'en:x-linked intellectual disability cantagrel type'
(id=9102628 ; fe=en:x-linked intellectual disability cantagrel type ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=4073 creation date=2017-10-29 touchdate=2025-12-20 05:49:10.000)

≈ 180 relations sortantes en:x-linked intellectual disability cantagrel type -- r_associated #0: 43 / 1 -> en:moderate mental retardation (i.q. 35-49) n1=en:x-linked intellectual disability cantagrel type | n2=en:moderate mental retardation (i.q. 35-49) | rel=r_associated | relid=0 | w=43 en:x-linked intellectual disability cantagrel type -- r_associated #0: 42 / 0.977 -> en:kaufman oculocerebrofacial syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:kaufman oculocerebrofacial syndrome | rel=r_associated | relid=0 | w=42 en:x-linked intellectual disability cantagrel type -- r_associated #0: 41 / 0.953 -> en:orotic aciduria n1=en:x-linked intellectual disability cantagrel type | n2=en:orotic aciduria | rel=r_associated | relid=0 | w=41 en:x-linked intellectual disability cantagrel type -- r_associated #0: 40 / 0.93 -> en:aicardi's syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:aicardi's syndrome | rel=r_associated | relid=0 | w=40 en:x-linked intellectual disability cantagrel type -- r_associated #0: 40 / 0.93 -> en:coffin-siris syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:coffin-siris syndrome | rel=r_associated | relid=0 | w=40 en:x-linked intellectual disability cantagrel type -- r_associated #0: 40 / 0.93 -> en:de barsy syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:de barsy syndrome | rel=r_associated | relid=0 | w=40 en:x-linked intellectual disability cantagrel type -- r_associated #0: 40 / 0.93 -> en:lowry maclean syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:lowry maclean syndrome | rel=r_associated | relid=0 | w=40 en:x-linked intellectual disability cantagrel type -- r_associated #0: 40 / 0.93 -> en:moloney syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:moloney syndrome | rel=r_associated | relid=0 | w=40 en:x-linked intellectual disability cantagrel type -- r_associated #0: 40 / 0.93 -> en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment n1=en:x-linked intellectual disability cantagrel type | n2=en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment | rel=r_associated | relid=0 | w=40 en:x-linked intellectual disability cantagrel type -- r_associated #0: 39 / 0.907 -> en:adolescent x-linked adrenoleukodystrophy n1=en:x-linked intellectual disability cantagrel type | n2=en:adolescent x-linked adrenoleukodystrophy | rel=r_associated | relid=0 | w=39 en:x-linked intellectual disability cantagrel type -- r_associated #0: 39 / 0.907 -> en:gurrieri sammito bellussi syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:gurrieri sammito bellussi syndrome | rel=r_associated | relid=0 | w=39 en:x-linked intellectual disability cantagrel type -- r_associated #0: 39 / 0.907 -> en:intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome | rel=r_associated | relid=0 | w=39 en:x-linked intellectual disability cantagrel type -- r_associated #0: 38 / 0.884 -> en:glycogen storage disease type vi n1=en:x-linked intellectual disability cantagrel type | n2=en:glycogen storage disease type vi | rel=r_associated | relid=0 | w=38 en:x-linked intellectual disability cantagrel type -- r_associated #0: 37 / 0.86 -> en:muscular dystrophy, duchenne n1=en:x-linked intellectual disability cantagrel type | n2=en:muscular dystrophy, duchenne | rel=r_associated | relid=0 | w=37 en:x-linked intellectual disability cantagrel type -- r_associated #0: 37 / 0.86 -> en:optic atrophy 2 (disorder) n1=en:x-linked intellectual disability cantagrel type | n2=en:optic atrophy 2 (disorder) | rel=r_associated | relid=0 | w=37 en:x-linked intellectual disability cantagrel type -- r_associated #0: 37 / 0.86 -> en:spondyloepiphyseal dysplasia tarda kohn type n1=en:x-linked intellectual disability cantagrel type | n2=en:spondyloepiphyseal dysplasia tarda kohn type | rel=r_associated | relid=0 | w=37 en:x-linked intellectual disability cantagrel type -- r_associated #0: 36 / 0.837 -> en:huntington disease n1=en:x-linked intellectual disability cantagrel type | n2=en:huntington disease | rel=r_associated | relid=0 | w=36 en:x-linked intellectual disability cantagrel type -- r_associated #0: 35 / 0.814 -> en:androgen-insensitivity syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:androgen-insensitivity syndrome | rel=r_associated | relid=0 | w=35 en:x-linked intellectual disability cantagrel type -- r_associated #0: 35 / 0.814 -> en:atkin syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:atkin syndrome | rel=r_associated | relid=0 | w=35 en:x-linked intellectual disability cantagrel type -- r_associated #0: 35 / 0.814 -> en:bornholm eye disease n1=en:x-linked intellectual disability cantagrel type | n2=en:bornholm eye disease | rel=r_associated | relid=0 | w=35 en:x-linked intellectual disability cantagrel type -- r_associated #0: 35 / 0.814 -> en:chronic granulomatous disease n1=en:x-linked intellectual disability cantagrel type | n2=en:chronic granulomatous disease | rel=r_associated | relid=0 | w=35 en:x-linked intellectual disability cantagrel type -- r_associated #0: 35 / 0.814 -> en:dermoids of cornea n1=en:x-linked intellectual disability cantagrel type | n2=en:dermoids of cornea | rel=r_associated | relid=0 | w=35 en:x-linked intellectual disability cantagrel type -- r_associated #0: 35 / 0.814 -> en:goniodysgenesis-mental retardation-short stature syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:goniodysgenesis-mental retardation-short stature syndrome | rel=r_associated | relid=0 | w=35 en:x-linked intellectual disability cantagrel type -- r_associated #0: 35 / 0.814 -> en:holoprosencephaly with fetal akinesia-hypokinesia sequence n1=en:x-linked intellectual disability cantagrel type | n2=en:holoprosencephaly with fetal akinesia-hypokinesia sequence | rel=r_associated | relid=0 | w=35 en:x-linked intellectual disability cantagrel type -- r_associated #0: 35 / 0.814 -> en:marfanoid mental retardation syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:marfanoid mental retardation syndrome | rel=r_associated | relid=0 | w=35 en:x-linked intellectual disability cantagrel type -- r_associated #0: 35 / 0.814 -> en:mental retardation, x-linked, with short stature, hypogonadism, and abnormal gait n1=en:x-linked intellectual disability cantagrel type | n2=en:mental retardation, x-linked, with short stature, hypogonadism, and abnormal gait | rel=r_associated | relid=0 | w=35 en:x-linked intellectual disability cantagrel type -- r_associated #0: 35 / 0.814 -> en:nutritional mental retardation n1=en:x-linked intellectual disability cantagrel type | n2=en:nutritional mental retardation | rel=r_associated | relid=0 | w=35 en:x-linked intellectual disability cantagrel type -- r_associated #0: 35 / 0.814 -> en:ornithine carbamoyltransferase deficiency n1=en:x-linked intellectual disability cantagrel type | n2=en:ornithine carbamoyltransferase deficiency | rel=r_associated | relid=0 | w=35 en:x-linked intellectual disability cantagrel type -- r_associated #0: 35 / 0.814 -> en:orofaciodigital syndrome 5 n1=en:x-linked intellectual disability cantagrel type | n2=en:orofaciodigital syndrome 5 | rel=r_associated | relid=0 | w=35 en:x-linked intellectual disability cantagrel type -- r_associated #0: 35 / 0.814 -> en:other mental retardation n1=en:x-linked intellectual disability cantagrel type | n2=en:other mental retardation | rel=r_associated | relid=0 | w=35 en:x-linked intellectual disability cantagrel type -- r_associated #0: 35 / 0.814 -> en:savant syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:savant syndrome | rel=r_associated | relid=0 | w=35 en:x-linked intellectual disability cantagrel type -- r_associated #0: 35 / 0.814 -> en:shprintzen-goldberg syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:shprintzen-goldberg syndrome | rel=r_associated | relid=0 | w=35 en:x-linked intellectual disability cantagrel type -- r_associated #0: 35 / 0.814 -> en:x-linked intellectual disability stocco dos santos type n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked intellectual disability stocco dos santos type | rel=r_associated | relid=0 | w=35 en:x-linked intellectual disability cantagrel type -- r_associated #0: 35 / 0.814 -> en:x-linked intellectual disability with ataxia and apraxia syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked intellectual disability with ataxia and apraxia syndrome | rel=r_associated | relid=0 | w=35 en:x-linked intellectual disability cantagrel type -- r_associated #0: 34 / 0.791 -> en:brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia n1=en:x-linked intellectual disability cantagrel type | n2=en:brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia | rel=r_associated | relid=0 | w=34 en:x-linked intellectual disability cantagrel type -- r_associated #0: 34 / 0.791 -> en:glucose-6-phosphate dehydrogenase deficiency anemia n1=en:x-linked intellectual disability cantagrel type | n2=en:glucose-6-phosphate dehydrogenase deficiency anemia | rel=r_associated | relid=0 | w=34 en:x-linked intellectual disability cantagrel type -- r_associated #0: 34 / 0.791 -> en:lipodystrophy, intellectual disability, deafness syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:lipodystrophy, intellectual disability, deafness syndrome | rel=r_associated | relid=0 | w=34 en:x-linked intellectual disability cantagrel type -- r_associated #0: 34 / 0.791 -> en:microcephalus and intellectual disability with phalangeal and neurological anomaly syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:microcephalus and intellectual disability with phalangeal and neurological anomaly syndrome | rel=r_associated | relid=0 | w=34 en:x-linked intellectual disability cantagrel type -- r_associated #0: 34 / 0.791 -> en:neutropenia, severe congenital, x-linked n1=en:x-linked intellectual disability cantagrel type | n2=en:neutropenia, severe congenital, x-linked | rel=r_associated | relid=0 | w=34 en:x-linked intellectual disability cantagrel type -- r_associated #0: 34 / 0.791 -> en:placental steroid sulfatase deficiency n1=en:x-linked intellectual disability cantagrel type | n2=en:placental steroid sulfatase deficiency | rel=r_associated | relid=0 | w=34 en:x-linked intellectual disability cantagrel type -- r_associated #0: 34 / 0.791 -> en:severe mental retardation (i.q. 20-34) n1=en:x-linked intellectual disability cantagrel type | n2=en:severe mental retardation (i.q. 20-34) | rel=r_associated | relid=0 | w=34 en:x-linked intellectual disability cantagrel type -- r_associated #0: 34 / 0.791 -> en:uveal coloboma with cleft lip and palate and intellectual disability syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:uveal coloboma with cleft lip and palate and intellectual disability syndrome | rel=r_associated | relid=0 | w=34 en:x-linked intellectual disability cantagrel type -- r_associated #0: 34 / 0.791 -> en:wiskott-aldrich syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:wiskott-aldrich syndrome | rel=r_associated | relid=0 | w=34 en:x-linked intellectual disability cantagrel type -- r_associated #0: 34 / 0.791 -> en:x-linked intellectual disability miles carpenter type n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked intellectual disability miles carpenter type | rel=r_associated | relid=0 | w=34 en:x-linked intellectual disability cantagrel type -- r_associated #0: 32 / 0.744 -> en:bardet-biedl syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:bardet-biedl syndrome | rel=r_associated | relid=0 | w=32 en:x-linked intellectual disability cantagrel type -- r_associated #0: 32 / 0.744 -> en:congenital hypoplasia of ulna and intellectual disability syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:congenital hypoplasia of ulna and intellectual disability syndrome | rel=r_associated | relid=0 | w=32 en:x-linked intellectual disability cantagrel type -- r_associated #0: 32 / 0.744 -> en:cooper jabs syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:cooper jabs syndrome | rel=r_associated | relid=0 | w=32 en:x-linked intellectual disability cantagrel type -- r_associated #0: 32 / 0.744 -> en:digitorenocerebral syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:digitorenocerebral syndrome | rel=r_associated | relid=0 | w=32 en:x-linked intellectual disability cantagrel type -- r_associated #0: 32 / 0.744 -> en:mental retardation syndrome, belgian type n1=en:x-linked intellectual disability cantagrel type | n2=en:mental retardation syndrome, belgian type | rel=r_associated | relid=0 | w=32 en:x-linked intellectual disability cantagrel type -- r_associated #0: 32 / 0.744 -> en:mental retardation, skeletal dysplasia, and abducens palsy n1=en:x-linked intellectual disability cantagrel type | n2=en:mental retardation, skeletal dysplasia, and abducens palsy | rel=r_associated | relid=0 | w=32 en:x-linked intellectual disability cantagrel type -- r_associated #0: 32 / 0.744 -> en:mental retardation, x-linked, syndromic, christianson type n1=en:x-linked intellectual disability cantagrel type | n2=en:mental retardation, x-linked, syndromic, christianson type | rel=r_associated | relid=0 | w=32 en:x-linked intellectual disability cantagrel type -- r_associated #0: 32 / 0.744 -> en:mowat-wilson syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:mowat-wilson syndrome | rel=r_associated | relid=0 | w=32 en:x-linked intellectual disability cantagrel type -- r_associated #0: 32 / 0.744 -> en:renpenning syndrome 1 n1=en:x-linked intellectual disability cantagrel type | n2=en:renpenning syndrome 1 | rel=r_associated | relid=0 | w=32 en:x-linked intellectual disability cantagrel type -- r_associated #0: 32 / 0.744 -> en:severe x-linked intellectual disability gustavson type n1=en:x-linked intellectual disability cantagrel type | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=32 en:x-linked intellectual disability cantagrel type -- r_associated #0: 32 / 0.744 -> en:tranebjaerg svejgaard syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:tranebjaerg svejgaard syndrome | rel=r_associated | relid=0 | w=32 en:x-linked intellectual disability cantagrel type -- r_associated #0: 32 / 0.744 -> en:x-linked congenital dyserythropoietic anemia with thrombocytopenia n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked congenital dyserythropoietic anemia with thrombocytopenia | rel=r_associated | relid=0 | w=32 en:x-linked intellectual disability cantagrel type -- r_associated #0: 32 / 0.744 -> en:x-linked dominant chondrodysplasia chassaing lacombe type n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked dominant chondrodysplasia chassaing lacombe type | rel=r_associated | relid=0 | w=32 en:x-linked intellectual disability cantagrel type -- r_associated #0: 32 / 0.744 -> en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome | rel=r_associated | relid=0 | w=32 en:x-linked intellectual disability cantagrel type -- r_associated #0: 32 / 0.744 -> en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome | rel=r_associated | relid=0 | w=32 en:x-linked intellectual disability cantagrel type -- r_associated #0: 31 / 0.721 -> en:alpha-thalassemia/mental retardation syndrome, nondeletion type, x-linked n1=en:x-linked intellectual disability cantagrel type | n2=en:alpha-thalassemia/mental retardation syndrome, nondeletion type, x-linked | rel=r_associated | relid=0 | w=31 en:x-linked intellectual disability cantagrel type -- r_associated #0: 31 / 0.721 -> en:borderline mental retardation (i.q. 70-85) n1=en:x-linked intellectual disability cantagrel type | n2=en:borderline mental retardation (i.q. 70-85) | rel=r_associated | relid=0 | w=31 en:x-linked intellectual disability cantagrel type -- r_associated #0: 31 / 0.721 -> en:cerebrofaciothoracic dysplasia n1=en:x-linked intellectual disability cantagrel type | n2=en:cerebrofaciothoracic dysplasia | rel=r_associated | relid=0 | w=31 en:x-linked intellectual disability cantagrel type -- r_associated #0: 31 / 0.721 -> en:corpus callosum, agenesis of, with facial anomalies and robin sequence n1=en:x-linked intellectual disability cantagrel type | n2=en:corpus callosum, agenesis of, with facial anomalies and robin sequence | rel=r_associated | relid=0 | w=31 en:x-linked intellectual disability cantagrel type -- r_associated #0: 31 / 0.721 -> en:fraxe intellectual disability syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:fraxe intellectual disability syndrome | rel=r_associated | relid=0 | w=31 en:x-linked intellectual disability cantagrel type -- r_associated #0: 31 / 0.721 -> en:glycogen storage disease type viii n1=en:x-linked intellectual disability cantagrel type | n2=en:glycogen storage disease type viii | rel=r_associated | relid=0 | w=31 en:x-linked intellectual disability cantagrel type -- r_associated #0: 31 / 0.721 -> en:juberg-marsidi syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:juberg-marsidi syndrome | rel=r_associated | relid=0 | w=31 en:x-linked intellectual disability cantagrel type -- r_associated #0: 31 / 0.721 -> en:kapur toriello syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:kapur toriello syndrome | rel=r_associated | relid=0 | w=31 en:x-linked intellectual disability cantagrel type -- r_associated #0: 31 / 0.721 -> en:muscular dystrophy, emery-dreifuss n1=en:x-linked intellectual disability cantagrel type | n2=en:muscular dystrophy, emery-dreifuss | rel=r_associated | relid=0 | w=31 en:x-linked intellectual disability cantagrel type -- r_associated #0: 31 / 0.721 -> en:ocular albinism, type ii n1=en:x-linked intellectual disability cantagrel type | n2=en:ocular albinism, type ii | rel=r_associated | relid=0 | w=31 en:x-linked intellectual disability cantagrel type -- r_associated #0: 31 / 0.721 -> en:ossification anomaly with psychomotor developmental delay syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:ossification anomaly with psychomotor developmental delay syndrome | rel=r_associated | relid=0 | w=31 en:x-linked intellectual disability cantagrel type -- r_associated #0: 31 / 0.721 -> en:pashayan syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:pashayan syndrome | rel=r_associated | relid=0 | w=31 en:x-linked intellectual disability cantagrel type -- r_associated #0: 31 / 0.721 -> en:perniola krajewska carnevale syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:perniola krajewska carnevale syndrome | rel=r_associated | relid=0 | w=31 en:x-linked intellectual disability cantagrel type -- r_associated #0: 31 / 0.721 -> en:waisman syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:waisman syndrome | rel=r_associated | relid=0 | w=31 en:x-linked intellectual disability cantagrel type -- r_associated #0: 31 / 0.721 -> en:wilson turner syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:wilson turner syndrome | rel=r_associated | relid=0 | w=31 en:x-linked intellectual disability cantagrel type -- r_associated #0: 30 / 0.698 -> en:achalasia microcephaly n1=en:x-linked intellectual disability cantagrel type | n2=en:achalasia microcephaly | rel=r_associated | relid=0 | w=30 en:x-linked intellectual disability cantagrel type -- r_associated #0: 30 / 0.698 -> en:alport syndrome, x-linked n1=en:x-linked intellectual disability cantagrel type | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=30 en:x-linked intellectual disability cantagrel type -- r_associated #0: 30 / 0.698 -> en:ataxia, fatal x-linked, with deafness and loss of vision n1=en:x-linked intellectual disability cantagrel type | n2=en:ataxia, fatal x-linked, with deafness and loss of vision | rel=r_associated | relid=0 | w=30 en:x-linked intellectual disability cantagrel type -- r_associated #0: 30 / 0.698 -> en:childhood cerebral x-linked adrenoleukodystrophy n1=en:x-linked intellectual disability cantagrel type | n2=en:childhood cerebral x-linked adrenoleukodystrophy | rel=r_associated | relid=0 | w=30 en:x-linked intellectual disability cantagrel type -- r_associated #0: 30 / 0.698 -> en:dyskeratosis congenita n1=en:x-linked intellectual disability cantagrel type | n2=en:dyskeratosis congenita | rel=r_associated | relid=0 | w=30 en:x-linked intellectual disability cantagrel type -- r_associated #0: 30 / 0.698 -> en:fitzsimmons-mclachlan-gilbert syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:fitzsimmons-mclachlan-gilbert syndrome | rel=r_associated | relid=0 | w=30 en:x-linked intellectual disability cantagrel type -- r_associated #0: 30 / 0.698 -> en:hall riggs syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:hall riggs syndrome | rel=r_associated | relid=0 | w=30 en:x-linked intellectual disability cantagrel type -- r_associated #0: 30 / 0.698 -> en:lubs x-linked mental retardation syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:lubs x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=30 en:x-linked intellectual disability cantagrel type -- r_associated #0: 30 / 0.698 -> en:menkes kinky hair syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:menkes kinky hair syndrome | rel=r_associated | relid=0 | w=30 en:x-linked intellectual disability cantagrel type -- r_associated #0: 30 / 0.698 -> en:mental retardation, x-linked n1=en:x-linked intellectual disability cantagrel type | n2=en:mental retardation, x-linked | rel=r_associated | relid=0 | w=30 en:x-linked intellectual disability cantagrel type -- r_associated #0: 30 / 0.698 -> en:microcephaly microcornea syndrome seemanova type n1=en:x-linked intellectual disability cantagrel type | n2=en:microcephaly microcornea syndrome seemanova type | rel=r_associated | relid=0 | w=30 en:x-linked intellectual disability cantagrel type -- r_associated #0: 30 / 0.698 -> en:microphthalmia, syndromic 2 n1=en:x-linked intellectual disability cantagrel type | n2=en:microphthalmia, syndromic 2 | rel=r_associated | relid=0 | w=30 en:x-linked intellectual disability cantagrel type -- r_associated #0: 30 / 0.698 -> en:ohdo syndrome, maat-kievit-brunner type n1=en:x-linked intellectual disability cantagrel type | n2=en:ohdo syndrome, maat-kievit-brunner type | rel=r_associated | relid=0 | w=30 en:x-linked intellectual disability cantagrel type -- r_associated #0: 30 / 0.698 -> en:orofaciodigital syndrome 9 n1=en:x-linked intellectual disability cantagrel type | n2=en:orofaciodigital syndrome 9 | rel=r_associated | relid=0 | w=30 en:x-linked intellectual disability cantagrel type -- r_associated #0: 30 / 0.698 -> en:smith-magenis syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:smith-magenis syndrome | rel=r_associated | relid=0 | w=30 en:x-linked intellectual disability cantagrel type -- r_associated #0: 30 / 0.698 -> en:trisomy 10p n1=en:x-linked intellectual disability cantagrel type | n2=en:trisomy 10p | rel=r_associated | relid=0 | w=30 en:x-linked intellectual disability cantagrel type -- r_associated #0: 30 / 0.698 -> en:x-linked intellectual disability and epilepsy with progressive joint contracture and facial dysmorphism syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked intellectual disability and epilepsy with progressive joint contracture and facial dysmorphism syndrome | rel=r_associated | relid=0 | w=30 en:x-linked intellectual disability cantagrel type -- r_associated #0: 29 / 0.674 -> en:al gazali sabrinathan nair syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:al gazali sabrinathan nair syndrome | rel=r_associated | relid=0 | w=29 en:x-linked intellectual disability cantagrel type -- r_associated #0: 29 / 0.674 -> en:arachnodactyly and intellectual disability with facial dysmorphism syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:arachnodactyly and intellectual disability with facial dysmorphism syndrome | rel=r_associated | relid=0 | w=29 en:x-linked intellectual disability cantagrel type -- r_associated #0: 29 / 0.674 -> en:cantalamessa baldini ambrosi syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:cantalamessa baldini ambrosi syndrome | rel=r_associated | relid=0 | w=29 en:x-linked intellectual disability cantagrel type -- r_associated #0: 29 / 0.674 -> en:mild mental retardation n1=en:x-linked intellectual disability cantagrel type | n2=en:mild mental retardation | rel=r_associated | relid=0 | w=29 en:x-linked intellectual disability cantagrel type -- r_associated #0: 29 / 0.674 -> en:x-linked intellectual disability armfield type n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=29 en:x-linked intellectual disability cantagrel type -- r_associated #0: 29 / 0.674 -> en:x-linked intellectual disability shrimpton type n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked intellectual disability shrimpton type | rel=r_associated | relid=0 | w=29 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:3-methylglutaconic aciduria type 2 n1=en:x-linked intellectual disability cantagrel type | n2=en:3-methylglutaconic aciduria type 2 | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:albinism, ocular, with late-onset sensorineural deafness (disorder) n1=en:x-linked intellectual disability cantagrel type | n2=en:albinism, ocular, with late-onset sensorineural deafness (disorder) | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:aldred syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:aldred syndrome | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:biemond syndrome type 2 n1=en:x-linked intellectual disability cantagrel type | n2=en:biemond syndrome type 2 | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:brunner syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:brunner syndrome | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:choroideremia n1=en:x-linked intellectual disability cantagrel type | n2=en:choroideremia | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:chromosome xq27.3q28 duplication syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:chromosome xq27.3q28 duplication syndrome | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:classical phenylketonuria n1=en:x-linked intellectual disability cantagrel type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:craniofrontonasal dysplasia n1=en:x-linked intellectual disability cantagrel type | n2=en:craniofrontonasal dysplasia | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:deafness-hypogonadism syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:deafness-hypogonadism syndrome | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:dent's disease n1=en:x-linked intellectual disability cantagrel type | n2=en:dent's disease | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:ectodermal dysplasia with blindness syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:ectodermal dysplasia with blindness syndrome | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:fragile x syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:fragile x syndrome | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:hemophilia a n1=en:x-linked intellectual disability cantagrel type | n2=en:hemophilia a | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:hemophilia b n1=en:x-linked intellectual disability cantagrel type | n2=en:hemophilia b | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:hydrocephalus with obesity and hypogonadism syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:hydrocephalus with obesity and hypogonadism syndrome | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:hyperphosphatasia with mental retardation n1=en:x-linked intellectual disability cantagrel type | n2=en:hyperphosphatasia with mental retardation | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:ichthyosis, x-linked n1=en:x-linked intellectual disability cantagrel type | n2=en:ichthyosis, x-linked | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:microphthalmia, syndromic 7 n1=en:x-linked intellectual disability cantagrel type | n2=en:microphthalmia, syndromic 7 | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:spinocerebellar ataxia, x-linked 3 n1=en:x-linked intellectual disability cantagrel type | n2=en:spinocerebellar ataxia, x-linked 3 | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:syndromic x-linked intellectual disability type 11 n1=en:x-linked intellectual disability cantagrel type | n2=en:syndromic x-linked intellectual disability type 11 | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:viljoen kallis voges syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:viljoen kallis voges syndrome | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:x-linked combined immunodeficiency diseases n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked combined immunodeficiency diseases | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 28 / 0.651 -> en:x-linked hydrocephalus syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked hydrocephalus syndrome | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability cantagrel type -- r_associated #0: 27 / 0.628 -> en:17q11.2 microduplication syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:17q11.2 microduplication syndrome | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability cantagrel type -- r_associated #0: 27 / 0.628 -> en:angiokeratoma corporis diffusum n1=en:x-linked intellectual disability cantagrel type | n2=en:angiokeratoma corporis diffusum | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability cantagrel type -- r_associated #0: 27 / 0.628 -> en:anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability cantagrel type -- r_associated #0: 27 / 0.628 -> en:bulbo-spinal atrophy, x-linked n1=en:x-linked intellectual disability cantagrel type | n2=en:bulbo-spinal atrophy, x-linked | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability cantagrel type -- r_associated #0: 27 / 0.628 -> en:dyserythropoietic anemia with thrombocytopenia n1=en:x-linked intellectual disability cantagrel type | n2=en:dyserythropoietic anemia with thrombocytopenia | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability cantagrel type -- r_associated #0: 27 / 0.628 -> en:female restricted epilepsy with intellectual disability syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:female restricted epilepsy with intellectual disability syndrome | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability cantagrel type -- r_associated #0: 27 / 0.628 -> en:glycogen storage disease type iib n1=en:x-linked intellectual disability cantagrel type | n2=en:glycogen storage disease type iib | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability cantagrel type -- r_associated #0: 27 / 0.628 -> en:hernandez aguirre-negrete syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:hernandez aguirre-negrete syndrome | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability cantagrel type -- r_associated #0: 27 / 0.628 -> en:kosztolanyi syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:kosztolanyi syndrome | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability cantagrel type -- r_associated #0: 27 / 0.628 -> en:lesch-nyhan syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:lesch-nyhan syndrome | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability cantagrel type -- r_associated #0: 27 / 0.628 -> en:prader-willi habitus, osteopenia, and camptodactyly n1=en:x-linked intellectual disability cantagrel type | n2=en:prader-willi habitus, osteopenia, and camptodactyly | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability cantagrel type -- r_associated #0: 27 / 0.628 -> en:primary ciliary dyskinesia and retinitis pigmentosa syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:primary ciliary dyskinesia and retinitis pigmentosa syndrome | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability cantagrel type -- r_associated #0: 27 / 0.628 -> en:scholte syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:scholte syndrome | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability cantagrel type -- r_associated #0: 27 / 0.628 -> en:simpson-golabi-behmel syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:simpson-golabi-behmel syndrome | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability cantagrel type -- r_associated #0: 27 / 0.628 -> en:wolf-hirschhorn syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:wolf-hirschhorn syndrome | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability cantagrel type -- r_associated #0: 27 / 0.628 -> en:x-linked adrenal hypoplasia congenita n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked adrenal hypoplasia congenita | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability cantagrel type -- r_associated #0: 27 / 0.628 -> en:x-linked epilepsy with learning disability and behavior disorder syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked epilepsy with learning disability and behavior disorder syndrome | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability cantagrel type -- r_associated #0: 27 / 0.628 -> en:x-linked intellectual disability turner type n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked intellectual disability turner type | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability cantagrel type -- r_associated #0: 27 / 0.628 -> en:x-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability cantagrel type -- r_associated #0: 26 / 0.605 -> en:brachydactyly, type a1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation n1=en:x-linked intellectual disability cantagrel type | n2=en:brachydactyly, type a1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation | rel=r_associated | relid=0 | w=26 en:x-linked intellectual disability cantagrel type -- r_associated #0: 26 / 0.605 -> en:histidinemia n1=en:x-linked intellectual disability cantagrel type | n2=en:histidinemia | rel=r_associated | relid=0 | w=26 en:x-linked intellectual disability cantagrel type -- r_associated #0: 26 / 0.605 -> en:laurence-moon syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:laurence-moon syndrome | rel=r_associated | relid=0 | w=26 en:x-linked intellectual disability cantagrel type -- r_associated #0: 26 / 0.605 -> en:leukoencephalopathy, cystic, without megalencephaly n1=en:x-linked intellectual disability cantagrel type | n2=en:leukoencephalopathy, cystic, without megalencephaly | rel=r_associated | relid=0 | w=26 en:x-linked intellectual disability cantagrel type -- r_associated #0: 26 / 0.605 -> en:masa syndrome (disorder) n1=en:x-linked intellectual disability cantagrel type | n2=en:masa syndrome (disorder) | rel=r_associated | relid=0 | w=26 en:x-linked intellectual disability cantagrel type -- r_associated #0: 26 / 0.605 -> en:myopathy, x-linked, with excessive autophagy (disorder) n1=en:x-linked intellectual disability cantagrel type | n2=en:myopathy, x-linked, with excessive autophagy (disorder) | rel=r_associated | relid=0 | w=26 en:x-linked intellectual disability cantagrel type -- r_associated #0: 26 / 0.605 -> en:neuronal ceroid-lipofuscinoses n1=en:x-linked intellectual disability cantagrel type | n2=en:neuronal ceroid-lipofuscinoses | rel=r_associated | relid=0 | w=26 en:x-linked intellectual disability cantagrel type -- r_associated #0: 26 / 0.605 -> en:oto-palato-digital syndrome type 1 n1=en:x-linked intellectual disability cantagrel type | n2=en:oto-palato-digital syndrome type 1 | rel=r_associated | relid=0 | w=26 en:x-linked intellectual disability cantagrel type -- r_associated #0: 26 / 0.605 -> en:pallister w syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:pallister w syndrome | rel=r_associated | relid=0 | w=26 en:x-linked intellectual disability cantagrel type -- r_associated #0: 26 / 0.605 -> en:sesame syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:sesame syndrome | rel=r_associated | relid=0 | w=26 en:x-linked intellectual disability cantagrel type -- r_associated #0: 26 / 0.605 -> en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour n1=en:x-linked intellectual disability cantagrel type | n2=en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour | rel=r_associated | relid=0 | w=26 en:x-linked intellectual disability cantagrel type -- r_associated #0: 26 / 0.605 -> en:x-linked intellectual disability schimke type n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked intellectual disability schimke type | rel=r_associated | relid=0 | w=26 en:x-linked intellectual disability cantagrel type -- r_associated #0: 26 / 0.605 -> en:x-linked intellectual disability wilson type n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked intellectual disability wilson type | rel=r_associated | relid=0 | w=26 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:12q14 microdeletion syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:12q14 microdeletion syndrome | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:1p21.3 microdeletion syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:1p21.3 microdeletion syndrome | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:aniridia and intellectual disability syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:aniridia and intellectual disability syndrome | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:brachioskeletogenital syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:brachioskeletogenital syndrome | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:chitayat meunier hodgkinson syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:chitayat meunier hodgkinson syndrome | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:chromosome xp22.3 microdeletion syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:chromosome xp22.3 microdeletion syndrome | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:congenital cataract with ataxia and deafness syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:congenital cataract with ataxia and deafness syndrome | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:congenital disorder of glycosylation type 1s n1=en:x-linked intellectual disability cantagrel type | n2=en:congenital disorder of glycosylation type 1s | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:ferro-cerebro-cutaneous syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:ferro-cerebro-cutaneous syndrome | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:fountain syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:fountain syndrome | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:fried syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:fried syndrome | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:mental retardation spasticity ectrodactyly n1=en:x-linked intellectual disability cantagrel type | n2=en:mental retardation spasticity ectrodactyly | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:piussan lenaerts mathieu syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:piussan lenaerts mathieu syndrome | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:ppp2r5d-related intellectual disability n1=en:x-linked intellectual disability cantagrel type | n2=en:ppp2r5d-related intellectual disability | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:trisomy xq28 syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:trisomy xq28 syndrome | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability pai type n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked intellectual disability pai type | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability seemanova type n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked intellectual disability seemanova type | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability stevenson type n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked intellectual disability stevenson type | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability stoll type n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked intellectual disability stoll type | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability van esch type n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked intellectual disability van esch type | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability cantagrel type -- r_associated #0: 20 / 0.465 -> en:x-linked intellectual disability with acromegaly and hyperactivity syndrome n1=en:x-linked intellectual disability cantagrel type | n2=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | rel=r_associated | relid=0 | w=20

≈ 189 relations entrantes en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome --- r_associated #0: 42 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=42 en:scholte syndrome --- r_associated #0: 37 --> en:x-linked intellectual disability cantagrel type n1=en:scholte syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=37 en:12q14 microdeletion syndrome --- r_associated #0: 35 --> en:x-linked intellectual disability cantagrel type n1=en:12q14 microdeletion syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=35 en:ectodermal dysplasia with blindness syndrome --- r_associated #0: 35 --> en:x-linked intellectual disability cantagrel type n1=en:ectodermal dysplasia with blindness syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=35 en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome --- r_associated #0: 35 --> en:x-linked intellectual disability cantagrel type n1=en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=35 en:spondyloepiphyseal dysplasia tarda kohn type --- r_associated #0: 35 --> en:x-linked intellectual disability cantagrel type n1=en:spondyloepiphyseal dysplasia tarda kohn type | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=35 en:primary ciliary dyskinesia and retinitis pigmentosa syndrome --- r_associated #0: 34 --> en:x-linked intellectual disability cantagrel type n1=en:primary ciliary dyskinesia and retinitis pigmentosa syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=34 en:17q11.2 microduplication syndrome --- r_associated #0: 32 --> en:x-linked intellectual disability cantagrel type n1=en:17q11.2 microduplication syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=32 en:cooper jabs syndrome --- r_associated #0: 32 --> en:x-linked intellectual disability cantagrel type n1=en:cooper jabs syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=32 en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome --- r_associated #0: 32 --> en:x-linked intellectual disability cantagrel type n1=en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=32 en:hall riggs syndrome --- r_associated #0: 32 --> en:x-linked intellectual disability cantagrel type n1=en:hall riggs syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=32 en:trisomy xq28 syndrome --- r_associated #0: 32 --> en:x-linked intellectual disability cantagrel type n1=en:trisomy xq28 syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=32 en:aniridia and intellectual disability syndrome --- r_associated #0: 31 --> en:x-linked intellectual disability cantagrel type n1=en:aniridia and intellectual disability syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=31 en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome --- r_associated #0: 31 --> en:x-linked intellectual disability cantagrel type n1=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=31 en:fried syndrome --- r_associated #0: 31 --> en:x-linked intellectual disability cantagrel type n1=en:fried syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=31 en:ppp2r5d-related intellectual disability --- r_associated #0: 31 --> en:x-linked intellectual disability cantagrel type n1=en:ppp2r5d-related intellectual disability | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=31 en:x-linked intellectual disability van esch type --- r_associated #0: 31 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked intellectual disability van esch type | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=31 en:fountain syndrome --- r_associated #0: 30 --> en:x-linked intellectual disability cantagrel type n1=en:fountain syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=30 en:x-linked intellectual disability pai type --- r_associated #0: 30 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked intellectual disability pai type | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=30 en:x-linked intellectual disability with acromegaly and hyperactivity syndrome --- r_associated #0: 30 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=30 en:brachioskeletogenital syndrome --- r_associated #0: 29 --> en:x-linked intellectual disability cantagrel type n1=en:brachioskeletogenital syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=29 en:congenital cataract with ataxia and deafness syndrome --- r_associated #0: 29 --> en:x-linked intellectual disability cantagrel type n1=en:congenital cataract with ataxia and deafness syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=29 en:mental retardation spasticity ectrodactyly --- r_associated #0: 29 --> en:x-linked intellectual disability cantagrel type n1=en:mental retardation spasticity ectrodactyly | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=29 en:piussan lenaerts mathieu syndrome --- r_associated #0: 29 --> en:x-linked intellectual disability cantagrel type n1=en:piussan lenaerts mathieu syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=29 en:1p21.3 microdeletion syndrome --- r_associated #0: 28 --> en:x-linked intellectual disability cantagrel type n1=en:1p21.3 microdeletion syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=28 en:ferro-cerebro-cutaneous syndrome --- r_associated #0: 28 --> en:x-linked intellectual disability cantagrel type n1=en:ferro-cerebro-cutaneous syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=28 en:x-linked intellectual disability armfield type --- r_associated #0: 28 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=28 en:arachnodactyly and intellectual disability with facial dysmorphism syndrome --- r_associated #0: 27 --> en:x-linked intellectual disability cantagrel type n1=en:arachnodactyly and intellectual disability with facial dysmorphism syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=27 en:chitayat meunier hodgkinson syndrome --- r_associated #0: 27 --> en:x-linked intellectual disability cantagrel type n1=en:chitayat meunier hodgkinson syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=27 en:chromosome xp22.3 microdeletion syndrome --- r_associated #0: 27 --> en:x-linked intellectual disability cantagrel type n1=en:chromosome xp22.3 microdeletion syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=27 en:kosztolanyi syndrome --- r_associated #0: 27 --> en:x-linked intellectual disability cantagrel type n1=en:kosztolanyi syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability seemanova type --- r_associated #0: 27 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked intellectual disability seemanova type | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability stevenson type --- r_associated #0: 27 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked intellectual disability stevenson type | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability stoll type --- r_associated #0: 27 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked intellectual disability stoll type | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=27 en:x-linked intellectual disability with ataxia and apraxia syndrome --- r_associated #0: 27 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked intellectual disability with ataxia and apraxia syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=27 en:congenital disorder of glycosylation type 1s --- r_associated #0: 26 --> en:x-linked intellectual disability cantagrel type n1=en:congenital disorder of glycosylation type 1s | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=26 en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome --- r_associated #0: 26 --> en:x-linked intellectual disability cantagrel type n1=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=26 en:x-linked intellectual disability miles carpenter type --- r_associated #0: 26 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked intellectual disability miles carpenter type | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=26 en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome --- r_associated #0: 26 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=26 en:3-methylglutaconic aciduria type 2 --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:3-methylglutaconic aciduria type 2 | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:achalasia microcephaly --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:achalasia microcephaly | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:adolescent x-linked adrenoleukodystrophy --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:adolescent x-linked adrenoleukodystrophy | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:aicardi's syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:aicardi's syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:al gazali sabrinathan nair syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:al gazali sabrinathan nair syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:albinism, ocular, with late-onset sensorineural deafness (disorder) --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:albinism, ocular, with late-onset sensorineural deafness (disorder) | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:aldred syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:aldred syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:alpha-thalassemia/mental retardation syndrome, nondeletion type, x-linked --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:alpha-thalassemia/mental retardation syndrome, nondeletion type, x-linked | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:alport syndrome, x-linked --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:alport syndrome, x-linked | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:androgen-insensitivity syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:androgen-insensitivity syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:angiokeratoma corporis diffusum --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:angiokeratoma corporis diffusum | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:ataxia, fatal x-linked, with deafness and loss of vision --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:ataxia, fatal x-linked, with deafness and loss of vision | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:atkin syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:atkin syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:bardet-biedl syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:bardet-biedl syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:biemond syndrome type 2 --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:biemond syndrome type 2 | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:borderline mental retardation (i.q. 70-85) --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:borderline mental retardation (i.q. 70-85) | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:bornholm eye disease --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:bornholm eye disease | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:brachydactyly, type a1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:brachydactyly, type a1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:brunner syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:brunner syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:bulbo-spinal atrophy, x-linked --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:bulbo-spinal atrophy, x-linked | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:cantalamessa baldini ambrosi syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:cantalamessa baldini ambrosi syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:cerebrofaciothoracic dysplasia --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:cerebrofaciothoracic dysplasia | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:childhood cerebral x-linked adrenoleukodystrophy --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:childhood cerebral x-linked adrenoleukodystrophy | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:choroideremia --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:choroideremia | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:chromosome xq27.3q28 duplication syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:chromosome xq27.3q28 duplication syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:chronic granulomatous disease --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:chronic granulomatous disease | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:classical phenylketonuria --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:classical phenylketonuria | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:coffin-siris syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:coffin-siris syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:congenital hypoplasia of ulna and intellectual disability syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:congenital hypoplasia of ulna and intellectual disability syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:corpus callosum, agenesis of, with facial anomalies and robin sequence --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:corpus callosum, agenesis of, with facial anomalies and robin sequence | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:craniofrontonasal dysplasia --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:craniofrontonasal dysplasia | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:de barsy syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:de barsy syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:deafness-hypogonadism syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:deafness-hypogonadism syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:dent's disease --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:dent's disease | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:dermoids of cornea --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:dermoids of cornea | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:digitorenocerebral syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:digitorenocerebral syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:dyserythropoietic anemia with thrombocytopenia --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:dyserythropoietic anemia with thrombocytopenia | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:dyskeratosis congenita --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:dyskeratosis congenita | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:female restricted epilepsy with intellectual disability syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:female restricted epilepsy with intellectual disability syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:fitzsimmons-mclachlan-gilbert syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:fitzsimmons-mclachlan-gilbert syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:fragile x syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:fragile x syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:fraxe intellectual disability syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:fraxe intellectual disability syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:glucose-6-phosphate dehydrogenase deficiency anemia --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:glucose-6-phosphate dehydrogenase deficiency anemia | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:glycogen storage disease type iib --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:glycogen storage disease type iib | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:glycogen storage disease type vi --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:glycogen storage disease type vi | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:glycogen storage disease type viii --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:glycogen storage disease type viii | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:goniodysgenesis-mental retardation-short stature syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:goniodysgenesis-mental retardation-short stature syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:gurrieri sammito bellussi syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:gurrieri sammito bellussi syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:hemophilia a --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:hemophilia a | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:hemophilia b --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:hemophilia b | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:hernandez aguirre-negrete syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:hernandez aguirre-negrete syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:histidinemia --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:histidinemia | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:holoprosencephaly with fetal akinesia-hypokinesia sequence --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:holoprosencephaly with fetal akinesia-hypokinesia sequence | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:huntington disease --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:huntington disease | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:hydrocephalus with obesity and hypogonadism syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:hydrocephalus with obesity and hypogonadism syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:hyperphosphatasia with mental retardation --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:hyperphosphatasia with mental retardation | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:ichthyosis, x-linked --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:ichthyosis, x-linked | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:juberg-marsidi syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:juberg-marsidi syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:kapur toriello syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:kapur toriello syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:kaufman oculocerebrofacial syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:kaufman oculocerebrofacial syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:laurence-moon syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:laurence-moon syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:lesch-nyhan syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:lesch-nyhan syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:leukoencephalopathy, cystic, without megalencephaly --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:leukoencephalopathy, cystic, without megalencephaly | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:lipodystrophy, intellectual disability, deafness syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:lipodystrophy, intellectual disability, deafness syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:lowry maclean syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:lowry maclean syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:lubs x-linked mental retardation syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:lubs x-linked mental retardation syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:marfanoid mental retardation syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:marfanoid mental retardation syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:masa syndrome (disorder) --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:masa syndrome (disorder) | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:menkes kinky hair syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:menkes kinky hair syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:mental retardation syndrome, belgian type --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:mental retardation syndrome, belgian type | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:mental retardation, skeletal dysplasia, and abducens palsy --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:mental retardation, skeletal dysplasia, and abducens palsy | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:mental retardation, x-linked --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:mental retardation, x-linked | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:mental retardation, x-linked, syndromic, christianson type --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:mental retardation, x-linked, syndromic, christianson type | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:mental retardation, x-linked, with short stature, hypogonadism, and abnormal gait --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:mental retardation, x-linked, with short stature, hypogonadism, and abnormal gait | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:microcephalus and intellectual disability with phalangeal and neurological anomaly syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:microcephalus and intellectual disability with phalangeal and neurological anomaly syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:microcephaly microcornea syndrome seemanova type --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:microcephaly microcornea syndrome seemanova type | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:microphthalmia, syndromic 2 --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:microphthalmia, syndromic 2 | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:microphthalmia, syndromic 7 --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:microphthalmia, syndromic 7 | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:mild mental retardation --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:mild mental retardation | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:moderate mental retardation (i.q. 35-49) --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:moderate mental retardation (i.q. 35-49) | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:moloney syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:moloney syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:mowat-wilson syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:mowat-wilson syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:muscular dystrophy, duchenne --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:muscular dystrophy, duchenne | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:muscular dystrophy, emery-dreifuss --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:muscular dystrophy, emery-dreifuss | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:myopathy, x-linked, with excessive autophagy (disorder) --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:myopathy, x-linked, with excessive autophagy (disorder) | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:neuronal ceroid-lipofuscinoses --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:neuronal ceroid-lipofuscinoses | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:neutropenia, severe congenital, x-linked --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:neutropenia, severe congenital, x-linked | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:nutritional mental retardation --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:nutritional mental retardation | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:ocular albinism, type ii --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:ocular albinism, type ii | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:ohdo syndrome, maat-kievit-brunner type --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:ohdo syndrome, maat-kievit-brunner type | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:optic atrophy 2 (disorder) --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:optic atrophy 2 (disorder) | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:ornithine carbamoyltransferase deficiency --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:ornithine carbamoyltransferase deficiency | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:orofaciodigital syndrome 5 --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:orofaciodigital syndrome 5 | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:orofaciodigital syndrome 9 --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:orofaciodigital syndrome 9 | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:orotic aciduria --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:orotic aciduria | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:ossification anomaly with psychomotor developmental delay syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:ossification anomaly with psychomotor developmental delay syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:other mental retardation --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:other mental retardation | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:oto-palato-digital syndrome type 1 --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:oto-palato-digital syndrome type 1 | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:pallister w syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:pallister w syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:pashayan syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:pashayan syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:perniola krajewska carnevale syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:perniola krajewska carnevale syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:placental steroid sulfatase deficiency --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:placental steroid sulfatase deficiency | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:prader-willi habitus, osteopenia, and camptodactyly --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:prader-willi habitus, osteopenia, and camptodactyly | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:renpenning syndrome 1 --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:renpenning syndrome 1 | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:savant syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:savant syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:sesame syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:sesame syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:severe mental retardation (i.q. 20-34) --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:severe mental retardation (i.q. 20-34) | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:severe x-linked intellectual disability gustavson type --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:severe x-linked intellectual disability gustavson type | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:shprintzen-goldberg syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:shprintzen-goldberg syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:simpson-golabi-behmel syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:simpson-golabi-behmel syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:smith-magenis syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:smith-magenis syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia, x-linked 3 --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:spinocerebellar ataxia, x-linked 3 | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:syndromic x-linked intellectual disability type 11 --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:syndromic x-linked intellectual disability type 11 | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:tranebjaerg svejgaard syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:tranebjaerg svejgaard syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:trisomy 10p --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:trisomy 10p | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:uveal coloboma with cleft lip and palate and intellectual disability syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:uveal coloboma with cleft lip and palate and intellectual disability syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:viljoen kallis voges syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:viljoen kallis voges syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:waisman syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:waisman syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:wilson turner syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:wilson turner syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:wiskott-aldrich syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:wiskott-aldrich syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:wolf-hirschhorn syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:wolf-hirschhorn syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:x-linked adrenal hypoplasia congenita --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked adrenal hypoplasia congenita | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:x-linked combined immunodeficiency diseases --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked combined immunodeficiency diseases | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:x-linked congenital dyserythropoietic anemia with thrombocytopenia --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked congenital dyserythropoietic anemia with thrombocytopenia | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:x-linked dominant chondrodysplasia chassaing lacombe type --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked dominant chondrodysplasia chassaing lacombe type | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:x-linked epilepsy with learning disability and behavior disorder syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked epilepsy with learning disability and behavior disorder syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:x-linked hydrocephalus syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked hydrocephalus syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability and epilepsy with progressive joint contracture and facial dysmorphism syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked intellectual disability and epilepsy with progressive joint contracture and facial dysmorphism syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability schimke type --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked intellectual disability schimke type | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability shrimpton type --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked intellectual disability shrimpton type | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability stocco dos santos type --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked intellectual disability stocco dos santos type | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability turner type --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked intellectual disability turner type | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability wilson type --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked intellectual disability wilson type | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 en:x-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome --- r_associated #0: 20 --> en:x-linked intellectual disability cantagrel type n1=en:x-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=20 céroïdes lipofuscinoses neuronales --- r_associated #0: 10 --> en:x-linked intellectual disability cantagrel type n1=céroïdes lipofuscinoses neuronales | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=10 céroïdes-lipofuscinoses neuronales --- r_associated #0: 10 --> en:x-linked intellectual disability cantagrel type n1=céroïdes-lipofuscinoses neuronales | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=10 en:Aicardi's syndrome --- r_associated #0: 10 --> en:x-linked intellectual disability cantagrel type n1=en:Aicardi's syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=10 en:Smith-Magenis syndrome --- r_associated #0: 10 --> en:x-linked intellectual disability cantagrel type n1=en:Smith-Magenis syndrome | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=10 syndrome de Viljoen-Kallis-Voges --- r_associated #0: 10 --> en:x-linked intellectual disability cantagrel type n1=syndrome de Viljoen-Kallis-Voges | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=10 syndrome de microcéphalie-brachydactylie-déficience intellectuelle --- r_associated #0: 10 --> en:x-linked intellectual disability cantagrel type n1=syndrome de microcéphalie-brachydactylie-déficience intellectuelle | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=10 céroïdes lipofuschinoses neuronales --- r_associated #0: 5 --> en:x-linked intellectual disability cantagrel type n1=céroïdes lipofuschinoses neuronales | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=5 dystrophie musculaire d'Emery-Dreifuss --- r_associated #0: 5 --> en:x-linked intellectual disability cantagrel type n1=dystrophie musculaire d'Emery-Dreifuss | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=5 dystrophie musculaire de Duchenne --- r_associated #0: 5 --> en:x-linked intellectual disability cantagrel type n1=dystrophie musculaire de Duchenne | n2=en:x-linked intellectual disability cantagrel type | rel=r_associated | relid=0 | w=5