Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Dysostosis multiplex, and the rest of your genome, with one test.
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Get my Genome Test22 genes linked to Dysostosis multiplex
Changes in these genes cause rare conditions in which Dysostosis multiplex 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 |
|---|---|---|
| FUCA1alpha-L-fucosidase 1 | Always | In 2 conditions |
| GALNSgalactosamine (N-acetyl)-6-sulfatase | Always | In 1 condition |
| GLB1galactosidase beta 1 | Always | In 4 conditions |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Always | In 2 conditions |
| IDUAalpha-L-iduronidase | Always | In 3 conditions |
| NAGLUN-acetyl-alpha-glucosaminidase | Always | In 1 condition |
| VPS33AVPS33A core subunit of CORVET and HOPS complexes | Always | In 2 conditions |
| GNEglucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | Very often (80–99%) | In 1 condition |
| GUSBglucuronidase beta | Very often (80–99%) | In 1 condition |
| MAN2B1mannosidase alpha class 2B member 1 | Very often (80–99%) | In 2 conditions |
| NEU1neuraminidase 1 | Very often (80–99%) | In 4 conditions |
| IDSiduronate 2-sulfatase | Often (30–79%) | In 1 condition |
| FGFR1fibroblast growth factor receptor 1 | Sometimes (5–29%) | In 1 condition |
| KRASKRas proto-oncogene, GTPase | Sometimes (5–29%) | In 1 condition |
| AGAaspartylglucosaminidase | Not recorded | In 1 condition |
| ARSBarylsulfatase B | Not recorded | In 1 condition |
| CTSAcathepsin A | Not recorded | In 1 condition |
| GNPTGN-acetylglucosamine-1-phosphate transferase subunit gamma | Not recorded | In 1 condition |
| GNSglucosamine (N-acetyl)-6-sulfatase | Not recorded | In 1 condition |
| HGSNATheparan-alpha-glucosaminide N-acetyltransferase | Not recorded | In 1 condition |
| SGSHN-sulfoglucosamine sulfohydrolase | Not recorded | In 1 condition |
| SUMF1sulfatase modifying factor 1 | 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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