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Summary Literature (0)
DOID:0070070 - autosomal dominant non-syndromic intellectual disability 40


Disease Ontology Definition:An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of MYT1L on chromosome 2p25.3.

Synonyms: MRD40, autosomal dominant mental retardation 40

Xenbase Genes : champ1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014699 - intellectual disability, autosomal dominant 40


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)