A particular human disease, caused by deletion of part of chromosome 11, and causing aniridia and other problems.

(medicine) A rare X-linked recessive disease characterized by eczema, thrombocytopenia, immune deficiency, and bloody diarrhea.

(medicine, gastroenterology) A syndrome associated with consumption of the westernized version of Chinese food, characterized by various symptoms such as burning and tingling sensations, rapid heartbeat, and drowsiness, and tentatively ascribed to monosodium glutamate found in the food.

(medicine, informal) A hypertensive crisis caused by the ingestion of foods high in tyramine (such as some cheeses) while the monoamine metabolism is compromised by the use of monoamine oxidase inhibitors.

A genetic disorder of the connective tissue that causes defects in the heart valves and aorta.

A form of sleep paralysis in which the sleeper sees a figure resembling a witch sitting on them while still in bed.

hypotonia

(idiomatic) hypotonia

(genetics) A type of genetic interaction in which two (or more) mutations which are not lethal when occurring singly in a cell are lethal when they occur together in the same cell.

toxic epidermal necrolysis