SLC26A2-related skeletal dysplasia
MONDO:0100592Any skeletal disorder in which the cause of the disease is a variant in the SLC26A2 gene. This includes SLC26A2-related achondrogenesis, SLC26A2-related atelosteogenesis, SLC26A2-related diastrophic dysplasia, and SLC26A2-related multiple epiphyseal dysplasia.
2 clinical trials for this condition and its sub-types, 0 tagged with SLC26A2-related skeletal dysplasia itself.
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Sub-types of SLC26A2-related skeletal dysplasia
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Diastrophic dysplasia 2 trials
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Achondrogenesis type IB 0 trials
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Atelosteogenesis type II 0 trials
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Multiple epiphyseal dysplasia type 4 0 trials