Hemarthrosis

Summary

Hemarthrosis (MONDO:0004431) is a disease and 5 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: 5

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	hemarthrosis
Mondo ID	MONDO:0004431
EFO	EFO:1001344
MeSH	D006395
DOID	DOID:801
ICD-10-CM	M25.0
SNOMED CT	81808003
UMLS	C0018924
MedGen	5479
Anatomy (UBERON)	UBERON:0002101
Is cancer (heuristic)	no

Also known as: haemarthrosis of shoulder joint · haemarthrosis of the ankle and foot · haemarthrosis of the pelvic region and thigh · hemarthrosis involving ankle and foot · hemarthrosis involving forearm · hemarthrosis involving hand · hemarthrosis involving lower leg · hemarthrosis involving pelvic region and thigh · hemarthrosis involving shoulder region · hemarthrosis involving upper arm · hemarthrosis of forearm · hemarthrosis of hand · hemarthrosis of lower leg · hemarthrosis of shoulder · hemarthrosis of the ankle and foot · hemarthrosis of the forearm · hemarthrosis of the hand · hemarthrosis of the lower leg · hemarthrosis of the pelvic region and thigh · hemarthrosis of the upper arm (+1 more)

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 disorder › skeletal system disorder › arthropathy › hemarthrosis

Related subtypes (23): transient arthropathy, synovial plica syndrome, hypermobility syndrome, Tietze syndrome, neurogenic arthropathy, Behcet syndrome arthropathy, ankylosis, bursitis, synovium neoplasm, hydrarthrosis, articular cartilage disorder, 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: 5.

Phase distribution (across all retrieved trials)

Phase	Trials
Not specified	3
PHASE4	2

Top trials by phase / activity

NCT	Phase	Status	Title
NCT07332910	PHASE4	NOT_YET_RECRUITING	Study the Anti-inflammatory Effect of Tranexamic Acid When Used in Anterior Cruciate Ligament Reconstruction.
NCT01748201	PHASE4	COMPLETED	Viscosupplementation in Patients With Hemophilic Arthropathy
NCT05629130	Not specified	RECRUITING	Embolization in Hereditary Coagulopathies
NCT05687331	Not specified	UNKNOWN	Changes in the Immunomodulatory Properties of Adipose Stromal Cells Due to Hemarthrosis After Knee Injury
NCT06543368	Not specified	COMPLETED	Low-Cost Platelet-Rich Plasma for Hemarthropathy