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- B4ad489cddce1aa10b9f85f5556ae925f hasDbXref "Orphanet:330" @default.
- B4ad489cddce1aa10b9f85f5556ae925f type Axiom @default.
- B4ad489cddce1aa10b9f85f5556ae925f annotatedProperty IAO_0000115 @default.
- B4ad489cddce1aa10b9f85f5556ae925f annotatedSource MONDO_0009315 @default.
- B4ad489cddce1aa10b9f85f5556ae925f annotatedTarget "Congenital factor XII deficiency is an autosomal recessive systemic dysfunction of the hemostatic pathway, that is due to a defect in the coagulation factor XII (FXII or Hageman factor), and is either asymptomatic or characterized by a prolonged activated partial thromboplastin time and an increased risk for thromboembolism. FXII deficiency is strongly associated with primary recurrent abortions." @default.