Genopathy
Gene-Disorder Association · Article
Gene
MT-CO2
Mitochondrially Encoded Cytochrome C Oxidase II
Disorder
Leber Hereditary Optic Neuropathy, Modifier Of
First reported 1950
Key publication · disorder Molybdenum deficiency in Dunkirk silty clay loam.Science (New York, N.Y.) · 1950
Manually curated
Association Review

In brief

The association between MT-CO2 (Mitochondrially Encoded Cytochrome C Oxidase II) and Leber Hereditary Optic Neuropathy, Modifier Of is a manually-curated gene–disease association, with its 2 contributing sources — 1 of them expert-curated — recording pathogenic and likely-pathogenic variants.

Sources 2
Clinical variants 2
Symptoms 28
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

2 sources

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

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03
MT-CO2

The gene

1 source summary

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

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04
Leber Hereditary Optic Neuropathy, Modifier Of

The disorder

14 database identifiers

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

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05
Phenotype

Clinical features

26 clinical features

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

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06
ClinVar and variant evidence

Genetic basis

2 clinical variants

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

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07
Mechanism overlap

Shared mechanisms

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

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08
Provenance

References & sources

8 references

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

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