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Very long chain acyl-CoA dehydrogenase deficiency

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Data Correlations | 1 study

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Genes category icon Genes
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ACADVL 100 100
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Biogroups category icon Biogroups
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Mitochondrial Fatty Acid Betaoxidat… 100 100
Fatty Acid Metabolism 98 98
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Individual Studies

  • OMIM - Congenital disorder

    Homo sapiens Homo sapiens | Mutations/Phenotypic   Mutations/Phenotypic

    This study contains curated human phenotype data extracted from OMIM. Additional computational processing and curation of the phenotype data was performed to further organize and group data from related phenotypes into unifying disease categories.

    Source: NextBio Library/Mutation and Phenotypic data
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Associated Researchers

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Thought leaders and organizations working on research involving very long chain acyl-coa dehydrogenase (vlcad) deficiency.

View All Author iconAuthors
  • U Spiekerkoetter
  • Ertan Mayatepek
  • Seiji Yamaguchi
  • R J A Wanders
  • A W Strauss
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  • Rigshospitalet, Denmark
  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDD…
  • Assistance Publique - Hôpitaux de Paris
View All Affiliations icon Organizations
  • University Children's Hospital
  • University of Alabama - Birmingham
  • University of Pittsburgh
  • National University Hospital
  • University of Rochester

Clinical Trials | 3 trials

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Community

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