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loading...| Preferred Name |
Factor I Deficiency |
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| Synonyms |
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| Definitions |
A usually inherited blood coagulation disorder characterized by the partial or complete absence of fibrinogen in the blood, resulting in bleeding. |
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| ID |
http://purl.obolibrary.org/obo/NCIT_C26692 |
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| ALT_DEFINITION |
A coagulation disorder characterized by the partial or complete absence of fibrinogen (factor I) activity in the blood. |
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| code |
C26692 |
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| Contributing_Source |
MedDRA NICHD |
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| definition |
A usually inherited blood coagulation disorder characterized by the partial or complete absence of fibrinogen in the blood, resulting in bleeding. |
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| in_subset |
http://purl.obolibrary.org/obo/NCIT_C90259 |
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| label |
Factor I Deficiency |
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| Legacy Concept Name |
Factor_I_Deficiency |
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| Maps_To |
Hypofibrinogenemia |
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| NCI_META_CUI |
CL480897 |
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| Preferred_Name |
Factor I Deficiency |
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| prefixIRI |
NCIT:C26692 |
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| prefLabel |
Factor I Deficiency |
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| Semantic_Type |
Disease or Syndrome |
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| subClassOf |
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