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Items: 3

1.

Hereditary factor X deficiency disease

A rare inherited bleeding disorder with a decreased antigen and/or activity of factor X (FX) and characterized by mild to severe bleeding symptoms. [from ORDO]

MedGen UID:
543976
Concept ID:
C0272327
Disease or Syndrome
2.

Congenital factor VII deficiency

A rare, genetic, congenital vitamin K-dependant coagulation factor deficiency disorder characterized by decreased levels or absence of coagulation factor VII (FVII), resulting in bleeding diathesis of variable severity. [from ORDO]

MedGen UID:
473015
Concept ID:
C0272320
Disease or Syndrome
3.

Intramuscular hematoma

Blood clot formed within muscle tissue following leakage of blood into the tissue. [from HPO]

MedGen UID:
777032
Concept ID:
C0240412
Finding; Pathologic Function
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