is a rare congenital condition with absent lower half of a limb.

is an abnormal pregnancy with placental tissue overgrowth, no fetus.

is a congenital uterine difference with a complete dividing wall (septum).

is a rare chromosome change involving multiple breaks, affecting health or fertility.

is a genetic brain-development disorder with malformations, seizures, developmental delays.

is a genetic brain-development condition causing seizures and developmental delays.

is a rare genetic brain-development disorder causing cortical malformations, seizures, developmental delays.

is a rare genetic condition causing brain malformations, developmental delays, and seizures.

is a rare genetic brain-development disorder causing seizures and developmental delays.

is a rare genetic disorder causing brain malformations, seizures, and developmental delays.

is inherited, causing progressive leg stiffness (spasticity) and other neurological problems.

is a rare, severe genetic bone-cartilage disorder, often fatal at birth.

is a focal epilepsy causing impaired awareness during seizures (focal impaired awareness).

is chronic nerve-related pain affecting a limb after injury or surgery.

is persistent limb pain after injury without nerve damage, causing swelling, sensitivity.

is chronic pain after nerve injury, with color changes and sensitivity.

is a rare condition of abnormal vessels with tissue overgrowth and anomalies.

is a problem after transplant, including rejection, infections, medication effects.

is a treatment-related issue during hemodialysis that harms health or comfort.

include infections, organ problems, and graft-versus-host disease (GVHD), sometimes long-term.

is a rare blood vessel tumor, locally aggressive, seldom spreads distantly.

is a rare cancer with two distinct lymphomas in one person.

is a behavior disorder in youth with persistent aggression and rule violations.

is a congenital disorder causing outer-ear malformations and conductive hearing loss.