SNOMED Definition:
(Full definition may include Is A relationships NOT present in Subset) |
|
Is a |
|
Factor VIII deficiency (disorder) |
|
Is a |
|
Hemophilia (disorder) |
|
Is a |
|
Hereditary coagulation factor deficiency (disorder) |
|
Is a |
|
X-linked hereditary disease (disorder) |
Group 1 |
|
Has interpretation (attribute) |
|
Abnormal (qualifier value) |
|
Interprets (attribute) |
|
Hemostatic function (observable entity) |
|
This concept's defining relationships are necessary but do not sufficiently define it (a.k.a. primitive).
|
Default Descriptions (Synonyms):
Hide DescriptionIDs
|
|
Synonym: |
AHG deficiency disease [47361014] |
|
Synonym: |
Sex-linked factor VIII deficiency [47362019] |
|
Synonym: |
Congenital factor VIII deficiency disease [47363012] |
|
Fully specified name: |
Hereditary factor VIII deficiency disease (disorder) [2787090010] |
|
Synonym: |
Hemophilia A [47356012] |
|
Synonym: |
Haemophilia A [483814018] |
|
Synonym: |
Classical haemophilia [483815017] |
|
Synonym: |
Hereditary factor VIII deficiency disease [47359017] |
|
Synonym: |
Congenital factor VIII deficiency [1225870016] |
|
Synonym: |
Classical hemophilia [47360010] |
|
Fully specified name: |
Hemophilia A (disorder) [758956015] |
|
Synonym: |
Haemophilia A, NOS [47364018] |
|
Synonym: |
Hemophilia A, NOS [47358013] |