69483-6LOINC 2.82
F9 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method
F9 gene Fam Mut Anl Bld/T
Definition
- This term is used for confirming a diagnosis of hemophilia B (factor IX deficiency) in males and identifying carrier females in families where an F9 (factor IX) mutation has been previously identified in affected individual. Mutation analysis only includes testing for the known familial mutation.
Component
- F9 gene mutation analysis limited to known familial mutations
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Find
Scale
- Doc
Method
- Molgen
Related names
- Blood; Christmas factor; Coagulation Factor 9 gene; coagulation factor IX; Coagulation Factor IX gene; Document; Fam Mut Anl; Finding; Findings; FIX; Genetics; HEMB; Heredity; Heritable; Inherited; LMTED; LTD; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutation; Mutations; Muts;
P19; PCR; Point in time; PTC; Random; THPH8; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- Blood
- Christmas factor
- Coagulation Factor 9 gene
- coagulation factor IX
- Coagulation Factor IX gene
- Document
- Fam Mut Anl
- Finding
- Findings
- FIX
- Genetics
- HEMB
- Heredity
- Heritable
- Inherited
- LMTED
- LTD
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mutation
- Mutations
- Muts
- P19
- PCR
- Point in time
- PTC
- Random
- THPH8
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue