Retinitis Pigmentosa 7, Digenic MeSH Supplementary Concept Data 2024

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Concepts

MeSH Supplementary: Retinitis Pigmentosa 7, Digenic
Unique ID: C567263
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567263
Registry Number: 0
Heading Mapped to: *Retinitis Pigmentosa
Frequency: 0
Note: digenic mutations in PRPH2 (RDS) and ROM1
Date of Entry: 2012/11/05

Retinitis Pigmentosa 7, Digenic Preferred

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