Summary Literature (0)

DOID:0070065 - autosomal dominant intellectual developmental disorder 35

Disease Ontology Definition:An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the PPP2R5D gene on chromosome 6p21.1.

Synonyms: MRD35, autosomal dominant mental retardation 35, autosomal dominant non-syndromic intellectual disability 35,

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014602 - intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee