|
DOID:0070066 - autosomal dominant intellectual developmental disorder 36
Disease Ontology Definition:An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the PPP2R1A gene on chromosome 19q13.41.
Synonyms: MRD36, autosomal dominant mental retardation 36, autosomal dominant non-syndromic intellectual disability 36,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0014605 - microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee