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Achromatopsia incomplete, X-linked MeSH Supplementary Concept Data 2022


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 Preferred
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