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"

11 matching diseasesClear search ×

Congenital coronary artery aneurysm

Congenital coronary aneurysm

ORPHA:95491

Congenital anomaly of the coronary sinus

ORPHA:95500

Congenital aortopulmonary window

Congenital aortopulmonary artery fistula · Congenital aortopulmonary septal defect

ORPHA:2037

Congenital left ventricular aneurysm

ORPHA:1055

Congenital patent ductus arteriosus aneurysm

ORPHA:99072

Congenital primary aphakia

ORPHA:83461

Congenital pulmonary vein atresia

Congenital PVA · CPVA

ORPHA:99126

Congenital pulmonary veins anomaly

ORPHA:98729

Congenital thrombotic thrombocytopenic purpura

Congenital ADAMTS-13 deficiency · Congenital TTP

ORPHA:93583

Coronary artery congenital malformation

ORPHA:1081

Hereditary pulmonary alveolar proteinosis

Congenital PAP · Congenital pulmonary alveolar proteinosis

ORPHA:264675