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Up to: Hereditary neurological disease · Inborn mitochondrial metabolism disorder
HSD10 mitochondrial disease
A rare, life-threatening neurometabolic disease characterized by a progressive neurodegenerative course, epilepsy, retinopathy and progressive cardiomyopathy.
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HSD10 disease, atypical type 0 trials
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HSD10 disease, infantile type 0 trials
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HSD10 disease, neonatal type 0 trials