Search Ontology:
Human Disease
retinitis pigmentosa 11
- Term ID
- DOID:0110408
- Synonyms
-
- RP11
- Definition
- A retinitis pigmentosa that has_material_basis_in mutation in the PRPF31 gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/11545739
- References
-
- ICD10CM:H35.5
- MESH:C563991
- MIM:600138
- Ontology
- Human Disease ( DOID:0110408 )
- is a type of
-
Other Pages
Genes Involved
Zebrafish Models