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Mitochondrial trifunctional protein deficiency

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Data Correlations | 2 studies

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Genes category icon Genes
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HADHB 100 100
HADHA 80 80
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Biogroups category icon Biogroups
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Cyclin E Destruction Pathway 100 100
Fatty Acid Elongation In Mitochondr… 99 99
Bile Acid Biosynthesis 96 96
Fatty Acid Metabolism 96 96
Valine Leucine and Isoleucine Degra… 96 96
Caprolactam Degradation 89 89
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Individual Studies

  • Mouse Phenotypes - Metabolic disease

    Mus musculus Mus musculus | Mutations/Phenotypic   Mutations/Phenotypic

    This study contains curated mouse gene mutation data extracted from the Mouse Genome Database (MGD) at The Jackson Laboratory, Bar Harbor, Maine. Additional computational processing and curation of mouse phenotype data was performed to further organize and group data from related phenotypes into uni…

    Source: NextBio Library/Mutation and Phenotypic data

  • 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 long chain 3-hydroxyacyl-coa dehydrogenase deficiency.

View All Author iconAuthors
  • J V Leonard
  • H Pihko
  • M J Bennett
  • A A M Morris
  • A M Lund
View All Affiliations icon Organizations
  • University of Helsinki
  • University of Texas Southwestern Medical Center
  • Oregon Health and Science University
  • Helsinki University Central Hospital
  • Sungkyunkwan University School of Medicine

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