77073-5LOINC 2.82
ATP5A1 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method
ATP5A1 Fam Mut Anl Bld/T
Component
- ATP5A1 gene mutation analysis limited to known familial mutations
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Find
Scale
- Doc
Method
- Molgen
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; Fam Mut Anl; Finding; Findings; Genetics; hATP1; HEL-S-123m; Heredity; Heritable; Inherited; LMTED; LTD; MC5DN4; Mitochondrial ATP synthase; Mitochondrial complex V deficiency nuclear type 4; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; MOM2; Mut; Mutation; Mutations; Muts; OMR; ORM; PCR; Point in time; Random; 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
- Fam Mut Anl
- Finding
- Findings
- Genetics
- hATP1
- HEL-S-123m
- Heredity
- Heritable
- Inherited
- LMTED
- LTD
- MC5DN4
- Mitochondrial ATP synthase
- Mitochondrial complex V deficiency nuclear type 4
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- MOM2
- Mut
- Mutation
- Mutations
- Muts
- OMR
- ORM
- PCR
- Point in time
- Random
- Tissue
- Tissue, unspecified
- WB
- Whole blood
1 further terms