Trait
Severe lactic acidosis
A severe form of lactic acidemia.
Summary
- Body system
- Laboratory abnormality
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page$trait$nameRead the genes linked to Severe lactic acidosis, and the rest of your genome, with one test.
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Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Björnstad SyndromeReads 1 of these genesBCS1LAbout this report →
- Primary Mitochondrial DiseaseReads 9 of these genesCOX16NDUFS4SLC25A4TSFMBCS1LLRPPRCAbout this report →
- Leigh SyndromeReads 6 of these genesNDUFS4TSFMTRMULRPPRCNDUFS2PDHA1About this report →
- Fontaine Progeroid SyndromeReads 1 of these genesSLC25A4About this report →
Show 3 more reports
- Rare Hereditary Peripheral NeuropathiesReads 7 of these genesNDUFS4TSFMTRMULRPPRCNDUFS2RRM2BAbout this report →
- Syndromic and Metabolic CardiomyopathiesReads 1 of these genesSLC25A4About this report →
- Pyruvate Dehydrogenase & Pyruvate Carboxylase DeficiencyReads 1 of these genesPDHA1About this report →
Read the genes linked to Severe lactic acidosis, and the rest of your genome, with one test.
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Get my Genome Test14 genes linked to Severe lactic acidosis
Changes in these genes cause rare conditions in which Severe lactic acidosis is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| COX16cytochrome c oxidase assembly factor COX16 | Always | In 1 condition |
| NDUFS4NADH:ubiquinone oxidoreductase subunit S4 | Always | In 1 condition |
| SLC25A4solute carrier family 25 member 4 | Always | In 1 condition |
| TSFMTs translation elongation factor, mitochondrial | Always | In 1 condition |
| UQCC3ubiquinol-cytochrome c reductase complex assembly factor 3 | Always | In 1 condition |
| BCS1LBCS1 ubiquinol-cytochrome c reductase complex chaperone | Often (30–79%) | In 1 condition |
| MT-TEmitochondrially encoded tRNA-Glu (GAA/G) | Often (30–79%) | In 1 condition |
| MT-TTmitochondrially encoded tRNA-Thr (ACN) | Often (30–79%) | In 1 condition |
| TRMUtRNA mitochondrial 2-thiouridylase | Often (30–79%) | In 1 condition |
| LRPPRCleucine rich pentatricopeptide repeat containing | Sometimes (5–29%) | In 1 condition |
| NDUFS2NADH:ubiquinone oxidoreductase core subunit S2 | Sometimes (5–29%) | In 1 condition |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Sometimes (5–29%) | In 1 condition |
| PDHA1pyruvate dehydrogenase E1 subunit alpha 1 | Not recorded | In 1 condition |
| SLC25A26solute carrier family 25 member 26 | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.19-9814e911.
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