Multiple mitochondrial dysfunctions syndrome 3
MONDO:0014132Any fatal multiple mitochondrial dysfunctions syndrome in which the cause of the disease is a mutation in the IBA57 gene.
Also known as: IBA57 deficiency, IBA57 fatal multiple mitochondrial dysfunctions syndrome, fatal multiple mitochondrial dysfunctions syndrome caused by mutation in IBA57, multiple mitochondrial dysfunctions syndrome 3, multiple mitochondrial dysfunctions syndrome type 3, MMDS3
50 clinical trials for this condition and its sub-types.
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Disease
(618)
Metabolic disease
(215)
Hereditary disease
(172)
Inherited lipid metabolism disorder
(165)
Inborn mitochondrial metabolism disorder
(57)
Inborn errors of metabolism
(42)
Mitochondrial disease
(39)
Human disease
(14)
Developmental defect during embryogenesis
(7)
Inherited fatty acid metabolism disorder
(6)