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Summary Literature (0)
DOID:0070048 - autosomal dominant non-syndromic intellectual disability 18


Disease Ontology Definition:An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of GATAD2B on chromosome 1q21.3.

Synonyms: MRD18, autosomal dominant mental retardation 18

Xenbase Genes : gatad2b

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014034 - severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome

OMIM:
OMIM:615074 - GAND SYNDROME; GAND

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)