Dyschromatosis universalis hereditaria 3
MONDO:0014169Any dyschromatosis universalis hereditaria in which the cause of the disease is a mutation in the ABCB6 gene.
Also known as: ABCB6 dyschromatosis universalis hereditaria, dyschromatosis universalis hereditaria 3, dyschromatosis universalis hereditaria caused by mutation in ABCB6, dyschromatosis universalis hereditaria type 3, DUH3
8 clinical trials for this condition and its sub-types.
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Disease
(618)
Hereditary disease
(172)
Skin disorder
(123)
Human disease
(14)
Hyperpigmentation of the skin
(11)
Skin pigmentation disorder
(11)
Hereditary skin disorder
(5)
Disease of genetic or genomic mechanism
(2)
Dyschromatosis universalis hereditaria
(1)
Disease by body system or component
(0)