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autism, susceptibility to, X-linked 2
Disease Summary
Associated Targets (24)
Tbio
19
Tchem
2
Tdark
2
Tclin
1
Mondo Description A class of genetic disorders resulting in intellectual disability that is associated either with mutations of genes located on the X chromosome or aberrations in the structure of the X chromosome (sex chromosome aberrations).
Uniprot Description A complex multifactorial, pervasive developmental disorder characterized by impairments in reciprocal social interaction and communication, restricted and stereotyped patterns of interests and activities, and the presence of developmental abnormalities by 3 years of age. Most individuals with autism also manifest moderate mental retardation.
Mondo Term and Equivalent IDs
MONDO:0010341: autism, susceptibility to, X-linked 2
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
MESH:D038901
OMIM:300495
MONDO:0010341
High level summary of knowledge for a disease, including descriptions and datasource references.