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3-alpha-hydroxyacyl-CoA dehydrogenase deficiency
Disease Summary
Associated Targets (1)
Tbio
1
Uniprot Description An autosomal recessive, metabolic disorder with various clinical presentations including hypoglycemia, hepatoencephalopathy, myopathy or cardiomyopathy, and in some cases sudden death.
DataSource References
UniProt Disease: OMIM:231530
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
UniProt Disease
High level summary of knowledge for a disease, including descriptions and datasource references.