Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Pallister W syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked recessive sensory neuropathy |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Ocular albinism, type I |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Chondrodysplasia punctata, X-linked recessive type |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked recessive intellectual disability and macrocephaly with ciliary dysfunction syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked intellectual disability with seizure and psoriasis syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked cone dysfunction syndrome with myopia (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Hydrocephalus with obesity and hypogonadism syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Deficiency of monoamine oxidase A (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked intellectual disability with ataxia and apraxia syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Chromosome Xp11.3 microdeletion syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
SCARF syndrome |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked intellectual disability with cubitus valgus and dysmorphism syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Microphthalmia with ankyloblepharon and intellectual disability syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked epilepsy with learning disability and behavior disorder syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked intellectual disability Shrimpton type |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked intellectual disability Pai type (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
N syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked spasticity, intellectual disability, epilepsy syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked severe congenital neutropenia (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Arts syndrome |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Juberg Marsidi syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Intellectual disability, developmental delay, contracture syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Alpha thalassemia X-linked intellectual disability syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked Charcot-Marie-Tooth disease type 4 |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked Charcot-Marie-Tooth disease type 3 |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Abruzzo Erickson syndrome |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked spastic paraplegia type 2 (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked Charcot-Marie-Tooth disease type 5 (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked endothelial dystrophy of cornea (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked myopathy with excessive autophagy (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked hereditary sensory and autonomic neuropathy with deafness (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Deafness and intellectual disability Martin Probst type syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Pierre Robin sequence faciodigital anomaly syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Bullous dystrophy macular type (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked Charcot-Marie-Tooth disease type 2 (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Holoprosencephaly sequence with hypokinesia and congenital joint contracture syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Hoyeraal-Hreidarsson syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Deafness and hypogonadism syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked intellectual disability Van Esch type (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked intellectual disability and hypotonia with facial dysmorphism and aggressive behavior syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked spinocerebellar ataxia type 3 (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Aland Islands eye disease (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked intellectual disability Cilliers type (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked spondyloepimetaphyseal dysplasia (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked parkinsonism with spasticity syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Xq12-q13.3 duplication syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked progressive cerebellar ataxia |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked spinocerebellar ataxia type 4 (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked osteoporosis with fractures |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Xp22.13p22.2 duplication syndrome |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Snyder-Robinson syndrome |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked intellectual disability Seemanova type (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked intellectual disability Siderius type (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked intellectual disability Stevenson type (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked intellectual disability Stocco Dos Santos type (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked intellectual disability Stoll type (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked intellectual disability Schimke type (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked intellectual disability Miles Carpenter type (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked intellectual disability Cantagrel type (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked intellectual disability Armfield type (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked intellectual disability Nascimento type (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked retinal dysplasia (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
3-Methylglutaconic aciduria type 2 |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Agenesis of corpus callosum and abnormal genitalia syndrome |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Cerebellum agenesis with hydrocephaly |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Albinism with deafness syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Borjeson-Forssman-Lehmann syndrome |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Atrophia bulborum hereditaria |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Bulbospinal neuronopathy |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Blue cone monochromatism (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Beta thalassemia X-linked thrombocytopenia syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Brachytelephalangic chondrodysplasia punctata (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Cutis laxa, x-linked |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Congenital adrenal hypoplasia, X-linked |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
CK syndrome |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Contiguous ABCD1 DXS1357E deletion syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Chromosome Xq27.3q28 duplication syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Choroideremia |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Congenital disorder of glycosylation type 1y |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Congenital disorder of glycosylation type 1s |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Danon disease |
Is a |
False |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Deafness-dystonia-optic neuronopathy syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Dent's disease (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
X-linked Ehlers-Danlos syndrome |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Distal Xq28 microduplication syndrome |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Early-onset X-linked optic atrophy (disorder) |
Is a |
False |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Early onset parkinsonism and intellectual disability syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Ferro-cerebro-cutaneous syndrome |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Fried syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
FRAXE intellectual disability syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
L1 syndrome |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Hyperekplexia epilepsy syndrome (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|
Infantile epileptic dyskinetic encephalopathy (disorder) |
Is a |
True |
X-linked recessive hereditary disease |
Inferred relationship |
Some |
|