Genopathy
Gene-Disorder Association · Article
Gene
PDSS1
Decaprenyl Diphosphate Synthase Subunit 1
Manually curated
Association Review

In brief

The association between PDSS1 (Decaprenyl Diphosphate Synthase Subunit 1) and Coenzyme Q10 Deficiency Disease is reported, with clinical genetic testing available.

Sources 1
Clinical variants 4
Symptoms 2
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
PDSS1

The gene

1 source summary

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

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04
Coenzyme Q10 Deficiency Disease

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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05
ClinVar and variant evidence

Genetic basis

4 clinical variants

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

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06
Mechanism overlap

Shared mechanisms

1 shared pathway

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

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07
Provenance

References & sources

9 references

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

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