loading...| Preferred Name |
Hemophilia |
|
| Synonyms |
|
|
| ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Hemophilia |
|
| ID |
C3093 |
|
| NCI_Definition |
A deficiency or abnormality of a blood coagulation factor characterized by the tendency to spontaneous or exaggerated post-traumatic hemorrhage, Hemophilia is typically a hereditary disorder but, rarely, may be acquired. Inherited coagulation factor-deficient hemophilias include hemophilia A or classic hemophilia (factor VIII deficiency) hemophilia B or Christmas disease (factor IX deficiency), and hemophilia C (factor XI deficiency). In individuals without hereditary hemophilia A, factor VIII inhibitors may occur spontaneously as autoantibodies, resulting in a condition known as 'acquired hemophilia.' Approximately 10 % of patients with acquired hemophilia have an underlying malignancy. |
|
| NCI_PT |
Hemophilia |
|
| NICHD_Definition |
_ |
|
| prefixIRI |
Hemophilia |
|
| prefLabel |
Hemophilia |
|
| Subset_Association1 |
NICHD Pediatric Terminology |
|
| Subset_Association2 |
Neonatal Research Network Terminology |
|
| SYN | ||
| subClassOf |
http://www.owl-ontologies.com/Ontology1358660052.owl#Congenital_Coagulation_Defect |