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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H02658 | X-linked congenital hemolytic anemia | ... congenital hemolytic anemia (HACXL) is a recently reported hemolytic anemia caused by mutations in the ATP11C. ATP11C encodes a major flippase in human erythrocytes. Flippase transports phospholipids from ... | Hematologic disease | ATP11C [HSA:286410] [KO:K26934] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |