Search Ontology:
Human Disease
retinitis pigmentosa 35
- Term ID
- DOID:0110357
- Synonyms
-
- RP35
- Definition
- A retinitis pigmentosa that has_material_basis_in mutation in the SEMA4A gene on chromosome 1q22. https://www.ncbi.nlm.nih.gov/pubmed/16199541
- References
-
- ICD10CM:H35.5
- MESH:C565206
- MIM:610282
- Ontology
- Human Disease ( DOID:0110357 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models