Trait
Ketoacidosis
Acidosis resulting from accumulation of ketone bodies.
Summary
- Body system
- Laboratory abnormality
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Ketoacidosis, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test21 genes linked to Ketoacidosis
Changes in these genes cause rare conditions in which Ketoacidosis 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 |
|---|---|---|
| CYC1cytochrome c1 | Always | In 1 condition |
| DBTdihydrolipoamide branched chain transacylase E2 | Always | In 1 condition |
| DLDdihydrolipoamide dehydrogenase | Always | In 1 condition |
| MMADHCmetabolism of cobalamin associated D | Always | In 1 condition |
| MRPL3mitochondrial ribosomal protein L3 | Always | In 1 condition |
| SLC16A1solute carrier family 16 member 1 | Always | In 1 condition |
| OXCT13-oxoacid CoA-transferase 1 | Very often (80–99%) | In 1 condition |
| ACAT1acetyl-CoA acetyltransferase 1 | Often (30–79%) | In 1 condition |
| ATP5F1DATP synthase F1 subunit delta | Often (30–79%) | In 1 condition |
| ACSF3acyl-CoA synthetase family member 3 | Sometimes (5–29%) | In 2 conditions |
| EIF2AK3eukaryotic translation initiation factor 2 alpha kinase 3 | Sometimes (5–29%) | In 1 condition |
| IARS2isoleucyl-tRNA synthetase 2, mitochondrial | Sometimes (5–29%) | In 1 condition |
| SUGCTsuccinyl-CoA:glutarate-CoA transferase | Sometimes (5–29%) | In 1 condition |
| CA5Acarbonic anhydrase 5A | Not recorded | In 1 condition |
| GKglycerol kinase | Not recorded | In 1 condition |
| HNF1AHNF1 homeobox A | Not recorded | In 1 condition |
| IL6interleukin 6 | Not recorded | In 1 condition |
| IVDisovaleryl-CoA dehydrogenase | Not recorded | In 1 condition |
| KCNJ11potassium inwardly rectifying channel subfamily J member 11 | Not recorded | In 1 condition |
| MCCC2methylcrotonyl-CoA carboxylase subunit 2 | Not recorded | In 1 condition |
| PAX4paired box 4 | 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.
Narrower traits
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 2026.10.16-c6eea6bf.
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks