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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H02350 | Dyschromatosis universalis hereditaria | ... pigmentary disorders characterized by asymptomatic hypo- and hyper-pigmented macules of irregular size and shape which appear early in life. At least two causative genes, ABCB6 and SASH1, have been reported. | Skin disease |
(DUH1) SASH1 [HSA:23328] [KO:K23705] (DUH3) ABCB6 [HSA:10058] [KO:K05661] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |