Genopathy
Gene-Disorder Association · Article
Gene
MYP11
Myopia 11 (High Grade, Autosomal Dominant)
Disorder
Myopia 11, Autosomal Dominant
First reported 1977
Key publication · disorder Acquired myopia in 11-year-old children.British medical journal · 1977
Manually curated
Association Review

In brief

The association between MYP11 (Myopia 11 (High Grade, Autosomal Dominant)) and Myopia 11, Autosomal Dominant 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
Myopia 11, Autosomal Dominant

The disorder

5 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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