combined oxidative phosphorylation deficiency 57
MONDO:0859337Mondo
Findings
No curated finding names combined oxidative phosphorylation deficiency 57 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 infancy · Infantile onset · Neonatal onset · Neonatal death · Third trimester onset
HPO, annotations 2026-09-02
Features
31 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.
- Decreased activity of mitochondrial complex IHPOHP:0011923
- 1 of 1 reported patient
- Decreased activity of mitochondrial complex IIIHPOHP:0011924
- 1 of 1 reported patient
- Decreased activity of mitochondrial complex IVHPOHP:0008347
- 1 of 1 reported patient
- Developmental regressionHPOHP:0002376
- 1 of 1 reported patient
- Global developmental delayHPOHP:0001263
- 1 of 1 reported patient
- Bull's eye maculopathyHPOHP:0011504
- 3 of 4 reported patients
- HypotoniaHPOHP:0001252
- 3 of 4 reported patients
- Cerebral atrophyHPOHP:0002059
- 2 of 4 reported patients
- DystoniaHPOHP:0001332
- 2 of 4 reported patients
- MyoclonusHPOHP:0001336
- 2 of 4 reported patients
- ApneaHPOHP:0002104
- 1 of 4 reported patients
- Cardiac arrestHPOHP:0001695
- 1 of 4 reported patients
Show the remaining 19
- Central diabetes insipidusHPOHP:0000863
- 1 of 4 reported patients
- Central hypoventilationHPOHP:0007110
- 1 of 4 reported patients
- Diabetes insipidusHPOHP:0000873
- 1 of 4 reported patients
- Epileptic encephalopathyHPOHP:0200134
- 1 of 4 reported patients
- Feeding difficultiesHPOHP:0011968
- 1 of 4 reported patients
- Fetal pleural effusionHPOHP:0025676
- 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.
- CRLS1HGNC:16148
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2023
- Limited · Ambry Genetics · Autosomal recessive · 2023
- Limited · G2P · Autosomal recessive · 2025