Trait
Limited hip movement
A decreased ability to move the femur at the hip joint associated with a decreased range of motion of the hip.
Summary
- Body system
- Abnormality of the musculoskeletal system
This page as data
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Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Hereditary Multiple OsteochondromasReads 2 of these genesEXT1EXT2About this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 3 of these genesCOMPCOL2A1MATN3About this report →
- AlkaptonuriaReads 1 of these genesHGDAbout this report →
- Primary Failure of Tooth EruptionReads 1 of these genesPTH1RAbout this report →
Show 17 more reports
- Restrictive Dermopathy (ZMPSTE24)Reads 1 of these genesZMPSTE24About this report →
- TRPV4-Related Skeletal DysplasiasReads 1 of these genesTRPV4About this report →
- Otospondylomegaepiphyseal Dysplasia (OSMED)Reads 1 of these genesCOL2A1About this report →
- LipodystrophyReads 2 of these genesLMNAZMPSTE24About this report →
- Limb-Girdle Muscular DystrophyReads 3 of these genesTTNLMNADYSFAbout this report →
- Achondrogenesis panelReads 1 of these genesCOL2A1About this report →
- Distal MyopathiesReads 2 of these genesTTNDYSFAbout this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Dilated CardiomyopathyReads 2 of these genesTTNLMNAAbout this report →
- Myofibrillar MyopathiesReads 1 of these genesTTNAbout this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesTRPV4LMNAAbout this report →
- Congenital MyopathiesReads 1 of these genesTTNAbout this report →
- VitreoretinopathyReads 1 of these genesCOL2A1About this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesTRPV4LMNAAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesNIPA1About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesEXT2About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesNIPA1About this report →
Read the genes linked to Limited hip movement, and the rest of your genome, with one test.
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Get my Genome Test15 genes linked to Limited hip movement
Changes in these genes cause rare conditions in which Limited hip movement 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 |
|---|---|---|
| COMPcartilage oligomeric matrix protein | Always | In 1 condition |
| FILIP1filamin A interacting protein 1 | Always | In 1 condition |
| COL2A1collagen type II alpha 1 chain | Often (30–79%) | In 3 conditions |
| HGDhomogentisate 1,2-dioxygenase | Often (30–79%) | In 1 condition |
| NIPA1NIPA magnesium transporter 1 | Often (30–79%) | In 1 condition |
| PTH1Rparathyroid hormone 1 receptor | Often (30–79%) | In 1 condition |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Often (30–79%) | In 1 condition |
| TTNtitin | Often (30–79%) | In 1 condition |
| EXT1exostosin glycosyltransferase 1 | Sometimes (5–29%) | In 1 condition |
| EXT2exostosin glycosyltransferase 2 | Sometimes (5–29%) | In 1 condition |
| LMNAlamin A/C | Sometimes (5–29%) | In 1 condition |
| MATN3matrilin 3 | Sometimes (5–29%) | In 1 condition |
| ZMPSTE24zinc metallopeptidase STE24 | Sometimes (5–29%) | In 1 condition |
| DYSFdysferlin | Rarely (1–4%) | In 1 condition |
| GPC6glypican 6 | 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.
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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 2026.10.19-9814e911.
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