Hypermobility syndrome

disease
On this page

Summary

Hypermobility syndrome (MONDO:0001798) is a disease and 16 clinical trials. A subtype of arthropathy — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 16

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namehypermobility syndrome
Mondo IDMONDO:0001798
DOIDDOID:13781
ICD-10-CMM35.7
SNOMED CT85551004
UMLSC0152093
MedGen508885
Is cancer (heuristic)no

Disease family

This is a subtype of arthropathy. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by body system or component › musculoskeletal system disorderskeletal system disorderarthropathyhypermobility syndrome

Related subtypes (23): transient arthropathy, synovial plica syndrome, Tietze syndrome, neurogenic arthropathy, Behcet syndrome arthropathy, ankylosis, bursitis, synovium neoplasm, hydrarthrosis, articular cartilage disorder, hemarthrosis, tenosynovitis, ganglion or cyst of synovium/tendon/bursa, spondyloarthropathy, temporomandibular joint disorder, arthritic joint disease, de Quervain disease, frozen shoulder, patellofemoral pain syndrome, secondary hypertrophic osteoarthropathy, shoulder impingement syndrome, crystal arthropathy, vertebral joint disorder

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 16.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified14
PHASE41
PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT07020455PHASE4COMPLETEDIs the Combine Prolotherapy More Effective Than the Traditional Prolotherapy in Patients With Temporomandibular Joint Hypermobility?
NCT02869373PHASE2COMPLETEDSpinal Stabilization Exercise Effects in Hypermobility
NCT05698446Not specifiedRECRUITINGComparison of MBR + Suture Tape, MBR, and Anatomic Reconstruction for CLAI in GJL Cases: A Prospective Cohort Study
NCT05871216Not specifiedRECRUITINGFunctional Instability in Patients Suffering From Collagen Disease and Joint Hypermobility
NCT06277401Not specifiedRECRUITINGExercise in Patients With Hypermobile Joints and Knee Pain
NCT07044999Not specifiedNOT_YET_RECRUITINGEvaluation of Balance and Physical Performance Under Dual Task Conditions in Individuals With and Without Generalized Joint Hypermobility
NCT07294014Not specifiedRECRUITINGInvestigation of Medial Longitudinal Arch and Foot Function in Patients With Lipedema
NCT07438873Not specifiedNOT_YET_RECRUITINGDynamic Lycra Garments for Hip Dysplasia Feasibility Study
NCT04666896Not specifiedTERMINATEDPatient-based Care Versus Standard Care for Patients With hEDS/HSD and Multidirectional Shoulder Instability
NCT04734041Not specifiedCOMPLETEDIntegrative Medicine for Hypermobility Spectrum Disorder and Ehlers-Danlos Syndromes (IMforHSDandEDS)
NCT04934267Not specifiedUNKNOWNThe Effect of Joint Hypermobility Syndrome on Delayed Onset of Muscle Soreness and Recovery Time
NCT04972565Not specifiedCOMPLETEDDyspnea in Hypermobile Ehlers-Danlos Syndrome and Hypermobility Spectrum Disorder
NCT05685199Not specifiedTERMINATEDIdentifying the Determinants of Bleeding and Hypermobility in Patients With Heavy Menstrual Bleeding
NCT05800262Not specifiedCOMPLETEDDynamic Stability Exercises in Patients With Hypermobile Ehlers-Danlos Syndrome and Hypermobility Spectrum Disorder
NCT06325345Not specifiedUNKNOWNRCT of Gut-directed Hypnotherapy in Ehlers-Danlos Syndromes and Generalized Hypermobility Spectrum Disorders
NCT06918613Not specifiedCOMPLETEDUltrasonographic Evaluation of the Effects of Different Wrist Positions on the Median Nerve in Patients With Generalized Joint Hypermobility

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.