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 ×

Renal pseudohypoaldosteronism type 1

Renal PHA1 · Autosomal dominant pseudohypoaldosteronism type 1

ORPHA:171871

Fibromuscular dysplasia of the renal arteries

Renal artery fibromuscular dysplasia · Renal FMD

ORPHA:698043

Pseudohypoaldosteronism type 1

PHA1 · PHA type 1

ORPHA:756