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"

18 matching diseasesClear search ×

Rare congenital anomaly of ventricular septum

Congenital ventricular septal anomaly · Congenital anomaly of interventricular communication

ORPHA:474347

Atrioventricular septal defect

AVSD · Atrioventricular canal defect

ORPHA:98722

Atrioventricular valve anomaly

ORPHA:98720

Complete atrioventricular septal defect

CAVC · Complete atrioventricular canal defect

ORPHA:1329

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 coronary sinus

ORPHA:95500

Congenital anomaly of the great veins

ORPHA:363189

Congenital anomaly of the inferior vena cava

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

ORPHA:95499

Congenital anomaly of the tricuspid valve chordae

Congenital anomaly of tricuspid chordae tendineae · Congenital anomaly of tricuspid tendinous chords

ORPHA:99055

Congenital heart block

Congenital atrioventricular block

ORPHA:60041

Congenital left ventricular aneurysm

ORPHA:1055

Congenital pericardium anomaly

ORPHA:2846

Congenital pulmonary veins anomaly

ORPHA:98729

Congenital pulmonary venous return anomaly

Congenital pulmonary venous connection anomaly

ORPHA:3090

Congenital systemic veins anomaly

ORPHA:3091

Congenital total pulmonary venous return anomaly

ORPHA:99125

Congenital urachal anomaly

ORPHA:435743