Search Ontology:
Human Disease
autosomal recessive intellectual developmental disorder 76
- Term ID
- DOID:0081235
- Synonyms
-
- Definition
- An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the GRIA1 gene on chromosome 5q33. https://pubmed.ncbi.nlm.nih.gov/35675825/
- References
- Ontology
- Human Disease ( DOID:0081235 )
- is a type of
-
Other Pages
Genes Involved
Zebrafish Models