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"

5 matching diseasesClear search ×

Acquired methemoglobinemia

Drug-induced methemoglobinemia

ORPHA:464453

Autosomal recessive methemoglobinemia

ORPHA:621

Drug-induced autoimmune hemolytic anemia

Drug-induced AIHA

ORPHA:90037

Hemoglobin M disease

M hemoglobinopathy · Autosomal dominant methemoglobinemia

ORPHA:330041

Methemoglobinemia-related cyanosis

ORPHA:707993