Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)
MONDO:0014943Any mitochondrial DNA depletion syndrome in which the cause of the disease is a mutation in the TFAM gene.
Also known as: TFAM mitochondrial DNA depletion syndrome, mitochondrial DNA depletion syndrome 15 (hepatocerebral type), mitochondrial DNA depletion syndrome caused by mutation in TFAM, MTDPS15
40 clinical trials for this condition and its sub-types.
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Disease
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Metabolic disease
(215)
Hereditary disease
(172)
Inborn mitochondrial metabolism disorder
(57)
Inborn errors of metabolism
(42)
Mitochondrial disease
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Human disease
(14)
Developmental defect during embryogenesis
(7)
Mitochondrial DNA depletion syndrome
(3)
Mitochondrial oxidative phosphorylation disorder
(3)