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 ×

Rare congenital anomaly of ventricular septum

Congenital ventricular septal anomaly · Congenital anomaly of interventricular communication

ORPHA:474347

Congenital anomaly of hepatic vein

ORPHA:95507

Congenital anomaly of superior vena cava

Congenital anomaly of superior caval vein · Congenital anomaly of the SVC

ORPHA:95498

Congenital anomaly of the inferior vena cava

Congenital anomaly of the IVC · Congenital anomaly of the inferior caval vein

ORPHA:95499

Congenital Gerbode defect

Left ventricular-to-right atrial communication

ORPHA:99095

Congenital heart block

Congenital atrioventricular block

ORPHA:60041

Congenital left ventricular aneurysm

ORPHA:1055

Congenital retinal arteriovenous communication

Congenital arteriovenous anastomoses of the retina · Congenital arteriovenous communication of the retina

ORPHA:353334

Interatrial communication

ASD · Atrial septal defect

ORPHA:1478

Rare atrial defect and interatrial communication

Atrial defect and interauricular communication

ORPHA:98727