Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Hypophosphatemic rickets, and the rest of your genome, with one test.
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Get my Genome Test25 genes linked to Hypophosphatemic rickets
Changes in these genes cause rare conditions in which Hypophosphatemic rickets 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 |
|---|---|---|
| DMP1dentin matrix acidic phosphoprotein 1 | Always | In 2 conditions |
| ENPP1ectonucleotide pyrophosphatase/phosphodiesterase 1 | Always | In 4 conditions |
| NDUFAF6NADH:ubiquinone oxidoreductase complex assembly factor 6 | Always | In 2 conditions |
| PHEXphosphate regulating endopeptidase X-linked | Always | In 1 condition |
| SLC34A3solute carrier family 34 member 3 | Always | In 2 conditions |
| SLC34A1solute carrier family 34 member 1 | Very often (80–99%) | In 2 conditions |
| ABCC6ATP binding cassette subfamily C member 6 | Often (30–79%) | In 3 conditions |
| CTNScystinosin, lysosomal cystine transporter | Often (30–79%) | In 1 condition |
| EHHADHenoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase | Often (30–79%) | In 1 condition |
| GATMglycine amidinotransferase | Often (30–79%) | In 1 condition |
| HNF4Ahepatocyte nuclear factor 4 alpha | Often (30–79%) | In 1 condition |
| HRASHRas proto-oncogene, GTPase | Sometimes (5–29%) | In 2 conditions |
| POLRMTRNA polymerase mitochondrial | Sometimes (5–29%) | In 1 condition |
| ALKALK receptor tyrosine kinase | Rarely (1–4%) | In 1 condition |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Rarely (1–4%) | In 1 condition |
| NAB2NGFI-A binding protein 2 | Rarely (1–4%) | In 1 condition |
| NRASNRAS proto-oncogene, GTPase | Rarely (1–4%) | In 2 conditions |
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Rarely (1–4%) | In 1 condition |
| SOX5SRY-box transcription factor 5 | Rarely (1–4%) | In 1 condition |
| STAT6signal transducer and activator of transcription 6 | Rarely (1–4%) | In 1 condition |
| ZEB2zinc finger E-box binding homeobox 2 | Rarely (1–4%) | In 1 condition |
| CLCN5Cl-/H+ antiporter 5 | Not recorded | In 1 condition |
| FAHfumarylacetoacetate hydrolase | Not recorded | In 1 condition |
| FGF23fibroblast growth factor 23 | Not recorded | In 1 condition |
| KRASKRas proto-oncogene, GTPase | 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 2026.10.16-c6eea6bf.
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