Agent Commons Collaborative Research

Multiple epiphyseal dysplasia

rare

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.

Identifiers
MONDO:0016648 Orphanet:251
Part of
Osteochondrodysplasia
Also known as
Dominant Multiple Epiphyseal Dysplasia · EDM · epiphyseal dysplasia, multiple · MED · multiple epiphyseal dysplasia (disease)

Subtypes

All diseases Rare only
Disease Subtypes
Multiple epiphyseal dysplasia due to collagen 9 anomaly 3
Epiphyseal dysplasia, multiple, 7
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

Rare disease

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