21667-1LOINC 2.82
F5 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
F5 gene Mut Anl Bld/T
Component
- F5 gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Activated protein C cofactor; APC; Blood; Coagulation Factor V - Leiden gene; coagulation factor V (proaccelerin, labile factor); FVL; Genetics; Heredity; Heritable; Identity or presence; Inherited; Labile factor; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; PCCF; PCR; Point in time; Proaccelerin gene; Random; RPRGL1; THPH2; Thrombophilia; Tissue; Tissue, unspecified; UniversalLabOrders; WB; Whole blood; Whole blood or Tissue
Index terms
- Activated protein C cofactor
- APC
- Blood
- coagulation factor V (proaccelerin, labile factor)
- Coagulation Factor V - Leiden gene
- F5 gene targeted mutation analysis
- FVL
- Genetics
- Heredity
- Heritable
- Identity or presence
- Inherited
- Labile factor
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- Nominal
- PCCF
- PCR
- Point in time
- Proaccelerin gene
- Random
- RPRGL1
- THPH2
- Thrombophilia
- Tissue
- Tissue, unspecified
- UniversalLabOrders
- WB
- Whole blood
- Whole blood or Tissue