is a rare, benign smooth muscle tumor of the genital skin.

is a rare inherited disorder affecting protein sugar attachment and development.

is an inherited condition that raises risk of blood cancers.

is a rare genetic disorder causing loose skin, developmental delays, eye issues.

is a serious transplant complication causing blood clots and kidney damage.

causes painful thumb-side wrist tendon swelling, making gripping and lifting harder.

is a rare, severe xeroderma pigmentosum with sun sensitivity and neurologic problems.

is a rare inherited condition causing hearing and vision loss with hypopigmentation.

is a rare genetic condition affecting inner ears, outer ears, and teeth.

is a rare genetic condition causing hearing loss and facial differences.

is a rare genetic condition causing deafness, dystonia, and vision loss.

is a genetic condition causing hearing loss, ear changes, and facial weakness.

is a genetic syndrome causing hearing loss, weak enamel, and nail abnormalities.

is a rare genetic syndrome affecting hearing, brain, nerves, weight, and heart.

causes hearing loss, bone growth abnormalities, and short stature.

is a rare syndrome causing hearing loss, genital differences, and bone fusion.

is a rare condition causing hearing loss and delayed or absent puberty.

is a rare genetic condition causing hearing loss and infertility.

is an inherited condition causing hearing loss, developmental delay, and learning difficulties.

is a rare genetic condition with hearing loss, lymphedema, increased leukemia risk.

is a rare genetic condition causing hearing loss and missing teeth.

is a rare genetic condition causing hearing loss and abnormal nails.

is a rare inherited disorder causing deafness, bowel pouches, and neuropathy.

is a rare condition causing hearing loss, patchy skin depigmentation, and achalasia.