency | rel=r_associated | relid=0 | w=30
  348. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:paraganglioma and gastric stromal sarcoma
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:paraganglioma and gastric stromal sarcoma | rel=r_associated | relid=0 | w=30
  349. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:peripheral resistance to thyroid hormone
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:peripheral resistance to thyroid hormone | rel=r_associated | relid=0 | w=30
  350. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:platelet-type von willebrand disease
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:platelet-type von willebrand disease | rel=r_associated | relid=0 | w=30
  351. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:primary pigmented nodular adrenocortical disease
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:primary pigmented nodular adrenocortical disease | rel=r_associated | relid=0 | w=30
  352. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:pseudohypoparathyroidism type 1c
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:pseudohypoparathyroidism type 1c | rel=r_associated | relid=0 | w=30
  353. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:reis-bucklers' corneal dystrophy
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:reis-bucklers' corneal dystrophy | rel=r_associated | relid=0 | w=30
  354. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:spinocerebellar ataxia 17
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia 17 | rel=r_associated | relid=0 | w=30
  355. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:spinocerebellar ataxia 36
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia 36 | rel=r_associated | relid=0 | w=30
  356. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:spinocerebellar ataxia type 5
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia type 5 | rel=r_associated | relid=0 | w=30
  357. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:spondylocostal dysostosis 4, autosomal dominant
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spondylocostal dysostosis 4, autosomal dominant | rel=r_associated | relid=0 | w=30
  358. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:syndactyly, type iii
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:syndactyly, type iii | rel=r_associated | relid=0 | w=30
  359. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:syndactyly, type v
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:syndactyly, type v | rel=r_associated | relid=0 | w=30
  360. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:tarsal-carpal coalition syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:tarsal-carpal coalition syndrome | rel=r_associated | relid=0 | w=30
  361. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 30 / 0.698 -> en:x-linked intellectual disability van esch type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:x-linked intellectual disability van esch type | rel=r_associated | relid=0 | w=30
  362. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:ablepharon-macrostomia syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:ablepharon-macrostomia syndrome | rel=r_associated | relid=0 | w=29
  363. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:acute intermittent porphyria
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:acute intermittent porphyria | rel=r_associated | relid=0 | w=29
  364. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:amelogenesis imperfecta, type ib
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:amelogenesis imperfecta, type ib | rel=r_associated | relid=0 | w=29
  365. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:angioedemas, hereditary
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:angioedemas, hereditary | rel=r_associated | relid=0 | w=29
  366. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:apert syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:apert syndrome | rel=r_associated | relid=0 | w=29
  367. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:autosomal dominant hyperinsulinism due to sur1 deficiency
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant hyperinsulinism due to sur1 deficiency | rel=r_associated | relid=0 | w=29
  368. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:bannayan-riley-ruvalcaba syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:bannayan-riley-ruvalcaba syndrome | rel=r_associated | relid=0 | w=29
  369. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:bilateral pheochromocytoma and islet cell adenoma of the pancreas
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:bilateral pheochromocytoma and islet cell adenoma of the pancreas | rel=r_associated | relid=0 | w=29
  370. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:cerebral hemorrhage with amyloidosis, hereditary, dutch type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:cerebral hemorrhage with amyloidosis, hereditary, dutch type | rel=r_associated | relid=0 | w=29
  371. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:cerebrooculonasal syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:cerebrooculonasal syndrome | rel=r_associated | relid=0 | w=29
  372. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:char syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:char syndrome | rel=r_associated | relid=0 | w=29
  373. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:charcot-marie-tooth disease, autosomal dominant, type 2k
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:charcot-marie-tooth disease, autosomal dominant, type 2k | rel=r_associated | relid=0 | w=29
  374. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:choreoathetosis/spasticity, episodic
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:choreoathetosis/spasticity, episodic | rel=r_associated | relid=0 | w=29
  375. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=29
  376. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:cochleosaccular degeneration of the inner ear and progressive cataracts
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:cochleosaccular degeneration of the inner ear and progressive cataracts | rel=r_associated | relid=0 | w=29
  377. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:congenital nephrogenic diabetes insipidus
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:congenital nephrogenic diabetes insipidus | rel=r_associated | relid=0 | w=29
  378. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:cutis laxa, autosomal dominant
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:cutis laxa, autosomal dominant | rel=r_associated | relid=0 | w=29
  379. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:dahlberg borer newcomer syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:dahlberg borer newcomer syndrome | rel=r_associated | relid=0 | w=29
  380. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:deafness enamel hypoplasia nail defects
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:deafness enamel hypoplasia nail defects | rel=r_associated | relid=0 | w=29
  381. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:deafness-craniofacial syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:deafness-craniofacial syndrome | rel=r_associated | relid=0 | w=29
  382. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:dentatorubral-pallidoluysian atrophy
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:dentatorubral-pallidoluysian atrophy | rel=r_associated | relid=0 | w=29
  383. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:developmental absence of tooth
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:developmental absence of tooth | rel=r_associated | relid=0 | w=29
  384. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:enterokinase deficiency
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:enterokinase deficiency | rel=r_associated | relid=0 | w=29
  385. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:familial digital arthropathy and brachydactyly syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:familial digital arthropathy and brachydactyly syndrome | rel=r_associated | relid=0 | w=29
  386. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:familial papillary thyroid carcinoma with renal papillary neoplasia syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:familial papillary thyroid carcinoma with renal papillary neoplasia syndrome | rel=r_associated | relid=0 | w=29
  387. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:freeman-sheldon syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:freeman-sheldon syndrome | rel=r_associated | relid=0 | w=29
  388. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:frontotemporal dementia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:frontotemporal dementia | rel=r_associated | relid=0 | w=29
  389. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:hawkinsinuria
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hawkinsinuria | rel=r_associated | relid=0 | w=29
  390. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:hereditary breast and ovarian cancer syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary breast and ovarian cancer syndrome | rel=r_associated | relid=0 | w=29
  391. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:hereditary elliptocytosis due to abnormal protein 4.1
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary elliptocytosis due to abnormal protein 4.1 | rel=r_associated | relid=0 | w=29
  392. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:hereditary gingival fibromatosis
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary gingival fibromatosis | rel=r_associated | relid=0 | w=29
  393. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:hereditary papillary renal carcinoma
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary papillary renal carcinoma | rel=r_associated | relid=0 | w=29
  394. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:juvenile cataract, microcornea, renal glucosuria syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:juvenile cataract, microcornea, renal glucosuria syndrome | rel=r_associated | relid=0 | w=29
  395. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:kapur toriello syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:kapur toriello syndrome | rel=r_associated | relid=0 | w=29
  396. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:keratosis palmoplantaris papulosa
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:keratosis palmoplantaris papulosa | rel=r_associated | relid=0 | w=29
  397. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:mullerian duct and limb anomalies syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:mullerian duct and limb anomalies syndrome | rel=r_associated | relid=0 | w=29
  398. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:neurofibromatosis 1
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:neurofibromatosis 1 | rel=r_associated | relid=0 | w=29
  399. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:oculodental syndrome rutherfurd syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29
  400. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:odontotrichoungual-digital-palmar syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:odontotrichoungual-digital-palmar syndrome | rel=r_associated | relid=0 | w=29
  401. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:pancreas agenesis, dorsal
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:pancreas agenesis, dorsal | rel=r_associated | relid=0 | w=29
  402. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:parastremmatic dwarfism
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:parastremmatic dwarfism | rel=r_associated | relid=0 | w=29
  403. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:parietal foramina
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:parietal foramina | rel=r_associated | relid=0 | w=29
  404. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:pitt-hopkins syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:pitt-hopkins syndrome | rel=r_associated | relid=0 | w=29
  405. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:popliteal pterygium syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:popliteal pterygium syndrome | rel=r_associated | relid=0 | w=29
  406. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:progressive heterotopic heteroplasia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:progressive heterotopic heteroplasia | rel=r_associated | relid=0 | w=29
  407. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:proteus-like syndrome (disorder)
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:proteus-like syndrome (disorder) | rel=r_associated | relid=0 | w=29
  408. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:pseudohypoaldosteronism, type 1, recessive form
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:pseudohypoaldosteronism, type 1, recessive form | rel=r_associated | relid=0 | w=29
  409. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:scalp-ear-nipple syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:scalp-ear-nipple syndrome | rel=r_associated | relid=0 | w=29
  410. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:sellars beighton syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:sellars beighton syndrome | rel=r_associated | relid=0 | w=29
  411. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:simpson-golabi-behmel syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:simpson-golabi-behmel syndrome | rel=r_associated | relid=0 | w=29
  412. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:spinocerebellar ataxia 11
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia 11 | rel=r_associated | relid=0 | w=29
  413. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:spinocerebellar ataxia 15
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia 15 | rel=r_associated | relid=0 | w=29
  414. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:spinocerebellar ataxia 30
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia 30 | rel=r_associated | relid=0 | w=29
  415. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:spinocerebellar ataxia type 4
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia type 4 | rel=r_associated | relid=0 | w=29
  416. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:spondyloepiphyseal dysplasia-brachydactyly and distinctive speech
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spondyloepiphyseal dysplasia-brachydactyly and distinctive speech | rel=r_associated | relid=0 | w=29
  417. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:spondyloepiphyseal dysplasia, kimberley type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spondyloepiphyseal dysplasia, kimberley type | rel=r_associated | relid=0 | w=29
  418. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:trichohepatoenteric syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:trichohepatoenteric syndrome | rel=r_associated | relid=0 | w=29
  419. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 29 / 0.674 -> en:zimmerman laband syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:zimmerman laband syndrome | rel=r_associated | relid=0 | w=29
  420. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:aase smith syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:aase smith syndrome | rel=r_associated | relid=0 | w=28
  421. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | rel=r_associated | relid=0 | w=28
  422. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:alpha-fetoprotein, hereditary persistence of
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:alpha-fetoprotein, hereditary persistence of | rel=r_associated | relid=0 | w=28
  423. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:aniridia and intellectual disability syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:aniridia and intellectual disability syndrome | rel=r_associated | relid=0 | w=28
  424. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:aniridia, ptosis, intellectual disability, familial obesity syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | rel=r_associated | relid=0 | w=28
  425. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:autoimmune lymphoproliferative syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autoimmune lymphoproliferative syndrome | rel=r_associated | relid=0 | w=28
  426. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:autosomal dominant charcot-marie-tooth disease type 2a1
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant charcot-marie-tooth disease type 2a1 | rel=r_associated | relid=0 | w=28
  427. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:autosomal dominant charcot-marie-tooth disease type 2m
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant charcot-marie-tooth disease type 2m | rel=r_associated | relid=0 | w=28
  428. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder)
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) | rel=r_associated | relid=0 | w=28
  429. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:autosomal dominant pterygium of conjunctiva
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant pterygium of conjunctiva | rel=r_associated | relid=0 | w=28
  430. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:bilateral microtia with deafness and cleft palate syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:bilateral microtia with deafness and cleft palate syndrome | rel=r_associated | relid=0 | w=28
  431. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:bilateral multiple fibroadenoma of breast
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:bilateral multiple fibroadenoma of breast | rel=r_associated | relid=0 | w=28
  432. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:blepharoptosis, myopia, ectopia lentis syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:blepharoptosis, myopia, ectopia lentis syndrome | rel=r_associated | relid=0 | w=28
  433. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:brachydactyly with hypertension
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:brachydactyly with hypertension | rel=r_associated | relid=0 | w=28
  434. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:brachydactyly, type a1 (disorder)
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:brachydactyly, type a1 (disorder) | rel=r_associated | relid=0 | w=28
  435. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:cardiac anomaly and heterotaxy syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:cardiac anomaly and heterotaxy syndrome | rel=r_associated | relid=0 | w=28
  436. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:charcot-marie-tooth disease, axonal, type 2g
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:charcot-marie-tooth disease, axonal, type 2g | rel=r_associated | relid=0 | w=28
  437. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:chorioretinal atrophy, progressive bifocal
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:chorioretinal atrophy, progressive bifocal | rel=r_associated | relid=0 | w=28
  438. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:congenital dyserythropoietic anemia, type iii
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:congenital dyserythropoietic anemia, type iii | rel=r_associated | relid=0 | w=28
  439. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:congenital sucrase-isomaltase deficiency
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:congenital sucrase-isomaltase deficiency | rel=r_associated | relid=0 | w=28
  440. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:craniosynostosis, philadelphia type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:craniosynostosis, philadelphia type | rel=r_associated | relid=0 | w=28
  441. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | rel=r_associated | relid=0 | w=28
  442. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:dyschondrosteosis and nephritis syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:dyschondrosteosis and nephritis syndrome | rel=r_associated | relid=0 | w=28
  443. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:epilepsy, myoclonic, benign adult familial, type 2
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:epilepsy, myoclonic, benign adult familial, type 2 | rel=r_associated | relid=0 | w=28
  444. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:familial amyloid polyneuropathy, type v
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:familial amyloid polyneuropathy, type v | rel=r_associated | relid=0 | w=28
  445. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:familial partial lipodystrophy, type 2
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:familial partial lipodystrophy, type 2 | rel=r_associated | relid=0 | w=28
  446. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:genitopatellar syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:genitopatellar syndrome | rel=r_associated | relid=0 | w=28
  447. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:glycogen storage disease 0, liver
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:glycogen storage disease 0, liver | rel=r_associated | relid=0 | w=28
  448. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:hereditary elliptocytosis due to deficiency of protein 4.1
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary elliptocytosis due to deficiency of protein 4.1 | rel=r_associated | relid=0 | w=28
  449. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:hereditary myopathy with early respiratory failure
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary myopathy with early respiratory failure | rel=r_associated | relid=0 | w=28
  450. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:hereditary sensory and autonomic neuropathy type 1b
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary sensory and autonomic neuropathy type 1b | rel=r_associated | relid=0 | w=28
  451. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:hyperinsulinemic hypoglycemia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hyperinsulinemic hypoglycemia | rel=r_associated | relid=0 | w=28
  452. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:inclusion body myopathy with early-onset paget disease and frontotemporal dementia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:inclusion body myopathy with early-onset paget disease and frontotemporal dementia | rel=r_associated | relid=0 | w=28
  453. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:kallmann syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:kallmann syndrome | rel=r_associated | relid=0 | w=28
  454. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:macular dystrophy, concentric annular
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:macular dystrophy, concentric annular | rel=r_associated | relid=0 | w=28
  455. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:may-hegglin anomaly
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:may-hegglin anomaly | rel=r_associated | relid=0 | w=28
  456. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:nance-horan syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:nance-horan syndrome | rel=r_associated | relid=0 | w=28
  457. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:oculodigitoesophagoduodenal syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:oculodigitoesophagoduodenal syndrome | rel=r_associated | relid=0 | w=28
  458. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:omphalocele cleft palate syndrome lethal
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:omphalocele cleft palate syndrome lethal | rel=r_associated | relid=0 | w=28
  459. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:papillon-lefevre disease
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:papillon-lefevre disease | rel=r_associated | relid=0 | w=28
  460. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:pelvis-shoulder dysplasia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:pelvis-shoulder dysplasia | rel=r_associated | relid=0 | w=28
  461. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:periodontitis co-occurrent with genetic disorder
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:periodontitis co-occurrent with genetic disorder | rel=r_associated | relid=0 | w=28
  462. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:reardon hall slaney syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:reardon hall slaney syndrome | rel=r_associated | relid=0 | w=28
  463. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:rotor syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:rotor syndrome | rel=r_associated | relid=0 | w=28
  464. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:schilbach-rott syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:schilbach-rott syndrome | rel=r_associated | relid=0 | w=28
  465. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:scholte syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:scholte syndrome | rel=r_associated | relid=0 | w=28
  466. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:short stature, pituitary and cerebellar defect and small sella turcica syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:short stature, pituitary and cerebellar defect and small sella turcica syndrome | rel=r_associated | relid=0 | w=28
  467. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:shprintzen-goldberg syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:shprintzen-goldberg syndrome | rel=r_associated | relid=0 | w=28
  468. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:spinocerebellar ataxia 21
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia 21 | rel=r_associated | relid=0 | w=28
  469. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:spinocerebellar ataxia 8
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia 8 | rel=r_associated | relid=0 | w=28
  470. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:spinocerebellar ataxia type 35
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia type 35 | rel=r_associated | relid=0 | w=28
  471. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:split-hand with congenital nystagmus, fundal changes, and cataracts
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:split-hand with congenital nystagmus, fundal changes, and cataracts | rel=r_associated | relid=0 | w=28
  472. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:spondyloepimetaphyseal dysplasia, missouri type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spondyloepimetaphyseal dysplasia, missouri type | rel=r_associated | relid=0 | w=28
  473. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:spondylometaphyseal dysplasia with dentinogenesis imperfecta
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spondylometaphyseal dysplasia with dentinogenesis imperfecta | rel=r_associated | relid=0 | w=28
  474. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:spondyloperipheral dysplasia short ulna
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spondyloperipheral dysplasia short ulna | rel=r_associated | relid=0 | w=28
  475. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:steatocystoma multiplex with natal tooth syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:steatocystoma multiplex with natal tooth syndrome | rel=r_associated | relid=0 | w=28
  476. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:steinfeld syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:steinfeld syndrome | rel=r_associated | relid=0 | w=28
  477. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:turcot syndrome (disorder)
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:turcot syndrome (disorder) | rel=r_associated | relid=0 | w=28
  478. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:uveal coloboma with cleft lip and palate and intellectual disability syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:uveal coloboma with cleft lip and palate and intellectual disability syndrome | rel=r_associated | relid=0 | w=28
  479. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:white platelet syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:white platelet syndrome | rel=r_associated | relid=0 | w=28
  480. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:whyte hemingway carpal tarsal phalangeal osteolyses
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:whyte hemingway carpal tarsal phalangeal osteolyses | rel=r_associated | relid=0 | w=28
  481. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:x-linked adrenal hypoplasia congenita
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:x-linked adrenal hypoplasia congenita | rel=r_associated | relid=0 | w=28
  482. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:x-linked intellectual disability cilliers type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:x-linked intellectual disability cilliers type | rel=r_associated | relid=0 | w=28
  483. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 28 / 0.651 -> en:yorifuji okuno syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:yorifuji okuno syndrome | rel=r_associated | relid=0 | w=28
  484. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:acanthosis nigricans and insulin resistance with muscle cramp and acral enlargement syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:acanthosis nigricans and insulin resistance with muscle cramp and acral enlargement syndrome | rel=r_associated | relid=0 | w=27
  485. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:acropectoral syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:acropectoral syndrome | rel=r_associated | relid=0 | w=27
  486. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:adrenal gland hyperplasia ii
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:adrenal gland hyperplasia ii | rel=r_associated | relid=0 | w=27
  487. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:alport syndrome, autosomal dominant
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:alport syndrome, autosomal dominant | rel=r_associated | relid=0 | w=27
  488. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:ameloonychohypohidrotic syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:ameloonychohypohidrotic syndrome | rel=r_associated | relid=0 | w=27
  489. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:aniridia and absent patella
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:aniridia and absent patella | rel=r_associated | relid=0 | w=27
  490. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:arthrogryposis, distal, type 1
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:arthrogryposis, distal, type 1 | rel=r_associated | relid=0 | w=27
  491. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:autosomal dominant ichthyosis vulgaris
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant ichthyosis vulgaris | rel=r_associated | relid=0 | w=27
  492. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:autosomal dominant oculocutaneous albinism
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant oculocutaneous albinism | rel=r_associated | relid=0 | w=27
  493. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:autosomal dominant variant form of albumin
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant variant form of albumin | rel=r_associated | relid=0 | w=27
  494. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:basal cell nevus syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:basal cell nevus syndrome | rel=r_associated | relid=0 | w=27
  495. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:cataract, congenital, cerulean type 1
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:cataract, congenital, cerulean type 1 | rel=r_associated | relid=0 | w=27
  496. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:charcot-marie-tooth disease, axonal, type 2l (disorder)
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:charcot-marie-tooth disease, axonal, type 2l (disorder) | rel=r_associated | relid=0 | w=27
  497. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:charcot-marie-tooth disease, axonal, type 2n
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:charcot-marie-tooth disease, axonal, type 2n | rel=r_associated | relid=0 | w=27
  498. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:chronic atrial and intestinal dysrhythmia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:chronic atrial and intestinal dysrhythmia | rel=r_associated | relid=0 | w=27
  499. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:corneal dystrophy, congenital stromal
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:corneal dystrophy, congenital stromal | rel=r_associated | relid=0 | w=27
  500. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:czech dysplasia, metatarsal type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:czech dysplasia, metatarsal type | rel=r_associated | relid=0 | w=27
  501. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:dysphasia, familial developmental
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:dysphasia, familial developmental | rel=r_associated | relid=0 | w=27
  502. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:ehlers-danlos syndrome, type i
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:ehlers-danlos syndrome, type i | rel=r_associated | relid=0 | w=27
  503. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:erythrokeratodermia with ataxia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:erythrokeratodermia with ataxia | rel=r_associated | relid=0 | w=27
  504. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:familial adrenocortical hypoplasia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:familial adrenocortical hypoplasia | rel=r_associated | relid=0 | w=27
  505. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:frontotemporal dementia, chromosome 3-linked
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:frontotemporal dementia, chromosome 3-linked | rel=r_associated | relid=0 | w=27
  506. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:glomerulopathy with fibronectin deposits 2 (disorder)
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:glomerulopathy with fibronectin deposits 2 (disorder) | rel=r_associated | relid=0 | w=27
  507. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:hamartoma syndrome, multiple
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hamartoma syndrome, multiple | rel=r_associated | relid=0 | w=27
  508. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:hemochromatosis, type 4
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hemochromatosis, type 4 | rel=r_associated | relid=0 | w=27
  509. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:hereditary elliptocytosis due to beta spectrin defect in self-association
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary elliptocytosis due to beta spectrin defect in self-association | rel=r_associated | relid=0 | w=27
  510. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=27
  511. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:hereditary sensory autonomic neuropathy, type 1
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary sensory autonomic neuropathy, type 1 | rel=r_associated | relid=0 | w=27
  512. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:heterozygous methylenetetrahydrofolate reductase mutation
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:heterozygous methylenetetrahydrofolate reductase mutation | rel=r_associated | relid=0 | w=27
  513. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:hip dysplasia, beukes type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hip dysplasia, beukes type | rel=r_associated | relid=0 | w=27
  514. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:homozygous methylenetetrahydrofolate reductase mutation
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:homozygous methylenetetrahydrofolate reductase mutation | rel=r_associated | relid=0 | w=27
  515. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:hypogonadism with prune belly syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hypogonadism with prune belly syndrome | rel=r_associated | relid=0 | w=27
  516. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:ichthyosis congenita with biliary atresia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:ichthyosis congenita with biliary atresia | rel=r_associated | relid=0 | w=27
  517. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:jackson-weiss syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:jackson-weiss syndrome | rel=r_associated | relid=0 | w=27
  518. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:keratoacanthoma familial
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:keratoacanthoma familial | rel=r_associated | relid=0 | w=27
  519. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:lymphedema and cerebral arteriovenous anomaly syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:lymphedema and cerebral arteriovenous anomaly syndrome | rel=r_associated | relid=0 | w=27
  520. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:martsolf syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:martsolf syndrome | rel=r_associated | relid=0 | w=27
  521. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:melanoma astrocytoma syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:melanoma astrocytoma syndrome | rel=r_associated | relid=0 | w=27
  522. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:metabolic syndrome x
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:metabolic syndrome x | rel=r_associated | relid=0 | w=27
  523. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:microcephaly deafness syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:microcephaly deafness syndrome | rel=r_associated | relid=0 | w=27
  524. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:moloney syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:moloney syndrome | rel=r_associated | relid=0 | w=27
  525. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:moyamoya disease with early onset achalasia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:moyamoya disease with early onset achalasia | rel=r_associated | relid=0 | w=27
  526. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:muckle-wells syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:muckle-wells syndrome | rel=r_associated | relid=0 | w=27
  527. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:nicolaides baraitser syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:nicolaides baraitser syndrome | rel=r_associated | relid=0 | w=27
  528. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:optic atrophy, autosomal dominant
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:optic atrophy, autosomal dominant | rel=r_associated | relid=0 | w=27
  529. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:osteogenesis imperfecta, levin type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:osteogenesis imperfecta, levin type | rel=r_associated | relid=0 | w=27
  530. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:overgrowth, macrocephaly, facial dysmorphism syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:overgrowth, macrocephaly, facial dysmorphism syndrome | rel=r_associated | relid=0 | w=27
  531. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:pancreatic triacylglycerol lipase deficiency
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:pancreatic triacylglycerol lipase deficiency | rel=r_associated | relid=0 | w=27
  532. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:persistent hyperinsulinemic hypoglycemia of infancy
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:persistent hyperinsulinemic hypoglycemia of infancy | rel=r_associated | relid=0 | w=27
  533. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:reticulate acropigmentation of kitamura
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:reticulate acropigmentation of kitamura | rel=r_associated | relid=0 | w=27
  534. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:santos mateus leal syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:santos mateus leal syndrome | rel=r_associated | relid=0 | w=27
  535. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:schaap taylor baraitser syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:schaap taylor baraitser syndrome | rel=r_associated | relid=0 | w=27
  536. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:schnyder crystalline corneal dystrophy
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:schnyder crystalline corneal dystrophy | rel=r_associated | relid=0 | w=27
  537. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:short fifth metacarpal insulin resistance syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:short fifth metacarpal insulin resistance syndrome | rel=r_associated | relid=0 | w=27
  538. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:spinocerebellar ataxia 10
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia 10 | rel=r_associated | relid=0 | w=27
  539. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:spinocerebellar ataxia 31 (disorder)
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia 31 (disorder) | rel=r_associated | relid=0 | w=27
  540. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:spinocerebellar ataxia type 32
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia type 32 | rel=r_associated | relid=0 | w=27
  541. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:spondylometaphyseal dysplasia, algerian type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spondylometaphyseal dysplasia, algerian type | rel=r_associated | relid=0 | w=27
  542. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:steatocystoma multiplex
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:steatocystoma multiplex | rel=r_associated | relid=0 | w=27
  543. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:ulna metaphyseal dysplasia syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:ulna metaphyseal dysplasia syndrome | rel=r_associated | relid=0 | w=27
  544. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:wellesley carman french syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:wellesley carman french syndrome | rel=r_associated | relid=0 | w=27
  545. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> en:zlotogora-ogur syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:zlotogora-ogur syndrome | rel=r_associated | relid=0 | w=27
  546. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 27 / 0.628 -> protéine
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=protéine | rel=r_associated | relid=0 | w=27
  547. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:adult onset non-insulinoma persistent hyperinsulinemic hypoglycemia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:adult onset non-insulinoma persistent hyperinsulinemic hypoglycemia | rel=r_associated | relid=0 | w=26
  548. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:advanced sleep-phase syndrome, familial
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:advanced sleep-phase syndrome, familial | rel=r_associated | relid=0 | w=26
  549. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:amelogenesis imperfecta
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:amelogenesis imperfecta | rel=r_associated | relid=0 | w=26
  550. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:amyloid neuropathies, familial
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:amyloid neuropathies, familial | rel=r_associated | relid=0 | w=26
  551. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:andersen syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:andersen syndrome | rel=r_associated | relid=0 | w=26
  552. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:ankylosing vertebral hyperostosis with tylosis syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:ankylosing vertebral hyperostosis with tylosis syndrome | rel=r_associated | relid=0 | w=26
  553. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:atelosteogenesis, type 1
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:atelosteogenesis, type 1 | rel=r_associated | relid=0 | w=26
  554. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:autosomal dominant familial woolly hair
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant familial woolly hair | rel=r_associated | relid=0 | w=26
  555. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:autosomal dominant hyperinsulinism due to kir6.2 deficiency
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant hyperinsulinism due to kir6.2 deficiency | rel=r_associated | relid=0 | w=26
  556. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:autosomal dominant palmoplantar keratoderma and congenital alopecia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:autosomal dominant palmoplantar keratoderma and congenital alopecia | rel=r_associated | relid=0 | w=26
  557. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:brachydactyly, type a2
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:brachydactyly, type a2 | rel=r_associated | relid=0 | w=26
  558. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:brachyolmia type 3
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:brachyolmia type 3 | rel=r_associated | relid=0 | w=26
  559. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:charcot-marie-tooth disease, axonal, type 2e (disorder)
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:charcot-marie-tooth disease, axonal, type 2e (disorder) | rel=r_associated | relid=0 | w=26
  560. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:cleft palate with short stature and vertebral anomaly syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:cleft palate with short stature and vertebral anomaly syndrome | rel=r_associated | relid=0 | w=26
  561. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:combined pituitary hormone deficiency genetic form
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:combined pituitary hormone deficiency genetic form | rel=r_associated | relid=0 | w=26
  562. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:cutaneous photosensitivity and lethal colitis syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:cutaneous photosensitivity and lethal colitis syndrome | rel=r_associated | relid=0 | w=26
  563. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:diffuse palmoplantar keratoderma and acrocyanosis syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:diffuse palmoplantar keratoderma and acrocyanosis syndrome | rel=r_associated | relid=0 | w=26
  564. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:doughnut lesions of skull, familial
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:doughnut lesions of skull, familial | rel=r_associated | relid=0 | w=26
  565. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:epiphyseal dysplasia, multiple, 1
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:epiphyseal dysplasia, multiple, 1 | rel=r_associated | relid=0 | w=26
  566. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:familial cerebral cavernous malformation
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:familial cerebral cavernous malformation | rel=r_associated | relid=0 | w=26
  567. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:fechtner syndrome (disorder)
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:fechtner syndrome (disorder) | rel=r_associated | relid=0 | w=26
  568. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:foxg1 syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:foxg1 syndrome | rel=r_associated | relid=0 | w=26
  569. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:generalized myotonia of thomsen
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:generalized myotonia of thomsen | rel=r_associated | relid=0 | w=26
  570. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:glomuvenous malformations
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:glomuvenous malformations | rel=r_associated | relid=0 | w=26
  571. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:glucose transporter protein type 1 deficiency syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:glucose transporter protein type 1 deficiency syndrome | rel=r_associated | relid=0 | w=26
  572. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:heart-hand syndrome, slovenian type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:heart-hand syndrome, slovenian type | rel=r_associated | relid=0 | w=26
  573. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:hereditary cerebral amyloid angiopathy, icelandic type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary cerebral amyloid angiopathy, icelandic type | rel=r_associated | relid=0 | w=26
  574. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:hereditary multiple exostoses
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary multiple exostoses | rel=r_associated | relid=0 | w=26
  575. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:heritable pulmonary arterial hypertension due to bmpr2 mutation
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:heritable pulmonary arterial hypertension due to bmpr2 mutation | rel=r_associated | relid=0 | w=26
  576. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:hunter-mcalpine craniosynostosis syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hunter-mcalpine craniosynostosis syndrome | rel=r_associated | relid=0 | w=26
  577. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:hyperinsulinemic hypoglycemia, familial, 7
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hyperinsulinemic hypoglycemia, familial, 7 | rel=r_associated | relid=0 | w=26
  578. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:hyperinsulinism due to hnf1a deficiency
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hyperinsulinism due to hnf1a deficiency | rel=r_associated | relid=0 | w=26
  579. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:hyperpigmentation, familial progressive
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hyperpigmentation, familial progressive | rel=r_associated | relid=0 | w=26
  580. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:hyperuricemia, anemia, renal failure syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hyperuricemia, anemia, renal failure syndrome | rel=r_associated | relid=0 | w=26
  581. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:hypogonadotropic hypogonadism with frontoparietal alopecia syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hypogonadotropic hypogonadism with frontoparietal alopecia syndrome | rel=r_associated | relid=0 | w=26
  582. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:kbg syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:kbg syndrome | rel=r_associated | relid=0 | w=26
  583. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:loeys-dietz syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:loeys-dietz syndrome | rel=r_associated | relid=0 | w=26
  584. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:lopes gorlin syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:lopes gorlin syndrome | rel=r_associated | relid=0 | w=26
  585. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:mesomelic dwarfism reinhardt pfeiffer type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:mesomelic dwarfism reinhardt pfeiffer type | rel=r_associated | relid=0 | w=26
  586. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:multiple endocrine neoplasia type 2a
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:multiple endocrine neoplasia type 2a | rel=r_associated | relid=0 | w=26
  587. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:muscular dystrophy, oculopharyngeal
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:muscular dystrophy, oculopharyngeal | rel=r_associated | relid=0 | w=26
  588. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:myopathy, distal 2
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:myopathy, distal 2 | rel=r_associated | relid=0 | w=26
  589. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:najjar syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:najjar syndrome | rel=r_associated | relid=0 | w=26
  590. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:neurofibromatosis 2
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:neurofibromatosis 2 | rel=r_associated | relid=0 | w=26
  591. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:oculopalatocerebral syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:oculopalatocerebral syndrome | rel=r_associated | relid=0 | w=26
  592. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome | rel=r_associated | relid=0 | w=26
  593. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:polycystic liver disease
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:polycystic liver disease | rel=r_associated | relid=0 | w=26
  594. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:potassium aggravated myotonia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:potassium aggravated myotonia | rel=r_associated | relid=0 | w=26
  595. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:pten hamartoma tumor syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:pten hamartoma tumor syndrome | rel=r_associated | relid=0 | w=26
  596. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:self-induced hyperinsulinemia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:self-induced hyperinsulinemia | rel=r_associated | relid=0 | w=26
  597. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:short stature with valvular heart disease and characteristic facies syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:short stature with valvular heart disease and characteristic facies syndrome | rel=r_associated | relid=0 | w=26
  598. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:shprintzen omphalocele syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:shprintzen omphalocele syndrome | rel=r_associated | relid=0 | w=26
  599. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:spinocerebellar ataxia 20
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia 20 | rel=r_associated | relid=0 | w=26
  600. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:spinocerebellar ataxia type 1
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia type 1 | rel=r_associated | relid=0 | w=26
  601. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:spinocerebellar ataxia type 6 (disorder)
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia type 6 (disorder) | rel=r_associated | relid=0 | w=26
  602. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:spinocerebellar ataxia type 7
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spinocerebellar ataxia type 7 | rel=r_associated | relid=0 | w=26
  603. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:spondyloepiphyseal dysplasia reardon type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spondyloepiphyseal dysplasia reardon type | rel=r_associated | relid=0 | w=26
  604. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:spondyloepiphyseal dysplasia, maroteaux type
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:spondyloepiphyseal dysplasia, maroteaux type | rel=r_associated | relid=0 | w=26
  605. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:syndactyly, type iv
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:syndactyly, type iv | rel=r_associated | relid=0 | w=26
  606. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:syndromic orbital border hypoplasia
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:syndromic orbital border hypoplasia | rel=r_associated | relid=0 | w=26
  607. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:synpolydactyly
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:synpolydactyly | rel=r_associated | relid=0 | w=26
  608. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:ulnar-mammary syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:ulnar-mammary syndrome | rel=r_associated | relid=0 | w=26
  609. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:x-linked intellectual disability with precocious puberty and obesity syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:x-linked intellectual disability with precocious puberty and obesity syndrome | rel=r_associated | relid=0 | w=26
  610. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 26 / 0.605 -> en:xanthomatosis, cerebrotendinous
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:xanthomatosis, cerebrotendinous | rel=r_associated | relid=0 | w=26
  611. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 20 / 0.465 -> en:chronic diarrhea with villous atrophy syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:chronic diarrhea with villous atrophy syndrome | rel=r_associated | relid=0 | w=20
  612. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 20 / 0.465 -> en:corneal dystrophy, subepithelial mucinous
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:corneal dystrophy, subepithelial mucinous | rel=r_associated | relid=0 | w=20
  613. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 20 / 0.465 -> en:epiphyseal dysplasia, multiple, 2
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:epiphyseal dysplasia, multiple, 2 | rel=r_associated | relid=0 | w=20
  614. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 20 / 0.465 -> en:ferro-cerebro-cutaneous syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:ferro-cerebro-cutaneous syndrome | rel=r_associated | relid=0 | w=20
  615. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 20 / 0.465 -> en:ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis | rel=r_associated | relid=0 | w=20
  616. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 20 / 0.465 -> en:insulin growth factor i deficiency
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:insulin growth factor i deficiency | rel=r_associated | relid=0 | w=20
  617. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 20 / 0.465 -> en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome | rel=r_associated | relid=0 | w=20
  618. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 20 / 0.465 -> en:piussan lenaerts mathieu syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:piussan lenaerts mathieu syndrome | rel=r_associated | relid=0 | w=20
  619. en:hyperinsulinism due to uncoupling protein 2 deficiency -- r_associated #0: 20 / 0.465 -> en:pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome
    n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome | rel=r_associated | relid=0 | w=20
≈ 661 relations entrantes

  1. en:gracile bone dysplasia --- r_associated #0: 43 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:gracile bone dysplasia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=43
  2. en:insulin growth factor i deficiency --- r_associated #0: 36 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:insulin growth factor i deficiency | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=36
  3. en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome --- r_associated #0: 35 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=35
  4. en:morava mehes syndrome --- r_associated #0: 35 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:morava mehes syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=35
  5. en:polydactyly, preaxial ii (disorder) --- r_associated #0: 35 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:polydactyly, preaxial ii (disorder) | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=35
  6. en:cleidorhizomelic syndrome --- r_associated #0: 34 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:cleidorhizomelic syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=34
  7. en:corneal dystrophy, subepithelial mucinous --- r_associated #0: 34 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:corneal dystrophy, subepithelial mucinous | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=34
  8. en:czech dysplasia, metatarsal type --- r_associated #0: 34 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:czech dysplasia, metatarsal type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=34
  9. en:ehlers-danlos syndrome vascular-like type --- r_associated #0: 34 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:ehlers-danlos syndrome vascular-like type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=34
  10. en:epiphyseal dysplasia, multiple, 2 --- r_associated #0: 34 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:epiphyseal dysplasia, multiple, 2 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=34
  11. en:halal syndrome --- r_associated #0: 34 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:halal syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=34
  12. en:hereditary sensory and autonomic neuropathy type 1b --- r_associated #0: 34 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary sensory and autonomic neuropathy type 1b | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=34
  13. en:pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome --- r_associated #0: 34 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=34
  14. en:steatocystoma multiplex with natal tooth syndrome --- r_associated #0: 34 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:steatocystoma multiplex with natal tooth syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=34
  15. en:17q11.2 microduplication syndrome --- r_associated #0: 32 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:17q11.2 microduplication syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=32
  16. en:aniridia, ptosis, intellectual disability, familial obesity syndrome --- r_associated #0: 32 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=32
  17. en:autosomal dominant focal dystonia dyt25 type --- r_associated #0: 32 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant focal dystonia dyt25 type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=32
  18. en:cardiac anomaly and heterotaxy syndrome --- r_associated #0: 32 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:cardiac anomaly and heterotaxy syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=32
  19. en:craniosynostosis with facial dysmorphism and brachydactyly syndrome --- r_associated #0: 32 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:craniosynostosis with facial dysmorphism and brachydactyly syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=32
  20. en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome --- r_associated #0: 32 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=32
  21. en:hyperuricemia, anemia, renal failure syndrome --- r_associated #0: 32 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hyperuricemia, anemia, renal failure syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=32
  22. en:x-linked intellectual disability van esch type --- r_associated #0: 32 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:x-linked intellectual disability van esch type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=32
  23. en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein --- r_associated #0: 31 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=31
  24. en:aphalangy and syndactyly with microcephaly syndrome --- r_associated #0: 31 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:aphalangy and syndactyly with microcephaly syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=31
  25. en:autosomal dominant palmoplantar keratoderma and congenital alopecia --- r_associated #0: 31 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant palmoplantar keratoderma and congenital alopecia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=31
  26. en:moyamoya disease with early onset achalasia --- r_associated #0: 31 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:moyamoya disease with early onset achalasia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=31
  27. en:piussan lenaerts mathieu syndrome --- r_associated #0: 31 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:piussan lenaerts mathieu syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=31
  28. en:primary pigmented nodular adrenocortical disease --- r_associated #0: 31 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:primary pigmented nodular adrenocortical disease | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=31
  29. en:short fifth metacarpal insulin resistance syndrome --- r_associated #0: 31 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:short fifth metacarpal insulin resistance syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=31
  30. en:autosomal dominant charcot-marie-tooth disease type 2m --- r_associated #0: 30 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant charcot-marie-tooth disease type 2m | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=30
  31. en:chronic diarrhea with villous atrophy syndrome --- r_associated #0: 30 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:chronic diarrhea with villous atrophy syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=30
  32. en:familial median cleft of upper and lower lip --- r_associated #0: 30 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:familial median cleft of upper and lower lip | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=30
  33. en:hyperinsulinism due to insulin receptor deficiency --- r_associated #0: 30 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hyperinsulinism due to insulin receptor deficiency | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=30
  34. en:najjar syndrome --- r_associated #0: 30 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:najjar syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=30
  35. en:scholte syndrome --- r_associated #0: 30 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:scholte syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=30
  36. en:spinocerebellar ataxia type 37 --- r_associated #0: 30 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia type 37 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=30
  37. en:timothy syndrome type 2 --- r_associated #0: 30 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:timothy syndrome type 2 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=30
  38. en:absence of fingerprints with congenital milia syndrome --- r_associated #0: 29 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:absence of fingerprints with congenital milia syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=29
  39. en:cutaneous photosensitivity and lethal colitis syndrome --- r_associated #0: 29 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:cutaneous photosensitivity and lethal colitis syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=29
  40. en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome --- r_associated #0: 29 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=29
  41. en:ferro-cerebro-cutaneous syndrome --- r_associated #0: 29 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:ferro-cerebro-cutaneous syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=29
  42. en:hyperinsulinism due to focal adenomatous hyperplasia --- r_associated #0: 29 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hyperinsulinism due to focal adenomatous hyperplasia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=29
  43. en:ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis --- r_associated #0: 29 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=29
  44. en:aniridia and intellectual disability syndrome --- r_associated #0: 28 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:aniridia and intellectual disability syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=28
  45. en:bamforth syndrome --- r_associated #0: 28 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:bamforth syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=28
  46. en:spinocerebellar ataxia type 32 --- r_associated #0: 28 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia type 32 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=28
  47. en:tubular renal disease with cardiomyopathy syndrome --- r_associated #0: 28 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:tubular renal disease with cardiomyopathy syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=28
  48. en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges --- r_associated #0: 27 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=27
  49. en:hyperinsulinism due to hnf1a deficiency --- r_associated #0: 27 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hyperinsulinism due to hnf1a deficiency | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=27
  50. en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome --- r_associated #0: 27 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=27
  51. en:preaxial deficiency, postaxial polydactyly and hypospadias --- r_associated #0: 27 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:preaxial deficiency, postaxial polydactyly and hypospadias | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=27
  52. en:acro-dermato-ungual-lacrimal-tooth syndrome --- r_associated #0: 26 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:acro-dermato-ungual-lacrimal-tooth syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=26
  53. en:autosomal dominant beta2-microglobulinic amyloidosis --- r_associated #0: 26 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant beta2-microglobulinic amyloidosis | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=26
  54. en:bethlem myopathy 1 --- r_associated #0: 26 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:bethlem myopathy 1 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=26
  55. en:brachytelephalangy, facial dysmorphism, kallmann syndrome --- r_associated #0: 26 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:brachytelephalangy, facial dysmorphism, kallmann syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=26
  56. en:cataract glaucoma syndrome --- r_associated #0: 26 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:cataract glaucoma syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=26
  57. en:diffuse palmoplantar keratoderma and acrocyanosis syndrome --- r_associated #0: 26 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:diffuse palmoplantar keratoderma and acrocyanosis syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=26
  58. en:dyschondrosteosis and nephritis syndrome --- r_associated #0: 26 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:dyschondrosteosis and nephritis syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=26
  59. en:hereditary isolated hypoparathyroidism due to agenesis of parathyroid gland --- r_associated #0: 26 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary isolated hypoparathyroidism due to agenesis of parathyroid gland | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=26
  60. en:x-linked intellectual disability with acromegaly and hyperactivity syndrome --- r_associated #0: 26 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=26
  61. dysplasie olfacto-génitale --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=dysplasie olfacto-génitale | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  62. dysplasie olfactogénitale --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=dysplasie olfactogénitale | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  63. dysplasie olfactogénitale de De Morsier --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=dysplasie olfactogénitale de De Morsier | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  64. démence fronto-temporale --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=démence fronto-temporale | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  65. en:3-hydroxyacyl-coa dehydrogenase deficiency --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:3-hydroxyacyl-coa dehydrogenase deficiency | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  66. en:aase smith syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:aase smith syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  67. en:ablepharon-macrostomia syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:ablepharon-macrostomia syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  68. en:abruzzo erickson syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:abruzzo erickson syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  69. en:acanthosis nigricans and insulin resistance with muscle cramp and acral enlargement syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:acanthosis nigricans and insulin resistance with muscle cramp and acral enlargement syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  70. en:achalasia microcephaly --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:achalasia microcephaly | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  71. en:ackerman syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:ackerman syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  72. en:acrodysostosis --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:acrodysostosis | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  73. en:acromegaloid facial appearance syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:acromegaloid facial appearance syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  74. en:acromicric dysplasia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:acromicric dysplasia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  75. en:acropectoral syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:acropectoral syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  76. en:acropectorovertebral dysplasia, f-form --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:acropectorovertebral dysplasia, f-form | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  77. en:acute intermittent porphyria --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:acute intermittent porphyria | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  78. en:adrenal gland hyperplasia ii --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:adrenal gland hyperplasia ii | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  79. en:adrenoleukodystrophy --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:adrenoleukodystrophy | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  80. en:adult onset autosomal dominant leukodystrophy --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:adult onset autosomal dominant leukodystrophy | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  81. en:adult onset non-insulinoma persistent hyperinsulinemic hypoglycemia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:adult onset non-insulinoma persistent hyperinsulinemic hypoglycemia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  82. en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  83. en:advanced sleep-phase syndrome, familial --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:advanced sleep-phase syndrome, familial | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  84. en:al gazali hirschsprung syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:al gazali hirschsprung syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  85. en:alagille syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:alagille syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  86. en:alimentary hyperinsulinemia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:alimentary hyperinsulinemia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  87. en:alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  88. en:alopecia, epilepsy, pyorrhea, mental subnormality --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:alopecia, epilepsy, pyorrhea, mental subnormality | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  89. en:alpha 1-antitrypsin deficiency --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:alpha 1-antitrypsin deficiency | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  90. en:alpha-fetoprotein, hereditary persistence of --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:alpha-fetoprotein, hereditary persistence of | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  91. en:alpha-methylacyl-coa racemase deficiency --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:alpha-methylacyl-coa racemase deficiency | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  92. en:alport syndrome, autosomal dominant --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:alport syndrome, autosomal dominant | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  93. en:amelogenesis imperfecta --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:amelogenesis imperfecta | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  94. en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  95. en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  96. en:amelogenesis imperfecta, type ib --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:amelogenesis imperfecta, type ib | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  97. en:ameloonychohypohidrotic syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:ameloonychohypohidrotic syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  98. en:amyloid neuropathies, familial --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:amyloid neuropathies, familial | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  99. en:andersen syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:andersen syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  100. en:angel shaped phalangoepiphyseal dysplasia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:angel shaped phalangoepiphyseal dysplasia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  101. en:angioedemas, hereditary --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:angioedemas, hereditary | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  102. en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  103. en:aniridia and absent patella --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:aniridia and absent patella | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  104. en:ankylosing vertebral hyperostosis with tylosis syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:ankylosing vertebral hyperostosis with tylosis syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  105. en:apert syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:apert syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  106. en:aplasia of lacrimal and salivary glands --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:aplasia of lacrimal and salivary glands | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  107. en:arthrogryposis, distal, type 1 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:arthrogryposis, distal, type 1 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  108. en:atelosteogenesis, type 1 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:atelosteogenesis, type 1 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  109. en:auriculo-condylar syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:auriculo-condylar syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  110. en:autoimmune lymphoproliferative syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autoimmune lymphoproliferative syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  111. en:autosomal dominant charcot-marie-tooth disease type 2a1 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant charcot-marie-tooth disease type 2a1 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  112. en:autosomal dominant charcot-marie-tooth disease type 2c --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant charcot-marie-tooth disease type 2c | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  113. en:autosomal dominant cystoid macular edema --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant cystoid macular edema | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  114. en:autosomal dominant deficiency of plasminogen --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant deficiency of plasminogen | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  115. en:autosomal dominant epidermolysis bullosa simplex --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant epidermolysis bullosa simplex | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  116. en:autosomal dominant excess of transthyretin --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant excess of transthyretin | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  117. en:autosomal dominant familial woolly hair --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant familial woolly hair | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  118. en:autosomal dominant hyperinsulinism due to kir6.2 deficiency --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant hyperinsulinism due to kir6.2 deficiency | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  119. en:autosomal dominant hyperinsulinism due to sur1 deficiency --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant hyperinsulinism due to sur1 deficiency | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  120. en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  121. en:autosomal dominant hypophosphatemic bone disease --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant hypophosphatemic bone disease | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  122. en:autosomal dominant ichthyosis --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant ichthyosis | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  123. en:autosomal dominant ichthyosis vulgaris --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant ichthyosis vulgaris | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  124. en:autosomal dominant idiopathic familial dystonia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant idiopathic familial dystonia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  125. en:autosomal dominant intermediate charcot-marie-tooth disease type e --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant intermediate charcot-marie-tooth disease type e | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  126. en:autosomal dominant late onset basal ganglia degeneration --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant late onset basal ganglia degeneration | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  127. en:autosomal dominant macrothrombocytopenia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant macrothrombocytopenia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  128. en:autosomal dominant muscular dystrophy not predominantly limb girdle --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant muscular dystrophy not predominantly limb girdle | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  129. en:autosomal dominant muscular dystrophy with limb girdle distribution --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant muscular dystrophy with limb girdle distribution | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  130. en:autosomal dominant mutilating keratoderma --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant mutilating keratoderma | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  131. en:autosomal dominant oculocutaneous albinism --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant oculocutaneous albinism | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  132. en:autosomal dominant polycystic kidney disease --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant polycystic kidney disease | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  133. en:autosomal dominant progressive nephropathy with hypertension --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant progressive nephropathy with hypertension | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  134. en:autosomal dominant pterygium of conjunctiva --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant pterygium of conjunctiva | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  135. en:autosomal dominant retinitis pigmentosa --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant retinitis pigmentosa | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  136. en:autosomal dominant variant form of albumin --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:autosomal dominant variant form of albumin | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  137. en:avascular necrosis of femur head --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:avascular necrosis of femur head | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  138. en:bannayan-riley-ruvalcaba syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:bannayan-riley-ruvalcaba syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  139. en:basal cell nevus syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:basal cell nevus syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  140. en:beare-stevenson cutis gyrata syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:beare-stevenson cutis gyrata syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  141. en:beckwith-wiedemann syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:beckwith-wiedemann syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  142. en:behavioral variant of frontotemporal dementia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:behavioral variant of frontotemporal dementia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  143. en:benign autosomal dominant osteopetrosis --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:benign autosomal dominant osteopetrosis | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  144. en:bilateral microtia with deafness and cleft palate syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:bilateral microtia with deafness and cleft palate syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  145. en:bilateral multiple fibroadenoma of breast --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:bilateral multiple fibroadenoma of breast | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  146. en:bilateral pheochromocytoma and islet cell adenoma of the pancreas --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:bilateral pheochromocytoma and islet cell adenoma of the pancreas | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  147. en:bixler christian gorlin syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:bixler christian gorlin syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  148. en:blau syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:blau syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  149. en:blepharo-cheilo-dontic syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:blepharo-cheilo-dontic syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  150. en:blepharoptosis, myopia, ectopia lentis syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:blepharoptosis, myopia, ectopia lentis syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  151. en:blindness, scoliosis, arachnodactyly syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:blindness, scoliosis, arachnodactyly syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  152. en:book syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:book syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  153. en:bork stender schmidt syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:bork stender schmidt syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  154. en:brachydactyly type a5 nail dysplasia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:brachydactyly type a5 nail dysplasia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  155. en:brachydactyly type a6 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:brachydactyly type a6 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  156. en:brachydactyly types b and e combined --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:brachydactyly types b and e combined | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  157. en:brachydactyly with hypertension --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:brachydactyly with hypertension | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  158. en:brachydactyly with syndactyly zhao type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:brachydactyly with syndactyly zhao type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  159. en:brachydactyly, type a1 (disorder) --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:brachydactyly, type a1 (disorder) | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  160. en:brachydactyly, type a2 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:brachydactyly, type a2 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  161. en:brachymesophalangy 2 and 5 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:brachymesophalangy 2 and 5 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  162. en:brachymorphism-onychodysplasia-dysphalangism syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:brachymorphism-onychodysplasia-dysphalangism syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  163. en:brachyolmia type 3 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:brachyolmia type 3 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  164. en:branchio-oto-renal syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:branchio-oto-renal syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  165. en:branchiogenic-deafness syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:branchiogenic-deafness syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  166. en:brooke-spiegler syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:brooke-spiegler syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  167. en:burn-mckeown syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:burn-mckeown syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  168. en:cap myopathy --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:cap myopathy | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  169. en:capillary malformation-arteriovenous malformation (disorder) --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:capillary malformation-arteriovenous malformation (disorder) | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  170. en:carnevale hernandez castillo syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:carnevale hernandez castillo syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  171. en:cataract, congenital, cerulean type 1 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:cataract, congenital, cerulean type 1 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  172. en:centronuclear myopathy 1 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:centronuclear myopathy 1 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  173. en:cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  174. en:cerebral hemorrhage with amyloidosis, hereditary, dutch type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:cerebral hemorrhage with amyloidosis, hereditary, dutch type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  175. en:cerebrooculonasal syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:cerebrooculonasal syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  176. en:char syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:char syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  177. en:charcot-marie-tooth disease type 2d --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:charcot-marie-tooth disease type 2d | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  178. en:charcot-marie-tooth disease, autosomal dominant, type 2k --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:charcot-marie-tooth disease, autosomal dominant, type 2k | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  179. en:charcot-marie-tooth disease, axonal, type 2b (disorder) --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:charcot-marie-tooth disease, axonal, type 2b (disorder) | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  180. en:charcot-marie-tooth disease, axonal, type 2e (disorder) --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:charcot-marie-tooth disease, axonal, type 2e (disorder) | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  181. en:charcot-marie-tooth disease, axonal, type 2f --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:charcot-marie-tooth disease, axonal, type 2f | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  182. en:charcot-marie-tooth disease, axonal, type 2g --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:charcot-marie-tooth disease, axonal, type 2g | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  183. en:charcot-marie-tooth disease, axonal, type 2l (disorder) --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:charcot-marie-tooth disease, axonal, type 2l (disorder) | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  184. en:charcot-marie-tooth disease, axonal, type 2n --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:charcot-marie-tooth disease, axonal, type 2n | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  185. en:charcot-marie-tooth disease, type 2j --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:charcot-marie-tooth disease, type 2j | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  186. en:choreoathetosis, hypothyroidism, and neonatal respiratory distress --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:choreoathetosis, hypothyroidism, and neonatal respiratory distress | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  187. en:choreoathetosis/spasticity, episodic --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:choreoathetosis/spasticity, episodic | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  188. en:chorioretinal atrophy, progressive bifocal --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:chorioretinal atrophy, progressive bifocal | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  189. en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  190. en:chromosome 11p11.2 deletion syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:chromosome 11p11.2 deletion syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  191. en:chromosome 17q21.31 deletion syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:chromosome 17q21.31 deletion syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  192. en:chromosome 22q11.2 microduplication syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:chromosome 22q11.2 microduplication syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  193. en:chromosome 3q29 deletion syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:chromosome 3q29 deletion syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  194. en:chronic atrial and intestinal dysrhythmia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:chronic atrial and intestinal dysrhythmia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  195. en:cleft palate with short stature and vertebral anomaly syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:cleft palate with short stature and vertebral anomaly syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  196. en:cleidocranial dysplasia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:cleidocranial dysplasia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  197. en:coach syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:coach syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  198. en:cochleosaccular degeneration of the inner ear and progressive cataracts --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:cochleosaccular degeneration of the inner ear and progressive cataracts | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  199. en:cole disease --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:cole disease | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  200. en:coloboma of macula with type b brachydactyly --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:coloboma of macula with type b brachydactyly | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  201. en:combined d-2- and l-2-hydroxyglutaric aciduria --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:combined d-2- and l-2-hydroxyglutaric aciduria | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  202. en:combined pituitary hormone deficiency genetic form --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:combined pituitary hormone deficiency genetic form | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  203. en:congenital adrenal hyperplasia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:congenital adrenal hyperplasia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  204. en:congenital bile acid synthesis defect type 3 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:congenital bile acid synthesis defect type 3 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  205. en:congenital dyserythropoietic anemia type iv --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:congenital dyserythropoietic anemia type iv | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  206. en:congenital dyserythropoietic anemia, type iii --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:congenital dyserythropoietic anemia, type iii | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  207. en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  208. en:congenital nephrogenic diabetes insipidus --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:congenital nephrogenic diabetes insipidus | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  209. en:congenital pancreatic enterokinase deficiency --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:congenital pancreatic enterokinase deficiency | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  210. en:congenital reticular ichthyosiform erythroderma --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:congenital reticular ichthyosiform erythroderma | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  211. en:congenital sucrase-isomaltase deficiency --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:congenital sucrase-isomaltase deficiency | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  212. en:corneal dystrophy, congenital stromal --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:corneal dystrophy, congenital stromal | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  213. en:corneal dystrophy, posterior amorphous --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:corneal dystrophy, posterior amorphous | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  214. en:craniofacial conodysplasia syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:craniofacial conodysplasia syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  215. en:craniofacial deafness hand syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:craniofacial deafness hand syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  216. en:craniosynostosis with dandy-walker malformation and hydrocephalus syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:craniosynostosis with dandy-walker malformation and hydrocephalus syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  217. en:craniosynostosis, philadelphia type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:craniosynostosis, philadelphia type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  218. en:craniosynostosis, type 2 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:craniosynostosis, type 2 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  219. en:crigler najjar syndrome, type 1 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:crigler najjar syndrome, type 1 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  220. en:crouzon syndrome with acanthosis nigricans (disorder) --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  221. en:currarino triad --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:currarino triad | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  222. en:cutis laxa, autosomal dominant --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:cutis laxa, autosomal dominant | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  223. en:dahlberg borer newcomer syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:dahlberg borer newcomer syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  224. en:de toni-debre-fanconi syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:de toni-debre-fanconi syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  225. en:deafness enamel hypoplasia nail defects --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:deafness enamel hypoplasia nail defects | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  226. en:deafness-craniofacial syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:deafness-craniofacial syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  227. en:deafness-hypogonadism syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:deafness-hypogonadism syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  228. en:dentatorubral-pallidoluysian atrophy --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:dentatorubral-pallidoluysian atrophy | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  229. en:dentin dyspalsia, shields type 2 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:dentin dyspalsia, shields type 2 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  230. en:dermoodontodysplasia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:dermoodontodysplasia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  231. en:developmental absence of tooth --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:developmental absence of tooth | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  232. en:developmental malformation, deafness, dystonia syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:developmental malformation, deafness, dystonia syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  233. en:diarrhea 4, malabsorptive, congenital --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:diarrhea 4, malabsorptive, congenital | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  234. en:dicer1 syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:dicer1 syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  235. en:dominant autosomal hereditary disorder, complete penetrance --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:dominant autosomal hereditary disorder, complete penetrance | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  236. en:dominant autosomal hereditary disorder, incomplete penetrance --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:dominant autosomal hereditary disorder, incomplete penetrance | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  237. en:dominant beta-thalassemia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:dominant beta-thalassemia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  238. en:dopa-responsive dystonia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:dopa-responsive dystonia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  239. en:doughnut lesions of skull, familial --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:doughnut lesions of skull, familial | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  240. en:drug-induced hyperinsulinemia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:drug-induced hyperinsulinemia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  241. en:dyskeratosis congenita, autosomal dominant --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:dyskeratosis congenita, autosomal dominant | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  242. en:dysphasia, familial developmental --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:dysphasia, familial developmental | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  243. en:dysplasia, saddan --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:dysplasia, saddan | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  244. en:dystonia 12 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:dystonia 12 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  245. en:dystrophia myotonica 2 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:dystrophia myotonica 2 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  246. en:ectodermal dysplasia with natal teeth, turnpenny type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:ectodermal dysplasia with natal teeth, turnpenny type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  247. en:ectopic hyperinsulinism --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:ectopic hyperinsulinism | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  248. en:edict syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:edict syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  249. en:ehlers-danlos syndrome, type i --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:ehlers-danlos syndrome, type i | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  250. en:enterokinase deficiency --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:enterokinase deficiency | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  251. en:epidermolysis bullosa simplex with pyloric atresia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:epidermolysis bullosa simplex with pyloric atresia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  252. en:epilepsy, myoclonic, benign adult familial, type 2 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:epilepsy, myoclonic, benign adult familial, type 2 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  253. en:epiphyseal dysplasia, multiple, 1 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:epiphyseal dysplasia, multiple, 1 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  254. en:episodic ataxia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:episodic ataxia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  255. en:epithelial recurrent erosion dystrophy --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:epithelial recurrent erosion dystrophy | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  256. en:erythrokeratodermia with ataxia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:erythrokeratodermia with ataxia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  257. en:familial adenomatous polyposis --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:familial adenomatous polyposis | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  258. en:familial adrenocortical hypoplasia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:familial adrenocortical hypoplasia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  259. en:familial alzheimer-like prion disease --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:familial alzheimer-like prion disease | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  260. en:familial amyloid polyneuropathy, type v --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:familial amyloid polyneuropathy, type v | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  261. en:familial arthrogryposis-cholestatic hepatorenal syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:familial arthrogryposis-cholestatic hepatorenal syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  262. en:familial benign neonatal epilepsy --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:familial benign neonatal epilepsy | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  263. en:familial cerebral cavernous malformation --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:familial cerebral cavernous malformation | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  264. en:familial creutzfeldt-jakob --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:familial creutzfeldt-jakob | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  265. en:familial digital arthropathy and brachydactyly syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:familial digital arthropathy and brachydactyly syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  266. en:familial encephalopathy with neuroserpin inclusion bodies --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:familial encephalopathy with neuroserpin inclusion bodies | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  267. en:familial hemiplegic migraine --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:familial hemiplegic migraine | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  268. en:familial hypoaldosteronism --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:familial hypoaldosteronism | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  269. en:familial hypodontia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:familial hypodontia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  270. en:familial isolated arrhythmogenic right ventricular dysplasia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:familial isolated arrhythmogenic right ventricular dysplasia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  271. en:familial non-autoimmune autosomal dominant hyperthyroidism --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:familial non-autoimmune autosomal dominant hyperthyroidism | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  272. en:familial osteochondritis dissecans --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:familial osteochondritis dissecans | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  273. en:familial papillary thyroid carcinoma with renal papillary neoplasia syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:familial papillary thyroid carcinoma with renal papillary neoplasia syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  274. en:familial partial lipodystrophy, type 2 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:familial partial lipodystrophy, type 2 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  275. en:familial spontaneous pneumothorax --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:familial spontaneous pneumothorax | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  276. en:familial thyroid dyshormonogenesis --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:familial thyroid dyshormonogenesis | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  277. en:fasting hyperinsulinemia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:fasting hyperinsulinemia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  278. en:fechtner syndrome (disorder) --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:fechtner syndrome (disorder) | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  279. en:feigenbaum bergeron richardson syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:feigenbaum bergeron richardson syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  280. en:fibrodysplasia ossificans progressiva --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:fibrodysplasia ossificans progressiva | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  281. en:fibular aplasia and ectrodactyly syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:fibular aplasia and ectrodactyly syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  282. en:foxg1 syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:foxg1 syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  283. en:freeman-sheldon syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:freeman-sheldon syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  284. en:frontotemporal dementia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:frontotemporal dementia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  285. en:frontotemporal dementia, chromosome 3-linked --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:frontotemporal dementia, chromosome 3-linked | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  286. en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  287. en:functional hyperinsulinism --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:functional hyperinsulinism | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  288. en:gemss syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:gemss syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  289. en:generalized epilepsy and paroxysmal dyskinesia syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:generalized epilepsy and paroxysmal dyskinesia syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  290. en:generalized myotonia of thomsen --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:generalized myotonia of thomsen | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  291. en:geniospasm 1 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:geniospasm 1 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  292. en:genitopatellar syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:genitopatellar syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  293. en:glomerulopathy with fibronectin deposits 2 (disorder) --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:glomerulopathy with fibronectin deposits 2 (disorder) | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  294. en:glomuvenous malformations --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:glomuvenous malformations | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  295. en:glucocorticoid deficiency with achalasia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:glucocorticoid deficiency with achalasia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  296. en:glucose transporter protein type 1 deficiency syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:glucose transporter protein type 1 deficiency syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  297. en:glutamate dehydrogenase 1 hyperinsulinism --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:glutamate dehydrogenase 1 hyperinsulinism | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  298. en:glycogen storage disease 0, liver --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:glycogen storage disease 0, liver | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  299. en:glycogen storage disease, hepatic form --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:glycogen storage disease, hepatic form | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  300. en:goldberg-shprintzen megacolon syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:goldberg-shprintzen megacolon syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  301. en:goniodysgenesis-mental retardation-short stature syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:goniodysgenesis-mental retardation-short stature syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  302. en:grayson wilbrandt corneal dystrophy --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:grayson wilbrandt corneal dystrophy | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  303. en:haim-munk syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:haim-munk syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  304. en:hamartoma syndrome, multiple --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hamartoma syndrome, multiple | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  305. en:hand foot uterus syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hand foot uterus syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  306. en:haspeslagh fryns muelenaere syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:haspeslagh fryns muelenaere syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  307. en:hawkinsinuria --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hawkinsinuria | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  308. en:heart-hand syndrome, slovenian type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:heart-hand syndrome, slovenian type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  309. en:hemochromatosis, type 4 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hemochromatosis, type 4 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  310. en:hepatolenticular degeneration --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hepatolenticular degeneration | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  311. en:hereditary adrenal unresponsiveness to corticotropin --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary adrenal unresponsiveness to corticotropin | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  312. en:hereditary benign intraepithelial dyskeratosis --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary benign intraepithelial dyskeratosis | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  313. en:hereditary breast and ovarian cancer syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary breast and ovarian cancer syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  314. en:hereditary cerebral amyloid angiopathy, icelandic type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary cerebral amyloid angiopathy, icelandic type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  315. en:hereditary cystatin c amyloid angiopathy --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary cystatin c amyloid angiopathy | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  316. en:hereditary diffuse gastric adenocarcinoma --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary diffuse gastric adenocarcinoma | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  317. en:hereditary elliptocytosis due to abnormal protein 4.1 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary elliptocytosis due to abnormal protein 4.1 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  318. en:hereditary elliptocytosis due to alpha spectrin defect --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary elliptocytosis due to alpha spectrin defect | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  319. en:hereditary elliptocytosis due to beta spectrin defect in self-association --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary elliptocytosis due to beta spectrin defect in self-association | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  320. en:hereditary elliptocytosis due to deficiency of protein 4.1 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary elliptocytosis due to deficiency of protein 4.1 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  321. en:hereditary gastrogenic lactose intolerance --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary gastrogenic lactose intolerance | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  322. en:hereditary gingival fibromatosis --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary gingival fibromatosis | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  323. en:hereditary glucocorticoid resistance --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary glucocorticoid resistance | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  324. en:hereditary isolated hypoparathyroidism due to impaired parathormone secretion --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary isolated hypoparathyroidism due to impaired parathormone secretion | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  325. en:hereditary motor and sensory neuropathy type i --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary motor and sensory neuropathy type i | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  326. en:hereditary multiple exostoses --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary multiple exostoses | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  327. en:hereditary myopathy with early respiratory failure --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary myopathy with early respiratory failure | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  328. en:hereditary nonpolyposis colorectal cancer --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary nonpolyposis colorectal cancer | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  329. en:hereditary oculoleptomeningeal amyloid angiopathy --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  330. en:hereditary pancreatitis --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary pancreatitis | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  331. en:hereditary papillary renal carcinoma --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary papillary renal carcinoma | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  332. en:hereditary sensory autonomic neuropathy, type 1 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary sensory autonomic neuropathy, type 1 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  333. en:hereditary stomatocytosis --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary stomatocytosis | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  334. en:hereditary systemic amyloidosis --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary systemic amyloidosis | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  335. en:hereditary vascular retinopathy --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary vascular retinopathy | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  336. en:hereditary vitamin d dependency syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hereditary vitamin d dependency syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  337. en:heritable pulmonary arterial hypertension due to bmpr2 mutation --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:heritable pulmonary arterial hypertension due to bmpr2 mutation | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  338. en:heterozygous methylenetetrahydrofolate reductase mutation --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:heterozygous methylenetetrahydrofolate reductase mutation | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  339. en:hip dysplasia, beukes type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hip dysplasia, beukes type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  340. en:hirschsprung disease with type d brachydactyly syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hirschsprung disease with type d brachydactyly syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  341. en:hnsha due to triosephosphate isomerase deficiency --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hnsha due to triosephosphate isomerase deficiency | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  342. en:holt-oram syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:holt-oram syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  343. en:homozygous methylenetetrahydrofolate reductase mutation --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:homozygous methylenetetrahydrofolate reductase mutation | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  344. en:hunter-mcalpine craniosynostosis syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hunter-mcalpine craniosynostosis syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  345. en:huntington disease-like 2 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:huntington disease-like 2 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  346. en:hyaline dystrophy of bruch's membrane --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hyaline dystrophy of bruch's membrane | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  347. en:hydrocephalus with obesity and hypogonadism syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hydrocephalus with obesity and hypogonadism syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  348. en:hyperferritinemia, hereditary, with congenital cataracts --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hyperferritinemia, hereditary, with congenital cataracts | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  349. en:hyperinsulinemia due to insulinoma --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hyperinsulinemia due to insulinoma | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  350. en:hyperinsulinemic hypoglycemia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hyperinsulinemic hypoglycemia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  351. en:hyperinsulinemic hypoglycemia, familial, 7 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hyperinsulinemic hypoglycemia, familial, 7 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  352. en:hyperinsulinism due to deficiency of glucokinase --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hyperinsulinism due to deficiency of glucokinase | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  353. en:hyperinsulinism due to hnf4a deficiency --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hyperinsulinism due to hnf4a deficiency | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  354. en:hyperparathyroidism-jaw tumor syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hyperparathyroidism-jaw tumor syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  355. en:hyperpigmentation, familial progressive --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hyperpigmentation, familial progressive | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  356. en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  357. en:hypogonadism with prune belly syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hypogonadism with prune belly syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  358. en:hypogonadism-cataract syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hypogonadism-cataract syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  359. en:hypogonadotropic hypogonadism with frontoparietal alopecia syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hypogonadotropic hypogonadism with frontoparietal alopecia syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  360. en:hypomagnesemia 1, intestinal --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hypomagnesemia 1, intestinal | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  361. en:hypoparathyroidism - autosomal dominant --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hypoparathyroidism - autosomal dominant | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  362. en:hypoplastic tibia and postaxial polydactyly syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hypoplastic tibia and postaxial polydactyly syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  363. en:hypothyroidism due to mutation in transcription factor of pituitary development --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hypothyroidism due to mutation in transcription factor of pituitary development | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  364. en:hypotrichosis simplex of scalp --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:hypotrichosis simplex of scalp | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  365. en:iatrogenic hyperinsulinism --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:iatrogenic hyperinsulinism | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  366. en:ichthyosis congenita with biliary atresia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:ichthyosis congenita with biliary atresia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  367. en:ichthyosis, cyclic, with epidermolytic hyperkeratosis --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:ichthyosis, cyclic, with epidermolytic hyperkeratosis | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  368. en:idiopathic transient neonatal hyperinsulinemia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:idiopathic transient neonatal hyperinsulinemia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  369. en:image syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:image syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  370. en:impaired glucose tolerance with hyperinsulism --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:impaired glucose tolerance with hyperinsulism | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  371. en:inclusion body myopathy with early-onset paget disease and frontotemporal dementia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:inclusion body myopathy with early-onset paget disease and frontotemporal dementia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  372. en:inherited disorder of thyroid metabolism --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:inherited disorder of thyroid metabolism | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  373. en:insulin autoimmune syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:insulin autoimmune syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  374. en:insulin resistance --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:insulin resistance | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  375. en:insulin-dependent diabetes mellitus secretory diarrhea syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:insulin-dependent diabetes mellitus secretory diarrhea syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  376. en:intestinal epithelial dysplasia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:intestinal epithelial dysplasia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  377. en:intestinal lipofuscinosis --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:intestinal lipofuscinosis | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  378. en:iris coloboma with ptosis, hypertelorism, and mental retardation --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:iris coloboma with ptosis, hypertelorism, and mental retardation | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  379. en:isolated autosomal dominant hypomagnesemia glaudemans type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:isolated autosomal dominant hypomagnesemia glaudemans type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  380. en:isolated cryptophthalmos --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:isolated cryptophthalmos | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  381. en:jackson-weiss syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:jackson-weiss syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  382. en:jaundice, chronic idiopathic --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:jaundice, chronic idiopathic | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  383. en:johnson neuroectodermal syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:johnson neuroectodermal syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  384. en:jones syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:jones syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  385. en:juvenile cataract, microcornea, renal glucosuria syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:juvenile cataract, microcornea, renal glucosuria syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  386. en:kallmann syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:kallmann syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  387. en:kapur toriello syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:kapur toriello syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  388. en:kbg syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:kbg syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  389. en:keratitis, hereditary --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:keratitis, hereditary | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  390. en:keratoacanthoma familial --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:keratoacanthoma familial | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  391. en:keratoderma, palmoplantar, diffuse --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:keratoderma, palmoplantar, diffuse | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  392. en:keratosis palmoplantaris papulosa --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:keratosis palmoplantaris papulosa | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  393. en:lactase deficiency, congenital --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:lactase deficiency, congenital | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  394. en:ladda zonana ramer syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:ladda zonana ramer syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  395. en:lamellar ichthyosis, autosomal dominant form --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:lamellar ichthyosis, autosomal dominant form | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  396. en:late-onset retinal degeneration (disorder) --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:late-onset retinal degeneration (disorder) | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  397. en:laurin-sandrow syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:laurin-sandrow syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  398. en:leopard syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:leopard syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  399. en:leukodystrophy, dysmyelinating, with oligodontia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:leukodystrophy, dysmyelinating, with oligodontia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  400. en:leukodystrophy, hypomyelinating, with hypodontia and hypogonadotropic hypogonadism --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:leukodystrophy, hypomyelinating, with hypodontia and hypogonadotropic hypogonadism | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  401. en:leukokeratosis, hereditary mucosal --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:leukokeratosis, hereditary mucosal | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  402. en:leukotriene c4 synthase deficiency --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:leukotriene c4 synthase deficiency | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  403. en:li-fraumeni syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:li-fraumeni syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  404. en:liddle syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:liddle syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  405. en:limb-mammary syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:limb-mammary syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  406. en:lissencephaly due to tuba1a (tubulin alpha 1a) mutation --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:lissencephaly due to tuba1a (tubulin alpha 1a) mutation | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  407. en:loeys-dietz syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:loeys-dietz syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  408. en:lopes gorlin syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:lopes gorlin syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  409. en:lowry maclean syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:lowry maclean syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  410. en:lowry yong syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:lowry yong syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  411. en:lubani al saleh teebi syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:lubani al saleh teebi syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  412. en:lung fibrosis, immunodeficiency, 46,xx gonadal dysgenesis syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:lung fibrosis, immunodeficiency, 46,xx gonadal dysgenesis syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  413. en:lymphedema and cerebral arteriovenous anomaly syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:lymphedema and cerebral arteriovenous anomaly syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  414. en:macular coloboma, cleft palate, hallux valgus syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:macular coloboma, cleft palate, hallux valgus syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  415. en:macular dystrophy, concentric annular --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:macular dystrophy, concentric annular | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  416. en:mammary-digital-nail syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:mammary-digital-nail syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  417. en:mandibulofacial dysostosis --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:mandibulofacial dysostosis | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  418. en:marfan syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:marfan syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  419. en:martsolf syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:martsolf syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  420. en:may-hegglin anomaly --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:may-hegglin anomaly | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  421. en:mcpherson clemens syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:mcpherson clemens syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  422. en:median nodule of upper lip --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:median nodule of upper lip | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  423. en:melanoma astrocytoma syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:melanoma astrocytoma syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  424. en:mental retardation, x-linked, syndromic 7 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:mental retardation, x-linked, syndromic 7 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  425. en:mesomelic dwarfism reinhardt pfeiffer type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:mesomelic dwarfism reinhardt pfeiffer type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  426. en:mesomelic dysplasia, kantaputra type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:mesomelic dysplasia, kantaputra type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  427. en:metabolic syndrome x --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:metabolic syndrome x | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  428. en:metaphyseal dysplasia, braun-tinschert type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:metaphyseal dysplasia, braun-tinschert type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  429. en:microcephaly deafness syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:microcephaly deafness syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  430. en:microcornea with glaucoma and absent frontal sinus syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:microcornea with glaucoma and absent frontal sinus syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  431. en:microphthalmia, syndromic 3 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:microphthalmia, syndromic 3 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  432. en:microphthalmia, syndromic 5 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:microphthalmia, syndromic 5 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  433. en:microphthalmia, syndromic 6 (disorder) --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:microphthalmia, syndromic 6 (disorder) | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  434. en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  435. en:mitochondrial neurogastrointestinal encephalomyopathy syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  436. en:mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  437. en:moderate steroid 21-hydroxylase deficiency --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:moderate steroid 21-hydroxylase deficiency | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  438. en:moloney syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:moloney syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  439. en:mowat-wilson syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:mowat-wilson syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  440. en:muckle-wells syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:muckle-wells syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  441. en:mucopolysaccharidosis ii --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:mucopolysaccharidosis ii | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  442. en:mullerian duct and limb anomalies syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:mullerian duct and limb anomalies syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  443. en:multiple endocrine neoplasia type 1 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:multiple endocrine neoplasia type 1 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  444. en:multiple endocrine neoplasia type 2a --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:multiple endocrine neoplasia type 2a | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  445. en:multiple endocrine neoplasia type 2b --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:multiple endocrine neoplasia type 2b | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  446. en:multiple epiphyseal dysplasia beighton type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:multiple epiphyseal dysplasia beighton type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  447. en:multiple epiphyseal dysplasia type 5 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:multiple epiphyseal dysplasia type 5 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  448. en:multiple gastrointestinal atresias (disorder) --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:multiple gastrointestinal atresias (disorder) | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  449. en:muscular dystrophy, oculopharyngeal --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:muscular dystrophy, oculopharyngeal | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  450. en:myopathy, distal 2 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:myopathy, distal 2 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  451. en:myopathy, distal, tateyama type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:myopathy, distal, tateyama type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  452. en:nance-horan syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:nance-horan syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  453. en:nemaline myopathy 3 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:nemaline myopathy 3 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  454. en:neurofibromatosis 1 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:neurofibromatosis 1 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  455. en:neurofibromatosis 2 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:neurofibromatosis 2 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  456. en:neurofibromatosis, type 1-like syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:neurofibromatosis, type 1-like syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  457. en:neuronal intestinal pseudoobstruction --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:neuronal intestinal pseudoobstruction | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  458. en:neuropathy, hereditary motor and sensory, okinawa type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:neuropathy, hereditary motor and sensory, okinawa type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  459. en:neuropathy, hereditary thermosensitive --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:neuropathy, hereditary thermosensitive | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  460. en:nicolaides baraitser syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:nicolaides baraitser syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  461. en:noonan syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:noonan syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  462. en:north american indian childhood cirrhosis --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:north american indian childhood cirrhosis | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  463. en:oculocerebral syndrome with hypopigmentation --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:oculocerebral syndrome with hypopigmentation | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  464. en:oculodental syndrome rutherfurd syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  465. en:oculodigitoesophagoduodenal syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:oculodigitoesophagoduodenal syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  466. en:oculootoradial syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:oculootoradial syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  467. en:oculopalatocerebral syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:oculopalatocerebral syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  468. en:odontoma dysphagia syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:odontoma dysphagia syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  469. en:odontotrichoungual-digital-palmar syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:odontotrichoungual-digital-palmar syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  470. en:ohdo syndrome, maat-kievit-brunner type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:ohdo syndrome, maat-kievit-brunner type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  471. en:okihiro syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:okihiro syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  472. en:omphalocele cleft palate syndrome lethal --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:omphalocele cleft palate syndrome lethal | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  473. en:optic atrophy, autosomal dominant --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:optic atrophy, autosomal dominant | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  474. en:osteogenesis imperfecta, levin type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:osteogenesis imperfecta, levin type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  475. en:osteopoikilosis and dacryocystitis --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:osteopoikilosis and dacryocystitis | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  476. en:osteosclerosis, developmental delay, craniosynostosis syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:osteosclerosis, developmental delay, craniosynostosis syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  477. en:other hyperinsulinism --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:other hyperinsulinism | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  478. en:overgrowth, macrocephaly, facial dysmorphism syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:overgrowth, macrocephaly, facial dysmorphism syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  479. en:palmoplantar keratoderma with deafness --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:palmoplantar keratoderma with deafness | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  480. en:pancreas agenesis, dorsal --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:pancreas agenesis, dorsal | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  481. en:pancreatic colipase deficiency --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:pancreatic colipase deficiency | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  482. en:pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  483. en:pancreatic triacylglycerol lipase deficiency --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:pancreatic triacylglycerol lipase deficiency | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  484. en:papillon-lefevre disease --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:papillon-lefevre disease | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  485. en:paraganglioma and gastric stromal sarcoma --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:paraganglioma and gastric stromal sarcoma | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  486. en:parastremmatic dwarfism --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:parastremmatic dwarfism | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  487. en:parietal foramina --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:parietal foramina | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  488. en:paroxysmal extreme pain disorder --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:paroxysmal extreme pain disorder | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  489. en:pelvis-shoulder dysplasia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:pelvis-shoulder dysplasia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  490. en:periodontitis co-occurrent with genetic disorder --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:periodontitis co-occurrent with genetic disorder | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  491. en:peripheral resistance to thyroid hormone --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:peripheral resistance to thyroid hormone | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  492. en:persistent hyperinsulinemic hypoglycemia of infancy --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:persistent hyperinsulinemic hypoglycemia of infancy | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  493. en:peutz-jeghers syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:peutz-jeghers syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  494. en:pfeiffer syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:pfeiffer syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  495. en:phosphoserine aminotransferase deficiency --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:phosphoserine aminotransferase deficiency | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  496. en:piebaldism --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:piebaldism | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  497. en:pitt-hopkins syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:pitt-hopkins syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  498. en:pituitary adenoma, familial isolated (disorder) --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:pituitary adenoma, familial isolated (disorder) | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  499. en:platelet-type von willebrand disease --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:platelet-type von willebrand disease | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  500. en:polycystic liver disease --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:polycystic liver disease | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  501. en:popliteal pterygium syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:popliteal pterygium syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  502. en:potassium aggravated myotonia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:potassium aggravated myotonia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  503. en:progressive heterotopic heteroplasia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:progressive heterotopic heteroplasia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  504. en:progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  505. en:proteus-like syndrome (disorder) --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:proteus-like syndrome (disorder) | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  506. en:pseudohypoaldosteronism, type 1, dominant form --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:pseudohypoaldosteronism, type 1, dominant form | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  507. en:pseudohypoaldosteronism, type 1, recessive form --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:pseudohypoaldosteronism, type 1, recessive form | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  508. en:pseudohypoparathyroidism type 1c --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:pseudohypoparathyroidism type 1c | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  509. en:pten hamartoma tumor syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:pten hamartoma tumor syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  510. en:radial hypoplasia, triphalangeal thumbs and hypospadias --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:radial hypoplasia, triphalangeal thumbs and hypospadias | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  511. en:radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  512. en:reardon hall slaney syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:reardon hall slaney syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  513. en:reis-bucklers' corneal dystrophy --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:reis-bucklers' corneal dystrophy | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  514. en:reticulate acropigmentation of kitamura --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:reticulate acropigmentation of kitamura | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  515. en:roch leri mesosomatous lipomatosis --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:roch leri mesosomatous lipomatosis | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  516. en:rombo syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:rombo syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  517. en:rotor syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:rotor syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  518. en:rudd klimek syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:rudd klimek syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  519. en:santos mateus leal syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:santos mateus leal syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  520. en:scalp-ear-nipple syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:scalp-ear-nipple syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  521. en:schaap taylor baraitser syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:schaap taylor baraitser syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  522. en:schilbach-rott syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:schilbach-rott syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  523. en:schnyder crystalline corneal dystrophy --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:schnyder crystalline corneal dystrophy | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  524. en:sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  525. en:self-induced hyperinsulinemia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:self-induced hyperinsulinemia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  526. en:sellars beighton syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:sellars beighton syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  527. en:severe steroid 21-hydroxylase deficiency --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:severe steroid 21-hydroxylase deficiency | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  528. en:short stature with valvular heart disease and characteristic facies syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:short stature with valvular heart disease and characteristic facies syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  529. en:short stature, pituitary and cerebellar defect and small sella turcica syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:short stature, pituitary and cerebellar defect and small sella turcica syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  530. en:shprintzen omphalocele syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:shprintzen omphalocele syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  531. en:shprintzen-goldberg syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:shprintzen-goldberg syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  532. en:shwachman-diamond syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:shwachman-diamond syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  533. en:simpson-golabi-behmel syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:simpson-golabi-behmel syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  534. en:small patella syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:small patella syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  535. en:sohval soffer syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:sohval soffer syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  536. en:sotos' syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:sotos' syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  537. en:spinocerebellar ataxia 10 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia 10 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  538. en:spinocerebellar ataxia 11 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia 11 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  539. en:spinocerebellar ataxia 12 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia 12 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  540. en:spinocerebellar ataxia 13 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia 13 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  541. en:spinocerebellar ataxia 14 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia 14 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  542. en:spinocerebellar ataxia 15 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia 15 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  543. en:spinocerebellar ataxia 17 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia 17 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  544. en:spinocerebellar ataxia 18 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia 18 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  545. en:spinocerebellar ataxia 20 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia 20 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  546. en:spinocerebellar ataxia 21 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia 21 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  547. en:spinocerebellar ataxia 23 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia 23 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  548. en:spinocerebellar ataxia 25 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia 25 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  549. en:spinocerebellar ataxia 26 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia 26 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  550. en:spinocerebellar ataxia 27 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia 27 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  551. en:spinocerebellar ataxia 28 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia 28 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  552. en:spinocerebellar ataxia 29 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia 29 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  553. en:spinocerebellar ataxia 30 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia 30 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  554. en:spinocerebellar ataxia 31 (disorder) --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia 31 (disorder) | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  555. en:spinocerebellar ataxia 36 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia 36 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  556. en:spinocerebellar ataxia 8 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia 8 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  557. en:spinocerebellar ataxia type 1 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia type 1 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  558. en:spinocerebellar ataxia type 19 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia type 19 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  559. en:spinocerebellar ataxia type 2 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia type 2 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  560. en:spinocerebellar ataxia type 35 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia type 35 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  561. en:spinocerebellar ataxia type 4 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia type 4 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  562. en:spinocerebellar ataxia type 5 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia type 5 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  563. en:spinocerebellar ataxia type 6 (disorder) --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia type 6 (disorder) | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  564. en:spinocerebellar ataxia type 7 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spinocerebellar ataxia type 7 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  565. en:split-hand with congenital nystagmus, fundal changes, and cataracts --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:split-hand with congenital nystagmus, fundal changes, and cataracts | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  566. en:split-hand-foot malformation with long bone deficiency 1 --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:split-hand-foot malformation with long bone deficiency 1 | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  567. en:spondylocostal dysostosis 4, autosomal dominant --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spondylocostal dysostosis 4, autosomal dominant | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  568. en:spondyloepimetaphyseal dysplasia, missouri type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spondyloepimetaphyseal dysplasia, missouri type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  569. en:spondyloepiphyseal dysplasia macdermot type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spondyloepiphyseal dysplasia macdermot type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  570. en:spondyloepiphyseal dysplasia reardon type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spondyloepiphyseal dysplasia reardon type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  571. en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  572. en:spondyloepiphyseal dysplasia, kimberley type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spondyloepiphyseal dysplasia, kimberley type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  573. en:spondyloepiphyseal dysplasia, maroteaux type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spondyloepiphyseal dysplasia, maroteaux type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  574. en:spondyloepiphyseal dysplasia-brachydactyly and distinctive speech --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spondyloepiphyseal dysplasia-brachydactyly and distinctive speech | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  575. en:spondylometaphyseal dysplasia with dentinogenesis imperfecta --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spondylometaphyseal dysplasia with dentinogenesis imperfecta | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  576. en:spondylometaphyseal dysplasia, algerian type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spondylometaphyseal dysplasia, algerian type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  577. en:spondyloperipheral dysplasia short ulna --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:spondyloperipheral dysplasia short ulna | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  578. en:stapes ankylosis with broad thumb and toes (disorder) --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:stapes ankylosis with broad thumb and toes (disorder) | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  579. en:steatocystoma multiplex --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:steatocystoma multiplex | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  580. en:steinfeld syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:steinfeld syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  581. en:sting-associated vasculopathy with onset in infancy --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:sting-associated vasculopathy with onset in infancy | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  582. en:strudwick syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:strudwick syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  583. en:syndactyly, type i --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:syndactyly, type i | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  584. en:syndactyly, type iii --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:syndactyly, type iii | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  585. en:syndactyly, type iv --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:syndactyly, type iv | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  586. en:syndactyly, type v --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:syndactyly, type v | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  587. en:syndrome, branchio-oculo-facial --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:syndrome, branchio-oculo-facial | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  588. en:syndromic orbital border hypoplasia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:syndromic orbital border hypoplasia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  589. en:synpolydactyly --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:synpolydactyly | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  590. en:tarsal-carpal coalition syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:tarsal-carpal coalition syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  591. en:teebi naguib al awadi syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:teebi naguib al awadi syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  592. en:thickened earlobe with conductive deafness syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:thickened earlobe with conductive deafness syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  593. en:thiel-behnke corneal dystrophy --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:thiel-behnke corneal dystrophy | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  594. en:timothy syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:timothy syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  595. en:transthyretin related familial amyloid cardiomyopathy --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:transthyretin related familial amyloid cardiomyopathy | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  596. en:trichohepatoenteric syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:trichohepatoenteric syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  597. en:trigonocephaly with broad thumb syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:trigonocephaly with broad thumb syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  598. en:tungland bellman syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:tungland bellman syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  599. en:turcot syndrome (disorder) --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:turcot syndrome (disorder) | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  600. en:ulna metaphyseal dysplasia syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:ulna metaphyseal dysplasia syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  601. en:ulnar-mammary syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:ulnar-mammary syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  602. en:upington disease --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:upington disease | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  603. en:urban schosser spohn syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:urban schosser spohn syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  604. en:uveal coloboma with cleft lip and palate and intellectual disability syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:uveal coloboma with cleft lip and palate and intellectual disability syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  605. en:vasculopathy, retinal, with cerebral leukodystrophy --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:vasculopathy, retinal, with cerebral leukodystrophy | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  606. en:visceral myopathy familial external ophthalmoplegia --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:visceral myopathy familial external ophthalmoplegia | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  607. en:visceral myopathy, familial --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:visceral myopathy, familial | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  608. en:vitelliform macular dystrophy --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:vitelliform macular dystrophy | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  609. en:vitreoretinochoroidopathy (disorder) --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:vitreoretinochoroidopathy (disorder) | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  610. en:waardenburg syndrome, type 4a --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:waardenburg syndrome, type 4a | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  611. en:wellesley carman french syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:wellesley carman french syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  612. en:white platelet syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:white platelet syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  613. en:whyte hemingway carpal tarsal phalangeal osteolyses --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:whyte hemingway carpal tarsal phalangeal osteolyses | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  614. en:wnt4 mullerian aplasia and ovarian dysfunction --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:wnt4 mullerian aplasia and ovarian dysfunction | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  615. en:wt limb blood syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:wt limb blood syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  616. en:x-linked adrenal hypoplasia congenita --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:x-linked adrenal hypoplasia congenita | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  617. en:x-linked intellectual disability cilliers type --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:x-linked intellectual disability cilliers type | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  618. en:x-linked intellectual disability with precocious puberty and obesity syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:x-linked intellectual disability with precocious puberty and obesity syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  619. en:xanthomatosis, cerebrotendinous --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:xanthomatosis, cerebrotendinous | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  620. en:yorifuji okuno syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:yorifuji okuno syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  621. en:zimmerman laband syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:zimmerman laband syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  622. en:zlotogora-ogur syndrome --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=en:zlotogora-ogur syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  623. hypogonadisme avec anosmie --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=hypogonadisme avec anosmie | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  624. protéine --- r_associated #0: 20 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=protéine | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20
  625. Kallman --- r_associated #0: 15 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=Kallman | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=15
  626. aclasie diaphysaire --- r_associated #0: 15 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=aclasie diaphysaire | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=15
  627. chondrodysplasie héréditaire déformante --- r_associated #0: 15 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=chondrodysplasie héréditaire déformante | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=15
  628. exostose héréditaire multiple --- r_associated #0: 15 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=exostose héréditaire multiple | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=15
  629. syndrome de Kallman-de Morsier --- r_associated #0: 15 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=syndrome de Kallman-de Morsier | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=15
  630. syndrome de de Morsier-Kallmann --- r_associated #0: 15 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=syndrome de de Morsier-Kallmann | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=15
  631. absence d'empreintes digitales avec syndrome de milia congénital --- r_associated #0: 10 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=absence d'empreintes digitales avec syndrome de milia congénital | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=10
  632. amélogenèse imparfaite --- r_associated #0: 10 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=amélogenèse imparfaite | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=10
  633. arachnodactylie --- r_associated #0: 10 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=arachnodactylie | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=10
  634. chondrodysplasie déformante héréditaire --- r_associated #0: 10 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=chondrodysplasie déformante héréditaire | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=10
  635. hypoparathyroïdie isolée héréditaire due à une sécrétion altérée de parathormone --- r_associated #0: 10 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=hypoparathyroïdie isolée héréditaire due à une sécrétion altérée de parathormone | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=10
  636. maladie de Bessel-Hagen --- r_associated #0: 10 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=maladie de Bessel-Hagen | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=10
  637. maladie exostosante multiple --- r_associated #0: 10 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=maladie exostosante multiple | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=10
  638. maladie ostéogénique --- r_associated #0: 10 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=maladie ostéogénique | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=10
  639. piebaldisme --- r_associated #0: 10 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=piebaldisme | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=10
  640. piébaldisme --- r_associated #0: 10 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=piébaldisme | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=10
  641. proteine --- r_associated #0: 10 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=proteine | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=10
  642. résistance à l'insuline --- r_associated #0: 10 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=résistance à l'insuline | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=10
  643. steatocystoma multiplex --- r_associated #0: 10 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=steatocystoma multiplex | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=10
  644. stéatocystomes multiples --- r_associated #0: 10 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=stéatocystomes multiples | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=10
  645. syndrome de bor --- r_associated #0: 10 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=syndrome de bor | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=10
  646. syndrome de de Morsier --- r_associated #0: 10 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=syndrome de de Morsier | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=10
  647. syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire --- r_associated #0: 10 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=10
  648. syndrome des hamartomes multiples lié à PTEN --- r_associated #0: 10 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=syndrome des hamartomes multiples lié à PTEN | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=10
  649. syndrome héréditaire de cancer du sein et de l'ovaire --- r_associated #0: 10 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=syndrome héréditaire de cancer du sein et de l'ovaire | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=10
  650. syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire --- r_associated #0: 10 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=10
  651. chimiorésistance à l'insuline --- r_associated #0: 5 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=chimiorésistance à l'insuline | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=5
  652. dystrophie musculaire oculo-pharyngée --- r_associated #0: 5 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=dystrophie musculaire oculo-pharyngée | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=5
  653. dystrophie musculaire oculopharyngée --- r_associated #0: 5 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=dystrophie musculaire oculopharyngée | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=5
  654. forme génétique de déficience combinée en hormones hypophysaires --- r_associated #0: 5 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=forme génétique de déficience combinée en hormones hypophysaires | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=5
  655. gigantisme cérébral --- r_associated #0: 5 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=gigantisme cérébral | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=5
  656. insulino-résistance --- r_associated #0: 5 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=insulino-résistance | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=5
  657. insulinorésistance --- r_associated #0: 5 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=insulinorésistance | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=5
  658. maladie des exostoses multiples --- r_associated #0: 5 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=maladie des exostoses multiples | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=5
  659. neuropathie sensitive héréditaire dominante de type i --- r_associated #0: 5 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=neuropathie sensitive héréditaire dominante de type i | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=5
  660. syndrome lymphoprolifératif avec autoimmunité --- r_associated #0: 5 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=syndrome lymphoprolifératif avec autoimmunité | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=5
  661. syndrome olfacto-génital --- r_associated #0: 5 --> en:hyperinsulinism due to uncoupling protein 2 deficiency
    n1=syndrome olfacto-génital | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | 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