De la chapelle dysplasia

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
DE LA CHAPELLE DYSPLASIA
C1850555
SLC26A2 Causal — Disgenet
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with De la chapelle dysplasia.
5 View disease cluster →
Diastrophic dysplasia 1 shared geneSLC26A2 Related via 1 shared gene including SLC26A2. Diastrophic dysplasia, broad bone-platyspondylic variant 1 shared geneSLC26A2 Related via 1 shared gene including SLC26A2. Ear disease 1 shared geneSLC26A2 Related via 1 shared gene including SLC26A2. SLC26A2-related skeletal dysplasia 1 shared geneSLC26A2 Related via 1 shared gene including SLC26A2. Atelosteogenesis 1 shared geneSLC26A2 Related via 1 shared gene including SLC26A2.