Genopathy
Gene-Disorder Association · Article
Gene
USH1H
Usher Syndrome 1H (Autosomal Recessive)
First reported 1989
Manually curated
Association Review

In brief

The association between USH1H (Usher Syndrome 1H (Autosomal Recessive)) and Usher Syndrome, Type Ih is a manually-curated gene–disease association, supported by a single expert-curated source.

Sources 1
Clinical variants 0
Symptoms 0
Compounds 0
Trials 0
Publications 0
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

1 source

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

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03
Usher Syndrome, Type Ih

The disorder

6 database identifiers

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

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04
Provenance

References & sources

1 reference

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

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