Cone-Rod Dystrophy, X-Linked, Type 1 MeSH Supplementary Concept Data 2025

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Concepts

MeSH Supplementary: Cone-Rod Dystrophy, X-Linked, Type 1
Unique ID: C564438
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564438
Entry Term(s): CORDX1
Registry Numbers: 0
Heading Mapped to: *Retinitis Pigmentosa; *Genetic Diseases, X-Linked
Frequency: 0
Note: mutation in RPGR
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Cone-Rod Dystrophy, X-Linked, Type 1 Preferred

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