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Diseases

Genetic and Rare Diseases Information Center (GARD)

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3-alpha hydroxyacyl-CoA dehydrogenase deficiency


Other Names for this Disease
  • 3-hydroxylacyl-CoA dehydrogenase deficiency
  • HADH deficiency
  • M/SCHAD
  • Medium and short chain 3-hydroxyacyl-CoA dehydrogenase deficiency
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Overview


These Web pages are updated as the Genetic and Rare Diseases Information Center receives questions and as new information becomes available. If you don’t see many information resources on this page, it may be because the Information Center hasn’t yet received a question about this condition.

Your Questions Answered
by the Genetic and Rare Diseases Information Center

Please contact us with your questions about 3-alpha hydroxyacyl-CoA dehydrogenase deficiency. We will answer your question and update these pages with new resources and information.

Basic Information

  • The Screening, Technology And Research in Genetics (STAR-G) Project has a fact sheet on this condition, which was written specifically for families that have received a diagnosis as a result of newborn screening. This fact sheet provides general information about the condition and answers questions that are of particular concern to parents.

In Depth Information

  • The Online Mendelian Inheritance in Man (OMIM) is an catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine. 
  • Orphanet is a European reference portal for information on rare diseases and orphan drugs.  Access to this database is free of charge.
  • PubMed is a searchable database of medical literature and lists journal articles that discuss 3-alpha hydroxyacyl-CoA dehydrogenase deficiency. Click on the link to view a sample search on this topic.