Search Ontology:
Human Disease
cone-rod dystrophy 13
- Term ID
- DOID:0111016
- Synonyms
-
- CORD13
- Definition
- A cone-rod dystrophy that has_material_basis_in mutation in the RPGRIP1 gene on chromosome 14q11.2. https://www.ncbi.nlm.nih.gov/pubmed/12920076
- References
- Ontology
- Human Disease ( DOID:0111016 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models