Sheldon-hall syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
SHELDON-HALL SYNDROME
1147MONDO:0011128
TNNT3 Causal
23401156
GWAS catalog, Orphanet
All5 Causal1 Unknown4
Related Diseases Diseases that share the most curated genes with Sheldon-hall syndrome.
5 View disease cluster →
Digitotalar dysmorphism 5 shared genesMYH3, TPM2, NALCN, TNNI2, TNNT3 Related via 5 shared genes including MYH3, TPM2, NALCN. Distal arthrogryposis 5 shared genesMYH3, TPM2, NALCN, TNNI2, TNNT3 Related via 5 shared genes including MYH3, TPM2, NALCN. Contractures, pterygia, and spondylocarpotarsal fusion syndrome 1 shared geneMYH3 Related via 1 shared gene including MYH3. Contractures, pterygia, and variable skeletal fusions syndrome 1 shared geneMYH3 Related via 1 shared gene including MYH3. TPM2-related myopathy 1 shared geneTPM2 Related via 1 shared gene including TPM2.