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hearing loss, autosomal recessive

MONDO:0019588

Also known as: hearing loss, autosomal recessive, autosomal recessive isolated neurosensory deafness type DFNB, autosomal recessive isolated sensorineural deafness type DFNB, autosomal recessive non-syndromic neurosensory deafness type DFNB, autosomal recessive non-syndromic sensorineural deafness type DFNB

MONDO:
MONDO:0019588
Orphanet:
90636
Rare disease110 associated genes

Description

Autosomal recessive form of nonsyndromic deafness.

Associated genes

+100 more genes — install the extension to see the full list inline on any page.

External references

Sources: MONDO (CC BY 4.0), Open Targets (CC0), Orphanet (CC BY 4.0).

Not for sole clinical decision-making. Always verify against primary sources.