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Disease Ontology Browser
Asperger syndrome (DOID:0050432)
Alliance: disease page
Alt IDs: OMIM:300494, OMIM:300497, OMIM:608631, OMIM:608638, OMIM:608781, OMIM:609954, ICD10CM:F84.5, MESH:D020817, NCI:C97159, ORDO:1162, UMLS_CUI:C0236792
Definition: An autism spectrum disorder that is characterized by significant difficulties in social interaction, along with restricted and repetitive patterns of behavior and interests. It differs from other autism spectrum disorders by its relative preservation of linguistic and cognitive development.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
MGI 6.14
The Jackson Laboratory