Search results for s-adenosylhomocysteine

312 hits were found for s-adenosylhomocysteine

# Family MCID Name MIFTS Score
1
HYP814 Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency 34 81.114
2
HYP003 Hypermethioninemia 51 22.852
3
HMC014 Homocysteinemia 52 13.318
4
VCC001 Vaccinia 47 7.336
5
P VSC007 Vascular Disease 63 7.240
6
P LVR013 Liver Disease 69 6.939
7
ADN001 Adenosine Deaminase Deficiency 59 6.565
8
STM007 Stomatitis 54 6.062
9
P HMC002 Homocystinuria 53 5.841
10
NNL005 Non-Alcoholic Fatty Liver Disease 63 5.732
11
P MYP004 Myopathy 67 5.687
12
c CHR684 Chronic Kidney Disease 69 5.200
13
P NRB001 Neuroblastoma 66 4.946
14
FTT001 Fatty Liver Disease 62 4.617
15
HYP241 Hypermethioninemia Due to Adenosine Kinase Deficiency 37 4.572
16
P HYP265 Hypotonia 42 4.524
17
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 4.373
18
P HPT023 Hepatocellular Carcinoma 96 4.182
19
ATH013 Atherosclerosis Susceptibility 63 4.027
20
NRL016 Neural Tube Defects 81 3.734
21
PYR009 Pyridoxine Deficiency Anemia 35 3.570
22
VTM002 Vitamin B12 Deficiency 48 3.510
23
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 3.457
24
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 50 3.434
25
P KDN018 Kidney Disease 72 3.434
26
GLY015 Glycine N-Methyltransferase Deficiency 40 3.419
27
CMB007 Combined Immunodeficiency 57 3.294
28
SVR004 Severe Combined Immunodeficiency 72 3.294
29
MLD018 Mild Cognitive Impairment 48 3.177
30
P LKM062 Leukemia, Acute Lymphoblastic 69 3.177
31
URM002 Uremia 47 3.144
32
CHL045 Choline Deficiency Disease 39 3.144
33
LYM017 Lyme Disease 62 3.054
34
CYS001 Cystic Fibrosis 78 3.052
35
END086 End Stage Renal Disease 52 3.052
36
PYR016 Pyridoxine Deficiency 29 3.052
37
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 49 3.033
38
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 47 2.773
39
BRK010 Burkitt Lymphoma 66 2.612
40
THR024 Thrombosis 56 2.612
41
48X005 48,xyyy 39 2.612
42
HYP266 Hypoxia 57 2.612
43
P ART021 Arteriosclerosis 54 2.553
44
HMN044 Human Immunodeficiency Virus Type 1 78 2.429
45
ATS010 Autosomal Recessive Disease 42 2.429
46
CHL014 Cholera 62 2.429
47
LSC001 Lesch-Nyhan Syndrome 62 2.407
48
P PRK057 Parkinson Disease, Late-Onset 80 2.407
49
c MCR130 Microvascular Complications of Diabetes 6 41 2.407
50
c MCR120 Microvascular Complications of Diabetes 7 47 2.407
51
P ALC033 Alcohol Use Disorder 61 2.407
52
LYM027 Lymphopenia 56 2.407
53
c MCR113 Microvascular Complications of Diabetes 3 52 2.407
54
c MCR133 Microvascular Complications of Diabetes 4 41 2.407
55
P ENC018 Encephalopathy 62 2.407
56
DWN001 Down Syndrome 70 2.261
57
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 2.246
58
NNL006 Non-Alcoholic Steatohepatitis 54 2.246
59
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 2.246
60
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 2.246
61
c ACT134 Acute Liver Failure 59 2.213
62
IMM167 Immune Deficiency Disease 78 2.213
63
HPT004 Hepatic Coma 43 2.213
64
CRN030 Coronary Stenosis 50 2.213
65
HLX001 Helix Syndrome 48 2.213
66
HPT019 Hepatic Encephalopathy 59 2.213
67
P MCR010 Microcephaly 60 2.213
68
c THR092 Thrombophilia Due to Thrombin Defect 74 2.064
69
PRP027 Peripheral Vascular Disease 71 2.064
70
EXT007 Extracutaneous Mastocytoma 38 2.064
71
YLL002 Yellow Fever 61 2.064
72
MST004 Mast Cell Neoplasm 42 2.064
73
MGL001 Megaloblastic Anemia 58 2.064
74
P HML002 Hemolytic Anemia 62 1.930
75
PLS011 Plasmacytoma 56 1.930
76
P HRD011 Hereditary Spherocytosis 64 1.930
77
c INH030 Inherited Retinal Disorder 28 1.847
78
NRM022 Neurometabolic Disease 24 1.847
79
P RTT002 Rett Syndrome 79 1.847
80
P PHC003 Pheochromocytoma 69 1.847
81
P ATX030 Ataxia-Telangiectasia 80 1.847
82
CLR108 Colorectal Adenoma 64 1.847
83
P CHN012 Chondrosarcoma 57 1.847
84
FCT007 Factor Vii Deficiency 64 1.847
85
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 1.847
86
ADR040 Adrenal Gland Pheochromocytoma 46 1.847
87
P PRK039 Parkinsonism 55 1.847
88
FND002 Fundus Dystrophy 55 1.847
89
c HPT001 Hepatitis C 62 1.847
90
ADN018 Adenoma 59 1.847
91
P RTN016 Retinal Degeneration 52 1.847
92
TLN003 Telangiectasis 51 1.847
93
CRY003 Cryptosporidiosis 56 1.847
94
P RSP003 Respiratory Failure 74 1.847
95
P EYD002 Eye Disease 57 1.847
96
P RTN018 Retinal Disease 53 1.847
97
SQM006 Squamous Cell Carcinoma 60 1.847
98
P CRD246 Cardiovascular System Disease 56 1.840
99
P ATS364 Autism 69 1.804
100
MSL001 Measles 61 1.804
101
ACT098 Acute Erythroid Leukemia 55 1.670
102
c HYP836 Hypercholesterolemia, Familial, 1 73 1.670
103
P HRP006 Herpes Simplex 65 1.670
104
CHC001 Chickenpox 57 1.670
105
MTH011 Methionine Adenosyltransferase Deficiency 18 1.670
106
STR077 Streptococcal Toxic-Shock Syndrome 35 1.565
107
P MYS005 Myositis 56 1.565
108
P EXN002 Exanthem 58 1.565
109
DFC004 Deficiency Anemia 74 1.565
110
ACT119 Acute Promyelocytic Leukemia 62 1.565
111
ESP021 Esophageal Cancer 83 1.565
112
CLR109 Colorectal Adenocarcinoma 50 1.565
113
P TRM003 Tremor 48 1.565
114
GLL048 Glial Tumor 52 1.565
115
47X002 47,xyy 48 1.565
116
TRC003 Trichomoniasis 53 1.565
117
IMP004 Impetigo 48 1.565
118
c DLT002 Dilated Cardiomyopathy 78 1.565
119
PNC001 Pancytopenia 53 1.565
120
TXC005 Toxic Shock Syndrome 62 1.565
121
P END033 Endocarditis 58 1.565
122
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 1.565
123
PHR003 Pharyngitis 58 1.565
124
IRN002 Iron Metabolism Disease 57 1.565
125
P MTR003 Mitral Valve Stenosis 53 1.565
126
HMP009 Haemophilus Influenzae 41 1.565
127
GLM045 Glioma 63 1.565
128
c LKM061 Leukemia, Acute Myeloid 83 1.524
129
MTH074 Methionine Adenosyltransferase I/iii Deficiency 42 1.524
130
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.524
131
c ATS007 Autism Spectrum Disorder 72 1.363
132
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 48 1.363
133
P PRS040 Prostate Cancer 95 1.363
134
P NRP001 Neuropathy 60 1.363
135
HYP066 Hyperglycemia 61 1.363
136
P HYP086 Hypothyroidism 69 1.363
137
CHL068 Cholestasis 61 1.363
138
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 34 1.363
139
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 1.264
140
HNM002 Hinman Syndrome 27 1.264
141
c CNG415 Congenital Disorder of Glycosylation, Type Ia 59 1.264
142
HYD038 Hydrops Fetalis, Nonimmune 59 1.264
143
ADP007 Adie Pupil 40 1.264
144
ADL002 Adult Syndrome 70 1.264
145
P MYC084 Mycobacterium Tuberculosis 1 68 1.181
146
PPL052 Papillomatosis, Confluent and Reticulated 34 1.181
147
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 1.181
148
P CLR023 Colorectal Cancer 100 1.181
149
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 1.181
150
EPD015 Epidemic Typhus 44 1.181
151
MLR004 Malaria 80 1.181
152
WLS001 Wilson Disease 70 1.181
153
THR100 Thrombocytopenic Purpura, Autoimmune 61 1.181
154
P RTN024 Retinoblastoma 73 1.181
155
P RHB003 Rhabdomyosarcoma 66 1.181
156
P LKM002 Leukemia 67 1.181
157
P ADN016 Adenocarcinoma 63 1.181
158
CHL123 Chlamydia 58 1.181
159
c INH020 Inherited Metabolic Disorder 48 1.181
160
CRB039 Cerebrovascular Disease 66 1.181
161
P HYP076 Hyperthyroidism 53 1.181
162
PLC008 Placenta Disease 49 1.181
163
PRP030 Purpura 54 1.181
164
VSC002 Vascular Dementia 60 1.181
165
HYP056 Hypoglycemia 65 1.181
166
CHR178 Chromosomal Triplication 34 1.181
167
END072 Endotheliitis 36 1.159
168
P ALZ034 Alzheimer Disease 87 0.964
169
ART140 Arteries, Anomalies of 53 0.964
170
ANN002 Anencephaly 57 0.964
171
AGN016 Aging 54 0.964
172
LPP008 Lipoprotein Quantitative Trait Locus 65 0.964
173
P CTN015 Cutaneous T Cell Lymphoma 48 0.964
174
c PCH010 Pachyonychia Congenita 3 43 0.964
175
MYL069 Myeloma, Multiple 77 0.964
176
OCL069 Ocular Motor Apraxia 57 0.964
177
P HYP750 Hypertriglyceridemia, Familial 62 0.964
178
TRM010 Traumatic Brain Injury 51 0.964
179
P MYL006 Myeloid Leukemia 61 0.964
180
P MVM001 Movement Disease 61 0.964
181
OVR059 Ovary Adenocarcinoma 49 0.964
182
ALC006 Alcoholic Hepatitis 61 0.964
183
c ACT027 Acute Pancreatitis 60 0.964
184
SPT005 Spotted Fever 49 0.964
185
P PNC044 Pancreatitis 61 0.964
186
P THR015 Thrombophilia 51 0.964
187
c ATS204 Autosomal Recessive Non-Syndromic Intellectual Disability 48 0.964
188
HYP060 Hyperinsulinism 54 0.964
189
P MYC008 Myocarditis 59 0.964
190
CYT002 Cytokine Deficiency 43 0.964
191
EXN003 Exencephaly 30 0.964
192
OVR094 Ovarian Epithelial Cancer 39 0.964
193
c PRG020 Paragangliomas 3 39 0.883
194
P CNG436 Congenital Disorder of Deglycosylation 51 0.883
195
NWC001 Newcastle Disease 47 0.883
196
PTH003 Pathologic Nystagmus 52 0.883
197
ANX004 Anoxia 40 0.682
198
c BCT007 Bacterial Meningitis 55 0.682
199
P DBT005 Diabetes Insipidus 54 0.682
200
VNZ002 Venezuelan Equine Encephalitis 46 0.682
201
PRN071 Parenteral Nutrition-Associated Cholestasis 23 0.682
202
NNS045 Non-Specific Syndromic Intellectual Disability 42 0.682
204
PNM013 Pneumococcal Meningitis 43 0.682
205
P THL005 Thalassemia 56 0.682
206
P OVR082 Overgrowth Syndrome 49 0.682
207
P BLD134 Bladder Cancer 79 0.682
208
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.682
209
c OTP006 Otopalatodigital Syndrome, Type I 60 0.682
210
PRS129 Prostatic Hyperplasia, Benign 49 0.682
211
c SCL052 Scleroderma, Familial Progressive 61 0.682
212
KR002 Kuru 45 0.682
213
c MTC063 Mitochondrial Dna Depletion Syndrome 3 51 0.682
214
END057 Endometrial Cancer 72 0.682
215
P OVR042 Ovarian Cancer 88 0.682
216
ATM095 Autoimmune Disease 61 0.682
217
P BRS047 Breast Cancer 98 0.682
218
ALC007 Alcohol Dependence 66 0.682
219
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.682
220
P PLM037 Pulmonary Hypertension 72 0.682
221
MNT001 Mantle Cell Lymphoma 67 0.682
222
VRL003 Variola Major 43 0.682
223
BTN004 Biotin Deficiency 45 0.682
224
P PLY014 Polycystic Kidney Disease 69 0.682
225
SBJ001 Subjective Cognitive Decline 30 0.682
226
MYL020 Myelomeningocele 51 0.682
227
P LYM118 Lymphoma 67 0.682
228
CHR103 Charge Syndrome 66 0.682
229
CRN264 Craniosynostosis with Fibular Aplasia 29 0.682
230
VSC053 Visceral Steatosis, Congenital 34 0.682
231
c TYR012 Tyrosinemia, Type I 61 0.682
232
P STS008 Sotos Syndrome 1 60 0.682
233
HSH003 Hashimoto Thyroiditis 60 0.682
234
c DPH024 Diaphragmatic Hernia, Congenital 64 0.682
235
c GRV009 Graves Disease 2 14 0.682
236
P CTR177 Citrullinemia, Type Ii, Adult-Onset 55 0.682
237
CRP030 Corpus Callosum, Agenesis of, with Facial Anomalies and Cerebellar Ataxia 37 0.682
238
P MJR001 Major Depressive Disorder 68 0.682
239
CFF002 Coffin-Lowry Syndrome 60 0.682
240
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 68 0.682
241
HYP114 Hypertensive Nephropathy 36 0.682
242
c HYD064 Hydrocephalus, Congenital, 1 51 0.682
243
PLY158 Polyglucosan Body Neuropathy, Adult Form 39 0.682
244
GLC012 Galactosialidosis 56 0.682
245
c PNC106 Pancreatic Agenesis 1 51 0.682
246
c TBR025 Tuberous Sclerosis 1 84 0.682
247
c HYP595 Hypertension, Essential 85 0.682
248
P MYC007 Myocardial Infarction 70 0.682
249
BCT022 Bacterial Infectious Disease 56 0.682
250
PRM329 Premature Aging 36 0.682
251
PRT037 Pertussis 65 0.682
252
c ACT073 Acute Leukemia 58 0.682
253
CWP001 Cowpox 45 0.682
254
P BCL017 B-Cell Lymphoma 59 0.682
255
P MSC003 Muscular Atrophy 52 0.682
256
BRN004 Brain Edema 54 0.682
257
P EMB005 Embryonal Rhabdomyosarcoma 53 0.682
258
CRC021 Carcinosarcoma 64 0.682
259
P NRC002 Narcolepsy 56 0.682
260
P TYR004 Tyrosinemia 50 0.682
261
P DBT009 Diabetes Mellitus 67 0.682
262
SML019 Smallpox 55 0.682
263
PST092 Posttransplant Acute Limbic Encephalitis 28 0.682
264
P ALP008 Alopecia 54 0.682
265
GLB002 Glioblastoma 67 0.682
266
P OPT006 Optic Nerve Disease 58 0.682
267
MNK002 Monkeypox 41 0.682
268
TRT001 Teratocarcinoma 42 0.682
269
P SKN015 Skin Carcinoma 71 0.682
270
MNT002 Mental Depression 57 0.682
271
P CCK001 Cockayne Syndrome 68 0.682
272
P MMP001 Mumps 57 0.682
273
P LNG064 Lung Cancer Susceptibility 3 70 0.682
274
c PRC016 Pre-Eclampsia 65 0.682
275
P GRV001 Graves' Disease 55 0.682
276
P SPN046 Spinal Muscular Atrophy 63 0.682
277
CRT013 Carotid Stenosis 51 0.682
278
PPL022 Papilloma 53 0.682
279
HRY003 Hairy Cell Leukemia 61 0.682
280
PRS021 Prostatic Adenoma 43 0.682
281
SQM002 Squamous Cell Papilloma 46 0.682
282
PSY004 Psychotic Disorder 66 0.682
283
BCL002 B Cell Deficiency 41 0.682
284
P HMR003 Hemorrhagic Disease 59 0.682
285
P TBR001 Tuberous Sclerosis 69 0.682
286
P GLY013 Glycogen Storage Disease 60 0.682
287
DPH001 Diphtheria 59 0.682
288
RBS001 Rabies 58 0.682
289
PRS045 Prostatic Hypertrophy 53 0.682
290
TRC008 Trachoma 53 0.682
291
KRT002 Keratomalacia 55 0.682
292
THY030 Thyroid Gland Disease 50 0.682
293
CPP004 Copper Deficiency Myelopathy 28 0.682
294
PLM031 Poliomyelitis 63 0.682
295
P PRP019 Peripheral Nervous System Disease 58 0.682
296
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.682
297
LPD008 Lipid Metabolism Disorder 62 0.682
298
P TCD001 Tic Disorder 49 0.682
299
GST045 Gastroenteritis 58 0.682
300
GNR003 Generalized Atherosclerosis 43 0.682
301
PNC034 Pancreas Disease 50 0.682
302
P PLY019 Polyneuropathy 52 0.682
303
HMN048 Human Papillomavirus Infectious Disease 46 0.682
304
P MNN013 Meningitis 65 0.682
305
c LKM005 Leukemia, T-Cell, Chronic 34 0.682
306
SFT003 Soft Tissue Sarcoma 57 0.682
307
DPR016 Depression 65 0.682
308
CRT055 Creatine Deficiency Syndromes 37 0.682
309
P MTC069 Mitochondrial Disorders 57 0.682
310
BRN071 Brain Injury 50 0.682
311
DWR001 Dwarfism 44 0.682
312
PNF002 Painful Legs and Moving Toes Syndrome 14 0.682
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