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Albinism MeSH Descriptor Data 2021


MeSH Heading
Albinism
Tree Number(s)
C11.270.040
C16.320.290.040
C16.320.565.100.102
C16.320.850.080
C17.800.621.440.102
C17.800.827.080
C18.452.648.100.102
Unique ID
D000417
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D000417
Annotation
general or unspecified; prefer specifics
Scope Note
General term for a number of inherited defects of amino acid metabolism in which there is a deficiency or absence of pigment in the eyes, skin, or hair.
NLM Classification #
WR 267
See Also
Chediak-Higashi Syndrome
Date Established
1966/01/01
Date of Entry
1999/01/01
Revision Date
2016/07/01
Albinism Preferred
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