multiple epiphyseal dysplasia
MONDO:0016648Mondo
Findings
No curated finding names multiple epiphyseal dysplasia yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Multiple epiphyseal dysplasias (MED/EDMs) are characterized by epiphyseal anomalies causing joint pain early in life, recurrent osteochondritis and early arthrosis. The EDMs are a heterogeneous group of diseases with variable expression classed as MED/EDMs 1-6.
Definition from the Mondo Disease Ontology (MONDO:0016648), read 2026-09-29. CC BY 4.0.
Features
1 feature
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, hp/releases/2026-09-01.
- ArthralgiaMondoHP:0002829
Where it sits
- A kind of
- Narrower terms (10)
- epiphyseal dysplasia, multiple, 7
- multiple epiphyseal dysplasia due to collagen 9 anomaly
- multiple epiphyseal dysplasia type 1
- multiple epiphyseal dysplasia type 4
- multiple epiphyseal dysplasia type 5
- multiple epiphyseal dysplasia, Al-Gazali type
- multiple epiphyseal dysplasia, Beighton type
- multiple epiphyseal dysplasia, Lowry type
- multiple epiphyseal dysplasia, with miniepiphyses
- multiple epiphyseal dysplasia, with severe proximal femoral dysplasia
Other names
5 names
Resolves to: multiple epiphyseal dysplasia
- Also called
- Dominant Multiple Epiphyseal DysplasiaEDMMEDmultiple epiphyseal dysplasia (disease)Polyepiphyseal dysplasia