is a rare genetic skin disorder causing ring-shaped blisters and scaling.

is a chronic inflammatory skin condition causing ring-shaped, itchy purple patches.

is a birth defect where pancreatic tissue encircles the duodenum, causing blockage.

is a genetic muscle disorder causing progressive hip and shoulder weakness.

is a rare genetic condition where all teeth fail to develop.

is a sexually transmitted infection from HPV causing genital or anal warts.

is a congenital heart defect where coronary arteries arise abnormally.

is a rare birth defect of coronary arteries affecting heart blood flow.

is a heart artery birth difference where the right coronary arises unusually.

is a rare birth (congenital) heart defect reducing oxygen to heart muscle.

is a rare congenital heart defect disrupting the heart’s oxygen-rich blood supply.

involves irregular timing of puberty and menstrual periods due to hormonal disruptions.

is a genetic disorder affecting puberty and menstrual cycle development.

is a rare heart defect affecting coronary artery openings and blood flow.

is a spinal condition where tail-end cord thread (filum terminale) is abnormal.

affects heart valve support structures (chordae, papillary muscles), impairing mitral function.

is a right heart valve abnormality affecting tricuspid supports, causing leakage.

is a rare genetic condition causing absence of all fingernails and toenails.

is a rare genetic disorder with absent nails and darkened body folds.

is a rare genetic disorder causing absent nails (anonychia) and microcephaly.

is a rare genetic condition causing absent or abnormally formed nails.

is a rare genetic disorder with absent eyes and other anomalies.

is a rare genetic condition affecting eye development, heart, and skeleton.

is a rare genetic syndrome affecting eye development and the esophagus.