Usher syndrome type 1

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Usher syndrome type 1
MYO7A Causal — ClinGen
USH1C Causal — ClinGen —
All2 Causal2 Unknown0
Related Diseases Diseases that share the most curated genes with Usher syndrome type 1.
5 View disease cluster →
Pendred syndrome 1 shared geneMYO7A Related via 1 shared gene including MYO7A. Congenital nystagmus 1 shared geneMYO7A Related via 1 shared gene including MYO7A. Retinitis pigmentosa-deafness syndrome 1 shared geneMYO7A Related via 1 shared gene including MYO7A. Usher syndrome 2 shared genesMYO7A, USH1C Related via 2 shared genes including MYO7A, USH1C. Hereditary hearing loss 2 shared genesMYO7A, USH1C Related via 2 shared genes including MYO7A, USH1C.