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mitochondrial DNA depletion syndrome 9
Summary
- Synonym
-
- fatal infantile lactic acidosis
- Definition
- A mitochondrial DNA depletion syndrome that is characterized by infantile onset of hypotonia, lactic acidosis, severe psychomotor retardation, progressive neurologic deterioration, and excretion of methylmalonic acid, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the alpha subunit of the succinate-CoA ligase gene on chromosome 2p11.
- Super Class
- autosomal recessive disease mitochondrial DNA depletion syndrome
External Links
- Disease Ontology
- DOID:0080128
- Mondo Disease Ontology
- MeSH
- ORDO
- OMIM
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002093 | Respiratory insufficiency |
| HP:0001252 | Hypotonia |
| HP:0002643 | Neonatal respiratory distress |
| HP:0001522 | Death in infancy |
| HP:0000365 | Hearing impairment |
| HP:0001270 | Motor delay |
| HP:0002421 | Poor head control |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0001284 | Areflexia |
| HP:0001511 | Intrauterine growth retardation |
