Catalog
Multiple epiphyseal dysplasias
Link to WHO Definition
Multiple epiphyseal dysplasias – http://id.who.int/icd/entity/2009123831
Multiple epiphyseal dysplasias (MED/EDMs) are characterised 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.
Parents
Children
- Multiple epiphyseal dysplasia, Beighton type
- Multiple epiphyseal dysplasia, Al-Gazali type
- Multiple epiphyseal dysplasia with severe proximal femoral dysplasia
- Multiple epiphyseal dysplasia type 4
- Multiple epiphyseal dysplasia with miniepiphyses
- Wolcott-Rallison syndrome
- Multiple epiphyseal dysplasia type 1
- Multiple epiphyseal dysplasia type 5
- Multiple epiphyseal dysplasia due to collagen 9 anomaly