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"

4 matching diseasesClear search ×

Hirschsprung disease

Aganglionic megacolon · Congenital intestinal aganglionosis

ORPHA:388

Congenital intestinal transport defect

ORPHA:104003

Congenital microcoria

Congenital miosis

ORPHA:566

Congenital ptosis

ORPHA:91411