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Disease

Hearing loss, autosomal recessive

Also known as 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+6 more

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, autosomal recessive nonsyndromic deafness, autosomal recessive nonsyndromic genetic deafness, deafness, autosomal recessive, deafness, neurosensory nonsyndromic recessive, DFN, nonsyndromic deafness, autosomal recessive, nonsyndromic genetic deafness, autosomal recessive.

12
Associated genes
2
Related proteins

What's happening now

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Associated genes

12 matches

Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.

OTOF0.81CDH230.75TMPRSS30.73TRIOBP0.73OTOGL0.73TECTA0.73MARVELD20.73PTPRQ0.72MYO15A0.72LOXHD10.71GRXCR10.71MPZL20.71

Disease biology

2 matches

Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.

Hepatocyte growth factorvia HGF0.61Sphingosine 1-phosphate receptor 2via S1PR20.57

Reference

Authoritative identity, definition & identifiers.

Synonyms

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, autosomal recessive nonsyndromic deafness, autosomal recessive nonsyndromic genetic deafness, deafness, autosomal recessive, deafness, neurosensory nonsyndromic recessive, DFN, nonsyndromic deafness, autosomal recessive, nonsyndromic genetic deafness, autosomal recessive

References & data sources
  • Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
  • Related entities are derived from literature co-mention (studied together) — associative, not causal.