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 ×

Hemoglobin M disease

M hemoglobinopathy · Autosomal dominant methemoglobinemia

ORPHA:330041

Genetic hemoglobinopathy

ORPHA:466066

Hemoglobinopathy

ORPHA:68364

Homozygous hemoglobin O Arab disease

Homozygous O Arab hemoglobinopathy

ORPHA:700111

Myeloid hemopathy

ORPHA:171895