Search results for s-adenosylmethionine

225 hits were found for s-adenosylmethionine

# Family MCID Name MIFTS Score
1
P LVR013 Liver Disease 68 0.439
2
CHL068 Cholestasis 61 0.341
3
HMC014 Homocysteinemia 53 0.310
4
OST012 Osteoarthritis 78 0.293
5
LVR012 Liver Cirrhosis 62 0.293
6
P HPT023 Hepatocellular Carcinoma 100 0.285
7
DPR016 Depression 63 0.276
8
FTT001 Fatty Liver Disease 61 0.266
9
SLP001 Sleeping Sickness 54 0.266
10
TRY001 Trypanosomiasis 50 0.266
11
P HMC002 Homocystinuria 53 0.225
12
P CLR023 Colorectal Cancer 99 0.213
13
P ALZ034 Alzheimer Disease 88 0.213
14
P MJR001 Major Depressive Disorder 68 0.213
15
MNT002 Mental Depression 58 0.213
16
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.201
17
NNL006 Non-Alcoholic Steatohepatitis 54 0.201
18
P INT099 Intrahepatic Cholestasis of Pregnancy 51 0.188
19
P NRB001 Neuroblastoma 72 0.174
20
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.174
21
PNM001 Pneumocystosis 59 0.174
22
P BRS047 Breast Cancer 97 0.159
23
P BLD134 Bladder Cancer 79 0.159
24
P PNM007 Pneumonia 68 0.159
25
FBR047 Fibromyalgia 58 0.159
26
P ALC033 Alcohol Use Disorder 58 0.159
27
P TRM003 Tremor 54 0.159
28
HYP003 Hypermethioninemia 40 0.159
29
P KDN018 Kidney Disease 72 0.142
30
P VSC007 Vascular Disease 63 0.142
31
ISC004 Ischemia 58 0.142
32
P NRP001 Neuropathy 56 0.142
33
ALC009 Alcoholic Liver Cirrhosis 53 0.142
34
VLV047 Volvulus of Midgut 49 0.142
35
VCC001 Vaccinia 49 0.142
36
VTM002 Vitamin B12 Deficiency 48 0.142
37
MTH074 Methionine Adenosyltransferase I/iii Deficiency 42 0.142
38
PYR009 Pyridoxine Deficiency Anemia 34 0.142
39
P PRK057 Parkinson Disease, Late-Onset 78 0.123
40
P LKM002 Leukemia 68 0.123
41
P HPT021 Hepatitis 67 0.123
42
OST159 Osteogenic Sarcoma 66 0.123
43
CHG001 Chagas Disease 66 0.123
44
P DYS154 Dystonia 65 0.123
45
P ADN016 Adenocarcinoma 64 0.123
46
MDD011 Mood Disorder 62 0.123
47
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.123
48
P FBR017 Fibrosarcoma 56 0.123
49
STM007 Stomatitis 50 0.123
50
47X002 47,xyy 49 0.123
51
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.123
52
P VSC018 Visceral Steatosis 33 0.123
53
HYP241 Hypermethioninemia Due to Adenosine Kinase Deficiency 32 0.123
54
MTH011 Methionine Adenosyltransferase Deficiency 18 0.123
55
P PNC035 Pancreatic Cancer 84 0.101
56
P GST053 Gastric Cancer 83 0.101
57
MLR004 Malaria 81 0.101
58
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.101
59
P SCH015 Schizophrenia 74 0.101
60
SVR004 Severe Combined Immunodeficiency 73 0.101
61
c CHR684 Chronic Kidney Disease 70 0.101
62
PLM001 Pulmonary Tuberculosis 69 0.101
63
P MLN008 Melanoma 69 0.101
64
P LKM062 Leukemia, Acute Lymphoblastic 69 0.101
65
ART002 Arts Syndrome 64 0.101
66
LSH001 Leishmaniasis 63 0.101
67
LSC001 Lesch-Nyhan Syndrome 62 0.101
68
ALC006 Alcoholic Hepatitis 61 0.101
69
CHL014 Cholera 59 0.101
70
P PRP019 Peripheral Nervous System Disease 58 0.101
71
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 56 0.101
72
c CHL134 Cholestasis, Benign Recurrent Intrahepatic, 1 56 0.101
73
P ART021 Arteriosclerosis 54 0.101
74
c MCR113 Microvascular Complications of Diabetes 3 52 0.101
75
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.101
76
HYP014 Hyperuricemia 52 0.101
77
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 52 0.101
78
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.101
79
CLR109 Colorectal Adenocarcinoma 51 0.101
80
END086 End Stage Renal Disease 51 0.101
81
c BCT013 Bacterial Pneumonia 48 0.101
82
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 48 0.101
83
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.101
84
c MCR120 Microvascular Complications of Diabetes 7 47 0.101
85
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.101
86
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.101
87
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.101
88
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.101
89
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.101
90
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.101
91
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.101
92
P KLZ004 Kala-Azar 1 41 0.101
93
c MCR130 Microvascular Complications of Diabetes 6 41 0.101
94
c MCR133 Microvascular Complications of Diabetes 4 41 0.101
95
CHL045 Choline Deficiency Disease 39 0.101
96
P LNG032 Lung Cancer 98 0.071
97
ESP021 Esophageal Cancer 90 0.071
98
P OVR042 Ovarian Cancer 88 0.071
99
NRL016 Neural Tube Defects 82 0.071
100
CYS001 Cystic Fibrosis 81 0.071
101
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.071
102
P RTT002 Rett Syndrome 80 0.071
103
P LKM071 Leukemia, Chronic Lymphocytic 79 0.071
104
IMM167 Immune Deficiency Disease 78 0.071
105
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.071
106
c HMC039 Hemochromatosis, Type 1 74 0.071
107
CRH001 Crohn's Disease 74 0.071
108
c HYP836 Hypercholesterolemia, Familial, 1 73 0.071
109
ULC004 Ulcerative Colitis 73 0.071
110
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.071
111
c HPT073 Hepatitis C Virus 72 0.071
112
P PHC003 Pheochromocytoma 71 0.071
113
HMN044 Human Immunodeficiency Virus Type 1 71 0.071
114
DFC004 Deficiency Anemia 70 0.071
115
BRN024 Bronchitis 68 0.071
116
P THR014 Thrombocytopenia 67 0.071
117
PSY004 Psychotic Disorder 67 0.071
118
c MGR028 Migraine with or Without Aura 1 67 0.071
119
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.071
120
ALC007 Alcohol Dependence 66 0.071
121
P HRP006 Herpes Simplex 65 0.071
122
ATH013 Atherosclerosis Susceptibility 65 0.071
123
P DBT009 Diabetes Mellitus 64 0.071
124
GT001 Gout 64 0.071
125
CLR108 Colorectal Adenoma 64 0.071
126
P HML002 Hemolytic Anemia 63 0.071
127
c PRC016 Pre-Eclampsia 63 0.071
128
P NTR004 Neutropenia 63 0.071
129
TRN015 Transient Cerebral Ischemia 63 0.071
130
c HPT001 Hepatitis C 62 0.071
131
c BRN108 Branchiootic Syndrome 1 62 0.071
132
c SVR001 Severe Acute Respiratory Syndrome 62 0.071
133
LPP008 Lipoprotein Quantitative Trait Locus 62 0.071
134
P HYP750 Hypertriglyceridemia, Familial 62 0.071
135
P ART023 Arthropathy 62 0.071
136
ALL026 Allergic Hypersensitivity Disease 62 0.071
137
TXC005 Toxic Shock Syndrome 62 0.071
138
P PRM006 Primary Biliary Cirrhosis 62 0.071
139
MSL001 Measles 62 0.071
140
c SCL052 Scleroderma, Familial Progressive 61 0.071
141
P PNC044 Pancreatitis 61 0.071
142
DPH001 Diphtheria 60 0.071
143
HPT019 Hepatic Encephalopathy 60 0.071
144
ACQ007 Acquired Immunodeficiency Syndrome 60 0.071
145
LNG099 Lung Disease 60 0.071
146
P HRD011 Hereditary Spherocytosis 60 0.071
147
P MCR010 Microcephaly 59 0.071
148
c HPT016 Hepatitis B 59 0.071
149
CHL123 Chlamydia 59 0.071
150
ADN018 Adenoma 59 0.071
151
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.071
152
ADR005 Adrenal Carcinoma 58 0.071
153
NWB001 Newborn Respiratory Distress Syndrome 58 0.071
154
P BNC003 Bone Cancer 58 0.071
155
P GLL018 Gallbladder Cancer 57 0.071
156
P GLL020 Gallbladder Disease 57 0.071
157
IRN002 Iron Metabolism Disease 57 0.071
158
P EXN002 Exanthem 57 0.071
159
CYT008 Cytomegalovirus Infection 57 0.071
160
HYP266 Hypoxia 57 0.071
161
P BPL003 Bipolar Disorder 56 0.071
162
LST001 Listeriosis 56 0.071
163
c ACT134 Acute Liver Failure 56 0.071
164
ERY051 Erythroleukemia, Familial 56 0.071
165
AGN016 Aging 56 0.071
166
P GST044 Gastritis 56 0.071
167
VSC003 Visceral Leishmaniasis 55 0.071
168
P SBS003 Substance Abuse 55 0.071
169
P INF037 Inflammatory Bowel Disease 54 0.071
170
DBT010 Diabetic Neuropathy 54 0.071
171
TRC003 Trichomoniasis 53 0.071
172
c GLL024 Gallbladder Disease 1 53 0.071
173
OVR059 Ovary Adenocarcinoma 53 0.071
174
DMY004 Demyelinating Disease 52 0.071
175
ART140 Arteries, Anomalies of 52 0.071
176
P CNG436 Congenital Disorder of Deglycosylation 52 0.071
177
PTH003 Pathologic Nystagmus 52 0.071
178
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.071
179
TRM010 Traumatic Brain Injury 51 0.071
180
c MTC063 Mitochondrial Dna Depletion Syndrome 3 51 0.071
181
MNN009 Meningoencephalitis 49 0.071
182
BRN071 Brain Injury 49 0.071
183
CRY014 Cryptococcal Meningitis 48 0.071
184
SPL018 Splenomegaly 48 0.071
185
HLX001 Helix Syndrome 47 0.071
186
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 47 0.071
187
ADN001 Adenosine Deaminase Deficiency 47 0.071
188
c INH020 Inherited Metabolic Disorder 47 0.071
189
SRT004 Serotonin Syndrome 47 0.071
190
ADR040 Adrenal Gland Pheochromocytoma 46 0.071
191
EPD015 Epidemic Typhus 45 0.071
192
HPT004 Hepatic Coma 45 0.071
193
URL001 Urolithiasis 45 0.071
194
ASP008 Aspiration Pneumonitis 45 0.071
195
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.071
196
P CHR345 Chronic Pain 44 0.071
197
c PCH010 Pachyonychia Congenita 3 44 0.071
198
CVD001 Covid-19 44 0.071
199
ADN022 Adenylosuccinase Deficiency 44 0.071
200
CRB090 Cerebral Hypoxia 44 0.071
201
NNS032 Non-Syndromic X-Linked Intellectual Disability 43 0.071
202
P HYP265 Hypotonia 43 0.071
203
SNL007 Senile Cataract 42 0.071
204
49X006 49, Xxxxy Syndrome 41 0.071
205
c MJR024 Major Affective Disorder 9 41 0.071
206
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.071
207
MLY001 Molybdenum Cofactor Deficiency 40 0.071
208
UTR043 Uterine Sarcoma 39 0.071
209
GLY015 Glycine N-Methyltransferase Deficiency 39 0.071
210
SYN089 Syndromic X-Linked Intellectual Disability Snyder Type 39 0.071
211
48X005 48,xyyy 39 0.071
212
MNT310 Mental Retardation, X-Linked, Syndromic, Snyder-Robinson Type 38 0.071
213
c MJR022 Major Affective Disorder 8 38 0.071
214
CRT055 Creatine Deficiency Syndromes 38 0.071
215
HMM004 Hamamy Syndrome 37 0.071
216
CRY036 Cryptogenic Cirrhosis 36 0.071
217
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.071
218
SPS016 Spasmodic Dysphonia 31 0.071
219
PYR016 Pyridoxine Deficiency 30 0.071
220
DSR074 Disorder of Purine Metabolism 29 0.071
221
SPS134 Spasmodic Dystonia 27 0.071
222
CHL079 Children's Interstitial Lung Disease 26 0.071
223
c PRM243 Primary Bone Cancer 24 0.071
224
c CHR121 Charcot-Marie-Tooth Neuropathy X Type 5 15 0.071
225
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 13 0.071
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