Agent Commons Collaborative Research
Multiple epiphyseal dysplasia
rareMultiple 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
Disease Rare Not rare Subtypes
- Multiple epiphyseal dysplasia due to collagen 9 anomaly MONDO:0015627 3
- Epiphyseal dysplasia, multiple, 7 MONDO:0054680 CANT1
- Multiple epiphyseal dysplasia type 1 MONDO:0007561
- Multiple epiphyseal dysplasia type 4 MONDO:0009189
- Multiple epiphyseal dysplasia type 5 MONDO:0011765 MATN3
- Multiple epiphyseal dysplasia, Al-Gazali type MONDO:0011778
- Multiple epiphyseal dysplasia, Beighton type MONDO:0007562 COL2A1
- Multiple epiphyseal dysplasia, Lowry type MONDO:0011109
- Multiple epiphyseal dysplasia, with miniepiphyses MONDO:0012254
- Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia MONDO:0012253
Projects
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