is a rare genetic disorder with eye, hair, and anorectal anomalies.

is a rare genetic condition affecting the eyes, hair, and development.

is a rare genetic disorder affecting the teeth, nails, and hair.

is a rare genetic condition (ectodermal dysplasia) affecting teeth, nails, skin.

is a rare genetic condition affecting teeth, hair, nails, fingers, and palms.

is a rare genetic condition affecting bone growth, teeth, and height.

is abnormal breakdown of tooth structure that can loosen or damage teeth.

is a milder hypophosphatasia variant causing early tooth loss and dental defects.

is a rare genetic disorder affecting teeth and brain white matter.

is a rare genetic syndrome affecting the teeth, aorta, and esophagus.

is a rare genetic condition affecting teeth, nails, hair, and skin.

is a rare genetic condition affecting teeth, hair, and limb development.

is a parasitic roundworm infection that causes painful intestinal nodules.

cause sudden return of Parkinson’s symptoms despite oral medicines.

is a rare X-linked genetic disorder causing developmental delays and heart arrhythmias.

is a rare, inherited, nonprogressive night blindness with normal daylight vision.

is a rare inherited eye disorder causing lifelong night blindness.

is a rare inherited eye disorder causing lifelong night blindness.

is a rare genetic condition affecting development, growth, and multiple organs.

is a rare genetic condition with forearm/thumb differences and limited eye movements.

is a rare genetic condition affecting the arms, eyes, and hearing.

is a rare genetic condition affecting limb, eye, hearing, and kidney development.

is swelling and irritation of the fluid-filled sac over the elbow.

is a usually benign brain tumor near the nerves for smell.