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Dyschromatosis symmetrica hereditaria

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Name:
Dyschromatosis symmetrica hereditaria
Description:
A rare genodermatosis characterized by the presence of the mixture of hyperpigmented and hypopigmented macules of approximately 5mm in diameter, principally located on the extremities and limbs.
ORPHAcode:
41
Synonyms:
Acropigmentation of Dohi
XREF(s):
Orphanet
ICD-10
MeSH
OMIM
Analyte(s):
ADAR
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14