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DOID:0070063 - autosomal dominant intellectual developmental disorder 33
Disease Ontology Definition:An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the DPP6 gene on chromosome 7q36.2.
Synonyms: MRD33, autosomal dominant mental retardation 33, autosomal dominant non-syndromic intellectual disability 33,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0014580 - intellectual disability, autosomal dominant 33 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee