Any 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.
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osteochondrodysplasia
MONDO:0005516
diaphyseal medullary stenosis-bone malignancy syndrome
MONDO:0007205
fibular aplasia-ectrodactyly syndrome
MONDO:0007225
cerebrocostomandibular syndrome
MONDO:0007301
cleidorhizomelic syndrome
MONDO:0007341
dyschondrosteosis-nephritis syndrome
MONDO:0007482