≈ 1106 relations sortantes
- en:mmih syndrome --
r_associated #0: 43 / 1 ->
en:basilar artery syndrome
n1=en:mmih syndrome | n2=en:basilar artery syndrome | rel=r_associated | relid=0 | w=43
- en:mmih syndrome --
r_associated #0: 43 / 1 ->
en:turner syndrome
n1=en:mmih syndrome | n2=en:turner syndrome | rel=r_associated | relid=0 | w=43
- en:mmih syndrome --
r_associated #0: 42 / 0.977 ->
en:acrodermatitis
n1=en:mmih syndrome | n2=en:acrodermatitis | rel=r_associated | relid=0 | w=42
- en:mmih syndrome --
r_associated #0: 42 / 0.977 ->
en:colon
n1=en:mmih syndrome | n2=en:colon | rel=r_associated | relid=0 | w=42
- en:mmih syndrome --
r_associated #0: 41 / 0.953 ->
en:congenital central hypoventilation
n1=en:mmih syndrome | n2=en:congenital central hypoventilation | rel=r_associated | relid=0 | w=41
- en:mmih syndrome --
r_associated #0: 40 / 0.93 ->
en:waardenburg syndrome
n1=en:mmih syndrome | n2=en:waardenburg syndrome | rel=r_associated | relid=0 | w=40
- en:mmih syndrome --
r_associated #0: 38 / 0.884 ->
en:17q21 microdeletion syndrome
n1=en:mmih syndrome | n2=en:17q21 microdeletion syndrome | rel=r_associated | relid=0 | w=38
- en:mmih syndrome --
r_associated #0: 38 / 0.884 ->
en:cadasil syndrome
n1=en:mmih syndrome | n2=en:cadasil syndrome | rel=r_associated | relid=0 | w=38
- en:mmih syndrome --
r_associated #0: 38 / 0.884 ->
en:cryopyrin-associated periodic syndrome
n1=en:mmih syndrome | n2=en:cryopyrin-associated periodic syndrome | rel=r_associated | relid=0 | w=38
- en:mmih syndrome --
r_associated #0: 38 / 0.884 ->
en:premenstrual syndrome
n1=en:mmih syndrome | n2=en:premenstrual syndrome | rel=r_associated | relid=0 | w=38
- en:mmih syndrome --
r_associated #0: 37 / 0.86 ->
en:diffuse cerebral sclerosis of schilder
n1=en:mmih syndrome | n2=en:diffuse cerebral sclerosis of schilder | rel=r_associated | relid=0 | w=37
- en:mmih syndrome --
r_associated #0: 36 / 0.837 ->
en:achenbach syndrome
n1=en:mmih syndrome | n2=en:achenbach syndrome | rel=r_associated | relid=0 | w=36
- en:mmih syndrome --
r_associated #0: 36 / 0.837 ->
en:bartter syndrome
n1=en:mmih syndrome | n2=en:bartter syndrome | rel=r_associated | relid=0 | w=36
- en:mmih syndrome --
r_associated #0: 36 / 0.837 ->
en:behcet syndrome
n1=en:mmih syndrome | n2=en:behcet syndrome | rel=r_associated | relid=0 | w=36
- en:mmih syndrome --
r_associated #0: 36 / 0.837 ->
en:cardiorenal syndrome
n1=en:mmih syndrome | n2=en:cardiorenal syndrome | rel=r_associated | relid=0 | w=36
- en:mmih syndrome --
r_associated #0: 35 / 0.814 ->
en:acatalasemia
n1=en:mmih syndrome | n2=en:acatalasemia | rel=r_associated | relid=0 | w=35
- en:mmih syndrome --
r_associated #0: 35 / 0.814 ->
en:angelman syndrome
n1=en:mmih syndrome | n2=en:angelman syndrome | rel=r_associated | relid=0 | w=35
- en:mmih syndrome --
r_associated #0: 35 / 0.814 ->
en:arnold-chiari malformation
n1=en:mmih syndrome | n2=en:arnold-chiari malformation | rel=r_associated | relid=0 | w=35
- en:mmih syndrome --
r_associated #0: 35 / 0.814 ->
en:autoinflammatory syndrome
n1=en:mmih syndrome | n2=en:autoinflammatory syndrome | rel=r_associated | relid=0 | w=35
- en:mmih syndrome --
r_associated #0: 35 / 0.814 ->
en:berardinelli-seip congenital lipodystrophy
n1=en:mmih syndrome | n2=en:berardinelli-seip congenital lipodystrophy | rel=r_associated | relid=0 | w=35
- en:mmih syndrome --
r_associated #0: 35 / 0.814 ->
en:cerebrooculofacioskeletal syndrome
n1=en:mmih syndrome | n2=en:cerebrooculofacioskeletal syndrome | rel=r_associated | relid=0 | w=35
- en:mmih syndrome --
r_associated #0: 35 / 0.814 ->
en:coffin-lowry syndrome
n1=en:mmih syndrome | n2=en:coffin-lowry syndrome | rel=r_associated | relid=0 | w=35
- en:mmih syndrome --
r_associated #0: 35 / 0.814 ->
en:complete trisomy 18 syndrome
n1=en:mmih syndrome | n2=en:complete trisomy 18 syndrome | rel=r_associated | relid=0 | w=35
- en:mmih syndrome --
r_associated #0: 35 / 0.814 ->
en:congenital varicella syndrome
n1=en:mmih syndrome | n2=en:congenital varicella syndrome | rel=r_associated | relid=0 | w=35
- en:mmih syndrome --
r_associated #0: 35 / 0.814 ->
en:cranioectodermal dysplasia
n1=en:mmih syndrome | n2=en:cranioectodermal dysplasia | rel=r_associated | relid=0 | w=35
- en:mmih syndrome --
r_associated #0: 35 / 0.814 ->
en:crigler-najjar syndrome
n1=en:mmih syndrome | n2=en:crigler-najjar syndrome | rel=r_associated | relid=0 | w=35
- en:mmih syndrome --
r_associated #0: 35 / 0.814 ->
en:down syndrome
n1=en:mmih syndrome | n2=en:down syndrome | rel=r_associated | relid=0 | w=35
- en:mmih syndrome --
r_associated #0: 35 / 0.814 ->
en:drug- and toxin-induced pulmonary arterial hypertension
n1=en:mmih syndrome | n2=en:drug- and toxin-induced pulmonary arterial hypertension | rel=r_associated | relid=0 | w=35
- en:mmih syndrome --
r_associated #0: 35 / 0.814 ->
en:dubin-johnson syndrome
n1=en:mmih syndrome | n2=en:dubin-johnson syndrome | rel=r_associated | relid=0 | w=35
- en:mmih syndrome --
r_associated #0: 35 / 0.814 ->
en:episodic pain syndrome, familial, 3
n1=en:mmih syndrome | n2=en:episodic pain syndrome, familial, 3 | rel=r_associated | relid=0 | w=35
- en:mmih syndrome --
r_associated #0: 35 / 0.814 ->
en:evans syndrome
n1=en:mmih syndrome | n2=en:evans syndrome | rel=r_associated | relid=0 | w=35
- en:mmih syndrome --
r_associated #0: 35 / 0.814 ->
en:kallmann syndrome
n1=en:mmih syndrome | n2=en:kallmann syndrome | rel=r_associated | relid=0 | w=35
- en:mmih syndrome --
r_associated #0: 35 / 0.814 ->
en:organic brain syndrome
n1=en:mmih syndrome | n2=en:organic brain syndrome | rel=r_associated | relid=0 | w=35
- en:mmih syndrome --
r_associated #0: 35 / 0.814 ->
en:respiratory distress syndrome
n1=en:mmih syndrome | n2=en:respiratory distress syndrome | rel=r_associated | relid=0 | w=35
- en:mmih syndrome --
r_associated #0: 35 / 0.814 ->
en:reye syndrome
n1=en:mmih syndrome | n2=en:reye syndrome | rel=r_associated | relid=0 | w=35
- en:mmih syndrome --
r_associated #0: 34 / 0.791 ->
en:5 alpha steroid reductase 2 deficiency
n1=en:mmih syndrome | n2=en:5 alpha steroid reductase 2 deficiency | rel=r_associated | relid=0 | w=34
- en:mmih syndrome --
r_associated #0: 34 / 0.791 ->
en:acute coronary syndrome
n1=en:mmih syndrome | n2=en:acute coronary syndrome | rel=r_associated | relid=0 | w=34
- en:mmih syndrome --
r_associated #0: 34 / 0.791 ->
en:alpha-1 antitrypsin deficiency
n1=en:mmih syndrome | n2=en:alpha-1 antitrypsin deficiency | rel=r_associated | relid=0 | w=34
- en:mmih syndrome --
r_associated #0: 34 / 0.791 ->
en:andersen syndrome
n1=en:mmih syndrome | n2=en:andersen syndrome | rel=r_associated | relid=0 | w=34
- en:mmih syndrome --
r_associated #0: 34 / 0.791 ->
en:bonnevie-ullrich syndrome
n1=en:mmih syndrome | n2=en:bonnevie-ullrich syndrome | rel=r_associated | relid=0 | w=34
- en:mmih syndrome --
r_associated #0: 34 / 0.791 ->
en:brown-sequard syndrome
n1=en:mmih syndrome | n2=en:brown-sequard syndrome | rel=r_associated | relid=0 | w=34
- en:mmih syndrome --
r_associated #0: 34 / 0.791 ->
en:capgras syndrome
n1=en:mmih syndrome | n2=en:capgras syndrome | rel=r_associated | relid=0 | w=34
- en:mmih syndrome --
r_associated #0: 34 / 0.791 ->
en:carbohydrate-deficient glycoprotein syndrome
n1=en:mmih syndrome | n2=en:carbohydrate-deficient glycoprotein syndrome | rel=r_associated | relid=0 | w=34
- en:mmih syndrome --
r_associated #0: 34 / 0.791 ->
en:chediak-higashi syndrome
n1=en:mmih syndrome | n2=en:chediak-higashi syndrome | rel=r_associated | relid=0 | w=34
- en:mmih syndrome --
r_associated #0: 34 / 0.791 ->
en:chromosome 2q37 deletion syndrome
n1=en:mmih syndrome | n2=en:chromosome 2q37 deletion syndrome | rel=r_associated | relid=0 | w=34
- en:mmih syndrome --
r_associated #0: 34 / 0.791 ->
en:compartment syndrome
n1=en:mmih syndrome | n2=en:compartment syndrome | rel=r_associated | relid=0 | w=34
- en:mmih syndrome --
r_associated #0: 34 / 0.791 ->
en:congenital anomaly of abdominal wall
n1=en:mmih syndrome | n2=en:congenital anomaly of abdominal wall | rel=r_associated | relid=0 | w=34
- en:mmih syndrome --
r_associated #0: 34 / 0.791 ->
en:dextrocardia
n1=en:mmih syndrome | n2=en:dextrocardia | rel=r_associated | relid=0 | w=34
- en:mmih syndrome --
r_associated #0: 34 / 0.791 ->
en:dry eye syndrome
n1=en:mmih syndrome | n2=en:dry eye syndrome | rel=r_associated | relid=0 | w=34
- en:mmih syndrome --
r_associated #0: 34 / 0.791 ->
en:eisenmenger syndrome
n1=en:mmih syndrome | n2=en:eisenmenger syndrome | rel=r_associated | relid=0 | w=34
- en:mmih syndrome --
r_associated #0: 34 / 0.791 ->
en:erythropoietic protoporphyria
n1=en:mmih syndrome | n2=en:erythropoietic protoporphyria | rel=r_associated | relid=0 | w=34
- en:mmih syndrome --
r_associated #0: 34 / 0.791 ->
en:fatal familial insomnia
n1=en:mmih syndrome | n2=en:fatal familial insomnia | rel=r_associated | relid=0 | w=34
- en:mmih syndrome --
r_associated #0: 34 / 0.791 ->
en:gastroschisis
n1=en:mmih syndrome | n2=en:gastroschisis | rel=r_associated | relid=0 | w=34
- en:mmih syndrome --
r_associated #0: 34 / 0.791 ->
en:meckel diverticulitis
n1=en:mmih syndrome | n2=en:meckel diverticulitis | rel=r_associated | relid=0 | w=34
- en:mmih syndrome --
r_associated #0: 34 / 0.791 ->
en:prune belly syndrome
n1=en:mmih syndrome | n2=en:prune belly syndrome | rel=r_associated | relid=0 | w=34
- en:mmih syndrome --
r_associated #0: 34 / 0.791 ->
en:situs inversus abdominalis
n1=en:mmih syndrome | n2=en:situs inversus abdominalis | rel=r_associated | relid=0 | w=34
- en:mmih syndrome --
r_associated #0: 34 / 0.791 ->
en:zollinger ellison syndrome
n1=en:mmih syndrome | n2=en:zollinger ellison syndrome | rel=r_associated | relid=0 | w=34
- en:mmih syndrome --
r_associated #0: 32 / 0.744 ->
en:acrocallosal syndrome
n1=en:mmih syndrome | n2=en:acrocallosal syndrome | rel=r_associated | relid=0 | w=32
- en:mmih syndrome --
r_associated #0: 32 / 0.744 ->
en:aicardi syndrome
n1=en:mmih syndrome | n2=en:aicardi syndrome | rel=r_associated | relid=0 | w=32
- en:mmih syndrome --
r_associated #0: 32 / 0.744 ->
en:antithrombin iii deficiency
n1=en:mmih syndrome | n2=en:antithrombin iii deficiency | rel=r_associated | relid=0 | w=32
- en:mmih syndrome --
r_associated #0: 32 / 0.744 ->
en:autosomal recessive hypohidrotic ectodermal dysplasia
n1=en:mmih syndrome | n2=en:autosomal recessive hypohidrotic ectodermal dysplasia | rel=r_associated | relid=0 | w=32
- en:mmih syndrome --
r_associated #0: 32 / 0.744 ->
en:chorea
n1=en:mmih syndrome | n2=en:chorea | rel=r_associated | relid=0 | w=32
- en:mmih syndrome --
r_associated #0: 32 / 0.744 ->
en:congenital digestive system disorder
n1=en:mmih syndrome | n2=en:congenital digestive system disorder | rel=r_associated | relid=0 | w=32
- en:mmih syndrome --
r_associated #0: 32 / 0.744 ->
en:congenital urinary system abnormality
n1=en:mmih syndrome | n2=en:congenital urinary system abnormality | rel=r_associated | relid=0 | w=32
- en:mmih syndrome --
r_associated #0: 32 / 0.744 ->
en:darier disease
n1=en:mmih syndrome | n2=en:darier disease | rel=r_associated | relid=0 | w=32
- en:mmih syndrome --
r_associated #0: 32 / 0.744 ->
en:diencephalic syndrome of infancy
n1=en:mmih syndrome | n2=en:diencephalic syndrome of infancy | rel=r_associated | relid=0 | w=32
- en:mmih syndrome --
r_associated #0: 32 / 0.744 ->
en:familial partial lipodystrophy
n1=en:mmih syndrome | n2=en:familial partial lipodystrophy | rel=r_associated | relid=0 | w=32
- en:mmih syndrome --
r_associated #0: 32 / 0.744 ->
en:holt-oram syndrome
n1=en:mmih syndrome | n2=en:holt-oram syndrome | rel=r_associated | relid=0 | w=32
- en:mmih syndrome --
r_associated #0: 32 / 0.744 ->
en:multiple congenital anomalies
n1=en:mmih syndrome | n2=en:multiple congenital anomalies | rel=r_associated | relid=0 | w=32
- en:mmih syndrome --
r_associated #0: 31 / 0.721 ->
en:adiposis dolorosa
n1=en:mmih syndrome | n2=en:adiposis dolorosa | rel=r_associated | relid=0 | w=31
- en:mmih syndrome --
r_associated #0: 31 / 0.721 ->
en:argininemia
n1=en:mmih syndrome | n2=en:argininemia | rel=r_associated | relid=0 | w=31
- en:mmih syndrome --
r_associated #0: 31 / 0.721 ->
en:beta-methylcrotonylglycinuria
n1=en:mmih syndrome | n2=en:beta-methylcrotonylglycinuria | rel=r_associated | relid=0 | w=31
- en:mmih syndrome --
r_associated #0: 31 / 0.721 ->
en:caroli disease
n1=en:mmih syndrome | n2=en:caroli disease | rel=r_associated | relid=0 | w=31
- en:mmih syndrome --
r_associated #0: 31 / 0.721 ->
en:cogan-reese syndrome
n1=en:mmih syndrome | n2=en:cogan-reese syndrome | rel=r_associated | relid=0 | w=31
- en:mmih syndrome --
r_associated #0: 31 / 0.721 ->
en:empty sella syndrome
n1=en:mmih syndrome | n2=en:empty sella syndrome | rel=r_associated | relid=0 | w=31
- en:mmih syndrome --
r_associated #0: 31 / 0.721 ->
en:erythromelalgia
n1=en:mmih syndrome | n2=en:erythromelalgia | rel=r_associated | relid=0 | w=31
- en:mmih syndrome --
r_associated #0: 31 / 0.721 ->
en:klinefelter syndrome
n1=en:mmih syndrome | n2=en:klinefelter syndrome | rel=r_associated | relid=0 | w=31
- en:mmih syndrome --
r_associated #0: 31 / 0.721 ->
en:menkes disease
n1=en:mmih syndrome | n2=en:menkes disease | rel=r_associated | relid=0 | w=31
- en:mmih syndrome --
r_associated #0: 31 / 0.721 ->
en:umbilical malformation
n1=en:mmih syndrome | n2=en:umbilical malformation | rel=r_associated | relid=0 | w=31
- en:mmih syndrome --
r_associated #0: 31 / 0.721 ->
en:wiskott-aldrich syndrome
n1=en:mmih syndrome | n2=en:wiskott-aldrich syndrome | rel=r_associated | relid=0 | w=31
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:acquired immunodeficiency syndrome
n1=en:mmih syndrome | n2=en:acquired immunodeficiency syndrome | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:ainhum
n1=en:mmih syndrome | n2=en:ainhum | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:alport syndrome
n1=en:mmih syndrome | n2=en:alport syndrome | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:amniotic band syndrome
n1=en:mmih syndrome | n2=en:amniotic band syndrome | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:aprosencephaly
n1=en:mmih syndrome | n2=en:aprosencephaly | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:arthrogryposis
n1=en:mmih syndrome | n2=en:arthrogryposis | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:bardet-biedl syndrome
n1=en:mmih syndrome | n2=en:bardet-biedl syndrome | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:campomelic dysplasia
n1=en:mmih syndrome | n2=en:campomelic dysplasia | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:cataplexy
n1=en:mmih syndrome | n2=en:cataplexy | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:chromosome 15q11-q13 duplication syndrome
n1=en:mmih syndrome | n2=en:chromosome 15q11-q13 duplication syndrome | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:cockayne syndrome
n1=en:mmih syndrome | n2=en:cockayne syndrome | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:congenital absence of bladder
n1=en:mmih syndrome | n2=en:congenital absence of bladder | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:congenital genitourinary tract anomalies nec
n1=en:mmih syndrome | n2=en:congenital genitourinary tract anomalies nec | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:congenital hernia
n1=en:mmih syndrome | n2=en:congenital hernia | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:craniosynostosis
n1=en:mmih syndrome | n2=en:craniosynostosis | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:deafness, autosomal recessive 28
n1=en:mmih syndrome | n2=en:deafness, autosomal recessive 28 | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:dysfunctional elimination syndrome
n1=en:mmih syndrome | n2=en:dysfunctional elimination syndrome | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:fanconi syndrome
n1=en:mmih syndrome | n2=en:fanconi syndrome | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:hereditary mucosal leukokeratosis
n1=en:mmih syndrome | n2=en:hereditary mucosal leukokeratosis | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:leigh disease
n1=en:mmih syndrome | n2=en:leigh disease | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:maroteaux-lamy syndrome
n1=en:mmih syndrome | n2=en:maroteaux-lamy syndrome | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:mobius syndrome
n1=en:mmih syndrome | n2=en:mobius syndrome | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:nephrotic syndrome
n1=en:mmih syndrome | n2=en:nephrotic syndrome | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:plague
n1=en:mmih syndrome | n2=en:plague | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:progressive familial intrahepatic cholestasis
n1=en:mmih syndrome | n2=en:progressive familial intrahepatic cholestasis | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:prolidase deficiency
n1=en:mmih syndrome | n2=en:prolidase deficiency | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:sudden infant death syndrome
n1=en:mmih syndrome | n2=en:sudden infant death syndrome | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:syndrome of apparent mineralocorticoid excess
n1=en:mmih syndrome | n2=en:syndrome of apparent mineralocorticoid excess | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:tarsal tunnel syndrome
n1=en:mmih syndrome | n2=en:tarsal tunnel syndrome | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:treacher collins syndrome
n1=en:mmih syndrome | n2=en:treacher collins syndrome | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:uveomeningoencephalitic syndrome
n1=en:mmih syndrome | n2=en:uveomeningoencephalitic syndrome | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:vitelliform macular dystrophy
n1=en:mmih syndrome | n2=en:vitelliform macular dystrophy | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
en:wolfram syndrome
n1=en:mmih syndrome | n2=en:wolfram syndrome | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 30 / 0.698 ->
paralysies périodiques familiales
n1=en:mmih syndrome | n2=paralysies périodiques familiales | rel=r_associated | relid=0 | w=30
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:22q telomere deletion syndrome
n1=en:mmih syndrome | n2=en:22q telomere deletion syndrome | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:acute respiratory distress syndrome
n1=en:mmih syndrome | n2=en:acute respiratory distress syndrome | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:alagille syndrome
n1=en:mmih syndrome | n2=en:alagille syndrome | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:allgrove syndrome
n1=en:mmih syndrome | n2=en:allgrove syndrome | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:anhidrotic ectodermal dysplasia 1
n1=en:mmih syndrome | n2=en:anhidrotic ectodermal dysplasia 1 | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:antiphospholipid syndrome
n1=en:mmih syndrome | n2=en:antiphospholipid syndrome | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:argininosuccinic aciduria
n1=en:mmih syndrome | n2=en:argininosuccinic aciduria | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:auditory perceptual disorder
n1=en:mmih syndrome | n2=en:auditory perceptual disorder | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:bloom syndrome
n1=en:mmih syndrome | n2=en:bloom syndrome | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:calciphylaxis
n1=en:mmih syndrome | n2=en:calciphylaxis | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:cervicocranial syndrome
n1=en:mmih syndrome | n2=en:cervicocranial syndrome | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:chilblains
n1=en:mmih syndrome | n2=en:chilblains | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:congenital hourglass bladder
n1=en:mmih syndrome | n2=en:congenital hourglass bladder | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:cytokine release syndrome
n1=en:mmih syndrome | n2=en:cytokine release syndrome | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:d-glyceric aciduria
n1=en:mmih syndrome | n2=en:d-glyceric aciduria | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:deletion 18p syndrome
n1=en:mmih syndrome | n2=en:deletion 18p syndrome | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:digeorge syndrome
n1=en:mmih syndrome | n2=en:digeorge syndrome | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:ehlers-danlos syndrome
n1=en:mmih syndrome | n2=en:ehlers-danlos syndrome | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:fibromyalgia
n1=en:mmih syndrome | n2=en:fibromyalgia | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:fragile x syndrome
n1=en:mmih syndrome | n2=en:fragile x syndrome | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:hyperlysinemia
n1=en:mmih syndrome | n2=en:hyperlysinemia | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:hyperviscosity syndrome
n1=en:mmih syndrome | n2=en:hyperviscosity syndrome | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:lysosomal storage disease
n1=en:mmih syndrome | n2=en:lysosomal storage disease | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:myositis
n1=en:mmih syndrome | n2=en:myositis | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:neonatal progeroid syndrome
n1=en:mmih syndrome | n2=en:neonatal progeroid syndrome | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:papillon-lefevre syndrome
n1=en:mmih syndrome | n2=en:papillon-lefevre syndrome | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:pediatric terminology
n1=en:mmih syndrome | n2=en:pediatric terminology | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:poland syndrome
n1=en:mmih syndrome | n2=en:poland syndrome | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:prader-willi syndrome
n1=en:mmih syndrome | n2=en:prader-willi syndrome | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:wernicke-korsakoff syndrome
n1=en:mmih syndrome | n2=en:wernicke-korsakoff syndrome | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
en:xyy syndrome
n1=en:mmih syndrome | n2=en:xyy syndrome | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 29 / 0.674 ->
vessie
(anatomie)
n1=en:mmih syndrome | n2=vessie (anatomie) | rel=r_associated | relid=0 | w=29
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
anomalie congénitale
n1=en:mmih syndrome | n2=anomalie congénitale | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:abetalipoproteinemia
n1=en:mmih syndrome | n2=en:abetalipoproteinemia | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:acromegaly
n1=en:mmih syndrome | n2=en:acromegaly | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:alpha thalassemia x-linked mental retardation syndrome
n1=en:mmih syndrome | n2=en:alpha thalassemia x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:aniridia
n1=en:mmih syndrome | n2=en:aniridia | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:atrophic muscular disorder
n1=en:mmih syndrome | n2=en:atrophic muscular disorder | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:barth syndrome
n1=en:mmih syndrome | n2=en:barth syndrome | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:complex regional pain syndrome i
n1=en:mmih syndrome | n2=en:complex regional pain syndrome i | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:congenital cyst of bladder
n1=en:mmih syndrome | n2=en:congenital cyst of bladder | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:congenital malformation syndrome
n1=en:mmih syndrome | n2=en:congenital malformation syndrome | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:cushing syndrome
n1=en:mmih syndrome | n2=en:cushing syndrome | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:cutis laxa
n1=en:mmih syndrome | n2=en:cutis laxa | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:cytochrome-c oxidase deficiency
n1=en:mmih syndrome | n2=en:cytochrome-c oxidase deficiency | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:diffuse infiltrative lymphocytosis syndrome
n1=en:mmih syndrome | n2=en:diffuse infiltrative lymphocytosis syndrome | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:ectodermal dysplasia
n1=en:mmih syndrome | n2=en:ectodermal dysplasia | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:ectromelia
n1=en:mmih syndrome | n2=en:ectromelia | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:endocrine syndrome
n1=en:mmih syndrome | n2=en:endocrine syndrome | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:factor v leiden
n1=en:mmih syndrome | n2=en:factor v leiden | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:feingold syndrome
n1=en:mmih syndrome | n2=en:feingold syndrome | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:genetic disorder
n1=en:mmih syndrome | n2=en:genetic disorder | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:goldenhar syndrome
n1=en:mmih syndrome | n2=en:goldenhar syndrome | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:hmg-coa lyase deficiency
n1=en:mmih syndrome | n2=en:hmg-coa lyase deficiency | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:imperforate anus
n1=en:mmih syndrome | n2=en:imperforate anus | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:kernicterus
n1=en:mmih syndrome | n2=en:kernicterus | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:leopard syndrome
n1=en:mmih syndrome | n2=en:leopard syndrome | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:li-fraumeni syndrome
n1=en:mmih syndrome | n2=en:li-fraumeni syndrome | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:methionine adenosyltransferase deficiency
n1=en:mmih syndrome | n2=en:methionine adenosyltransferase deficiency | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:paroxysmal extreme pain disorder
n1=en:mmih syndrome | n2=en:paroxysmal extreme pain disorder | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:tay-sachs disease
n1=en:mmih syndrome | n2=en:tay-sachs disease | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 28 / 0.651 ->
en:vertebral artery syndrome
n1=en:mmih syndrome | n2=en:vertebral artery syndrome | rel=r_associated | relid=0 | w=28
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
côlon
n1=en:mmih syndrome | n2=côlon | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:adenine phosphoribosyltransferase deficiency
n1=en:mmih syndrome | n2=en:adenine phosphoribosyltransferase deficiency | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:alkaptonuria
n1=en:mmih syndrome | n2=en:alkaptonuria | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:alstrom syndrome
n1=en:mmih syndrome | n2=en:alstrom syndrome | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:carnitine palmitoyltransferase i deficiency
n1=en:mmih syndrome | n2=en:carnitine palmitoyltransferase i deficiency | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:churg-strauss syndrome
n1=en:mmih syndrome | n2=en:churg-strauss syndrome | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:congenital amegakaryocytic thrombocytopenia
n1=en:mmih syndrome | n2=en:congenital amegakaryocytic thrombocytopenia | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:congenital cortical hyperostosis
n1=en:mmih syndrome | n2=en:congenital cortical hyperostosis | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:congenital pain insensitivity
n1=en:mmih syndrome | n2=en:congenital pain insensitivity | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:cystinuria
n1=en:mmih syndrome | n2=en:cystinuria | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:dumping syndrome
n1=en:mmih syndrome | n2=en:dumping syndrome | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:dyschromatosis symmetrica hereditaria
n1=en:mmih syndrome | n2=en:dyschromatosis symmetrica hereditaria | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:gitelman syndrome
n1=en:mmih syndrome | n2=en:gitelman syndrome | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:hair tourniquet
n1=en:mmih syndrome | n2=en:hair tourniquet | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:hand foot uterus syndrome
n1=en:mmih syndrome | n2=en:hand foot uterus syndrome | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:jackson-weiss syndrome
n1=en:mmih syndrome | n2=en:jackson-weiss syndrome | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:laurence-moon syndrome
n1=en:mmih syndrome | n2=en:laurence-moon syndrome | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:leri-weill dyschondrosteosis
n1=en:mmih syndrome | n2=en:leri-weill dyschondrosteosis | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:liddle syndrome
n1=en:mmih syndrome | n2=en:liddle syndrome | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:lubs x-linked mental retardation syndrome
n1=en:mmih syndrome | n2=en:lubs x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:marfan syndrome
n1=en:mmih syndrome | n2=en:marfan syndrome | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:neural tube defect
n1=en:mmih syndrome | n2=en:neural tube defect | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:ossification of posterior longitudinal ligament
n1=en:mmih syndrome | n2=en:ossification of posterior longitudinal ligament | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:persistent cloaca
n1=en:mmih syndrome | n2=en:persistent cloaca | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:piebaldism
n1=en:mmih syndrome | n2=en:piebaldism | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:simpson golabi behmel syndrome type 1
n1=en:mmih syndrome | n2=en:simpson golabi behmel syndrome type 1 | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:sjogren syndrome
n1=en:mmih syndrome | n2=en:sjogren syndrome | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:smith-magenis syndrome
n1=en:mmih syndrome | n2=en:smith-magenis syndrome | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:sotos syndrome
n1=en:mmih syndrome | n2=en:sotos syndrome | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:temporomandibular joint dysfunction syndrome
n1=en:mmih syndrome | n2=en:temporomandibular joint dysfunction syndrome | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:tourette syndrome
n1=en:mmih syndrome | n2=en:tourette syndrome | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
en:walker-warburg syndrome
n1=en:mmih syndrome | n2=en:walker-warburg syndrome | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 27 / 0.628 ->
maladie de Marfan
n1=en:mmih syndrome | n2=maladie de Marfan | rel=r_associated | relid=0 | w=27
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:achromatopsia
n1=en:mmih syndrome | n2=en:achromatopsia | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:albright's hereditary osteodystrophy
n1=en:mmih syndrome | n2=en:albright's hereditary osteodystrophy | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:aortic coarctation
n1=en:mmih syndrome | n2=en:aortic coarctation | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:biotinidase deficiency
n1=en:mmih syndrome | n2=en:biotinidase deficiency | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:cartilage hair hypoplasia
n1=en:mmih syndrome | n2=en:cartilage hair hypoplasia | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:central sleep apnea syndrome
n1=en:mmih syndrome | n2=en:central sleep apnea syndrome | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:cloacal exstrophy
n1=en:mmih syndrome | n2=en:cloacal exstrophy | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:congenital
n1=en:mmih syndrome | n2=en:congenital | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:congenital dilatation of bladder
n1=en:mmih syndrome | n2=en:congenital dilatation of bladder | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:congenital disorder of deglycosylation
n1=en:mmih syndrome | n2=en:congenital disorder of deglycosylation | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:congenital fiber-type disproportion
n1=en:mmih syndrome | n2=en:congenital fiber-type disproportion | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:congenital hypoplasia of bladder
n1=en:mmih syndrome | n2=en:congenital hypoplasia of bladder | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:congenital uterovesical fistula
n1=en:mmih syndrome | n2=en:congenital uterovesical fistula | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:conn syndrome
n1=en:mmih syndrome | n2=en:conn syndrome | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:cryptophthalmos syndrome
n1=en:mmih syndrome | n2=en:cryptophthalmos syndrome | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:dentatorubral-pallidoluysian atrophy
n1=en:mmih syndrome | n2=en:dentatorubral-pallidoluysian atrophy | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:dialyzer first use syndrome
n1=en:mmih syndrome | n2=en:dialyzer first use syndrome | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:donohue syndrome
n1=en:mmih syndrome | n2=en:donohue syndrome | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:familial dysautonomia
n1=en:mmih syndrome | n2=en:familial dysautonomia | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:familial juvenile nephronophthisis
n1=en:mmih syndrome | n2=en:familial juvenile nephronophthisis | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:felty syndrome
n1=en:mmih syndrome | n2=en:felty syndrome | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:focal dermal hypoplasia
n1=en:mmih syndrome | n2=en:focal dermal hypoplasia | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:gastrointestinal tract disorders congenital nec
n1=en:mmih syndrome | n2=en:gastrointestinal tract disorders congenital nec | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:hereditary angioedema
n1=en:mmih syndrome | n2=en:hereditary angioedema | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:kearns-sayre syndrome
n1=en:mmih syndrome | n2=en:kearns-sayre syndrome | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:maple syrup urine disease
n1=en:mmih syndrome | n2=en:maple syrup urine disease | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:microcephaly and chorioretinopathy, autosomal recessive, type 1
n1=en:mmih syndrome | n2=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:monosomy 13q syndrome
n1=en:mmih syndrome | n2=en:monosomy 13q syndrome | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:omphalocele
n1=en:mmih syndrome | n2=en:omphalocele | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:pseudotumor cerebri
n1=en:mmih syndrome | n2=en:pseudotumor cerebri | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:pyruvate carboxylase deficiency
n1=en:mmih syndrome | n2=en:pyruvate carboxylase deficiency | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:robinow syndrome
n1=en:mmih syndrome | n2=en:robinow syndrome | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
en:transposition of great vessels
n1=en:mmih syndrome | n2=en:transposition of great vessels | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
peste
(maladie)
n1=en:mmih syndrome | n2=peste (maladie) | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 26 / 0.605 ->
syndrome
n1=en:mmih syndrome | n2=syndrome | rel=r_associated | relid=0 | w=26
- en:mmih syndrome --
r_associated #0: 25 / 0.581 ->
en:acrodermatitis enteropathica
n1=en:mmih syndrome | n2=en:acrodermatitis enteropathica | rel=r_associated | relid=0 | w=25
- en:mmih syndrome --
r_associated #0: 25 / 0.581 ->
en:beare-stevenson cutis gyrata syndrome
n1=en:mmih syndrome | n2=en:beare-stevenson cutis gyrata syndrome | rel=r_associated | relid=0 | w=25
- en:mmih syndrome --
r_associated #0: 25 / 0.581 ->
en:bladder
n1=en:mmih syndrome | n2=en:bladder | rel=r_associated | relid=0 | w=25
- en:mmih syndrome --
r_associated #0: 25 / 0.581 ->
en:fisher syndrome
n1=en:mmih syndrome | n2=en:fisher syndrome | rel=r_associated | relid=0 | w=25
- en:mmih syndrome --
r_associated #0: 25 / 0.581 ->
en:hereditary orotic aciduria
n1=en:mmih syndrome | n2=en:hereditary orotic aciduria | rel=r_associated | relid=0 | w=25
- en:mmih syndrome --
r_associated #0: 25 / 0.581 ->
en:hunter syndrome
n1=en:mmih syndrome | n2=en:hunter syndrome | rel=r_associated | relid=0 | w=25
- en:mmih syndrome --
r_associated #0: 25 / 0.581 ->
en:kleine-levin syndrome
n1=en:mmih syndrome | n2=en:kleine-levin syndrome | rel=r_associated | relid=0 | w=25
- en:mmih syndrome --
r_associated #0: 25 / 0.581 ->
en:long-chain acyl-coa dehydrogenase deficiency
n1=en:mmih syndrome | n2=en:long-chain acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=25
- en:mmih syndrome --
r_associated #0: 25 / 0.581 ->
en:mitochondrial trifunctional protein deficiency
n1=en:mmih syndrome | n2=en:mitochondrial trifunctional protein deficiency | rel=r_associated | relid=0 | w=25
- en:mmih syndrome --
r_associated #0: 25 / 0.581 ->
en:nail-patella syndrome
n1=en:mmih syndrome | n2=en:nail-patella syndrome | rel=r_associated | relid=0 | w=25
- en:mmih syndrome --
r_associated #0: 25 / 0.581 ->
en:nephrocalcinosis
n1=en:mmih syndrome | n2=en:nephrocalcinosis | rel=r_associated | relid=0 | w=25
- en:mmih syndrome --
r_associated #0: 25 / 0.581 ->
en:norrie syndrome
n1=en:mmih syndrome | n2=en:norrie syndrome | rel=r_associated | relid=0 | w=25
- en:mmih syndrome --
r_associated #0: 25 / 0.581 ->
en:pelizaeus-merzbacher disease
n1=en:mmih syndrome | n2=en:pelizaeus-merzbacher disease | rel=r_associated | relid=0 | w=25
- en:mmih syndrome --
r_associated #0: 25 / 0.581 ->
en:restless leg syndrome
n1=en:mmih syndrome | n2=en:restless leg syndrome | rel=r_associated | relid=0 | w=25
- en:mmih syndrome --
r_associated #0: 25 / 0.581 ->
maladie héréditaire
n1=en:mmih syndrome | n2=maladie héréditaire | rel=r_associated | relid=0 | w=25
- en:mmih syndrome --
r_associated #0: 25 / 0.581 ->
syndrome de Marfan
n1=en:mmih syndrome | n2=syndrome de Marfan | rel=r_associated | relid=0 | w=25
- en:mmih syndrome --
r_associated #0: 24 / 0.558 ->
en:allan-herndon-dudley syndrome
n1=en:mmih syndrome | n2=en:allan-herndon-dudley syndrome | rel=r_associated | relid=0 | w=24
- en:mmih syndrome --
r_associated #0: 24 / 0.558 ->
en:benign mucous membrane pemphigoid
n1=en:mmih syndrome | n2=en:benign mucous membrane pemphigoid | rel=r_associated | relid=0 | w=24
- en:mmih syndrome --
r_associated #0: 24 / 0.558 ->
en:blau syndrome
n1=en:mmih syndrome | n2=en:blau syndrome | rel=r_associated | relid=0 | w=24
- en:mmih syndrome --
r_associated #0: 24 / 0.558 ->
en:cerebrotendinous xanthomatosis
n1=en:mmih syndrome | n2=en:cerebrotendinous xanthomatosis | rel=r_associated | relid=0 | w=24
- en:mmih syndrome --
r_associated #0: 24 / 0.558 ->
en:congenital inguinal hernia
n1=en:mmih syndrome | n2=en:congenital inguinal hernia | rel=r_associated | relid=0 | w=24
- en:mmih syndrome --
r_associated #0: 24 / 0.558 ->
en:fox-fordyce disease
n1=en:mmih syndrome | n2=en:fox-fordyce disease | rel=r_associated | relid=0 | w=24
- en:mmih syndrome --
r_associated #0: 24 / 0.558 ->
en:frontotemporal dementia
n1=en:mmih syndrome | n2=en:frontotemporal dementia | rel=r_associated | relid=0 | w=24
- en:mmih syndrome --
r_associated #0: 24 / 0.558 ->
en:gerstmann-straussler-scheinker disease
n1=en:mmih syndrome | n2=en:gerstmann-straussler-scheinker disease | rel=r_associated | relid=0 | w=24
- en:mmih syndrome --
r_associated #0: 24 / 0.558 ->
en:hirschsprung's disease and allied congenital conditions
n1=en:mmih syndrome | n2=en:hirschsprung's disease and allied congenital conditions | rel=r_associated | relid=0 | w=24
- en:mmih syndrome --
r_associated #0: 24 / 0.558 ->
en:kabuki syndrome
n1=en:mmih syndrome | n2=en:kabuki syndrome | rel=r_associated | relid=0 | w=24
- en:mmih syndrome --
r_associated #0: 24 / 0.558 ->
en:lesch-nyhan syndrome
n1=en:mmih syndrome | n2=en:lesch-nyhan syndrome | rel=r_associated | relid=0 | w=24
- en:mmih syndrome --
r_associated #0: 24 / 0.558 ->
en:myotonic disorder
n1=en:mmih syndrome | n2=en:myotonic disorder | rel=r_associated | relid=0 | w=24
- en:mmih syndrome --
r_associated #0: 24 / 0.558 ->
en:persistent urogenital sinus
n1=en:mmih syndrome | n2=en:persistent urogenital sinus | rel=r_associated | relid=0 | w=24
- en:mmih syndrome --
r_associated #0: 24 / 0.558 ->
en:renal coloboma syndrome
n1=en:mmih syndrome | n2=en:renal coloboma syndrome | rel=r_associated | relid=0 | w=24
- en:mmih syndrome --
r_associated #0: 24 / 0.558 ->
en:sheehan syndrome
n1=en:mmih syndrome | n2=en:sheehan syndrome | rel=r_associated | relid=0 | w=24
- en:mmih syndrome --
r_associated #0: 24 / 0.558 ->
en:x-linked creatine transporter deficiency
n1=en:mmih syndrome | n2=en:x-linked creatine transporter deficiency | rel=r_associated | relid=0 | w=24
- en:mmih syndrome --
r_associated #0: 24 / 0.558 ->
maladie génétique
n1=en:mmih syndrome | n2=maladie génétique | rel=r_associated | relid=0 | w=24
- en:mmih syndrome --
r_associated #0: 23 / 0.535 ->
anomalie héréditaire
n1=en:mmih syndrome | n2=anomalie héréditaire | rel=r_associated | relid=0 | w=23
- en:mmih syndrome --
r_associated #0: 23 / 0.535 ->
en:congenital rectovesical fistula
n1=en:mmih syndrome | n2=en:congenital rectovesical fistula | rel=r_associated | relid=0 | w=23
- en:mmih syndrome --
r_associated #0: 23 / 0.535 ->
en:displaced ureteric orifice
n1=en:mmih syndrome | n2=en:displaced ureteric orifice | rel=r_associated | relid=0 | w=23
- en:mmih syndrome --
r_associated #0: 23 / 0.535 ->
en:familial periodic paralysis
n1=en:mmih syndrome | n2=en:familial periodic paralysis | rel=r_associated | relid=0 | w=23
- en:mmih syndrome --
r_associated #0: 23 / 0.535 ->
en:hereditary fructose intolerance
n1=en:mmih syndrome | n2=en:hereditary fructose intolerance | rel=r_associated | relid=0 | w=23
- en:mmih syndrome --
r_associated #0: 23 / 0.535 ->
en:melnick-fraser syndrome
n1=en:mmih syndrome | n2=en:melnick-fraser syndrome | rel=r_associated | relid=0 | w=23
- en:mmih syndrome --
r_associated #0: 23 / 0.535 ->
en:morquio syndrome
n1=en:mmih syndrome | n2=en:morquio syndrome | rel=r_associated | relid=0 | w=23
- en:mmih syndrome --
r_associated #0: 23 / 0.535 ->
en:mowat-wilson syndrome
n1=en:mmih syndrome | n2=en:mowat-wilson syndrome | rel=r_associated | relid=0 | w=23
- en:mmih syndrome --
r_associated #0: 23 / 0.535 ->
en:multiple gastrointestinal atresias (disorder)
n1=en:mmih syndrome | n2=en:multiple gastrointestinal atresias (disorder) | rel=r_associated | relid=0 | w=23
- en:mmih syndrome --
r_associated #0: 23 / 0.535 ->
en:netherton syndrome
n1=en:mmih syndrome | n2=en:netherton syndrome | rel=r_associated | relid=0 | w=23
- en:mmih syndrome --
r_associated #0: 23 / 0.535 ->
en:noonan syndrome
n1=en:mmih syndrome | n2=en:noonan syndrome | rel=r_associated | relid=0 | w=23
- en:mmih syndrome --
r_associated #0: 23 / 0.535 ->
en:pseudoachondroplasia
n1=en:mmih syndrome | n2=en:pseudoachondroplasia | rel=r_associated | relid=0 | w=23
- en:mmih syndrome --
r_associated #0: 23 / 0.535 ->
en:rett syndrome
n1=en:mmih syndrome | n2=en:rett syndrome | rel=r_associated | relid=0 | w=23
- en:mmih syndrome --
r_associated #0: 23 / 0.535 ->
en:sandifer's syndrome
n1=en:mmih syndrome | n2=en:sandifer's syndrome | rel=r_associated | relid=0 | w=23
- en:mmih syndrome --
r_associated #0: 23 / 0.535 ->
en:sirenomelia
n1=en:mmih syndrome | n2=en:sirenomelia | rel=r_associated | relid=0 | w=23
- en:mmih syndrome --
r_associated #0: 23 / 0.535 ->
en:stevens-johnson syndrome
n1=en:mmih syndrome | n2=en:stevens-johnson syndrome | rel=r_associated | relid=0 | w=23
- en:mmih syndrome --
r_associated #0: 23 / 0.535 ->
en:trigger finger disorder
n1=en:mmih syndrome | n2=en:trigger finger disorder | rel=r_associated | relid=0 | w=23
- en:mmih syndrome --
r_associated #0: 23 / 0.535 ->
en:von hippel-lindau syndrome
n1=en:mmih syndrome | n2=en:von hippel-lindau syndrome | rel=r_associated | relid=0 | w=23
- en:mmih syndrome --
r_associated #0: 22 / 0.512 ->
en:alpha-methylacyl-coa racemase deficiency
n1=en:mmih syndrome | n2=en:alpha-methylacyl-coa racemase deficiency | rel=r_associated | relid=0 | w=22
- en:mmih syndrome --
r_associated #0: 22 / 0.512 ->
en:burning mouth syndrome
n1=en:mmih syndrome | n2=en:burning mouth syndrome | rel=r_associated | relid=0 | w=22
- en:mmih syndrome --
r_associated #0: 22 / 0.512 ->
en:congenital abnormality
n1=en:mmih syndrome | n2=en:congenital abnormality | rel=r_associated | relid=0 | w=22
- en:mmih syndrome --
r_associated #0: 22 / 0.512 ->
en:idiopathic congenital megacolon (disorder)
n1=en:mmih syndrome | n2=en:idiopathic congenital megacolon (disorder) | rel=r_associated | relid=0 | w=22
- en:mmih syndrome --
r_associated #0: 22 / 0.512 ->
en:melas syndrome
n1=en:mmih syndrome | n2=en:melas syndrome | rel=r_associated | relid=0 | w=22
- en:mmih syndrome --
r_associated #0: 22 / 0.512 ->
en:periodic fever, aphthous stomatitis, pharyngitis, adenitis syndrome
n1=en:mmih syndrome | n2=en:periodic fever, aphthous stomatitis, pharyngitis, adenitis syndrome | rel=r_associated | relid=0 | w=22
- en:mmih syndrome --
r_associated #0: 22 / 0.512 ->
en:red man syndrome
n1=en:mmih syndrome | n2=en:red man syndrome | rel=r_associated | relid=0 | w=22
- en:mmih syndrome --
r_associated #0: 22 / 0.512 ->
en:vacterl association
n1=en:mmih syndrome | n2=en:vacterl association | rel=r_associated | relid=0 | w=22
- en:mmih syndrome --
r_associated #0: 22 / 0.512 ->
en:wolf-hirschhorn syndrome
n1=en:mmih syndrome | n2=en:wolf-hirschhorn syndrome | rel=r_associated | relid=0 | w=22
- en:mmih syndrome --
r_associated #0: 22 / 0.512 ->
en:x-linked bulbar-muscular atrophy
n1=en:mmih syndrome | n2=en:x-linked bulbar-muscular atrophy | rel=r_associated | relid=0 | w=22
- en:mmih syndrome --
r_associated #0: 22 / 0.512 ->
en:zellweger syndrome
n1=en:mmih syndrome | n2=en:zellweger syndrome | rel=r_associated | relid=0 | w=22
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
agénésie vésicale
n1=en:mmih syndrome | n2=agénésie vésicale | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:accessory bladder
n1=en:mmih syndrome | n2=en:accessory bladder | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:anencephaly
n1=en:mmih syndrome | n2=en:anencephaly | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:autosomal dominant optic atrophy
n1=en:mmih syndrome | n2=en:autosomal dominant optic atrophy | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:cauda equina syndrome
n1=en:mmih syndrome | n2=en:cauda equina syndrome | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:choroideremia
n1=en:mmih syndrome | n2=en:choroideremia | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:cleidocranial dysplasia
n1=en:mmih syndrome | n2=en:cleidocranial dysplasia | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:congenital prolapse of bladder
n1=en:mmih syndrome | n2=en:congenital prolapse of bladder | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:congenital structural myopathy
n1=en:mmih syndrome | n2=en:congenital structural myopathy | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:ectrodactyly
n1=en:mmih syndrome | n2=en:ectrodactyly | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:ellis-van creveld syndrome
n1=en:mmih syndrome | n2=en:ellis-van creveld syndrome | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:hyperganglionosis
n1=en:mmih syndrome | n2=en:hyperganglionosis | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:jervell and lange nielsen syndrome
n1=en:mmih syndrome | n2=en:jervell and lange nielsen syndrome | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:n-acetylglutamate synthase deficiency
n1=en:mmih syndrome | n2=en:n-acetylglutamate synthase deficiency | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:neoplastic syndrome
n1=en:mmih syndrome | n2=en:neoplastic syndrome | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:neuroacanthocytosis
n1=en:mmih syndrome | n2=en:neuroacanthocytosis | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:osteochondrodysplasia
n1=en:mmih syndrome | n2=en:osteochondrodysplasia | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:primary vesicoureteric reflux
n1=en:mmih syndrome | n2=en:primary vesicoureteric reflux | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:pseudotrisomy 13 syndrome
n1=en:mmih syndrome | n2=en:pseudotrisomy 13 syndrome | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:sanfilippo syndrome
n1=en:mmih syndrome | n2=en:sanfilippo syndrome | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:stein-leventhal syndrome
n1=en:mmih syndrome | n2=en:stein-leventhal syndrome | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:synpolydactyly
n1=en:mmih syndrome | n2=en:synpolydactyly | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:toxic shock syndrome
n1=en:mmih syndrome | n2=en:toxic shock syndrome | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
en:xerophthalmia
n1=en:mmih syndrome | n2=en:xerophthalmia | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 21 / 0.488 ->
syndrome de Walker-Warburg
n1=en:mmih syndrome | n2=syndrome de Walker-Warburg | rel=r_associated | relid=0 | w=21
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
acidémie glutarique de type 1
n1=en:mmih syndrome | n2=acidémie glutarique de type 1 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
acidurie glutarique de type 1
n1=en:mmih syndrome | n2=acidurie glutarique de type 1 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
acrodermatite entéropathique
n1=en:mmih syndrome | n2=acrodermatite entéropathique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
acrodermatitis enteropathica
n1=en:mmih syndrome | n2=acrodermatitis enteropathica | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
acromégalie
n1=en:mmih syndrome | n2=acromégalie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
acromégalie, plis cutanés de la face et du cuir chevelu, et leucomes cornéens
n1=en:mmih syndrome | n2=acromégalie, plis cutanés de la face et du cuir chevelu, et leucomes cornéens | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
acromegaly
n1=en:mmih syndrome | n2=acromegaly | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
agnosie
n1=en:mmih syndrome | n2=agnosie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
aïnhum
n1=en:mmih syndrome | n2=aïnhum | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
ainhum
n1=en:mmih syndrome | n2=ainhum | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
albinisme
n1=en:mmih syndrome | n2=albinisme | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
albinisme oculocutané de type mutant jaune
n1=en:mmih syndrome | n2=albinisme oculocutané de type mutant jaune | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
anasarque foetal
n1=en:mmih syndrome | n2=anasarque foetal | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
anasarque foeto-placentaire
n1=en:mmih syndrome | n2=anasarque foeto-placentaire | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
anasarque foetoplacentaire
n1=en:mmih syndrome | n2=anasarque foetoplacentaire | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
anencéphalie
n1=en:mmih syndrome | n2=anencéphalie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
aniridie partielle avec agénésie rénale unilatérale et retard psychomoteur
n1=en:mmih syndrome | n2=aniridie partielle avec agénésie rénale unilatérale et retard psychomoteur | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
aniridie, ataxie cérébelleuse et déficience mentale
n1=en:mmih syndrome | n2=aniridie, ataxie cérébelleuse et déficience mentale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
anomalie d'Ebstein
n1=en:mmih syndrome | n2=anomalie d'Ebstein | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
anomalie du développement
n1=en:mmih syndrome | n2=anomalie du développement | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
anti-sida
n1=en:mmih syndrome | n2=anti-sida | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
antisida
n1=en:mmih syndrome | n2=antisida | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
aphasie primaire progressive
n1=en:mmih syndrome | n2=aphasie primaire progressive | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
aphasie progressive primaire
n1=en:mmih syndrome | n2=aphasie progressive primaire | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
aphasies primaires progressives
n1=en:mmih syndrome | n2=aphasies primaires progressives | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
aplasie de la paroi abdominale
n1=en:mmih syndrome | n2=aplasie de la paroi abdominale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
arachnodactylie
n1=en:mmih syndrome | n2=arachnodactylie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
arthrogrypose
n1=en:mmih syndrome | n2=arthrogrypose | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
association toxoplasmose, rubéole, cytomégalovirus et herpès chez un nouveau-né
n1=en:mmih syndrome | n2=association toxoplasmose, rubéole, cytomégalovirus et herpès chez un nouveau-né | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
atélectasie congestive
n1=en:mmih syndrome | n2=atélectasie congestive | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
atransferrinémie
n1=en:mmih syndrome | n2=atransferrinémie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
atrophie optique autosomique dominante
n1=en:mmih syndrome | n2=atrophie optique autosomique dominante | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
cataplexie
n1=en:mmih syndrome | n2=cataplexie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
cétoacidurie à chaînes ramifiées
n1=en:mmih syndrome | n2=cétoacidurie à chaînes ramifiées | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
choc au poumon
n1=en:mmih syndrome | n2=choc au poumon | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
choc toxique staphylococcique
n1=en:mmih syndrome | n2=choc toxique staphylococcique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
cholestases intrahépatiques progressives familiales
n1=en:mmih syndrome | n2=cholestases intrahépatiques progressives familiales | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
chondrodysplasia punctata
n1=en:mmih syndrome | n2=chondrodysplasia punctata | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
chondrodysplasie léthale avec brièveté des côtes
n1=en:mmih syndrome | n2=chondrodysplasie léthale avec brièveté des côtes | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
coarctation aortique
n1=en:mmih syndrome | n2=coarctation aortique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
congénital
n1=en:mmih syndrome | n2=congénital | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
congenital
n1=en:mmih syndrome | n2=congenital | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
congénitale
n1=en:mmih syndrome | n2=congénitale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
contractures congénitales et arachnodactylie
n1=en:mmih syndrome | n2=contractures congénitales et arachnodactylie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
crânio-sténose
n1=en:mmih syndrome | n2=crânio-sténose | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
craniosténose
n1=en:mmih syndrome | n2=craniosténose | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
crâniosténose
n1=en:mmih syndrome | n2=crâniosténose | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
craniosynostose
n1=en:mmih syndrome | n2=craniosynostose | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
crâniosynostose
n1=en:mmih syndrome | n2=crâniosynostose | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
cysticercose
n1=en:mmih syndrome | n2=cysticercose | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
cysticercose cérébrale
n1=en:mmih syndrome | n2=cysticercose cérébrale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
cysticercose du système nerveux central
n1=en:mmih syndrome | n2=cysticercose du système nerveux central | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
cysticercose neurologique
n1=en:mmih syndrome | n2=cysticercose neurologique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
cysticercoses
n1=en:mmih syndrome | n2=cysticercoses | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
déficience congénitale
n1=en:mmih syndrome | n2=déficience congénitale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
déficit congénital en mégacaryocytes
n1=en:mmih syndrome | n2=déficit congénital en mégacaryocytes | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
déficit en biotinidase
n1=en:mmih syndrome | n2=déficit en biotinidase | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
déficit en céto-acide décarboxylase
n1=en:mmih syndrome | n2=déficit en céto-acide décarboxylase | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
déficit en cytochrome oxydase
n1=en:mmih syndrome | n2=déficit en cytochrome oxydase | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
déficit en cytochrome-c oxydase
n1=en:mmih syndrome | n2=déficit en cytochrome-c oxydase | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
déficit en prolidase
n1=en:mmih syndrome | n2=déficit en prolidase | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
déficit en protéine trifonctionnelle mitochondriale
n1=en:mmih syndrome | n2=déficit en protéine trifonctionnelle mitochondriale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
déficit en pyruvate carboxylase
n1=en:mmih syndrome | n2=déficit en pyruvate carboxylase | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
déformation congénitale
n1=en:mmih syndrome | n2=déformation congénitale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
démence fronto-temporale
n1=en:mmih syndrome | n2=démence fronto-temporale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
démence frontotemporale
n1=en:mmih syndrome | n2=démence frontotemporale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
dentine opalescente héréditaire
n1=en:mmih syndrome | n2=dentine opalescente héréditaire | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
dentinogénèse imparfaite
n1=en:mmih syndrome | n2=dentinogénèse imparfaite | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
DentinoGenesis Imperfecta
n1=en:mmih syndrome | n2=DentinoGenesis Imperfecta | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
dentinogenesis imperfecta
n1=en:mmih syndrome | n2=dentinogenesis imperfecta | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
détresse respiratoire
n1=en:mmih syndrome | n2=détresse respiratoire | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
dextrocardie
n1=en:mmih syndrome | n2=dextrocardie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
difformité congénitale
n1=en:mmih syndrome | n2=difformité congénitale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
distomatoses pulmonaires
n1=en:mmih syndrome | n2=distomatoses pulmonaires | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
Duane (syndrome de)
n1=en:mmih syndrome | n2=Duane (syndrome de) | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
dumping syndrome
n1=en:mmih syndrome | n2=dumping syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
dysérythropoïèse congénitale
n1=en:mmih syndrome | n2=dysérythropoïèse congénitale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
dysostose craniofaciale
n1=en:mmih syndrome | n2=dysostose craniofaciale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
dysostose enchondrale héréditaire
n1=en:mmih syndrome | n2=dysostose enchondrale héréditaire | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
dysplasie campomélique
n1=en:mmih syndrome | n2=dysplasie campomélique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
dysplasie cléido-crânienne
n1=en:mmih syndrome | n2=dysplasie cléido-crânienne | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
dysplasie cléidocrânienne
n1=en:mmih syndrome | n2=dysplasie cléidocrânienne | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
dysplasie ectodermique
n1=en:mmih syndrome | n2=dysplasie ectodermique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental
n1=en:mmih syndrome | n2=dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
dysplasie ectodermique, ectrodactylie et dystrophie maculaire
n1=en:mmih syndrome | n2=dysplasie ectodermique, ectrodactylie et dystrophie maculaire | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
dysplasie frontonasale
n1=en:mmih syndrome | n2=dysplasie frontonasale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
dystrophie neuro-axonale infantile
n1=en:mmih syndrome | n2=dystrophie neuro-axonale infantile | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
dystrophie neuroaxonale
n1=en:mmih syndrome | n2=dystrophie neuroaxonale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
dystrophie neuroaxonale de Seitelberger
n1=en:mmih syndrome | n2=dystrophie neuroaxonale de Seitelberger | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
dystrophie neuroaxonale infantile
n1=en:mmih syndrome | n2=dystrophie neuroaxonale infantile | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
dystrophie orbitaire congénitale
n1=en:mmih syndrome | n2=dystrophie orbitaire congénitale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
dystrophies neuroaxonales
n1=en:mmih syndrome | n2=dystrophies neuroaxonales | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie)
n1=en:mmih syndrome | n2=ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
ectrodactylie
n1=en:mmih syndrome | n2=ectrodactylie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:10p13-p14 deletion syndrome
n1=en:mmih syndrome | n2=en:10p13-p14 deletion syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:abstinence syndrome
n1=en:mmih syndrome | n2=en:abstinence syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:achard syndrome
n1=en:mmih syndrome | n2=en:achard syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:achondrogenesis
n1=en:mmih syndrome | n2=en:achondrogenesis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:acquired hyperostosis syndrome
n1=en:mmih syndrome | n2=en:acquired hyperostosis syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:acrodysostosis 1
n1=en:mmih syndrome | n2=en:acrodysostosis 1 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:acyl-coa dehydrogenase, short-chain deficiency
n1=en:mmih syndrome | n2=en:acyl-coa dehydrogenase, short-chain deficiency | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:adenocutanemucous syndrome
n1=en:mmih syndrome | n2=en:adenocutanemucous syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:adrenal cytomegaly
n1=en:mmih syndrome | n2=en:adrenal cytomegaly | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:agnosia
n1=en:mmih syndrome | n2=en:agnosia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:aids
n1=en:mmih syndrome | n2=en:aids | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:AIDS
n1=en:mmih syndrome | n2=en:AIDS | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:AIDS awareness
n1=en:mmih syndrome | n2=en:AIDS awareness | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:albinism
n1=en:mmih syndrome | n2=en:albinism | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:alice in wonderland syndrome
n1=en:mmih syndrome | n2=en:alice in wonderland syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Alice in Wonderland syndrome
n1=en:mmih syndrome | n2=en:Alice in Wonderland syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Alice in wonderland Syndrome
n1=en:mmih syndrome | n2=en:Alice in wonderland Syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:alligator skin
n1=en:mmih syndrome | n2=en:alligator skin | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:alveolar proteinosis
n1=en:mmih syndrome | n2=en:alveolar proteinosis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:amyoplasia congenita
n1=en:mmih syndrome | n2=en:amyoplasia congenita | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:anasarca
n1=en:mmih syndrome | n2=en:anasarca | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:and mental retardation
n1=en:mmih syndrome | n2=en:and mental retardation | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Angelman syndrome
n1=en:mmih syndrome | n2=en:Angelman syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:anterior plagiocephalies, synostotic
n1=en:mmih syndrome | n2=en:anterior plagiocephalies, synostotic | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:anti-AIDS
n1=en:mmih syndrome | n2=en:anti-AIDS | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:aortic arch syndrome
n1=en:mmih syndrome | n2=en:aortic arch syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:apl differentiation syndrome
n1=en:mmih syndrome | n2=en:apl differentiation syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:arachnodactily
n1=en:mmih syndrome | n2=en:arachnodactily | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:arachnodactyly
n1=en:mmih syndrome | n2=en:arachnodactyly | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:arakawa syndrome ii
n1=en:mmih syndrome | n2=en:arakawa syndrome ii | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:arnold chiari malformation
n1=en:mmih syndrome | n2=en:arnold chiari malformation | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:arnold-chiari deformity
n1=en:mmih syndrome | n2=en:arnold-chiari deformity | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:arrhythmogenic right ventricular dysplasia
n1=en:mmih syndrome | n2=en:arrhythmogenic right ventricular dysplasia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:ataxia-telangiectasisa-like disorder 1
n1=en:mmih syndrome | n2=en:ataxia-telangiectasisa-like disorder 1 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:atransferrinemia
n1=en:mmih syndrome | n2=en:atransferrinemia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:atypical hemolytic uremic syndrome
n1=en:mmih syndrome | n2=en:atypical hemolytic uremic syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:autoimmune polyendocrinopathy syndrome
n1=en:mmih syndrome | n2=en:autoimmune polyendocrinopathy syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:autoimmune polyglandular syndrome
n1=en:mmih syndrome | n2=en:autoimmune polyglandular syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:autosomal dominant congenital deafness with onychodystrophy
n1=en:mmih syndrome | n2=en:autosomal dominant congenital deafness with onychodystrophy | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:bernard-soulier syndrome
n1=en:mmih syndrome | n2=en:bernard-soulier syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:bile acid synthesis defect
n1=en:mmih syndrome | n2=en:bile acid synthesis defect | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:birth defect
n1=en:mmih syndrome | n2=en:birth defect | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:black death
n1=en:mmih syndrome | n2=en:black death | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Black death
n1=en:mmih syndrome | n2=en:Black death | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:black plague
n1=en:mmih syndrome | n2=en:black plague | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:brain iron accumulation type i syndrome
n1=en:mmih syndrome | n2=en:brain iron accumulation type i syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:branched-chain ketoaciduria
n1=en:mmih syndrome | n2=en:branched-chain ketoaciduria | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Caffey's disease
n1=en:mmih syndrome | n2=en:Caffey's disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:campomelic dwarfism
n1=en:mmih syndrome | n2=en:campomelic dwarfism | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:carbonic anhydrase i deficiency
n1=en:mmih syndrome | n2=en:carbonic anhydrase i deficiency | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:cardio-facio-cutaneous syndrome
n1=en:mmih syndrome | n2=en:cardio-facio-cutaneous syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:cardiofaciocutaneous syndrome
n1=en:mmih syndrome | n2=en:cardiofaciocutaneous syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:cat-eye syndrome
n1=en:mmih syndrome | n2=en:cat-eye syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:cataplexia
n1=en:mmih syndrome | n2=en:cataplexia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:cataplexis
n1=en:mmih syndrome | n2=en:cataplexis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:cerebral gigantism
n1=en:mmih syndrome | n2=en:cerebral gigantism | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:cerebral tuberculosis
n1=en:mmih syndrome | n2=en:cerebral tuberculosis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:charge syndrome
n1=en:mmih syndrome | n2=en:charge syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:child's sudden death
n1=en:mmih syndrome | n2=en:child's sudden death | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:chondrodysplasia punctata
n1=en:mmih syndrome | n2=en:chondrodysplasia punctata | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:chromosome 16p11.2 deletion syndrome
n1=en:mmih syndrome | n2=en:chromosome 16p11.2 deletion syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:chromosome 16p12.1 deletion syndrome
n1=en:mmih syndrome | n2=en:chromosome 16p12.1 deletion syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:chronic infantile neurological cutaneous and articular syndrome
n1=en:mmih syndrome | n2=en:chronic infantile neurological cutaneous and articular syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:classical maple syrup urine disease
n1=en:mmih syndrome | n2=en:classical maple syrup urine disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:codas syndrome
n1=en:mmih syndrome | n2=en:codas syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:coloboma and anal atresia syndrome
n1=en:mmih syndrome | n2=en:coloboma and anal atresia syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:combined lipase deficiency
n1=en:mmih syndrome | n2=en:combined lipase deficiency | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:complete trisomy 13 syndrome
n1=en:mmih syndrome | n2=en:complete trisomy 13 syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:complex regional pain syndrome ii
n1=en:mmih syndrome | n2=en:complex regional pain syndrome ii | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:congenital anomaly
n1=en:mmih syndrome | n2=en:congenital anomaly | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:congenital bilateral aplasia of the vas deferens
n1=en:mmih syndrome | n2=en:congenital bilateral aplasia of the vas deferens | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:congenital defect
n1=en:mmih syndrome | n2=en:congenital defect | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:congenital dyserythropoietic anemia
n1=en:mmih syndrome | n2=en:congenital dyserythropoietic anemia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:congenital malformation
n1=en:mmih syndrome | n2=en:congenital malformation | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:congenital porphyria
n1=en:mmih syndrome | n2=en:congenital porphyria | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:congenital stenosis of large intestine
n1=en:mmih syndrome | n2=en:congenital stenosis of large intestine | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:congenital ureterovesical junction obstruction
n1=en:mmih syndrome | n2=en:congenital ureterovesical junction obstruction | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:connexin 26 gene anomaly
n1=en:mmih syndrome | n2=en:connexin 26 gene anomaly | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:cor triatriatum
n1=en:mmih syndrome | n2=en:cor triatriatum | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:cortical dysplasia-focal epilepsy syndrome
n1=en:mmih syndrome | n2=en:cortical dysplasia-focal epilepsy syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:cot death
n1=en:mmih syndrome | n2=en:cot death | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:craniofacial dysostosis
n1=en:mmih syndrome | n2=en:craniofacial dysostosis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:cri du chat syndrome
n1=en:mmih syndrome | n2=en:cri du chat syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:crib death
n1=en:mmih syndrome | n2=en:crib death | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:cysticercosis
n1=en:mmih syndrome | n2=en:cysticercosis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:cysticercus disease
n1=en:mmih syndrome | n2=en:cysticercus disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:de toni-debre-fanconi syndrome
n1=en:mmih syndrome | n2=en:de toni-debre-fanconi syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:deafness, autosomal recessive 1a
n1=en:mmih syndrome | n2=en:deafness, autosomal recessive 1a | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:deafness, autosomal recessive 49
n1=en:mmih syndrome | n2=en:deafness, autosomal recessive 49 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Degos's syndrome
n1=en:mmih syndrome | n2=en:Degos's syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:delayed foetal renal development
n1=en:mmih syndrome | n2=en:delayed foetal renal development | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:deletion 18q syndrome
n1=en:mmih syndrome | n2=en:deletion 18q syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:dentinogenesis imperfecta
n1=en:mmih syndrome | n2=en:dentinogenesis imperfecta | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Dercum's disease
n1=en:mmih syndrome | n2=en:Dercum's disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:developmental fault
n1=en:mmih syndrome | n2=en:developmental fault | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Devergie's disease
n1=en:mmih syndrome | n2=en:Devergie's disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:didymosis aplasticosebacea
n1=en:mmih syndrome | n2=en:didymosis aplasticosebacea | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:dihydropyrimidine dehydrogenase deficiency
n1=en:mmih syndrome | n2=en:dihydropyrimidine dehydrogenase deficiency | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:disease aids
n1=en:mmih syndrome | n2=en:disease aids | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Diskinson's syndrome
n1=en:mmih syndrome | n2=en:Diskinson's syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:distal monosomy 10q syndrome
n1=en:mmih syndrome | n2=en:distal monosomy 10q syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:double cortex syndrome
n1=en:mmih syndrome | n2=en:double cortex syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Down syndrome
n1=en:mmih syndrome | n2=en:Down syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:dravet syndrome
n1=en:mmih syndrome | n2=en:dravet syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:drug hypersensitivity syndrome
n1=en:mmih syndrome | n2=en:drug hypersensitivity syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:duane syndrome
n1=en:mmih syndrome | n2=en:duane syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Duane's syndrome
n1=en:mmih syndrome | n2=en:Duane's syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Dubin-Sprinz disease
n1=en:mmih syndrome | n2=en:Dubin-Sprinz disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:dumping stomach
n1=en:mmih syndrome | n2=en:dumping stomach | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:dysequilibrium syndrome
n1=en:mmih syndrome | n2=en:dysequilibrium syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:ebstein anomaly
n1=en:mmih syndrome | n2=en:ebstein anomaly | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:eiken type chondrodysplasia
n1=en:mmih syndrome | n2=en:eiken type chondrodysplasia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:erythermalgia
n1=en:mmih syndrome | n2=en:erythermalgia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:erythropoietic porphyria
n1=en:mmih syndrome | n2=en:erythropoietic porphyria | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:erythropoietic uroporphyria
n1=en:mmih syndrome | n2=en:erythropoietic uroporphyria | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:escobar syndrome
n1=en:mmih syndrome | n2=en:escobar syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:exomphalos
n1=en:mmih syndrome | n2=en:exomphalos | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:familial atypical hemolytic uremic syndrome
n1=en:mmih syndrome | n2=en:familial atypical hemolytic uremic syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:familial hypertrophic cardiomyopathy
n1=en:mmih syndrome | n2=en:familial hypertrophic cardiomyopathy | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:farber lipogranulomatosis
n1=en:mmih syndrome | n2=en:farber lipogranulomatosis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:ferro-cerebro-cutaneous syndrome
n1=en:mmih syndrome | n2=en:ferro-cerebro-cutaneous syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:fetal hydantoin syndrome
n1=en:mmih syndrome | n2=en:fetal hydantoin syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:fetal megacystis
n1=en:mmih syndrome | n2=en:fetal megacystis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:fetal retinoid syndrome
n1=en:mmih syndrome | n2=en:fetal retinoid syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:fibrodysplasia ossificans progressiva
n1=en:mmih syndrome | n2=en:fibrodysplasia ossificans progressiva | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:fish skin disease
n1=en:mmih syndrome | n2=en:fish skin disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:fragile X syndrome
n1=en:mmih syndrome | n2=en:fragile X syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:fragile x tremor/ataxia syndrome
n1=en:mmih syndrome | n2=en:fragile x tremor/ataxia syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:frohlich syndrome
n1=en:mmih syndrome | n2=en:frohlich syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:frontonasal dysplasia
n1=en:mmih syndrome | n2=en:frontonasal dysplasia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:gangrenous stomatitis
n1=en:mmih syndrome | n2=en:gangrenous stomatitis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:gargoylism
n1=en:mmih syndrome | n2=en:gargoylism | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:generalized arterial calcification of infancy 1
n1=en:mmih syndrome | n2=en:generalized arterial calcification of infancy 1 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:genetic condition
n1=en:mmih syndrome | n2=en:genetic condition | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:genetic disease
n1=en:mmih syndrome | n2=en:genetic disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:genetic illness
n1=en:mmih syndrome | n2=en:genetic illness | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:gigantism and hyperplastic visceromegaly
n1=en:mmih syndrome | n2=en:gigantism and hyperplastic visceromegaly | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:glanzmann thrombasthenia
n1=en:mmih syndrome | n2=en:glanzmann thrombasthenia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:glucose-6-phosphate dehydrogenase deficiency
n1=en:mmih syndrome | n2=en:glucose-6-phosphate dehydrogenase deficiency | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:glutaric acidemia type 1
n1=en:mmih syndrome | n2=en:glutaric acidemia type 1 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:glutaric aciduria type 1
n1=en:mmih syndrome | n2=en:glutaric aciduria type 1 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:glutaric aciduria, type 1
n1=en:mmih syndrome | n2=en:glutaric aciduria, type 1 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:glycogen storage disease
n1=en:mmih syndrome | n2=en:glycogen storage disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Goltz syndrome
n1=en:mmih syndrome | n2=en:Goltz syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:gray baby syndrome
n1=en:mmih syndrome | n2=en:gray baby syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:gray platelet syndrome
n1=en:mmih syndrome | n2=en:gray platelet syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Gray platelet syndrome
n1=en:mmih syndrome | n2=en:Gray platelet syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:greig syndrome
n1=en:mmih syndrome | n2=en:greig syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:griscelli syndrome type 2
n1=en:mmih syndrome | n2=en:griscelli syndrome type 2 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Guillain-Barre syndrome
n1=en:mmih syndrome | n2=en:Guillain-Barre syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:guillain-barre syndrome
n1=en:mmih syndrome | n2=en:guillain-barre syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:hallermann syndrome
n1=en:mmih syndrome | n2=en:hallermann syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:hansenarium
n1=en:mmih syndrome | n2=en:hansenarium | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:hantavirus pulmonary syndrome
n1=en:mmih syndrome | n2=en:hantavirus pulmonary syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:hard skin syndrome parana type
n1=en:mmih syndrome | n2=en:hard skin syndrome parana type | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:hartnup disease
n1=en:mmih syndrome | n2=en:hartnup disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:hematomphalus
n1=en:mmih syndrome | n2=en:hematomphalus | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:hereditary coproporphyria
n1=en:mmih syndrome | n2=en:hereditary coproporphyria | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:hereditary disease
n1=en:mmih syndrome | n2=en:hereditary disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:hereditary hyperbilirubinemia
n1=en:mmih syndrome | n2=en:hereditary hyperbilirubinemia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:hereditary persistence of fetal hemoglobin
n1=en:mmih syndrome | n2=en:hereditary persistence of fetal hemoglobin | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:heritable pulmonary arterial hypertension
n1=en:mmih syndrome | n2=en:heritable pulmonary arterial hypertension | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:hermansky-pudlak syndrome
n1=en:mmih syndrome | n2=en:hermansky-pudlak syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:heterotaxy syndrome
n1=en:mmih syndrome | n2=en:heterotaxy syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:heterotaxy syndrome with asplenia
n1=en:mmih syndrome | n2=en:heterotaxy syndrome with asplenia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:high molecular weight kininogen deficiency
n1=en:mmih syndrome | n2=en:high molecular weight kininogen deficiency | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:holmes-adie syndrome
n1=en:mmih syndrome | n2=en:holmes-adie syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:holocarboxylase synthetase deficiency
n1=en:mmih syndrome | n2=en:holocarboxylase synthetase deficiency | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:holoprosencephaly
n1=en:mmih syndrome | n2=en:holoprosencephaly | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:horner syndrome
n1=en:mmih syndrome | n2=en:horner syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:hurler syndrome
n1=en:mmih syndrome | n2=en:hurler syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Hurler syndrome
n1=en:mmih syndrome | n2=en:Hurler syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Hurler's disease
n1=en:mmih syndrome | n2=en:Hurler's disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Hurler's syndome
n1=en:mmih syndrome | n2=en:Hurler's syndome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:hyaline membrane syndrome
n1=en:mmih syndrome | n2=en:hyaline membrane syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:hydrops fetalis
n1=en:mmih syndrome | n2=en:hydrops fetalis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:hydrops foetalis
n1=en:mmih syndrome | n2=en:hydrops foetalis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:hymenolepiasis
n1=en:mmih syndrome | n2=en:hymenolepiasis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:hyperpipecolatemia
n1=en:mmih syndrome | n2=en:hyperpipecolatemia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:hypohidrotic ectodermal dysplasia with immune deficiency
n1=en:mmih syndrome | n2=en:hypohidrotic ectodermal dysplasia with immune deficiency | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:hypopituitarism
n1=en:mmih syndrome | n2=en:hypopituitarism | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:hypoxaemia
n1=en:mmih syndrome | n2=en:hypoxaemia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:ichthyosis
n1=en:mmih syndrome | n2=en:ichthyosis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:idiopathic hypersomnolence
n1=en:mmih syndrome | n2=en:idiopathic hypersomnolence | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:immune deficiency syndrome
n1=en:mmih syndrome | n2=en:immune deficiency syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:immunodeficiency with hyper-igm type 2
n1=en:mmih syndrome | n2=en:immunodeficiency with hyper-igm type 2 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:infantile convulsions and paroxysmal choreoathetosis, familial
n1=en:mmih syndrome | n2=en:infantile convulsions and paroxysmal choreoathetosis, familial | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:infantile neuroaxonal dystrophy
n1=en:mmih syndrome | n2=en:infantile neuroaxonal dystrophy | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:inspissated bile syndrome
n1=en:mmih syndrome | n2=en:inspissated bile syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:insufficient breast milk syndrome
n1=en:mmih syndrome | n2=en:insufficient breast milk syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:insulin receptor mutation - associated insulin resistance syndromes
n1=en:mmih syndrome | n2=en:insulin receptor mutation - associated insulin resistance syndromes | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:intestinal pseudo-obstruction
n1=en:mmih syndrome | n2=en:intestinal pseudo-obstruction | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:jacobsen syndrome
n1=en:mmih syndrome | n2=en:jacobsen syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:juvenile x-linked retinoschisis
n1=en:mmih syndrome | n2=en:juvenile x-linked retinoschisis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Kawasaki disease
n1=en:mmih syndrome | n2=en:Kawasaki disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:kawasaki disease
n1=en:mmih syndrome | n2=en:kawasaki disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Kawasaki's syndrome
n1=en:mmih syndrome | n2=en:Kawasaki's syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:kenny-caffey syndrome type 2
n1=en:mmih syndrome | n2=en:kenny-caffey syndrome type 2 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:kimura disease
n1=en:mmih syndrome | n2=en:kimura disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Klinefelter syndrome
n1=en:mmih syndrome | n2=en:Klinefelter syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Korsakoff syndrome
n1=en:mmih syndrome | n2=en:Korsakoff syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:korsakoff syndrome
n1=en:mmih syndrome | n2=en:korsakoff syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:kshv inflammatory cytokine syndrome
n1=en:mmih syndrome | n2=en:kshv inflammatory cytokine syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:lazar-house
n1=en:mmih syndrome | n2=en:lazar-house | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:leper colony
n1=en:mmih syndrome | n2=en:leper colony | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:leprosary
n1=en:mmih syndrome | n2=en:leprosary | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:leprosy
n1=en:mmih syndrome | n2=en:leprosy | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:leriche syndrome
n1=en:mmih syndrome | n2=en:leriche syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:lethal multiple pterygium syndrome
n1=en:mmih syndrome | n2=en:lethal multiple pterygium syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:lethal neonatal rigidity and multifocal seizure syndrome
n1=en:mmih syndrome | n2=en:lethal neonatal rigidity and multifocal seizure syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:leucinosis
n1=en:mmih syndrome | n2=en:leucinosis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:levocardia
n1=en:mmih syndrome | n2=en:levocardia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:lig4 syndrome
n1=en:mmih syndrome | n2=en:lig4 syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:lipase hypersecretion syndrome
n1=en:mmih syndrome | n2=en:lipase hypersecretion syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:lissencephaly
n1=en:mmih syndrome | n2=en:lissencephaly | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
n1=en:mmih syndrome | n2=en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:lupus anticoagulant disorder
n1=en:mmih syndrome | n2=en:lupus anticoagulant disorder | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:macroglossia
n1=en:mmih syndrome | n2=en:macroglossia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:macrophage activation syndrome
n1=en:mmih syndrome | n2=en:macrophage activation syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:major physical defect
n1=en:mmih syndrome | n2=en:major physical defect | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:malabsorption syndrome
n1=en:mmih syndrome | n2=en:malabsorption syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:malignant atrophic papulosis
n1=en:mmih syndrome | n2=en:malignant atrophic papulosis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:malignant hyperthermia syndrome
n1=en:mmih syndrome | n2=en:malignant hyperthermia syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:mallory-weiss syndrome
n1=en:mmih syndrome | n2=en:mallory-weiss syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:maple-tree syrup disease
n1=en:mmih syndrome | n2=en:maple-tree syrup disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:marburg virus disease
n1=en:mmih syndrome | n2=en:marburg virus disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Marfan's disease
n1=en:mmih syndrome | n2=en:Marfan's disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:marfan's syndrome
n1=en:mmih syndrome | n2=en:marfan's syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Marfan's syndrome
n1=en:mmih syndrome | n2=en:Marfan's syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:marshall syndrome
n1=en:mmih syndrome | n2=en:marshall syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:maternal diabetes and deafness syndrome
n1=en:mmih syndrome | n2=en:maternal diabetes and deafness syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:maternal uniparental disomy chromosome 14 syndrome
n1=en:mmih syndrome | n2=en:maternal uniparental disomy chromosome 14 syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:meckel-gruber syndrome
n1=en:mmih syndrome | n2=en:meckel-gruber syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:meconium aspiration syndrome
n1=en:mmih syndrome | n2=en:meconium aspiration syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:meconium plug syndrome
n1=en:mmih syndrome | n2=en:meconium plug syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:meesmann corneal dystrophy
n1=en:mmih syndrome | n2=en:meesmann corneal dystrophy | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:meningeal tuberculosis
n1=en:mmih syndrome | n2=en:meningeal tuberculosis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:mental retardation, autosomal dominant 9
n1=en:mmih syndrome | n2=en:mental retardation, autosomal dominant 9 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:mental retardation, autosomal recessive 34
n1=en:mmih syndrome | n2=en:mental retardation, autosomal recessive 34 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome
n1=en:mmih syndrome | n2=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:metabolic syndrome
n1=en:mmih syndrome | n2=en:metabolic syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:miller-dieker syndrome
n1=en:mmih syndrome | n2=en:miller-dieker syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:mitochondrial dna depletion syndrome 12
n1=en:mmih syndrome | n2=en:mitochondrial dna depletion syndrome 12 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:mitochondrial neurogastrointestingal encephalopathy
n1=en:mmih syndrome | n2=en:mitochondrial neurogastrointestingal encephalopathy | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:mucocutaneous lymph node syndrome
n1=en:mmih syndrome | n2=en:mucocutaneous lymph node syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:mucolipidosis type iii gamma
n1=en:mmih syndrome | n2=en:mucolipidosis type iii gamma | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:mullerian inhibiting factor deficiency
n1=en:mmih syndrome | n2=en:mullerian inhibiting factor deficiency | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:mullerian-renal-cervical spine syndrome
n1=en:mmih syndrome | n2=en:mullerian-renal-cervical spine syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:multicentric osteolysis, nodulosis, and arthropathy
n1=en:mmih syndrome | n2=en:multicentric osteolysis, nodulosis, and arthropathy | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:multiple acyl-coa dehydrogenase deficiency
n1=en:mmih syndrome | n2=en:multiple acyl-coa dehydrogenase deficiency | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:multiple vascular disruption syndrome
n1=en:mmih syndrome | n2=en:multiple vascular disruption syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies)
n1=en:mmih syndrome | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:myhre syndrome
n1=en:mmih syndrome | n2=en:myhre syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:myitis
n1=en:mmih syndrome | n2=en:myitis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:myokymia
n1=en:mmih syndrome | n2=en:myokymia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:nelson syndrome
n1=en:mmih syndrome | n2=en:nelson syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:neurocysticercosis
n1=en:mmih syndrome | n2=en:neurocysticercosis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:neurological cysticercosis
n1=en:mmih syndrome | n2=en:neurological cysticercosis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:neuronal intranuclear inclusion disease
n1=en:mmih syndrome | n2=en:neuronal intranuclear inclusion disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:neuropathy, hereditary sensory and autonomic, type vii
n1=en:mmih syndrome | n2=en:neuropathy, hereditary sensory and autonomic, type vii | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:neurotoxicity syndrome
n1=en:mmih syndrome | n2=en:neurotoxicity syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:noma
n1=en:mmih syndrome | n2=en:noma | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:non-trisomic autosomal aneuploidy
n1=en:mmih syndrome | n2=en:non-trisomic autosomal aneuploidy | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:nystagmus
n1=en:mmih syndrome | n2=en:nystagmus | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:obstructive sleep apnea syndrome
n1=en:mmih syndrome | n2=en:obstructive sleep apnea syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:oculo-respiratory syndrome
n1=en:mmih syndrome | n2=en:oculo-respiratory syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:oculorespiratory syndrome
n1=en:mmih syndrome | n2=en:oculorespiratory syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:odontogenesis imperfecta
n1=en:mmih syndrome | n2=en:odontogenesis imperfecta | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:oeis complex
n1=en:mmih syndrome | n2=en:oeis complex | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:ombilical hernia
n1=en:mmih syndrome | n2=en:ombilical hernia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:onychoosteodysostosis
n1=en:mmih syndrome | n2=en:onychoosteodysostosis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:ophthalmoneuritis
n1=en:mmih syndrome | n2=en:ophthalmoneuritis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:opitz g/bbb syndrome
n1=en:mmih syndrome | n2=en:opitz g/bbb syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:optic neuritis
n1=en:mmih syndrome | n2=en:optic neuritis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:orofacial cleft 1
n1=en:mmih syndrome | n2=en:orofacial cleft 1 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:orofaciodigital syndrome type 6
n1=en:mmih syndrome | n2=en:orofaciodigital syndrome type 6 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:osteopetrosis with renal tubular acidosis
n1=en:mmih syndrome | n2=en:osteopetrosis with renal tubular acidosis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:osteopoecilia
n1=en:mmih syndrome | n2=en:osteopoecilia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:osteopoikilosis
n1=en:mmih syndrome | n2=en:osteopoikilosis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:overgrowth syndrome
n1=en:mmih syndrome | n2=en:overgrowth syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:pachyonychia congenita
n1=en:mmih syndrome | n2=en:pachyonychia congenita | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:pain agnosia
n1=en:mmih syndrome | n2=en:pain agnosia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:palmar-plantar erythodysthesia
n1=en:mmih syndrome | n2=en:palmar-plantar erythodysthesia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:panuveitis
n1=en:mmih syndrome | n2=en:panuveitis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:paragonimiasis
n1=en:mmih syndrome | n2=en:paragonimiasis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:pearson marrow-pancreas syndrome
n1=en:mmih syndrome | n2=en:pearson marrow-pancreas syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:pena-shokeir syndrome
n1=en:mmih syndrome | n2=en:pena-shokeir syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:penta x syndrome
n1=en:mmih syndrome | n2=en:penta x syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:pentalogy of cantrell
n1=en:mmih syndrome | n2=en:pentalogy of cantrell | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:periodic fever syndrome
n1=en:mmih syndrome | n2=en:periodic fever syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:peritoneal panniculitis
n1=en:mmih syndrome | n2=en:peritoneal panniculitis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:persistent fetal circulation
n1=en:mmih syndrome | n2=en:persistent fetal circulation | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:perthes disease
n1=en:mmih syndrome | n2=en:perthes disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:pettigrew syndrome
n1=en:mmih syndrome | n2=en:pettigrew syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:physical defect
n1=en:mmih syndrome | n2=en:physical defect | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Pick's disease
n1=en:mmih syndrome | n2=en:Pick's disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:pick's disease
n1=en:mmih syndrome | n2=en:pick's disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:pierre robin syndrome
n1=en:mmih syndrome | n2=en:pierre robin syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:pityriasis rubra pilaris
n1=en:mmih syndrome | n2=en:pityriasis rubra pilaris | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:plasma kallikrein deficiency
n1=en:mmih syndrome | n2=en:plasma kallikrein deficiency | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:plummer-vinson syndrome
n1=en:mmih syndrome | n2=en:plummer-vinson syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Plummer-Vinson syndrome
n1=en:mmih syndrome | n2=en:Plummer-Vinson syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:porphyria cutanea tarda
n1=en:mmih syndrome | n2=en:porphyria cutanea tarda | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:potocki-shaffer syndrome
n1=en:mmih syndrome | n2=en:potocki-shaffer syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:potter syndrome
n1=en:mmih syndrome | n2=en:potter syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Prader-Willi syndrome
n1=en:mmih syndrome | n2=en:Prader-Willi syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:primary carnitine deficiency
n1=en:mmih syndrome | n2=en:primary carnitine deficiency | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:primary progressive aphasia
n1=en:mmih syndrome | n2=en:primary progressive aphasia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:progeria
n1=en:mmih syndrome | n2=en:progeria | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:progressive bulbar palsy
n1=en:mmih syndrome | n2=en:progressive bulbar palsy | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:progressive supranuclear palsy
n1=en:mmih syndrome | n2=en:progressive supranuclear palsy | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:pulmonary alveolar proteinosis
n1=en:mmih syndrome | n2=en:pulmonary alveolar proteinosis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:pulmonary shunting
n1=en:mmih syndrome | n2=en:pulmonary shunting | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:pyramidal tract dysfunction
n1=en:mmih syndrome | n2=en:pyramidal tract dysfunction | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:pyruvate dehydrogenase deficiency
n1=en:mmih syndrome | n2=en:pyruvate dehydrogenase deficiency | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:respiratory distress
n1=en:mmih syndrome | n2=en:respiratory distress | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:reversible posterior leukoencephalopathy syndrome
n1=en:mmih syndrome | n2=en:reversible posterior leukoencephalopathy syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:rhizomelic dysplasia
n1=en:mmih syndrome | n2=en:rhizomelic dysplasia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:rieger syndrome type 1
n1=en:mmih syndrome | n2=en:rieger syndrome type 1 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:roberts syndrome
n1=en:mmih syndrome | n2=en:roberts syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:russell-silver syndrome
n1=en:mmih syndrome | n2=en:russell-silver syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:sacral agenesis
n1=en:mmih syndrome | n2=en:sacral agenesis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:sarcitis
n1=en:mmih syndrome | n2=en:sarcitis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:scheie syndrome
n1=en:mmih syndrome | n2=en:scheie syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:schinzel-giedion midface-retraction syndrome
n1=en:mmih syndrome | n2=en:schinzel-giedion midface-retraction syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:schock lung
n1=en:mmih syndrome | n2=en:schock lung | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:schwartz-jampel syndrome
n1=en:mmih syndrome | n2=en:schwartz-jampel syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:scleromyxedema
n1=en:mmih syndrome | n2=en:scleromyxedema | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:segmented intestine
n1=en:mmih syndrome | n2=en:segmented intestine | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Seitelberger's disease
n1=en:mmih syndrome | n2=en:Seitelberger's disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:selective antibody deficiency with normal immunoglobulins
n1=en:mmih syndrome | n2=en:selective antibody deficiency with normal immunoglobulins | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:septo-optic dysplasia
n1=en:mmih syndrome | n2=en:septo-optic dysplasia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Sheehan's syndrome
n1=en:mmih syndrome | n2=en:Sheehan's syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:short bowel syndrome
n1=en:mmih syndrome | n2=en:short bowel syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:short rib-polydactyly syndrome
n1=en:mmih syndrome | n2=en:short rib-polydactyly syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:short stature homeobox deficiency
n1=en:mmih syndrome | n2=en:short stature homeobox deficiency | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:shprintzen-goldberg craniosynostosis syndrome
n1=en:mmih syndrome | n2=en:shprintzen-goldberg craniosynostosis syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:shy-drager syndrome
n1=en:mmih syndrome | n2=en:shy-drager syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:sicca syndrome
n1=en:mmih syndrome | n2=en:sicca syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:sick euthyroid syndrome
n1=en:mmih syndrome | n2=en:sick euthyroid syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:SIDS
n1=en:mmih syndrome | n2=en:SIDS | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:sids
n1=en:mmih syndrome | n2=en:sids | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:single central incisor syndrome
n1=en:mmih syndrome | n2=en:single central incisor syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:situs inversus
n1=en:mmih syndrome | n2=en:situs inversus | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:situs inversus viscerum
n1=en:mmih syndrome | n2=en:situs inversus viscerum | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:situs mutatus
n1=en:mmih syndrome | n2=en:situs mutatus | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:sjogren-larsson syndrome
n1=en:mmih syndrome | n2=en:sjogren-larsson syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:somnolence syndrome
n1=en:mmih syndrome | n2=en:somnolence syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Soto's syndrome
n1=en:mmih syndrome | n2=en:Soto's syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Sotos' syndrome
n1=en:mmih syndrome | n2=en:Sotos' syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:sotos' syndrome
n1=en:mmih syndrome | n2=en:sotos' syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:spondyloepimetaphyseal dysplasia with joint laxity type 2
n1=en:mmih syndrome | n2=en:spondyloepimetaphyseal dysplasia with joint laxity type 2 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:stargardt disease
n1=en:mmih syndrome | n2=en:stargardt disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Stargardt disease
n1=en:mmih syndrome | n2=en:Stargardt disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Stevens-Johnson syndrome
n1=en:mmih syndrome | n2=en:Stevens-Johnson syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Stokes-Adams syndrome
n1=en:mmih syndrome | n2=en:Stokes-Adams syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:stokes-adams syndrome
n1=en:mmih syndrome | n2=en:stokes-adams syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:subacute sclerosing panencephalitis
n1=en:mmih syndrome | n2=en:subacute sclerosing panencephalitis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:sudden infant death
n1=en:mmih syndrome | n2=en:sudden infant death | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:sudden unexplained death in childhood
n1=en:mmih syndrome | n2=en:sudden unexplained death in childhood | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:sudden unexplained infant death
n1=en:mmih syndrome | n2=en:sudden unexplained infant death | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:sunset syndrome
n1=en:mmih syndrome | n2=en:sunset syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:superior mesenteric artery syndrome
n1=en:mmih syndrome | n2=en:superior mesenteric artery syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:surfactant protein deficiency
n1=en:mmih syndrome | n2=en:surfactant protein deficiency | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:systemic inflammatory response syndrome
n1=en:mmih syndrome | n2=en:systemic inflammatory response syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:takotsubo cardiomyopathy
n1=en:mmih syndrome | n2=en:takotsubo cardiomyopathy | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Tay-Sachs disease
n1=en:mmih syndrome | n2=en:Tay-Sachs disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:tempi syndrome
n1=en:mmih syndrome | n2=en:tempi syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:teratosis
n1=en:mmih syndrome | n2=en:teratosis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:thiamin-responsive maple syrup urine disease
n1=en:mmih syndrome | n2=en:thiamin-responsive maple syrup urine disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:thrombocytopenia 2
n1=en:mmih syndrome | n2=en:thrombocytopenia 2 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:thyroid dysgenesis
n1=en:mmih syndrome | n2=en:thyroid dysgenesis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:thyroid hormone resistance syndrome
n1=en:mmih syndrome | n2=en:thyroid hormone resistance syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:tissue kallikrein deficiency
n1=en:mmih syndrome | n2=en:tissue kallikrein deficiency | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:togaviridae infection
n1=en:mmih syndrome | n2=en:togaviridae infection | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:tolosa-hunt syndrome
n1=en:mmih syndrome | n2=en:tolosa-hunt syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:torch syndrome
n1=en:mmih syndrome | n2=en:torch syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Townes-Brocks syndrome
n1=en:mmih syndrome | n2=en:Townes-Brocks syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:townes-brocks syndrome
n1=en:mmih syndrome | n2=en:townes-brocks syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Toxic Shock Syndrome
n1=en:mmih syndrome | n2=en:Toxic Shock Syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:tracheobronchomegaly
n1=en:mmih syndrome | n2=en:tracheobronchomegaly | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:trichorhinophalangeal syndrome type ii
n1=en:mmih syndrome | n2=en:trichorhinophalangeal syndrome type ii | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:trichorhinophalangeal syndrome type II
n1=en:mmih syndrome | n2=en:trichorhinophalangeal syndrome type II | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:trichothiodystrophy
n1=en:mmih syndrome | n2=en:trichothiodystrophy | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:triple a syndrome
n1=en:mmih syndrome | n2=en:triple a syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Triple a syndrome
n1=en:mmih syndrome | n2=en:Triple a syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:triploidy syndrome
n1=en:mmih syndrome | n2=en:triploidy syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:trisomy 14 mosaicism
n1=en:mmih syndrome | n2=en:trisomy 14 mosaicism | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:tuberculosis of meninges (cerebral)(spinal)
n1=en:mmih syndrome | n2=en:tuberculosis of meninges (cerebral)(spinal) | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:tuberculosis, meningeal
n1=en:mmih syndrome | n2=en:tuberculosis, meningeal | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:tuberculous hypertrophic pachymeningitides
n1=en:mmih syndrome | n2=en:tuberculous hypertrophic pachymeningitides | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:tuberculous leptomeningitis
n1=en:mmih syndrome | n2=en:tuberculous leptomeningitis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:tuberculous meningitis
n1=en:mmih syndrome | n2=en:tuberculous meningitis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:tubulointerstitial nephritis and uveitis
n1=en:mmih syndrome | n2=en:tubulointerstitial nephritis and uveitis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:twiddler's syndrome
n1=en:mmih syndrome | n2=en:twiddler's syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:type a 14
n1=en:mmih syndrome | n2=en:type a 14 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Umbilical hernia
n1=en:mmih syndrome | n2=en:Umbilical hernia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:umbilical hernia
n1=en:mmih syndrome | n2=en:umbilical hernia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:urea cycle metabolism disorder
n1=en:mmih syndrome | n2=en:urea cycle metabolism disorder | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:variegate porphyria
n1=en:mmih syndrome | n2=en:variegate porphyria | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:visceral myopathy
n1=en:mmih syndrome | n2=en:visceral myopathy | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:wallerian degeneration
n1=en:mmih syndrome | n2=en:wallerian degeneration | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:waterhouse-friderichsen syndrome
n1=en:mmih syndrome | n2=en:waterhouse-friderichsen syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:wegener granulomatosis
n1=en:mmih syndrome | n2=en:wegener granulomatosis | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:whipple disease
n1=en:mmih syndrome | n2=en:whipple disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Whipple disease
n1=en:mmih syndrome | n2=en:Whipple disease | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Williams syndrome
n1=en:mmih syndrome | n2=en:Williams syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:williams syndrome
n1=en:mmih syndrome | n2=en:williams syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:wilms tumor 1 gene syndromes
n1=en:mmih syndrome | n2=en:wilms tumor 1 gene syndromes | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:x-linked dominant hypophosphatemic rickets
n1=en:mmih syndrome | n2=en:x-linked dominant hypophosphatemic rickets | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:xerophtalmy
n1=en:mmih syndrome | n2=en:xerophtalmy | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:xxxy and xxxxy syndrome
n1=en:mmih syndrome | n2=en:xxxy and xxxxy syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:yellow nail syndrome
n1=en:mmih syndrome | n2=en:yellow nail syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
en:Zellweger syndrome
n1=en:mmih syndrome | n2=en:Zellweger syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
érythermalgie
n1=en:mmih syndrome | n2=érythermalgie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
erythromelalgia
n1=en:mmih syndrome | n2=erythromelalgia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
érythromélalgie
n1=en:mmih syndrome | n2=érythromélalgie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
examen non précisé, méningite tuberculeuse
n1=en:mmih syndrome | n2=examen non précisé, méningite tuberculeuse | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
exomphale
n1=en:mmih syndrome | n2=exomphale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
exomphale congénitale
n1=en:mmih syndrome | n2=exomphale congénitale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
exstrophie cloacale
n1=en:mmih syndrome | n2=exstrophie cloacale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
fibromyalgie
n1=en:mmih syndrome | n2=fibromyalgie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
gigantisme cérébral
n1=en:mmih syndrome | n2=gigantisme cérébral | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
glycogénose
n1=en:mmih syndrome | n2=glycogénose | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
Goltz
n1=en:mmih syndrome | n2=Goltz | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale
n1=en:mmih syndrome | n2=hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
hernie ombilicale
n1=en:mmih syndrome | n2=hernie ombilicale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
hernie ombilicale congénitale
n1=en:mmih syndrome | n2=hernie ombilicale congénitale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
hernies ombilicales
n1=en:mmih syndrome | n2=hernies ombilicales | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
hétérotaxie
n1=en:mmih syndrome | n2=hétérotaxie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
holoprosencéphalie
n1=en:mmih syndrome | n2=holoprosencéphalie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
holoprosencéphalie de type 2
n1=en:mmih syndrome | n2=holoprosencéphalie de type 2 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
holoprosencéphalie de type 3
n1=en:mmih syndrome | n2=holoprosencéphalie de type 3 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
holoprosencéphalie de type 4
n1=en:mmih syndrome | n2=holoprosencéphalie de type 4 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
holoprosencéphalie familiale alobaire de type 1
n1=en:mmih syndrome | n2=holoprosencéphalie familiale alobaire de type 1 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
hydrops foetoplacentaire
n1=en:mmih syndrome | n2=hydrops foetoplacentaire | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
hypertrophie staturale avec macroglossie et omphalocèle
n1=en:mmih syndrome | n2=hypertrophie staturale avec macroglossie et omphalocèle | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
hypoplasie dermique en aires
n1=en:mmih syndrome | n2=hypoplasie dermique en aires | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
hypoplasie dermique focale
n1=en:mmih syndrome | n2=hypoplasie dermique focale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
hypoxémie
n1=en:mmih syndrome | n2=hypoxémie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
ichthyose
n1=en:mmih syndrome | n2=ichthyose | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
ichtyose
n1=en:mmih syndrome | n2=ichtyose | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
ichtyose folliculaire, atrichie et photophobie
n1=en:mmih syndrome | n2=ichtyose folliculaire, atrichie et photophobie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
ichtyose, affection neurologique spastique, et oligophrénie
n1=en:mmih syndrome | n2=ichtyose, affection neurologique spastique, et oligophrénie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
ictère nucléaire
n1=en:mmih syndrome | n2=ictère nucléaire | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
idiotie spastique amaurotique axonale
n1=en:mmih syndrome | n2=idiotie spastique amaurotique axonale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
imperforation anale
n1=en:mmih syndrome | n2=imperforation anale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
imperforation de l'anus
n1=en:mmih syndrome | n2=imperforation de l'anus | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
inflammation musculaire
n1=en:mmih syndrome | n2=inflammation musculaire | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
insensibilité congénitale à la douleur de type III
n1=en:mmih syndrome | n2=insensibilité congénitale à la douleur de type III | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
insuffisance pulmonaire post-traumatique
n1=en:mmih syndrome | n2=insuffisance pulmonaire post-traumatique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
insuffisance respiratoire, problème respiratoire
n1=en:mmih syndrome | n2=insuffisance respiratoire, problème respiratoire | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
intolérance au fructose
n1=en:mmih syndrome | n2=intolérance au fructose | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
lèpre
n1=en:mmih syndrome | n2=lèpre | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
léproserie
n1=en:mmih syndrome | n2=léproserie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
leprosy
n1=en:mmih syndrome | n2=leprosy | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
leptoméningite tuberculeuse
n1=en:mmih syndrome | n2=leptoméningite tuberculeuse | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
leucinose
n1=en:mmih syndrome | n2=leucinose | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
lévocardie
n1=en:mmih syndrome | n2=lévocardie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
lipodystrophie partielle familiale
n1=en:mmih syndrome | n2=lipodystrophie partielle familiale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
lissencéphalie
n1=en:mmih syndrome | n2=lissencéphalie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
macroglossie
n1=en:mmih syndrome | n2=macroglossie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie à virus de Marburg
n1=en:mmih syndrome | n2=maladie à virus de Marburg | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie congénitale
n1=en:mmih syndrome | n2=maladie congénitale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
Maladie congénitale
n1=en:mmih syndrome | n2=Maladie congénitale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie de Caffey
n1=en:mmih syndrome | n2=maladie de Caffey | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie de Dercum
n1=en:mmih syndrome | n2=maladie de Dercum | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie de dercum
n1=en:mmih syndrome | n2=maladie de dercum | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie de dubin-johnson
n1=en:mmih syndrome | n2=maladie de dubin-johnson | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie de hurler
n1=en:mmih syndrome | n2=maladie de hurler | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie de Hurler
n1=en:mmih syndrome | n2=maladie de Hurler | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie de Kawasaki
n1=en:mmih syndrome | n2=maladie de Kawasaki | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie de marfan
n1=en:mmih syndrome | n2=maladie de marfan | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie de Perthes
n1=en:mmih syndrome | n2=maladie de Perthes | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie de Seitelberger
n1=en:mmih syndrome | n2=maladie de Seitelberger | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie de seitelberger
n1=en:mmih syndrome | n2=maladie de seitelberger | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie de Tay-Sachs
n1=en:mmih syndrome | n2=maladie de Tay-Sachs | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie de tay-sachs
n1=en:mmih syndrome | n2=maladie de tay-sachs | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie de Tay-sachs
n1=en:mmih syndrome | n2=maladie de Tay-sachs | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
Maladie de Whipple
n1=en:mmih syndrome | n2=Maladie de Whipple | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie de whipple
n1=en:mmih syndrome | n2=maladie de whipple | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie de Whipple
n1=en:mmih syndrome | n2=maladie de Whipple | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie des épiphyses ponctuées
n1=en:mmih syndrome | n2=maladie des épiphyses ponctuées | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie des urines à l'odeur de sirop d'érable
n1=en:mmih syndrome | n2=maladie des urines à l'odeur de sirop d'érable | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie des urines avec odeur de sirop erable
n1=en:mmih syndrome | n2=maladie des urines avec odeur de sirop erable | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie du cri du chat
n1=en:mmih syndrome | n2=maladie du cri du chat | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie du sirop d'érable
n1=en:mmih syndrome | n2=maladie du sirop d'érable | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladie lysosomique de surcharge
n1=en:mmih syndrome | n2=maladie lysosomique de surcharge | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
maladies des bandes amniotiques
n1=en:mmih syndrome | n2=maladies des bandes amniotiques | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
malformation
n1=en:mmih syndrome | n2=malformation | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
malformation congénitale
n1=en:mmih syndrome | n2=malformation congénitale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
malformation d'Arnold-Chiari
n1=en:mmih syndrome | n2=malformation d'Arnold-Chiari | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
Malformation d'Arnold-Chiari
n1=en:mmih syndrome | n2=Malformation d'Arnold-Chiari | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
malformation d'arnold-chiari
n1=en:mmih syndrome | n2=malformation d'arnold-chiari | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
malformations congénitales du corps calleux
n1=en:mmih syndrome | n2=malformations congénitales du corps calleux | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
méningite tuberculeuse
n1=en:mmih syndrome | n2=méningite tuberculeuse | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
méningite tuberculeuse examen non précisé
n1=en:mmih syndrome | n2=méningite tuberculeuse examen non précisé | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
mésentérique supérieure (syndrome de l'artère)
n1=en:mmih syndrome | n2=mésentérique supérieure (syndrome de l'artère) | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
microdélétion 5q35
n1=en:mmih syndrome | n2=microdélétion 5q35 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
mort subite du nourrisson
n1=en:mmih syndrome | n2=mort subite du nourrisson | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
myocardiopathie de tako-tsubo
n1=en:mmih syndrome | n2=myocardiopathie de tako-tsubo | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
myokymie
n1=en:mmih syndrome | n2=myokymie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
myopathie viscérale familiale avec ophtalmoplégie externe
n1=en:mmih syndrome | n2=myopathie viscérale familiale avec ophtalmoplégie externe | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
myosite
n1=en:mmih syndrome | n2=myosite | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
myosites
n1=en:mmih syndrome | n2=myosites | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
nanisme campomélique
n1=en:mmih syndrome | n2=nanisme campomélique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
néphrocalcinose
n1=en:mmih syndrome | n2=néphrocalcinose | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
neuro-acanthocytose
n1=en:mmih syndrome | n2=neuro-acanthocytose | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
neurocysticercose
n1=en:mmih syndrome | n2=neurocysticercose | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
neuropathie optique
n1=en:mmih syndrome | n2=neuropathie optique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
nevrilème
n1=en:mmih syndrome | n2=nevrilème | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
névrite optique
n1=en:mmih syndrome | n2=névrite optique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
noma
n1=en:mmih syndrome | n2=noma | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
nystagmus congénital isolé
n1=en:mmih syndrome | n2=nystagmus congénital isolé | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
oedème du poumon non cardiogénique
n1=en:mmih syndrome | n2=oedème du poumon non cardiogénique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
oedème pulmonaire non cardiogénique
n1=en:mmih syndrome | n2=oedème pulmonaire non cardiogénique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
omphalocèle
n1=en:mmih syndrome | n2=omphalocèle | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
omphalocèles
n1=en:mmih syndrome | n2=omphalocèles | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
ongles jaunes (syndrome des)
n1=en:mmih syndrome | n2=ongles jaunes (syndrome des) | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
onycho-ostéodysostose
n1=en:mmih syndrome | n2=onycho-ostéodysostose | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
onycho-patellaire (syndrome)
n1=en:mmih syndrome | n2=onycho-patellaire (syndrome) | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
ophtalmorhino-stomatoxérose
n1=en:mmih syndrome | n2=ophtalmorhino-stomatoxérose | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
ostéochondrodysplasie
n1=en:mmih syndrome | n2=ostéochondrodysplasie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
ostéochondrodysplasies
n1=en:mmih syndrome | n2=ostéochondrodysplasies | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
ostéopétrose avec acidose rénale tubulaire
n1=en:mmih syndrome | n2=ostéopétrose avec acidose rénale tubulaire | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
ostéopoecilie
n1=en:mmih syndrome | n2=ostéopoecilie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
pachyméningite hypertrophique tuberculeuse
n1=en:mmih syndrome | n2=pachyméningite hypertrophique tuberculeuse | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
pachyonychie congénitale de Jadassohn-Lewandowsky
n1=en:mmih syndrome | n2=pachyonychie congénitale de Jadassohn-Lewandowsky | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
panencéphalite subaiguë sclérosante
n1=en:mmih syndrome | n2=panencéphalite subaiguë sclérosante | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
panuvéite
n1=en:mmih syndrome | n2=panuvéite | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
papulose atrophiante maligne de Degos
n1=en:mmih syndrome | n2=papulose atrophiante maligne de Degos | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
paragonimiase
n1=en:mmih syndrome | n2=paragonimiase | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
paragonimose
n1=en:mmih syndrome | n2=paragonimose | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
paralysie périodique familiale
n1=en:mmih syndrome | n2=paralysie périodique familiale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
paralysie supranucléaire progressive
n1=en:mmih syndrome | n2=paralysie supranucléaire progressive | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
pathologie congénitale
n1=en:mmih syndrome | n2=pathologie congénitale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
pemphigoïde bénigne des muqueuses
n1=en:mmih syndrome | n2=pemphigoïde bénigne des muqueuses | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
peste
n1=en:mmih syndrome | n2=peste | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
peste noire
n1=en:mmih syndrome | n2=peste noire | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
phacomatose congenitale
n1=en:mmih syndrome | n2=phacomatose congenitale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
piébaldisme
n1=en:mmih syndrome | n2=piébaldisme | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
piebaldisme
n1=en:mmih syndrome | n2=piebaldisme | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
pityriasis rubra pilaire
n1=en:mmih syndrome | n2=pityriasis rubra pilaire | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
Pityriasis rubra pilaire
n1=en:mmih syndrome | n2=Pityriasis rubra pilaire | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
Plummer-Vinson (syndrome de)
n1=en:mmih syndrome | n2=Plummer-Vinson (syndrome de) | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
porphyrie cutanée tardive
n1=en:mmih syndrome | n2=porphyrie cutanée tardive | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
porphyrie érythropoïétique
n1=en:mmih syndrome | n2=porphyrie érythropoïétique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
poumon de choc
n1=en:mmih syndrome | n2=poumon de choc | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
poumon de choc traumatique
n1=en:mmih syndrome | n2=poumon de choc traumatique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
poumon du vietnam
n1=en:mmih syndrome | n2=poumon du vietnam | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
présentation sacro-iliaque droite antérieure
n1=en:mmih syndrome | n2=présentation sacro-iliaque droite antérieure | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
progeria
n1=en:mmih syndrome | n2=progeria | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
progéria
n1=en:mmih syndrome | n2=progéria | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
protéinose alvéolaire
n1=en:mmih syndrome | n2=protéinose alvéolaire | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
protéinose alvéolaire pulmonaire
n1=en:mmih syndrome | n2=protéinose alvéolaire pulmonaire | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
protoproporphyrie érythropoïétique
n1=en:mmih syndrome | n2=protoproporphyrie érythropoïétique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
psychose de korsakoff
n1=en:mmih syndrome | n2=psychose de korsakoff | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
queue de cheval (syndrome de la)
n1=en:mmih syndrome | n2=queue de cheval (syndrome de la) | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
red man syndrome
n1=en:mmih syndrome | n2=red man syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
S.I.D.A.
n1=en:mmih syndrome | n2=S.I.D.A. | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
Sars
n1=en:mmih syndrome | n2=Sars | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
scléromyxoedème d'Arndt-Gottron
n1=en:mmih syndrome | n2=scléromyxoedème d'Arndt-Gottron | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
Seitelberger
n1=en:mmih syndrome | n2=Seitelberger | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
Seitelberger (maladie de)
n1=en:mmih syndrome | n2=Seitelberger (maladie de) | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
septo-optic dysplasia
n1=en:mmih syndrome | n2=septo-optic dysplasia | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
sicca syndrome
n1=en:mmih syndrome | n2=sicca syndrome | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
SIDA
n1=en:mmih syndrome | n2=SIDA | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
Silver-Russell (syndrome de)
n1=en:mmih syndrome | n2=Silver-Russell (syndrome de) | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
sirénomélie
n1=en:mmih syndrome | n2=sirénomélie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
sirop d'érable (urine à odeur de)
n1=en:mmih syndrome | n2=sirop d'érable (urine à odeur de) | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
situs inversus
n1=en:mmih syndrome | n2=situs inversus | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
Sotos (syndrome de)
n1=en:mmih syndrome | n2=Sotos (syndrome de) | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome adéno-cutanéo-muqueux
n1=en:mmih syndrome | n2=syndrome adéno-cutanéo-muqueux | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome adénocutanéomuqueux
n1=en:mmih syndrome | n2=syndrome adénocutanéomuqueux | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome cérébro-oculo-faciosquelettique
n1=en:mmih syndrome | n2=syndrome cérébro-oculo-faciosquelettique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome coronarien aigu
n1=en:mmih syndrome | n2=syndrome coronarien aigu | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome d'Adair-Dighton
n1=en:mmih syndrome | n2=syndrome d'Adair-Dighton | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome d'Alagille
n1=en:mmih syndrome | n2=syndrome d'Alagille | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome d'Alice au pays des merveilles
n1=en:mmih syndrome | n2=syndrome d'Alice au pays des merveilles | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome d'Alport
n1=en:mmih syndrome | n2=syndrome d'Alport | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome d'alport
n1=en:mmih syndrome | n2=syndrome d'alport | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome d'angelman
n1=en:mmih syndrome | n2=syndrome d'angelman | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
Syndrome d'Angelman
n1=en:mmih syndrome | n2=Syndrome d'Angelman | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome d'Angelman
n1=en:mmih syndrome | n2=syndrome d'Angelman | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome d'immunodéficience acquise
n1=en:mmih syndrome | n2=syndrome d'immunodéficience acquise | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de bile épaisse
n1=en:mmih syndrome | n2=syndrome de bile épaisse | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de bride amniotique
n1=en:mmih syndrome | n2=syndrome de bride amniotique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de chasse
n1=en:mmih syndrome | n2=syndrome de chasse | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de détresse respiratoire
n1=en:mmih syndrome | n2=syndrome de détresse respiratoire | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de détresse respiratoire aiguë
n1=en:mmih syndrome | n2=syndrome de détresse respiratoire aiguë | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de détresse respiratoire aigüe
n1=en:mmih syndrome | n2=syndrome de détresse respiratoire aigüe | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
Syndrome de détresse respiratoire aiguë
n1=en:mmih syndrome | n2=Syndrome de détresse respiratoire aiguë | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de douleur extrême paroxystique
n1=en:mmih syndrome | n2=syndrome de douleur extrême paroxystique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de Duane
n1=en:mmih syndrome | n2=syndrome de Duane | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de duane
n1=en:mmih syndrome | n2=syndrome de duane | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de dubin-johnson
n1=en:mmih syndrome | n2=syndrome de dubin-johnson | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de Dubin-Johnson
n1=en:mmih syndrome | n2=syndrome de Dubin-Johnson | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de fragilité du chromosome X
n1=en:mmih syndrome | n2=syndrome de fragilité du chromosome X | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de Goltz
n1=en:mmih syndrome | n2=syndrome de Goltz | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de goltz
n1=en:mmih syndrome | n2=syndrome de goltz | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de Jacobsen
n1=en:mmih syndrome | n2=syndrome de Jacobsen | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de jadassohn-lewandowsky
n1=en:mmih syndrome | n2=syndrome de jadassohn-lewandowsky | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de Jadassohn-Lewandowsky
n1=en:mmih syndrome | n2=syndrome de Jadassohn-Lewandowsky | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de Kawasaki
n1=en:mmih syndrome | n2=syndrome de Kawasaki | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de kawasaki
n1=en:mmih syndrome | n2=syndrome de kawasaki | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de Kelly-Paterson
n1=en:mmih syndrome | n2=syndrome de Kelly-Paterson | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de l'arc aortique
n1=en:mmih syndrome | n2=syndrome de l'arc aortique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de l'homme rouge
n1=en:mmih syndrome | n2=syndrome de l'homme rouge | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de l'immunodéficience acquise
n1=en:mmih syndrome | n2=syndrome de l'immunodéficience acquise | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de la crosse aortique
n1=en:mmih syndrome | n2=syndrome de la crosse aortique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de la mort subite du nourrisson
n1=en:mmih syndrome | n2=syndrome de la mort subite du nourrisson | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
Syndrome de la queue de cheval
n1=en:mmih syndrome | n2=Syndrome de la queue de cheval | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de la queue de cheval
n1=en:mmih syndrome | n2=syndrome de la queue de cheval | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de Laurence-Moon
n1=en:mmih syndrome | n2=syndrome de Laurence-Moon | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de malabsorption
n1=en:mmih syndrome | n2=syndrome de malabsorption | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de marfan
n1=en:mmih syndrome | n2=syndrome de marfan | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de Martin-Bell
n1=en:mmih syndrome | n2=syndrome de Martin-Bell | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de membrane hyaline
n1=en:mmih syndrome | n2=syndrome de membrane hyaline | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
Syndrome de Plummer-Vinson
n1=en:mmih syndrome | n2=Syndrome de Plummer-Vinson | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de Plummer-Vinson
n1=en:mmih syndrome | n2=syndrome de Plummer-Vinson | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de plummer-vinson
n1=en:mmih syndrome | n2=syndrome de plummer-vinson | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de réaction inflammatoire généralisée
n1=en:mmih syndrome | n2=syndrome de réaction inflammatoire généralisée | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de rétraction du globe oculaire
n1=en:mmih syndrome | n2=syndrome de rétraction du globe oculaire | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de Rett
n1=en:mmih syndrome | n2=syndrome de Rett | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
Syndrome de Rett
n1=en:mmih syndrome | n2=Syndrome de Rett | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de rett
n1=en:mmih syndrome | n2=syndrome de rett | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de Sheehan
n1=en:mmih syndrome | n2=syndrome de Sheehan | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de Shy-Drager
n1=en:mmih syndrome | n2=syndrome de Shy-Drager | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de shy-drager
n1=en:mmih syndrome | n2=syndrome de shy-drager | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
Syndrome de Shy-Drager
n1=en:mmih syndrome | n2=Syndrome de Shy-Drager | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de Silver-Russell
n1=en:mmih syndrome | n2=syndrome de Silver-Russell | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de silver-russell
n1=en:mmih syndrome | n2=syndrome de silver-russell | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de soto
n1=en:mmih syndrome | n2=syndrome de soto | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de Sotos
n1=en:mmih syndrome | n2=syndrome de Sotos | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de sotos
n1=en:mmih syndrome | n2=syndrome de sotos | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de Stilling-Türk-Duane
n1=en:mmih syndrome | n2=syndrome de Stilling-Türk-Duane | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de Türk-Stilling-Duane
n1=en:mmih syndrome | n2=syndrome de Türk-Stilling-Duane | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de türk-stilling-duane
n1=en:mmih syndrome | n2=syndrome de türk-stilling-duane | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de Vogt-Koyanagi-Harada
n1=en:mmih syndrome | n2=syndrome de Vogt-Koyanagi-Harada | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
Syndrome de Vogt-Koyanagi-Harada
n1=en:mmih syndrome | n2=Syndrome de Vogt-Koyanagi-Harada | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome de Williams
n1=en:mmih syndrome | n2=syndrome de Williams | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome des brides amniotiques
n1=en:mmih syndrome | n2=syndrome des brides amniotiques | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome des yeux de chat
n1=en:mmih syndrome | n2=syndrome des yeux de chat | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome du bébé gris
n1=en:mmih syndrome | n2=syndrome du bébé gris | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome du canal tarsien
n1=en:mmih syndrome | n2=syndrome du canal tarsien | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome du choc toxique
n1=en:mmih syndrome | n2=syndrome du choc toxique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome du grêle court
n1=en:mmih syndrome | n2=syndrome du grêle court | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome du tunnel tarsien
n1=en:mmih syndrome | n2=syndrome du tunnel tarsien | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome gris du nourrisson
n1=en:mmih syndrome | n2=syndrome gris du nourrisson | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome hétérotaxique
n1=en:mmih syndrome | n2=syndrome hétérotaxique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome inflammatoire aigu systémique
n1=en:mmih syndrome | n2=syndrome inflammatoire aigu systémique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome lympho-cutanéo-muqueux
n1=en:mmih syndrome | n2=syndrome lympho-cutanéo-muqueux | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome métabolique
n1=en:mmih syndrome | n2=syndrome métabolique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome sec
n1=en:mmih syndrome | n2=syndrome sec | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome TORCH
n1=en:mmih syndrome | n2=syndrome TORCH | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome torch
n1=en:mmih syndrome | n2=syndrome torch | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome tricho-rhino-phalangien de type 2
n1=en:mmih syndrome | n2=syndrome tricho-rhino-phalangien de type 2 | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome tricho-rhino-phalangien de type II
n1=en:mmih syndrome | n2=syndrome tricho-rhino-phalangien de type II | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
syndrome tricho-rhino-phalangien de type ii
n1=en:mmih syndrome | n2=syndrome tricho-rhino-phalangien de type ii | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
tare congénitale
n1=en:mmih syndrome | n2=tare congénitale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
toxémie staphylococcique
n1=en:mmih syndrome | n2=toxémie staphylococcique | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
TPN ou NADP
n1=en:mmih syndrome | n2=TPN ou NADP | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
trachéo-bronchomégalie
n1=en:mmih syndrome | n2=trachéo-bronchomégalie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
trichothiodystrophie
n1=en:mmih syndrome | n2=trichothiodystrophie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
tuberculose des méninges
n1=en:mmih syndrome | n2=tuberculose des méninges | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
tuberculose méningée
n1=en:mmih syndrome | n2=tuberculose méningée | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
tunnel tarsien (syndrome du)
n1=en:mmih syndrome | n2=tunnel tarsien (syndrome du) | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
Türk-Stilling-Duane (syndrome de)
n1=en:mmih syndrome | n2=Türk-Stilling-Duane (syndrome de) | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
une anomalie congénitale
n1=en:mmih syndrome | n2=une anomalie congénitale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
van Bogaert (xanthomatose cérébrotendineuse de)
n1=en:mmih syndrome | n2=van Bogaert (xanthomatose cérébrotendineuse de) | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
varicelle congénitale
n1=en:mmih syndrome | n2=varicelle congénitale | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
vessie
n1=en:mmih syndrome | n2=vessie | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
vice de conformation
n1=en:mmih syndrome | n2=vice de conformation | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
Walker-Warburg (syndrome de)
n1=en:mmih syndrome | n2=Walker-Warburg (syndrome de) | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
wallérienne (dégénérescence)
n1=en:mmih syndrome | n2=wallérienne (dégénérescence) | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
Whipple (maladie de)
n1=en:mmih syndrome | n2=Whipple (maladie de) | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
xanthique (lithiase)
n1=en:mmih syndrome | n2=xanthique (lithiase) | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
xanthomatose cérébro-tendineuse
n1=en:mmih syndrome | n2=xanthomatose cérébro-tendineuse | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
xanthomatose cérébrotendineuse
n1=en:mmih syndrome | n2=xanthomatose cérébrotendineuse | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
xanthomatose cérébrotendineuse de Van Bogaert
n1=en:mmih syndrome | n2=xanthomatose cérébrotendineuse de Van Bogaert | rel=r_associated | relid=0 | w=20
- en:mmih syndrome --
r_associated #0: 20 / 0.465 ->
yellow nail syndrome
n1=en:mmih syndrome | n2=yellow nail syndrome | rel=r_associated | relid=0 | w=20
| ≈ 1666 relations entrantes
- en:maple syrup urine disease ---
r_associated #0: 696 -->
en:mmih syndrome
n1=en:maple syrup urine disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=696
- leucinose ---
r_associated #0: 609.18 -->
en:mmih syndrome
n1=leucinose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=609.18
- maladie du sirop d'érable ---
r_associated #0: 604.37 -->
en:mmih syndrome
n1=maladie du sirop d'érable | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=604.37
- en:branched-chain ketoaciduria ---
r_associated #0: 520 -->
en:mmih syndrome
n1=en:branched-chain ketoaciduria | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=520
- peste
(maladie) ---
r_associated #0: 492 -->
en:mmih syndrome
n1=peste (maladie) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=492
- en:plague ---
r_associated #0: 488 -->
en:mmih syndrome
n1=en:plague | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=488
- anomalie congénitale ---
r_associated #0: 429 -->
en:mmih syndrome
n1=anomalie congénitale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=429
- en:congenital abnormality ---
r_associated #0: 427 -->
en:mmih syndrome
n1=en:congenital abnormality | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=427
- maladie héréditaire ---
r_associated #0: 391 -->
en:mmih syndrome
n1=maladie héréditaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=391
- en:hereditary disease ---
r_associated #0: 390 -->
en:mmih syndrome
n1=en:hereditary disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=390
- maladie génétique ---
r_associated #0: 386 -->
en:mmih syndrome
n1=maladie génétique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=386
- syndrome de Goltz ---
r_associated #0: 385 -->
en:mmih syndrome
n1=syndrome de Goltz | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=385
- Goltz ---
r_associated #0: 383 -->
en:mmih syndrome
n1=Goltz | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=383
- hypoplasie dermique focale ---
r_associated #0: 383 -->
en:mmih syndrome
n1=hypoplasie dermique focale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=383
- hypoplasie dermique en aires ---
r_associated #0: 381 -->
en:mmih syndrome
n1=hypoplasie dermique en aires | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=381
- en:focal dermal hypoplasia ---
r_associated #0: 380 -->
en:mmih syndrome
n1=en:focal dermal hypoplasia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=380
- malformation congénitale ---
r_associated #0: 356 -->
en:mmih syndrome
n1=malformation congénitale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=356
- en:SIDS ---
r_associated #0: 355 -->
en:mmih syndrome
n1=en:SIDS | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=355
- en:cot death ---
r_associated #0: 355 -->
en:mmih syndrome
n1=en:cot death | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=355
- en:genetic disease ---
r_associated #0: 355 -->
en:mmih syndrome
n1=en:genetic disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=355
- mort subite du nourrisson ---
r_associated #0: 355 -->
en:mmih syndrome
n1=mort subite du nourrisson | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=355
- en:sudden infant death syndrome ---
r_associated #0: 353 -->
en:mmih syndrome
n1=en:sudden infant death syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=353
- en:congenital anomaly ---
r_associated #0: 351 -->
en:mmih syndrome
n1=en:congenital anomaly | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=351
- syndrome de la mort subite du nourrisson ---
r_associated #0: 345 -->
en:mmih syndrome
n1=syndrome de la mort subite du nourrisson | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=345
- omphalocèle ---
r_associated #0: 328 -->
en:mmih syndrome
n1=omphalocèle | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=328
- en:omphalocele ---
r_associated #0: 324 -->
en:mmih syndrome
n1=en:omphalocele | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=324
- exomphale ---
r_associated #0: 320 -->
en:mmih syndrome
n1=exomphale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=320
- hernie ombilicale congénitale ---
r_associated #0: 320 -->
en:mmih syndrome
n1=hernie ombilicale congénitale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=320
- omphalocèles ---
r_associated #0: 316 -->
en:mmih syndrome
n1=omphalocèles | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=316
- atélectasie congestive ---
r_associated #0: 315 -->
en:mmih syndrome
n1=atélectasie congestive | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=315
- exomphale congénitale ---
r_associated #0: 315 -->
en:mmih syndrome
n1=exomphale congénitale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=315
- syndrome du choc toxique ---
r_associated #0: 315 -->
en:mmih syndrome
n1=syndrome du choc toxique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=315
- en:toxic shock syndrome ---
r_associated #0: 314 -->
en:mmih syndrome
n1=en:toxic shock syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=314
- choc au poumon ---
r_associated #0: 310 -->
en:mmih syndrome
n1=choc au poumon | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=310
- en:congenital defect ---
r_associated #0: 310 -->
en:mmih syndrome
n1=en:congenital defect | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=310
- hernie ombilicale ---
r_associated #0: 310 -->
en:mmih syndrome
n1=hernie ombilicale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=310
- poumon du vietnam ---
r_associated #0: 310 -->
en:mmih syndrome
n1=poumon du vietnam | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=310
- insuffisance pulmonaire post-traumatique ---
r_associated #0: 306 -->
en:mmih syndrome
n1=insuffisance pulmonaire post-traumatique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=306
- en:genetic disorder ---
r_associated #0: 305 -->
en:mmih syndrome
n1=en:genetic disorder | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=305
- en:umbilical hernia ---
r_associated #0: 305 -->
en:mmih syndrome
n1=en:umbilical hernia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=305
- oedème pulmonaire non cardiogénique ---
r_associated #0: 304 -->
en:mmih syndrome
n1=oedème pulmonaire non cardiogénique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=304
- oedème du poumon non cardiogénique ---
r_associated #0: 302 -->
en:mmih syndrome
n1=oedème du poumon non cardiogénique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=302
- en:acute respiratory distress syndrome ---
r_associated #0: 301 -->
en:mmih syndrome
n1=en:acute respiratory distress syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=301
- hernies ombilicales ---
r_associated #0: 301 -->
en:mmih syndrome
n1=hernies ombilicales | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=301
- poumon de choc traumatique ---
r_associated #0: 300 -->
en:mmih syndrome
n1=poumon de choc traumatique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=300
- déformation congénitale ---
r_associated #0: 296 -->
en:mmih syndrome
n1=déformation congénitale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=296
- déficience congénitale ---
r_associated #0: 295 -->
en:mmih syndrome
n1=déficience congénitale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=295
- en:Toxic Shock Syndrome ---
r_associated #0: 295 -->
en:mmih syndrome
n1=en:Toxic Shock Syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=295
- crânio-sténose ---
r_associated #0: 288 -->
en:mmih syndrome
n1=crânio-sténose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=288
- en:craniosynostosis ---
r_associated #0: 287 -->
en:mmih syndrome
n1=en:craniosynostosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=287
- crâniosynostose ---
r_associated #0: 286 -->
en:mmih syndrome
n1=crâniosynostose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=286
- craniosynostose ---
r_associated #0: 285 -->
en:mmih syndrome
n1=craniosynostose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=285
- en:marfan syndrome ---
r_associated #0: 285 -->
en:mmih syndrome
n1=en:marfan syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=285
- Sars ---
r_associated #0: 284 -->
en:mmih syndrome
n1=Sars | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=284
- crâniosténose ---
r_associated #0: 284 -->
en:mmih syndrome
n1=crâniosténose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=284
- anomalie héréditaire ---
r_associated #0: 281 -->
en:mmih syndrome
n1=anomalie héréditaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=281
- maladie de Marfan ---
r_associated #0: 281 -->
en:mmih syndrome
n1=maladie de Marfan | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=281
- syndrome de Marfan ---
r_associated #0: 281 -->
en:mmih syndrome
n1=syndrome de Marfan | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=281
- en:classical maple syrup urine disease ---
r_associated #0: 280 -->
en:mmih syndrome
n1=en:classical maple syrup urine disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=280
- en:thiamin-responsive maple syrup urine disease ---
r_associated #0: 280 -->
en:mmih syndrome
n1=en:thiamin-responsive maple syrup urine disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=280
- déficit en céto-acide décarboxylase ---
r_associated #0: 275 -->
en:mmih syndrome
n1=déficit en céto-acide décarboxylase | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=275
- maladie des urines à l'odeur de sirop d'érable ---
r_associated #0: 275 -->
en:mmih syndrome
n1=maladie des urines à l'odeur de sirop d'érable | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=275
- syndrome de détresse respiratoire aigüe ---
r_associated #0: 274 -->
en:mmih syndrome
n1=syndrome de détresse respiratoire aigüe | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=274
- maladie des urines avec odeur de sirop erable ---
r_associated #0: 270 -->
en:mmih syndrome
n1=maladie des urines avec odeur de sirop erable | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=270
- poumon de choc ---
r_associated #0: 268 -->
en:mmih syndrome
n1=poumon de choc | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=268
- en:crib death ---
r_associated #0: 265 -->
en:mmih syndrome
n1=en:crib death | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=265
- méningite tuberculeuse ---
r_associated #0: 258 -->
en:mmih syndrome
n1=méningite tuberculeuse | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=258
- en:meningeal tuberculosis ---
r_associated #0: 255 -->
en:mmih syndrome
n1=en:meningeal tuberculosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=255
- en:tuberculosis of meninges (cerebral)(spinal) ---
r_associated #0: 255 -->
en:mmih syndrome
n1=en:tuberculosis of meninges (cerebral)(spinal) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=255
- examen non précisé, méningite tuberculeuse ---
r_associated #0: 255 -->
en:mmih syndrome
n1=examen non précisé, méningite tuberculeuse | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=255
- leptoméningite tuberculeuse ---
r_associated #0: 255 -->
en:mmih syndrome
n1=leptoméningite tuberculeuse | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=255
- tuberculose des méninges ---
r_associated #0: 255 -->
en:mmih syndrome
n1=tuberculose des méninges | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=255
- tuberculose méningée ---
r_associated #0: 255 -->
en:mmih syndrome
n1=tuberculose méningée | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=255
- arachnodactylie ---
r_associated #0: 251 -->
en:mmih syndrome
n1=arachnodactylie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=251
- en:tuberculosis, meningeal ---
r_associated #0: 250 -->
en:mmih syndrome
n1=en:tuberculosis, meningeal | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=250
- en:tuberculous hypertrophic pachymeningitides ---
r_associated #0: 250 -->
en:mmih syndrome
n1=en:tuberculous hypertrophic pachymeningitides | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=250
- en:tuberculous leptomeningitis ---
r_associated #0: 250 -->
en:mmih syndrome
n1=en:tuberculous leptomeningitis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=250
- syndrome de chasse ---
r_associated #0: 250 -->
en:mmih syndrome
n1=syndrome de chasse | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=250
- syndrome de détresse respiratoire aiguë ---
r_associated #0: 250 -->
en:mmih syndrome
n1=syndrome de détresse respiratoire aiguë | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=250
- en:dumping syndrome ---
r_associated #0: 247 -->
en:mmih syndrome
n1=en:dumping syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=247
- pachyméningite hypertrophique tuberculeuse ---
r_associated #0: 245 -->
en:mmih syndrome
n1=pachyméningite hypertrophique tuberculeuse | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=245
- en:arachnodactyly ---
r_associated #0: 231 -->
en:mmih syndrome
n1=en:arachnodactyly | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=231
- en:genetic condition ---
r_associated #0: 210 -->
en:mmih syndrome
n1=en:genetic condition | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=210
- en:primary progressive aphasia ---
r_associated #0: 210 -->
en:mmih syndrome
n1=en:primary progressive aphasia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=210
- méningite tuberculeuse examen non précisé ---
r_associated #0: 210 -->
en:mmih syndrome
n1=méningite tuberculeuse examen non précisé | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=210
- aphasie primaire progressive ---
r_associated #0: 209 -->
en:mmih syndrome
n1=aphasie primaire progressive | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=209
- en:gray baby syndrome ---
r_associated #0: 208 -->
en:mmih syndrome
n1=en:gray baby syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=208
- aphasies primaires progressives ---
r_associated #0: 206 -->
en:mmih syndrome
n1=aphasies primaires progressives | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=206
- difformité congénitale ---
r_associated #0: 205 -->
en:mmih syndrome
n1=difformité congénitale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=205
- syndrome du bébé gris ---
r_associated #0: 205 -->
en:mmih syndrome
n1=syndrome du bébé gris | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=205
- maladie congénitale ---
r_associated #0: 201 -->
en:mmih syndrome
n1=maladie congénitale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=201
- syndrome gris du nourrisson ---
r_associated #0: 200 -->
en:mmih syndrome
n1=syndrome gris du nourrisson | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=200
- côlon ---
r_associated #0: 197 -->
en:mmih syndrome
n1=côlon | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=197
- en:colon ---
r_associated #0: 196 -->
en:mmih syndrome
n1=en:colon | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=196
- pathologie congénitale ---
r_associated #0: 195 -->
en:mmih syndrome
n1=pathologie congénitale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=195
- craniosténose ---
r_associated #0: 185 -->
en:mmih syndrome
n1=craniosténose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=185
- en:aortic coarctation ---
r_associated #0: 183 -->
en:mmih syndrome
n1=en:aortic coarctation | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=183
- coarctation aortique ---
r_associated #0: 180 -->
en:mmih syndrome
n1=coarctation aortique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=180
- en:walker-warburg syndrome ---
r_associated #0: 180 -->
en:mmih syndrome
n1=en:walker-warburg syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=180
- aphasie progressive primaire ---
r_associated #0: 179 -->
en:mmih syndrome
n1=aphasie progressive primaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=179
- agénésie vésicale ---
r_associated #0: 178 -->
en:mmih syndrome
n1=agénésie vésicale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=178
- syndrome de Walker-Warburg ---
r_associated #0: 178 -->
en:mmih syndrome
n1=syndrome de Walker-Warburg | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=178
- en:pyruvate carboxylase deficiency ---
r_associated #0: 175 -->
en:mmih syndrome
n1=en:pyruvate carboxylase deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=175
- déficit en pyruvate carboxylase ---
r_associated #0: 174 -->
en:mmih syndrome
n1=déficit en pyruvate carboxylase | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=174
- en:congenital absence of bladder ---
r_associated #0: 174 -->
en:mmih syndrome
n1=en:congenital absence of bladder | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=174
- cysticercose cérébrale ---
r_associated #0: 171 -->
en:mmih syndrome
n1=cysticercose cérébrale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=171
- cysticercose du système nerveux central ---
r_associated #0: 168 -->
en:mmih syndrome
n1=cysticercose du système nerveux central | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=168
- paralysies périodiques familiales ---
r_associated #0: 168 -->
en:mmih syndrome
n1=paralysies périodiques familiales | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=168
- en:familial periodic paralysis ---
r_associated #0: 166 -->
en:mmih syndrome
n1=en:familial periodic paralysis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=166
- en:zellweger syndrome ---
r_associated #0: 166 -->
en:mmih syndrome
n1=en:zellweger syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=166
- en:Zellweger syndrome ---
r_associated #0: 165 -->
en:mmih syndrome
n1=en:Zellweger syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=165
- paralysie périodique familiale ---
r_associated #0: 165 -->
en:mmih syndrome
n1=paralysie périodique familiale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=165
- syndrome d'Alport ---
r_associated #0: 164 -->
en:mmih syndrome
n1=syndrome d'Alport | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=164
- Syndrome de Vogt-Koyanagi-Harada ---
r_associated #0: 161 -->
en:mmih syndrome
n1=Syndrome de Vogt-Koyanagi-Harada | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=161
- atrophie optique autosomique dominante ---
r_associated #0: 160 -->
en:mmih syndrome
n1=atrophie optique autosomique dominante | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=160
- cysticercose neurologique ---
r_associated #0: 160 -->
en:mmih syndrome
n1=cysticercose neurologique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=160
- en:Diskinson's syndrome ---
r_associated #0: 160 -->
en:mmih syndrome
n1=en:Diskinson's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=160
- en:neurocysticercosis ---
r_associated #0: 159 -->
en:mmih syndrome
n1=en:neurocysticercosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=159
- cysticercose ---
r_associated #0: 155 -->
en:mmih syndrome
n1=cysticercose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=155
- cysticercoses ---
r_associated #0: 155 -->
en:mmih syndrome
n1=cysticercoses | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=155
- en:cysticercosis ---
r_associated #0: 155 -->
en:mmih syndrome
n1=en:cysticercosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=155
- neurocysticercose ---
r_associated #0: 155 -->
en:mmih syndrome
n1=neurocysticercose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=155
- malformation d'Arnold-Chiari ---
r_associated #0: 151 -->
en:mmih syndrome
n1=malformation d'Arnold-Chiari | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=151
- en:arnold chiari malformation ---
r_associated #0: 145 -->
en:mmih syndrome
n1=en:arnold chiari malformation | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=145
- en:arnold-chiari malformation ---
r_associated #0: 142 -->
en:mmih syndrome
n1=en:arnold-chiari malformation | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=142
- ostéochondrodysplasies ---
r_associated #0: 141 -->
en:mmih syndrome
n1=ostéochondrodysplasies | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=141
- syndrome de Türk-Stilling-Duane ---
r_associated #0: 140 -->
en:mmih syndrome
n1=syndrome de Türk-Stilling-Duane | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=140
- en:osteochondrodysplasia ---
r_associated #0: 139 -->
en:mmih syndrome
n1=en:osteochondrodysplasia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=139
- en:duane syndrome ---
r_associated #0: 136 -->
en:mmih syndrome
n1=en:duane syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=136
- syndrome de Duane ---
r_associated #0: 136 -->
en:mmih syndrome
n1=syndrome de Duane | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=136
- érythermalgie ---
r_associated #0: 135 -->
en:mmih syndrome
n1=érythermalgie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=135
- en:angelman syndrome ---
r_associated #0: 134 -->
en:mmih syndrome
n1=en:angelman syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=134
- en:erythromelalgia ---
r_associated #0: 134 -->
en:mmih syndrome
n1=en:erythromelalgia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=134
- en:congenital malformation ---
r_associated #0: 130 -->
en:mmih syndrome
n1=en:congenital malformation | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=130
- syndrome d'Angelman ---
r_associated #0: 130 -->
en:mmih syndrome
n1=syndrome d'Angelman | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=130
- érythromélalgie ---
r_associated #0: 130 -->
en:mmih syndrome
n1=érythromélalgie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=130
- syndrome de duane ---
r_associated #0: 128 -->
en:mmih syndrome
n1=syndrome de duane | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=128
- en:whipple disease ---
r_associated #0: 126 -->
en:mmih syndrome
n1=en:whipple disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=126
- maladie de Whipple ---
r_associated #0: 125 -->
en:mmih syndrome
n1=maladie de Whipple | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=125
- erythromelalgia ---
r_associated #0: 124 -->
en:mmih syndrome
n1=erythromelalgia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=124
- en:birth defect ---
r_associated #0: 120 -->
en:mmih syndrome
n1=en:birth defect | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=120
- ostéopétrose avec acidose rénale tubulaire ---
r_associated #0: 117 -->
en:mmih syndrome
n1=ostéopétrose avec acidose rénale tubulaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=117
- en:osteopetrosis with renal tubular acidosis ---
r_associated #0: 116 -->
en:mmih syndrome
n1=en:osteopetrosis with renal tubular acidosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=116
- démence frontotemporale ---
r_associated #0: 115 -->
en:mmih syndrome
n1=démence frontotemporale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=115
- démence fronto-temporale ---
r_associated #0: 113 -->
en:mmih syndrome
n1=démence fronto-temporale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=113
- idiotie spastique amaurotique axonale ---
r_associated #0: 113 -->
en:mmih syndrome
n1=idiotie spastique amaurotique axonale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=113
- dystrophie neuroaxonale infantile ---
r_associated #0: 112 -->
en:mmih syndrome
n1=dystrophie neuroaxonale infantile | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=112
- dystrophie neuroaxonale ---
r_associated #0: 110 -->
en:mmih syndrome
n1=dystrophie neuroaxonale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=110
- en:genetic illness ---
r_associated #0: 110 -->
en:mmih syndrome
n1=en:genetic illness | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=110
- en:piebaldism ---
r_associated #0: 108 -->
en:mmih syndrome
n1=en:piebaldism | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=108
- maladie de Caffey ---
r_associated #0: 107 -->
en:mmih syndrome
n1=maladie de Caffey | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=107
- dystrophie neuro-axonale infantile ---
r_associated #0: 106 -->
en:mmih syndrome
n1=dystrophie neuro-axonale infantile | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=106
- en:pulmonary shunting ---
r_associated #0: 105 -->
en:mmih syndrome
n1=en:pulmonary shunting | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=105
- piebaldisme ---
r_associated #0: 105 -->
en:mmih syndrome
n1=piebaldisme | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=105
- piébaldisme ---
r_associated #0: 104 -->
en:mmih syndrome
n1=piébaldisme | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=104
- anencéphalie ---
r_associated #0: 101 -->
en:mmih syndrome
n1=anencéphalie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=101
- dystrophie neuroaxonale de Seitelberger ---
r_associated #0: 101 -->
en:mmih syndrome
n1=dystrophie neuroaxonale de Seitelberger | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=101
- syndrome des brides amniotiques ---
r_associated #0: 101 -->
en:mmih syndrome
n1=syndrome des brides amniotiques | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=101
- en:frontotemporal dementia ---
r_associated #0: 100 -->
en:mmih syndrome
n1=en:frontotemporal dementia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=100
- en:yellow nail syndrome ---
r_associated #0: 100 -->
en:mmih syndrome
n1=en:yellow nail syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=100
- lissencéphalie ---
r_associated #0: 100 -->
en:mmih syndrome
n1=lissencéphalie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=100
- syndrome de Rett ---
r_associated #0: 100 -->
en:mmih syndrome
n1=syndrome de Rett | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=100
- en:amniotic band syndrome ---
r_associated #0: 99 -->
en:mmih syndrome
n1=en:amniotic band syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=99
- en:lissencephaly ---
r_associated #0: 99 -->
en:mmih syndrome
n1=en:lissencephaly | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=99
- en:rett syndrome ---
r_associated #0: 99 -->
en:mmih syndrome
n1=en:rett syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=99
- aïnhum ---
r_associated #0: 98 -->
en:mmih syndrome
n1=aïnhum | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=98
- en:anencephaly ---
r_associated #0: 98 -->
en:mmih syndrome
n1=en:anencephaly | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=98
- yellow nail syndrome ---
r_associated #0: 98 -->
en:mmih syndrome
n1=yellow nail syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=98
- syndrome de soto ---
r_associated #0: 97 -->
en:mmih syndrome
n1=syndrome de soto | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=97
- gigantisme cérébral ---
r_associated #0: 96 -->
en:mmih syndrome
n1=gigantisme cérébral | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=96
- maladies des bandes amniotiques ---
r_associated #0: 96 -->
en:mmih syndrome
n1=maladies des bandes amniotiques | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=96
- cataplexie ---
r_associated #0: 95 -->
en:mmih syndrome
n1=cataplexie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=95
- en:ainhum ---
r_associated #0: 95 -->
en:mmih syndrome
n1=en:ainhum | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=95
- en:sotos syndrome ---
r_associated #0: 95 -->
en:mmih syndrome
n1=en:sotos syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=95
- sicca syndrome ---
r_associated #0: 95 -->
en:mmih syndrome
n1=sicca syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=95
- syndrome adénocutanéomuqueux ---
r_associated #0: 94 -->
en:mmih syndrome
n1=syndrome adénocutanéomuqueux | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=94
- en:alice in wonderland syndrome ---
r_associated #0: 93 -->
en:mmih syndrome
n1=en:alice in wonderland syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=93
- en:cataplexy ---
r_associated #0: 92 -->
en:mmih syndrome
n1=en:cataplexy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=92
- dumping syndrome ---
r_associated #0: 91 -->
en:mmih syndrome
n1=dumping syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=91
- en:sicca syndrome ---
r_associated #0: 91 -->
en:mmih syndrome
n1=en:sicca syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=91
- maladie de Seitelberger ---
r_associated #0: 91 -->
en:mmih syndrome
n1=maladie de Seitelberger | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=91
- syndrome de bride amniotique ---
r_associated #0: 91 -->
en:mmih syndrome
n1=syndrome de bride amniotique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=91
- ainhum ---
r_associated #0: 90 -->
en:mmih syndrome
n1=ainhum | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=90
- en:Alice in Wonderland syndrome ---
r_associated #0: 90 -->
en:mmih syndrome
n1=en:Alice in Wonderland syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=90
- en:Angelman syndrome ---
r_associated #0: 90 -->
en:mmih syndrome
n1=en:Angelman syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=90
- en:Umbilical hernia ---
r_associated #0: 90 -->
en:mmih syndrome
n1=en:Umbilical hernia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=90
- en:jacobsen syndrome ---
r_associated #0: 90 -->
en:mmih syndrome
n1=en:jacobsen syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=90
- en:septo-optic dysplasia ---
r_associated #0: 90 -->
en:mmih syndrome
n1=en:septo-optic dysplasia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=90
- en:sotos' syndrome ---
r_associated #0: 90 -->
en:mmih syndrome
n1=en:sotos' syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=90
- protéinose alvéolaire ---
r_associated #0: 90 -->
en:mmih syndrome
n1=protéinose alvéolaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=90
- protéinose alvéolaire pulmonaire ---
r_associated #0: 90 -->
en:mmih syndrome
n1=protéinose alvéolaire pulmonaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=90
- syndrome de Kawasaki ---
r_associated #0: 90 -->
en:mmih syndrome
n1=syndrome de Kawasaki | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=90
- septo-optic dysplasia ---
r_associated #0: 89 -->
en:mmih syndrome
n1=septo-optic dysplasia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=89
- syndrome de Jacobsen ---
r_associated #0: 89 -->
en:mmih syndrome
n1=syndrome de Jacobsen | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=89
- nanisme campomélique ---
r_associated #0: 88 -->
en:mmih syndrome
n1=nanisme campomélique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=88
- en:pulmonary alveolar proteinosis ---
r_associated #0: 87 -->
en:mmih syndrome
n1=en:pulmonary alveolar proteinosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=87
- Seitelberger ---
r_associated #0: 86 -->
en:mmih syndrome
n1=Seitelberger | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=86
- maladie de Kawasaki ---
r_associated #0: 86 -->
en:mmih syndrome
n1=maladie de Kawasaki | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=86
- en:kawasaki disease ---
r_associated #0: 85 -->
en:mmih syndrome
n1=en:kawasaki disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=85
- leprosy ---
r_associated #0: 85 -->
en:mmih syndrome
n1=leprosy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=85
- tare congénitale ---
r_associated #0: 85 -->
en:mmih syndrome
n1=tare congénitale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=85
- en:leprosy ---
r_associated #0: 84 -->
en:mmih syndrome
n1=en:leprosy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=84
- dentinogenesis imperfecta ---
r_associated #0: 83 -->
en:mmih syndrome
n1=dentinogenesis imperfecta | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=83
- en:dentinogenesis imperfecta ---
r_associated #0: 82 -->
en:mmih syndrome
n1=en:dentinogenesis imperfecta | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=82
- syndrome du canal tarsien ---
r_associated #0: 82 -->
en:mmih syndrome
n1=syndrome du canal tarsien | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=82
- Malformation d'Arnold-Chiari ---
r_associated #0: 80 -->
en:mmih syndrome
n1=Malformation d'Arnold-Chiari | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=80
- en:cerebral tuberculosis ---
r_associated #0: 80 -->
en:mmih syndrome
n1=en:cerebral tuberculosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=80
- en:infantile neuroaxonal dystrophy ---
r_associated #0: 80 -->
en:mmih syndrome
n1=en:infantile neuroaxonal dystrophy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=80
- en:tarsal tunnel syndrome ---
r_associated #0: 80 -->
en:mmih syndrome
n1=en:tarsal tunnel syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=80
- syndrome adéno-cutanéo-muqueux ---
r_associated #0: 80 -->
en:mmih syndrome
n1=syndrome adéno-cutanéo-muqueux | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=80
- syndrome d'Alice au pays des merveilles ---
r_associated #0: 80 -->
en:mmih syndrome
n1=syndrome d'Alice au pays des merveilles | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=80
- syndrome de Sotos ---
r_associated #0: 80 -->
en:mmih syndrome
n1=syndrome de Sotos | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=80
- syndrome lympho-cutanéo-muqueux ---
r_associated #0: 80 -->
en:mmih syndrome
n1=syndrome lympho-cutanéo-muqueux | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=80
- syndrome tricho-rhino-phalangien de type ii ---
r_associated #0: 80 -->
en:mmih syndrome
n1=syndrome tricho-rhino-phalangien de type ii | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=80
- syndrome de türk-stilling-duane ---
r_associated #0: 79 -->
en:mmih syndrome
n1=syndrome de türk-stilling-duane | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=79
- en:red man syndrome ---
r_associated #0: 78 -->
en:mmih syndrome
n1=en:red man syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=78
- syndrome de l'homme rouge ---
r_associated #0: 76 -->
en:mmih syndrome
n1=syndrome de l'homme rouge | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=76
- syndrome tricho-rhino-phalangien de type 2 ---
r_associated #0: 76 -->
en:mmih syndrome
n1=syndrome tricho-rhino-phalangien de type 2 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=76
- dystrophies neuroaxonales ---
r_associated #0: 75 -->
en:mmih syndrome
n1=dystrophies neuroaxonales | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=75
- en:trichorhinophalangeal syndrome type ii ---
r_associated #0: 74 -->
en:mmih syndrome
n1=en:trichorhinophalangeal syndrome type ii | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=74
- albinisme ---
r_associated #0: 72 -->
en:mmih syndrome
n1=albinisme | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=72
- en:Whipple disease ---
r_associated #0: 72 -->
en:mmih syndrome
n1=en:Whipple disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=72
- en:fragile x syndrome ---
r_associated #0: 71 -->
en:mmih syndrome
n1=en:fragile x syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=71
- en:torch syndrome ---
r_associated #0: 71 -->
en:mmih syndrome
n1=en:torch syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=71
- Syndrome d'Angelman ---
r_associated #0: 70 -->
en:mmih syndrome
n1=Syndrome d'Angelman | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=70
- anasarque foetal ---
r_associated #0: 70 -->
en:mmih syndrome
n1=anasarque foetal | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=70
- détresse respiratoire ---
r_associated #0: 70 -->
en:mmih syndrome
n1=détresse respiratoire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=70
- en:fragile X syndrome ---
r_associated #0: 70 -->
en:mmih syndrome
n1=en:fragile X syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=70
- malformation d'arnold-chiari ---
r_associated #0: 70 -->
en:mmih syndrome
n1=malformation d'arnold-chiari | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=70
- en:albinism ---
r_associated #0: 69 -->
en:mmih syndrome
n1=en:albinism | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=69
- en:korsakoff syndrome ---
r_associated #0: 69 -->
en:mmih syndrome
n1=en:korsakoff syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=69
- en:oculo-respiratory syndrome ---
r_associated #0: 69 -->
en:mmih syndrome
n1=en:oculo-respiratory syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=69
- en:Korsakoff syndrome ---
r_associated #0: 68 -->
en:mmih syndrome
n1=en:Korsakoff syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=68
- en:oculorespiratory syndrome ---
r_associated #0: 68 -->
en:mmih syndrome
n1=en:oculorespiratory syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=68
- en:respiratory distress syndrome ---
r_associated #0: 68 -->
en:mmih syndrome
n1=en:respiratory distress syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=68
- syndrome torch ---
r_associated #0: 67 -->
en:mmih syndrome
n1=syndrome torch | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=67
- en:hydrops fetalis ---
r_associated #0: 66 -->
en:mmih syndrome
n1=en:hydrops fetalis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=66
- syndrome TORCH ---
r_associated #0: 66 -->
en:mmih syndrome
n1=syndrome TORCH | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=66
- syndrome de Plummer-Vinson ---
r_associated #0: 66 -->
en:mmih syndrome
n1=syndrome de Plummer-Vinson | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=66
- Syndrome de Rett ---
r_associated #0: 65 -->
en:mmih syndrome
n1=Syndrome de Rett | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=65
- association toxoplasmose, rubéole, cytomégalovirus et herpès chez un nouveau-né ---
r_associated #0: 65 -->
en:mmih syndrome
n1=association toxoplasmose, rubéole, cytomégalovirus et herpès chez un nouveau-né | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=65
- en:Plummer-Vinson syndrome ---
r_associated #0: 65 -->
en:mmih syndrome
n1=en:Plummer-Vinson syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=65
- inflammation musculaire ---
r_associated #0: 65 -->
en:mmih syndrome
n1=inflammation musculaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=65
- syndrome de détresse respiratoire ---
r_associated #0: 65 -->
en:mmih syndrome
n1=syndrome de détresse respiratoire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=65
- syndrome de fragilité du chromosome X ---
r_associated #0: 65 -->
en:mmih syndrome
n1=syndrome de fragilité du chromosome X | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=65
- syndrome d'angelman ---
r_associated #0: 64 -->
en:mmih syndrome
n1=syndrome d'angelman | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=64
- syndrome de Kelly-Paterson ---
r_associated #0: 64 -->
en:mmih syndrome
n1=syndrome de Kelly-Paterson | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=64
- en:erythermalgia ---
r_associated #0: 63 -->
en:mmih syndrome
n1=en:erythermalgia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=63
- en:hurler syndrome ---
r_associated #0: 63 -->
en:mmih syndrome
n1=en:hurler syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=63
- situs inversus ---
r_associated #0: 63 -->
en:mmih syndrome
n1=situs inversus | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=63
- en:russell-silver syndrome ---
r_associated #0: 62 -->
en:mmih syndrome
n1=en:russell-silver syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=62
- queue de cheval (syndrome de la) ---
r_associated #0: 62 -->
en:mmih syndrome
n1=queue de cheval (syndrome de la) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=62
- en:dubin-johnson syndrome ---
r_associated #0: 61 -->
en:mmih syndrome
n1=en:dubin-johnson syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=61
- myosite ---
r_associated #0: 61 -->
en:mmih syndrome
n1=myosite | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=61
- syndrome de Silver-Russell ---
r_associated #0: 61 -->
en:mmih syndrome
n1=syndrome de Silver-Russell | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=61
- DentinoGenesis Imperfecta ---
r_associated #0: 60 -->
en:mmih syndrome
n1=DentinoGenesis Imperfecta | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=60
- acromégalie ---
r_associated #0: 60 -->
en:mmih syndrome
n1=acromégalie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=60
- en:Hurler syndrome ---
r_associated #0: 60 -->
en:mmih syndrome
n1=en:Hurler syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=60
- en:Kawasaki disease ---
r_associated #0: 60 -->
en:mmih syndrome
n1=en:Kawasaki disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=60
- en:Klinefelter syndrome ---
r_associated #0: 60 -->
en:mmih syndrome
n1=en:Klinefelter syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=60
- en:Sotos' syndrome ---
r_associated #0: 60 -->
en:mmih syndrome
n1=en:Sotos' syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=60
- en:situs inversus ---
r_associated #0: 60 -->
en:mmih syndrome
n1=en:situs inversus | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=60
- hypertrophie staturale avec macroglossie et omphalocèle ---
r_associated #0: 60 -->
en:mmih syndrome
n1=hypertrophie staturale avec macroglossie et omphalocèle | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=60
- syndrome de dubin-johnson ---
r_associated #0: 60 -->
en:mmih syndrome
n1=syndrome de dubin-johnson | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=60
- en:cauda equina syndrome ---
r_associated #0: 59 -->
en:mmih syndrome
n1=en:cauda equina syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=59
- en:guillain-barre syndrome ---
r_associated #0: 59 -->
en:mmih syndrome
n1=en:guillain-barre syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=59
- syndrome d'alport ---
r_associated #0: 59 -->
en:mmih syndrome
n1=syndrome d'alport | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=59
- syndrome de silver-russell ---
r_associated #0: 59 -->
en:mmih syndrome
n1=syndrome de silver-russell | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=59
- en:Guillain-Barre syndrome ---
r_associated #0: 58 -->
en:mmih syndrome
n1=en:Guillain-Barre syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=58
- en:glutaric acidemia type 1 ---
r_associated #0: 58 -->
en:mmih syndrome
n1=en:glutaric acidemia type 1 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=58
- en:acromegaly ---
r_associated #0: 57 -->
en:mmih syndrome
n1=en:acromegaly | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=57
- en:klinefelter syndrome ---
r_associated #0: 56 -->
en:mmih syndrome
n1=en:klinefelter syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=56
- syndrome de la queue de cheval ---
r_associated #0: 56 -->
en:mmih syndrome
n1=syndrome de la queue de cheval | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=56
- syndrome de rett ---
r_associated #0: 56 -->
en:mmih syndrome
n1=syndrome de rett | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=56
- dystrophies neuro-axonales ---
r_associated #0: 55 -->
en:mmih syndrome
n1=dystrophies neuro-axonales | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=55
- acidurie glutarique de type 1 ---
r_associated #0: 54 -->
en:mmih syndrome
n1=acidurie glutarique de type 1 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=54
- algodystrophies ---
r_associated #0: 54 -->
en:mmih syndrome
n1=algodystrophies | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=54
- en:cat-eye syndrome ---
r_associated #0: 54 -->
en:mmih syndrome
n1=en:cat-eye syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=54
- en:down syndrome ---
r_associated #0: 54 -->
en:mmih syndrome
n1=en:down syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=54
- en:myositis ---
r_associated #0: 54 -->
en:mmih syndrome
n1=en:myositis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=54
- peste ---
r_associated #0: 54 -->
en:mmih syndrome
n1=peste | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=54
- syndrome des yeux de chat ---
r_associated #0: 54 -->
en:mmih syndrome
n1=syndrome des yeux de chat | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=54
- vice de conformation ---
r_associated #0: 54 -->
en:mmih syndrome
n1=vice de conformation | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=54
- en:pick's disease ---
r_associated #0: 53 -->
en:mmih syndrome
n1=en:pick's disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=53
- dysplasie cléidocrânienne ---
r_associated #0: 52 -->
en:mmih syndrome
n1=dysplasie cléidocrânienne | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=52
- en:alport syndrome ---
r_associated #0: 52 -->
en:mmih syndrome
n1=en:alport syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=52
- en:physical defect ---
r_associated #0: 52 -->
en:mmih syndrome
n1=en:physical defect | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=52
- dentine opalescente héréditaire ---
r_associated #0: 51 -->
en:mmih syndrome
n1=dentine opalescente héréditaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=51
- en:Marfan's syndrome ---
r_associated #0: 51 -->
en:mmih syndrome
n1=en:Marfan's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=51
- en:cardio-facio-cutaneous syndrome ---
r_associated #0: 51 -->
en:mmih syndrome
n1=en:cardio-facio-cutaneous syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=51
- en:mucocutaneous lymph node syndrome ---
r_associated #0: 51 -->
en:mmih syndrome
n1=en:mucocutaneous lymph node syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=51
- en:tay-sachs disease ---
r_associated #0: 51 -->
en:mmih syndrome
n1=en:tay-sachs disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=51
- red man syndrome ---
r_associated #0: 51 -->
en:mmih syndrome
n1=red man syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=51
- syndrome de Vogt-Koyanagi-Harada ---
r_associated #0: 51 -->
en:mmih syndrome
n1=syndrome de Vogt-Koyanagi-Harada | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=51
- trachéo-bronchomégalie ---
r_associated #0: 51 -->
en:mmih syndrome
n1=trachéo-bronchomégalie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=51
- xanthomatose cérébro-tendineuse ---
r_associated #0: 51 -->
en:mmih syndrome
n1=xanthomatose cérébro-tendineuse | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=51
- xanthomatose cérébrotendineuse ---
r_associated #0: 51 -->
en:mmih syndrome
n1=xanthomatose cérébrotendineuse | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=51
- SIDA ---
r_associated #0: 50 -->
en:mmih syndrome
n1=SIDA | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- Syndrome de la queue de cheval ---
r_associated #0: 50 -->
en:mmih syndrome
n1=Syndrome de la queue de cheval | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- acidémie glutarique de type 1 ---
r_associated #0: 50 -->
en:mmih syndrome
n1=acidémie glutarique de type 1 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- acrodermatite entéropathique ---
r_associated #0: 50 -->
en:mmih syndrome
n1=acrodermatite entéropathique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- anomalie du développement ---
r_associated #0: 50 -->
en:mmih syndrome
n1=anomalie du développement | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- anti-sida ---
r_associated #0: 50 -->
en:mmih syndrome
n1=anti-sida | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- antisida ---
r_associated #0: 50 -->
en:mmih syndrome
n1=antisida | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- cœur triatrial ---
r_associated #0: 50 -->
en:mmih syndrome
n1=cœur triatrial | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- congénitale ---
r_associated #0: 50 -->
en:mmih syndrome
n1=congénitale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- dysplasie cléido-crânienne ---
r_associated #0: 50 -->
en:mmih syndrome
n1=dysplasie cléido-crânienne | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- en:AIDS ---
r_associated #0: 50 -->
en:mmih syndrome
n1=en:AIDS | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- en:Down syndrome ---
r_associated #0: 50 -->
en:mmih syndrome
n1=en:Down syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- en:Pick's disease ---
r_associated #0: 50 -->
en:mmih syndrome
n1=en:Pick's disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- en:Tay-Sachs disease ---
r_associated #0: 50 -->
en:mmih syndrome
n1=en:Tay-Sachs disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- en:congenital ---
r_associated #0: 50 -->
en:mmih syndrome
n1=en:congenital | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- en:macroglossia ---
r_associated #0: 50 -->
en:mmih syndrome
n1=en:macroglossia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- en:plummer-vinson syndrome ---
r_associated #0: 50 -->
en:mmih syndrome
n1=en:plummer-vinson syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- en:respiratory distress ---
r_associated #0: 50 -->
en:mmih syndrome
n1=en:respiratory distress | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- en:schock lung ---
r_associated #0: 50 -->
en:mmih syndrome
n1=en:schock lung | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- en:tracheobronchomegaly ---
r_associated #0: 50 -->
en:mmih syndrome
n1=en:tracheobronchomegaly | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- hydrops fœtoplacentaire ---
r_associated #0: 50 -->
en:mmih syndrome
n1=hydrops fœtoplacentaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- névrite optique ---
r_associated #0: 50 -->
en:mmih syndrome
n1=névrite optique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- syndrome d'immunodéficience acquise ---
r_associated #0: 50 -->
en:mmih syndrome
n1=syndrome d'immunodéficience acquise | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- syndrome du tunnel tarsien ---
r_associated #0: 50 -->
en:mmih syndrome
n1=syndrome du tunnel tarsien | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- syndrome hétérotaxique ---
r_associated #0: 50 -->
en:mmih syndrome
n1=syndrome hétérotaxique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- toxémie staphylococcique ---
r_associated #0: 50 -->
en:mmih syndrome
n1=toxémie staphylococcique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- tunnel tarsien (syndrome du) ---
r_associated #0: 50 -->
en:mmih syndrome
n1=tunnel tarsien (syndrome du) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=50
- acromegaly ---
r_associated #0: 49 -->
en:mmih syndrome
n1=acromegaly | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=49
- en:alveolar proteinosis ---
r_associated #0: 49 -->
en:mmih syndrome
n1=en:alveolar proteinosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=49
- en:cardiofaciocutaneous syndrome ---
r_associated #0: 49 -->
en:mmih syndrome
n1=en:cardiofaciocutaneous syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=49
- hydrops foetoplacentaire ---
r_associated #0: 49 -->
en:mmih syndrome
n1=hydrops foetoplacentaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=49
- syndrome de Dubin-Johnson ---
r_associated #0: 49 -->
en:mmih syndrome
n1=syndrome de Dubin-Johnson | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=49
- syndrome tricho-rhino-phalangien de type II ---
r_associated #0: 49 -->
en:mmih syndrome
n1=syndrome tricho-rhino-phalangien de type II | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=49
- anasarque foeto-placentaire ---
r_associated #0: 48 -->
en:mmih syndrome
n1=anasarque foeto-placentaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=48
- en:AIDS awareness ---
r_associated #0: 48 -->
en:mmih syndrome
n1=en:AIDS awareness | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=48
- en:cerebrotendinous xanthomatosis ---
r_associated #0: 48 -->
en:mmih syndrome
n1=en:cerebrotendinous xanthomatosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=48
- en:gigantism and hyperplastic visceromegaly ---
r_associated #0: 48 -->
en:mmih syndrome
n1=en:gigantism and hyperplastic visceromegaly | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=48
- en:ophthalmoneuritis ---
r_associated #0: 48 -->
en:mmih syndrome
n1=en:ophthalmoneuritis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=48
- sirop d'érable (urine à odeur de) ---
r_associated #0: 48 -->
en:mmih syndrome
n1=sirop d'érable (urine à odeur de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=48
- syndrome de shy-drager ---
r_associated #0: 48 -->
en:mmih syndrome
n1=syndrome de shy-drager | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=48
- en:Kawasaki's syndrome ---
r_associated #0: 47 -->
en:mmih syndrome
n1=en:Kawasaki's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=47
- en:acrodermatitis enteropathica ---
r_associated #0: 47 -->
en:mmih syndrome
n1=en:acrodermatitis enteropathica | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=47
- nevrilème ---
r_associated #0: 47 -->
en:mmih syndrome
n1=nevrilème | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=47
- syndrome de marfan ---
r_associated #0: 47 -->
en:mmih syndrome
n1=syndrome de marfan | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=47
- S.I.D.A. ---
r_associated #0: 46 -->
en:mmih syndrome
n1=S.I.D.A. | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=46
- Syndrome de Shy-Drager ---
r_associated #0: 46 -->
en:mmih syndrome
n1=Syndrome de Shy-Drager | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=46
- coeur triatrial ---
r_associated #0: 46 -->
en:mmih syndrome
n1=coeur triatrial | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=46
- congenital ---
r_associated #0: 46 -->
en:mmih syndrome
n1=congenital | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=46
- en:chondrodysplasia punctata ---
r_associated #0: 46 -->
en:mmih syndrome
n1=en:chondrodysplasia punctata | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=46
- en:heterotaxy syndrome ---
r_associated #0: 46 -->
en:mmih syndrome
n1=en:heterotaxy syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=46
- maladie de marfan ---
r_associated #0: 46 -->
en:mmih syndrome
n1=maladie de marfan | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=46
- pityriasis rubra pilaire ---
r_associated #0: 46 -->
en:mmih syndrome
n1=pityriasis rubra pilaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=46
- syndrome coronarien aigu ---
r_associated #0: 46 -->
en:mmih syndrome
n1=syndrome coronarien aigu | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=46
- syndrome de Shy-Drager ---
r_associated #0: 46 -->
en:mmih syndrome
n1=syndrome de Shy-Drager | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=46
- wallérienne (dégénérescence) ---
r_associated #0: 46 -->
en:mmih syndrome
n1=wallérienne (dégénérescence) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=46
- anasarque foetoplacentaire ---
r_associated #0: 45 -->
en:mmih syndrome
n1=anasarque foetoplacentaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=45
- en:optic neuritis ---
r_associated #0: 45 -->
en:mmih syndrome
n1=en:optic neuritis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=45
- en:situs mutatus ---
r_associated #0: 45 -->
en:mmih syndrome
n1=en:situs mutatus | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=45
- en:wallerian degeneration ---
r_associated #0: 45 -->
en:mmih syndrome
n1=en:wallerian degeneration | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=45
- maladie de Hurler ---
r_associated #0: 45 -->
en:mmih syndrome
n1=maladie de Hurler | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=45
- psychose de korsakoff ---
r_associated #0: 45 -->
en:mmih syndrome
n1=psychose de korsakoff | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=45
- scléromyxœdème d'Arndt-Gottron ---
r_associated #0: 45 -->
en:mmih syndrome
n1=scléromyxœdème d'Arndt-Gottron | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=45
- xanthomatose cérébrotendineuse de Van Bogaert ---
r_associated #0: 45 -->
en:mmih syndrome
n1=xanthomatose cérébrotendineuse de Van Bogaert | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=45
- en:acute coronary syndrome ---
r_associated #0: 44 -->
en:mmih syndrome
n1=en:acute coronary syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=44
- en:adrenal cytomegaly ---
r_associated #0: 44 -->
en:mmih syndrome
n1=en:adrenal cytomegaly | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=44
- en:pityriasis rubra pilaris ---
r_associated #0: 44 -->
en:mmih syndrome
n1=en:pityriasis rubra pilaris | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=44
- en:segmented intestine ---
r_associated #0: 44 -->
en:mmih syndrome
n1=en:segmented intestine | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=44
- en:trichorhinophalangeal syndrome type II ---
r_associated #0: 44 -->
en:mmih syndrome
n1=en:trichorhinophalangeal syndrome type II | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=44
- protoproporphyrie érythropoïétique ---
r_associated #0: 44 -->
en:mmih syndrome
n1=protoproporphyrie érythropoïétique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=44
- syndrome de goltz ---
r_associated #0: 44 -->
en:mmih syndrome
n1=syndrome de goltz | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=44
- syndrome de sotos ---
r_associated #0: 44 -->
en:mmih syndrome
n1=syndrome de sotos | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=44
- syndrome inflammatoire aigu systémique ---
r_associated #0: 44 -->
en:mmih syndrome
n1=syndrome inflammatoire aigu systémique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=44
- Syndrome de détresse respiratoire aiguë ---
r_associated #0: 43 -->
en:mmih syndrome
n1=Syndrome de détresse respiratoire aiguë | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=43
- en:17q21 microdeletion syndrome ---
r_associated #0: 43 -->
en:mmih syndrome
n1=en:17q21 microdeletion syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=43
- en:argininosuccinic aciduria ---
r_associated #0: 43 -->
en:mmih syndrome
n1=en:argininosuccinic aciduria | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=43
- en:bladder ---
r_associated #0: 43 -->
en:mmih syndrome
n1=en:bladder | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=43
- en:de toni-debre-fanconi syndrome ---
r_associated #0: 43 -->
en:mmih syndrome
n1=en:de toni-debre-fanconi syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=43
- en:meesmann corneal dystrophy ---
r_associated #0: 43 -->
en:mmih syndrome
n1=en:meesmann corneal dystrophy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=43
- en:norrie syndrome ---
r_associated #0: 43 -->
en:mmih syndrome
n1=en:norrie syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=43
- en:stokes-adams syndrome ---
r_associated #0: 43 -->
en:mmih syndrome
n1=en:stokes-adams syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=43
- en:wilms tumor 1 gene syndromes ---
r_associated #0: 43 -->
en:mmih syndrome
n1=en:wilms tumor 1 gene syndromes | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=43
- imperforation de l'anus ---
r_associated #0: 43 -->
en:mmih syndrome
n1=imperforation de l'anus | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=43
- syndrome de Jadassohn-Lewandowsky ---
r_associated #0: 43 -->
en:mmih syndrome
n1=syndrome de Jadassohn-Lewandowsky | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=43
- varicelle congénitale ---
r_associated #0: 43 -->
en:mmih syndrome
n1=varicelle congénitale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=43
- chondrodysplasia punctata ---
r_associated #0: 42 -->
en:mmih syndrome
n1=chondrodysplasia punctata | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=42
- en:adenocutanemucous syndrome ---
r_associated #0: 42 -->
en:mmih syndrome
n1=en:adenocutanemucous syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=42
- en:congenital varicella syndrome ---
r_associated #0: 42 -->
en:mmih syndrome
n1=en:congenital varicella syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=42
- en:glutaric aciduria, type 1 ---
r_associated #0: 42 -->
en:mmih syndrome
n1=en:glutaric aciduria, type 1 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=42
- en:ichthyosis ---
r_associated #0: 42 -->
en:mmih syndrome
n1=en:ichthyosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=42
- en:neuronal intranuclear inclusion disease ---
r_associated #0: 42 -->
en:mmih syndrome
n1=en:neuronal intranuclear inclusion disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=42
- en:shy-drager syndrome ---
r_associated #0: 42 -->
en:mmih syndrome
n1=en:shy-drager syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=42
- en:teratosis ---
r_associated #0: 42 -->
en:mmih syndrome
n1=en:teratosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=42
- en:wiskott-aldrich syndrome ---
r_associated #0: 42 -->
en:mmih syndrome
n1=en:wiskott-aldrich syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=42
- ichtyose ---
r_associated #0: 42 -->
en:mmih syndrome
n1=ichtyose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=42
- phacomatose congenitale ---
r_associated #0: 42 -->
en:mmih syndrome
n1=phacomatose congenitale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=42
- scléromyxoedème d'Arndt-Gottron ---
r_associated #0: 42 -->
en:mmih syndrome
n1=scléromyxoedème d'Arndt-Gottron | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=42
- trichothiodystrophie ---
r_associated #0: 42 -->
en:mmih syndrome
n1=trichothiodystrophie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=42
- vessie
(anatomie) ---
r_associated #0: 42 -->
en:mmih syndrome
n1=vessie (anatomie) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=42
- Syndrome de Plummer-Vinson ---
r_associated #0: 41 -->
en:mmih syndrome
n1=Syndrome de Plummer-Vinson | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=41
- Weir Mitchell ---
r_associated #0: 41 -->
en:mmih syndrome
n1=Weir Mitchell | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=41
- agnosie ---
r_associated #0: 41 -->
en:mmih syndrome
n1=agnosie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=41
- distomatoses pulmonaires ---
r_associated #0: 41 -->
en:mmih syndrome
n1=distomatoses pulmonaires | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=41
- déficit en prolidase ---
r_associated #0: 41 -->
en:mmih syndrome
n1=déficit en prolidase | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=41
- en:alpha thalassemia x-linked mental retardation syndrome ---
r_associated #0: 41 -->
en:mmih syndrome
n1=en:alpha thalassemia x-linked mental retardation syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=41
- en:major physical defect ---
r_associated #0: 41 -->
en:mmih syndrome
n1=en:major physical defect | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=41
- en:multiple gastrointestinal atresias (disorder) ---
r_associated #0: 41 -->
en:mmih syndrome
n1=en:multiple gastrointestinal atresias (disorder) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=41
- en:pearson marrow-pancreas syndrome ---
r_associated #0: 41 -->
en:mmih syndrome
n1=en:pearson marrow-pancreas syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=41
- en:rieger syndrome type 1 ---
r_associated #0: 41 -->
en:mmih syndrome
n1=en:rieger syndrome type 1 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=41
- imperforation anale ---
r_associated #0: 41 -->
en:mmih syndrome
n1=imperforation anale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=41
- porphyrie cutanée tardive ---
r_associated #0: 41 -->
en:mmih syndrome
n1=porphyrie cutanée tardive | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=41
- porphyrie érythropoïétique ---
r_associated #0: 41 -->
en:mmih syndrome
n1=porphyrie érythropoïétique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=41
- syndrome de kawasaki ---
r_associated #0: 41 -->
en:mmih syndrome
n1=syndrome de kawasaki | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=41
- syndrome sec ---
r_associated #0: 41 -->
en:mmih syndrome
n1=syndrome sec | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=41
- Silver-Russell (syndrome de) ---
r_associated #0: 40 -->
en:mmih syndrome
n1=Silver-Russell (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- Walker-Warburg (syndrome de) ---
r_associated #0: 40 -->
en:mmih syndrome
n1=Walker-Warburg (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- Whipple (maladie de) ---
r_associated #0: 40 -->
en:mmih syndrome
n1=Whipple (maladie de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- anasarque fœtoplacentaire ---
r_associated #0: 40 -->
en:mmih syndrome
n1=anasarque fœtoplacentaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- dentinogénèse imparfaite ---
r_associated #0: 40 -->
en:mmih syndrome
n1=dentinogénèse imparfaite | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- dysplasie olfacto-génitale ---
r_associated #0: 40 -->
en:mmih syndrome
n1=dysplasie olfacto-génitale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) ---
r_associated #0: 40 -->
en:mmih syndrome
n1=ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental (dysplasie) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- en:acquired immunodeficiency syndrome ---
r_associated #0: 40 -->
en:mmih syndrome
n1=en:acquired immunodeficiency syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- en:agnosia ---
r_associated #0: 40 -->
en:mmih syndrome
n1=en:agnosia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- en:black death ---
r_associated #0: 40 -->
en:mmih syndrome
n1=en:black death | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- en:black plague ---
r_associated #0: 40 -->
en:mmih syndrome
n1=en:black plague | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- en:cockayne syndrome ---
r_associated #0: 40 -->
en:mmih syndrome
n1=en:cockayne syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- en:dextrocardia ---
r_associated #0: 40 -->
en:mmih syndrome
n1=en:dextrocardia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- en:disease aids ---
r_associated #0: 40 -->
en:mmih syndrome
n1=en:disease aids | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- en:displaced ureteric orifice ---
r_associated #0: 40 -->
en:mmih syndrome
n1=en:displaced ureteric orifice | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- en:double cortex syndrome ---
r_associated #0: 40 -->
en:mmih syndrome
n1=en:double cortex syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- en:ectodermal dysplasia ---
r_associated #0: 40 -->
en:mmih syndrome
n1=en:ectodermal dysplasia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- en:erythropoietic porphyria ---
r_associated #0: 40 -->
en:mmih syndrome
n1=en:erythropoietic porphyria | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- en:erythropoietic protoporphyria ---
r_associated #0: 40 -->
en:mmih syndrome
n1=en:erythropoietic protoporphyria | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- en:frohlich syndrome ---
r_associated #0: 40 -->
en:mmih syndrome
n1=en:frohlich syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- en:immune deficiency syndrome ---
r_associated #0: 40 -->
en:mmih syndrome
n1=en:immune deficiency syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- en:insufficient breast milk syndrome ---
r_associated #0: 40 -->
en:mmih syndrome
n1=en:insufficient breast milk syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- en:metabolic syndrome ---
r_associated #0: 40 -->
en:mmih syndrome
n1=en:metabolic syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- en:neurological cysticercosis ---
r_associated #0: 40 -->
en:mmih syndrome
n1=en:neurological cysticercosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- en:scleromyxedema ---
r_associated #0: 40 -->
en:mmih syndrome
n1=en:scleromyxedema | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- en:systemic inflammatory response syndrome ---
r_associated #0: 40 -->
en:mmih syndrome
n1=en:systemic inflammatory response syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- en:trichothiodystrophy ---
r_associated #0: 40 -->
en:mmih syndrome
n1=en:trichothiodystrophy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- en:x-linked creatine transporter deficiency ---
r_associated #0: 40 -->
en:mmih syndrome
n1=en:x-linked creatine transporter deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- hypoxémie ---
r_associated #0: 40 -->
en:mmih syndrome
n1=hypoxémie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- intolérance au fructose ---
r_associated #0: 40 -->
en:mmih syndrome
n1=intolérance au fructose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- lèpre ---
r_associated #0: 40 -->
en:mmih syndrome
n1=lèpre | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- maladie de Dercum ---
r_associated #0: 40 -->
en:mmih syndrome
n1=maladie de Dercum | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- maladie de Tay-sachs ---
r_associated #0: 40 -->
en:mmih syndrome
n1=maladie de Tay-sachs | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- maladie de tay-sachs ---
r_associated #0: 40 -->
en:mmih syndrome
n1=maladie de tay-sachs | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- peste noire ---
r_associated #0: 40 -->
en:mmih syndrome
n1=peste noire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- syndrome de douleur extrême paroxystique ---
r_associated #0: 40 -->
en:mmih syndrome
n1=syndrome de douleur extrême paroxystique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- syndrome de l'immunodéficience acquise ---
r_associated #0: 40 -->
en:mmih syndrome
n1=syndrome de l'immunodéficience acquise | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- syndrome du grêle court ---
r_associated #0: 40 -->
en:mmih syndrome
n1=syndrome du grêle court | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=40
- Pityriasis rubra pilaire ---
r_associated #0: 39 -->
en:mmih syndrome
n1=Pityriasis rubra pilaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=39
- Sotos (syndrome de) ---
r_associated #0: 39 -->
en:mmih syndrome
n1=Sotos (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=39
- Türk-Stilling-Duane (syndrome de) ---
r_associated #0: 39 -->
en:mmih syndrome
n1=Türk-Stilling-Duane (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=39
- en:Stokes-Adams syndrome ---
r_associated #0: 39 -->
en:mmih syndrome
n1=en:Stokes-Adams syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=39
- en:adiposis dolorosa ---
r_associated #0: 39 -->
en:mmih syndrome
n1=en:adiposis dolorosa | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=39
- en:donohue syndrome ---
r_associated #0: 39 -->
en:mmih syndrome
n1=en:donohue syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=39
- en:dysequilibrium syndrome ---
r_associated #0: 39 -->
en:mmih syndrome
n1=en:dysequilibrium syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=39
- en:hereditary orotic aciduria ---
r_associated #0: 39 -->
en:mmih syndrome
n1=en:hereditary orotic aciduria | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=39
- en:pachyonychia congenita ---
r_associated #0: 39 -->
en:mmih syndrome
n1=en:pachyonychia congenita | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=39
- en:paragonimiasis ---
r_associated #0: 39 -->
en:mmih syndrome
n1=en:paragonimiasis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=39
- en:paroxysmal extreme pain disorder ---
r_associated #0: 39 -->
en:mmih syndrome
n1=en:paroxysmal extreme pain disorder | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=39
- en:porphyria cutanea tarda ---
r_associated #0: 39 -->
en:mmih syndrome
n1=en:porphyria cutanea tarda | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=39
- en:progressive bulbar palsy ---
r_associated #0: 39 -->
en:mmih syndrome
n1=en:progressive bulbar palsy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=39
- en:single central incisor syndrome ---
r_associated #0: 39 -->
en:mmih syndrome
n1=en:single central incisor syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=39
- hétérotaxie ---
r_associated #0: 39 -->
en:mmih syndrome
n1=hétérotaxie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=39
- mésentérique supérieure (syndrome de l'artère) ---
r_associated #0: 39 -->
en:mmih syndrome
n1=mésentérique supérieure (syndrome de l'artère) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=39
- neuropathie optique ---
r_associated #0: 39 -->
en:mmih syndrome
n1=neuropathie optique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=39
- onycho-ostéodysostose ---
r_associated #0: 39 -->
en:mmih syndrome
n1=onycho-ostéodysostose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=39
- syndrome d'Adair-Dighton ---
r_associated #0: 39 -->
en:mmih syndrome
n1=syndrome d'Adair-Dighton | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=39
- syndrome d'Alagille ---
r_associated #0: 39 -->
en:mmih syndrome
n1=syndrome d'Alagille | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=39
- en:Black death ---
r_associated #0: 38 -->
en:mmih syndrome
n1=en:Black death | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=38
- en:cataplexia ---
r_associated #0: 38 -->
en:mmih syndrome
n1=en:cataplexia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=38
- en:cleidocranial dysplasia ---
r_associated #0: 38 -->
en:mmih syndrome
n1=en:cleidocranial dysplasia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=38
- en:conn syndrome ---
r_associated #0: 38 -->
en:mmih syndrome
n1=en:conn syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=38
- en:fibromyalgia ---
r_associated #0: 38 -->
en:mmih syndrome
n1=en:fibromyalgia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=38
- en:variegate porphyria ---
r_associated #0: 38 -->
en:mmih syndrome
n1=en:variegate porphyria | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=38
- hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale ---
r_associated #0: 38 -->
en:mmih syndrome
n1=hamartoblastome hypothalamique, hypopituitarisme, imperforation anale et polydactylie post-axiale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=38
- holoprosencéphalie de type 4 ---
r_associated #0: 38 -->
en:mmih syndrome
n1=holoprosencéphalie de type 4 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=38
- ichtyose, affection neurologique spastique, et oligophrénie ---
r_associated #0: 38 -->
en:mmih syndrome
n1=ichtyose, affection neurologique spastique, et oligophrénie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=38
- léproserie ---
r_associated #0: 38 -->
en:mmih syndrome
n1=léproserie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=38
- maladie des épiphyses ponctuées ---
r_associated #0: 38 -->
en:mmih syndrome
n1=maladie des épiphyses ponctuées | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=38
- noma ---
r_associated #0: 38 -->
en:mmih syndrome
n1=noma | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=38
- nystagmus congénital isolé ---
r_associated #0: 38 -->
en:mmih syndrome
n1=nystagmus congénital isolé | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=38
- van Bogaert (xanthomatose cérébrotendineuse de) ---
r_associated #0: 38 -->
en:mmih syndrome
n1=van Bogaert (xanthomatose cérébrotendineuse de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=38
- dysplasie ectodermique ---
r_associated #0: 37 -->
en:mmih syndrome
n1=dysplasie ectodermique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=37
- en:acatalasemia ---
r_associated #0: 37 -->
en:mmih syndrome
n1=en:acatalasemia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=37
- en:allgrove syndrome ---
r_associated #0: 37 -->
en:mmih syndrome
n1=en:allgrove syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=37
- en:arakawa syndrome ii ---
r_associated #0: 37 -->
en:mmih syndrome
n1=en:arakawa syndrome ii | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=37
- en:arnold-chiari deformity ---
r_associated #0: 37 -->
en:mmih syndrome
n1=en:arnold-chiari deformity | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=37
- en:cranioectodermal dysplasia ---
r_associated #0: 37 -->
en:mmih syndrome
n1=en:cranioectodermal dysplasia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=37
- en:gangrenous stomatitis ---
r_associated #0: 37 -->
en:mmih syndrome
n1=en:gangrenous stomatitis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=37
- en:hereditary fructose intolerance ---
r_associated #0: 37 -->
en:mmih syndrome
n1=en:hereditary fructose intolerance | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=37
- en:holoprosencephaly ---
r_associated #0: 37 -->
en:mmih syndrome
n1=en:holoprosencephaly | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=37
- en:imperforate anus ---
r_associated #0: 37 -->
en:mmih syndrome
n1=en:imperforate anus | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=37
- en:maple-tree syrup disease ---
r_associated #0: 37 -->
en:mmih syndrome
n1=en:maple-tree syrup disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=37
- en:prolidase deficiency ---
r_associated #0: 37 -->
en:mmih syndrome
n1=en:prolidase deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=37
- en:sheehan syndrome ---
r_associated #0: 37 -->
en:mmih syndrome
n1=en:sheehan syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=37
- en:situs inversus viscerum ---
r_associated #0: 37 -->
en:mmih syndrome
n1=en:situs inversus viscerum | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=37
- en:sudden unexplained death in childhood ---
r_associated #0: 37 -->
en:mmih syndrome
n1=en:sudden unexplained death in childhood | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=37
- en:superior mesenteric artery syndrome ---
r_associated #0: 37 -->
en:mmih syndrome
n1=en:superior mesenteric artery syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=37
- en:von hippel-lindau syndrome ---
r_associated #0: 37 -->
en:mmih syndrome
n1=en:von hippel-lindau syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=37
- holoprosencéphalie ---
r_associated #0: 37 -->
en:mmih syndrome
n1=holoprosencéphalie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=37
- ichtyose folliculaire, atrichie et photophobie ---
r_associated #0: 37 -->
en:mmih syndrome
n1=ichtyose folliculaire, atrichie et photophobie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=37
- macroglossie ---
r_associated #0: 37 -->
en:mmih syndrome
n1=macroglossie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=37
- myocardiopathie de tako-tsubo ---
r_associated #0: 37 -->
en:mmih syndrome
n1=myocardiopathie de tako-tsubo | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=37
- syndrome de bile épaisse ---
r_associated #0: 37 -->
en:mmih syndrome
n1=syndrome de bile épaisse | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=37
- dysostose craniofaciale ---
r_associated #0: 36 -->
en:mmih syndrome
n1=dysostose craniofaciale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=36
- déficit en protéine trifonctionnelle mitochondriale ---
r_associated #0: 36 -->
en:mmih syndrome
n1=déficit en protéine trifonctionnelle mitochondriale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=36
- en:Duane's syndrome ---
r_associated #0: 36 -->
en:mmih syndrome
n1=en:Duane's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=36
- en:Gray platelet syndrome ---
r_associated #0: 36 -->
en:mmih syndrome
n1=en:Gray platelet syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=36
- en:cataplexis ---
r_associated #0: 36 -->
en:mmih syndrome
n1=en:cataplexis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=36
- en:exomphalos ---
r_associated #0: 36 -->
en:mmih syndrome
n1=en:exomphalos | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=36
- en:inspissated bile syndrome ---
r_associated #0: 36 -->
en:mmih syndrome
n1=en:inspissated bile syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=36
- en:kallmann syndrome ---
r_associated #0: 36 -->
en:mmih syndrome
n1=en:kallmann syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=36
- en:nail-patella syndrome ---
r_associated #0: 36 -->
en:mmih syndrome
n1=en:nail-patella syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=36
- en:penta x syndrome ---
r_associated #0: 36 -->
en:mmih syndrome
n1=en:penta x syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=36
- en:short bowel syndrome ---
r_associated #0: 36 -->
en:mmih syndrome
n1=en:short bowel syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=36
- en:takotsubo cardiomyopathy ---
r_associated #0: 36 -->
en:mmih syndrome
n1=en:takotsubo cardiomyopathy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=36
- holoprosencéphalie de type 3 ---
r_associated #0: 36 -->
en:mmih syndrome
n1=holoprosencéphalie de type 3 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=36
- ichthyose ---
r_associated #0: 36 -->
en:mmih syndrome
n1=ichthyose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=36
- ongles jaunes (syndrome des) ---
r_associated #0: 36 -->
en:mmih syndrome
n1=ongles jaunes (syndrome des) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=36
- ostéochondrodysplasie ---
r_associated #0: 36 -->
en:mmih syndrome
n1=ostéochondrodysplasie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=36
- sirénomélie ---
r_associated #0: 36 -->
en:mmih syndrome
n1=sirénomélie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=36
- syndrome de Sheehan ---
r_associated #0: 36 -->
en:mmih syndrome
n1=syndrome de Sheehan | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=36
- arthrogrypose ---
r_associated #0: 35 -->
en:mmih syndrome
n1=arthrogrypose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- congénital ---
r_associated #0: 35 -->
en:mmih syndrome
n1=congénital | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- dysostose crânio-faciale ---
r_associated #0: 35 -->
en:mmih syndrome
n1=dysostose crânio-faciale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:Prader-Willi syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:Prader-Willi syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:Triple a syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:Triple a syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:acrodysostosis 1 ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:acrodysostosis 1 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:alpha-1 antitrypsin deficiency ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:alpha-1 antitrypsin deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:aortic arch syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:aortic arch syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:argininemia ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:argininemia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:arrhythmogenic right ventricular dysplasia ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:arrhythmogenic right ventricular dysplasia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:arthrogryposis ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:arthrogryposis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:autoimmune polyendocrinopathy syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:autoimmune polyendocrinopathy syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:barth syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:barth syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:berardinelli-seip congenital lipodystrophy ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:berardinelli-seip congenital lipodystrophy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:blau syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:blau syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:cadasil syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:cadasil syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:cerebrooculofacioskeletal syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:cerebrooculofacioskeletal syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:chromosome 15q11-q13 duplication syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:chromosome 15q11-q13 duplication syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:congenital malformation syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:congenital malformation syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:cushing syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:cushing syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:deafness, autosomal recessive 1a ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:deafness, autosomal recessive 1a | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:dravet syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:dravet syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:dyschromatosis symmetrica hereditaria ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:dyschromatosis symmetrica hereditaria | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:endocrine syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:endocrine syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:fetal retinoid syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:fetal retinoid syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:gastrointestinal tract disorders congenital nec ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:gastrointestinal tract disorders congenital nec | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:hartnup disease ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:hartnup disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:hereditary coproporphyria ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:hereditary coproporphyria | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:hereditary hyperbilirubinemia ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:hereditary hyperbilirubinemia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:hermansky-pudlak syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:hermansky-pudlak syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:heterotaxy ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:heterotaxy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:high molecular weight kininogen deficiency ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:high molecular weight kininogen deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:hyperlysinemia ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:hyperlysinemia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:infantile convulsions and paroxysmal choreoathetosis, familial ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:infantile convulsions and paroxysmal choreoathetosis, familial | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:intestinal pseudo-obstruction ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:intestinal pseudo-obstruction | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:laurence-moon syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:laurence-moon syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:leigh disease ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:leigh disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:macrophage activation syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:macrophage activation syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:miller-dieker syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:miller-dieker syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:mitochondrial neurogastrointestingal encephalopathy ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:mitochondrial neurogastrointestingal encephalopathy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:multiple acyl-coa dehydrogenase deficiency ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:multiple acyl-coa dehydrogenase deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:multiple vascular disruption syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:multiple vascular disruption syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:periodic fever, aphthous stomatitis, pharyngitis, adenitis syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:periodic fever, aphthous stomatitis, pharyngitis, adenitis syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:persistent cloaca ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:persistent cloaca | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:persistent fetal circulation ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:persistent fetal circulation | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:poland syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:poland syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:prader-willi syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:prader-willi syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:progeria ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:progeria | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:restless leg syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:restless leg syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:sirenomelia ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:sirenomelia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:situs inversus abdominalis ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:situs inversus abdominalis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:somnolence syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:somnolence syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:stargardt disease ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:stargardt disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:subacute sclerosing panencephalitis ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:subacute sclerosing panencephalitis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:townes-brocks syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:townes-brocks syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:triple a syndrome ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:triple a syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:tubulointerstitial nephritis and uveitis ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:tubulointerstitial nephritis and uveitis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- en:xerophthalmia ---
r_associated #0: 35 -->
en:mmih syndrome
n1=en:xerophthalmia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- progeria ---
r_associated #0: 35 -->
en:mmih syndrome
n1=progeria | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- progéria ---
r_associated #0: 35 -->
en:mmih syndrome
n1=progéria | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- syndrome cérébro-oculo-faciosquelettique ---
r_associated #0: 35 -->
en:mmih syndrome
n1=syndrome cérébro-oculo-faciosquelettique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- syndrome de l'arc aortique ---
r_associated #0: 35 -->
en:mmih syndrome
n1=syndrome de l'arc aortique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- syndrome de la crosse aortique ---
r_associated #0: 35 -->
en:mmih syndrome
n1=syndrome de la crosse aortique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- syndrome de plummer-vinson ---
r_associated #0: 35 -->
en:mmih syndrome
n1=syndrome de plummer-vinson | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- trachéobronchomégalie ---
r_associated #0: 35 -->
en:mmih syndrome
n1=trachéobronchomégalie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=35
- Plummer-Vinson (syndrome de) ---
r_associated #0: 34 -->
en:mmih syndrome
n1=Plummer-Vinson (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- Seitelberger (maladie de) ---
r_associated #0: 34 -->
en:mmih syndrome
n1=Seitelberger (maladie de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- dysplasie frontonasale ---
r_associated #0: 34 -->
en:mmih syndrome
n1=dysplasie frontonasale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- ectrodactylie ---
r_associated #0: 34 -->
en:mmih syndrome
n1=ectrodactylie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:10p13-p14 deletion syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:10p13-p14 deletion syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:5 alpha steroid reductase 2 deficiency ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:5 alpha steroid reductase 2 deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:Soto's syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:Soto's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:accessory bladder ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:accessory bladder | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:acrodermatitis ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:acrodermatitis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:alkaptonuria ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:alkaptonuria | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:allan-herndon-dudley syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:allan-herndon-dudley syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:alpha-methylacyl-coa racemase deficiency ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:alpha-methylacyl-coa racemase deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:autosomal recessive hypohidrotic ectodermal dysplasia ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:autosomal recessive hypohidrotic ectodermal dysplasia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:beta-methylcrotonylglycinuria ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:beta-methylcrotonylglycinuria | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:bile acid synthesis defect ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:bile acid synthesis defect | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:biotinidase deficiency ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:biotinidase deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:carbonic anhydrase i deficiency ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:carbonic anhydrase i deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:child's sudden death ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:child's sudden death | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:chromosome 16p11.2 deletion syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:chromosome 16p11.2 deletion syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:chronic infantile neurological cutaneous and articular syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:chronic infantile neurological cutaneous and articular syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:codas syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:codas syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:congenital hypoplasia of bladder ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:congenital hypoplasia of bladder | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:congenital urinary system abnormality ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:congenital urinary system abnormality | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:cortical dysplasia-focal epilepsy syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:cortical dysplasia-focal epilepsy syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:craniofacial dysostosis ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:craniofacial dysostosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:cri du chat syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:cri du chat syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:cryptophthalmos syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:cryptophthalmos syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:fragile x tremor/ataxia syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:fragile x tremor/ataxia syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:gitelman syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:gitelman syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:glanzmann thrombasthenia ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:glanzmann thrombasthenia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:goldenhar syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:goldenhar syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:greig syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:greig syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:heritable pulmonary arterial hypertension ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:heritable pulmonary arterial hypertension | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:hirschsprung's disease and allied congenital conditions ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:hirschsprung's disease and allied congenital conditions | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:holmes-adie syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:holmes-adie syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:horner syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:horner syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:hyaline membrane syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:hyaline membrane syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:hymenolepiasis ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:hymenolepiasis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:hyperviscosity syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:hyperviscosity syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:jackson-weiss syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:jackson-weiss syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:jervell and lange nielsen syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:jervell and lange nielsen syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:long-chain 3-hydroxyacyl-coa dehydrogenase deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:lupus anticoagulant disorder ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:lupus anticoagulant disorder | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:marshall syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:marshall syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:mowat-wilson syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:mowat-wilson syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:mullerian inhibiting factor deficiency ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:mullerian inhibiting factor deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:neural tube defect ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:neural tube defect | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:neuroacanthocytosis ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:neuroacanthocytosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:orofaciodigital syndrome type 6 ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:orofaciodigital syndrome type 6 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:pena-shokeir syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:pena-shokeir syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:short stature homeobox deficiency ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:short stature homeobox deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:shprintzen-goldberg craniosynostosis syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:shprintzen-goldberg craniosynostosis syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:sick euthyroid syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:sick euthyroid syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:sudden unexplained infant death ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:sudden unexplained infant death | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:tempi syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:tempi syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:thrombocytopenia 2 ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:thrombocytopenia 2 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:urea cycle metabolism disorder ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:urea cycle metabolism disorder | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- en:waardenburg syndrome ---
r_associated #0: 34 -->
en:mmih syndrome
n1=en:waardenburg syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- insensibilité congénitale à la douleur de type III ---
r_associated #0: 34 -->
en:mmih syndrome
n1=insensibilité congénitale à la douleur de type III | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- maladie à virus de Marburg ---
r_associated #0: 34 -->
en:mmih syndrome
n1=maladie à virus de Marburg | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- myopathie viscérale familiale avec ophtalmoplégie externe ---
r_associated #0: 34 -->
en:mmih syndrome
n1=myopathie viscérale familiale avec ophtalmoplégie externe | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- onycho-patellaire (syndrome) ---
r_associated #0: 34 -->
en:mmih syndrome
n1=onycho-patellaire (syndrome) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- papulose atrophiante maligne de Degos ---
r_associated #0: 34 -->
en:mmih syndrome
n1=papulose atrophiante maligne de Degos | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- syndrome de Laurence-Moon ---
r_associated #0: 34 -->
en:mmih syndrome
n1=syndrome de Laurence-Moon | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- syndrome de rétraction du globe oculaire ---
r_associated #0: 34 -->
en:mmih syndrome
n1=syndrome de rétraction du globe oculaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=34
- anasarque ---
r_associated #0: 33 -->
en:mmih syndrome
n1=anasarque | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=33
- dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental ---
r_associated #0: 33 -->
en:mmih syndrome
n1=dysplasie ectodermique-fente labiopalatine-déformation des mains et des pieds avec retard mental | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=33
- dystrophie orbitaire congénitale ---
r_associated #0: 33 -->
en:mmih syndrome
n1=dystrophie orbitaire congénitale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=33
- en:frontonasal dysplasia ---
r_associated #0: 33 -->
en:mmih syndrome
n1=en:frontonasal dysplasia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=33
- en:gray platelet syndrome ---
r_associated #0: 33 -->
en:mmih syndrome
n1=en:gray platelet syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=33
- en:marburg virus disease ---
r_associated #0: 33 -->
en:mmih syndrome
n1=en:marburg virus disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=33
- en:mitochondrial trifunctional protein deficiency ---
r_associated #0: 33 -->
en:mmih syndrome
n1=en:mitochondrial trifunctional protein deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=33
- en:tuberculous meningitis ---
r_associated #0: 33 -->
en:mmih syndrome
n1=en:tuberculous meningitis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=33
- en:visceral myopathy ---
r_associated #0: 33 -->
en:mmih syndrome
n1=en:visceral myopathy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=33
- maladie de seitelberger ---
r_associated #0: 33 -->
en:mmih syndrome
n1=maladie de seitelberger | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=33
- maladie lysosomique de surcharge ---
r_associated #0: 33 -->
en:mmih syndrome
n1=maladie lysosomique de surcharge | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=33
- neuro-acanthocytose ---
r_associated #0: 33 -->
en:mmih syndrome
n1=neuro-acanthocytose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=33
- ophtalmorhino-stomatoxérose ---
r_associated #0: 33 -->
en:mmih syndrome
n1=ophtalmorhino-stomatoxérose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=33
- panencéphalite subaiguë sclérosante ---
r_associated #0: 33 -->
en:mmih syndrome
n1=panencéphalite subaiguë sclérosante | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=33
- syndrome de jadassohn-lewandowsky ---
r_associated #0: 33 -->
en:mmih syndrome
n1=syndrome de jadassohn-lewandowsky | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=33
- syndrome métabolique ---
r_associated #0: 33 -->
en:mmih syndrome
n1=syndrome métabolique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=33
- Maladie congénitale ---
r_associated #0: 32 -->
en:mmih syndrome
n1=Maladie congénitale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- dysplasie ectodermique, ectrodactylie et dystrophie maculaire ---
r_associated #0: 32 -->
en:mmih syndrome
n1=dysplasie ectodermique, ectrodactylie et dystrophie maculaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:22q telomere deletion syndrome ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:22q telomere deletion syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:acquired hyperostosis syndrome ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:acquired hyperostosis syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:acrocallosal syndrome ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:acrocallosal syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:acyl-coa dehydrogenase, short-chain deficiency ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:acyl-coa dehydrogenase, short-chain deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:atransferrinemia ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:atransferrinemia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:autoinflammatory syndrome ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:autoinflammatory syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:bonnevie-ullrich syndrome ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:bonnevie-ullrich syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:burning mouth syndrome ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:burning mouth syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:calciphylaxis ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:calciphylaxis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:caroli disease ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:caroli disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:cerebral gigantism ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:cerebral gigantism | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:chromosome 16p12.1 deletion syndrome ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:chromosome 16p12.1 deletion syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:cloacal exstrophy ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:cloacal exstrophy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:coffin-lowry syndrome ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:coffin-lowry syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:cogan-reese syndrome ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:cogan-reese syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:complex regional pain syndrome ii ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:complex regional pain syndrome ii | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:congenital bilateral aplasia of the vas deferens ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:congenital bilateral aplasia of the vas deferens | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:congenital fiber-type disproportion ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:congenital fiber-type disproportion | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:congenital hourglass bladder ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:congenital hourglass bladder | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:congenital rectovesical fistula ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:congenital rectovesical fistula | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:drug- and toxin-induced pulmonary arterial hypertension ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:drug- and toxin-induced pulmonary arterial hypertension | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:dumping stomach ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:dumping stomach | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:ebstein anomaly ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:ebstein anomaly | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:familial dysautonomia ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:familial dysautonomia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:familial partial lipodystrophy ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:familial partial lipodystrophy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:fibrodysplasia ossificans progressiva ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:fibrodysplasia ossificans progressiva | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:fox-fordyce disease ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:fox-fordyce disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:generalized arterial calcification of infancy 1 ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:generalized arterial calcification of infancy 1 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:hereditary persistence of fetal hemoglobin ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:hereditary persistence of fetal hemoglobin | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:heterotaxy syndrome with asplenia ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:heterotaxy syndrome with asplenia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:hyperpipecolatemia ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:hyperpipecolatemia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:immunodeficiency with hyper-igm type 2 ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:immunodeficiency with hyper-igm type 2 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:juvenile x-linked retinoschisis ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:juvenile x-linked retinoschisis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:kabuki syndrome ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:kabuki syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:leucinosis ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:leucinosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:lysosomal storage disease ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:lysosomal storage disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:malignant atrophic papulosis ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:malignant atrophic papulosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:mallory-weiss syndrome ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:mallory-weiss syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:methionine adenosyltransferase deficiency ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:methionine adenosyltransferase deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:microcephaly and chorioretinopathy, autosomal recessive, type 1 ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:microcephaly and chorioretinopathy, autosomal recessive, type 1 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:n-acetylglutamate synthase deficiency ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:n-acetylglutamate synthase deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:nelson syndrome ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:nelson syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:ombilical hernia ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:ombilical hernia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:primary vesicoureteric reflux ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:primary vesicoureteric reflux | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:pseudotrisomy 13 syndrome ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:pseudotrisomy 13 syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:sacral agenesis ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:sacral agenesis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:spondyloepimetaphyseal dysplasia with joint laxity type 2 ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:spondyloepimetaphyseal dysplasia with joint laxity type 2 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:stein-leventhal syndrome ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:stein-leventhal syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:surfactant protein deficiency ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:surfactant protein deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:vitelliform macular dystrophy ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:vitelliform macular dystrophy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:wegener granulomatosis ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:wegener granulomatosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:wolfram syndrome ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:wolfram syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- en:x-linked bulbar-muscular atrophy ---
r_associated #0: 32 -->
en:mmih syndrome
n1=en:x-linked bulbar-muscular atrophy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- holoprosencéphalie de type 2 ---
r_associated #0: 32 -->
en:mmih syndrome
n1=holoprosencéphalie de type 2 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- syndrome sapho ---
r_associated #0: 32 -->
en:mmih syndrome
n1=syndrome sapho | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=32
- Syndrome de Marfan ---
r_associated #0: 31 -->
en:mmih syndrome
n1=Syndrome de Marfan | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- anomalie d'Ebstein ---
r_associated #0: 31 -->
en:mmih syndrome
n1=anomalie d'Ebstein | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- dextrocardie ---
r_associated #0: 31 -->
en:mmih syndrome
n1=dextrocardie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- dysérythropoïèse congénitale ---
r_associated #0: 31 -->
en:mmih syndrome
n1=dysérythropoïèse congénitale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:Devergie's disease ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:Devergie's disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:Goltz syndrome ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:Goltz syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:Marfan's disease ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:Marfan's disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:abstinence syndrome ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:abstinence syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:albright's hereditary osteodystrophy ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:albright's hereditary osteodystrophy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:anterior plagiocephalies, synostotic ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:anterior plagiocephalies, synostotic | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:atrophic muscular disorder ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:atrophic muscular disorder | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:atypical hemolytic uremic syndrome ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:atypical hemolytic uremic syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:auditory perceptual disorder ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:auditory perceptual disorder | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:autosomal dominant congenital deafness with onychodystrophy ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:autosomal dominant congenital deafness with onychodystrophy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:carnitine palmitoyltransferase i deficiency ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:carnitine palmitoyltransferase i deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:congenital disorder of deglycosylation ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:congenital disorder of deglycosylation | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:congenital dyserythropoietic anemia ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:congenital dyserythropoietic anemia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:congenital structural myopathy ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:congenital structural myopathy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:crigler-najjar syndrome ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:crigler-najjar syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:d-glyceric aciduria ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:d-glyceric aciduria | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:deafness, autosomal recessive 49 ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:deafness, autosomal recessive 49 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:dentatorubral-pallidoluysian atrophy ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:dentatorubral-pallidoluysian atrophy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:didymosis aplasticosebacea ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:didymosis aplasticosebacea | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:feingold syndrome ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:feingold syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:fetal hydantoin syndrome ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:fetal hydantoin syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:fisher syndrome ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:fisher syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:gerstmann-straussler-scheinker disease ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:gerstmann-straussler-scheinker disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:hereditary angioedema ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:hereditary angioedema | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:hmg-coa lyase deficiency ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:hmg-coa lyase deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:hunter syndrome ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:hunter syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:hypohidrotic ectodermal dysplasia with immune deficiency ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:hypohidrotic ectodermal dysplasia with immune deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:insulin receptor mutation - associated insulin resistance syndromes ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:insulin receptor mutation - associated insulin resistance syndromes | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:kearns-sayre syndrome ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:kearns-sayre syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:kernicterus ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:kernicterus | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:lesch-nyhan syndrome ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:lesch-nyhan syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:malignant hyperthermia syndrome ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:malignant hyperthermia syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:maternal diabetes and deafness syndrome ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:maternal diabetes and deafness syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:maternal uniparental disomy chromosome 14 syndrome ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:maternal uniparental disomy chromosome 14 syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:melas syndrome ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:melas syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:melnick-fraser syndrome ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:melnick-fraser syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:mental retardation, autosomal recessive 34 ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:mental retardation, autosomal recessive 34 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:multicentric osteolysis, nodulosis, and arthropathy ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:multicentric osteolysis, nodulosis, and arthropathy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:nephrocalcinosis ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:nephrocalcinosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:palmar-plantar erythodysthesia ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:palmar-plantar erythodysthesia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:panuveitis ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:panuveitis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:peritoneal panniculitis ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:peritoneal panniculitis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:plasma kallikrein deficiency ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:plasma kallikrein deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:sandifer's syndrome ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:sandifer's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:simpson golabi behmel syndrome type 1 ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:simpson golabi behmel syndrome type 1 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:synpolydactyly ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:synpolydactyly | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:temporomandibular joint dysfunction syndrome ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:temporomandibular joint dysfunction syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:thyroid dysgenesis ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:thyroid dysgenesis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:vacterl association ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:vacterl association | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:wernicke-korsakoff syndrome ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:wernicke-korsakoff syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- en:xxxy and xxxxy syndrome ---
r_associated #0: 31 -->
en:mmih syndrome
n1=en:xxxy and xxxxy syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- exstrophie cloacale ---
r_associated #0: 31 -->
en:mmih syndrome
n1=exstrophie cloacale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- holoprosencéphalie familiale alobaire de type 1 ---
r_associated #0: 31 -->
en:mmih syndrome
n1=holoprosencéphalie familiale alobaire de type 1 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- ictère nucléaire ---
r_associated #0: 31 -->
en:mmih syndrome
n1=ictère nucléaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- lipodystrophie partielle familiale ---
r_associated #0: 31 -->
en:mmih syndrome
n1=lipodystrophie partielle familiale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- maladie de whipple ---
r_associated #0: 31 -->
en:mmih syndrome
n1=maladie de whipple | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- malformation d'Ebstein ---
r_associated #0: 31 -->
en:mmih syndrome
n1=malformation d'Ebstein | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- myokymie ---
r_associated #0: 31 -->
en:mmih syndrome
n1=myokymie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- myosites ---
r_associated #0: 31 -->
en:mmih syndrome
n1=myosites | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- néphrocalcinose ---
r_associated #0: 31 -->
en:mmih syndrome
n1=néphrocalcinose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- ostéopoecilie ---
r_associated #0: 31 -->
en:mmih syndrome
n1=ostéopoecilie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- pachyonychie congénitale de Jadassohn-Lewandowsky ---
r_associated #0: 31 -->
en:mmih syndrome
n1=pachyonychie congénitale de Jadassohn-Lewandowsky | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- panuvéite ---
r_associated #0: 31 -->
en:mmih syndrome
n1=panuvéite | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- paragonimiase ---
r_associated #0: 31 -->
en:mmih syndrome
n1=paragonimiase | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- paragonimose ---
r_associated #0: 31 -->
en:mmih syndrome
n1=paragonimose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- pemphigoïde bénigne des muqueuses ---
r_associated #0: 31 -->
en:mmih syndrome
n1=pemphigoïde bénigne des muqueuses | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- syndrome de Martin-Bell ---
r_associated #0: 31 -->
en:mmih syndrome
n1=syndrome de Martin-Bell | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- syndrome de Stilling-Türk-Duane ---
r_associated #0: 31 -->
en:mmih syndrome
n1=syndrome de Stilling-Türk-Duane | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- syndrome de malabsorption ---
r_associated #0: 31 -->
en:mmih syndrome
n1=syndrome de malabsorption | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=31
- Syndrome d'Alagille ---
r_associated #0: 30 -->
en:mmih syndrome
n1=Syndrome d'Alagille | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- aniridie, ataxie cérébelleuse et déficience mentale ---
r_associated #0: 30 -->
en:mmih syndrome
n1=aniridie, ataxie cérébelleuse et déficience mentale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- chondrodysplasie léthale avec brièveté des côtes ---
r_associated #0: 30 -->
en:mmih syndrome
n1=chondrodysplasie léthale avec brièveté des côtes | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- contractures congénitales et arachnodactylie ---
r_associated #0: 30 -->
en:mmih syndrome
n1=contractures congénitales et arachnodactylie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- cétoacidurie à chaînes ramifiées ---
r_associated #0: 30 -->
en:mmih syndrome
n1=cétoacidurie à chaînes ramifiées | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- dysostose enchondrale héréditaire ---
r_associated #0: 30 -->
en:mmih syndrome
n1=dysostose enchondrale héréditaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- déficit en biotinidase ---
r_associated #0: 30 -->
en:mmih syndrome
n1=déficit en biotinidase | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- déficit en cytochrome oxydase ---
r_associated #0: 30 -->
en:mmih syndrome
n1=déficit en cytochrome oxydase | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- déficit en cytochrome-c oxydase ---
r_associated #0: 30 -->
en:mmih syndrome
n1=déficit en cytochrome-c oxydase | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:Alice in wonderland Syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:Alice in wonderland Syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:Dercum's disease ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:Dercum's disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:Dubin-Sprinz disease ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:Dubin-Sprinz disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:Townes-Brocks syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:Townes-Brocks syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:and mental retardation ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:and mental retardation | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:andersen syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:andersen syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:arachnodactily ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:arachnodactily | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:behcet syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:behcet syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:cardiorenal syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:cardiorenal syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:chilblains ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:chilblains | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:combined lipase deficiency ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:combined lipase deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:complete trisomy 18 syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:complete trisomy 18 syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:complex regional pain syndrome i ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:complex regional pain syndrome i | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:congenital amegakaryocytic thrombocytopenia ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:congenital amegakaryocytic thrombocytopenia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:congenital cyst of bladder ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:congenital cyst of bladder | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:congenital dilatation of bladder ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:congenital dilatation of bladder | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:congenital porphyria ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:congenital porphyria | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:congenital uterovesical fistula ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:congenital uterovesical fistula | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:connexin 26 gene anomaly ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:connexin 26 gene anomaly | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:cytochrome-c oxidase deficiency ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:cytochrome-c oxidase deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:delayed foetal renal development ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:delayed foetal renal development | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:deletion 18p syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:deletion 18p syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:developmental fault ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:developmental fault | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:diencephalic syndrome of infancy ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:diencephalic syndrome of infancy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:diffuse infiltrative lymphocytosis syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:diffuse infiltrative lymphocytosis syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:digeorge syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:digeorge syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:dry eye syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:dry eye syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:ectrodactyly ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:ectrodactyly | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:ehlers-danlos syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:ehlers-danlos syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:episodic pain syndrome, familial, 3 ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:episodic pain syndrome, familial, 3 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:erythropoietic uroporphyria ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:erythropoietic uroporphyria | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:familial hypertrophic cardiomyopathy ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:familial hypertrophic cardiomyopathy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:fanconi syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:fanconi syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:felty syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:felty syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:glycogen storage disease ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:glycogen storage disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:griscelli syndrome type 2 ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:griscelli syndrome type 2 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:hand foot uterus syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:hand foot uterus syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:hantavirus pulmonary syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:hantavirus pulmonary syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:hypopituitarism ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:hypopituitarism | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:langer-giedion syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:langer-giedion syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:lipase hypersecretion syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:lipase hypersecretion syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:meconium plug syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:meconium plug syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:mobius syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:mobius syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:multiple congenital anomalies ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:multiple congenital anomalies | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:myotonic disorder ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:myotonic disorder | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:neuropathy, hereditary sensory and autonomic, type vii ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:neuropathy, hereditary sensory and autonomic, type vii | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:non-trisomic autosomal aneuploidy ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:non-trisomic autosomal aneuploidy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:obstructive sleep apnea syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:obstructive sleep apnea syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:odontogenesis imperfecta ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:odontogenesis imperfecta | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:onychoosteodysostosis ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:onychoosteodysostosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:osteopoecilia ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:osteopoecilia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:pain agnosia ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:pain agnosia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:pentalogy of cantrell ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:pentalogy of cantrell | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:perthes disease ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:perthes disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:pettigrew syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:pettigrew syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:progressive familial intrahepatic cholestasis ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:progressive familial intrahepatic cholestasis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:progressive supranuclear palsy ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:progressive supranuclear palsy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:pyruvate dehydrogenase deficiency ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:pyruvate dehydrogenase deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:sarcitis ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:sarcitis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:schinzel-giedion midface-retraction syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:schinzel-giedion midface-retraction syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:schwartz-jampel syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:schwartz-jampel syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:short rib-polydactyly syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:short rib-polydactyly syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:sids ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:sids | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:stevens-johnson syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:stevens-johnson syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:vertebral artery syndrome ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:vertebral artery syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- en:x-linked dominant hypophosphatemic rickets ---
r_associated #0: 30 -->
en:mmih syndrome
n1=en:x-linked dominant hypophosphatemic rickets | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- maladie de Perthes ---
r_associated #0: 30 -->
en:mmih syndrome
n1=maladie de Perthes | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- maladie de Tay-Sachs ---
r_associated #0: 30 -->
en:mmih syndrome
n1=maladie de Tay-Sachs | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- maladie de hurler ---
r_associated #0: 30 -->
en:mmih syndrome
n1=maladie de hurler | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- maladie du cri du chat ---
r_associated #0: 30 -->
en:mmih syndrome
n1=maladie du cri du chat | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- malformation ---
r_associated #0: 30 -->
en:mmih syndrome
n1=malformation | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- malformations congénitales du corps calleux ---
r_associated #0: 30 -->
en:mmih syndrome
n1=malformations congénitales du corps calleux | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- paralysie supranucléaire progressive ---
r_associated #0: 30 -->
en:mmih syndrome
n1=paralysie supranucléaire progressive | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- présentation sacro-iliaque droite antérieure ---
r_associated #0: 30 -->
en:mmih syndrome
n1=présentation sacro-iliaque droite antérieure | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- xanthique (lithiase) ---
r_associated #0: 30 -->
en:mmih syndrome
n1=xanthique (lithiase) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=30
- TPN ou NADP ---
r_associated #0: 29 -->
en:mmih syndrome
n1=TPN ou NADP | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- albinisme oculocutané de type mutant jaune ---
r_associated #0: 29 -->
en:mmih syndrome
n1=albinisme oculocutané de type mutant jaune | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- aniridie partielle avec agénésie rénale unilatérale et retard psychomoteur ---
r_associated #0: 29 -->
en:mmih syndrome
n1=aniridie partielle avec agénésie rénale unilatérale et retard psychomoteur | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:Stargardt disease ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:Stargardt disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:Williams syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:Williams syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:achenbach syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:achenbach syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:amyoplasia congenita ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:amyoplasia congenita | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:anasarca ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:anasarca | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:anhidrotic ectodermal dysplasia 1 ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:anhidrotic ectodermal dysplasia 1 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:apl differentiation syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:apl differentiation syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:autoimmune polyglandular syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:autoimmune polyglandular syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:autosomal dominant optic atrophy ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:autosomal dominant optic atrophy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:bardet-biedl syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:bardet-biedl syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:beare-stevenson cutis gyrata syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:beare-stevenson cutis gyrata syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:bernard-soulier syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:bernard-soulier syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:cervicocranial syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:cervicocranial syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:charge syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:charge syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:churg-strauss syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:churg-strauss syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:congenital inguinal hernia ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:congenital inguinal hernia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:cysticercus disease ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:cysticercus disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:darier disease ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:darier disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:deafness, autosomal recessive 28 ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:deafness, autosomal recessive 28 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:dihydropyrimidine dehydrogenase deficiency ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:dihydropyrimidine dehydrogenase deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:empty sella syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:empty sella syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:familial atypical hemolytic uremic syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:familial atypical hemolytic uremic syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:fish skin disease ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:fish skin disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:hyperganglionosis ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:hyperganglionosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:leprosary ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:leprosary | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:leri-weill dyschondrosteosis ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:leri-weill dyschondrosteosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:leriche syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:leriche syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:lig4 syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:lig4 syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:lubs x-linked mental retardation syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:lubs x-linked mental retardation syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:marfan's syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:marfan's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:meconium aspiration syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:meconium aspiration syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:mullerian-renal-cervical spine syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:mullerian-renal-cervical spine syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:neonatal progeroid syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:neonatal progeroid syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:nystagmus ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:nystagmus | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:papillon-lefevre syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:papillon-lefevre syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:pediatric terminology ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:pediatric terminology | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:periodic fever syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:periodic fever syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:persistent urogenital sinus ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:persistent urogenital sinus | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:potocki-shaffer syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:potocki-shaffer syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:potter syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:potter syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:pyramidal tract dysfunction ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:pyramidal tract dysfunction | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:renal coloboma syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:renal coloboma syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:reye syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:reye syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:rhizomelic dysplasia ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:rhizomelic dysplasia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:robinow syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:robinow syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:sanfilippo syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:sanfilippo syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:selective antibody deficiency with normal immunoglobulins ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:selective antibody deficiency with normal immunoglobulins | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:sunset syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:sunset syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:syndrome of apparent mineralocorticoid excess ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:syndrome of apparent mineralocorticoid excess | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:type a 14 ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:type a 14 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:uveomeningoencephalitic syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:uveomeningoencephalitic syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:williams syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:williams syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:wolf-hirschhorn syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:wolf-hirschhorn syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:xerophtalmy ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:xerophtalmy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- en:zollinger ellison syndrome ---
r_associated #0: 29 -->
en:mmih syndrome
n1=en:zollinger ellison syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- glycogénose ---
r_associated #0: 29 -->
en:mmih syndrome
n1=glycogénose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- maladie de dubin-johnson ---
r_associated #0: 29 -->
en:mmih syndrome
n1=maladie de dubin-johnson | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- syndrome de Williams ---
r_associated #0: 29 -->
en:mmih syndrome
n1=syndrome de Williams | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- syndrome de réaction inflammatoire généralisée ---
r_associated #0: 29 -->
en:mmih syndrome
n1=syndrome de réaction inflammatoire généralisée | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- une anomalie congénitale ---
r_associated #0: 29 -->
en:mmih syndrome
n1=une anomalie congénitale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=29
- aplasie de la paroi abdominale ---
r_associated #0: 28 -->
en:mmih syndrome
n1=aplasie de la paroi abdominale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- atransferrinémie ---
r_associated #0: 28 -->
en:mmih syndrome
n1=atransferrinémie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- cholestases intrahépatiques progressives familiales ---
r_associated #0: 28 -->
en:mmih syndrome
n1=cholestases intrahépatiques progressives familiales | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:Seitelberger's disease ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:Seitelberger's disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:Stevens-Johnson syndrome ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:Stevens-Johnson syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:achromatopsia ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:achromatopsia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:aicardi syndrome ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:aicardi syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:aniridia ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:aniridia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:anti-AIDS ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:anti-AIDS | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:aprosencephaly ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:aprosencephaly | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:ataxia-telangiectasisa-like disorder 1 ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:ataxia-telangiectasisa-like disorder 1 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:bartter syndrome ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:bartter syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:benign mucous membrane pemphigoid ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:benign mucous membrane pemphigoid | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:chorea ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:chorea | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:congenital cortical hyperostosis ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:congenital cortical hyperostosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:congenital pain insensitivity ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:congenital pain insensitivity | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:congenital prolapse of bladder ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:congenital prolapse of bladder | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:congenital ureterovesical junction obstruction ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:congenital ureterovesical junction obstruction | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:deletion 18q syndrome ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:deletion 18q syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:drug hypersensitivity syndrome ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:drug hypersensitivity syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:escobar syndrome ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:escobar syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:evans syndrome ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:evans syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:factor v leiden ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:factor v leiden | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:ferro-cerebro-cutaneous syndrome ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:ferro-cerebro-cutaneous syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:gargoylism ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:gargoylism | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:glutaric aciduria type 1 ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:glutaric aciduria type 1 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:hair tourniquet ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:hair tourniquet | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:hansenarium ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:hansenarium | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:liddle syndrome ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:liddle syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:maroteaux-lamy syndrome ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:maroteaux-lamy syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:mitochondrial dna depletion syndrome 12 ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:mitochondrial dna depletion syndrome 12 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:mucolipidosis type iii gamma ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:mucolipidosis type iii gamma | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:nephrotic syndrome ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:nephrotic syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:noma ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:noma | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:oeis complex ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:oeis complex | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:ossification of posterior longitudinal ligament ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:ossification of posterior longitudinal ligament | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:osteopoikilosis ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:osteopoikilosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:pelizaeus-merzbacher disease ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:pelizaeus-merzbacher disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:prune belly syndrome ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:prune belly syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:trigger finger disorder ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:trigger finger disorder | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- en:xyy syndrome ---
r_associated #0: 28 -->
en:mmih syndrome
n1=en:xyy syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=28
- Maladie de Whipple ---
r_associated #0: 27 -->
en:mmih syndrome
n1=Maladie de Whipple | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- Syndrome coronarien aigu ---
r_associated #0: 27 -->
en:mmih syndrome
n1=Syndrome coronarien aigu | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- acrodermatitis enteropathica ---
r_associated #0: 27 -->
en:mmih syndrome
n1=acrodermatitis enteropathica | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- choc toxique staphylococcique ---
r_associated #0: 27 -->
en:mmih syndrome
n1=choc toxique staphylococcique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- déficit congénital en mégacaryocytes ---
r_associated #0: 27 -->
en:mmih syndrome
n1=déficit congénital en mégacaryocytes | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:Degos's syndrome ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:Degos's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:Hurler's disease ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:Hurler's disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:Hurler's syndome ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:Hurler's syndome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:Sheehan's syndrome ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:Sheehan's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:adenine phosphoribosyltransferase deficiency ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:adenine phosphoribosyltransferase deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:alagille syndrome ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:alagille syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:alligator skin ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:alligator skin | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:brain iron accumulation type i syndrome ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:brain iron accumulation type i syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:congenital anomaly of abdominal wall ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:congenital anomaly of abdominal wall | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:congenital genitourinary tract anomalies nec ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:congenital genitourinary tract anomalies nec | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:congenital stenosis of large intestine ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:congenital stenosis of large intestine | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:cor triatriatum ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:cor triatriatum | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:eiken type chondrodysplasia ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:eiken type chondrodysplasia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:ellis-van creveld syndrome ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:ellis-van creveld syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:farber lipogranulomatosis ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:farber lipogranulomatosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:fatal familial insomnia ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:fatal familial insomnia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:fetal megacystis ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:fetal megacystis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:glucose-6-phosphate dehydrogenase deficiency ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:glucose-6-phosphate dehydrogenase deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:hereditary mucosal leukokeratosis ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:hereditary mucosal leukokeratosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:holocarboxylase synthetase deficiency ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:holocarboxylase synthetase deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:holt-oram syndrome ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:holt-oram syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:hydrops foetalis ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:hydrops foetalis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:hypoxaemia ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:hypoxaemia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:idiopathic hypersomnolence ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:idiopathic hypersomnolence | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:kenny-caffey syndrome type 2 ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:kenny-caffey syndrome type 2 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:kshv inflammatory cytokine syndrome ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:kshv inflammatory cytokine syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:leopard syndrome ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:leopard syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:lethal multiple pterygium syndrome ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:lethal multiple pterygium syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:lethal neonatal rigidity and multifocal seizure syndrome ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:lethal neonatal rigidity and multifocal seizure syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:long-chain acyl-coa dehydrogenase deficiency ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:long-chain acyl-coa dehydrogenase deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:malabsorption syndrome ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:malabsorption syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:meckel-gruber syndrome ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:meckel-gruber syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:menkes disease ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:menkes disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:myhre syndrome ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:myhre syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:myitis ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:myitis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:myokymia ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:myokymia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:neurotoxicity syndrome ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:neurotoxicity syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:orofacial cleft 1 ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:orofacial cleft 1 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:reversible posterior leukoencephalopathy syndrome ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:reversible posterior leukoencephalopathy syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:roberts syndrome ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:roberts syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:smith-magenis syndrome ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:smith-magenis syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:thyroid hormone resistance syndrome ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:thyroid hormone resistance syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:togaviridae infection ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:togaviridae infection | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:transposition of great vessels ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:transposition of great vessels | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:trisomy ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:trisomy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:trisomy 14 mosaicism ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:trisomy 14 mosaicism | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- en:waterhouse-friderichsen syndrome ---
r_associated #0: 27 -->
en:mmih syndrome
n1=en:waterhouse-friderichsen syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- fibromyalgie ---
r_associated #0: 27 -->
en:mmih syndrome
n1=fibromyalgie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- microdélétion 5q35 ---
r_associated #0: 27 -->
en:mmih syndrome
n1=microdélétion 5q35 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- syndrome de membrane hyaline ---
r_associated #0: 27 -->
en:mmih syndrome
n1=syndrome de membrane hyaline | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- trisomie ---
r_associated #0: 27 -->
en:mmih syndrome
n1=trisomie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=27
- Duane (syndrome de) ---
r_associated #0: 26 -->
en:mmih syndrome
n1=Duane (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- acromégalie, plis cutanés de la face et du cuir chevelu, et leucomes cornéens ---
r_associated #0: 26 -->
en:mmih syndrome
n1=acromégalie, plis cutanés de la face et du cuir chevelu, et leucomes cornéens | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- dysplasie campomélique ---
r_associated #0: 26 -->
en:mmih syndrome
n1=dysplasie campomélique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:Caffey's disease ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:Caffey's disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:achard syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:achard syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:achondrogenesis ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:achondrogenesis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:aids ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:aids | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:alstrom syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:alstrom syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:antithrombin iii deficiency ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:antithrombin iii deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:campomelic dwarfism ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:campomelic dwarfism | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:campomelic dysplasia ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:campomelic dysplasia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:carbohydrate-deficient glycoprotein syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:carbohydrate-deficient glycoprotein syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:choroideremia ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:choroideremia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:chromosome 2q37 deletion syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:chromosome 2q37 deletion syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:coloboma and anal atresia syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:coloboma and anal atresia syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:compartment syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:compartment syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:complete trisomy 13 syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:complete trisomy 13 syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:congenital digestive system disorder ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:congenital digestive system disorder | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:dialyzer first use syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:dialyzer first use syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:distal monosomy 10q syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:distal monosomy 10q syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:dysfunctional elimination syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:dysfunctional elimination syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:familial juvenile nephronophthisis ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:familial juvenile nephronophthisis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:hallermann syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:hallermann syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:hard skin syndrome parana type ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:hard skin syndrome parana type | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:hematomphalus ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:hematomphalus | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:idiopathic congenital megacolon (disorder) ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:idiopathic congenital megacolon (disorder) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:kimura disease ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:kimura disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:kleine-levin syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:kleine-levin syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:lazar-house ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:lazar-house | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:leper colony ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:leper colony | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:levocardia ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:levocardia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:li-fraumeni syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:li-fraumeni syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:meckel diverticulitis ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:meckel diverticulitis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:mental retardation, autosomal dominant 9 ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:mental retardation, autosomal dominant 9 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:monosomy 13q syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:monosomy 13q syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:morquio syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:morquio syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:neoplastic syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:neoplastic syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:netherton syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:netherton syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:noonan syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:noonan syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:opitz g/bbb syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:opitz g/bbb syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:overgrowth syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:overgrowth syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:pierre robin syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:pierre robin syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:primary carnitine deficiency ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:primary carnitine deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:pseudoachondroplasia ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:pseudoachondroplasia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:pseudotumor cerebri ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:pseudotumor cerebri | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:scheie syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:scheie syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:sjogren-larsson syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:sjogren-larsson syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:sudden infant death ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:sudden infant death | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:tissue kallikrein deficiency ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:tissue kallikrein deficiency | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:tolosa-hunt syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:tolosa-hunt syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:treacher collins syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:treacher collins syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:triploidy syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:triploidy syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- en:twiddler's syndrome ---
r_associated #0: 26 -->
en:mmih syndrome
n1=en:twiddler's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- insuffisance respiratoire, problème respiratoire ---
r_associated #0: 26 -->
en:mmih syndrome
n1=insuffisance respiratoire, problème respiratoire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- lévocardie ---
r_associated #0: 26 -->
en:mmih syndrome
n1=lévocardie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- maladie de dercum ---
r_associated #0: 26 -->
en:mmih syndrome
n1=maladie de dercum | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- syndrome de la selle turcique vide ---
r_associated #0: 26 -->
en:mmih syndrome
n1=syndrome de la selle turcique vide | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- vessie ---
r_associated #0: 26 -->
en:mmih syndrome
n1=vessie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=26
- Hölmgren (triade de) ---
r_associated #0: 25 -->
en:mmih syndrome
n1=Hölmgren (triade de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- Kawasaki (maladie de) ---
r_associated #0: 25 -->
en:mmih syndrome
n1=Kawasaki (maladie de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- Maladie héréditaire ---
r_associated #0: 25 -->
en:mmih syndrome
n1=Maladie héréditaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- Seitelberger (dystrophie neuroaxonale de) ---
r_associated #0: 25 -->
en:mmih syndrome
n1=Seitelberger (dystrophie neuroaxonale de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- albinisme avec pigmentation minime ---
r_associated #0: 25 -->
en:mmih syndrome
n1=albinisme avec pigmentation minime | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- brides amniotiques (syndrome des) ---
r_associated #0: 25 -->
en:mmih syndrome
n1=brides amniotiques (syndrome des) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- choc toxique ---
r_associated #0: 25 -->
en:mmih syndrome
n1=choc toxique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- crosse aortique(syndrome de la) ---
r_associated #0: 25 -->
en:mmih syndrome
n1=crosse aortique(syndrome de la) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- dysostose crâniofaciale ---
r_associated #0: 25 -->
en:mmih syndrome
n1=dysostose crâniofaciale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- dysplasie olfactogénitale ---
r_associated #0: 25 -->
en:mmih syndrome
n1=dysplasie olfactogénitale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- en:Alagille's syndrome ---
r_associated #0: 25 -->
en:mmih syndrome
n1=en:Alagille's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- en:Angelman's syndrome ---
r_associated #0: 25 -->
en:mmih syndrome
n1=en:Angelman's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- en:Gitelman syndrome ---
r_associated #0: 25 -->
en:mmih syndrome
n1=en:Gitelman syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- en:Hebra's pityriasis ---
r_associated #0: 25 -->
en:mmih syndrome
n1=en:Hebra's pityriasis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- en:Köbberling's syndrome ---
r_associated #0: 25 -->
en:mmih syndrome
n1=en:Köbberling's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- en:Stein-Leventhal syndrome ---
r_associated #0: 25 -->
en:mmih syndrome
n1=en:Stein-Leventhal syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- en:Wegener granulomatosis ---
r_associated #0: 25 -->
en:mmih syndrome
n1=en:Wegener granulomatosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- en:bloom syndrome ---
r_associated #0: 25 -->
en:mmih syndrome
n1=en:bloom syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- en:cartilage hair hypoplasia ---
r_associated #0: 25 -->
en:mmih syndrome
n1=en:cartilage hair hypoplasia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- en:central sleep apnea syndrome ---
r_associated #0: 25 -->
en:mmih syndrome
n1=en:central sleep apnea syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- en:chondrodystrophia punctata ---
r_associated #0: 25 -->
en:mmih syndrome
n1=en:chondrodystrophia punctata | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- en:congenital central hypoventilation ---
r_associated #0: 25 -->
en:mmih syndrome
n1=en:congenital central hypoventilation | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- en:congenital hernia ---
r_associated #0: 25 -->
en:mmih syndrome
n1=en:congenital hernia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- en:cysticercal disease ---
r_associated #0: 25 -->
en:mmih syndrome
n1=en:cysticercal disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- en:dactylolysis spontanea ---
r_associated #0: 25 -->
en:mmih syndrome
n1=en:dactylolysis spontanea | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- en:ectromelia ---
r_associated #0: 25 -->
en:mmih syndrome
n1=en:ectromelia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- en:exumbilication ---
r_associated #0: 25 -->
en:mmih syndrome
n1=en:exumbilication | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- en:hereditary illness ---
r_associated #0: 25 -->
en:mmih syndrome
n1=en:hereditary illness | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- en:hypothalamic hamartoblastoma ---
r_associated #0: 25 -->
en:mmih syndrome
n1=en:hypothalamic hamartoblastoma | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- en:proctatresia ---
r_associated #0: 25 -->
en:mmih syndrome
n1=en:proctatresia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- en:sjogren syndrome ---
r_associated #0: 25 -->
en:mmih syndrome
n1=en:sjogren syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- granulomatose éosinophilique avec polyangéite ---
r_associated #0: 25 -->
en:mmih syndrome
n1=granulomatose éosinophilique avec polyangéite | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- hypogonadisme avec anosmie ---
r_associated #0: 25 -->
en:mmih syndrome
n1=hypogonadisme avec anosmie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- lichen ruber acuminatus ---
r_associated #0: 25 -->
en:mmih syndrome
n1=lichen ruber acuminatus | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=25
- DUGV ---
r_associated #0: 24 -->
en:mmih syndrome
n1=DUGV | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- SRAS ---
r_associated #0: 24 -->
en:mmih syndrome
n1=SRAS | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- en:Donohue syndrome ---
r_associated #0: 24 -->
en:mmih syndrome
n1=en:Donohue syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- en:Marburg virus disease ---
r_associated #0: 24 -->
en:mmih syndrome
n1=en:Marburg virus disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- en:Martin-Bell's syndrome ---
r_associated #0: 24 -->
en:mmih syndrome
n1=en:Martin-Bell's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- en:Waterhouse-Friderichsen syndrome ---
r_associated #0: 24 -->
en:mmih syndrome
n1=en:Waterhouse-Friderichsen syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- en:anal imperforation ---
r_associated #0: 24 -->
en:mmih syndrome
n1=en:anal imperforation | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- en:basilar artery syndrome ---
r_associated #0: 24 -->
en:mmih syndrome
n1=en:basilar artery syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- en:capgras syndrome ---
r_associated #0: 24 -->
en:mmih syndrome
n1=en:capgras syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- en:cystinuria ---
r_associated #0: 24 -->
en:mmih syndrome
n1=en:cystinuria | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- en:cytokine release syndrome ---
r_associated #0: 24 -->
en:mmih syndrome
n1=en:cytokine release syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- en:diffuse cerebral sclerosis of schilder ---
r_associated #0: 24 -->
en:mmih syndrome
n1=en:diffuse cerebral sclerosis of schilder | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- en:ichthyosis vera ---
r_associated #0: 24 -->
en:mmih syndrome
n1=en:ichthyosis vera | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- en:inherited disease ---
r_associated #0: 24 -->
en:mmih syndrome
n1=en:inherited disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- en:leprosarium ---
r_associated #0: 24 -->
en:mmih syndrome
n1=en:leprosarium | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- en:toxemia ---
r_associated #0: 24 -->
en:mmih syndrome
n1=en:toxemia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- en:turner syndrome ---
r_associated #0: 24 -->
en:mmih syndrome
n1=en:turner syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- en:umbilical malformation ---
r_associated #0: 24 -->
en:mmih syndrome
n1=en:umbilical malformation | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- en:zinc-deficiency type ---
r_associated #0: 24 -->
en:mmih syndrome
n1=en:zinc-deficiency type | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- hémicéphalie ---
r_associated #0: 24 -->
en:mmih syndrome
n1=hémicéphalie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- paragangliome (mise en évidence scintigraphique du) ---
r_associated #0: 24 -->
en:mmih syndrome
n1=paragangliome (mise en évidence scintigraphique du) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- pemphigus bénin des muqueuses ---
r_associated #0: 24 -->
en:mmih syndrome
n1=pemphigus bénin des muqueuses | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- psychose de Korsakoff ---
r_associated #0: 24 -->
en:mmih syndrome
n1=psychose de Korsakoff | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- souffrance respiratoire ---
r_associated #0: 24 -->
en:mmih syndrome
n1=souffrance respiratoire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- syndrome d'alagille ---
r_associated #0: 24 -->
en:mmih syndrome
n1=syndrome d'alagille | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- syndrome de Joubert-Boltshauser (syndrome de) ---
r_associated #0: 24 -->
en:mmih syndrome
n1=syndrome de Joubert-Boltshauser (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=24
- Goltz (syndrome de) ---
r_associated #0: 23 -->
en:mmih syndrome
n1=Goltz (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=23
- Marfan (maladie de) ---
r_associated #0: 23 -->
en:mmih syndrome
n1=Marfan (maladie de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=23
- albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception ---
r_associated #0: 23 -->
en:mmih syndrome
n1=albinisme oculocutané avec mèches noires, troubles intestinaux et surdité congénitale de perception | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=23
- anasarque f?toplacentaire ---
r_associated #0: 23 -->
en:mmih syndrome
n1=anasarque f?toplacentaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=23
- aniridie, microcornée et cataracte régressive ---
r_associated #0: 23 -->
en:mmih syndrome
n1=aniridie, microcornée et cataracte régressive | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=23
- en:CDA ---
r_associated #0: 23 -->
en:mmih syndrome
n1=en:CDA | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=23
- en:FPLD ---
r_associated #0: 23 -->
en:mmih syndrome
n1=en:FPLD | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=23
- en:Günther's disease ---
r_associated #0: 23 -->
en:mmih syndrome
n1=en:Günther's disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=23
- en:Laurence-Moon's syndrome ---
r_associated #0: 23 -->
en:mmih syndrome
n1=en:Laurence-Moon's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=23
- en:Seitelberger's neuroaxonal dystrophy ---
r_associated #0: 23 -->
en:mmih syndrome
n1=en:Seitelberger's neuroaxonal dystrophy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=23
- en:chediak-higashi syndrome ---
r_associated #0: 23 -->
en:mmih syndrome
n1=en:chediak-higashi syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=23
- en:craniostenosis ---
r_associated #0: 23 -->
en:mmih syndrome
n1=en:craniostenosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=23
- en:hand and foot deformity ---
r_associated #0: 23 -->
en:mmih syndrome
n1=en:hand and foot deformity | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=23
- en:organic brain syndrome ---
r_associated #0: 23 -->
en:mmih syndrome
n1=en:organic brain syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=23
- en:umbilical hiatus ---
r_associated #0: 23 -->
en:mmih syndrome
n1=en:umbilical hiatus | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=23
- en:yellow nail ---
r_associated #0: 23 -->
en:mmih syndrome
n1=en:yellow nail | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=23
- porphyrie (anesthésie chez un patient atteint de) ---
r_associated #0: 23 -->
en:mmih syndrome
n1=porphyrie (anesthésie chez un patient atteint de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=23
- syndrome de Zellweger ---
r_associated #0: 23 -->
en:mmih syndrome
n1=syndrome de Zellweger | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=23
- syndrome de sevrage ---
r_associated #0: 23 -->
en:mmih syndrome
n1=syndrome de sevrage | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=23
- Maladie de Tay-Sachs ---
r_associated #0: 22 -->
en:mmih syndrome
n1=Maladie de Tay-Sachs | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=22
- S.I.D.A ---
r_associated #0: 22 -->
en:mmih syndrome
n1=S.I.D.A | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=22
- dégénérescence wallérienne ---
r_associated #0: 22 -->
en:mmih syndrome
n1=dégénérescence wallérienne | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=22
- en:Dubin-Johnson's syndrome ---
r_associated #0: 22 -->
en:mmih syndrome
n1=en:Dubin-Johnson's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=22
- en:Feingold syndrome ---
r_associated #0: 22 -->
en:mmih syndrome
n1=en:Feingold syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=22
- en:Fox-Fordyce disease ---
r_associated #0: 22 -->
en:mmih syndrome
n1=en:Fox-Fordyce disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=22
- en:Leriche syndrome ---
r_associated #0: 22 -->
en:mmih syndrome
n1=en:Leriche syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=22
- en:antiphospholipid syndrome ---
r_associated #0: 22 -->
en:mmih syndrome
n1=en:antiphospholipid syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=22
- en:cleft lip and palate ---
r_associated #0: 22 -->
en:mmih syndrome
n1=en:cleft lip and palate | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=22
- en:cryopyrin-associated periodic syndrome ---
r_associated #0: 22 -->
en:mmih syndrome
n1=en:cryopyrin-associated periodic syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=22
- en:developmental anomaly ---
r_associated #0: 22 -->
en:mmih syndrome
n1=en:developmental anomaly | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=22
- en:eisenmenger syndrome ---
r_associated #0: 22 -->
en:mmih syndrome
n1=en:eisenmenger syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=22
- en:gastroschisis ---
r_associated #0: 22 -->
en:mmih syndrome
n1=en:gastroschisis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=22
- en:premenstrual syndrome ---
r_associated #0: 22 -->
en:mmih syndrome
n1=en:premenstrual syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=22
- en:tourette syndrome ---
r_associated #0: 22 -->
en:mmih syndrome
n1=en:tourette syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=22
- selle turcique vide ---
r_associated #0: 22 -->
en:mmih syndrome
n1=selle turcique vide | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=22
- syndrome hémolytique et urémique atypique ---
r_associated #0: 22 -->
en:mmih syndrome
n1=syndrome hémolytique et urémique atypique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=22
- FMD ---
r_associated #0: 21 -->
en:mmih syndrome
n1=FMD | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- Jacobsen (syndrome de) ---
r_associated #0: 21 -->
en:mmih syndrome
n1=Jacobsen (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- acatalasémie ---
r_associated #0: 21 -->
en:mmih syndrome
n1=acatalasémie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- acidurie argininosuccinique ---
r_associated #0: 21 -->
en:mmih syndrome
n1=acidurie argininosuccinique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- adipose douloureuse de Dercum ---
r_associated #0: 21 -->
en:mmih syndrome
n1=adipose douloureuse de Dercum | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- alcaptonurie ---
r_associated #0: 21 -->
en:mmih syndrome
n1=alcaptonurie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- aniridie ---
r_associated #0: 21 -->
en:mmih syndrome
n1=aniridie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- argininémie ---
r_associated #0: 21 -->
en:mmih syndrome
n1=argininémie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- calciphylaxie ---
r_associated #0: 21 -->
en:mmih syndrome
n1=calciphylaxie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- cholestase intrahépatique progressive familiale de type 1 ---
r_associated #0: 21 -->
en:mmih syndrome
n1=cholestase intrahépatique progressive familiale de type 1 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- choroïdérémie ---
r_associated #0: 21 -->
en:mmih syndrome
n1=choroïdérémie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- coproporphyrie héréditaire ---
r_associated #0: 21 -->
en:mmih syndrome
n1=coproporphyrie héréditaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- en:abetalipoproteinemia ---
r_associated #0: 21 -->
en:mmih syndrome
n1=en:abetalipoproteinemia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- en:acute respiratory distress ---
r_associated #0: 21 -->
en:mmih syndrome
n1=en:acute respiratory distress | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- en:anaerosis ---
r_associated #0: 21 -->
en:mmih syndrome
n1=en:anaerosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- en:brown-sequard syndrome ---
r_associated #0: 21 -->
en:mmih syndrome
n1=en:brown-sequard syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- en:cutis laxa ---
r_associated #0: 21 -->
en:mmih syndrome
n1=en:cutis laxa | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- en:megaloglossia ---
r_associated #0: 21 -->
en:mmih syndrome
n1=en:megaloglossia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- hypopituitarisme ---
r_associated #0: 21 -->
en:mmih syndrome
n1=hypopituitarisme | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- idiosyncrasie au fructose ---
r_associated #0: 21 -->
en:mmih syndrome
n1=idiosyncrasie au fructose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- odontogénèse imparfaite ---
r_associated #0: 21 -->
en:mmih syndrome
n1=odontogénèse imparfaite | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- syndrome cardio-facio-cutané ---
r_associated #0: 21 -->
en:mmih syndrome
n1=syndrome cardio-facio-cutané | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- syndrome de Churg-Strauss ---
r_associated #0: 21 -->
en:mmih syndrome
n1=syndrome de Churg-Strauss | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- syndrome de Prader-Willi ---
r_associated #0: 21 -->
en:mmih syndrome
n1=syndrome de Prader-Willi | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- syndrome des ongles jaunes ---
r_associated #0: 21 -->
en:mmih syndrome
n1=syndrome des ongles jaunes | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- triskélion ---
r_associated #0: 21 -->
en:mmih syndrome
n1=triskélion | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- xérophtalmie ---
r_associated #0: 21 -->
en:mmih syndrome
n1=xérophtalmie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=21
- ARTHROGRYPOSE ---
r_associated #0: 20 -->
en:mmih syndrome
n1=ARTHROGRYPOSE | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=20
- dysplasie olfactogénitale de De Morsier ---
r_associated #0: 20 -->
en:mmih syndrome
n1=dysplasie olfactogénitale de De Morsier | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=20
- syndrome ---
r_associated #0: 20 -->
en:mmih syndrome
n1=syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=20
- triploïdie ---
r_associated #0: 16 -->
en:mmih syndrome
n1=triploïdie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=16
- trisomie 21 ---
r_associated #0: 16 -->
en:mmih syndrome
n1=trisomie 21 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=16
- Albert (position d') ---
r_associated #0: 15 -->
en:mmih syndrome
n1=Albert (position d') | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- Anomalie d'Ebstein ---
r_associated #0: 15 -->
en:mmih syndrome
n1=Anomalie d'Ebstein | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- Arthrogrypose ---
r_associated #0: 15 -->
en:mmih syndrome
n1=Arthrogrypose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- Détresse respiratoire ---
r_associated #0: 15 -->
en:mmih syndrome
n1=Détresse respiratoire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- Giessen (test de) ---
r_associated #0: 15 -->
en:mmih syndrome
n1=Giessen (test de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- Intolérance au fructose ---
r_associated #0: 15 -->
en:mmih syndrome
n1=Intolérance au fructose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- Kallman ---
r_associated #0: 15 -->
en:mmih syndrome
n1=Kallman | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- Maladie de Marfan ---
r_associated #0: 15 -->
en:mmih syndrome
n1=Maladie de Marfan | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- Maladie génétique ---
r_associated #0: 15 -->
en:mmih syndrome
n1=Maladie génétique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- Malformation congénitale ---
r_associated #0: 15 -->
en:mmih syndrome
n1=Malformation congénitale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- Noma ---
r_associated #0: 15 -->
en:mmih syndrome
n1=Noma | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- Syndrome d'immunodéficience acquise ---
r_associated #0: 15 -->
en:mmih syndrome
n1=Syndrome d'immunodéficience acquise | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- Syndrome de Walker-Warburg ---
r_associated #0: 15 -->
en:mmih syndrome
n1=Syndrome de Walker-Warburg | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- Syndrome de sevrage ---
r_associated #0: 15 -->
en:mmih syndrome
n1=Syndrome de sevrage | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- acidoses lactiques (classification selon Cohen et Woods) ---
r_associated #0: 15 -->
en:mmih syndrome
n1=acidoses lactiques (classification selon Cohen et Woods) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- agglutinines froides (neuropathie à) ---
r_associated #0: 15 -->
en:mmih syndrome
n1=agglutinines froides (neuropathie à) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- cysticercoïde (larve) ---
r_associated #0: 15 -->
en:mmih syndrome
n1=cysticercoïde (larve) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- dysembryome (bénin, malin) ---
r_associated #0: 15 -->
en:mmih syndrome
n1=dysembryome (bénin, malin) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- dégénérescence wallerienne ---
r_associated #0: 15 -->
en:mmih syndrome
n1=dégénérescence wallerienne | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- démence (sémiologie) ---
r_associated #0: 15 -->
en:mmih syndrome
n1=démence (sémiologie) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- goltz ---
r_associated #0: 15 -->
en:mmih syndrome
n1=goltz | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- iceberg (signe de l') ---
r_associated #0: 15 -->
en:mmih syndrome
n1=iceberg (signe de l') | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- maladie à virus de marburg ---
r_associated #0: 15 -->
en:mmih syndrome
n1=maladie à virus de marburg | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- malentendant (enfant) ---
r_associated #0: 15 -->
en:mmih syndrome
n1=malentendant (enfant) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- osteopœcilie ---
r_associated #0: 15 -->
en:mmih syndrome
n1=osteopœcilie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- syndrome de Kallman-de Morsier ---
r_associated #0: 15 -->
en:mmih syndrome
n1=syndrome de Kallman-de Morsier | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- syndrome de Korsakoff ---
r_associated #0: 15 -->
en:mmih syndrome
n1=syndrome de Korsakoff | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- syndrome de Plummer-VInson ---
r_associated #0: 15 -->
en:mmih syndrome
n1=syndrome de Plummer-VInson | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- syndrome de de Morsier-Kallmann ---
r_associated #0: 15 -->
en:mmih syndrome
n1=syndrome de de Morsier-Kallmann | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- triple arthrodèse ---
r_associated #0: 15 -->
en:mmih syndrome
n1=triple arthrodèse | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- triple opération à la française ---
r_associated #0: 15 -->
en:mmih syndrome
n1=triple opération à la française | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- triptans ---
r_associated #0: 15 -->
en:mmih syndrome
n1=triptans | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- triquétrum ---
r_associated #0: 15 -->
en:mmih syndrome
n1=triquétrum | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- triradialis sulcus de Turner ---
r_associated #0: 15 -->
en:mmih syndrome
n1=triradialis sulcus de Turner | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- tris ---
r_associated #0: 15 -->
en:mmih syndrome
n1=tris | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- trismus ---
r_associated #0: 15 -->
en:mmih syndrome
n1=trismus | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- trisomie du bras court du chromosome 3 ---
r_associated #0: 15 -->
en:mmih syndrome
n1=trisomie du bras court du chromosome 3 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- xérophthalmie ---
r_associated #0: 15 -->
en:mmih syndrome
n1=xérophthalmie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=15
- aprosencéphalie ---
r_associated #0: 11 -->
en:mmih syndrome
n1=aprosencéphalie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=11
- dysautonomie familiale ---
r_associated #0: 11 -->
en:mmih syndrome
n1=dysautonomie familiale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=11
- insomnie familiale fatale ---
r_associated #0: 11 -->
en:mmih syndrome
n1=insomnie familiale fatale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=11
- lepréchaunisme ---
r_associated #0: 11 -->
en:mmih syndrome
n1=lepréchaunisme | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=11
- maladie de Fox-Fordyce ---
r_associated #0: 11 -->
en:mmih syndrome
n1=maladie de Fox-Fordyce | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=11
- mongolisme ---
r_associated #0: 11 -->
en:mmih syndrome
n1=mongolisme | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=11
- syndrome de Gitelman ---
r_associated #0: 11 -->
en:mmih syndrome
n1=syndrome de Gitelman | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=11
- syndrome de Warburg ---
r_associated #0: 11 -->
en:mmih syndrome
n1=syndrome de Warburg | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=11
- Acromégalie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Acromégalie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Agnosie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Agnosie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Albinisme ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Albinisme | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Alice au pays des merveilles (syndrome d') ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Alice au pays des merveilles (syndrome d') | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Anencéphalie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Anencéphalie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Angelman (syndrome d') ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Angelman (syndrome d') | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- CONGÉNITALE ---
r_associated #0: 10 -->
en:mmih syndrome
n1=CONGÉNITALE | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Cataplexie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Cataplexie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Craniosynostose ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Craniosynostose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Cysticercose ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Cysticercose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Côlon ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Côlon | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Dercum (maladie de) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Dercum (maladie de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Dubin-Johnson (syndrome de) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Dubin-Johnson (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Dugbe (virus) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Dugbe (virus) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Fibromyalgie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Fibromyalgie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Glycogénose ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Glycogénose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- HLP3 ---
r_associated #0: 10 -->
en:mmih syndrome
n1=HLP3 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- HPE3 ---
r_associated #0: 10 -->
en:mmih syndrome
n1=HPE3 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- HPE4 ---
r_associated #0: 10 -->
en:mmih syndrome
n1=HPE4 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Haltia-Santavuori (maladie de) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Haltia-Santavuori (maladie de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Hernie ombilicale ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Hernie ombilicale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Hurler (maladie de) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Hurler (maladie de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Hypopituitarisme ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Hypopituitarisme | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Hypoxémie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Hypoxémie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Insler et Bernstein (score cervical d') ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Insler et Bernstein (score cervical d') | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Laurence-Moon (syndrome de) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Laurence-Moon (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Levine-Critchley (syndrome de) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Levine-Critchley (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Lisfranc (fracture de) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Lisfranc (fracture de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Léproserie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Léproserie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Macroglossie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Macroglossie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Maladie de Kawasaki ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Maladie de Kawasaki | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Malformation ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Malformation | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Malformation d'Ebstein ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Malformation d'Ebstein | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Marburg (fièvre de) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Marburg (fièvre de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Martin-Bell (syndrome de) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Martin-Bell (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Mort subite du nourrisson ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Mort subite du nourrisson | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Myosite ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Myosite | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- PMDS ---
r_associated #0: 10 -->
en:mmih syndrome
n1=PMDS | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- PMI gene ---
r_associated #0: 10 -->
en:mmih syndrome
n1=PMI gene | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Panum (aire de) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Panum (aire de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Peste noire ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Peste noire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Pitt-Rogers-Danks (syndrome de) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Pitt-Rogers-Danks (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Progéria ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Progéria | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Sheehan (syndrome de) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Sheehan (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Shy-Drager (syndrome de) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Shy-Drager (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Sicard (opération de) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Sicard (opération de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Sipple (syndrome de) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Sipple (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Situs inversus ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Situs inversus | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Stargardt (maladie de ) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Stargardt (maladie de ) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Stilling-Türk-Duane (syndrome de) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Stilling-Türk-Duane (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Syndrome d'Immunodéficience Acquise ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Syndrome d'Immunodéficience Acquise | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Syndrome de Churg-Strauss ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Syndrome de Churg-Strauss | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Syndrome de Prader-Willi ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Syndrome de Prader-Willi | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Syndrome de Sheehan ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Syndrome de Sheehan | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Syndrome de Sotos ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Syndrome de Sotos | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Syndrome de détresse respiratoire ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Syndrome de détresse respiratoire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Syndrome de malabsorption ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Syndrome de malabsorption | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Syndrome du choc toxique ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Syndrome du choc toxique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Syndrome métabolique ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Syndrome métabolique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Townes-Brocks (syndrome de) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Townes-Brocks (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Trichothiodystrophie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Trichothiodystrophie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Trisomie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Trisomie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Vogt-Koyanagi-Harada (syndrome de) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Vogt-Koyanagi-Harada (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Wegener (granulomatose de) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Wegener (granulomatose de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- Yellen-Gomco (clamp de) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=Yellen-Gomco (clamp de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- a-bêta-lipoprotéinémie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=a-bêta-lipoprotéinémie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- achondrogénèses ---
r_associated #0: 10 -->
en:mmih syndrome
n1=achondrogénèses | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- achromatopsie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=achromatopsie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- alcalose métabolique (classification) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=alcalose métabolique (classification) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- allocations ---
r_associated #0: 10 -->
en:mmih syndrome
n1=allocations | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- angl. TBS ---
r_associated #0: 10 -->
en:mmih syndrome
n1=angl. TBS | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- angl. XLSA/A ---
r_associated #0: 10 -->
en:mmih syndrome
n1=angl. XLSA/A | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- aniline (intoxication par l') ---
r_associated #0: 10 -->
en:mmih syndrome
n1=aniline (intoxication par l') | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- association de tics vocaux et tics moteurs du syndrome de gilles de la tourette ---
r_associated #0: 10 -->
en:mmih syndrome
n1=association de tics vocaux et tics moteurs du syndrome de gilles de la tourette | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- chondrodysplasie ponctuée ---
r_associated #0: 10 -->
en:mmih syndrome
n1=chondrodysplasie ponctuée | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- coproantigènes (recherche de) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=coproantigènes (recherche de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- cutis laxa ---
r_associated #0: 10 -->
en:mmih syndrome
n1=cutis laxa | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- distance interpédiculaire (mesure de la) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=distance interpédiculaire (mesure de la) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- dysplasie frontométaphysaire ---
r_associated #0: 10 -->
en:mmih syndrome
n1=dysplasie frontométaphysaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- dysplasie génitale ---
r_associated #0: 10 -->
en:mmih syndrome
n1=dysplasie génitale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- dysplasie iridodentaire ---
r_associated #0: 10 -->
en:mmih syndrome
n1=dysplasie iridodentaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- ectodermitis erosiva pluriorificialis ---
r_associated #0: 10 -->
en:mmih syndrome
n1=ectodermitis erosiva pluriorificialis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- ectodermose ---
r_associated #0: 10 -->
en:mmih syndrome
n1=ectodermose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- ectodermose érosive pluriorificielle de Fiessinger-Rendu ---
r_associated #0: 10 -->
en:mmih syndrome
n1=ectodermose érosive pluriorificielle de Fiessinger-Rendu | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- ectoenzyme ---
r_associated #0: 10 -->
en:mmih syndrome
n1=ectoenzyme | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- ectomie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=ectomie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- ectomorphie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=ectomorphie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- ectoparasite ---
r_associated #0: 10 -->
en:mmih syndrome
n1=ectoparasite | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- ectoparasitose ---
r_associated #0: 10 -->
en:mmih syndrome
n1=ectoparasitose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- ectopie cardiaque ---
r_associated #0: 10 -->
en:mmih syndrome
n1=ectopie cardiaque | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- ectopie des procès ciliaires ---
r_associated #0: 10 -->
en:mmih syndrome
n1=ectopie des procès ciliaires | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- ectopie du cristallin ---
r_associated #0: 10 -->
en:mmih syndrome
n1=ectopie du cristallin | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:5p minus syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:5p minus syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:5q microdeletion ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:5q microdeletion | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Albert's position ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Albert's position | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Albright's hereditary osteodystrophy ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Albright's hereditary osteodystrophy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Cogan-Reese syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Cogan-Reese syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Colon ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Colon | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Crouzon's disease ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Crouzon's disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Crouzon?s disease ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Crouzon?s disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Down's ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Down's | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Down's syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Down's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:FrontoMetaphyseal Dysplasia ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:FrontoMetaphyseal Dysplasia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Harada's disease ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Harada's disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Holt-Oram syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Holt-Oram syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Jadassohn-Lewandowsky syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Jadassohn-Lewandowsky syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Korsakoff''s syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Korsakoff''s syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Korsakoff's syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Korsakoff's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:LEOPARD syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:LEOPARD syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Lejeune's syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Lejeune's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:MELAS syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:MELAS syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:NHSA III ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:NHSA III | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:PWS ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:PWS | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Perthes' disease ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Perthes' disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Riley-Day's syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Riley-Day's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Schmorl's jaundice ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Schmorl's jaundice | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Schridde's disease ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Schridde's disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Shy-Drager's syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Shy-Drager's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Smith-Magenis syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Smith-Magenis syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Sotos's syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Sotos's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Stilling-Türk-Duane's syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Stilling-Türk-Duane's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Tay Sachs' disease ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Tay Sachs' disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Vogt Koyanagi Harada's syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Vogt Koyanagi Harada's syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:WBS ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:WBS | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Williams' syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Williams' syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:Williams-Beuren syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:Williams-Beuren syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:abdominal wall aplasia ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:abdominal wall aplasia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:acquired immune deficiency syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:acquired immune deficiency syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:acromegalia ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:acromegalia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:adactylia ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:adactylia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:alcaptonuria ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:alcaptonuria | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:anaesthesia for porphyria ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:anaesthesia for porphyria | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:and oligophrenia ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:and oligophrenia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:and photophobia syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:and photophobia syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:and postaxil polydactylie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:and postaxil polydactylie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:atresia ani ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:atresia ani | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:atrichia ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:atrichia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:bilirubin encephalopathy ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:bilirubin encephalopathy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:cacomorphosis ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:cacomorphosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:cancrum oris ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:cancrum oris | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:cat cry disease ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:cat cry disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:cat cry syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:cat cry syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:chromosome 5p deletion syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:chromosome 5p deletion syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:congenital insensitivity to pain type III ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:congenital insensitivity to pain type III | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:contractural arachnodactyly ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:contractural arachnodactyly | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:ectrodactyly and macular dystrophy ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:ectrodactyly and macular dystrophy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:eds ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:eds | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:ehlers danlos syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:ehlers danlos syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:erythroblastosis fetalis ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:erythroblastosis fetalis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:familial ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:familial | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:follicularis ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:follicularis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:glycogenosis ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:glycogenosis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:green monkey virus disease ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:green monkey virus disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:hereditary sensory and autonomic neuropathy type III ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:hereditary sensory and autonomic neuropathy type III | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:homogentisuria ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:homogentisuria | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:hypoacousic child ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:hypoacousic child | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:hypoxemia ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:hypoxemia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:infectious gangrene of the mouth ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:infectious gangrene of the mouth | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:intestinal malabsorption ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:intestinal malabsorption | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:irideremia ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:irideremia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:leper house ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:leper house | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:minimal pigment type ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:minimal pigment type | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:nuclear icterus ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:nuclear icterus | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:nuclear jaundice ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:nuclear jaundice | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:optic neuropathy ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:optic neuropathy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:patterson-kelly syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:patterson-kelly syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:peripheral neuropathy in cold agglutinin disease ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:peripheral neuropathy in cold agglutinin disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:right sacrum anterior position ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:right sacrum anterior position | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:sign of the iceberg ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:sign of the iceberg | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:spastic neurologic disorder ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:spastic neurologic disorder | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:stress cardiomyopathy ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:stress cardiomyopathy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:substance withdrawal syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:substance withdrawal syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:trisomy 21 ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:trisomy 21 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:type 1 ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:type 1 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:type 2 ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:type 2 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:type 3 ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:type 3 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:type 4 ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:type 4 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:weaning syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:weaning syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:with external ophthalmoplegia ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:with external ophthalmoplegia | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:withdrawal syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:withdrawal syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:xanthine lithiasis ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:xanthine lithiasis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:xanthonychia syndrome ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:xanthonychia syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- en:xanthonychie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=en:xanthonychie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- fente nasolabiopalatine ---
r_associated #0: 10 -->
en:mmih syndrome
n1=fente nasolabiopalatine | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- gastroschisis ---
r_associated #0: 10 -->
en:mmih syndrome
n1=gastroschisis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- glycogénique (surcharge et infiltration) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=glycogénique (surcharge et infiltration) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle ---
r_associated #0: 10 -->
en:mmih syndrome
n1=hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- holocentromère ---
r_associated #0: 10 -->
en:mmih syndrome
n1=holocentromère | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- holocentromérique ---
r_associated #0: 10 -->
en:mmih syndrome
n1=holocentromérique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- holocrine ---
r_associated #0: 10 -->
en:mmih syndrome
n1=holocrine | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- holodiastolique ---
r_associated #0: 10 -->
en:mmih syndrome
n1=holodiastolique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- holoenzyme ---
r_associated #0: 10 -->
en:mmih syndrome
n1=holoenzyme | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- hologamie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=hologamie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- hologynique ---
r_associated #0: 10 -->
en:mmih syndrome
n1=hologynique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- holomérocrine ---
r_associated #0: 10 -->
en:mmih syndrome
n1=holomérocrine | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- holophrase ---
r_associated #0: 10 -->
en:mmih syndrome
n1=holophrase | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- holoproencéphalie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=holoproencéphalie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- hypoesthésie cornéenne, anomalie rétinienne, surdité neurosensorielle, anomalie du faciès, persistance du canal artériel et retard mental ---
r_associated #0: 10 -->
en:mmih syndrome
n1=hypoesthésie cornéenne, anomalie rétinienne, surdité neurosensorielle, anomalie du faciès, persistance du canal artériel et retard mental | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- hypohypophysie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=hypohypophysie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- hypostimulinie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=hypostimulinie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- impédance acoustique (symb. Z) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=impédance acoustique (symb. Z) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- laparoschisis ---
r_associated #0: 10 -->
en:mmih syndrome
n1=laparoschisis | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- maladie de Duhring ---
r_associated #0: 10 -->
en:mmih syndrome
n1=maladie de Duhring | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- maladie de Gilles de la Tourette ---
r_associated #0: 10 -->
en:mmih syndrome
n1=maladie de Gilles de la Tourette | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- maladie de Stargardt ---
r_associated #0: 10 -->
en:mmih syndrome
n1=maladie de Stargardt | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- maladie des tics ---
r_associated #0: 10 -->
en:mmih syndrome
n1=maladie des tics | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- maladie des tics de Gilles de la Tourette ---
r_associated #0: 10 -->
en:mmih syndrome
n1=maladie des tics de Gilles de la Tourette | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- maladies de gilles de la tourette ---
r_associated #0: 10 -->
en:mmih syndrome
n1=maladies de gilles de la tourette | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- mort imminente (expérience de la) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=mort imminente (expérience de la) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- neuroblastome (mise en évidence scintigraphique du) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=neuroblastome (mise en évidence scintigraphique du) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- nystagmus ---
r_associated #0: 10 -->
en:mmih syndrome
n1=nystagmus | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- nystagmus héréditaire vertical ---
r_associated #0: 10 -->
en:mmih syndrome
n1=nystagmus héréditaire vertical | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- nystagmus lié au sexe ---
r_associated #0: 10 -->
en:mmih syndrome
n1=nystagmus lié au sexe | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- nystagmus myoclonies ---
r_associated #0: 10 -->
en:mmih syndrome
n1=nystagmus myoclonies | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- néphritique (syndrome) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=néphritique (syndrome) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- omovertébral (os) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=omovertébral (os) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- ostéoporose-pseudogliome (syndrome) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=ostéoporose-pseudogliome (syndrome) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- paralysie périodique hypokaliémique familiale (maladie de Westphal) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=paralysie périodique hypokaliémique familiale (maladie de Westphal) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- paraplégie spastique dans la syphilis congénitale ---
r_associated #0: 10 -->
en:mmih syndrome
n1=paraplégie spastique dans la syphilis congénitale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- pluripotence ---
r_associated #0: 10 -->
en:mmih syndrome
n1=pluripotence | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- pluripotent ---
r_associated #0: 10 -->
en:mmih syndrome
n1=pluripotent | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- plurisegmentectomie hépatique ---
r_associated #0: 10 -->
en:mmih syndrome
n1=plurisegmentectomie hépatique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- pneumallergène ---
r_associated #0: 10 -->
en:mmih syndrome
n1=pneumallergène | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- pneumatisation de l'apophyse unciforme ---
r_associated #0: 10 -->
en:mmih syndrome
n1=pneumatisation de l'apophyse unciforme | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- pneumatisation du cornet moyen ---
r_associated #0: 10 -->
en:mmih syndrome
n1=pneumatisation du cornet moyen | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- pneumatocèle ---
r_associated #0: 10 -->
en:mmih syndrome
n1=pneumatocèle | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- pneumatose colique ---
r_associated #0: 10 -->
en:mmih syndrome
n1=pneumatose colique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- pneumaturie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=pneumaturie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- pneumectomie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=pneumectomie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- pneumoarthrographie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=pneumoarthrographie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- pneumobilie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=pneumobilie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- poumon (fonctions métaboliques du) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=poumon (fonctions métaboliques du) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- profondeur de l'anesthésie (stade de) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=profondeur de l'anesthésie (stade de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- prolidase (déficit en) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=prolidase (déficit en) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- protéine trifonctionnelle mitochondriale (déficit en) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=protéine trifonctionnelle mitochondriale (déficit en) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- quadriplégie spastique, rétinite pigmentaire et retard mental ---
r_associated #0: 10 -->
en:mmih syndrome
n1=quadriplégie spastique, rétinite pigmentaire et retard mental | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- rétinite pigmentaire et retard mental ---
r_associated #0: 10 -->
en:mmih syndrome
n1=rétinite pigmentaire et retard mental | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- seitelberger ---
r_associated #0: 10 -->
en:mmih syndrome
n1=seitelberger | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- sel biliaire ---
r_associated #0: 10 -->
en:mmih syndrome
n1=sel biliaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- sirtuine ---
r_associated #0: 10 -->
en:mmih syndrome
n1=sirtuine | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- sisi-test ---
r_associated #0: 10 -->
en:mmih syndrome
n1=sisi-test | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- sismothérapie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=sismothérapie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- situs inversus viscerum ---
r_associated #0: 10 -->
en:mmih syndrome
n1=situs inversus viscerum | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- situs mutatus ---
r_associated #0: 10 -->
en:mmih syndrome
n1=situs mutatus | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- souche de référence ---
r_associated #0: 10 -->
en:mmih syndrome
n1=souche de référence | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- souche transduite ---
r_associated #0: 10 -->
en:mmih syndrome
n1=souche transduite | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- syndrome de Duker-Weiss-Siber ---
r_associated #0: 10 -->
en:mmih syndrome
n1=syndrome de Duker-Weiss-Siber | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- syndrome de Feingold ---
r_associated #0: 10 -->
en:mmih syndrome
n1=syndrome de Feingold | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- syndrome de Gilles de la Tourette ---
r_associated #0: 10 -->
en:mmih syndrome
n1=syndrome de Gilles de la Tourette | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- syndrome de Leriche ---
r_associated #0: 10 -->
en:mmih syndrome
n1=syndrome de Leriche | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- syndrome de Stein-Leventhal-Cohen ---
r_associated #0: 10 -->
en:mmih syndrome
n1=syndrome de Stein-Leventhal-Cohen | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- syndrome de Stevens-Johnson ---
r_associated #0: 10 -->
en:mmih syndrome
n1=syndrome de Stevens-Johnson | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- syndrome de Townes-Brocks ---
r_associated #0: 10 -->
en:mmih syndrome
n1=syndrome de Townes-Brocks | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- syndrome de de Morsier ---
r_associated #0: 10 -->
en:mmih syndrome
n1=syndrome de de Morsier | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- syndrome de la Tourette ---
r_associated #0: 10 -->
en:mmih syndrome
n1=syndrome de la Tourette | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- syndrome de sheehan ---
r_associated #0: 10 -->
en:mmih syndrome
n1=syndrome de sheehan | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- syndrome de stress respiratoire de l'adulte ---
r_associated #0: 10 -->
en:mmih syndrome
n1=syndrome de stress respiratoire de l'adulte | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- syndrome de tourette ---
r_associated #0: 10 -->
en:mmih syndrome
n1=syndrome de tourette | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- syndrome de zellweger ---
r_associated #0: 10 -->
en:mmih syndrome
n1=syndrome de zellweger | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- syndrome des pouces en adduction-arthrogrypose (type Dundar) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=syndrome des pouces en adduction-arthrogrypose (type Dundar) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- syndrome des tics de Gilles de la Tourette ---
r_associated #0: 10 -->
en:mmih syndrome
n1=syndrome des tics de Gilles de la Tourette | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- syndrome du p(17)p11.2p11.2 ---
r_associated #0: 10 -->
en:mmih syndrome
n1=syndrome du p(17)p11.2p11.2 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- sélacien venimeux ---
r_associated #0: 10 -->
en:mmih syndrome
n1=sélacien venimeux | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- toxémie ---
r_associated #0: 10 -->
en:mmih syndrome
n1=toxémie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- triphosphopyridine-nucléotide ---
r_associated #0: 10 -->
en:mmih syndrome
n1=triphosphopyridine-nucléotide | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- trisomie 9p ---
r_associated #0: 10 -->
en:mmih syndrome
n1=trisomie 9p | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- trouble de gilles de la tourette ---
r_associated #0: 10 -->
en:mmih syndrome
n1=trouble de gilles de la tourette | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- varicelle (complications neurologiques de la) ---
r_associated #0: 10 -->
en:mmih syndrome
n1=varicelle (complications neurologiques de la) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=10
- dysencéphalie splanchnokystique ---
r_associated #0: 6 -->
en:mmih syndrome
n1=dysencéphalie splanchnokystique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=6
- trisomie 13 ---
r_associated #0: 6 -->
en:mmih syndrome
n1=trisomie 13 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=6
- trisomie 18 ---
r_associated #0: 6 -->
en:mmih syndrome
n1=trisomie 18 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=6
- Acinetobacter ---
r_associated #0: 5 -->
en:mmih syndrome
n1=Acinetobacter | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- Adair-Dighton (syndrome d') ---
r_associated #0: 5 -->
en:mmih syndrome
n1=Adair-Dighton (syndrome d') | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- Alagille (syndrome d') ---
r_associated #0: 5 -->
en:mmih syndrome
n1=Alagille (syndrome d') | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- Anasarque ---
r_associated #0: 5 -->
en:mmih syndrome
n1=Anasarque | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- Dumoulin (classification de) ---
r_associated #0: 5 -->
en:mmih syndrome
n1=Dumoulin (classification de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- Exomphale ---
r_associated #0: 5 -->
en:mmih syndrome
n1=Exomphale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- Korsakoff (syndrome de) ---
r_associated #0: 5 -->
en:mmih syndrome
n1=Korsakoff (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- Maladie du cri du chat ---
r_associated #0: 5 -->
en:mmih syndrome
n1=Maladie du cri du chat | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- Neurocysticercose ---
r_associated #0: 5 -->
en:mmih syndrome
n1=Neurocysticercose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- Neuropathie optique ---
r_associated #0: 5 -->
en:mmih syndrome
n1=Neuropathie optique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- Onsager (relation d') ---
r_associated #0: 5 -->
en:mmih syndrome
n1=Onsager (relation d') | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- Perthes (maladie de) ---
r_associated #0: 5 -->
en:mmih syndrome
n1=Perthes (maladie de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- Peste Noire ---
r_associated #0: 5 -->
en:mmih syndrome
n1=Peste Noire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- Tay-Sachs (maladie de) ---
r_associated #0: 5 -->
en:mmih syndrome
n1=Tay-Sachs (maladie de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- Williams (syndrome de) ---
r_associated #0: 5 -->
en:mmih syndrome
n1=Williams (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- abêtalipoprotéinémie ---
r_associated #0: 5 -->
en:mmih syndrome
n1=abêtalipoprotéinémie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- acidurie ---
r_associated #0: 5 -->
en:mmih syndrome
n1=acidurie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- acidurie 3-hydroxy-3-méthyl-glutarique ---
r_associated #0: 5 -->
en:mmih syndrome
n1=acidurie 3-hydroxy-3-méthyl-glutarique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- acidurie 3-méthylglutaconique ---
r_associated #0: 5 -->
en:mmih syndrome
n1=acidurie 3-méthylglutaconique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- acidurie 4-hydroxybutyrique ---
r_associated #0: 5 -->
en:mmih syndrome
n1=acidurie 4-hydroxybutyrique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- acidurie paradoxale ---
r_associated #0: 5 -->
en:mmih syndrome
n1=acidurie paradoxale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- acineux ---
r_associated #0: 5 -->
en:mmih syndrome
n1=acineux | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- acini ---
r_associated #0: 5 -->
en:mmih syndrome
n1=acini | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- acinus ---
r_associated #0: 5 -->
en:mmih syndrome
n1=acinus | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- acinus hépatique de Rappaport ---
r_associated #0: 5 -->
en:mmih syndrome
n1=acinus hépatique de Rappaport | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- agglutinines irrégulières ---
r_associated #0: 5 -->
en:mmih syndrome
n1=agglutinines irrégulières | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- agglutinogène ---
r_associated #0: 5 -->
en:mmih syndrome
n1=agglutinogène | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- agitation postopératoire ---
r_associated #0: 5 -->
en:mmih syndrome
n1=agitation postopératoire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- aglossie et adactylie ---
r_associated #0: 5 -->
en:mmih syndrome
n1=aglossie et adactylie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- aglycone ---
r_associated #0: 5 -->
en:mmih syndrome
n1=aglycone | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- agnosie chromatique ---
r_associated #0: 5 -->
en:mmih syndrome
n1=agnosie chromatique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- agnosie d'extensité ---
r_associated #0: 5 -->
en:mmih syndrome
n1=agnosie d'extensité | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- agnosie d'intensité ---
r_associated #0: 5 -->
en:mmih syndrome
n1=agnosie d'intensité | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- agnosie des couleurs ---
r_associated #0: 5 -->
en:mmih syndrome
n1=agnosie des couleurs | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- albinisme avec immunodéficience et troubles hématologiques ---
r_associated #0: 5 -->
en:mmih syndrome
n1=albinisme avec immunodéficience et troubles hématologiques | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- albinisme avec surdité ---
r_associated #0: 5 -->
en:mmih syndrome
n1=albinisme avec surdité | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- cri du chat (maladie du) ---
r_associated #0: 5 -->
en:mmih syndrome
n1=cri du chat (maladie du) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- duodénectomie ---
r_associated #0: 5 -->
en:mmih syndrome
n1=duodénectomie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- duodénite ---
r_associated #0: 5 -->
en:mmih syndrome
n1=duodénite | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- dysembryome cutané ---
r_associated #0: 5 -->
en:mmih syndrome
n1=dysembryome cutané | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- dysembryome de l'ovaire ---
r_associated #0: 5 -->
en:mmih syndrome
n1=dysembryome de l'ovaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- dysembryome testiculaire ---
r_associated #0: 5 -->
en:mmih syndrome
n1=dysembryome testiculaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- dysembryoplasie ---
r_associated #0: 5 -->
en:mmih syndrome
n1=dysembryoplasie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- dysembryoplasie neuro-épithéliale ---
r_associated #0: 5 -->
en:mmih syndrome
n1=dysembryoplasie neuro-épithéliale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- dysenterie ---
r_associated #0: 5 -->
en:mmih syndrome
n1=dysenterie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- dysenterie amibienne ---
r_associated #0: 5 -->
en:mmih syndrome
n1=dysenterie amibienne | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- dysentériforme ---
r_associated #0: 5 -->
en:mmih syndrome
n1=dysentériforme | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- dysentérique ---
r_associated #0: 5 -->
en:mmih syndrome
n1=dysentérique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- dysérythropoïèse ---
r_associated #0: 5 -->
en:mmih syndrome
n1=dysérythropoïèse | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- démence d'Alzheimer ---
r_associated #0: 5 -->
en:mmih syndrome
n1=démence d'Alzheimer | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- en:PFIC11 ---
r_associated #0: 5 -->
en:mmih syndrome
n1=en:PFIC11 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- en:Sachs' disease ---
r_associated #0: 5 -->
en:mmih syndrome
n1=en:Sachs' disease | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- en:cat's cry syndrome ---
r_associated #0: 5 -->
en:mmih syndrome
n1=en:cat's cry syndrome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- hypoxanthine-guanine-phosphoribosyl-transferase (déficit en) ---
r_associated #0: 5 -->
en:mmih syndrome
n1=hypoxanthine-guanine-phosphoribosyl-transferase (déficit en) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- ichtyophtalmie ---
r_associated #0: 5 -->
en:mmih syndrome
n1=ichtyophtalmie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- ichtyosarcotoxisme ---
r_associated #0: 5 -->
en:mmih syndrome
n1=ichtyosarcotoxisme | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- insectes (allergie aux) ---
r_associated #0: 5 -->
en:mmih syndrome
n1=insectes (allergie aux) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- malabsorption (syndrome de) ---
r_associated #0: 5 -->
en:mmih syndrome
n1=malabsorption (syndrome de) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- maladie de Duhring-Brocq ---
r_associated #0: 5 -->
en:mmih syndrome
n1=maladie de Duhring-Brocq | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- malf ormation dysraphique ---
r_associated #0: 5 -->
en:mmih syndrome
n1=malf ormation dysraphique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- malformation kystique adénomatoïde du poumon ---
r_associated #0: 5 -->
en:mmih syndrome
n1=malformation kystique adénomatoïde du poumon | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- malformation luxante de la hanche ---
r_associated #0: 5 -->
en:mmih syndrome
n1=malformation luxante de la hanche | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- malformation mamelonnaire ---
r_associated #0: 5 -->
en:mmih syndrome
n1=malformation mamelonnaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- malformation mammaire ---
r_associated #0: 5 -->
en:mmih syndrome
n1=malformation mammaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- malformation ombilicale ---
r_associated #0: 5 -->
en:mmih syndrome
n1=malformation ombilicale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- malformation utérine ---
r_associated #0: 5 -->
en:mmih syndrome
n1=malformation utérine | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- malformation vaginale ---
r_associated #0: 5 -->
en:mmih syndrome
n1=malformation vaginale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- malformation vasculaire cérébrale du nourrisson ---
r_associated #0: 5 -->
en:mmih syndrome
n1=malformation vasculaire cérébrale du nourrisson | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- malformations de la charnière occipitocervicale ---
r_associated #0: 5 -->
en:mmih syndrome
n1=malformations de la charnière occipitocervicale | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- mésentérite rétractile ---
r_associated #0: 5 -->
en:mmih syndrome
n1=mésentérite rétractile | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- mésentérite sclérosante ---
r_associated #0: 5 -->
en:mmih syndrome
n1=mésentérite sclérosante | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- neurinome bilatéral du nerf cochléaire (VIII) ---
r_associated #0: 5 -->
en:mmih syndrome
n1=neurinome bilatéral du nerf cochléaire (VIII) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- nystagmus (zone de moindre) ---
r_associated #0: 5 -->
en:mmih syndrome
n1=nystagmus (zone de moindre) | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- onychodysplasie ---
r_associated #0: 5 -->
en:mmih syndrome
n1=onychodysplasie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- onychogryphose ---
r_associated #0: 5 -->
en:mmih syndrome
n1=onychogryphose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- onycholyse ---
r_associated #0: 5 -->
en:mmih syndrome
n1=onycholyse | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- onycholyse candidosique ---
r_associated #0: 5 -->
en:mmih syndrome
n1=onycholyse candidosique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- onycholyse semi-lunaire partielle ---
r_associated #0: 5 -->
en:mmih syndrome
n1=onycholyse semi-lunaire partielle | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- onychomadèse ---
r_associated #0: 5 -->
en:mmih syndrome
n1=onychomadèse | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- onychomatricome ---
r_associated #0: 5 -->
en:mmih syndrome
n1=onychomatricome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- opération de Dunn ---
r_associated #0: 5 -->
en:mmih syndrome
n1=opération de Dunn | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- osteopoecilie ---
r_associated #0: 5 -->
en:mmih syndrome
n1=osteopoecilie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- paragnathe ---
r_associated #0: 5 -->
en:mmih syndrome
n1=paragnathe | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- pemphigoïde muqueux bénin ---
r_associated #0: 5 -->
en:mmih syndrome
n1=pemphigoïde muqueux bénin | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- porphyrie aigüe intermittente ---
r_associated #0: 5 -->
en:mmih syndrome
n1=porphyrie aigüe intermittente | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- porphyrie cutanée ---
r_associated #0: 5 -->
en:mmih syndrome
n1=porphyrie cutanée | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- porphyrie de Doss ---
r_associated #0: 5 -->
en:mmih syndrome
n1=porphyrie de Doss | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- sars ---
r_associated #0: 5 -->
en:mmih syndrome
n1=sars | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- syndrome d'Ehlers-Danlos ---
r_associated #0: 5 -->
en:mmih syndrome
n1=syndrome d'Ehlers-Danlos | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- syndrome de Dunnigan ---
r_associated #0: 5 -->
en:mmih syndrome
n1=syndrome de Dunnigan | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- syndrome de Kallmann ---
r_associated #0: 5 -->
en:mmih syndrome
n1=syndrome de Kallmann | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- syndrome de Kaposi-Juliusberg ---
r_associated #0: 5 -->
en:mmih syndrome
n1=syndrome de Kaposi-Juliusberg | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- syndrome de Kearns-Sayre ---
r_associated #0: 5 -->
en:mmih syndrome
n1=syndrome de Kearns-Sayre | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- syndrome de Kleine-Levin ---
r_associated #0: 5 -->
en:mmih syndrome
n1=syndrome de Kleine-Levin | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- syndrome de Klüver-Bucy ---
r_associated #0: 5 -->
en:mmih syndrome
n1=syndrome de Klüver-Bucy | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- syndrome de Reye ---
r_associated #0: 5 -->
en:mmih syndrome
n1=syndrome de Reye | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- syndrome de Waterhouse-Friderichsen ---
r_associated #0: 5 -->
en:mmih syndrome
n1=syndrome de Waterhouse-Friderichsen | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- syndrome de l'angle pontocérébelleux ---
r_associated #0: 5 -->
en:mmih syndrome
n1=syndrome de l'angle pontocérébelleux | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- syndrome de l'apex orbitaire ---
r_associated #0: 5 -->
en:mmih syndrome
n1=syndrome de l'apex orbitaire | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- syndrome de l'apophyse styloïde longue ---
r_associated #0: 5 -->
en:mmih syndrome
n1=syndrome de l'apophyse styloïde longue | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- syndrome de syndrome de Joubert-Boltshauser ---
r_associated #0: 5 -->
en:mmih syndrome
n1=syndrome de syndrome de Joubert-Boltshauser | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- syndrome olfacto-génital ---
r_associated #0: 5 -->
en:mmih syndrome
n1=syndrome olfacto-génital | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- syndromes du gène 1 de la tumeur de Wilms ---
r_associated #0: 5 -->
en:mmih syndrome
n1=syndromes du gène 1 de la tumeur de Wilms | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- triplet (CGG) n ---
r_associated #0: 5 -->
en:mmih syndrome
n1=triplet (CGG) n | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- trisomie 17p11.2 ---
r_associated #0: 5 -->
en:mmih syndrome
n1=trisomie 17p11.2 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- trisomie 8 ---
r_associated #0: 5 -->
en:mmih syndrome
n1=trisomie 8 | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- xanthoastrocytome pléomorphe ---
r_associated #0: 5 -->
en:mmih syndrome
n1=xanthoastrocytome pléomorphe | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- xanthochromie ---
r_associated #0: 5 -->
en:mmih syndrome
n1=xanthochromie | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- xanthochromie caroténique ---
r_associated #0: 5 -->
en:mmih syndrome
n1=xanthochromie caroténique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- xanthoerythrodermia perstans ---
r_associated #0: 5 -->
en:mmih syndrome
n1=xanthoerythrodermia perstans | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- xanthogranulome juvénile ---
r_associated #0: 5 -->
en:mmih syndrome
n1=xanthogranulome juvénile | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- xanthogranulome nécrobiotique ---
r_associated #0: 5 -->
en:mmih syndrome
n1=xanthogranulome nécrobiotique | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- xanthogranulome palpébral ---
r_associated #0: 5 -->
en:mmih syndrome
n1=xanthogranulome palpébral | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- xanthohistiocytome ---
r_associated #0: 5 -->
en:mmih syndrome
n1=xanthohistiocytome | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- xanthoma disseminatum ---
r_associated #0: 5 -->
en:mmih syndrome
n1=xanthoma disseminatum | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- xanthomatose ---
r_associated #0: 5 -->
en:mmih syndrome
n1=xanthomatose | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=5
- double point ---
r_associated #0: -20 -->
en:mmih syndrome
n1=double point | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=-20
- deux points ---
r_associated #0: -43 -->
en:mmih syndrome
n1=deux points | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=-43
- deux-points ---
r_associated #0: -45 -->
en:mmih syndrome
n1=deux-points | n2=en:mmih syndrome | rel=r_associated | relid=0 | w=-45
|