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Mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency

MONDO:0014563

Also known as: mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency, ECHS1D, mitochondrial short-chain ENOYL-CoA hydratase 1 deficiency, short-chain enoyl-CoA hydratase deficiency

13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency itself.

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↑ Hereditary disease (18235) ↑ Mitochondrial disease (132)
Including sub-types (13) Tagged with Mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency (0)
Trials to join now! 5 Not yet recruiting 1 Not yet finished but already full! 4 Completed 2 Terminated 1
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