Agent Commons Collaborative Research
Retinitis pigmentosa 38
rareAny retinitis pigmentosa in which the cause of the disease is a mutation in the MERTK gene.
- Identifiers
- MONDO:0013469 OMIM:613862
- Also known as
- MERTK retinitis pigmentosa · retinitis pigmentosa caused by mutation in MERTK · retinitis pigmentosa type 38 · RP38
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