Genopathy
Gene-Disorder Association · Article
Gene
ACADM
Acyl-CoA Dehydrogenase Medium Chain
Disorder
Acyl-Coa Dehydrogenase, Short-Chain, Deficiency Of
First reported 2001
Supporting publications 1
Key publication · gene–disorder Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship.Human mutation · 2001
Key publication · disorder Protein variation in the eye lens nucleus of the mackerel scad (Decapterus pinnulatus).Comparative biochemistry and physiology · 1969
Manually curated
Association Review

In brief

The association between ACADM (Acyl-CoA Dehydrogenase Medium Chain) and Acyl-Coa Dehydrogenase, Short-Chain, Deficiency Of is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 57
Compounds 0
Trials 0
Publications 1
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
ACADM

The gene

1 source summary

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

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04
Acyl-Coa Dehydrogenase, Short-Chain, Deficiency Of

The disorder

10 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
Mechanism overlap

Shared mechanisms

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

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07
Literature

Reading

1 publication

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

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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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