autosomal dominant intellectual developmental disorder 6

Summary

DOID:0070036 - autosomal dominant intellectual developmental disorder 6

Disease Ontology Definition:An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the GRIN2B gene on chromosome 12p13.1.

Synonyms: autosomal dominant mental retardation 6, autosomal dominant non-syndromic intellectual disability 6, MRD6

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

: grin2b

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013509 - lumbar vertebra cartilage element

MONDO:0013509 - lumbar vertebra cartilage element

MIM:

MIM:613970 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6

MIM:613970 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6

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)