Search results for S-Adenosylmethionine

81 hits were found for S-Adenosylmethionine

# Family MCID Name MIFTS Score
1
P HPT021 Hepatitis 69 0.259
2
P LVR013 Liver Disease 75 0.217
3
P INT001 Intrahepatic Cholestasis 59 0.217
4
CHL068 Cholestasis 59 0.217
5
P HMC002 Homocystinuria 50 0.164
6
HYP037 Hyperhomocysteinemia 50 0.164
7
P BRS047 Breast Cancer 100 0.142
8
P NRB001 Neuroblastoma 70 0.116
9
c HPT001 Hepatitis C 68 0.116
10
c HPT016 Hepatitis B 64 0.116
11
c HPT003 Hepatitis a 59 0.116
12
FTT001 Fatty Liver Disease 59 0.116
13
P ALC004 Alcohol Abuse 59 0.116
14
SBS003 Substance Abuse 54 0.116
15
TRY001 Trypanosomiasis 51 0.116
16
NNL002 Nonalcoholic Steatohepatitis 50 0.116
17
END072 Endotheliitis 42 0.116
18
NTR005 Nutritional Deficiency Disease 36 0.116
19
HMC014 Homocysteinemia 35 0.116
20
HYP241 Hypermethioninemia Due to Adenosine Kinase Deficiency 23 0.116
21
P LNG032 Lung Cancer 95 0.082
22
P ALZ034 Alzheimer Disease 92 0.082
23
P HPT023 Hepatocellular Carcinoma 92 0.082
24
MLR004 Malaria 83 0.082
25
HV1006 Hiv-1 80 0.082
26
P RTT002 Rett Syndrome 77 0.082
27
c HPT073 Hepatitis C Virus 73 0.082
28
P PHC003 Pheochromocytoma 71 0.082
29
LVR012 Liver Cirrhosis 67 0.082
30
P MYP004 Myopathy 67 0.082
31
VSC007 Vascular Disease 67 0.082
32
SRC014 Sarcoma 66 0.082
33
LNG099 Lung Disease 64 0.082
34
ALC007 Alcohol Dependence 63 0.082
35
MLN008 Melanoma 62 0.082
36
ISC004 Ischemia 61 0.082
37
MTH009 Mouth Disease 61 0.082
38
MDD011 Mood Disorder 61 0.082
39
P CLR108 Colorectal Adenoma 60 0.082
40
ALC006 Alcoholic Hepatitis 59 0.082
41
P NRP001 Neuropathy 59 0.082
42
ADN018 Adenoma 58 0.082
43
RHM027 Rheumatic Disease 58 0.082
44
CHY002 Chylomicron Retention Disease 57 0.082
45
NRM005 Neuromuscular Disease 56 0.082
46
P FBR017 Fibrosarcoma 56 0.082
47
TRN015 Transient Cerebral Ischemia 56 0.082
48
GST050 Gastrointestinal System Disease 56 0.082
49
END030 End Stage Renal Failure 55 0.082
50
c PND001 Pain Disorder 54 0.082
51
SLP005 Sleep Disorder 53 0.082
52
KRT002 Keratomalacia 52 0.082
53
c HPT015 Hepatitis D 52 0.082
54
P MSC033 Muscle Disorders 52 0.082
55
STM006 Stomach Disease 50 0.082
56
P CLL015 Collagen Disease 50 0.082
57
c ACT134 Acute Liver Failure 50 0.082
58
ALC009 Alcoholic Liver Cirrhosis 49 0.082
59
c INH020 Inherited Metabolic Disorder 49 0.082
60
AMN002 Amino Acid Metabolic Disorder 47 0.082
61
ACR041 Acromelic Frontonasal Dysostosis 45 0.082
62
ADN001 Adenosine Deaminase Deficiency 45 0.082
63
VTM002 Vitamin B12 Deficiency 44 0.082
64
UTR043 Uterine Sarcoma 44 0.082
65
BRT030 Birth Defects 43 0.082
66
TRC003 Trichomoniasis 41 0.082
67
NRN002 Neuronitis 41 0.082
68
CRB009 Cerebritis 39 0.082
69
MYF002 Myofascial Pain Syndrome 39 0.082
70
MLY001 Molybdenum Cofactor Deficiency 38 0.082
71
HYP003 Hypermethioninemia 37 0.082
72
VSC018 Visceral Steatosis 37 0.082
73
PYR016 Pyridoxine Deficiency 36 0.082
74
ALR002 Al-Raqad Syndrome 36 0.082
75
ALC003 Alcoholic Psychosis 33 0.082
76
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 33 0.082
77
ALC001 Alcohol-Related Birth Defect 31 0.082
78
VTM003 Vitamin Metabolic Disorder 30 0.082
79
HYP269 Hypermethioninemia, Persistent, Autosomal Dominant, Due to Methionine Adenosyltransferase I/iii Deficiency 29 0.082
80
PYR009 Pyridoxine Deficiency Anemia 18 0.082
81
INB001 Inborn Amino Acid Metabolism Disorder 12 0.082
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