autosomal dominant intellectual developmental disorder 8

Summary

DOID:0070038 - autosomal dominant intellectual developmental disorder 8

Disease Ontology Definition:An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the GRIN1 gene on chromosome 9q34.3.

Synonyms: autosomal dominant mental retardation 8, autosomal dominant non-syndromic intellectual disability 8, MRD8

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

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

: grin1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013655 - intellectual disability, autosomal dominant 8

MONDO:0013655 - intellectual disability, autosomal dominant 8

MIM:

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

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

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant intellectual developmental disorder (is_a)