Disease_Mapped_To_Gene
CTRP Terminology
CTRP Disease Terminology
Pediatric Hematology-Oncology Terminology
Cellosaurus Disease Terminology
Cellosaurus Terminology
mCode Terminology
mCode Elixhauser Coagulation Deficiency Value Set
Hemophilia A
An X-linked recessive deficiency of coagulation factor VIII characterized by a tendency to bleed. Hemophilia A, the most common type of hemophilia, occurs in approximately 1 in 4,000 to 1 in 5,000 live male births.
An inherited deficiency of coagulation factor VIII characterized by the tendency to spontaneous or exaggerated post-traumatic hemorrhage. Inherited as an X-linked recessive disease, hemophilia A is the most common hemophilia, occurring in approximately 1 in 10,000 male births.
C0019069
C27146
CTRP
Cellosaurus
Disease or Syndrome
Factor VIII Deficiency
Hemophilia A
Hemophilia A
Hemophilia A
Hemophilia_A
Hereditary Factor VIII Deficiency
Hereditary Factor VIII Deficiency Disease
Hereditary factor VIII deficiency
NICHD
mCode
F8 Gene
Hemophilia
NICHD Terminology
Hereditary Coagulation Factor Deficiency
Neonatal Research Network Terminology