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loading...| Preferred Name |
Factor_V_Leiden_Mutation |
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| Synonyms |
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| ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Factor_V_Leiden_Mutation |
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| ID |
C91334 |
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| NCI_Definition |
Human F5 Leiden allele is a variant form of the F5 gene that is located in the vicinity of 1q23 and is approximately 75 kb in length. This allele, which encodes coagulation factor V Leiden protein, is involved in hypercoagulability due to resistance to degradation by activated protein C. |
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| NCI_PT |
F5 Leiden Allele |
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| NICHD_Definition |
_ |
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| prefixIRI |
Factor_V_Leiden_Mutation |
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| prefLabel |
Factor_V_Leiden_Mutation |
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| Subset_Association1 |
NICHD Pediatric Terminology |
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| Subset_Association2 |
Neonatal Research Network Terminology |
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| SYN | ||
| subClassOf |
http://www.owl-ontologies.com/Ontology1358660052.owl#Congenital_Coagulation_Defect |
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