Hearing loss, autosomal recessive 119

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Subtype of: Hearing loss · Hearing loss, autosomal recessive
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
hearing loss, autosomal recessive 119
MONDO_0030480
AFG2B Causal
34626583 38554706
ClinGen, Open Targets —
All1 Causal1 Unknown0
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Sensorineural hearing loss-spastic quadriplegia–intellectual disability 1 shared geneAFG2B Related via 1 shared gene including AFG2B. Isolated sensorineural deafness 1 shared geneAFG2B Related via 1 shared gene including AFG2B. Nonsyndromic hearing loss 1 shared geneAFG2B Related via 1 shared gene including AFG2B. Deafness 1 shared geneAFG2B Related via 1 shared gene including AFG2B. Hearing loss 1 shared geneAFG2B Related via 1 shared gene including AFG2B.