Newfoundland Rod-Cone Dystrophy MeSH Supplementary Concept Data 2023

Details
Concepts

MeSH Supplementary: Newfoundland Rod-Cone Dystrophy
Unique ID: C564391
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564391
Registry Number: 0
Heading Mapped to: *Retinitis Pigmentosa
Frequency: 1
Note: RLBP1 protein, human mutation
Date of Entry: 2012/11/05

Newfoundland Rod-Cone Dystrophy Preferred

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