mitochondrial complex 5 (ATP synthase) deficiency, nuclear type 6
MONDO:0032869Mondo
Findings
No curated finding names mitochondrial complex 5 (ATP synthase) deficiency, nuclear type 6 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Death in childhood
HPO, annotations 2026-09-02
Features
8 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Developmental regressionHPOHP:0002376
- 4 of 4 reported patients
- AtaxiaHPOHP:0001251
- 3 of 4 reported patients
- ChoreaHPOHP:0002072
- 2 of 4 reported patients
- LethargyHPOHP:0001254
- 2 of 4 reported patients
- OphthalmoplegiaHPOHP:0000602
- 2 of 4 reported patients
- BradykinesiaHPOHP:0002067
- 1 of 4 reported patients
- HyperreflexiaHPOHP:0001347
- 1 of 4 reported patients
- Hypertrophic cardiomyopathyHPOHP:0001639
- 1 of 4 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- ATP5MKHGNC:30889
- Moderate · PanelApp Australia · Autosomal recessive · 2025