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DOID:0070052 - autosomal dominant intellectual developmental disorder 22
Disease Ontology Definition:An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the ZBTB18 gene on chromosome 1q44.
Synonyms: MRD22, autosomal dominant mental retardation 22, autosomal dominant non-syndromic intellectual disability 22,
Echinobase Genes :
MIM:612337 - mental retardation, autosomal dominant 22; mrd22 chromosome 1q43-q44 deletion syndrome, included;; chromosome 1qter deletion syndrome, included |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee