Genopathy
Gene-Disorder Association · Article
Gene
NYS2
Nystagmus 2, Congenital Autosomal Dominant
Disorder
Nystagmus 2, Congenital, Autosomal Dominant
First reported 1964
Key publication · disorder [A RARE TYPE OF HEREDITARY NYSTAGMUS WITH AUTOSOMAL-DOMINANT INHERITANCE AND SPECIAL PHENOMENON: VERTICAL NYSTAGMUS COMPONENT AND DISORDER OF THE VERTICAL AND HORIZONTAL OPTOKINETIC NYSTAGMUS].Acta genetica et statistica medica · 1964
Manually curated
Association Review

In brief

The association between NYS2 (Nystagmus 2, Congenital Autosomal Dominant) and Nystagmus 2, Congenital, Autosomal Dominant is a manually-curated gene–disease association, supported by a single expert-curated source.

Sources 1
Clinical variants 0
Symptoms 9
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
Nystagmus 2, Congenital, Autosomal Dominant

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
Phenotype

Clinical features

5 clinical features

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

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05
Provenance

References & sources

2 references

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

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