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DOID:0070053 - autosomal dominant intellectual developmental disorder 23
Disease Ontology Definition:An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the SETD5 gene on chromosome 3p25.3.
Synonyms: MRD23, autosomal dominant mental retardation 23, autosomal dominant non-syndromic intellectual disability 23,
Xenbase Genes : setd5
MONDO:0014336 - intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee