Multiple epiphyseal dysplasias

Description

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.

Index terms

Multiple epiphyseal dysplasias
dysplasia epiphysealis multiplex
multiple epiphyseal dysplasias NOS

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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

Exclusions from above levels

http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism

Sibling codes

LD24.60 – Pseudoachondroplasia
LD24.6Y – Other specified multiple epiphyseal dysplasia or pseudoachondroplasia

Foundation entity

Multiple epiphyseal dysplasias – http://id.who.int/icd/entity/2009123831

Allowed postcoordination axes

hasManifestation

Part of: LD24.6: Multiple epiphyseal dysplasia or pseudoachondroplasia › LD24: Syndromes with skeletal anomalies as a major feature › 20: Developmental anomalies