Cone-Rod Dystrophy 12 MeSH Supplementary Concept Data 2025

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Concepts

MeSH Supplementary: Cone-Rod Dystrophy 12
Unique ID: C567206
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567206
Entry Term(s): CORD12
Registry Numbers: 0
Heading Mapped to: *Retinitis Pigmentosa
Frequency: 1
Note: mutation in PROM1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Cone-Rod Dystrophy 12 Preferred

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