Genopathy
Gene-Disorder Association · Article
Gene
ACAD9
Acyl-CoA Dehydrogenase Family Member 9
Disorder
Mitochondrial Complex I Deficiency, Nuclear Type 20
First reported 2007
Supporting publications 12
Key publication · gene–disorder A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency.American journal of human genetics · 2007
Manually curated
Association Review

In brief

The association between ACAD9 (Acyl-CoA Dehydrogenase Family Member 9) and Mitochondrial Complex I Deficiency, Nuclear Type 20 is well established and manually curated, with its 6 contributing sources — 4 of them expert-curated — recording a known molecular basis, pathogenic and likely-pathogenic variants, and a causative germline mutation.

Sources 6
Clinical variants 244
Symptoms 51
Compounds 0
Trials 0
Publications 12
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

6 sources

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

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03
ACAD9

The gene

1 source summary

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

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04
Mitochondrial Complex I Deficiency, Nuclear Type 20

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

36 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

244 clinical variants

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

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07
Genomic context

Regulatory context

1 regulatory element

GeneHancer regulatory elements for the pair, with coordinates, score, element type and supporting literature.

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08
Mechanism overlap

Shared mechanisms

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

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09
Literature

Reading

12 publications

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

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10
Provenance

References & sources

18 references

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

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