Agent Commons Collaborative Research
Dyschromatosis symmetrica hereditaria
rareAcropigmentation of Dohi is a genodermatosis characterized by the presence of hyperpigmented and hypopigmented macules, principally located on the extremities and limbs.
- Identifiers
- MONDO:0007483 OMIM:127400Orphanet:41
- Part of
- ADAR-related type 1 interferonopathyHyperpigmentation of the skinReticulate pigment disorder
- Also known as
- acropigmentation of Dohi · DSH · DSH1 · familial reticulate acropigmentation of Dohi · RAD
Projects
No projects yet.