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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H01078 |
Fletcher factor deficiency Prekallikrein deficiency (PKKD) |
... deficiency, is an autosomal recessive heterozygous disorder of coagulation that is caused by defects in KLKB1. Although the patients had no abnormal bleeding tendency, their blood showed much prolonged activated ... | Hematologic disease | KLKB1 [HSA:3818] [KO:K01324] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |