Concept information
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Coagulation Protein Disorders
Preferred term
Factor XII Deficiency
Type
-
mesh:Descriptor
Definition
- An absence or reduced level of blood coagulation factor XII. It normally occurs in the absence of patient or family history of hemorrhagic disorders and is marked by prolonged clotting time.
Broader concept
Entry terms
- Coagulation Factor 12 Deficiency
- Deficiency, Factor 12
- Deficiency, Factor Twelve
- Deficiency, Factor XII
- Factor 12 Deficiency
- Factor Twelve Deficiency
- Hageman Factor Deficiency
- Hageman Trait
Allowable Qualifier(s)
- blood (Qualifier)
- cerebrospinal fluid (Qualifier)
- chemically induced (Qualifier)
- classification (Qualifier)
- complications (Qualifier)
- congenital (Qualifier)
- diagnosis (Qualifier)
- diagnostic imaging (Qualifier)
- diet therapy (Qualifier)
- drug therapy (Qualifier)
- economics (Qualifier)
- embryology (Qualifier)
- enzymology (Qualifier)
- epidemiology (Qualifier)
- ethnology (Qualifier)
- etiology (Qualifier)
- genetics (Qualifier)
- history (Qualifier)
- immunology (Qualifier)
- metabolism (Qualifier)
- microbiology (Qualifier)
- mortality (Qualifier)
- nursing (Qualifier)
- parasitology (Qualifier)
- pathology (Qualifier)
- physiopathology (Qualifier)
- prevention & control (Qualifier)
- psychology (Qualifier)
- radiotherapy (Qualifier)
- rehabilitation (Qualifier)
- surgery (Qualifier)
- therapy (Qualifier)
- urine (Qualifier)
- veterinary (Qualifier)
- virology (Qualifier)
In other languages
-
French
-
Déficit congénital en facteur Hageman
-
Déficit congénital en facteur XII
URI
http://data.loterre.fr/ark:/67375/JVR-PCJ659PX-T
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