Retinitis Pigmentosa 41 MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Retinitis Pigmentosa 41
Unique ID: C567422
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567422
Entry Term(s): Retinal Degeneration, Autosomal Recessive, Prominin-Related
Registry Numbers: 0
Heading Mapped to: *Retinitis Pigmentosa
Frequency: 0
Note: mutations in PROM1; aka RP41
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Retinitis Pigmentosa 41 Preferred

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