Autosomal recessive nonsyndromic hearing loss 102

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Subtype of: Hearing loss, autosomal recessive · Nonsyndromic hearing loss
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
autosomal recessive nonsyndromic hearing loss 102
MONDO:0014428
EPS8 Causal — ClinGen —
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Autosomal recessive nonsyndromic hearing loss 102.
5 View disease cluster →
Deafness, autosomal recessive, 102 1 shared geneEPS8 Related via 1 shared gene including EPS8. Isolated sensorineural deafness 1 shared geneEPS8 Related via 1 shared gene including EPS8. Nonsyndromic hearing loss 1 shared geneEPS8 Related via 1 shared gene including EPS8. Deafness 1 shared geneEPS8 Related via 1 shared gene including EPS8. Hearing loss 1 shared geneEPS8 Related via 1 shared gene including EPS8.