Digitotalar dysmorphism

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
DIGITOTALAR DYSMORPHISM
C1852085MONDO:0015240
MYBPC1 Unknown
20045868
Disgenet, Orphanet
MYH3 Unknown
23401156
Disgenet
NALCN Unknown
25683120
Disgenet, Orphanet
TNNI2 Unknown
23401156
ClinVar, Disgenet
TNNT3 Unknown
23401156
Disgenet, Orphanet
TPM2 Unknown
23401156
Disgenet, GWAS catalog
All6 Causal0 Unknown6
Related Diseases Diseases that share the most curated genes with Digitotalar dysmorphism.
5 View disease cluster →
Sheldon-hall syndrome 5 shared genesMYH3, TPM2, NALCN, TNNI2, TNNT3 Related via 5 shared genes including MYH3, TPM2, NALCN. Distal arthrogryposis 6 shared genesMYH3, TPM2, NALCN, TNNI2, TNNT3, MYBPC1 Related via 6 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.