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Retinitis Pigmentosa 41 MeSH Supplementary Concept Data 2022


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 Number
0
Heading Mapped to
*Retinitis Pigmentosa
Frequency
0
Note
mutations in PROM1; aka RP41
Date of Entry
2012/11/05
Retinitis Pigmentosa 41 Preferred
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