OPN1MW and X-Linked Cone Dysfunction Syndrome With Myopia: Association Evidence

At a glance

Association overview

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

Provenance

1 source

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

OPN1MW

1 source summary

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

X-Linked Cone Dysfunction Syndrome With Myopia

6 database identifiers

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

Literature

1 publication

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

Provenance

4 references

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