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 anomaly of the tricuspid valve chordae

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

ORPHA:99055

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 arteries

Congenital aorta, aortic arch or pulmonary arteries anomaly

ORPHA:98724

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 tricuspid malformation

ORPHA:98721

Congenital tricuspid stenosis

ORPHA:95459

Congenital urachal anomaly

ORPHA:435743

Rare congenital anomaly of ventricular septum

Congenital ventricular septal anomaly · Congenital anomaly of interventricular communication

ORPHA:474347