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Symptoms:
Glycogen Storage Disease Type VII; Glycogenosis 7; Tarui Disease
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Hierarchical
More information
disease
;
glycogen
;
glycogen storage disease
;
glycogen storage disease type vii
Active principles
Rating
Bibliogr.
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1
alpha-Glucosidases
100
+
2
Glucan 1,4-alpha-Glucosidase
84
+
3
Collagen Type VII
49
+
4
Creatine Kinase, MM Form
48
+
5
Glycogen
42
+
6
Phosphorylase Kinase
32
+
7
Glucose-6-Phosphatase
30
+
8
Starch
28
+
9
Glucose-6-Phosphate
21
+
10
Glucuronidase
18
+
11
Factor VII
16
+
12
Liver Glycogen
10
+
13
Granulocyte Colony-Stimulating Factor
9
+
14
Glycogen Synthase
9
+
15
1-Deoxynojirimycin
8
+
16
Recombinant Proteins
8
+
17
beta-N-Acetylhexosaminidases
7
+
18
Glucosylceramidase
7
+
19
Phosphorylase b
6
+
20
Phosphorylase a
5
+
21
Lactates
5
+
22
Dietary Carbohydrates
5
+
23
Glucose
4
+
24
Hexosaminidases
4
+
25
Blood Glucose
4
+
26
Lactic Acid
3
+
27
Glycogen Phosphorylase
3
+
28
Glycosaminoglycans
3
+
29
Amino Acids, Acidic
3
+
30
Glycogen Synthase Kinase 3
3
+
31
Glycosphingolipids
3
+
32
Glucosyltransferases
2
+
33
Factor VIIa
2
+
34
von Willebrand Factor
2
+
35
Deamino Arginine Vasopressin
2
+
36
Glucose Transport Proteins, Facilitative
2
+
37
Cerebroside-Sulfatase
1
+
38
Glucosylceramides
1
+
39
Insulin
1
+
40
Sterol Esterase
1
+
41
Mannosephosphates
1
+
42
Hexosaminidase B
1
+
43
Hexosaminidase A
1
+
44
Sulfur Isotopes
1
+
45
Hydrolases
1
+
46
Codon, Nonsense
1
+
47
Phosphorylases
1
+
48
Molecular Chaperones
1
+
49
Iduronidase
1
+
50
Autoantibodies
1
+
51
Factor VIII
1
+
52
alpha-Galactosidase
1
+
53
Glycogen Synthase Kinases
1
+
54
alpha-Mannosidase
1
+
55
Enzymes
1
+
56
beta-Glucosidase
1
+
57
Phytanic Acid
1
+
58
Triglycerides
1
+
59
Receptor, IGF Type 2
1
+
60
Glucosephosphates
1
+
61
Dextranase
1
+
62
Ristocetin
1
+
63
Naphthol AS D Esterase
1
+
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