35297-1LOINC 2.82
LMNA gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
LMNA gene Mut Anl Bld/T
Component
- LMNA gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Blood; CDCD1; CDDC; Charcot-Marie-Tooth disease, axonal, type 2B1; CMD1A; CMT2B1; EMD2; FPL; FPLD; FPLD2; Genetics; Heredity; Heritable; HGPS; IDC; Identity or presence; Inherited; lamin A/C; LDP1; LFP; LGMD1B; LMN1; LMNC; LMNL1; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; PCR; Point in time; PRO1; Progeria 1 (Hutchinson-Gilford type); Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- Blood
- CDCD1
- CDDC
- Charcot-Marie-Tooth disease, axonal, type 2B1
- CMD1A
- CMT2B1
- EMD2
- FPL
- FPLD
- FPLD2
- Genetics
- Heredity
- Heritable
- HGPS
- IDC
- Identity or presence
- Inherited
- lamin A/C
- LDP1
- LFP
- LGMD1B
- LMN1
- LMNA gene targeted mutation analysis
- LMNC
- LMNL1
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- Nominal
- PCR
- Point in time
- PRO1
- Progeria 1 (Hutchinson-Gilford type)
- Random
- Tissue
- Tissue, unspecified
3 further terms