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DOID:0070060 - autosomal dominant intellectual developmental disorder 30
Disease Ontology Definition:An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the ZMYND11 gene on chromosome 10p15.3.
Synonyms: MRD30, autosomal dominant mental retardation 30, autosomal dominant non-syndromic intellectual disability 30,
Echinobase Genes :
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal dominant intellectual developmental disorder (is_a),
autosomal dominant intellectual developmental disorder 29 (is_a)