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"

10 matching diseasesClear search ×

RAS-associated autoimmune leukoproliferative disease

RALD

ORPHA:268114

Familial hyperaldosteronism

FH

ORPHA:235936

Familial hyperaldosteronism type I

Dexamethasone-sensitive hypertension · FH-I

ORPHA:403

Familial hyperaldosteronism type II

FH-II · FH2

ORPHA:404

Familial hyperaldosteronism type III

FH-III · FH3

ORPHA:251274

Familial hyperaldosteronism type IV

FH4

ORPHA:642671

Genetic hyperaldosteronism

ORPHA:371861

OBSOLETE: Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency

ORPHA:248305

Primary hyperaldosteronism-seizures-neurological abnormalities syndrome

ORPHA:369929

Rare primary hyperaldosteronism

Rare primary aldosteronism

ORPHA:181415