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LD24.61 Multiple epiphyseal dysplasias

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

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.

code elsewhere

• Wolcott-Rallison syndrome  (5A13.6)

postcoordination

synonyms

• Multiple epiphyseal dysplasias
• dysplasia epiphysealis multiplex
• Multiple epiphyseal dysplasia type 1
• Multiple epiphyseal dysplasia type 4
• Multiple epiphyseal dysplasia type 5
• Multiple epiphyseal dysplasia due to collagen 9 anomaly
• Multiple epiphyseal dysplasia type 2
• Multiple epiphyseal dysplasia type 3
• Multiple epiphyseal dysplasia type 6
• Multiple epiphyseal dysplasia, Beighton type
• Multiple epiphyseal dysplasia with severe proximal femoral dysplasia
• Multiple epiphyseal dysplasia with miniepiphyses
• Multiple epiphyseal dysplasia, Al-Gazali type

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