Trait
Neonatal asphyxia
Respiratory failure in the newborn.
Summary
- Also called
- Asphyxia neonatorum
- Body system
- Abnormality of the respiratory system
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Neonatal asphyxia, and the rest of your genome, with one test.
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Get my Genome Test14 genes linked to Neonatal asphyxia
Changes in these genes cause rare conditions in which Neonatal asphyxia 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 |
|---|---|---|
| COG7component of oligomeric golgi complex 7 | Always | In 1 condition |
| SHPKsedoheptulokinase | Always | In 1 condition |
| SLC27A4solute carrier family 27 member 4 | Always | In 1 condition |
| YWHAZtyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta | Always | In 1 condition |
| ALDH7A1aldehyde dehydrogenase 7 family member A1 | Sometimes (5–29%) | In 1 condition |
| BIN1bridging integrator 1 | Sometimes (5–29%) | In 1 condition |
| DNM2dynamin 2 | Sometimes (5–29%) | In 1 condition |
| HSD3B2hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 | Sometimes (5–29%) | In 1 condition |
| MTMR14myotubularin related protein 14 | Sometimes (5–29%) | In 1 condition |
| MYF6myogenic factor 6 | Sometimes (5–29%) | In 1 condition |
| PLPBPpyridoxal phosphate binding protein | Sometimes (5–29%) | In 1 condition |
| RNF168ring finger protein 168 | Sometimes (5–29%) | In 1 condition |
| RYR1ryanodine receptor 1 | Sometimes (5–29%) | In 1 condition |
| GALK1galactokinase 1 | Rarely (1–4%) | 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 2026.10.16-c6eea6bf.
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