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Trait
Hip osteoarthritis
Summary
- Also called
- Osteoarthritis of hip
- Body system
- Abnormality of the musculoskeletal system
Hip osteoarthritisHP:0008843
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Read the genes linked to Hip osteoarthritis, and the rest of your genome, with one test.
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Get my Genome Test20 genes linked to Hip osteoarthritis
Changes in these genes cause rare conditions in which Hip osteoarthritis 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 |
|---|---|---|
| COL2A1collagen type II alpha 1 chain | Always | In 3 conditions |
| MAN2B2mannosidase alpha class 2B member 2 | Always | In 1 condition |
| PFN1profilin 1 | Always | In 1 condition |
| GDF5growth differentiation factor 5 | Often (30–79%) | In 1 condition |
| SMAD2SMAD family member 2 | Often (30–79%) | In 1 condition |
| TRAPPC2trafficking protein particle complex subunit 2 | Often (30–79%) | In 2 conditions |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Often (30–79%) | In 1 condition |
| ANKRD55ankyrin repeat domain 55 | Sometimes (5–29%) | In 1 condition |
| CD247CD247 molecule | Sometimes (5–29%) | In 1 condition |
| IL2RAinterleukin 2 receptor subunit alpha | Sometimes (5–29%) | In 1 condition |
| IL2RBinterleukin 2 receptor subunit beta | Sometimes (5–29%) | In 1 condition |
| PTPN2protein tyrosine phosphatase non-receptor type 2 | Sometimes (5–29%) | In 1 condition |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Sometimes (5–29%) | In 1 condition |
| SMAD3SMAD family member 3 | Sometimes (5–29%) | In 1 condition |
| STAT4signal transducer and activator of transcription 4 | Sometimes (5–29%) | In 1 condition |
| ACANaggrecan | Not recorded | In 1 condition |
| CLCN7Cl-/H+ antiporter 7 | Not recorded | In 1 condition |
| COMPcartilage oligomeric matrix protein | Not recorded | In 1 condition |
| FRZBfrizzled related protein | Not recorded | In 1 condition |
| HLA-Bmajor histocompatibility complex, class I, B | 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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