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Achromatopsia 5 MeSH Supplementary Concept Data 2022


MeSH Supplementary
Achromatopsia 5
Unique ID
C567759
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567759
Registry Number
0
Heading Mapped to
*Color Vision Defects
*Eye Diseases, Hereditary
Frequency
0
Date of Entry
2012/11/05
Achromatopsia 5 Preferred
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