Wolcott-rallison syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
WOLCOTT-RALLISON DYSPLASIA
EIF2AK3 Causal — ClinVar
WOLCOTT-RALLISON SYNDROME
1667C0432217MESH:C536739MONDO:0009192
EIF2AK3 Unknown
10932183 12960215 16813601 7551159
CTD, Disgenet, Orphanet
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Wolcott-rallison syndrome.
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Multiple epiphyseal dysplasia with early-onset diabetes mellitus 1 shared geneEIF2AK3 Related via 1 shared gene including EIF2AK3. Sialolithiasis 1 shared geneEIF2AK3 Related via 1 shared gene including EIF2AK3. Progressive supranuclear palsy 1 shared geneEIF2AK3 Related via 1 shared gene including EIF2AK3. Status epilepticus 1 shared geneEIF2AK3 Related via 1 shared gene including EIF2AK3. Connective tissue disease 1 shared geneEIF2AK3 Related via 1 shared gene including EIF2AK3.