autosomal dominant non-syndromic intellectual disability 21

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Summary

Literature (0)

DOID:0070051 - autosomal dominant non-syndromic intellectual disability 21

Disease Ontology Definition:An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of CTCF on chromosome 16q22.1.

Synonyms: MRD21, autosomal dominant mental retardation 21,

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

: ctcf

OMIM:

MIM:615502 - mental retardation, autosomal dominant 21; mrd21

MIM:615502 - mental retardation, autosomal dominant 21; mrd21

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)