is a genetic condition causing growth delays, limb differences, and learning challenges.

is a genetic disorder affecting development, with facial features and learning challenges.

is a rare genetic condition affecting growth, development, and sometimes behavior.

is a rare genetic condition affecting development, facial features, limbs, and learning.

is a genetic condition with developmental delays and distinctive features.

is a rare genetic disorder affecting cornea, skin, and bones.

is a congenital disorder of corneal development causing cloudy vision.

is an abnormal bulge in a heart artery, risking heart attack.

is an abnormal coronary artery connection to a heart chamber or vessel.

is a congenital heart condition where coronary arteries develop abnormally.

is a birth defect of heart arteries that can reduce blood flow.

is plaque buildup in heart arteries, limiting blood flow to heart.

involves brief heart artery spasms causing chest pain and reduced oxygen supply.

is narrowing or blockage of coronary artery openings at the aorta.

is re-narrowing of a treated heart artery after angioplasty or stenting.

is a rare congenital heart defect blocking coronary vein drainage.

is a rare narrowing of the heart's main vein, hindering drainage.

is narrowing of heart arteries reducing blood flow, causing chest pain.

is a blood clot blocking a heart artery, potentially causing heart attack.

is a viral respiratory illness causing fever, cough, and sometimes severe complications.

is a rare genetic immune disorder causing recurrent infections and T-cell lymphopenia.

is a rare genetic disorder causing absent corpus callosum and genital differences.

is a rare genetic disorder affecting brain, vision, jaw, and development.

is a genetic condition with missing corpus callosum, large head, wide-set eyes.