MeSH Browser

MeSH Supplementary: Achromatopsia incomplete, X-linked
Unique ID: C538165
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538165
Entry Term(s): Incomplete achromatopsia , X-linked; X-linked achromatopsia, incomplete
Registry Number: 0
Heading Mapped to: *Color Vision Defects; *Genetic Diseases, X-Linked
Frequency: 2
Date of Entry: 2010/06/25

Achromatopsia incomplete, X-linked MeSH Supplementary Concept Data 2024