Macular Dystrophy, Retinal, 2 MeSH Supplementary Concept Data 2025

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Concepts

MeSH Supplementary: Macular Dystrophy, Retinal, 2
Unique ID: C562746
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562746
Registry Numbers: 0
Heading Mapped to: *Corneal Dystrophies, Hereditary
Frequency: 2
Note: mutation in PROM1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Macular Dystrophy, Retinal, 2 Preferred

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