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*  Lysosomal storage disease
... storage disease Glycogen storage diseases Type II Pompe disease Type IIb Danon disease Other Cholesteryl ester storage disease ... Type A) MPS III B (Type B) MPS III C (Type C) MPS III D (Type D) Type IV (Morquio) MPS IVA (Type A) MPS IVB (Type B) Type VI ( ... glycoprotein storage disorders (E77.0-E77.1) mucolipidoses Also, glycogen storage disease type II (Pompe disease) is also a ... Type 4 Kufs disease / adult NCL (CLN4) Type 5 Finnish Variant / late infantile (CLN5) Type 6 Late infantile variant (CLN6) Type ...
*  Danon disease
... or glycogen storage disease Type IIb) is a metabolic disorder.Danon disease is an X-linked lysosomal and glycogen storage ... January 1981). "Lysosomal glycogen storage disease with normal acid maltase". Neurology. 31 (1): 51-7. doi:10.1212/wnl.31.1.51 ... Although the genetic cause of Danon Disease is known, the mechanism of disease is not well understood. Danon disease involves a ... including Pompe disease. Females In females the symptoms of Danon Disease are less severe. Common symptoms of Danon Disease in ...
*  List of MeSH codes (C16)
... glycogen storage disease type ii MeSH C16.320.565.202.449.510 --- glycogen storage disease type iib MeSH C16.320.565.202. ... glycogen storage disease type iib MeSH C16.320.322.217 --- glycogen storage disease type viii MeSH C16.320.322.233 --- ... glycogen storage disease type iv MeSH C16.320.565.202.449.560 --- glycogen storage disease type v MeSH C16.320.565.202.449.580 ... glycogen storage disease type vi MeSH C16.320.565.202.449.600 --- glycogen storage disease type vii MeSH C16.320.565.202. ...
*  List of MeSH codes (C14)
... glycogen storage disease type iib MeSH C14.280.238.510 --- kearns-sayer syndrome MeSH C14.280.238.615 --- myocardial ... intracranial arterial diseases MeSH C14.907.253.560.200 --- cerebral arterial diseases MeSH C14.907.253.560.200.175 --- cadasil ... mahaim-type MeSH C14.280.067.780.977 --- wolff-parkinson-white syndrome MeSH C14.280.067.829 --- sick sinus syndrome MeSH ... hippel-lindau disease MeSH C14.907.077.410 --- klippel-trenaunay-weber syndrome MeSH C14.907.077.850 --- sturge-weber syndrome ...
*  List of MeSH codes (C10)
... glycogen storage disease type iib MeSH C10.597.606.643.455.625 --- lesch-nyhan syndrome MeSH C10.597.606.643.455.687 --- menkes ... glycogen storage disease type ii MeSH C10.228.140.163.100.435.590 --- mucolipidoses MeSH C10.228.140.163.100.435.810 --- sialic ... leigh disease MeSH C10.228.140.163.100.425 --- lesch-nyhan syndrome MeSH C10.228.140.163.100.435 --- lysosomal storage diseases ... lewy body disease MeSH C10.228.662.600.400 --- parkinson disease MeSH C10.228.662.600.700 --- parkinson disease, secondary MeSH ...
*  List of MeSH codes (C18)
... glycogen storage disease type ii MeSH C18.452.648.202.449.510 --- glycogen storage disease type iib MeSH C18.452.648.202. ... glycogen storage disease type iv MeSH C18.452.648.202.449.560 --- glycogen storage disease type v MeSH C18.452.648.202.449.580 ... glycogen storage disease type vi MeSH C18.452.648.202.449.600 --- glycogen storage disease type vii MeSH C18.452.648.202. ... glycogen storage disease MeSH C18.452.648.202.449.448 --- glycogen storage disease type i MeSH C18.452.648.202.449.500 --- ...
*  ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases
Glycogen storage disease type II (Pompe's disease) Glycogen storage disease type III Glycogen storage disease type IV Glycogen ... type IIb or III Hyperbetalipoproteinaemia with prebetalipoproteinaemia Hypercholesterolaemia with endogenous hyperglyceridaemia ... Glycogen storage disease Glycogen storage disease type I (von Gierke's disease) ... Type 3) Bielschowsky-Jansky disease (Type 2) Kufs disease (Type 4) Spielmeyer-Vogt disease (Type 3) (E75.5) Other lipid storage ...
*  Vitamin B6
Cooking, storage, and processing losses of vitamin B6 vary and in some foods may be more than 50%, depending on the form of ... Evidence exists for decreased levels of vitamin B6 in women with type 1 diabetes and in patients with systemic inflammation, ... PLP is a required coenzyme of glycogen phosphorylase, the enzyme necessary for glycogenolysis to occur. PLP can catalyze ... Also, PLP influences expression of glycoprotein IIb by interacting with various transcription factors. The result is inhibition ...
*  Muscle
... s also keep a storage form of glucose in the form of glycogen. Glycogen can be rapidly converted to glucose when energy ... Type II, fast twitch muscle, has three major subtypes (IIa, IIx, and IIb) that vary in both contractile speed and force ... Other syndromes or conditions that can induce skeletal muscle atrophy are congestive heart disease and some diseases of the ... Type IIb is anaerobic, glycolytic, "white" muscle that is least dense in mitochondria and myoglobin. In small animals (e.g., ...
*  List of OMIM disorder codes
PGM1 Glycogen storage disease XV; 613507; GYG1 Glycogen storage disease type 0; 240600; GYS2 Glycogen storage disease, type ... SLC37A4 Glycogen storage disease Ic; 232240; SLC17A3 Glycogen storage disease II; 232300; GAA Glycogen storage disease IIb; ... AGL Glycogen storage disease IV; 232500; GBE1 Glycogen storage disease IXc; 613027; PHKG2 Glycogen storage disease of heart, ... PFKM Glycogen storage disease X; 261670; PGAM2 Glycogen storage disease XI; 612933; LDHA Glycogen storage disease XII; 611881; ...