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Summary Literature (0)
DOID:0070038 - autosomal dominant non-syndromic intellectual disability 8


Disease Ontology Definition:An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of GRIN1 on chromosome 9q34.3.

Synonyms: MRD8, autosomal dominant mental retardation 8

Xenbase Genes : grin1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013655 - intellectual disability, autosomal dominant 8

OMIM:
OMIM:614254 - NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD

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)