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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00844 |
Familial benign chronic pemphigus Hailey-Hailey disease |
... 20 and 40 years of age. In two third of all cases, positive family history is detected. Mutations in ATP2C1 that encodes a secretory pathway Ca2+/Mn2+-ATPase in the Golgi apparatus impair desmosomal keratinocyte ... | Congenital malformation | ATP2C1 [HSA:27032] [KO:K01537] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |