Optic atrophy with demyelinating disease of CNS
MONDO:0008132Also known as: optic atrophy with demyelinating disease of CNS
41 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
Disease
(618)
Metabolic disease
(215)
Hereditary disease
(172)
Inborn mitochondrial metabolism disorder
(57)
Inborn errors of metabolism
(42)
Mitochondrial disease
(39)
Human disease
(14)
Developmental defect during embryogenesis
(7)
Mitochondrial oxidative phosphorylation disorder
(3)
Disease of genetic or genomic mechanism
(2)