is a genetic kidney development disorder causing no urine (anuria) and hypotension.

is a rare fetal kidney disorder linked to twin-to-twin transfusion syndrome.

is a rare inherited disorder disrupting fetal kidney development, causing kidney failure.

is a group of inherited kidney disorders affecting the tubules' transport functions.

is a rare inherited disorder affecting kidney tubules, brain, and liver.

is a childhood kidney cancer that usually responds well to treatment.

is a rare genetic disorder affecting kidney, liver, and pancreas development.

is swelling under the skin caused by certain blood pressure medicines.

is high blood pressure caused by narrowed kidney arteries.

is a rare X-linked disorder causing developmental delays, intellectual disability, microcephaly.

is a noncancerous growth in the reproductive organs.

is cancer that starts in organs involved in reproduction, with varied symptoms.

affects the organs involved in sex, hormones, and having children.

is a rare genetic condition affecting brain development, learning, and behavior.

is an eye disease where drainage blockage can cause lasting vision loss.

is ongoing glaucoma caused by past corticosteroid use that can damage vision.

is advanced open-angle glaucoma with lasting vision loss from optic nerve damage.

is a rare genetic disorder causing reduced response to thyroid hormone.

is a rare genetic condition causing the body to resist thyroid hormone.

is a rare disorder where the body poorly responds to TRH.

is an immune reaction causing sneezing, congestion, cough, or wheezing.

is a smoking-related lung disease that causes inflammation and breathing problems.

is when lungs can't get enough oxygen or clear carbon dioxide.

is a birth defect where the lungs or airways develop abnormally.