77072-7LOINC 2.82
ATP5A1 gene full mutation analysis in Blood or Tissue by Sequencing
ATP5A1 Full Mut Anl Bld/T Seq
Component
- ATP5A1 gene full mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Find
Scale
- Doc
Method
- Sequencing
Related names
- ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1, cardiac muscle; ATP5A; ATP5AL2; ATPM; Blood; Combined oxidative phosphorylation deficiency-22; COXPD22; Document; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; hATP1; HEL-S-123m; Heredity; Heritable; high-throughput sequencing; HTS; Inherited; MC5DN4; Mitochondrial ATP synthase; Mitochondrial complex V deficiency nuclear type 4; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; MOM2; Mut; Mutations; Next generation sequencing; NGS; OMR; ORM; Point in time; Random; sequencing of entire coding region; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1, cardiac muscle
- ATP5A
- ATP5AL2
- ATPM
- Blood
- Combined oxidative phosphorylation deficiency-22
- COXPD22
- Document
- Finding
- Findings
- full gene sequencing
- Full Mut Anl
- Genetics
- hATP1
- HEL-S-123m
- Heredity
- Heritable
- high-throughput sequencing
- HTS
- Inherited
- MC5DN4
- Mitochondrial ATP synthase
- Mitochondrial complex V deficiency nuclear type 4
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- MOM2
- Mut
- Mutations
- Next generation sequencing
- NGS
- OMR
- ORM
- Point in time
- Random
- sequencing of entire coding region
- Tissue
- Tissue, unspecified
- WB
- Whole blood
1 further terms