Search Ontology:
Human Disease

autosomal recessive intellectual developmental disorder 6

Term ID
DOID:0081182
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
Ontology
Human Disease   ( DOID:0081182 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models