NC_012920.1(MT-ATP6):m.8764G>A AND Leigh syndrome
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 17, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000854317.1
Allele description [Variation Report for NC_012920.1(MT-ATP6):m.8764G>A]
NC_012920.1(MT-ATP6):m.8764G>A
Condition(s)
- Name:
- Leigh syndrome (NULS)
- Synonyms:
- Leigh Disease; Subacute necrotizing encephalopathy; Necrotizing encephalopathy infantile subacute of Leigh; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0009723; MedGen: C0023264; Orphanet: 506; OMIM: 256000
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Urostomy Obstruction
Urostomy ObstructionMedGen
-
Laryngeal Hemorrhage
Laryngeal HemorrhageMedGen
-
reflux
refluxMedGen
-
Rhinitis
RhinitisMedGen
-
Splenosis
SplenosisMedGen
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See more...Assertion and evidence details
Last Updated: May 19, 2024