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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:0002151 | Increased circulating lactate concentration |
| HP:0002197 | Generalized-onset seizure |
| HP:0002283 | Global brain atrophy |
| HP:0002305 | Athetosis |
| HP:0002448 | Progressive encephalopathy |
| HP:0002487 | Hyperkinetic movements |
| HP:0002490 | Increased CSF lactate |
| HP:0002540 | Inability to walk |
| HP:0002747 | Respiratory insufficiency due to muscle weakness |
| HP:0002912 | Methylmalonic acidemia |
