autosomal dominant intellectual developmental disorder

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Summary

Literature (0)

DOID:0060307 - autosomal dominant intellectual developmental disorder

Disease Ontology Definition:A intellectual disability characterized by an autosomal dominant inheritance pattern.

Synonyms: autosomal dominant mental retardation, autosomal dominant non-syndromic mental retardation,

Echinobase 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

: smarcb1, dync1h1, kansl1, ctcf

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

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

Parent(s): autosomal dominant disease (is_a), intellectual disability (is_a), non-syndromic intellectual disability (is_a)