ZFIN Human Disease: autosomal dominant intellectual developmental disorder 6

OBO ID: DOID:0070036

Term Name:	autosomal dominant intellectual developmental disorder 6		Search Ontology:
Synonyms:	autosomal dominant mental retardation 6 autosomal dominant non-syndromic intellectual disability 6 MRD6
Definition:	An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the GRIN2B gene on chromosome 12p13.1. https://www.ncbi.nlm.nih.gov/pubmed/20890276
References:	OMIM:613970
Ontology:	Human Disease ( DOID:0070036 )

Relationships

is a type of:	autosomal dominant intellectual developmental disorder autosomal dominant intellectual developmental disorder Show first 5 Terms

OTHER autosomal dominant intellectual developmental disorder 6 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
GRIN2B	grin2bb grin2ba	Intellectual developmental disorder, autosomal dominant 6, with or without seizures	613970

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None