Genopathy
Gene-Disorder Association · Article
Gene
MYH9
Myosin Heavy Chain 9
Disorder
Deafness, Autosomal Dominant 17
First reported 1997
Supporting publications 10
Key publication · gene–disorder A five-generation family with late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration.Audiology & neuro-otology · 1997
Key publication · disorder Saccule otoconia displacement into cochlea in cochleosaccular degeneration.Archives of otolaryngology (Chicago, Ill. : 1960) · 1980
Manually curated
Association Review

In brief

The association between MYH9 (Myosin Heavy Chain 9) and Deafness, Autosomal Dominant 17 is well established and manually curated, with its 3 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic variants, and causative variation.

Sources 3
Clinical variants 475
Symptoms 5
Compounds 0
Trials 0
Publications 10
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

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02
Provenance

Evidence and sources

3 sources

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

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03
MYH9

The gene

2 source summaries

A gene summary alongside the source descriptions it was distilled from.

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04
Deafness, Autosomal Dominant 17

The disorder

10 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

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05
Phenotype

Clinical features

1 clinical feature

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

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06
ClinVar and variant evidence

Genetic basis

475 clinical variants

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

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07
Mechanism overlap

Shared mechanisms

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

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08
Literature

Reading

10 publications

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

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09
Provenance

References & sources

14 references

Every source and publication cited across this dossier, as one numbered reference list.

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