Leber Congenital Amaurosis 10 MeSH Supplementary Concept Data 2025

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Concepts

MeSH Supplementary: Leber Congenital Amaurosis 10
Unique ID: C565720
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565720
Registry Numbers: 0
Heading Mapped to: *Leber Congenital Amaurosis
Frequency: 5
Note: associated with mutations on CEP290 PROTEIN, HUMAN gene
Date of Entry: 2012/11/05
Revision Date: 2022/04/25

Leber Congenital Amaurosis 10 Preferred

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