milroy disease
1Milroy disease — autosomal dominant primary lymphedema occurring at or soon after birth, caused by a mutation of chromosome locus 5q35.3; called also Nonne Milroy d. and Milroy l …
2Milroy disease (lymphedema) — Mil·roy disease (lymphedema) (milґroi) [William Forsyth Milroy, American physician, 1855–1942] see under disease …
3Nonne-Milroy disease — Milroy d …
4Milroy's disease — Classification and external resources ICD 10 Q82.0 ICD 9 757.0 …
5Nonne-Milroy disease — Non·ne Mil·roy disease (nonґə milґroi) [Max Nonne, German neurologist, 1861–1939; William Forsyth Milroy, American physician, 1855–1942] see under disease …
6Milroy's disease — Mil·roy s disease mil .rȯiz n a hereditary lymphedema esp. of the legs Milroy William Forsyth (1855 1942) American physician. Milroy specialized in internal medicine and was an authority on diseases of the heart and lungs. His most important… …
7Milroy's disease — see lymphoedema [W. F. Milroy (1855–1942), US physician] …
8Disease — Illness or sickness often characterized by typical patient problems (symptoms) and physical findings (signs). Disruption sequence: The events that occur when a fetus that is developing normally is subjected to a destructive agent such as the… …
9Milroy — William F., U.S. physician, 1855–1942. See M. disease …
10Milroy lymphedema — see under disease …
