Genopathy
Gene-Disorder Association · Article
Gene
CNNM4
Cyclin And CBS Domain Divalent Metal Cation Transport Mediator 4
Disorder
Cone Dystrophy
First reported 1974
Key publication · disorder Cone dystrophy with dominant inheritance.American journal of ophthalmology · 1974
Manually curated
Association Review

In brief

The association between CNNM4 (Cyclin And CBS Domain Divalent Metal Cation Transport Mediator 4) and Cone Dystrophy is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 1
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
CNNM4

The gene

1 source summary

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

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04
Cone Dystrophy

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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05
Provenance

References & sources

3 references

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

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