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GW0742 Compound  •  C1433139

Synonyms: GW0742 • GW 0742

Related concepts

# Entity Type Relation Support Relative specificity
1 Hepatomegaly Disease Known Explain
2 PPARD gene Gene Known Explain
3 Myopathy Disease Known Explain
4 NOS3 gene Gene Known Explain
5 AKT1 gene Gene Known Explain
6 perfluorobutyric acid Compound Inferred Explain
7 fumonisin B1 Compound Inferred Explain
8 dichlorfop-methyl Compound Inferred Explain
9 chlorobenzilate Compound Inferred Explain
10 isopropyl 4,4'-dibromobenzilate Compound Inferred Explain
11 systhane Compound Inferred Explain
12 1,4-bis(2-(3,5-dichloropyridyloxy))benzene Compound Inferred Explain
13 fenarimol Compound Inferred Explain
14 Dicofol Compound Inferred Explain
15 propiconazole Compound Inferred Explain
16 triadimefon Compound Inferred Explain
17 perfluorooctanoic acid Compound Inferred Explain
18 Pydrin Compound Inferred Explain
19 ADAMTSL2 gene Gene Inferred Explain
20 Dexpropranolol Compound Inferred Explain
21 Hypertrophy Disease Inferred Explain
22 TRIM37 gene Gene Inferred Explain
23 DDT (Insecticide) Compound Inferred Explain
24 zileuton Compound Inferred Explain
25 MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED Disease Inferred Explain
26 Phenobarbital Compound Inferred Explain
27 4-(3-(2-propyl-3-hydroxy-4-acetyl)phenoxy)propyloxyphenoxy acetic acid Compound Inferred Explain
28 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 7 Disease Inferred Explain
29 Eichsfeld type congenital muscular dystrophy Disease Inferred Explain
30 MYOPATHY, HYALINE BODY, AUTOSOMAL RECESSIVE Disease Inferred Explain
31 MYOPATHY, DISTAL, WITH EARLY RESPIRATORY FAILURE, AUTOSOMAL DOMINANT Disease Inferred Explain
32 MYOPATHY, MYOSIN STORAGE (disorder) Disease Inferred Explain
33 HEREDITARY MYOPATHY WITH EARLY RESPIRATORY FAILURE Disease Inferred Explain
34 MYOTILINOPATHY Disease Inferred Explain
35 Spheroid body myopathy Disease Inferred Explain
36 Congenital Fiber Type Disproportion Disease Inferred Explain
37 Filaminopathy, autosomal dominant Disease Inferred Explain
38 MYOSCLEROSIS, AUTOSOMAL RECESSIVE Disease Inferred Explain
39 ALPHA-B CRYSTALLINOPATHY Disease Inferred Explain
40 MYOPATHY, MYOFIBRILLAR, ZASP-RELATED Disease Inferred Explain
41 MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET Disease Inferred Explain
42 MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE Disease Inferred Explain
43 Nemaline myopathy 3 Disease Inferred Explain
44 Liver diseases Disease Inferred Explain
45 Fibromyalgia Disease Inferred Explain
46 Polymyalgia Rheumatica Disease Inferred Explain
47 Myofascial Pain Syndromes Disease Inferred Explain
48 MIR362 gene Gene Inferred Explain
49 NONAKA MYOPATHY Disease Inferred Explain
50 MIR382 gene Gene Inferred Explain
51 Tendinopathy Disease Inferred Explain
52 Bethlem myopathy Disease Inferred Explain
53 Myopathy, limb-girdle, with bone fragility Disease Inferred Explain
54 Congenital Structural Myopathy Disease Inferred Explain
55 MIR379 gene Gene Inferred Explain
56 MYOPATHY, DISTAL, WITH ONSET IN INFANCY Disease Inferred Explain
57 MYOPATHY, CENTRONUCLEAR, AUTOSOMAL DOMINANT Disease Inferred Explain
58 MIR487B gene Gene Inferred Explain
59 MIR495 gene Gene Inferred Explain
60 C1845120 Other Inferred Explain
61 NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY Disease Inferred Explain
62 Eosinophilia-Myalgia Syndrome Disease Inferred Explain
63 Compartment syndromes Disease Inferred Explain
64 Muscular Disorders, Atrophic Disease Inferred Explain
65 X-linked centronuclear myopathy Other Inferred Explain
66 Native American myopathy Disease Inferred Explain
67 Myomatous neoplasm Disease Inferred Explain
68 Craniomandibular Disorders Disease Inferred Explain
69 MITOCHONDRIAL MYOPATHY AND SIDEROBLASTIC ANEMIA Disease Inferred Explain
70 CARDIOMYOPATHY ASSOCIATED WITH MYOPATHY AND SUDDEN DEATH Disease Inferred Explain
71 MYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY (disorder) Disease Inferred Explain
72 Welander Distal Myopathy Disease Inferred Explain
73 Neuromuscular Diseases Disease Inferred Explain
74 MIR376A1 gene Gene Inferred Explain
75 EPIPHYSEAL DYSPLASIA, MULTIPLE, 3 Disease Inferred Explain
76 INCLUSION BODY MYOPATHY 3, AUTOSOMAL DOMINANT Disease Inferred Explain
77 Isaacs syndrome Disease Inferred Explain
78 MIR154 gene Gene Inferred Explain
79 Muscle Cramp Disease Inferred Explain
80 MIR99B gene Gene Inferred Explain
81 Chronic Fatigue Syndrome Disease Inferred Explain
82 MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE Disease Inferred Explain
83 TRIFUNCTIONAL PROTEIN DEFICIENCY Disease Inferred Explain
84 Myotonic Disorders Disease Inferred Explain
85 MIR432 gene Gene Inferred Explain
86 Muscle Rigidity Disease Inferred Explain
87 SECRETORY DIARRHEA, MYOPATHY, AND DEAFNESS Disease Inferred Explain
88 Contracture Other Inferred Explain
89 MYOPATHY, DISTAL 2 Disease Inferred Explain
90 Muscle Weakness Disease Inferred Explain
91 MIR381 gene Gene Inferred Explain
92 Iron Compound Inferred Explain
93 Rhabdomyolysis Disease Inferred Explain
94 MIR30C2 gene Gene Inferred Explain
95 MIR335 gene Gene Inferred Explain
96 Mitochondrial Myopathies Disease Inferred Explain
97 MIR130A gene Gene Inferred Explain
98 Familial Periodic Paralysis Disease Inferred Explain
99 Myopathies, Nemaline Disease Inferred Explain
100 MIR132 gene Gene Inferred Explain

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