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Disease Ontology Browser
chromosome 15q13.3 microdeletion syndrome (DOID:0060394)
Alliance: disease page
Synonyms: 15q13.3 microdeletion syndrome
Alt IDs: OMIM:612001, ICD10CM:Q93.5, MESH:C567439, ORDO:199318
Definition: A chromosomal deletion syndrome that is characterized by intellectual dsability, developmental delay, autism spectrum disorder and seizure, has_material_basis_in autosomal dominant inheritance of partial deletion of the long arm of chromosome 15.

Disease References using Mouse Models (5)
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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10/29/2024
MGI 6.24 		The Jackson Laboratory