'en:severe x-linked intellectual disability gustavson type'
(id=9102733 ; fe=en:severe x-linked intellectual disability gustavson type ; type=1 ; niveau=200 ;
luminosité=25 ;
somme entrante=2369 creation date=2017-10-29 touchdate=2024-09-19 01:01:31.000) ≈ 76 relations sortantes
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 25 / 1 ->
en:severe
n1=en:severe x-linked intellectual disability gustavson type | n2=en:severe | rel=r_associated | relid=0 | w=25
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:12q14 microdeletion syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:12q14 microdeletion syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:17q11.2 microduplication syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:17q11.2 microduplication syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:1p21.3 microdeletion syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:1p21.3 microdeletion syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:aniridia and intellectual disability syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:aniridia and intellectual disability syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:aniridia, ptosis, intellectual disability, familial obesity syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:aphalangy and syndactyly with microcephaly syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:aphalangy and syndactyly with microcephaly syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:arachnodactyly and intellectual disability with facial dysmorphism syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:arachnodactyly and intellectual disability with facial dysmorphism syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:arhinia, choanal atresia, and microphthalmia
n1=en:severe x-linked intellectual disability gustavson type | n2=en:arhinia, choanal atresia, and microphthalmia | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:autosomal dominant focal dystonia dyt25 type
n1=en:severe x-linked intellectual disability gustavson type | n2=en:autosomal dominant focal dystonia dyt25 type | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:brachioskeletogenital syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:brachioskeletogenital syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:brain calcification rajab type
n1=en:severe x-linked intellectual disability gustavson type | n2=en:brain calcification rajab type | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:brain malformation, congenital heart disease, postaxial polydactyly syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:brain malformation, congenital heart disease, postaxial polydactyly syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:cataract glaucoma syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:cataract glaucoma syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:chitayat meunier hodgkinson syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:chitayat meunier hodgkinson syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:chromosome xp22.3 microdeletion syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:chromosome xp22.3 microdeletion syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:congenital cataract with ataxia and deafness syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:congenital cataract with ataxia and deafness syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:congenital cerebral ventriculomegaly
n1=en:severe x-linked intellectual disability gustavson type | n2=en:congenital cerebral ventriculomegaly | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:congenital disorder of glycosylation type 1s
n1=en:severe x-linked intellectual disability gustavson type | n2=en:congenital disorder of glycosylation type 1s | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:cooper jabs syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:cooper jabs syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:deafness and myopia syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:deafness and myopia syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:disorder of eye co-occurrent and due to marfan syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:disorder of eye co-occurrent and due to marfan syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:dysmorphism, pectus carinatum, joint laxity syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:dysmorphism, pectus carinatum, joint laxity syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:ectodermal dysplasia with blindness syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:ectodermal dysplasia with blindness syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:ehlers-danlos syndrome kyphoscoliotic and deafness type
n1=en:severe x-linked intellectual disability gustavson type | n2=en:ehlers-danlos syndrome kyphoscoliotic and deafness type | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:epithelio-exfoliative colitis and deafness syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:epithelio-exfoliative colitis and deafness syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:fara chlupackova syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:fara chlupackova syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:ferro-cerebro-cutaneous syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:ferro-cerebro-cutaneous syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:fountain syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:fountain syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:fried syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:fried syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:glaucoma and sleep apnea syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:glaucoma and sleep apnea syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:halal syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:halal syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:hall riggs syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:hall riggs syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:hypertrichosis and acromegaloid facial appearance syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:hypertrichosis and acromegaloid facial appearance syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:hypomandibular faciocranial dysostosis
n1=en:severe x-linked intellectual disability gustavson type | n2=en:hypomandibular faciocranial dysostosis | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:insulin growth factor i deficiency
n1=en:severe x-linked intellectual disability gustavson type | n2=en:insulin growth factor i deficiency | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:juvenile amyotrophic lateral sclerosis
n1=en:severe x-linked intellectual disability gustavson type | n2=en:juvenile amyotrophic lateral sclerosis | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:kosztolanyi syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:kosztolanyi syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:lissencephaly type 3 familial fetal akinesia sequence syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:mental retardation spasticity ectrodactyly
n1=en:severe x-linked intellectual disability gustavson type | n2=en:mental retardation spasticity ectrodactyly | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:microcephaly albinism digital anomalies syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:microcephaly albinism digital anomalies syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:moyamoya disease with early onset achalasia
n1=en:severe x-linked intellectual disability gustavson type | n2=en:moyamoya disease with early onset achalasia | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:nablus mask-like facial syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:nablus mask-like facial syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:pigmented paravenous chorioretinal atrophy
n1=en:severe x-linked intellectual disability gustavson type | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:piussan lenaerts mathieu syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:piussan lenaerts mathieu syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:porencephaly
n1=en:severe x-linked intellectual disability gustavson type | n2=en:porencephaly | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:ppp2r5d-related intellectual disability
n1=en:severe x-linked intellectual disability gustavson type | n2=en:ppp2r5d-related intellectual disability | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:primary ciliary dyskinesia and retinitis pigmentosa syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:primary ciliary dyskinesia and retinitis pigmentosa syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:robinow-like syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:robinow-like syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:scholte syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:scholte syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:short stature syndrome, brussels type
n1=en:severe x-linked intellectual disability gustavson type | n2=en:short stature syndrome, brussels type | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:spondyloepiphyseal dysplasia tarda kohn type
n1=en:severe x-linked intellectual disability gustavson type | n2=en:spondyloepiphyseal dysplasia tarda kohn type | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:trisomy xq28 syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:trisomy xq28 syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:x-linked intellectual disability armfield type
n1=en:severe x-linked intellectual disability gustavson type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
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:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:x-linked intellectual disability miles carpenter type
n1=en:severe x-linked intellectual disability gustavson type | n2=en:x-linked intellectual disability miles carpenter type | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:x-linked intellectual disability pai type
n1=en:severe x-linked intellectual disability gustavson type | n2=en:x-linked intellectual disability pai type | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:x-linked intellectual disability seemanova type
n1=en:severe x-linked intellectual disability gustavson type | n2=en:x-linked intellectual disability seemanova type | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:x-linked intellectual disability stevenson type
n1=en:severe x-linked intellectual disability gustavson type | n2=en:x-linked intellectual disability stevenson type | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:x-linked intellectual disability stoll type
n1=en:severe x-linked intellectual disability gustavson type | n2=en:x-linked intellectual disability stoll type | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:x-linked intellectual disability van esch type
n1=en:severe x-linked intellectual disability gustavson type | n2=en:x-linked intellectual disability van esch type | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:x-linked intellectual disability with acromegaly and hyperactivity syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:x-linked intellectual disability with ataxia and apraxia syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:x-linked intellectual disability with ataxia and apraxia syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
en:yemenite deaf-blind hypopigmentation syndrome
n1=en:severe x-linked intellectual disability gustavson type | n2=en:yemenite deaf-blind hypopigmentation syndrome | rel=r_associated | relid=0 | w=20
- en:severe x-linked intellectual disability gustavson type --
r_associated #0: 20 / 0.8 ->
rétinite pigmentaire paraveineuse
n1=en:severe x-linked intellectual disability gustavson type | n2=rétinite pigmentaire paraveineuse | rel=r_associated | relid=0 | w=20
| ≈ 76 relations entrantes
- rétinite pigmentaire paraveineuse ---
r_associated #0: 42 -->
en:severe x-linked intellectual disability gustavson type
n1=rétinite pigmentaire paraveineuse | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=42
- en:ehlers-danlos syndrome kyphoscoliotic and deafness type ---
r_associated #0: 41 -->
en:severe x-linked intellectual disability gustavson type
n1=en:ehlers-danlos syndrome kyphoscoliotic and deafness type | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=41
- en:glaucoma and sleep apnea syndrome ---
r_associated #0: 41 -->
en:severe x-linked intellectual disability gustavson type
n1=en:glaucoma and sleep apnea syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=41
- en:x-linked intellectual disability seemanova type ---
r_associated #0: 41 -->
en:severe x-linked intellectual disability gustavson type
n1=en:x-linked intellectual disability seemanova type | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=41
- en:pigmented paravenous chorioretinal atrophy ---
r_associated #0: 40 -->
en:severe x-linked intellectual disability gustavson type
n1=en:pigmented paravenous chorioretinal atrophy | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=40
- en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome ---
r_associated #0: 40 -->
en:severe x-linked intellectual disability gustavson type
n1=en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=40
- en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome ---
r_associated #0: 39 -->
en:severe x-linked intellectual disability gustavson type
n1=en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=39
- en:trisomy xq28 syndrome ---
r_associated #0: 37 -->
en:severe x-linked intellectual disability gustavson type
n1=en:trisomy xq28 syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=37
- en:aphalangy and syndactyly with microcephaly syndrome ---
r_associated #0: 36 -->
en:severe x-linked intellectual disability gustavson type
n1=en:aphalangy and syndactyly with microcephaly syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=36
- en:fountain syndrome ---
r_associated #0: 36 -->
en:severe x-linked intellectual disability gustavson type
n1=en:fountain syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=36
- en:ppp2r5d-related intellectual disability ---
r_associated #0: 35 -->
en:severe x-linked intellectual disability gustavson type
n1=en:ppp2r5d-related intellectual disability | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=35
- en:spondyloepiphyseal dysplasia tarda kohn type ---
r_associated #0: 35 -->
en:severe x-linked intellectual disability gustavson type
n1=en:spondyloepiphyseal dysplasia tarda kohn type | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability pai type ---
r_associated #0: 35 -->
en:severe x-linked intellectual disability gustavson type
n1=en:x-linked intellectual disability pai type | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=35
- en:chitayat meunier hodgkinson syndrome ---
r_associated #0: 34 -->
en:severe x-linked intellectual disability gustavson type
n1=en:chitayat meunier hodgkinson syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=34
- en:congenital cerebral ventriculomegaly ---
r_associated #0: 34 -->
en:severe x-linked intellectual disability gustavson type
n1=en:congenital cerebral ventriculomegaly | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=34
- en:juvenile amyotrophic lateral sclerosis ---
r_associated #0: 34 -->
en:severe x-linked intellectual disability gustavson type
n1=en:juvenile amyotrophic lateral sclerosis | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=34
- en:piussan lenaerts mathieu syndrome ---
r_associated #0: 34 -->
en:severe x-linked intellectual disability gustavson type
n1=en:piussan lenaerts mathieu syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type ---
r_associated #0: 34 -->
en:severe x-linked intellectual disability gustavson type
n1=en:x-linked intellectual disability armfield type | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability with acromegaly and hyperactivity syndrome ---
r_associated #0: 34 -->
en:severe x-linked intellectual disability gustavson type
n1=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=34
- en:brachioskeletogenital syndrome ---
r_associated #0: 32 -->
en:severe x-linked intellectual disability gustavson type
n1=en:brachioskeletogenital syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=32
- en:chromosome xp22.3 microdeletion syndrome ---
r_associated #0: 32 -->
en:severe x-linked intellectual disability gustavson type
n1=en:chromosome xp22.3 microdeletion syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=32
- en:congenital disorder of glycosylation type 1s ---
r_associated #0: 32 -->
en:severe x-linked intellectual disability gustavson type
n1=en:congenital disorder of glycosylation type 1s | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=32
- en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome ---
r_associated #0: 32 -->
en:severe x-linked intellectual disability gustavson type
n1=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=32
- en:osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome ---
r_associated #0: 32 -->
en:severe x-linked intellectual disability gustavson type
n1=en:osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=32
- en:robinow-like syndrome ---
r_associated #0: 32 -->
en:severe x-linked intellectual disability gustavson type
n1=en:robinow-like syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=32
- en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome ---
r_associated #0: 32 -->
en:severe x-linked intellectual disability gustavson type
n1=en:severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome | 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 -->
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 stevenson type ---
r_associated #0: 32 -->
en:severe x-linked intellectual disability gustavson type
n1=en:x-linked intellectual disability stevenson type | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=32
- en:aniridia, ptosis, intellectual disability, familial obesity syndrome ---
r_associated #0: 31 -->
en:severe x-linked intellectual disability gustavson type
n1=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=31
- en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome ---
r_associated #0: 31 -->
en:severe x-linked intellectual disability gustavson type
n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=31
- en:cataract glaucoma syndrome ---
r_associated #0: 31 -->
en:severe x-linked intellectual disability gustavson type
n1=en:cataract glaucoma syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=31
- en:ectodermal dysplasia with blindness syndrome ---
r_associated #0: 31 -->
en:severe x-linked intellectual disability gustavson type
n1=en:ectodermal dysplasia with blindness syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=31
- en:epithelio-exfoliative colitis and deafness syndrome ---
r_associated #0: 31 -->
en:severe x-linked intellectual disability gustavson type
n1=en:epithelio-exfoliative colitis and deafness syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=31
- en:fried syndrome ---
r_associated #0: 31 -->
en:severe x-linked intellectual disability gustavson type
n1=en:fried syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=31
- en:moyamoya disease with early onset achalasia ---
r_associated #0: 31 -->
en:severe x-linked intellectual disability gustavson type
n1=en:moyamoya disease with early onset achalasia | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=31
- en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome ---
r_associated #0: 31 -->
en:severe x-linked intellectual disability gustavson type
n1=en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability stoll type ---
r_associated #0: 31 -->
en:severe x-linked intellectual disability gustavson type
n1=en:x-linked intellectual disability stoll type | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability with ataxia and apraxia syndrome ---
r_associated #0: 31 -->
en:severe x-linked intellectual disability gustavson type
n1=en:x-linked intellectual disability with ataxia and apraxia syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=31
- en:12q14 microdeletion syndrome ---
r_associated #0: 30 -->
en:severe x-linked intellectual disability gustavson type
n1=en:12q14 microdeletion syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=30
- en:aniridia and intellectual disability syndrome ---
r_associated #0: 30 -->
en:severe x-linked intellectual disability gustavson type
n1=en:aniridia and intellectual disability syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=30
- en:brain calcification rajab type ---
r_associated #0: 30 -->
en:severe x-linked intellectual disability gustavson type
n1=en:brain calcification rajab type | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=30
- en:brain malformation, congenital heart disease, postaxial polydactyly syndrome ---
r_associated #0: 30 -->
en:severe x-linked intellectual disability gustavson type
n1=en:brain malformation, congenital heart disease, postaxial polydactyly syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=30
- en:ferro-cerebro-cutaneous syndrome ---
r_associated #0: 30 -->
en:severe x-linked intellectual disability gustavson type
n1=en:ferro-cerebro-cutaneous syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=30
- en:halal syndrome ---
r_associated #0: 30 -->
en:severe x-linked intellectual disability gustavson type
n1=en:halal syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=30
- en:hypertrichosis and acromegaloid facial appearance syndrome ---
r_associated #0: 30 -->
en:severe x-linked intellectual disability gustavson type
n1=en:hypertrichosis and acromegaloid facial appearance syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=30
- en:scholte syndrome ---
r_associated #0: 30 -->
en:severe x-linked intellectual disability gustavson type
n1=en:scholte syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability miles carpenter type ---
r_associated #0: 30 -->
en:severe x-linked intellectual disability gustavson type
n1=en:x-linked intellectual disability miles carpenter type | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=30
- en:1p21.3 microdeletion syndrome ---
r_associated #0: 29 -->
en:severe x-linked intellectual disability gustavson type
n1=en:1p21.3 microdeletion syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=29
- en:autosomal dominant focal dystonia dyt25 type ---
r_associated #0: 29 -->
en:severe x-linked intellectual disability gustavson type
n1=en:autosomal dominant focal dystonia dyt25 type | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=29
- en:insulin growth factor i deficiency ---
r_associated #0: 29 -->
en:severe x-linked intellectual disability gustavson type
n1=en:insulin growth factor i deficiency | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=29
- en:lissencephaly type 3 familial fetal akinesia sequence syndrome ---
r_associated #0: 29 -->
en:severe x-linked intellectual disability gustavson type
n1=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability van esch type ---
r_associated #0: 29 -->
en:severe x-linked intellectual disability gustavson type
n1=en:x-linked intellectual disability van esch type | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=29
- en:arachnodactyly and intellectual disability with facial dysmorphism syndrome ---
r_associated #0: 28 -->
en:severe x-linked intellectual disability gustavson type
n1=en:arachnodactyly and intellectual disability with facial dysmorphism syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=28
- en:congenital cataract with ataxia and deafness syndrome ---
r_associated #0: 28 -->
en:severe x-linked intellectual disability gustavson type
n1=en:congenital cataract with ataxia and deafness syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=28
- en:deafness and myopia syndrome ---
r_associated #0: 28 -->
en:severe x-linked intellectual disability gustavson type
n1=en:deafness and myopia syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=28
- en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome ---
r_associated #0: 28 -->
en:severe x-linked intellectual disability gustavson type
n1=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=28
- en:dysmorphism, pectus carinatum, joint laxity syndrome ---
r_associated #0: 28 -->
en:severe x-linked intellectual disability gustavson type
n1=en:dysmorphism, pectus carinatum, joint laxity syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=28
- en:hall riggs syndrome ---
r_associated #0: 28 -->
en:severe x-linked intellectual disability gustavson type
n1=en:hall riggs syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=28
- en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome ---
r_associated #0: 28 -->
en:severe x-linked intellectual disability gustavson type
n1=en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=28
- en:short stature syndrome, brussels type ---
r_associated #0: 28 -->
en:severe x-linked intellectual disability gustavson type
n1=en:short stature syndrome, brussels type | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=28
- en:17q11.2 microduplication syndrome ---
r_associated #0: 27 -->
en:severe x-linked intellectual disability gustavson type
n1=en:17q11.2 microduplication syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=27
- en:disorder of eye co-occurrent and due to marfan syndrome ---
r_associated #0: 27 -->
en:severe x-linked intellectual disability gustavson type
n1=en:disorder of eye co-occurrent and due to marfan syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=27
- en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome ---
r_associated #0: 27 -->
en:severe x-linked intellectual disability gustavson type
n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=27
- en:primary ciliary dyskinesia and retinitis pigmentosa syndrome ---
r_associated #0: 27 -->
en:severe x-linked intellectual disability gustavson type
n1=en:primary ciliary dyskinesia and retinitis pigmentosa syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=27
- en:yemenite deaf-blind hypopigmentation syndrome ---
r_associated #0: 27 -->
en:severe x-linked intellectual disability gustavson type
n1=en:yemenite deaf-blind hypopigmentation syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=27
- en:arhinia, choanal atresia, and microphthalmia ---
r_associated #0: 26 -->
en:severe x-linked intellectual disability gustavson type
n1=en:arhinia, choanal atresia, and microphthalmia | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=26
- en:cooper jabs syndrome ---
r_associated #0: 26 -->
en:severe x-linked intellectual disability gustavson type
n1=en:cooper jabs syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=26
- en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome ---
r_associated #0: 26 -->
en:severe x-linked intellectual disability gustavson type
n1=en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=26
- en:fara chlupackova syndrome ---
r_associated #0: 26 -->
en:severe x-linked intellectual disability gustavson type
n1=en:fara chlupackova syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=26
- en:hypomandibular faciocranial dysostosis ---
r_associated #0: 26 -->
en:severe x-linked intellectual disability gustavson type
n1=en:hypomandibular faciocranial dysostosis | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=26
- en:kosztolanyi syndrome ---
r_associated #0: 26 -->
en:severe x-linked intellectual disability gustavson type
n1=en:kosztolanyi syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=26
- en:mental retardation spasticity ectrodactyly ---
r_associated #0: 26 -->
en:severe x-linked intellectual disability gustavson type
n1=en:mental retardation spasticity ectrodactyly | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=26
- en:microcephaly albinism digital anomalies syndrome ---
r_associated #0: 26 -->
en:severe x-linked intellectual disability gustavson type
n1=en:microcephaly albinism digital anomalies syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=26
- en:nablus mask-like facial syndrome ---
r_associated #0: 26 -->
en:severe x-linked intellectual disability gustavson type
n1=en:nablus mask-like facial syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=26
- en:porencephaly ---
r_associated #0: 26 -->
en:severe x-linked intellectual disability gustavson type
n1=en:porencephaly | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=26
- rétinite pigmentaire liée à la périphérine (pro219leu) ---
r_associated #0: 10 -->
en:severe x-linked intellectual disability gustavson type
n1=rétinite pigmentaire liée à la périphérine (pro219leu) | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=10
|