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Disease Ontology Browser
chromosome 15q11.2 deletion syndrome (DOID:0060393)
Alliance: disease page
Synonyms: 15q11.2 microdeletion syndrome
Alt IDs: OMIM:615656, ORDO:261183, UMLS_CUI:C3180937
Definition: A chromosomal deletion syndrome that is characterized by intellectual disbaility, dysmorphic facies, psychiatric illness and autism spectrum disorder, has_material_basis_in autosomal dominant inheritance of partial deletion of the long arm of chromosome 15.

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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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12/10/2024
MGI 6.24 		The Jackson Laboratory