68467-0LOINC 2.82
APOB+LDLR+PCSK9 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
APOB+LDLR+PCSK9 gene Mut Anl Bld/T
Component
- APOB+LDLR+PCSK9 gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Blood; Convertase subtilisin/kexin type 9 preproprotein; FH3; Genetics; HCHOLA3; Heredity; Heritable; Hypercholesterolemia, autosomal dominant 3; Identity or presence; Inherited; LDLCQ1; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; NARC1; NARC-1; Neural apoptosis regulated convertase 1; Neural apoptosis-regulated convertase 1; Nominal; PC9; PCR; Point in time; Proprotein convertase PC9; Proprotein convertase subtilisin/kexin type 9; Random; Subtilisin/kexin-like protease PC9; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- APOB+LDLR+PCSK9 gene targeted mutation analysis
- Blood
- Convertase subtilisin/kexin type 9 preproprotein
- FH3
- Genetics
- HCHOLA3
- Heredity
- Heritable
- Hypercholesterolemia, autosomal dominant 3
- Identity or presence
- Inherited
- LDLCQ1
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- NARC-1
- NARC1
- Neural apoptosis regulated convertase 1
- Neural apoptosis-regulated convertase 1
- Nominal
- PC9
- PCR
- Point in time
- Proprotein convertase PC9
- Proprotein convertase subtilisin/kexin type 9
- Random
- Subtilisin/kexin-like protease PC9
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue