42785-6LOINC 2.82
FGFR1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
FGFR1 gene Mut Anl Bld/T
Component
- FGFR1 gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Basic fibroblast growth factor receptor 1 precursor; BFGFR; bFGF-R-1; Blood; CD331; CEK; C-FGR; FGFBR; FGFR-1; fibroblast growth factor receptor 1; fibroblast growth factor receptor 1 (fms-related tyrosine kinase 2, Pfeiffer syndrome); FLG; FLT2; FLT-2; Genetics; H2; H3; H4; H5; HBGFR; Heredity; Heritable; HH2; HRTFDS; Identity or presence; Inherited; KAL2; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; N-SAM; OGD; PCR; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- Basic fibroblast growth factor receptor 1 precursor
- bFGF-R-1
- BFGFR
- Blood
- C-FGR
- CD331
- CEK
- FGFBR
- FGFR-1
- FGFR1 gene targeted mutation analysis
- fibroblast growth factor receptor 1
- fibroblast growth factor receptor 1 (fms-related tyrosine kinase 2, Pfeiffer syndrome)
- FLG
- FLT-2
- FLT2
- Genetics
- H2
- H3
- H4
- H5
- HBGFR
- Heredity
- Heritable
- HH2
- HRTFDS
- Identity or presence
- Inherited
- KAL2
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- N-SAM
- Nominal
- OGD
- PCR
- Point in time
6 further terms