ZFIN Human Disease: autosomal dominant intellectual developmental disorder 8

OBO ID: DOID:0070038

Term Name:	autosomal dominant intellectual developmental disorder 8		Search Ontology:
Synonyms:	autosomal dominant mental retardation 8 autosomal dominant non-syndromic intellectual disability 8 MRD8
Definition:	An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the GRIN1 gene on chromosome 9q34.3. https://www.ncbi.nlm.nih.gov/pubmed/21376300
References:	OMIM:614254
Ontology:	Human Disease ( DOID:0070038 )

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 8 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
GRIN1	grin1a grin1b	Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant	614254

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None