Disease

Nonsyndromic genetic hearing loss

Also known as nonsyndromic hereditary hearing loss, familial deafness, isolated genetic deafness, non-syndromic genetic deafness+3 more

nonsyndromic hereditary hearing loss, familial deafness, isolated genetic deafness, non-syndromic genetic deafness, nonsyndromic genetic deafness, nonsyndromic deafness, nonsyndromic hearing loss.

Associated genes

Related proteins

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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.

TECTA0.66 MYO60.66 MYO15A0.64 TMC10.63 LOXHD10.63 MYO7A0.60 CDH230.59 TMPRSS30.59 KCNQ40.57 OTOF0.57 SYNE40.54 CEACAM160.52

Disease biology

3 matches

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

Potassium voltage-gated channel subfamily KQT member 4via KCNQ40.57 ATP-sensitive inward rectifier potassium channel 10via KCNJ100.37 Sphingosine 1-phosphate receptor 2via S1PR20.37

Reference

Authoritative identity, definition & identifiers.

Synonyms

nonsyndromic hereditary hearing loss, familial deafness, isolated genetic deafness, non-syndromic genetic deafness, nonsyndromic genetic deafness, nonsyndromic deafness, nonsyndromic hearing loss

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.