mitochondrial complex IV deficiency, nuclear type 20
MONDO:0033655Mondo
Findings
No curated finding names mitochondrial complex IV deficiency, nuclear type 20 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 · Congenital onset · Infantile onset · Death in childhood
HPO, annotations 2026-09-02
Features
17 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.
- Elevated circulating hepatic transaminase concentrationHPOHP:0002910
- 2 of 2 reported patients
- Increased circulating lactate concentrationHPOHP:0002151
- 2 of 2 reported patients
- Pulmonary arterial hypertensionHPOHP:0002092
- 2 of 2 reported patients
- Deeply set eyeHPOHP:0000490
- 1 of 2 reported patients
- Frontal bossingHPOHP:0002007
- 1 of 2 reported patients
- HyperalaninemiaHPOHP:0003348
- 1 of 2 reported patients
- HyperprolinemiaHPOHP:0008358
- 1 of 2 reported patients
- LethargyHPOHP:0001254
- 1 of 2 reported patients
- Long eyelashesHPOHP:0000527
- 1 of 2 reported patients
- SynophrysHPOHP:0000664
- 1 of 2 reported patients
- Wide anterior fontanelHPOHP:0000260
- 1 of 2 reported patients
- Brisk reflexesHPOHP:0001348
Show the remaining 5
- CardiomegalyHPOHP:0001640
- Decreased activity of mitochondrial complex IVHPOHP:0008347
- Failure to thrive in infancyHPOHP:0001531
- HepatomegalyHPOHP:0002240
- HypotoniaHPOHP:0001252
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.
- COX5AHGNC:2267
- Limited · Ambry Genetics · Autosomal recessive · 2022
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2022
Where it sits
Other names
1 name
Resolves to: mitochondrial complex IV deficiency, nuclear type 20
- Also called
- MC4DN20