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epiphysiolysis of the hip (SCFE) - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

epiphysiolysis of the hip

MONDO:0018382

Also known as:SCFESUFEepiphysiolysis capitis femoris

Overview

Epiphysiolysis of the hip is a rare osteonecrosis disorder characterized by unilateral or bilateral disruption of the capital femoral physis with varying degrees of posterior epiphysis translation and simultaneous anterior metaphysis displacement. Patients typically present in pre-adolescence/adolescence with pain of variable intensity in varying locations (hip, groin, thigh, knee).

GeneticsAutosomal dominant

Clinical Presentation

Features include: Proximal femoral epiphysiolysis and Hip osteoarthritis.

Organ System	Phenotype Count	Example Features
Bones and joints	2	Proximal femoral epiphysiolysis, Hip osteoarthritis

Explore clinical features

Diagnosis

Biomarker and diagnostic research for epiphysiolysis of the hip has been reported in the published literature.

Prognosis

Estimated prevalence: Unknown (Unknown prevalence).

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for epiphysiolysis of the hip.

14 publications have been identified in PubMed for epiphysiolysis of the hip. Research spans Review / Meta-Analysis (36%), Case Report / Case Series (21%), and Clinical Trial Publication (21%).

Research Type	Count	% of Total
Research summaries	5	36%

Data assembled from 5 of 12 sources · Last updated Sep 20, 2026, 6:52 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

OMIM

Online Mendelian Inheritance in Man

OMIM:182260

Orphanet

European rare disease database

Orphanet:399329

GARD

Genetic and Rare Diseases Info Center

GARD:21666

Questions for Your Care Team

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epiphysiolysis of the hip

Overview

Clinical Presentation

Explore clinical features

Diagnosis

Prognosis

Research Landscape

Medical References

External Resources

OMIM

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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