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Dyschromatosis symmetrica hereditaria 1 MeSH Supplementary Concept Data 2025


MeSH Supplementary
Dyschromatosis symmetrica hereditaria 1
Unique ID
C535729
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C535729
Entry Term(s)
Dyschromatosis symmetrica hereditaria
Familial reticulate acropigmentation of Dohi
Reticulate acropigmentation of Dohi
Symmetric dyschromatosis of the extremities
Registry Numbers
0
Heading Mapped to
Pigmentation Disorders / congenital
Frequency
78
Note
A hereditary autosomal dominant condition primarily observed in persons of Chinese or Japanese descent. It is characterized by hyperpigmented and hypopigmented macules on the face and dorsal aspects of the extremities that appear in infancy or early childhood. Mutations in the ADAR gene have been identified. OMIM: 127400
Date of Entry
2010/08/25
Revision Date
2015/08/18
Dyschromatosis symmetrica hereditaria 1 Preferred
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