Cone-Rod Dystrophy, X-Linked, 3 MeSH Supplementary Concept Data 2025

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Concepts

MeSH Supplementary: Cone-Rod Dystrophy, X-Linked, 3
Unique ID: C564507
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564507
Entry Term(s): CORDX3
Registry Numbers: 0
Heading Mapped to: *Retinitis Pigmentosa; *Genetic Diseases, X-Linked
Frequency: 2
Note: mutation in CACNA1F
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Cone-Rod Dystrophy, X-Linked, 3 Preferred

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