Preferred Name | Dysfibrinogenemia | |
Synonyms |
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Definitions |
A coagulation disorder caused by abnormalities in fibrin that result in defective clot formation. This disorder may be inherited or acquired. |
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ID |
http://purl.obolibrary.org/obo/NCIT_C131659 |
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ALT_DEFINITION |
A coagulation disorder caused by abnormalities in fibrin that result in defective clot formation. This disorder may be inherited or acquired. |
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code |
C131659 |
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Contributing_Source |
NICHD |
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definition |
A coagulation disorder caused by abnormalities in fibrin that result in defective clot formation. This disorder may be inherited or acquired. |
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in_subset | ||
label |
Dysfibrinogenemia |
|
Preferred_Name |
Dysfibrinogenemia |
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prefixIRI |
NCIT:C131659 |
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prefLabel |
Dysfibrinogenemia |
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Semantic_Type |
Disease or Syndrome |
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UMLS_CUI |
C1260903 |
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subClassOf |
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