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mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Uniprot Description A severe, autosomal recessive inborn error affecting valine metabolism. Disease features include brain lesions in the basal ganglia, neurodegeneration, delayed psychomotor development, hypotonia, spasticity, and increased lactic acid in serum and cerebral serum fluid.
Mondo Term and Equivalent IDs
MONDO:0014563:  mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency
GARD:0013019: 
UMLS:C4225391: