Search results for Uridine diphosphate-N-acetylglucosamine

81 hits were found for Uridine diphosphate-N-acetylglucosamine

# Family MCID Name MIFTS Score
1
PRT037 Pertussis 49 2.795
2
P LNG032 Lung Cancer 98 2.688
3
P MCL001 Mucolipidosis 49 2.625
4
TRY001 Trypanosomiasis 50 2.575
5
SLP001 Sleeping Sickness 56 2.471
6
MNT002 Mental Depression 56 2.448
7
P ENC018 Encephalopathy 62 2.319
8
DYS015 Dysentery 50 2.254
9
c MCL062 Mucolipidosis Ii Alpha/beta 69 2.021
10
c MCL046 Mucolipidosis Iii Alpha/beta 61 2.002
11
c MCL016 Mucolipidosis Iii Gamma 49 2.002
12
P MYP004 Myopathy 67 1.963
13
c SML038 Small Cell Cancer of the Lung 69 1.921
14
P PNC035 Pancreatic Cancer 86 1.885
15
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.557
16
P HPT023 Hepatocellular Carcinoma 95 1.517
17
P EPL164 Epilepsy 70 1.484
18
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.435
19
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.435
20
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 1.435
21
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.435
22
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.435
23
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 1.435
24
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.435
25
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.435
26
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.435
27
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 1.435
28
LYM027 Lymphopenia 56 1.407
29
CLN015 Colon Adenocarcinoma 64 1.407
30
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.357
31
MLD018 Mild Cognitive Impairment 48 1.336
32
P ALZ034 Alzheimer Disease 87 1.324
33
ATS010 Autosomal Recessive Disease 42 1.301
34
HYP066 Hyperglycemia 60 1.281
35
P MYC084 Mycobacterium Tuberculosis 1 68 1.210
36
P ADN016 Adenocarcinoma 63 1.210
37
ANX004 Anoxia 40 1.170
38
LYS002 Lysosomal Storage Disease 51 1.167
39
P MSC005 Muscular Dystrophy 66 1.147
40
P GST053 Gastric Cancer 82 1.010
41
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.985
42
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.977
43
NRL016 Neural Tube Defects 81 0.977
44
P CRP001 Carpal Tunnel Syndrome 66 0.891
45
SLR001 Sialuria 48 0.787
46
NNK001 Nonaka Myopathy 58 0.657
47
P FRS004 Free Sialic Acid Storage Disorders 41 0.640
48
ATM095 Autoimmune Disease 61 0.636
49
BRK010 Burkitt Lymphoma 66 0.631
50
P LNG064 Lung Cancer Susceptibility 3 70 0.631
51
MYP120 Myopathy, Distal, with Rimmed Vacuoles 33 0.550
52
c MCR115 Microvascular Complications of Diabetes 5 65 0.523
53
IMM080 Immunodeficiency 23 51 0.507
54
c CNG411 Congenital Disorder of Glycosylation, Type in 66 0.492
55
P ATS364 Autism 72 0.475
56
ART103 Arthrogryposis, Mental Retardation, and Seizures 37 0.452
57
HYP458 Hyper Ige Syndrome 60 0.452
58
DRM006 Dermatitis 62 0.452
59
CNG506 Congenital Amyoplasia 27 0.452
60
P MCR010 Microcephaly 59 0.436
61
HYP060 Hyperinsulinism 53 0.414
62
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 0.414
63
WST001 West Syndrome 64 0.359
64
c ATS007 Autism Spectrum Disorder 72 0.359
65
P ATR011 Atrial Fibrillation 66 0.359
66
RTN020 Retinal Vascular Disease 45 0.359
67
P CNG001 Congenital Myasthenic Syndrome 68 0.359
68
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.359
69
c MSC169 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 1 61 0.320
70
c SPR089 Spermatogenic Failure 4 32 0.320
71
PRX085 Preaxial Hallucal Polydactyly 28 0.320
72
P DST002 Distal Arthrogryposis 63 0.320
73
c GLY008 Glycogen Storage Disease Ii 72 0.320
74
P SCL018 Scoliosis 57 0.320
75
BRT055 Breath-Holding Spells 26 0.320
76
CRD223 Cardiac Arrhythmia 63 0.320
77
P MYS079 Miyoshi Muscular Dystrophy 52 0.320
78
TRS001 Tarsal Tunnel Syndrome 26 0.320
79
QDR001 Quadriplegia 49 0.320
80
FTD001 Foot Drop 36 0.320
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