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"

3 matching diseasesClear search ×

Acquired prothrombin deficiency

Acquired hypoprothrombinemia

ORPHA:26348

Acquired methemoglobinemia

Drug-induced methemoglobinemia

ORPHA:464453

Congenital factor II deficiency

Dysprothrombinemia · Hypoprothrombinemia

ORPHA:325