Cone-Rod Dystrophy 13 MeSH Supplementary Concept Data 2024

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Concepts

MeSH Supplementary: Cone-Rod Dystrophy 13
Unique ID: C567698
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567698
Entry Term(s): CORD13
Registry Number: 0
Heading Mapped to: *Retinitis Pigmentosa
Frequency: 0
Note: mutation in RPGRIP1
Date of Entry: 2012/11/05

Cone-Rod Dystrophy 13 Preferred

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