autosomal dominant intellectual developmental disorder 22

Summary

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,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: zbtb18, znf238.2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012869 - intellectual disability, autosomal dominant 22

MONDO:0012869 - intellectual disability, autosomal dominant 22

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

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

Parent(s): autosomal dominant intellectual developmental disorder (is_a)