40341-0LOINC 2.82
MT-ATP6 gene m.8993T>G [Presence] in Blood or Tissue by Molecular genetics method
MT-ATP6 m.8993T>G Bld/T Ql
Component
- MT-ATP6 gene.m.8993T>G
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- PrThr
Scale
- Ord
Method
- Molgen
Related names
- ATP synthase 6; ATP synthase A chain; ATP6; ATPASE 6; Blood; Genetics; Heredity; Heritable; Inherited; L156R; Leigh syndrome; Leu156Pro; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; MTATP6; MT-ATP6 m.8993T>G; NARP syndrome; Neurogenic muscle weakness, ataxia and retinitis pigmentosa; Ordinal; PCR; Point in time; PR; QL; Qual; Qualitative; Random; Screen; T8993G; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- ATP synthase 6
- ATP synthase A chain
- ATP6
- ATPASE 6
- Blood
- G
- Genetics
- Heredity
- Heritable
- Inherited
- L156R
- Leigh syndrome
- Leu156Pro
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- MT-ATP6 gene.m.8993T>G
- MT-ATP6 m.8993T>
- MTATP6
- NARP syndrome
- Neurogenic muscle weakness, ataxia and retinitis pigmentosa
- Ordinal
- PCR
- Point in time
- PR
- QL
- Qual
- Qualitative
- Random
- Screen
- T8993G
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue