Deafness-onychodystrophy syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
AUTOSOMAL DOMINANT DEAFNESS - ONYCHODYSTROPHY SYNDROME
MONDO:0007420
ATP6V1B2 Causal
24913193 28396750
ClinVar, GWAS catalog
AUTOSOMAL DOMINANT DEAFNESS-ONYCHODYSTROPHY SYNDROME
79499
ATP6V1B2 Unknown
24913193
Orphanet
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Deafness-onychodystrophy syndrome.
5 View disease cluster →
Deafness with congenital onychodystrophy 1 shared geneATP6V1B2 Related via 1 shared gene including ATP6V1B2. Doors syndrome 1 shared geneATP6V1B2 Related via 1 shared gene including ATP6V1B2. Digitrenocerebral syndrome 1 shared geneATP6V1B2 Related via 1 shared gene including ATP6V1B2. Zimmermann-laband syndrome 1 shared geneATP6V1B2 Related via 1 shared gene including ATP6V1B2. Lymphoma 1 shared geneATP6V1B2 Related via 1 shared gene including ATP6V1B2.