is a rare genetic disorder causing brain ventriculomegaly and cystic kidneys.

causes trouble understanding spoken words despite normal hearing and speech.

is an extremely rare genetic condition affecting development and physical features.

is an allergic eye condition causing severe itching, redness, and light sensitivity.

is a recurring allergic eye inflammation, often affecting children seasonally.

is a rare, harmless wart-like skin growth with fatty immune cells.

is a slow-growing, low-grade type of squamous cell carcinoma.

is a rare birthmark-like blood vessel growth causing wart-like skin lesions.

is a rare blood vessel birthmark causing wart-like skin growths.

is a noncancerous skin birthmark causing raised, wart-like patches.

is a harmless wart-like growth caused by human papillomavirus infection.

is a rare disorder causing spine malformations, hormone and T-cell immune problems.

causes reduced blood flow to the brain, raising the risk of stroke.

causes extra vertebral segmentation and unusual facial and mouth development.

is an inherited disorder of fat metabolism causing hypoglycemia and heart/muscle problems.

is inflammation of the seminal vesicles, often causing pelvic pain.

is a group of conditions causing blisters on the skin and mucosa.

affects the inner ear and balance, causing dizziness, vertigo, and unsteadiness.

is a noncancerous growth in the vestibular glands near the vaginal opening.

is inner ear nerve inflammation causing sudden vertigo, nausea, and imbalance.

causes involuntary eye movements linked to inner ear or balance problems.

is a usually noncancerous tumor on the nerve linking ear and brain.

is a rare oral cancer affecting the area between lips and gums.

affects the nerve for hearing and balance, causing hearing loss or dizziness.