is an inherited disorder causing bone marrow failure and leukemia risk.

is an inherited thyroid condition causing an enlarged gland with multiple nodules.

is a rare inherited condition causing multiple benign fibrous skin growths.

is an inherited condition causing multiple benign fatty lumps under the skin.

is an inherited condition causing multiple usually benign tumors around the brain.

is an inherited condition causing multiple flat pink to red birthmarks.

is an inherited skin condition causing many small, benign hair follicle tumors.

is a rare inherited condition affecting tiny nasal hairs called cilia.

is an inherited kidney disease causing protein-rich urine and body swelling.

is an inherited thyroid cancer that does not arise from C cells.

causes painful calcium deposits around joints despite normal blood phosphate levels.

is a rare inherited condition causing omphalocele and distinctive facial features.

is a rare migraine type causing temporary weakness on one side.

is an inherited condition causing benign fibro-osseous tumors in the jawbones.

is an inherited joint disorder affecting bone and cartilage in growing children.

is a rare inherited disorder affecting bone growth and skeletal development.

is an inherited form of pancreatic cancer that runs in families.

is an inherited thyroid cancer affecting papillary or follicular thyroid cells.

is a rare inherited condition linked to thyroid and kidney tumors.

is a genetic disorder causing sudden, brief episodes of coordination loss.

is an inherited epilepsy causing seizures that start in one brain area.

is a rare genetic disorder causing limb fat loss and metabolic complications.

is an inherited condition where a fetal blood vessel stays open.

is an inherited disorder causing episodes of temporary muscle weakness or paralysis.