lipid storage disease — Any of a group of relatively rare hereditary disorders of fat metabolism in which enzyme defects cause distinctive types of lipids to accumulate. They include Tay Sachs disease, Gaucher disease, Niemann Pick disease, and Fabry disease. Several… … Universalium
Neutral lipid storage disease — Classification and external resources OMIM 275630 … Wikipedia
Inborn error of lipid metabolism — Classification and external resources Several fatty acid molecules ICD 10 E75 … Wikipedia
Inborn errors of lipid metabolism — ICD9|277.85 ICDO = OMIM = MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D008052 Numerous genetic disorders are caused by errors in fatty acid metabolism. These disorders may be described as fatty oxidation disorders or as a lipid… … Wikipedia
Lysosomal storage disease — The lysosomal storage diseases are a group of over forty human genetic disorders that result from defects in lysosomal function. [cite journal |author=Winchester B, Vellodi A, Young E |title=The molecular basis of lysosomal storage diseases and… … Wikipedia
Lipid — Structures of some common lipids. At the top are oleic acid[1] and cholesterol.[2] The middle structure is a triglyceride composed of oleoyl, stearoyl, and palmitoyl chains at … Wikipedia
Cholesteryl ester storage disease — Template:Cholesteryl Ester Storage Disease (CESD) Classification and external resources ICD 10 E75.5 ICD 9 272.7 … Wikipedia
Childhood disintegrative disorder — Classification and external resources ICD 10 F84.2 F84.3 ICD 9 299.10 299.11 Childhood dis … Wikipedia
Congenital disorder of glycosylation — Congenital disorders of glycosylation Classification and external resources ICD 10 E77.8 ICD 9 271.8 … Wikipedia
Genetic disorder — For a non technical introduction to the topic, see Introduction to genetics. Genetic disorder Classification and external resources MeSH D030342 A genetic disorder is an illness caused by abnormalities in genes or … Wikipedia
