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mitochondrial DNA depletion syndrome 5
Summary
- Synonym
-
- succinate-CoA ligase deficiency
- Definition
- A mitochondrial DNA depletion syndrome that is characterized by infantile onset of hypotonia, progressive neurologic deterioration, a hyperkinetic-dystonic movement disorder, external ophthalmoplegia, deafness, and variable renal tubular dysfunction, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the beta subunit of the succinate-CoA ligase gene on chromosome 13q14.
- Super Class
- autosomal recessive disease mitochondrial DNA depletion syndrome
External Links
- Disease Ontology
- DOID:0080124
- Mondo Disease Ontology
- MeSH
- OMIM
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P19971 | Thymidine phosphorylase | |
| P53597 | Succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial | |
| Q9P2R7 | Succinate--CoA ligase [ADP-forming] subunit beta, mitochondrial |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001257 | Spasticity |
| HP:0001270 | Motor delay |
| HP:0001332 | Dystonia |
| HP:0001349 | Facial diplegia |
| HP:0001508 | Failure to thrive |
| HP:0001518 | Small for gestational age |
| HP:0001935 | Microcytic anemia |
| HP:0002020 | Gastroesophageal reflux |
| HP:0002059 | Cerebral atrophy |
| HP:0002134 | Abnormal basal ganglia morphology |
