is a lymphatic system cancer, often curable with chemotherapy and radiation.

is a rare, aggressive lymphatic system cancer requiring prompt, specialized treatment.

is a rare classical Hodgkin lymphoma subtype affecting lymph nodes, usually curable.

is a subtype of Hodgkin lymphoma affecting lymph nodes; highly treatable.

is a common lymph node cancer with high cure rates.

is an inherited disorder causing high homocysteine, affecting eyes, bones, blood vessels.

is a rare brain development disorder with smooth cortex, seizures, significant delays.

is an inherited metabolic disorder impairing branched-chain amino acid breakdown.

is a fast-growing cancerous cerebellar brain tumor, usually in children.

is a rare inherited muscle disease causing early-onset weakness and breathing problems.

is a slow-growing skin T-cell lymphoma causing itchy patches and plaques.

is a usually slow-growing appendix tumor from hormone-producing cells, often found incidentally.

is a rare inherited metabolic disorder causing organic acid buildup and acidosis.

is a rare genetic brain disorder causing childhood-onset movement and vision problems.

is a genetic metabolic disorder impairing phenylalanine breakdown, requiring lifelong dietary management.

is a rare neurodegenerative disorder causing balance, eye movement, speech difficulties.

is a rare, aggressive lung cancer with mixed tissue features.

is a rare inflammatory skin disease causing painful, rapidly enlarging ulcers.

is a rare autoimmune neurological disorder causing progressive stiffness and spasms.

is a rare kidney cancer subtype, often slower-growing with better outcomes.

is an inflammatory muscle disease causing skin rash and muscle weakness.

is an inherited connective-tissue disorder with stretchy skin, fragile scars, hypermobile joints.

is a genetic connective tissue disorder causing hypermobile joints and elastic skin.

is a genetic connective tissue disorder causing joint hypermobility and fragile skin.