Congenital genu recurvatum
diseaseOn this page
Also known as genu recurvatumhyperextension deformity of kneehyperextension of knee deformity
Summary
Congenital genu recurvatum (MONDO:0017560) is a disease and 3 clinical trials. A subtype of congenital knee dislocation — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Clinical trials: 3
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | congenital genu recurvatum |
| Mondo ID | MONDO:0017560 |
| Orphanet | 295229 |
| ICD-11 | 1709221347 |
| NCIT | C103184 |
| SNOMED CT | 205063003 |
| UMLS | C0152235 |
| MedGen | 508941 |
| GARD | 0021225 |
| Is cancer (heuristic) | no |
Also known as: genu recurvatum · hyperextension deformity of knee · hyperextension of knee deformity
Disease family
This is a subtype of congenital knee dislocation. 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 developmental or physiological process › disorder of development or morphogenesis › congenital knee dislocation › congenital genu recurvatum
Related subtypes (1): congenital genu flexum
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: 3.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 3 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT06647082 | Not specified | NOT_YET_RECRUITING | Engaging Kids With Robotic Exoskeletons and Gamification |
| NCT07008521 | Not specified | ACTIVE_NOT_RECRUITING | UNIVERSAL EXERCISE UNIT and REBOUND THERAPY ON GENU RECURVATUM Cerebral Palsy Childeren |
| NCT02854189 | Not specified | COMPLETED | The Results of Oxford Unicompartmental Knee Arthroplasty in Patients With and Without Preoperative Genu Recurvatum |
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.