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Disease Ontology Browser
autosomal dominant intellectual developmental disorder 38 (DOID:0070068)
Alliance: disease page
Synonyms: autosomal dominant mental retardation 38; autosomal dominant non-syndromic intellectual disability 38; MRD38; PRELDS; psychomotor retardation, epilepsy, and language disability syndrome
Alt IDs: OMIM:616393
Definition: An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the EEF1A2 gene on chromosome 20q13.33.

Disease References using Mouse Models (1)
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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04/16/2024
MGI 6.23 		The Jackson Laboratory