Knowledge on rare diseases and orphan drugs
COVID-19 & Rare diseases
Rare Diseases Resources for Refugees/Displaced Persons
Search for a rare disease
Mitochondrial disease
ORPHA:68380
Classification level: Group of disorders
Prevalence: -
Inheritance: -
Age of onset:
UMLS: C0751651
MeSH: D028361
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
: produced/endorsed by ERN(s)
: produced/endorsed by FSMR(s)
General public
Guidelines
Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
- Research project(s) (83)
- Clinical trial(s) (12)
- Biobank(s) (14)
- Registry(ies) (33)
- Network of experts (9)
Newborn screening