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loading...| Preferred Name |
Factor I Deficiency |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C26692 |
| ALT_DEFINITION |
A coagulation disorder characterized by the partial or complete absence of fibrinogen (factor I) activity in the blood. |
| code |
C26692 |
| Concept_In_Subset |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C189762 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C118464 |
| Contributing_Source |
MedDRA NICHD |
| DEFINITION |
A usually inherited blood coagulation disorder characterized by the partial or complete absence of fibrinogen in the blood, resulting in bleeding. |
| FULL_SYN |
Hypofibrinogenemia Fibrinogen Deficiency Factor I Deficiency |
| label |
Factor I Deficiency |
| Legacy Concept Name |
Factor_I_Deficiency |
| Maps_To |
Hypofibrinogenemia |
| NCI_META_CUI |
CL480897 |
| Preferred_Name |
Factor I Deficiency |
| prefixIRI |
Thesaurus:C26692 |
| prefLabel |
Factor I Deficiency |
| Semantic_Type |
Disease or Syndrome |
| subClassOf |
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