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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

Xenbase Genes : ctcf

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014213 - intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome

OMIM:
OMIM:615502 - INTELLECTUAL DEVELOPMENTAL DISORDER, 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 non-syndromic intellectual disability (is_a)