is a congenital heart defect (ASD) causing flow between upper chambers.

is a congenital heart defect with a hole between upper chambers.

is a genetic heart condition with a hole between upper chambers.

is a congenital heart defect causing a hole between upper chambers.

is a congenital heart defect with a hole between upper chambers.

is a congenital heart defect causing a hole between upper chambers (atria).

is a congenital heart defect with a hole between atria.

is a genetic, congenital atrial septal defect causing abnormal blood flow (shunt).

is a bulging atrial septum, often incidental but may raise clot risk.

is a genetic heart condition causing atrial septal defects and rhythm problems.

is a congenital heart defect involving the coronary sinus, causing abnormal flow.

is a congenital heart defect: hole low in atrial septum near valves.

is a congenital heart defect with a hole between upper chambers.

is a congenital heart hole where veins enter, altering blood flow.

is a rare heart rhythm disorder where the atria stop contracting.

is a rare inherited rhythm disorder with absent atrial activity and bradycardia.

causes early, permanent hair loss and small bump-like skin lesions (papules).

is a heart rhythm problem where electrical signals slow or stop.

is a rare genetic disorder causing heart, eyelid, limb, and anal defects.

is a congenital heart defect affecting septa and atrioventricular valves.

is a congenital defect of the atrioventricular valves causing leakage or narrowing.

is a thinned, floppy eardrum that may sag and impair hearing.

is chronic inflammation thinning stomach lining, reducing acid and vitamin B12 absorption.

is tongue inflammation with papillae loss, causing smooth, red, sore tongue.