Search Ontology:
Human Disease
retinitis pigmentosa 19
- Term ID
- DOID:0110354
- Synonyms
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- RP19
- Definition
- A retinitis pigmentosa that has_material_basis_in mutation in the ABCA4 gene on chromosome 1p22. https://www.ncbi.nlm.nih.gov/pubmed/9425888
- References
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- ICD10CM:H35.5
- MESH:C566637
- MIM:601718
- Ontology
- Human Disease ( DOID:0110354 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models