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Deficiency of butyryl-CoA dehydrogenase

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Data Correlations | 1 study

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Genes category icon Genes
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ACADS 100 100
ACAD8 100 100
ACADSB 100 100
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Biogroups category icon Biogroups
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Beta-Oxidation of Fatty Acids 100 100
Fatty Acid Metabolism 97 97
Mitochondrial Fatty Acid Betaoxidat… 97 97
Beta-Alanine Metabolism 96 96
Butanoate Metabolism 96 96
Valine Leucine and Isoleucine Degra… 94 94
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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 short chain acyl-coa dehydrogenase deficiency.

View All Author iconAuthors
  • Niels Gregersen
  • Dietrich Matern
  • Jerry Vockley
  • N Gregersen
  • W J Rhead
View All Affiliations icon Organizations
  • Aarhus University Hospital and Faculty of Health Sciences
  • Aarhus University Hospital
  • Shanghai Jiaotong University School of Medicine
  • University of Massachusetts Medical School
  • Utrecht University

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