Wolman disease — a lysosomal storage disease caused by deficiency of the lysosomal sterol esterase, with onset in early infancy and death before one year of age. Clinical features include hepatosplenomegaly, steatorrhea, abdominal distention, anemia, inanition,… … Medical dictionary
Wolman-Krankheit — Klassifikation nach ICD 10 E75.5 Sonstige Störungen der Lipidspeicherung (inkl. Wolman Krankheit) … Deutsch Wikipedia
Wolman-Syndrom — Klassifikation nach ICD 10 E75.5 Sonstige Störungen der Lipidspeicherung (inkl. Wolman Krankheit) … Deutsch Wikipedia
primary familial xanthomatosis — Wolman xanthomatosis Wolman disease … Medical dictionary
Xanthomatosis — A condition in which fatty deposits occur in various parts of the body. These fatty deposits are called xanthomas or xanthomata and appear as yellowish firm nodules in the skin. Xanthomas are in themselves a harmless growth of tissue. However,… … Medical dictionary
Wolman — Moshe, 20th century Israeli neuropathologist, *1914. See W. disease, W. xanthomatosis … Medical dictionary
Morbus Wolman — Klassifikation nach ICD 10 E75.5 Sonstige Störungen der Lipidspeicherung (inkl. Wolman Krankheit) … Deutsch Wikipedia
Cerebrotendineous xanthomatosis — Classification and external resources ICD 10 E75.5 ICD 9 272.7 … Wikipedia
Disease — 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… … Medical dictionary
Cholesteryl ester storage disease — Template:Cholesteryl Ester Storage Disease (CESD) Classification and external resources ICD 10 E75.5 ICD 9 272.7 … Wikipedia
Inborn error of lipid metabolism — Classification and external resources Several fatty acid molecules ICD 10 E75 … Wikipedia