Search results for s-adenosylhomocysteine

314 hits were found for s-adenosylhomocysteine

# Family MCID Name MIFTS Score
1
HYP814 Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency 34 95.231
2
HYP003 Hypermethioninemia 51 20.816
3
HMC014 Homocysteinemia 52 6.569
4
P LVR013 Liver Disease 68 4.435
5
VCC001 Vaccinia 49 4.397
6
P VSC007 Vascular Disease 62 4.004
7
P MYP004 Myopathy 67 3.993
8
HYP241 Hypermethioninemia Due to Adenosine Kinase Deficiency 38 3.829
9
ADN001 Adenosine Deaminase Deficiency 59 3.626
10
STM007 Stomatitis 52 3.608
11
P HPT023 Hepatocellular Carcinoma 95 2.931
12
P HYP265 Hypotonia 42 2.752
13
P NRB001 Neuroblastoma 66 2.655
14
NNL005 Non-Alcoholic Fatty Liver Disease 63 2.605
15
P HMC002 Homocystinuria 52 2.605
16
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 48 2.506
17
ATH013 Atherosclerosis Susceptibility 63 2.330
18
PYR009 Pyridoxine Deficiency Anemia 35 2.216
19
c CHR684 Chronic Kidney Disease 73 2.166
20
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 2.064
21
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 2.011
22
LYM017 Lyme Disease 63 1.910
23
FTT001 Fatty Liver Disease 61 1.830
24
VTM002 Vitamin B12 Deficiency 48 1.813
25
GLY015 Glycine N-Methyltransferase Deficiency 40 1.803
26
CMB007 Combined Immunodeficiency 56 1.759
27
SVR004 Severe Combined Immunodeficiency 70 1.759
28
P LKM062 Leukemia, Acute Lymphoblastic 69 1.730
29
MLD018 Mild Cognitive Impairment 48 1.730
30
END086 End Stage Renal Disease 54 1.730
31
CYS001 Cystic Fibrosis 77 1.699
32
PYR016 Pyridoxine Deficiency 29 1.699
33
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 47 1.629
34
BRK010 Burkitt Lymphoma 65 1.589
35
THR024 Thrombosis 56 1.589
36
ATS010 Autosomal Recessive Disease 42 1.543
37
HMN044 Human Immunodeficiency Virus Type 1 76 1.543
38
CHL014 Cholera 62 1.543
39
HYP266 Hypoxia 56 1.543
40
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 50 1.542
41
P KDN018 Kidney Disease 71 1.519
42
HLX001 Helix Syndrome 47 1.489
43
IMM167 Immune Deficiency Disease 76 1.489
44
HPT019 Hepatic Encephalopathy 59 1.489
45
CRN030 Coronary Stenosis 50 1.489
46
P MCR010 Microcephaly 59 1.489
47
HPT004 Hepatic Coma 43 1.489
48
c ACT134 Acute Liver Failure 57 1.489
49
URM002 Uremia 47 1.447
50
CHL045 Choline Deficiency Disease 39 1.447
51
DFC004 Deficiency Anemia 74 1.419
52
PLS011 Plasmacytoma 56 1.419
53
P HRD011 Hereditary Spherocytosis 63 1.419
54
P HML002 Hemolytic Anemia 62 1.419
55
P CRD246 Cardiovascular System Disease 55 1.328
56
P ART021 Arteriosclerosis 53 1.300
57
HYD038 Hydrops Fetalis, Nonimmune 57 1.265
58
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 1.265
59
c CNG415 Congenital Disorder of Glycosylation, Type Ia 58 1.265
60
ADP007 Adie Pupil 40 1.265
61
ADL002 Adult Syndrome 69 1.265
62
HNM002 Hinman Syndrome 29 1.265
63
LSC001 Lesch-Nyhan Syndrome 62 1.263
64
c MCR133 Microvascular Complications of Diabetes 4 41 1.263
65
c MCR113 Microvascular Complications of Diabetes 3 52 1.263
66
c MCR130 Microvascular Complications of Diabetes 6 41 1.263
67
c MCR120 Microvascular Complications of Diabetes 7 47 1.263
68
P PRK057 Parkinson Disease, Late-Onset 79 1.263
69
P ALC033 Alcohol Use Disorder 67 1.263
70
LYM027 Lymphopenia 56 1.263
71
P ENC018 Encephalopathy 62 1.263
72
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 1.223
73
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.223
74
NNL006 Non-Alcoholic Steatohepatitis 54 1.223
75
AGN016 Aging 53 1.178
76
PRP027 Peripheral Vascular Disease 71 1.178
77
c THR092 Thrombophilia Due to Thrombin Defect 74 1.178
78
MST004 Mast Cell Neoplasm 41 1.178
79
MGL001 Megaloblastic Anemia 59 1.178
80
EXT007 Extracutaneous Mastocytoma 38 1.178
81
YLL002 Yellow Fever 61 1.178
82
48X005 48,xyyy 39 1.178
83
END072 Endotheliitis 36 1.158
84
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.124
85
P RTT002 Rett Syndrome 79 1.124
86
P ATX030 Ataxia-Telangiectasia 80 1.124
87
P CHN012 Chondrosarcoma 56 1.124
88
P PHC003 Pheochromocytoma 70 1.124
89
FCT007 Factor Vii Deficiency 64 1.124
90
ADR040 Adrenal Gland Pheochromocytoma 45 1.124
91
P RSP003 Respiratory Failure 73 1.124
92
P PRK039 Parkinsonism 55 1.124
93
CLR108 Colorectal Adenoma 63 1.124
94
SQM006 Squamous Cell Carcinoma 59 1.124
95
P EYD002 Eye Disease 57 1.124
96
ADN018 Adenoma 58 1.124
97
c HPT001 Hepatitis C 61 1.124
98
CRY003 Cryptosporidiosis 55 1.124
99
TLN003 Telangiectasis 51 1.124
100
P RTN018 Retinal Disease 53 1.124
101
P RTN016 Retinal Degeneration 52 1.124
102
FND002 Fundus Dystrophy 54 1.124
103
c INH030 Inherited Retinal Disorder 28 1.124
104
NRM022 Neurometabolic Disease 24 1.124
105
ACT119 Acute Promyelocytic Leukemia 62 1.053
106
P EXN002 Exanthem 58 1.053
107
P MYS005 Myositis 55 1.053
108
ESP021 Esophageal Cancer 84 1.053
109
STR077 Streptococcal Toxic-Shock Syndrome 34 1.053
110
CLR109 Colorectal Adenocarcinoma 50 1.053
111
PNC001 Pancytopenia 52 1.053
112
PHR003 Pharyngitis 57 1.053
113
TRC003 Trichomoniasis 53 1.053
114
IRN002 Iron Metabolism Disease 56 1.053
115
P MTR003 Mitral Valve Stenosis 53 1.053
116
P END033 Endocarditis 58 1.053
117
c DLT002 Dilated Cardiomyopathy 79 1.053
118
TXC005 Toxic Shock Syndrome 61 1.053
119
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 1.053
120
IMP004 Impetigo 48 1.053
121
GLM045 Glioma 62 1.053
122
47X002 47,xyy 47 1.053
123
HMP009 Haemophilus Influenzae 41 1.053
124
P TRM003 Tremor 50 1.053
125
GLL048 Glial Tumor 51 1.053
126
NRL016 Neural Tube Defects 80 0.931
127
c PRG020 Paragangliomas 3 39 0.883
128
P CNG436 Congenital Disorder of Deglycosylation 51 0.883
129
NWC001 Newcastle Disease 47 0.883
130
PTH003 Pathologic Nystagmus 52 0.883
131
DWN001 Down Syndrome 70 0.564
132
P ATS364 Autism 72 0.510
133
MSL001 Measles 61 0.450
134
c ATS007 Autism Spectrum Disorder 71 0.416
135
c HYP836 Hypercholesterolemia, Familial, 1 73 0.416
136
ACT098 Acute Erythroid Leukemia 55 0.416
137
MTH011 Methionine Adenosyltransferase Deficiency 18 0.416
138
CHC001 Chickenpox 56 0.416
139
P HRP006 Herpes Simplex 65 0.416
140
MTH074 Methionine Adenosyltransferase I/iii Deficiency 43 0.380
141
c LKM061 Leukemia, Acute Myeloid 83 0.380
142
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.380
143
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 36 0.380
144
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 48 0.340
145
CHL068 Cholestasis 61 0.340
146
P HYP086 Hypothyroidism 68 0.340
147
HYP066 Hyperglycemia 60 0.340
148
P NRP001 Neuropathy 59 0.340
149
MLR004 Malaria 77 0.294
150
PPL052 Papillomatosis, Confluent and Reticulated 34 0.294
151
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.294
152
P RTN024 Retinoblastoma 72 0.294
153
P CLR023 Colorectal Cancer 100 0.294
154
WLS001 Wilson Disease 70 0.294
155
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.294
156
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.294
157
P MYC084 Mycobacterium Tuberculosis 1 68 0.294
158
EPD015 Epidemic Typhus 44 0.294
159
CHL123 Chlamydia 58 0.294
160
P LKM002 Leukemia 65 0.294
161
PRP030 Purpura 54 0.294
162
P ADN016 Adenocarcinoma 63 0.294
163
P RHB003 Rhabdomyosarcoma 66 0.294
164
c INH020 Inherited Metabolic Disorder 47 0.294
165
CRB039 Cerebrovascular Disease 65 0.294
166
PLC008 Placenta Disease 48 0.294
167
VSC002 Vascular Dementia 59 0.294
168
P HYP076 Hyperthyroidism 53 0.294
169
CHR178 Chromosomal Triplication 33 0.294
170
HYP056 Hypoglycemia 65 0.294
171
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.240
172
P CTN015 Cutaneous T Cell Lymphoma 48 0.240
173
c ATS204 Autosomal Recessive Non-Syndromic Intellectual Disability 47 0.240
174
P ALZ034 Alzheimer Disease 87 0.240
175
ART140 Arteries, Anomalies of 52 0.240
176
P PRS040 Prostate Cancer 95 0.240
177
OCL069 Ocular Motor Apraxia 57 0.240
178
LPP008 Lipoprotein Quantitative Trait Locus 65 0.240
179
ANN002 Anencephaly 57 0.240
180
P HYP750 Hypertriglyceridemia, Familial 61 0.240
181
MYL069 Myeloma, Multiple 76 0.240
182
c PCH010 Pachyonychia Congenita 3 43 0.240
183
HYP060 Hyperinsulinism 53 0.240
184
P THR015 Thrombophilia 51 0.240
185
P MVM001 Movement Disease 61 0.240
186
P PNC044 Pancreatitis 61 0.240
187
c ACT027 Acute Pancreatitis 60 0.240
188
ALC006 Alcoholic Hepatitis 61 0.240
189
SPT005 Spotted Fever 49 0.240
190
OVR059 Ovary Adenocarcinoma 49 0.240
191
P MYL006 Myeloid Leukemia 60 0.240
192
P MYC008 Myocarditis 59 0.240
193
CYT002 Cytokine Deficiency 43 0.240
194
OVR094 Ovarian Epithelial Cancer 39 0.240
195
TRM010 Traumatic Brain Injury 50 0.240
196
EXN003 Exencephaly 30 0.240
197
MYL020 Myelomeningocele 51 0.170
198
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.170
199
P LYM118 Lymphoma 66 0.170
200
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.170
201
P OVR042 Ovarian Cancer 88 0.170
202
c SCL052 Scleroderma, Familial Progressive 60 0.170
203
c GLY007 Glycogen Storage Disease Iv 58 0.170
204
c HYD064 Hydrocephalus, Congenital, 1 51 0.170
205
KR002 Kuru 45 0.170
206
c MTC063 Mitochondrial Dna Depletion Syndrome 3 51 0.170
207
GLC012 Galactosialidosis 55 0.170
208
c OTP006 Otopalatodigital Syndrome, Type I 59 0.170
209
ALC007 Alcohol Dependence 65 0.170
210
P BLD134 Bladder Cancer 79 0.170
211
PLY158 Polyglucosan Body Neuropathy, Adult Form 39 0.170
212
c TYR012 Tyrosinemia, Type I 61 0.170
213
CFF002 Coffin-Lowry Syndrome 59 0.170
214
P BRS047 Breast Cancer 97 0.170
215
c GRV009 Graves Disease 2 14 0.170
216
P CTR177 Citrullinemia, Type Ii, Adult-Onset 56 0.170
217
VRL003 Variola Major 43 0.170
218
CRP030 Corpus Callosum, Agenesis of, with Facial Anomalies and Cerebellar Ataxia 37 0.170
219
P PLM037 Pulmonary Hypertension 69 0.170
220
HYP114 Hypertensive Nephropathy 35 0.170
221
c PNC106 Pancreatic Agenesis 1 51 0.170
222
CHR103 Charge Syndrome 65 0.170
223
CRN264 Craniosynostosis with Fibular Aplasia 29 0.170
224
c TBR025 Tuberous Sclerosis 1 84 0.170
225
HSH003 Hashimoto Thyroiditis 60 0.170
226
c DPH024 Diaphragmatic Hernia, Congenital 63 0.170
227
P STS008 Sotos Syndrome 1 62 0.170
228
P MYC007 Myocardial Infarction 69 0.170
229
P MJR001 Major Depressive Disorder 68 0.170
230
ATM095 Autoimmune Disease 61 0.170
231
c HYP595 Hypertension, Essential 84 0.170
232
VSC053 Visceral Steatosis, Congenital 35 0.170
233
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 68 0.170
234
END057 Endometrial Cancer 76 0.170
235
PRS129 Prostatic Hyperplasia, Benign 48 0.170
236
P LNG064 Lung Cancer Susceptibility 3 69 0.170
237
MNT001 Mantle Cell Lymphoma 65 0.170
238
BTN004 Biotin Deficiency 44 0.170
239
P MMP001 Mumps 56 0.170
240
HMN048 Human Papillomavirus Infectious Disease 45 0.170
241
RBS001 Rabies 57 0.170
242
TRC008 Trachoma 53 0.170
243
SBJ001 Subjective Cognitive Decline 29 0.170
244
DPH001 Diphtheria 59 0.170
245
P PLY014 Polycystic Kidney Disease 71 0.170
246
GNR003 Generalized Atherosclerosis 42 0.170
247
P HMR003 Hemorrhagic Disease 59 0.170
248
MNK002 Monkeypox 41 0.170
249
P TCD001 Tic Disorder 50 0.170
250
GLB002 Glioblastoma 67 0.170
251
PPL022 Papilloma 53 0.170
252
P GLY013 Glycogen Storage Disease 59 0.170
253
HRY003 Hairy Cell Leukemia 53 0.170
254
BCL002 B Cell Deficiency 40 0.170
255
P TBR001 Tuberous Sclerosis 69 0.170
256
P SPN046 Spinal Muscular Atrophy 62 0.170
257
BCT022 Bacterial Infectious Disease 55 0.170
258
BRN004 Brain Edema 54 0.170
259
P PRP019 Peripheral Nervous System Disease 57 0.170
260
CPP004 Copper Deficiency Myelopathy 28 0.170
261
LPD008 Lipid Metabolism Disorder 61 0.170
262
P EMB005 Embryonal Rhabdomyosarcoma 53 0.170
263
GST045 Gastroenteritis 58 0.170
264
P OPT006 Optic Nerve Disease 57 0.170
265
P PLY019 Polyneuropathy 52 0.170
266
SQM002 Squamous Cell Papilloma 45 0.170
267
PNC034 Pancreas Disease 49 0.170
268
PLM031 Poliomyelitis 62 0.170
269
THY030 Thyroid Gland Disease 50 0.170
270
CRC021 Carcinosarcoma 62 0.170
271
PRS021 Prostatic Adenoma 43 0.170
272
PSY004 Psychotic Disorder 66 0.170
273
TRT001 Teratocarcinoma 41 0.170
274
P SKN015 Skin Carcinoma 71 0.170
275
P CCK001 Cockayne Syndrome 67 0.170
276
P GRV001 Graves' Disease 54 0.170
277
c ACT073 Acute Leukemia 59 0.170
278
PRS045 Prostatic Hypertrophy 53 0.170
279
KRT002 Keratomalacia 54 0.170
280
CRT013 Carotid Stenosis 51 0.170
281
c PRC016 Pre-Eclampsia 64 0.170
282
MNT002 Mental Depression 56 0.170
283
PRT037 Pertussis 49 0.170
284
CRT055 Creatine Deficiency Syndromes 38 0.170
285
P TYR004 Tyrosinemia 49 0.170
286
P DBT009 Diabetes Mellitus 67 0.170
287
P NRC002 Narcolepsy 55 0.170
288
VNZ002 Venezuelan Equine Encephalitis 45 0.170
289
CWP001 Cowpox 44 0.170
290
P BCL017 B-Cell Lymphoma 57 0.170
291
P MSC003 Muscular Atrophy 52 0.170
292
P MTC069 Mitochondrial Disorders 57 0.170
293
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.170
294
c LKM005 Leukemia, T-Cell, Chronic 33 0.170
295
P THL005 Thalassemia 56 0.170
296
P DBT005 Diabetes Insipidus 54 0.170
297
c BCT007 Bacterial Meningitis 55 0.170
298
P MNN013 Meningitis 65 0.170
299
SML019 Smallpox 55 0.170
300
P ALP008 Alopecia 53 0.170
301
ANX004 Anoxia 40 0.170
302
PNF002 Painful Legs and Moving Toes Syndrome 14 0.170
303
PNM013 Pneumococcal Meningitis 43 0.170
304
SFT003 Soft Tissue Sarcoma 43 0.170
305
NNS045 Non-Specific Syndromic Intellectual Disability 41 0.170
307
PRN071 Parenteral Nutrition-Associated Cholestasis 23 0.170
308
DWR001 Dwarfism 44 0.170
309
BRN071 Brain Injury 50 0.170
310
GLY078 Glycogen Storage Disease Due to Glycogen Branching Enzyme Deficiency 38 0.170
311
DPR016 Depression 64 0.170
312
PST092 Posttransplant Acute Limbic Encephalitis 29 0.170
313
PRM329 Premature Aging 36 0.170
314
P OVR082 Overgrowth Syndrome 41 0.170
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