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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H01162 |
Scott syndrome Bleeding disorder platelet-type 7 (BDPLT7) |
Scott syndrome is a rare autosomal recessive congenital bleeding disorder caused by a defect in blood coagulation. When platelets are activated, a calcium-induced rearrangement of the platelet membrane ... | Hematologic disease | ANO6 [HSA:196527] [KO:K19500] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |