Cure My Disease

Don't miss your cure!

Home News Browse Soon ready About
Log in / Sign up

Browse

Explore conditions, clinical trials, and the organisations running them.

Conditions By category Trials Sponsors

← All categories

Up to: Disorder of organic acid metabolism · Inborn mitochondrial metabolism disorder · Inherited fatty acid metabolism disorder · Sulfur metabolism disease

Inherited lipoic acid biosynthesis defect

An inherited metabolic disease that is has its basis in the disruption of lipoate biosynthetic process.

0 trials tagged with this condition →

  • Pyruvate dehydrogenase E3 deficiency 1 trial
  • Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities 0 trials
  • Fatal multiple mitochondrial dysfunctions syndrome 0 trials Sub-types →
  • Lipoic acid synthetase deficiency 0 trials
  • Lipoyl transferase 1 deficiency 0 trials
  • Spasticity-ataxia-gait anomalies syndrome 0 trials

Cure My Disease

Helping patients find clinical trials that match their disease.

Why was Cure my disease built?

Explore

Home News Browse Glossary About Terms of use Contact us

This is a site from Cyber and Space