Search Ontology:
Human Disease
retinitis pigmentosa 2
- Term ID
- DOID:0110415
- Synonyms
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- RP2
- Definition
- A retinitis pigmentosa that has_material_basis_in mutation in the RP2 gene on chromosome Xp11.3. https://www.ncbi.nlm.nih.gov/pubmed/9697692
- References
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- ICD10CM:H35.5
- MESH:C567523
- MIM:312600
- Ontology
- Human Disease ( DOID:0110415 )
- is a type of
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Genes Involved
Zebrafish Models