Search Ontology:
Human Disease
retinitis pigmentosa 18
- Term ID
- DOID:0110356
- Synonyms
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- RP18
- Definition
- A retinitis pigmentosa that has_material_basis_in mutation in the PRPF3 gene on chromosome 1q21. https://www.ncbi.nlm.nih.gov/pubmed/11773002
- References
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- ICD10CM:H35.5
- MESH:C563320
- MIM:601414
- Ontology
- Human Disease ( DOID:0110356 )
- is a type of
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Genes Involved
Zebrafish Models