Search results for s-adenosylmethionine

122 hits were found for s-adenosylmethionine

# Family MCID Name MIFTS Score
1
P LVR013 Liver Disease 76 0.331
2
CHL068 Cholestasis 60 0.274
3
FTT001 Fatty Liver Disease 66 0.234
4
P NNL004 Nonalcoholic Fatty Liver Disease 56 0.219
5
P HPT021 Hepatitis 73 0.202
6
NNL002 Nonalcoholic Steatohepatitis 54 0.202
7
HMC014 Homocysteinemia 53 0.202
8
P ALZ034 Alzheimer Disease 87 0.185
9
GST050 Gastrointestinal System Disease 67 0.185
10
P INT099 Intrahepatic Cholestasis of Pregnancy 53 0.185
11
P HMC002 Homocystinuria 51 0.185
12
CHR158 Charles Bonnet Syndrome 26 0.185
13
P SBS003 Substance Abuse 60 0.165
14
INT052 Intestinal Volvulus 43 0.165
15
P BRS047 Breast Cancer 100 0.143
16
DPR016 Depression 72 0.143
17
P PNM007 Pneumonia 72 0.143
18
P ADN016 Adenocarcinoma 70 0.143
19
c HPT003 Hepatitis a 66 0.143
20
P FBR017 Fibrosarcoma 61 0.143
21
c FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.143
22
PNM001 Pneumocystosis 58 0.143
23
P VSC018 Visceral Steatosis 37 0.143
24
HYP241 Hypermethioninemia Due to Adenosine Kinase Deficiency 29 0.143
25
c HPT016 Hepatitis B 70 0.117
26
ALC007 Alcohol Dependence 69 0.117
27
P ALC004 Alcohol Abuse 68 0.117
28
LVR012 Liver Cirrhosis 67 0.117
29
ISC004 Ischemia 67 0.117
30
P MJR001 Major Depressive Disorder 67 0.117
31
MNT002 Mental Depression 65 0.117
32
P TRM003 Tremor 55 0.117
33
TRY001 Trypanosomiasis 55 0.117
34
c CHL134 Cholestasis, Benign Recurrent Intrahepatic, 1 54 0.117
35
CLR109 Colorectal Adenocarcinoma 54 0.117
36
SLP001 Sleeping Sickness 49 0.117
37
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 43 0.117
38
c APL023 Aplasia Cutis Congenita, Nonsyndromic 40 0.117
39
TRY004 Trypanosomiasis, Human East-African 26 0.117
40
MTH011 Methionine Adenosyltransferase Deficiency 16 0.117
41
P LNG032 Lung Cancer 99 0.083
42
P HPT023 Hepatocellular Carcinoma 96 0.083
43
P PRS040 Prostate Cancer 93 0.083
44
MLR004 Malaria 84 0.083
45
P PNC035 Pancreatic Cancer 82 0.083
46
P RTT002 Rett Syndrome 82 0.083
47
OST012 Osteoarthritis 80 0.083
48
P PRK057 Parkinson Disease, Late-Onset 76 0.083
49
PLY001 Polycythemia Vera 75 0.083
50
c HMC039 Hemochromatosis, Type 1 74 0.083
51
c CHR089 Chronic Kidney Failure 73 0.083
52
c HPT073 Hepatitis C Virus 72 0.083
53
VSC007 Vascular Disease 72 0.083
54
P PHC003 Pheochromocytoma 72 0.083
55
P LKM002 Leukemia 72 0.083
56
P KDN018 Kidney Disease 71 0.083
57
SRC014 Sarcoma 70 0.083
58
LNG099 Lung Disease 70 0.083
59
c HPT001 Hepatitis C 69 0.083
60
ALL026 Allergic Hypersensitivity Disease 68 0.083
61
P DBT009 Diabetes Mellitus 67 0.083
62
FBR047 Fibromyalgia 66 0.083
63
OST159 Osteogenic Sarcoma 66 0.083
64
P PRP019 Peripheral Nervous System Disease 66 0.083
65
RHM027 Rheumatic Disease 65 0.083
66
MSL001 Measles 65 0.083
67
P MYP004 Myopathy 64 0.083
68
ADN018 Adenoma 64 0.083
69
CLR108 Colorectal Adenoma 64 0.083
70
MLN008 Melanoma 63 0.083
71
P NRP001 Neuropathy 63 0.083
72
AGN016 Aging 63 0.083
73
HYP266 Hypoxia 63 0.083
74
ALC006 Alcoholic Hepatitis 62 0.083
75
HMN014 Human Immunodeficiency Virus Infectious Disease 62 0.083
76
NRM005 Neuromuscular Disease 61 0.083
77
END030 End Stage Renal Failure 60 0.083
78
P PNS012 Paine Syndrome 60 0.083
79
SLP005 Sleep Disorder 60 0.083
80
NTR005 Nutritional Deficiency Disease 59 0.083
81
NWB001 Newborn Respiratory Distress Syndrome 59 0.083
82
TRN015 Transient Cerebral Ischemia 59 0.083
83
c MCR113 Microvascular Complications of Diabetes 3 58 0.083
84
P MSC033 Muscle Disorders 57 0.083
85
RSP019 Respiratory Distress Syndrome in Premature Infants 56 0.083
86
OVR059 Ovary Adenocarcinoma 55 0.083
87
STM007 Stomatitis 53 0.083
88
MSC190 Muscular Disease 53 0.083
89
c ACT134 Acute Liver Failure 53 0.083
90
ALC009 Alcoholic Liver Cirrhosis 52 0.083
91
P CLL015 Collagen Disease 52 0.083
92
UTR043 Uterine Sarcoma 50 0.083
93
ADR040 Adrenal Gland Pheochromocytoma 49 0.083
94
AMN002 Amino Acid Metabolic Disorder 49 0.083
95
VTM002 Vitamin B12 Deficiency 48 0.083
96
ADN001 Adenosine Deaminase Deficiency 48 0.083
97
c INF145 Infantile Liver Failure Syndrome 1 47 0.083
98
LYM067 Lymphoid Leukemia 47 0.083
99
c MCR120 Microvascular Complications of Diabetes 7 46 0.083
100
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 46 0.083
101
ALP077 Alpha-Methylacetoacetic Aciduria 45 0.083
102
P JVN024 Juvenile Hereditary Hemochromatosis 44 0.083
103
TRC003 Trichomoniasis 44 0.083
104
c MCR130 Microvascular Complications of Diabetes 6 43 0.083
105
c MCR133 Microvascular Complications of Diabetes 4 43 0.083
106
MYF002 Myofascial Pain Syndrome 43 0.083
107
BWN003 Bowenoid Papulosis 42 0.083
108
c PRS136 Prostate Cancer, Hereditary, 6 40 0.083
109
CHL045 Choline Deficiency Disease 40 0.083
110
HYP003 Hypermethioninemia 40 0.083
111
MTH074 Methionine Adenosyltransferase I/iii Deficiency 39 0.083
112
MSC004 Muscle Tissue Disease 39 0.083
113
MLY001 Molybdenum Cofactor Deficiency 39 0.083
114
CRY036 Cryptogenic Cirrhosis 38 0.083
115
RSP007 Respiratory Distress Syndrome, Infant 37 0.083
116
c PRS130 Prostate Cancer, Hereditary, 8 37 0.083
117
BLD165 Blood Group, Colton System 34 0.083
118
PYR016 Pyridoxine Deficiency 33 0.083
119
NTR027 Neutrophil Actin Dysfunction 32 0.083
120
RPD005 Rapidly Involuting Congenital Hemangioma 25 0.083
121
AMN012 Aminoacidopathies 24 0.083
122
INB001 Inborn Amino Acid Metabolism Disorder 16 0.083
Content
Loading form....