Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

2 matching diseasesClear search ×

Mitochondrial oxidative phosphorylation disorder with no known mechanism

OXPHOS disease with no known mechanism

ORPHA:254822

Mitochondrial oxidative phosphorylation disorder

OXPHOS disease

ORPHA:223713