Dyschromatosis universalis hereditaria 3

MONDO:0014169

Any 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

2 clinical trials for this condition and its sub-types, 0 tagged with Dyschromatosis universalis hereditaria 3 itself.

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↑ Dyschromatosis universalis hereditaria (1)

Including sub-types (2) Tagged with Dyschromatosis universalis hereditaria 3 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.