MeSH Browser

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 MeSH Supplementary Concept Data 2025