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dyschromatosis symmetrica hereditaria

Disease Summary
Associated Targets (2)
Tbio

1

Tdark

1


GARD Rare
Mondo Description Acropigmentation of Dohi is a genodermatosis characterised by the presence of hyperpigmented and hypopigmented macules, principally located on the extremities and limbs.
Uniprot Description An autosomal dominant pigmentary genodermatosis characterized by a mixture of hyperpigmented and hypopigmented macules distributed on the face and the dorsal parts of the hands and feet, that appear in infancy or early childhood.
Disease Ontology Description A pigmentation disease characterized by progressively pigmented and depigmented macules, often mixed in a reticulate pattern, concentrated on the dorsal extremities.
Mondo Term and Equivalent IDs
MONDO:0007483:  dyschromatosis symmetrica hereditaria
EFO:0008878: 
GARD:0000334: 
MESH:C535729: 
NCIT:C118435: 
Orphanet:41: 
SCTID:239085000: 
UMLS:C0406775: