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- B726e7a05f52a264f0be4b32c01666126 hasDbXref "Orphanet:325" @default.
- B726e7a05f52a264f0be4b32c01666126 type Axiom @default.
- B726e7a05f52a264f0be4b32c01666126 annotatedProperty IAO_0000115 @default.
- B726e7a05f52a264f0be4b32c01666126 annotatedSource MONDO_0013361 @default.
- B726e7a05f52a264f0be4b32c01666126 annotatedTarget "Congenital factor II deficiency is an inherited bleeding disorder due to reduced activity of factor II (FII, prothrombin) and characterized by mucocutaneous bleeding symptoms." @default.