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DOID:0080233 - autosomal dominant intellectual developmental disorder 50
Disease Ontology Definition:An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the NAA15 gene on chromosome 4q31.
Synonyms: autosomal dominant intellectual developmental disorder-50 with behavioral abnormalities, autosomal dominant mental retardation 50,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0030916 - intellectual disability, autosomal dominant 50 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee