is an X-linked disorder causing developmental delay, intellectual disability, and seizures.

is a rare genetic disorder causing early-onset nerve and brain degeneration.

is a rare cancer with clear-looking cells, affecting kidneys, ovaries, uterus.

is a rare ovarian cancer sometimes associated with endometriosis.

is a rare, noncancerous gland tumor, often arising in salivary glands.

is a slow-growing skin cancer variant on sun-exposed areas, rarely spreading.

is a rare, slow-growing bone cancer arising from cartilage.

is a rare, usually benign ovarian tumor with cystic and fibrous tissue.

is a rare brain or spinal cord tumor from ependymal cells.

is a rare, usually benign sweat gland tumor causing slow-growing skin nodules.

is a rare kidney cancer subtype with slow growth and good prognosis.

is the most common kidney cancer, often found incidentally, potentially aggressive.

is a rare, aggressive soft tissue cancer, often near tendons.

is a rare childhood kidney cancer that can spread to bone.

is a rare skin cancer from squamous cells, often on sun-exposed areas.

is a rare urothelial bladder cancer with clear cells, often invasive.

is a congenital opening in the hard palate, affecting feeding, speech.

is a congenital condition with a split in the upper lip, repairable.

is a congenital split in upper lip and gum ridge (alveolus).

is a rare genetic condition with facial differences, heart defects, hearing loss.

is present at birth, with an opening in lip and/or palate.

is a rare genetic condition combining cleft lip and retinal disease (retinopathy).

is a birth difference with an opening in lip and/or palate.

is a rare genetic disorder causing cleft lip/palate, hearing loss, sacral lipomas.