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Biological and Environmental Research Ontology
Last uploaded:
December 23, 2022
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| Preferred Name | Hemophilia A | |
| Synonyms |
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| Definitions |
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. |
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| ID |
http://purl.obolibrary.org/obo/NCIT_C27146 |
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| ALT_DEFINITION |
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.
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| code |
C27146
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| Contributing_Source |
Cellosaurus CTRP NICHD
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|
| definition |
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.
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| Display_Name |
Hemophilia A
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| in_subset |
http://purl.obolibrary.org/obo/NCIT_C90259 http://purl.obolibrary.org/obo/NCIT_C116977 http://purl.obolibrary.org/obo/NCIT_C132009 http://purl.obolibrary.org/obo/NCIT_C165258 |
|
| label |
Hemophilia A
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| Legacy Concept Name |
Hemophilia_A
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| Preferred_Name |
Hemophilia A
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| prefixIRI |
NCIT:C27146
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| prefLabel |
Hemophilia A
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| Semantic_Type |
Disease or Syndrome
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| UMLS_CUI |
C0019069
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| subClassOf |
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