Transient arthropathy
diseaseOn this page
Also known as transient arthropathy involving forearmtransient arthropathy involving handtransient arthropathy involving lower legtransient arthropathy involving multiple sitestransient arthropathy involving pelvic region and thightransient arthropathy involving shoulder regiontransient arthropathy involving upper arm
Summary
Transient arthropathy (MONDO:0001429) is a disease. A subtype of arthropathy — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | transient arthropathy |
| Mondo ID | MONDO:0001429 |
| DOID | DOID:12084 |
| ICD-11 | 404860910 |
| NCIT | C35761 |
| SNOMED CT | 66191007 |
| UMLS | C0152083 |
| MedGen | 101813 |
| Is cancer (heuristic) | no |
Also known as: transient arthropathy involving forearm · transient arthropathy involving hand · transient arthropathy involving lower leg · transient arthropathy involving multiple sites · transient arthropathy involving pelvic region and thigh · transient arthropathy involving shoulder region · transient arthropathy involving upper arm
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 › transient arthropathy
Related subtypes (23): synovial plica syndrome, hypermobility 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
Subtypes (1): transient arthritis
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: 0.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.