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Dyschromatosis universalis hereditaria MeSH Supplementary Concept Data 2024


MeSH Supplementary
Dyschromatosis universalis hereditaria
Unique ID
C535730
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C535730
Heading Mapped to
Pigmentation Disorders / congenital
*Skin Diseases, Genetic
Frequency
29
Note
A rare herditary skin condition characterized by hyper- and hypopigmented macules of variable size and shape that appear in infancy or early childhood on the trunk, limbs, and sometimes the face. There may also be abnormalities affecting the hair, nails, and dermal connective tissue as well as nerves. OMIM: 127500
Date of Entry
2010/08/25
Revision Date
2016/09/29
Dyschromatosis universalis hereditaria Preferred
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