ZFIN Human Disease: autosomal recessive intellectual developmental disorder 6

OBO ID: DOID:0081182

Term Name:	autosomal recessive intellectual developmental disorder 6		Search Ontology:
Synonyms:
Definition:	An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the ionotropic glutamate receptor-6 gene (GRIK2) on chromosome 6q16. https://pubmed.ncbi.nlm.nih.gov/25039795/
References:	OMIM:611092
Ontology:	Human Disease ( DOID:0081182 )

Relationships

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

OTHER autosomal recessive intellectual developmental disorder 6 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
GRIK2	grik2	Intellectual developmental disorder, autosomal recessive 6	611092

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None