autosomal dominant intellectual developmental disorder 76 Disease Ontology Browser

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autosomal dominant intellectual developmental disorder 76 (DOID:0081468)
Alliance: disease page
Alt IDs: OMIM:621285
Definition: An autosomal dominant intellectual developmental disorder that is characterized by developmental delay, mildly to severely impaired intellectual development with speech and language deficits, and autism and that has_material_basis_in heterozygous mutation in the MARK2 gene on chromosome 11q13.

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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