'en:x-linked intellectual disability armfield type'
(id=9102758 ; fe=en:x-linked intellectual disability armfield type ; type=1 ; niveau=200 ;
luminosité=25 ;
somme entrante=7406 creation date=2017-10-29 touchdate=2025-08-21 12:09:40.000) ≈ 334 relations sortantes
- en:x-linked intellectual disability armfield type --
r_associated #0: 43 / 1 ->
en:alport syndrome, x-linked
n1=en:x-linked intellectual disability armfield type | n2=en:alport syndrome, x-linked | rel=r_associated | relid=0 | w=43
- en:x-linked intellectual disability armfield type --
r_associated #0: 43 / 1 ->
en:congenital malformation syndromes with metabolic disturbances
n1=en:x-linked intellectual disability armfield type | n2=en:congenital malformation syndromes with metabolic disturbances | rel=r_associated | relid=0 | w=43
- en:x-linked intellectual disability armfield type --
r_associated #0: 43 / 1 ->
en:intellectual disability with cataract and kyphosis syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:intellectual disability with cataract and kyphosis syndrome | rel=r_associated | relid=0 | w=43
- en:x-linked intellectual disability armfield type --
r_associated #0: 43 / 1 ->
en:mental retardation, x-linked
n1=en:x-linked intellectual disability armfield type | n2=en:mental retardation, x-linked | rel=r_associated | relid=0 | w=43
- en:x-linked intellectual disability armfield type --
r_associated #0: 43 / 1 ->
en:opitz trigonocephaly syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:opitz trigonocephaly syndrome | rel=r_associated | relid=0 | w=43
- en:x-linked intellectual disability armfield type --
r_associated #0: 43 / 1 ->
en:x-linked intellectual disability abidi type
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability abidi type | rel=r_associated | relid=0 | w=43
- en:x-linked intellectual disability armfield type --
r_associated #0: 42 / 0.977 ->
en:kosztolanyi syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:kosztolanyi syndrome | rel=r_associated | relid=0 | w=42
- en:x-linked intellectual disability armfield type --
r_associated #0: 42 / 0.977 ->
en:mental retardation, x-linked, with short stature, hypogonadism, and abnormal gait
n1=en:x-linked intellectual disability armfield type | n2=en:mental retardation, x-linked, with short stature, hypogonadism, and abnormal gait | rel=r_associated | relid=0 | w=42
- en:x-linked intellectual disability armfield type --
r_associated #0: 42 / 0.977 ->
en:x-linked dominant chondrodysplasia chassaing lacombe type
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked dominant chondrodysplasia chassaing lacombe type | rel=r_associated | relid=0 | w=42
- en:x-linked intellectual disability armfield type --
r_associated #0: 42 / 0.977 ->
en:x-linked lissencephaly
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked lissencephaly | rel=r_associated | relid=0 | w=42
- en:x-linked intellectual disability armfield type --
r_associated #0: 41 / 0.953 ->
en:brachioskeletogenital syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:brachioskeletogenital syndrome | rel=r_associated | relid=0 | w=41
- en:x-linked intellectual disability armfield type --
r_associated #0: 41 / 0.953 ->
en:brunner syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:brunner syndrome | rel=r_associated | relid=0 | w=41
- en:x-linked intellectual disability armfield type --
r_associated #0: 41 / 0.953 ->
en:hall riggs syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:hall riggs syndrome | rel=r_associated | relid=0 | w=41
- en:x-linked intellectual disability armfield type --
r_associated #0: 41 / 0.953 ->
en:malformation defect spectrum
n1=en:x-linked intellectual disability armfield type | n2=en:malformation defect spectrum | rel=r_associated | relid=0 | w=41
- en:x-linked intellectual disability armfield type --
r_associated #0: 41 / 0.953 ->
en:other mental retardation
n1=en:x-linked intellectual disability armfield type | n2=en:other mental retardation | rel=r_associated | relid=0 | w=41
- en:x-linked intellectual disability armfield type --
r_associated #0: 40 / 0.93 ->
en:uveal coloboma with cleft lip and palate and intellectual disability syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:uveal coloboma with cleft lip and palate and intellectual disability syndrome | rel=r_associated | relid=0 | w=40
- en:x-linked intellectual disability armfield type --
r_associated #0: 40 / 0.93 ->
en:x-linked intellectual disability pai type
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability pai type | rel=r_associated | relid=0 | w=40
- en:x-linked intellectual disability armfield type --
r_associated #0: 39 / 0.907 ->
en:alpha-thalassemia/mental retardation syndrome, nondeletion type, x-linked
n1=en:x-linked intellectual disability armfield type | n2=en:alpha-thalassemia/mental retardation syndrome, nondeletion type, x-linked | rel=r_associated | relid=0 | w=39
- en:x-linked intellectual disability armfield type --
r_associated #0: 39 / 0.907 ->
en:chronic granulomatous disease
n1=en:x-linked intellectual disability armfield type | n2=en:chronic granulomatous disease | rel=r_associated | relid=0 | w=39
- en:x-linked intellectual disability armfield type --
r_associated #0: 39 / 0.907 ->
en:glucose-6-phosphate dehydrogenase deficiency anemia
n1=en:x-linked intellectual disability armfield type | n2=en:glucose-6-phosphate dehydrogenase deficiency anemia | rel=r_associated | relid=0 | w=39
- en:x-linked intellectual disability armfield type --
r_associated #0: 39 / 0.907 ->
en:mental retardation syndrome, belgian type
n1=en:x-linked intellectual disability armfield type | n2=en:mental retardation syndrome, belgian type | rel=r_associated | relid=0 | w=39
- en:x-linked intellectual disability armfield type --
r_associated #0: 39 / 0.907 ->
en:microcephaly microcornea syndrome seemanova type
n1=en:x-linked intellectual disability armfield type | n2=en:microcephaly microcornea syndrome seemanova type | rel=r_associated | relid=0 | w=39
- en:x-linked intellectual disability armfield type --
r_associated #0: 39 / 0.907 ->
en:perniola krajewska carnevale syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:perniola krajewska carnevale syndrome | rel=r_associated | relid=0 | w=39
- en:x-linked intellectual disability armfield type --
r_associated #0: 39 / 0.907 ->
en:x-linked intellectual disability seemanova type
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability seemanova type | rel=r_associated | relid=0 | w=39
- en:x-linked intellectual disability armfield type --
r_associated #0: 38 / 0.884 ->
en:borderline mental retardation (i.q. 70-85)
n1=en:x-linked intellectual disability armfield type | n2=en:borderline mental retardation (i.q. 70-85) | rel=r_associated | relid=0 | w=38
- en:x-linked intellectual disability armfield type --
r_associated #0: 37 / 0.86 ->
en:corneal dystrophy, endothelial, x-linked
n1=en:x-linked intellectual disability armfield type | n2=en:corneal dystrophy, endothelial, x-linked | rel=r_associated | relid=0 | w=37
- en:x-linked intellectual disability armfield type --
r_associated #0: 37 / 0.86 ->
en:lissencephaly, x-linked, 2
n1=en:x-linked intellectual disability armfield type | n2=en:lissencephaly, x-linked, 2 | rel=r_associated | relid=0 | w=37
- en:x-linked intellectual disability armfield type --
r_associated #0: 37 / 0.86 ->
en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome | rel=r_associated | relid=0 | w=37
- en:x-linked intellectual disability armfield type --
r_associated #0: 36 / 0.837 ->
en:oculocerebrorenal syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:oculocerebrorenal syndrome | rel=r_associated | relid=0 | w=36
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:abruzzo erickson syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:abruzzo erickson syndrome | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:adolescent x-linked adrenoleukodystrophy
n1=en:x-linked intellectual disability armfield type | n2=en:adolescent x-linked adrenoleukodystrophy | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis
n1=en:x-linked intellectual disability armfield type | n2=en:alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:ayazi syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:ayazi syndrome | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:bornholm eye disease
n1=en:x-linked intellectual disability armfield type | n2=en:bornholm eye disease | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:brachydactyly, type a1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation
n1=en:x-linked intellectual disability armfield type | n2=en:brachydactyly, type a1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
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 armfield 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=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:cerebrofaciothoracic dysplasia
n1=en:x-linked intellectual disability armfield type | n2=en:cerebrofaciothoracic dysplasia | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:childhood cerebral x-linked adrenoleukodystrophy
n1=en:x-linked intellectual disability armfield type | n2=en:childhood cerebral x-linked adrenoleukodystrophy | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:congenital ectodermal dysplasia of face
n1=en:x-linked intellectual disability armfield type | n2=en:congenital ectodermal dysplasia of face | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia
n1=en:x-linked intellectual disability armfield type | n2=en:corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:dermoids of cornea
n1=en:x-linked intellectual disability armfield type | n2=en:dermoids of cornea | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:dyskeratosis congenita
n1=en:x-linked intellectual disability armfield type | n2=en:dyskeratosis congenita | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:fraxe intellectual disability syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:fraxe intellectual disability syndrome | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:goldberg-shprintzen megacolon syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:goldberg-shprintzen megacolon syndrome | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:goldenhar syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:goldenhar syndrome | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:harrod doman keele syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:harrod doman keele syndrome | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:kohlschutter tonz syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:kohlschutter tonz syndrome | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:lesch-nyhan syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:lesch-nyhan syndrome | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:mental retardation, x-linked, snyder-robinson type
n1=en:x-linked intellectual disability armfield type | n2=en:mental retardation, x-linked, snyder-robinson type | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:mucopolysaccharidosis ii
n1=en:x-linked intellectual disability armfield type | n2=en:mucopolysaccharidosis ii | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:orofaciodigital syndrome 9
n1=en:x-linked intellectual disability armfield type | n2=en:orofaciodigital syndrome 9 | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:orofaciodigital syndrome x
n1=en:x-linked intellectual disability armfield type | n2=en:orofaciodigital syndrome x | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:ossification anomaly with psychomotor developmental delay syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:ossification anomaly with psychomotor developmental delay syndrome | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:otopalatodigital syndrome, type ii
n1=en:x-linked intellectual disability armfield type | n2=en:otopalatodigital syndrome, type ii | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:periventricular heterotopia, x-linked
n1=en:x-linked intellectual disability armfield type | n2=en:periventricular heterotopia, x-linked | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:scholte syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:scholte syndrome | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:scott bryant graham syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:scott bryant graham syndrome | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:viljoen kallis voges syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:viljoen kallis voges syndrome | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:volcke soekarman syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:volcke soekarman syndrome | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:x-linked congenital dyserythropoietic anemia with thrombocytopenia
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked congenital dyserythropoietic anemia with thrombocytopenia | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:x-linked creatine transporter deficiency
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked creatine transporter deficiency | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:x-linked intellectual disability schimke type
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability schimke type | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:x-linked intellectual disability stoll type
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability stoll type | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:x-linked intellectual disability van esch type
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability van esch type | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:x-linked intellectual disability wilson type
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability wilson type | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 35 / 0.814 ->
en:x-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:adams oliver syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:adams oliver syndrome | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:aicardi's syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:aicardi's syndrome | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:androgen-insensitivity syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:androgen-insensitivity syndrome | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:aniridia and intellectual disability syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:aniridia and intellectual disability syndrome | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:ataxia, fatal x-linked, with deafness and loss of vision
n1=en:x-linked intellectual disability armfield type | n2=en:ataxia, fatal x-linked, with deafness and loss of vision | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:atkin syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:atkin syndrome | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:chromosome xq27.3q28 duplication syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:chromosome xq27.3q28 duplication syndrome | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:classical phenylketonuria
n1=en:x-linked intellectual disability armfield type | n2=en:classical phenylketonuria | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:de sanctis-cacchione syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:de sanctis-cacchione syndrome | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:der kaloustian mcintosh silver syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:der kaloustian mcintosh silver syndrome | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:digitorenocerebral syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:digitorenocerebral syndrome | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:dystonia 3, torsion, x-linked
n1=en:x-linked intellectual disability armfield type | n2=en:dystonia 3, torsion, x-linked | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:goniodysgenesis-mental retardation-short stature syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:goniodysgenesis-mental retardation-short stature syndrome | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:huntington disease
n1=en:x-linked intellectual disability armfield type | n2=en:huntington disease | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:klippel's disease
n1=en:x-linked intellectual disability armfield type | n2=en:klippel's disease | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity (disorder)
n1=en:x-linked intellectual disability armfield type | n2=en:mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity (disorder) | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:microphthalmia, syndromic 4 (disorder)
n1=en:x-linked intellectual disability armfield type | n2=en:microphthalmia, syndromic 4 (disorder) | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:microphthalmia, syndromic 7
n1=en:x-linked intellectual disability armfield type | n2=en:microphthalmia, syndromic 7 | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:neutropenia, severe congenital, x-linked
n1=en:x-linked intellectual disability armfield type | n2=en:neutropenia, severe congenital, x-linked | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:oculopalatocerebral syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:oculopalatocerebral syndrome | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:oto-palato-digital syndrome type 1
n1=en:x-linked intellectual disability armfield type | n2=en:oto-palato-digital syndrome type 1 | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:pallister w syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:pallister w syndrome | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
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 armfield type --
r_associated #0: 34 / 0.791 ->
en:shprintzen-goldberg syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:shprintzen-goldberg syndrome | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:spinocerebellar ataxia, x-linked 4
n1=en:x-linked intellectual disability armfield type | n2=en:spinocerebellar ataxia, x-linked 4 | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:trichodysplasia with amelogenesis imperfecta syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:trichodysplasia with amelogenesis imperfecta syndrome | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:trisomy 10p
n1=en:x-linked intellectual disability armfield type | n2=en:trisomy 10p | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:trisomy xq28 syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:trisomy xq28 syndrome | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:tuberous sclerosis
n1=en:x-linked intellectual disability armfield type | n2=en:tuberous sclerosis | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:waisman syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:waisman syndrome | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 34 / 0.791 ->
en:x-linked dyskeratosis congenita
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked dyskeratosis congenita | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:17q11.2 microduplication syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:17q11.2 microduplication syndrome | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:arthrogryposis multiplex congenita, distal, x-linked
n1=en:x-linked intellectual disability armfield type | n2=en:arthrogryposis multiplex congenita, distal, x-linked | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:bardet-biedl syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:bardet-biedl syndrome | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:branchial arch syndrome x-linked
n1=en:x-linked intellectual disability armfield type | n2=en:branchial arch syndrome x-linked | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:choroideremia
n1=en:x-linked intellectual disability armfield type | n2=en:choroideremia | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:chromosome 19q13.11 deletion syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:chromosome 19q13.11 deletion syndrome | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:congenital abnormality
n1=en:x-linked intellectual disability armfield type | n2=en:congenital abnormality | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:fitzsimmons-mclachlan-gilbert syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:fitzsimmons-mclachlan-gilbert syndrome | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:gaucher disease
n1=en:x-linked intellectual disability armfield type | n2=en:gaucher disease | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:klinefelter syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:klinefelter syndrome | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:lubs x-linked mental retardation syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:lubs x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:microcephalus and intellectual disability with phalangeal and neurological anomaly syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:microcephalus and intellectual disability with phalangeal and neurological anomaly syndrome | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:microcephaly deafness syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:microcephaly deafness syndrome | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:prieto badia mulas syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:prieto badia mulas syndrome | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:rett syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:rett syndrome | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:rosenthal-kloepfer syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:rosenthal-kloepfer syndrome | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:sohval soffer syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:sohval soffer syndrome | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:verloes gillerot fryns syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:verloes gillerot fryns syndrome | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:x-linked immunodeficiency with magnesium defect, epstein-barr virus infection and neoplasia
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked immunodeficiency with magnesium defect, epstein-barr virus infection and neoplasia | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:x-linked intellectual disability stocco dos santos type
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability stocco dos santos type | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:x-linked intellectual disability turner type
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability turner type | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:x-linked intellectual disability with ataxia and apraxia syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability with ataxia and apraxia syndrome | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:x-linked mendelian susceptibility to mycobacterial disease
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked mendelian susceptibility to mycobacterial disease | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:x-linked retinal dysplasia
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked retinal dysplasia | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 32 / 0.744 ->
en:zunich neuroectodermal syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:zunich neuroectodermal syndrome | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:al gazali aziz salem syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:al gazali aziz salem syndrome | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:angelman syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:angelman syndrome | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:angiokeratoma corporis diffusum
n1=en:x-linked intellectual disability armfield type | n2=en:angiokeratoma corporis diffusum | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:biemond syndrome type 2
n1=en:x-linked intellectual disability armfield type | n2=en:biemond syndrome type 2 | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:blepharophimosis syndrome ohdo type
n1=en:x-linked intellectual disability armfield type | n2=en:blepharophimosis syndrome ohdo type | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:borjeson-forssman-lehmann syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:borjeson-forssman-lehmann syndrome | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:cask related intellectual disability
n1=en:x-linked intellectual disability armfield type | n2=en:cask related intellectual disability | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:christ-siemens-touraine syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:christ-siemens-touraine syndrome | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:congenital nephrogenic diabetes insipidus
n1=en:x-linked intellectual disability armfield type | n2=en:congenital nephrogenic diabetes insipidus | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:congenital qualifier
n1=en:x-linked intellectual disability armfield type | n2=en:congenital qualifier | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:cooper jabs syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:cooper jabs syndrome | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:dandy-walker malformation with mental retardation, basal ganglia disease, and seizures
n1=en:x-linked intellectual disability armfield type | n2=en:dandy-walker malformation with mental retardation, basal ganglia disease, and seizures | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:hair defect with photosensitivity and mental retardation
n1=en:x-linked intellectual disability armfield type | n2=en:hair defect with photosensitivity and mental retardation | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:hemophilia a
n1=en:x-linked intellectual disability armfield type | n2=en:hemophilia a | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:histidinemia
n1=en:x-linked intellectual disability armfield type | n2=en:histidinemia | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:hydrocephalus with obesity and hypogonadism syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:hydrocephalus with obesity and hypogonadism syndrome | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:hypospadias-mental retardation syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:hypospadias-mental retardation syndrome | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:juberg-marsidi syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:juberg-marsidi syndrome | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:malformation association
n1=en:x-linked intellectual disability armfield type | n2=en:malformation association | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:menkes kinky hair syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:menkes kinky hair syndrome | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:mental retardation, skeletal dysplasia, and abducens palsy
n1=en:x-linked intellectual disability armfield type | n2=en:mental retardation, skeletal dysplasia, and abducens palsy | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:mental retardation, x-linked, syndromic 7
n1=en:x-linked intellectual disability armfield type | n2=en:mental retardation, x-linked, syndromic 7 | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:mohr-tranebjaerg syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:mohr-tranebjaerg syndrome | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:optic atrophy 2 (disorder)
n1=en:x-linked intellectual disability armfield type | n2=en:optic atrophy 2 (disorder) | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:orofaciodigital syndrome 5
n1=en:x-linked intellectual disability armfield type | n2=en:orofaciodigital syndrome 5 | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:placental steroid sulfatase deficiency
n1=en:x-linked intellectual disability armfield type | n2=en:placental steroid sulfatase deficiency | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:plagiocephaly and x-linked mental retardation
n1=en:x-linked intellectual disability armfield type | n2=en:plagiocephaly and x-linked mental retardation | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:severe mental retardation (i.q. 20-34)
n1=en:x-linked intellectual disability armfield type | n2=en:severe mental retardation (i.q. 20-34) | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:simpson-golabi-behmel syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:simpson-golabi-behmel syndrome | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:unspecified mental retardation; other impairments of behaviour
n1=en:x-linked intellectual disability armfield type | n2=en:unspecified mental retardation; other impairments of behaviour | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment
n1=en:x-linked intellectual disability armfield type | n2=en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:x-linked agammaglobulinemia
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked agammaglobulinemia | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:x-linked intellectual disability cilliers type
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability cilliers type | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:x-linked intellectual disability with acromegaly and hyperactivity syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:x-linked intellectual disability with cerebellar hypoplasia syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability with cerebellar hypoplasia syndrome | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:x-linked intellectual disability zorick type
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability zorick type | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 31 / 0.721 ->
en:x-linked recessive intellectual disability and macrocephaly with ciliary dysfunction syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked recessive intellectual disability and macrocephaly with ciliary dysfunction syndrome | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:bulbo-spinal atrophy, x-linked
n1=en:x-linked intellectual disability armfield type | n2=en:bulbo-spinal atrophy, x-linked | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:cahmr syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:cahmr syndrome | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:cardio-facio-cutaneous syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:cardio-facio-cutaneous syndrome | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:deafness-hypogonadism syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:deafness-hypogonadism syndrome | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:down syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:down syndrome | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:fried syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:fried syndrome | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:hemophilia b
n1=en:x-linked intellectual disability armfield type | n2=en:hemophilia b | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:homocystinuria
n1=en:x-linked intellectual disability armfield type | n2=en:homocystinuria | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:hydronephrosis, congenital, with cleft palate, characteristic facies, hypotonia, and mental retardation
n1=en:x-linked intellectual disability armfield type | n2=en:hydronephrosis, congenital, with cleft palate, characteristic facies, hypotonia, and mental retardation | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:kabuki make-up syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:kabuki make-up syndrome | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:malformation sequence
n1=en:x-linked intellectual disability armfield type | n2=en:malformation sequence | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:marfanoid mental retardation syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:marfanoid mental retardation syndrome | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:mcdonough syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:mcdonough syndrome | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:microphthalmia, syndromic 2
n1=en:x-linked intellectual disability armfield type | n2=en:microphthalmia, syndromic 2 | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:moloney syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:moloney syndrome | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:morm syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:morm syndrome | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:muscular dystrophy, duchenne
n1=en:x-linked intellectual disability armfield type | n2=en:muscular dystrophy, duchenne | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:nance-horan syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:nance-horan syndrome | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:ocular albinism, type ii
n1=en:x-linked intellectual disability armfield type | n2=en:ocular albinism, type ii | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:ornithine carbamoyltransferase deficiency
n1=en:x-linked intellectual disability armfield type | n2=en:ornithine carbamoyltransferase deficiency | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:smith-magenis syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:smith-magenis syndrome | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:winship viljoen leary syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:winship viljoen leary syndrome | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:x-linked intellectual disability with precocious puberty and obesity syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability with precocious puberty and obesity syndrome | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 30 / 0.698 ->
en:x-linked neurodegenerative syndrome bertini type
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked neurodegenerative syndrome bertini type | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:1p21.3 microdeletion syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:1p21.3 microdeletion syndrome | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:achalasia microcephaly
n1=en:x-linked intellectual disability armfield type | n2=en:achalasia microcephaly | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:albinism-deafness syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:albinism-deafness syndrome | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:albinism, ocular, with late-onset sensorineural deafness (disorder)
n1=en:x-linked intellectual disability armfield type | n2=en:albinism, ocular, with late-onset sensorineural deafness (disorder) | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:aldred syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:aldred syndrome | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:allan-herndon-dudley syndrome (ahds)
n1=en:x-linked intellectual disability armfield type | n2=en:allan-herndon-dudley syndrome (ahds) | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:cardio-acral-facial syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:cardio-acral-facial syndrome | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:coffin-siris syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:coffin-siris syndrome | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:congenital malformation syndromes associated with short stature
n1=en:x-linked intellectual disability armfield type | n2=en:congenital malformation syndromes associated with short stature | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:congenital malformation syndromes involving limbs
n1=en:x-linked intellectual disability armfield type | n2=en:congenital malformation syndromes involving limbs | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:corpus callosum, agenesis of, with facial anomalies and robin sequence
n1=en:x-linked intellectual disability armfield type | n2=en:corpus callosum, agenesis of, with facial anomalies and robin sequence | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:de barsy syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:de barsy syndrome | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:ectodermal dysplasia with blindness syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:ectodermal dysplasia with blindness syndrome | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:facial milia, lobate tongue, lingual and labial frenula syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:facial milia, lobate tongue, lingual and labial frenula syndrome | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:focal dermal hypoplasia
n1=en:x-linked intellectual disability armfield type | n2=en:focal dermal hypoplasia | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:glycogen storage disease type iib
n1=en:x-linked intellectual disability armfield type | n2=en:glycogen storage disease type iib | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:hyper-igm immunodeficiency syndrome, type 1
n1=en:x-linked intellectual disability armfield type | n2=en:hyper-igm immunodeficiency syndrome, type 1 | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:kapur toriello syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:kapur toriello syndrome | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:kaufman oculocerebrofacial syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:kaufman oculocerebrofacial syndrome | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:lowry maclean syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:lowry maclean syndrome | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:lujan fryns syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:lujan fryns syndrome | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:mental retardation with psychosis, pyramidal signs, and macroorchidism
n1=en:x-linked intellectual disability armfield type | n2=en:mental retardation with psychosis, pyramidal signs, and macroorchidism | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:mild mental retardation
n1=en:x-linked intellectual disability armfield type | n2=en:mild mental retardation | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:nutritional mental retardation
n1=en:x-linked intellectual disability armfield type | n2=en:nutritional mental retardation | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:ocular albinism, type i
n1=en:x-linked intellectual disability armfield type | n2=en:ocular albinism, type i | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:ohdo syndrome, maat-kievit-brunner type
n1=en:x-linked intellectual disability armfield type | n2=en:ohdo syndrome, maat-kievit-brunner type | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:orotic aciduria
n1=en:x-linked intellectual disability armfield type | n2=en:orotic aciduria | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:renpenning syndrome 1
n1=en:x-linked intellectual disability armfield type | n2=en:renpenning syndrome 1 | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:schaap taylor baraitser syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:schaap taylor baraitser syndrome | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:siderius x-linked mental retardation syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:siderius x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:syndromic x-linked intellectual disability due to jarid1c mutation
n1=en:x-linked intellectual disability armfield type | n2=en:syndromic x-linked intellectual disability due to jarid1c mutation | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:temtamy syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:temtamy syndrome | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour
n1=en:x-linked intellectual disability armfield type | n2=en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:unspecified mental retardation; without mention of impairment of behaviour
n1=en:x-linked intellectual disability armfield type | n2=en:unspecified mental retardation; without mention of impairment of behaviour | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:x-linked combined immunodeficiency diseases
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked combined immunodeficiency diseases | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:x-linked intellectual disability shrimpton type
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability shrimpton type | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 29 / 0.674 ->
en:x-linked sideroblastic anemia with spinocerebellar ataxia
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked sideroblastic anemia with spinocerebellar ataxia | rel=r_associated | relid=0 | w=29
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:3-methylglutaconic aciduria type 2
n1=en:x-linked intellectual disability armfield type | n2=en:3-methylglutaconic aciduria type 2 | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:acrocephalosyndactyly
n1=en:x-linked intellectual disability armfield type | n2=en:acrocephalosyndactyly | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:alopecia contractures dwarfism mental retardation
n1=en:x-linked intellectual disability armfield type | n2=en:alopecia contractures dwarfism mental retardation | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:beta thalassemia x-linked thrombocytopenia syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:beta thalassemia x-linked thrombocytopenia syndrome | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:congenital hypoplasia of ulna and intellectual disability syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:congenital hypoplasia of ulna and intellectual disability syndrome | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:congenital malformation syndromes affecting facial appearance
n1=en:x-linked intellectual disability armfield type | n2=en:congenital malformation syndromes affecting facial appearance | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:glycogen storage disease type vi
n1=en:x-linked intellectual disability armfield type | n2=en:glycogen storage disease type vi | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:gonadal dysgenesis xx type deafness
n1=en:x-linked intellectual disability armfield type | n2=en:gonadal dysgenesis xx type deafness | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:hernandez aguirre-negrete syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:hernandez aguirre-negrete syndrome | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:heterotopia, periventricular, ehlers-danlos variant
n1=en:x-linked intellectual disability armfield type | n2=en:heterotopia, periventricular, ehlers-danlos variant | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:holoprosencephaly with fetal akinesia-hypokinesia sequence
n1=en:x-linked intellectual disability armfield type | n2=en:holoprosencephaly with fetal akinesia-hypokinesia sequence | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:hyperphosphatasia with mental retardation
n1=en:x-linked intellectual disability armfield type | n2=en:hyperphosphatasia with mental retardation | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:karandikar maria kamble syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:karandikar maria kamble syndrome | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:laurence-moon syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:laurence-moon syndrome | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:masa syndrome (disorder)
n1=en:x-linked intellectual disability armfield type | n2=en:masa syndrome (disorder) | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:microphthalmia, syndromic 1
n1=en:x-linked intellectual disability armfield type | n2=en:microphthalmia, syndromic 1 | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:moderate mental retardation (i.q. 35-49)
n1=en:x-linked intellectual disability armfield type | n2=en:moderate mental retardation (i.q. 35-49) | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:mowat-wilson syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:mowat-wilson syndrome | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:myopathy, x-linked, with excessive autophagy (disorder)
n1=en:x-linked intellectual disability armfield type | n2=en:myopathy, x-linked, with excessive autophagy (disorder) | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:orofaciodigital syndrome 8
n1=en:x-linked intellectual disability armfield type | n2=en:orofaciodigital syndrome 8 | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:partington x-linked mental retardation syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:partington x-linked mental retardation syndrome | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:syndromic x-linked intellectual disability type 11
n1=en:x-linked intellectual disability armfield type | n2=en:syndromic x-linked intellectual disability type 11 | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:wiskott-aldrich syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:wiskott-aldrich syndrome | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:woods black norbury syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:woods black norbury syndrome | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:x-linked epilepsy with learning disability and behavior disorder syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked epilepsy with learning disability and behavior disorder syndrome | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:x-linked hydrocephalus syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked hydrocephalus syndrome | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
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:x-linked intellectual disability armfield type --
r_associated #0: 28 / 0.651 ->
en:x-linked intellectual disability with cubitus valgus and dysmorphism syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability with cubitus valgus and dysmorphism syndrome | rel=r_associated | relid=0 | w=28
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:ataxia with deafness and intellectual disability syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:ataxia with deafness and intellectual disability syndrome | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:brachymorphism-onychodysplasia-dysphalangism syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:brachymorphism-onychodysplasia-dysphalangism syndrome | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:cleft palate-lateral synechia syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:cleft palate-lateral synechia syndrome | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:dyserythropoietic anemia with thrombocytopenia
n1=en:x-linked intellectual disability armfield type | n2=en:dyserythropoietic anemia with thrombocytopenia | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:erythrokeratodermia variabilis 3 (disorder)
n1=en:x-linked intellectual disability armfield type | n2=en:erythrokeratodermia variabilis 3 (disorder) | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:female restricted epilepsy with intellectual disability syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:female restricted epilepsy with intellectual disability syndrome | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:glycogen storage disease type viii
n1=en:x-linked intellectual disability armfield type | n2=en:glycogen storage disease type viii | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:gurrieri sammito bellussi syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:gurrieri sammito bellussi syndrome | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:hydrocephalus with cerebellar agenesis
n1=en:x-linked intellectual disability armfield type | n2=en:hydrocephalus with cerebellar agenesis | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:ichthyosis, x-linked
n1=en:x-linked intellectual disability armfield type | n2=en:ichthyosis, x-linked | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:isolated noncompaction of the ventricular myocardium
n1=en:x-linked intellectual disability armfield type | n2=en:isolated noncompaction of the ventricular myocardium | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:ladda zonana ramer syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:ladda zonana ramer syndrome | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:lipodystrophy, intellectual disability, deafness syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:lipodystrophy, intellectual disability, deafness syndrome | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:lubani al saleh teebi syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:lubani al saleh teebi syndrome | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:martsolf syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:martsolf syndrome | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:mental retardation smith fineman myers type
n1=en:x-linked intellectual disability armfield type | n2=en:mental retardation smith fineman myers type | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:multiple system malformation syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:multiple system malformation syndrome | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:neuronal ceroid-lipofuscinoses
n1=en:x-linked intellectual disability armfield type | n2=en:neuronal ceroid-lipofuscinoses | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:norrie disease
n1=en:x-linked intellectual disability armfield type | n2=en:norrie disease | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:pfeiffer kapferer syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:pfeiffer kapferer syndrome | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:prader-willi habitus, osteopenia, and camptodactyly
n1=en:x-linked intellectual disability armfield type | n2=en:prader-willi habitus, osteopenia, and camptodactyly | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:prader-willi syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:prader-willi syndrome | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:primary ciliary dyskinesia and retinitis pigmentosa syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:primary ciliary dyskinesia and retinitis pigmentosa syndrome | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:severe x-linked mitochondrial encephalomyopathy
n1=en:x-linked intellectual disability armfield type | n2=en:severe x-linked mitochondrial encephalomyopathy | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:spondyloepiphyseal dysplasia tarda kohn type
n1=en:x-linked intellectual disability armfield type | n2=en:spondyloepiphyseal dysplasia tarda kohn type | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:wieacker-wolff syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:wieacker-wolff syndrome | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:wilson turner syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:wilson turner syndrome | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:x-linked adrenal hypoplasia congenita
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked adrenal hypoplasia congenita | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:x-linked hereditary sensory and autonomic neuropathy with deafness
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked hereditary sensory and autonomic neuropathy with deafness | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:x-linked intellectual disability stevenson type
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability stevenson type | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:x-linked lymphoproliferative disorder
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked lymphoproliferative disorder | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 27 / 0.628 ->
en:x-linked neurodegenerative syndrome hamel type
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked neurodegenerative syndrome hamel type | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:12q14 microdeletion syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:12q14 microdeletion syndrome | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:acrocephalopolysyndactyly type 2
n1=en:x-linked intellectual disability armfield type | n2=en:acrocephalopolysyndactyly type 2 | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:al gazali sabrinathan nair syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:al gazali sabrinathan nair syndrome | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:arachnodactyly and intellectual disability with facial dysmorphism syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:arachnodactyly and intellectual disability with facial dysmorphism syndrome | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:cantalamessa baldini ambrosi syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:cantalamessa baldini ambrosi syndrome | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:cerebrooculonasal syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:cerebrooculonasal syndrome | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:cleft palate with short stature and vertebral anomaly syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:cleft palate with short stature and vertebral anomaly syndrome | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:congenital cataract with ataxia and deafness syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:congenital cataract with ataxia and deafness syndrome | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:congenital malformation syndrome related to known exogenous cause
n1=en:x-linked intellectual disability armfield type | n2=en:congenital malformation syndrome related to known exogenous cause | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:craniofrontonasal dysplasia
n1=en:x-linked intellectual disability armfield type | n2=en:craniofrontonasal dysplasia | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:deafness and intellectual disability martin probst type syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:deafness and intellectual disability martin probst type syndrome | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:dent's disease
n1=en:x-linked intellectual disability armfield type | n2=en:dent's disease | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:dmd-associated dilated cardiomyopathy
n1=en:x-linked intellectual disability armfield type | n2=en:dmd-associated dilated cardiomyopathy | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:fine-lubinsky syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:fine-lubinsky syndrome | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:fountain syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:fountain syndrome | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:fragile x syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:fragile x syndrome | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:growth retardation, alopecia, pseudoanodontia and optic atrophy
n1=en:x-linked intellectual disability armfield type | n2=en:growth retardation, alopecia, pseudoanodontia and optic atrophy | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:leukoencephalopathy, cystic, without megalencephaly
n1=en:x-linked intellectual disability armfield type | n2=en:leukoencephalopathy, cystic, without megalencephaly | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:maple syrup urine disease
n1=en:x-linked intellectual disability armfield type | n2=en:maple syrup urine disease | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:mental retardation, x-linked, syndromic, christianson type
n1=en:x-linked intellectual disability armfield type | n2=en:mental retardation, x-linked, syndromic, christianson type | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:multiple congenital anomalies of fetus
n1=en:x-linked intellectual disability armfield type | n2=en:multiple congenital anomalies of fetus | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:muscular dystrophy, emery-dreifuss
n1=en:x-linked intellectual disability armfield type | n2=en:muscular dystrophy, emery-dreifuss | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:orofaciodigital syndrome 11
n1=en:x-linked intellectual disability armfield type | n2=en:orofaciodigital syndrome 11 | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:pashayan syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:pashayan syndrome | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:pelizaeus-merzbacher disease
n1=en:x-linked intellectual disability armfield type | n2=en:pelizaeus-merzbacher disease | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:profound intellectual disabilities
n1=en:x-linked intellectual disability armfield type | n2=en:profound intellectual disabilities | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:savant syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:savant syndrome | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:sesame syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:sesame syndrome | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:spinocerebellar ataxia, x-linked 3
n1=en:x-linked intellectual disability armfield type | n2=en:spinocerebellar ataxia, x-linked 3 | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:spondyloepiphyseal dysplasia tarda, x-linked
n1=en:x-linked intellectual disability armfield type | n2=en:spondyloepiphyseal dysplasia tarda, x-linked | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:tranebjaerg svejgaard syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:tranebjaerg svejgaard syndrome | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:wolf-hirschhorn syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:wolf-hirschhorn syndrome | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:x-linked intellectual disability and epilepsy with progressive joint contracture and facial dysmorphism syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability and epilepsy with progressive joint contracture and facial dysmorphism syndrome | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:x-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 26 / 0.605 ->
en:x-linked intellectual disability miles carpenter type
n1=en:x-linked intellectual disability armfield type | n2=en:x-linked intellectual disability miles carpenter type | rel=r_associated | relid=0 | w=26
- en:x-linked intellectual disability armfield type --
r_associated #0: 20 / 0.465 ->
en:chitayat meunier hodgkinson syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:chitayat meunier hodgkinson syndrome | rel=r_associated | relid=0 | w=20
- en:x-linked intellectual disability armfield type --
r_associated #0: 20 / 0.465 ->
en:chromosome xp22.3 microdeletion syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:chromosome xp22.3 microdeletion syndrome | rel=r_associated | relid=0 | w=20
- en:x-linked intellectual disability armfield type --
r_associated #0: 20 / 0.465 ->
en:congenital disorder of glycosylation type 1s
n1=en:x-linked intellectual disability armfield type | n2=en:congenital disorder of glycosylation type 1s | rel=r_associated | relid=0 | w=20
- en:x-linked intellectual disability armfield type --
r_associated #0: 20 / 0.465 ->
en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome | rel=r_associated | relid=0 | w=20
- en:x-linked intellectual disability armfield type --
r_associated #0: 20 / 0.465 ->
en:ferro-cerebro-cutaneous syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:ferro-cerebro-cutaneous syndrome | rel=r_associated | relid=0 | w=20
- en:x-linked intellectual disability armfield type --
r_associated #0: 20 / 0.465 ->
en:mental retardation spasticity ectrodactyly
n1=en:x-linked intellectual disability armfield type | n2=en:mental retardation spasticity ectrodactyly | rel=r_associated | relid=0 | w=20
- en:x-linked intellectual disability armfield type --
r_associated #0: 20 / 0.465 ->
en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | rel=r_associated | relid=0 | w=20
- en:x-linked intellectual disability armfield type --
r_associated #0: 20 / 0.465 ->
en:mycophenolate mofetil embryopathy
n1=en:x-linked intellectual disability armfield type | n2=en:mycophenolate mofetil embryopathy | rel=r_associated | relid=0 | w=20
- en:x-linked intellectual disability armfield type --
r_associated #0: 20 / 0.465 ->
en:piussan lenaerts mathieu syndrome
n1=en:x-linked intellectual disability armfield type | n2=en:piussan lenaerts mathieu syndrome | rel=r_associated | relid=0 | w=20
- en:x-linked intellectual disability armfield type --
r_associated #0: 20 / 0.465 ->
en:ppp2r5d-related intellectual disability
n1=en:x-linked intellectual disability armfield type | n2=en:ppp2r5d-related intellectual disability | rel=r_associated | relid=0 | w=20
| ≈ 359 relations entrantes
- en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome ---
r_associated #0: 39 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=39
- en:congenital disorder of glycosylation type 1s ---
r_associated #0: 36 -->
en:x-linked intellectual disability armfield type
n1=en:congenital disorder of glycosylation type 1s | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=36
- en:x-linked intellectual disability stoll type ---
r_associated #0: 36 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked intellectual disability stoll type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=36
- en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome ---
r_associated #0: 35 -->
en:x-linked intellectual disability armfield type
n1=en:deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=35
- en:mental retardation spasticity ectrodactyly ---
r_associated #0: 35 -->
en:x-linked intellectual disability armfield type
n1=en:mental retardation spasticity ectrodactyly | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=35
- en:piussan lenaerts mathieu syndrome ---
r_associated #0: 35 -->
en:x-linked intellectual disability armfield type
n1=en:piussan lenaerts mathieu syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=35
- en:ppp2r5d-related intellectual disability ---
r_associated #0: 35 -->
en:x-linked intellectual disability armfield type
n1=en:ppp2r5d-related intellectual disability | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=35
- en:trisomy xq28 syndrome ---
r_associated #0: 35 -->
en:x-linked intellectual disability armfield type
n1=en:trisomy xq28 syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=35
- en:x-linked intellectual disability pai type ---
r_associated #0: 35 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked intellectual disability pai type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=35
- en:congenital cataract with ataxia and deafness syndrome ---
r_associated #0: 34 -->
en:x-linked intellectual disability armfield type
n1=en:congenital cataract with ataxia and deafness syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=34
- en:ferro-cerebro-cutaneous syndrome ---
r_associated #0: 34 -->
en:x-linked intellectual disability armfield type
n1=en:ferro-cerebro-cutaneous syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=34
- en:fountain syndrome ---
r_associated #0: 34 -->
en:x-linked intellectual disability armfield type
n1=en:fountain syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=34
- en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome ---
r_associated #0: 34 -->
en:x-linked intellectual disability armfield type
n1=en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=34
- en:x-linked intellectual disability stevenson type ---
r_associated #0: 34 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked intellectual disability stevenson type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=34
- en:aniridia and intellectual disability syndrome ---
r_associated #0: 32 -->
en:x-linked intellectual disability armfield type
n1=en:aniridia and intellectual disability syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=32
- en:arachnodactyly and intellectual disability with facial dysmorphism syndrome ---
r_associated #0: 32 -->
en:x-linked intellectual disability armfield type
n1=en:arachnodactyly and intellectual disability with facial dysmorphism syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=32
- en:hall riggs syndrome ---
r_associated #0: 32 -->
en:x-linked intellectual disability armfield type
n1=en:hall riggs syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=32
- en:primary ciliary dyskinesia and retinitis pigmentosa syndrome ---
r_associated #0: 32 -->
en:x-linked intellectual disability armfield type
n1=en:primary ciliary dyskinesia and retinitis pigmentosa syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=32
- en:x-linked intellectual disability miles carpenter type ---
r_associated #0: 32 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked intellectual disability miles carpenter type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=32
- en:1p21.3 microdeletion syndrome ---
r_associated #0: 31 -->
en:x-linked intellectual disability armfield type
n1=en:1p21.3 microdeletion syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=31
- en:chitayat meunier hodgkinson syndrome ---
r_associated #0: 31 -->
en:x-linked intellectual disability armfield type
n1=en:chitayat meunier hodgkinson syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=31
- en:ectodermal dysplasia with blindness syndrome ---
r_associated #0: 31 -->
en:x-linked intellectual disability armfield type
n1=en:ectodermal dysplasia with blindness syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=31
- en:kosztolanyi syndrome ---
r_associated #0: 31 -->
en:x-linked intellectual disability armfield type
n1=en:kosztolanyi syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=31
- en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome ---
r_associated #0: 31 -->
en:x-linked intellectual disability armfield type
n1=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=31
- en:x-linked intellectual disability seemanova type ---
r_associated #0: 31 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked intellectual disability seemanova type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=31
- en:12q14 microdeletion syndrome ---
r_associated #0: 30 -->
en:x-linked intellectual disability armfield type
n1=en:12q14 microdeletion syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=30
- en:17q11.2 microduplication syndrome ---
r_associated #0: 30 -->
en:x-linked intellectual disability armfield type
n1=en:17q11.2 microduplication syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=30
- en:mycophenolate mofetil embryopathy ---
r_associated #0: 30 -->
en:x-linked intellectual disability armfield type
n1=en:mycophenolate mofetil embryopathy | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=30
- en:x-linked intellectual disability with ataxia and apraxia syndrome ---
r_associated #0: 30 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked intellectual disability with ataxia and apraxia syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=30
- en:brachioskeletogenital syndrome ---
r_associated #0: 29 -->
en:x-linked intellectual disability armfield type
n1=en:brachioskeletogenital syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=29
- en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome ---
r_associated #0: 29 -->
en:x-linked intellectual disability armfield type
n1=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | 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 -->
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 van esch type ---
r_associated #0: 29 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked intellectual disability van esch type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=29
- en:fried syndrome ---
r_associated #0: 28 -->
en:x-linked intellectual disability armfield type
n1=en:fried syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=28
- en:spondyloepiphyseal dysplasia tarda kohn type ---
r_associated #0: 28 -->
en:x-linked intellectual disability armfield type
n1=en:spondyloepiphyseal dysplasia tarda kohn type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=28
- en:cooper jabs syndrome ---
r_associated #0: 27 -->
en:x-linked intellectual disability armfield type
n1=en:cooper jabs syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=27
- en:x-linked intellectual disability with acromegaly and hyperactivity syndrome ---
r_associated #0: 27 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked intellectual disability with acromegaly and hyperactivity syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=27
- en:chromosome xp22.3 microdeletion syndrome ---
r_associated #0: 26 -->
en:x-linked intellectual disability armfield type
n1=en:chromosome xp22.3 microdeletion syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=26
- en:scholte syndrome ---
r_associated #0: 26 -->
en:x-linked intellectual disability armfield type
n1=en:scholte syndrome | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:x-linked intellectual disability, macrocephaly, macroorchidism syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=26
- leucinose ---
r_associated #0: 25 -->
en:x-linked intellectual disability armfield type
n1=leucinose | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=25
- en:3-methylglutaconic aciduria type 2 ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:3-methylglutaconic aciduria type 2 | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:abruzzo erickson syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:abruzzo erickson syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:achalasia microcephaly ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:achalasia microcephaly | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:acrocephalopolysyndactyly type 2 ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:acrocephalopolysyndactyly type 2 | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:acrocephalosyndactyly ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:acrocephalosyndactyly | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:adams oliver syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:adams oliver syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:adolescent x-linked adrenoleukodystrophy ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:adolescent x-linked adrenoleukodystrophy | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:aicardi's syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:aicardi's syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:al gazali aziz salem syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:al gazali aziz salem syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:al gazali sabrinathan nair syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:al gazali sabrinathan nair syndrome | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:albinism, ocular, with late-onset sensorineural deafness (disorder) | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:albinism-deafness syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:albinism-deafness syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:aldred syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:aldred syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:allan-herndon-dudley syndrome (ahds) ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:allan-herndon-dudley syndrome (ahds) | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:alopecia contractures dwarfism mental retardation ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:alopecia contractures dwarfism mental retardation | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:alpha-thalassemia/mental retardation syndrome, nondeletion type, x-linked | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:alport syndrome, x-linked ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:alport syndrome, x-linked | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:androgen-insensitivity syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:androgen-insensitivity syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:angelman syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:angelman syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:angiokeratoma corporis diffusum ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:angiokeratoma corporis diffusum | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:arthrogryposis multiplex congenita, distal, x-linked ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:arthrogryposis multiplex congenita, distal, x-linked | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:ataxia with deafness and intellectual disability syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:ataxia with deafness and intellectual disability syndrome | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:ataxia, fatal x-linked, with deafness and loss of vision | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:atkin syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:atkin syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:ayazi syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:ayazi syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:bardet-biedl syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:bardet-biedl syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:beta thalassemia x-linked thrombocytopenia syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:beta thalassemia x-linked thrombocytopenia syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:biemond syndrome type 2 ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:biemond syndrome type 2 | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:blepharophimosis syndrome ohdo type ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:blepharophimosis syndrome ohdo type | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:borderline mental retardation (i.q. 70-85) | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:borjeson-forssman-lehmann syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:borjeson-forssman-lehmann syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:bornholm eye disease ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:bornholm eye disease | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:brachydactyly, type a1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:brachymorphism-onychodysplasia-dysphalangism syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:brachymorphism-onychodysplasia-dysphalangism syndrome | n2=en:x-linked intellectual disability armfield 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 armfield 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 armfield type | rel=r_associated | relid=0 | w=20
- en:branchial arch syndrome x-linked ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:branchial arch syndrome x-linked | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:brunner syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:brunner syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:bulbo-spinal atrophy, x-linked ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:bulbo-spinal atrophy, x-linked | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:cahmr syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:cahmr syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:cantalamessa baldini ambrosi syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:cantalamessa baldini ambrosi syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:cardio-acral-facial syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:cardio-acral-facial syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:cardio-facio-cutaneous syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:cardio-facio-cutaneous syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:cardiofaciocutaneous syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:cardiofaciocutaneous syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:cask related intellectual disability ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:cask related intellectual disability | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:cerebrofaciothoracic dysplasia ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:cerebrofaciothoracic dysplasia | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:cerebrooculonasal syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:cerebrooculonasal syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:childhood cerebral x-linked adrenoleukodystrophy ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:childhood cerebral x-linked adrenoleukodystrophy | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:choroideremia ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:choroideremia | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:christ-siemens-touraine syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:christ-siemens-touraine syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:chromosome 19q13.11 deletion syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:chromosome 19q13.11 deletion syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:chromosome xq27.3q28 duplication syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:chromosome xq27.3q28 duplication syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:chronic granulomatous disease ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:chronic granulomatous disease | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:classical maple syrup urine disease ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:classical maple syrup urine disease | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:classical phenylketonuria ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:classical phenylketonuria | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:cleft palate with short stature and vertebral anomaly syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:cleft palate with short stature and vertebral anomaly syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:cleft palate-lateral synechia syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:cleft palate-lateral synechia syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:coffin-siris syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:coffin-siris syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:congenital abnormality ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:congenital abnormality | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:congenital ectodermal dysplasia of face ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:congenital ectodermal dysplasia of face | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:congenital hypoplasia of ulna and intellectual disability syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:congenital malformation syndrome related to known exogenous cause ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:congenital malformation syndrome related to known exogenous cause | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:congenital malformation syndromes affecting facial appearance ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:congenital malformation syndromes affecting facial appearance | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:congenital malformation syndromes associated with short stature ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:congenital malformation syndromes associated with short stature | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:congenital malformation syndromes involving limbs ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:congenital malformation syndromes involving limbs | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:congenital malformation syndromes with metabolic disturbances ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:congenital malformation syndromes with metabolic disturbances | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:congenital nephrogenic diabetes insipidus ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:congenital nephrogenic diabetes insipidus | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:congenital qualifier ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:congenital qualifier | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:corneal dystrophy, endothelial, x-linked ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:corneal dystrophy, endothelial, x-linked | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:corpus callosum, agenesis of, with facial anomalies and robin sequence | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:craniofrontonasal dysplasia ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:craniofrontonasal dysplasia | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:dandy-walker malformation with mental retardation, basal ganglia disease, and seizures ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:dandy-walker malformation with mental retardation, basal ganglia disease, and seizures | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:de barsy syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:de barsy syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:de sanctis-cacchione syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:de sanctis-cacchione syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:deafness and intellectual disability martin probst type syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:deafness and intellectual disability martin probst type syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:deafness-hypogonadism syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:deafness-hypogonadism syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:dent's disease ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:dent's disease | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:der kaloustian mcintosh silver syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:der kaloustian mcintosh silver syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:dermoids of cornea ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:dermoids of cornea | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:digitorenocerebral syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:digitorenocerebral syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:dmd-associated dilated cardiomyopathy ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:dmd-associated dilated cardiomyopathy | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:down syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:down syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:dyserythropoietic anemia with thrombocytopenia ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:dyserythropoietic anemia with thrombocytopenia | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:dyskeratosis congenita ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:dyskeratosis congenita | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:dystonia 3, torsion, x-linked ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:dystonia 3, torsion, x-linked | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:erythrokeratodermia variabilis 3 (disorder) ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:erythrokeratodermia variabilis 3 (disorder) | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:facial milia, lobate tongue, lingual and labial frenula syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:facial milia, lobate tongue, lingual and labial frenula syndrome | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:female restricted epilepsy with intellectual disability syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:fine-lubinsky syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:fine-lubinsky syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:fitzsimmons-mclachlan-gilbert syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:fitzsimmons-mclachlan-gilbert syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:focal dermal hypoplasia ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:focal dermal hypoplasia | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:fragile x syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:fragile x syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:fraxe intellectual disability syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:fraxe intellectual disability syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:gaucher disease ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:gaucher disease | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:glucose-6-phosphate dehydrogenase deficiency anemia ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:glucose-6-phosphate dehydrogenase deficiency anemia | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:glycogen storage disease type iib ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:glycogen storage disease type iib | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:glycogen storage disease type vi ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:glycogen storage disease type vi | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:glycogen storage disease type viii ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:glycogen storage disease type viii | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:goldberg-shprintzen megacolon syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:goldberg-shprintzen megacolon syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:goldenhar syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:goldenhar syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:gonadal dysgenesis xx type deafness ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:gonadal dysgenesis xx type deafness | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:goniodysgenesis-mental retardation-short stature syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:goniodysgenesis-mental retardation-short stature syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:growth retardation, alopecia, pseudoanodontia and optic atrophy ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:growth retardation, alopecia, pseudoanodontia and optic atrophy | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:gurrieri sammito bellussi syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:gurrieri sammito bellussi syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:hair defect with photosensitivity and mental retardation ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:hair defect with photosensitivity and mental retardation | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:harrod doman keele syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:harrod doman keele syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:hemophilia a ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:hemophilia a | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:hemophilia b ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:hemophilia b | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:hernandez aguirre-negrete syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:hernandez aguirre-negrete syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:heterotopia, periventricular, ehlers-danlos variant ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:heterotopia, periventricular, ehlers-danlos variant | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:histidinemia ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:histidinemia | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:holoprosencephaly with fetal akinesia-hypokinesia sequence ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:holoprosencephaly with fetal akinesia-hypokinesia sequence | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:homocystinuria ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:homocystinuria | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:huntington disease ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:huntington disease | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:hydrocephalus with cerebellar agenesis ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:hydrocephalus with cerebellar agenesis | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:hydrocephalus with obesity and hypogonadism syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:hydrocephalus with obesity and hypogonadism syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:hydronephrosis, congenital, with cleft palate, characteristic facies, hypotonia, and mental retardation ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:hydronephrosis, congenital, with cleft palate, characteristic facies, hypotonia, and mental retardation | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:hyper-igm immunodeficiency syndrome, type 1 ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:hyper-igm immunodeficiency syndrome, type 1 | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:hyperphosphatasia with mental retardation ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:hyperphosphatasia with mental retardation | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:hypospadias-mental retardation syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:hypospadias-mental retardation syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:ichthyosis, x-linked ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:ichthyosis, x-linked | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:intellectual disability with cataract and kyphosis syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:intellectual disability with cataract and kyphosis syndrome | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:isolated noncompaction of the ventricular myocardium ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:isolated noncompaction of the ventricular myocardium | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:juberg-marsidi syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:juberg-marsidi syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:kabuki make-up syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:kabuki make-up syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:kapur toriello syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:kapur toriello syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:karandikar maria kamble syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:karandikar maria kamble syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:kaufman oculocerebrofacial syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:kaufman oculocerebrofacial syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:klinefelter syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:klinefelter syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:klippel's disease ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:klippel's disease | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:kohlschutter tonz syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:kohlschutter tonz syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:ladda zonana ramer syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:ladda zonana ramer syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:laurence-moon syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:laurence-moon syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:lesch-nyhan syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:lesch-nyhan syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:leukoencephalopathy, cystic, without megalencephaly ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:leukoencephalopathy, cystic, without megalencephaly | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:lipodystrophy, intellectual disability, deafness syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:lipodystrophy, intellectual disability, deafness syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:lissencephaly, x-linked, 2 ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:lissencephaly, x-linked, 2 | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:lowry maclean syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:lowry maclean syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:lubani al saleh teebi syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:lubani al saleh teebi syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:lubs x-linked mental retardation syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:lubs x-linked mental retardation syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:lujan fryns syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:lujan fryns syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:malformation association ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:malformation association | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:malformation defect spectrum ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:malformation defect spectrum | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:malformation sequence ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:malformation sequence | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:maple syrup urine disease ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:maple syrup urine disease | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:marfanoid mental retardation syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:marfanoid mental retardation syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:martsolf syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:martsolf syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:masa syndrome (disorder) ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:masa syndrome (disorder) | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:mcdonough syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:mcdonough syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:menkes kinky hair syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:menkes kinky hair syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:mental retardation smith fineman myers type ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:mental retardation smith fineman myers type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:mental retardation syndrome, belgian type ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:mental retardation syndrome, belgian type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:mental retardation with psychosis, pyramidal signs, and macroorchidism ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:mental retardation with psychosis, pyramidal signs, and macroorchidism | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity (disorder) ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity (disorder) | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:mental retardation, skeletal dysplasia, and abducens palsy | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:mental retardation, x-linked ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:mental retardation, x-linked | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:mental retardation, x-linked, snyder-robinson type ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:mental retardation, x-linked, snyder-robinson type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:mental retardation, x-linked, syndromic 7 ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:mental retardation, x-linked, syndromic 7 | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:mental retardation, x-linked, syndromic, christianson type | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:mental retardation, x-linked, with short stature, hypogonadism, and abnormal gait | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:microcephalus and intellectual disability with phalangeal and neurological anomaly syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:microcephaly deafness syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:microcephaly deafness syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:microcephaly microcornea syndrome seemanova type ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:microcephaly microcornea syndrome seemanova type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:microphthalmia, syndromic 1 ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:microphthalmia, syndromic 1 | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:microphthalmia, syndromic 2 ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:microphthalmia, syndromic 2 | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:microphthalmia, syndromic 4 (disorder) ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:microphthalmia, syndromic 4 (disorder) | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:microphthalmia, syndromic 7 ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:microphthalmia, syndromic 7 | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:mild mental retardation ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:mild mental retardation | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:moderate mental retardation (i.q. 35-49) | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:mohr-tranebjaerg syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:mohr-tranebjaerg syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:moloney syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:moloney syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:morm syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:morm syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:mowat-wilson syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:mowat-wilson syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:mucopolysaccharidosis ii ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:mucopolysaccharidosis ii | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:multiple congenital anomalies of fetus ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:multiple congenital anomalies of fetus | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:multiple system malformation syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:multiple system malformation syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:muscular dystrophy, duchenne ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:muscular dystrophy, duchenne | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:muscular dystrophy, emery-dreifuss ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:muscular dystrophy, emery-dreifuss | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:myopathy, x-linked, with excessive autophagy (disorder) | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:nance-horan syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:nance-horan syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:neuronal ceroid-lipofuscinoses ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:neuronal ceroid-lipofuscinoses | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:neutropenia, severe congenital, x-linked ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:neutropenia, severe congenital, x-linked | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:norrie disease ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:norrie disease | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:nutritional mental retardation ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:nutritional mental retardation | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:ocular albinism, type i ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:ocular albinism, type i | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:ocular albinism, type ii ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:ocular albinism, type ii | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:oculocerebrorenal syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:oculocerebrorenal syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:oculopalatocerebral syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:oculopalatocerebral syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:ohdo syndrome, maat-kievit-brunner type ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:ohdo syndrome, maat-kievit-brunner type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:opitz trigonocephaly syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:opitz trigonocephaly syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:optic atrophy 2 (disorder) ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:optic atrophy 2 (disorder) | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:ornithine carbamoyltransferase deficiency ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:ornithine carbamoyltransferase deficiency | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndrome 11 ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:orofaciodigital syndrome 11 | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndrome 5 ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:orofaciodigital syndrome 5 | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndrome 8 ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:orofaciodigital syndrome 8 | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndrome 9 ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:orofaciodigital syndrome 9 | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:orofaciodigital syndrome x ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:orofaciodigital syndrome x | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:orotic aciduria ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:orotic aciduria | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:ossification anomaly with psychomotor developmental delay syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:osteopenia, myopia, hearing loss, intellectual disability, facial dysmorphism syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:other mental retardation ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:other mental retardation | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:oto-palato-digital syndrome type 1 ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:oto-palato-digital syndrome type 1 | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:otopalatodigital syndrome, type ii ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:otopalatodigital syndrome, type ii | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:pallister w syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:pallister w syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:partington x-linked mental retardation syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:partington x-linked mental retardation syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:pashayan syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:pashayan syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:pelizaeus-merzbacher disease ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:pelizaeus-merzbacher disease | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:periventricular heterotopia, x-linked ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:periventricular heterotopia, x-linked | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:perniola krajewska carnevale syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:perniola krajewska carnevale syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:pfeiffer kapferer syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:pfeiffer kapferer syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:placental steroid sulfatase deficiency ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:placental steroid sulfatase deficiency | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:plagiocephaly and x-linked mental retardation ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:plagiocephaly and x-linked mental retardation | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:prader-willi habitus, osteopenia, and camptodactyly ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:prader-willi habitus, osteopenia, and camptodactyly | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:prader-willi syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:prader-willi syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:prieto badia mulas syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:prieto badia mulas syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:profound intellectual disabilities ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:profound intellectual disabilities | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:renpenning syndrome 1 ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:renpenning syndrome 1 | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:rett syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:rett syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:rosenthal-kloepfer syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:rosenthal-kloepfer syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:savant syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:savant syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:schaap taylor baraitser syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:schaap taylor baraitser syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:scott bryant graham syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:scott bryant graham syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:sesame syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:sesame syndrome | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:severe mental retardation (i.q. 20-34) | 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 -->
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 mitochondrial encephalomyopathy ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:severe x-linked mitochondrial encephalomyopathy | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:shprintzen-goldberg syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:shprintzen-goldberg syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:siderius x-linked mental retardation syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:siderius x-linked mental retardation syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:simpson-golabi-behmel syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:simpson-golabi-behmel syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:smith-magenis syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:smith-magenis syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:sohval soffer syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:sohval soffer syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:spinocerebellar ataxia, x-linked 3 ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:spinocerebellar ataxia, x-linked 3 | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:spinocerebellar ataxia, x-linked 4 ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:spinocerebellar ataxia, x-linked 4 | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:spondyloepiphyseal dysplasia tarda, x-linked ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:spondyloepiphyseal dysplasia tarda, x-linked | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:syndromic x-linked intellectual disability due to jarid1c mutation ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:syndromic x-linked intellectual disability due to jarid1c mutation | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:syndromic x-linked intellectual disability type 11 | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:temtamy syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:temtamy syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:thiamin-responsive maple syrup urine disease ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:thiamin-responsive maple syrup urine disease | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:tranebjaerg svejgaard syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:tranebjaerg svejgaard syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:trichodysplasia with amelogenesis imperfecta syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:trichodysplasia with amelogenesis imperfecta syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:trisomy 10p ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:trisomy 10p | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:tuberous sclerosis ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:tuberous sclerosis | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:unspecified mental retardation; other impairments of behaviour ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:unspecified mental retardation; other impairments of behaviour | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:unspecified mental retardation; significant impairment of behaviour requiring attention or treatment | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:unspecified mental retardation; with the statement of no, or minimal, impairment of behaviour | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:unspecified mental retardation; without mention of impairment of behaviour ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:unspecified mental retardation; without mention of impairment of behaviour | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:uveal coloboma with cleft lip and palate and intellectual disability syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:verloes gillerot fryns syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:verloes gillerot fryns syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:viljoen kallis voges syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:viljoen kallis voges syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:volcke soekarman syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:volcke soekarman syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:waisman syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:waisman syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:wieacker-wolff syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:wieacker-wolff syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:wilson turner syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:wilson turner syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:winship viljoen leary syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:winship viljoen leary syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:wiskott-aldrich syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:wiskott-aldrich syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:wolf-hirschhorn syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:wolf-hirschhorn syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:woods black norbury syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:woods black norbury syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked adrenal hypoplasia congenita ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked adrenal hypoplasia congenita | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked agammaglobulinemia ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked agammaglobulinemia | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked combined immunodeficiency diseases ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked combined immunodeficiency diseases | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:x-linked congenital dyserythropoietic anemia with thrombocytopenia | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked creatine transporter deficiency ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked creatine transporter deficiency | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:x-linked dominant chondrodysplasia chassaing lacombe type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked dyskeratosis congenita ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked dyskeratosis congenita | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:x-linked epilepsy with learning disability and behavior disorder syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked hereditary sensory and autonomic neuropathy with deafness ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked hereditary sensory and autonomic neuropathy with deafness | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked hydrocephalus syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked hydrocephalus syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked immunodeficiency with magnesium defect, epstein-barr virus infection and neoplasia ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked immunodeficiency with magnesium defect, epstein-barr virus infection and neoplasia | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked intellectual disability abidi type ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked intellectual disability abidi type | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:x-linked intellectual disability and epilepsy with progressive joint contracture and facial dysmorphism syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked intellectual disability cilliers type ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked intellectual disability cilliers type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked intellectual disability schimke type ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked intellectual disability schimke type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked intellectual disability shrimpton type ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked intellectual disability shrimpton type | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:x-linked intellectual disability stocco dos santos type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked intellectual disability turner type ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked intellectual disability turner type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked intellectual disability wilson type ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked intellectual disability wilson type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked intellectual disability with cerebellar hypoplasia syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked intellectual disability with cerebellar hypoplasia syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked intellectual disability with cubitus valgus and dysmorphism syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked intellectual disability with cubitus valgus and dysmorphism syndrome | n2=en:x-linked intellectual disability armfield 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 armfield type
n1=en:x-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked intellectual disability with precocious puberty and obesity syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked intellectual disability with precocious puberty and obesity syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked intellectual disability zorick type ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked intellectual disability zorick type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked lissencephaly ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked lissencephaly | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked lymphoproliferative disorder ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked lymphoproliferative disorder | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked mendelian susceptibility to mycobacterial disease ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked mendelian susceptibility to mycobacterial disease | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked neurodegenerative syndrome bertini type ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked neurodegenerative syndrome bertini type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked neurodegenerative syndrome hamel type ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked neurodegenerative syndrome hamel type | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked recessive intellectual disability and macrocephaly with ciliary dysfunction syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked recessive intellectual disability and macrocephaly with ciliary dysfunction syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked retinal dysplasia ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked retinal dysplasia | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:x-linked sideroblastic anemia with spinocerebellar ataxia ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:x-linked sideroblastic anemia with spinocerebellar ataxia | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- en:zunich neuroectodermal syndrome ---
r_associated #0: 20 -->
en:x-linked intellectual disability armfield type
n1=en:zunich neuroectodermal syndrome | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=20
- déficit en céto-acide décarboxylase ---
r_associated #0: 15 -->
en:x-linked intellectual disability armfield type
n1=déficit en céto-acide décarboxylase | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=15
- Goltz ---
r_associated #0: 10 -->
en:x-linked intellectual disability armfield type
n1=Goltz | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=10
- céroïdes lipofuscinoses neuronales ---
r_associated #0: 10 -->
en:x-linked intellectual disability armfield type
n1=céroïdes lipofuscinoses neuronales | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=10
- céroïdes-lipofuscinoses neuronales ---
r_associated #0: 10 -->
en:x-linked intellectual disability armfield type
n1=céroïdes-lipofuscinoses neuronales | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=10
- déficience congénitale ---
r_associated #0: 10 -->
en:x-linked intellectual disability armfield type
n1=déficience congénitale | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=10
- déformation congénitale ---
r_associated #0: 10 -->
en:x-linked intellectual disability armfield type
n1=déformation congénitale | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=10
- hypoplasie dermique en aires ---
r_associated #0: 10 -->
en:x-linked intellectual disability armfield type
n1=hypoplasie dermique en aires | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=10
- hypoplasie dermique focale ---
r_associated #0: 10 -->
en:x-linked intellectual disability armfield type
n1=hypoplasie dermique focale | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=10
- maladie des urines à l'odeur de sirop d'érable ---
r_associated #0: 10 -->
en:x-linked intellectual disability armfield type
n1=maladie des urines à l'odeur de sirop d'érable | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=10
- maladie du sirop d'érable ---
r_associated #0: 10 -->
en:x-linked intellectual disability armfield type
n1=maladie du sirop d'érable | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=10
- syndrome de Goltz ---
r_associated #0: 10 -->
en:x-linked intellectual disability armfield type
n1=syndrome de Goltz | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=10
- syndrome de Rett ---
r_associated #0: 10 -->
en:x-linked intellectual disability armfield type
n1=syndrome de Rett | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=10
- syndrome de Viljoen-Kallis-Voges ---
r_associated #0: 10 -->
en:x-linked intellectual disability armfield type
n1=syndrome de Viljoen-Kallis-Voges | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=10
- syndrome de microcéphalie-brachydactylie-déficience intellectuelle ---
r_associated #0: 10 -->
en:x-linked intellectual disability armfield type
n1=syndrome de microcéphalie-brachydactylie-déficience intellectuelle | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=10
- anomalie congénitale ---
r_associated #0: 5 -->
en:x-linked intellectual disability armfield type
n1=anomalie congénitale | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=5
- céroïdes lipofuschinoses neuronales ---
r_associated #0: 5 -->
en:x-linked intellectual disability armfield type
n1=céroïdes lipofuschinoses neuronales | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=5
- dystrophie musculaire d'Emery-Dreifuss ---
r_associated #0: 5 -->
en:x-linked intellectual disability armfield type
n1=dystrophie musculaire d'Emery-Dreifuss | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=5
- dystrophie musculaire de Duchenne ---
r_associated #0: 5 -->
en:x-linked intellectual disability armfield type
n1=dystrophie musculaire de Duchenne | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=5
- en:congenital anomaly ---
r_associated #0: 5 -->
en:x-linked intellectual disability armfield type
n1=en:congenital anomaly | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=5
- maladie des urines avec odeur de sirop erable ---
r_associated #0: 5 -->
en:x-linked intellectual disability armfield type
n1=maladie des urines avec odeur de sirop erable | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=5
- malformation congénitale ---
r_associated #0: 5 -->
en:x-linked intellectual disability armfield type
n1=malformation congénitale | n2=en:x-linked intellectual disability armfield type | rel=r_associated | relid=0 | w=5
|