Search results for s-adenosylmethionine

623 hits were found for s-adenosylmethionine

# Family MCID Name MIFTS Score
1
NNL005 Non-Alcoholic Fatty Liver Disease 63 7.435
2
P LVR013 Liver Disease 68 7.135
3
FTT001 Fatty Liver Disease 61 6.566
4
HMC014 Homocysteinemia 52 6.350
5
P ALC033 Alcohol Use Disorder 67 5.717
6
CHL068 Cholestasis 61 5.148
7
NNL006 Non-Alcoholic Steatohepatitis 54 5.035
8
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 4.983
9
ALC007 Alcohol Dependence 65 4.917
10
P MJR001 Major Depressive Disorder 68 4.118
11
MNT002 Mental Depression 56 4.118
12
P HPT021 Hepatitis 68 3.987
13
DPR016 Depression 64 3.966
14
SLP001 Sleeping Sickness 56 3.907
15
HYP241 Hypermethioninemia Due to Adenosine Kinase Deficiency 38 3.782
16
P HMC002 Homocystinuria 52 3.778
17
TRY001 Trypanosomiasis 50 3.771
18
LVR012 Liver Cirrhosis 62 3.622
19
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 3.417
20
CHL045 Choline Deficiency Disease 39 3.346
21
MTH011 Methionine Adenosyltransferase Deficiency 18 3.143
22
HYP003 Hypermethioninemia 51 3.088
23
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 2.952
24
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 50 2.874
25
P INT099 Intrahepatic Cholestasis of Pregnancy 61 2.782
26
VTM002 Vitamin B12 Deficiency 48 2.721
27
ALC009 Alcoholic Liver Cirrhosis 54 2.708
28
P NRB001 Neuroblastoma 66 2.643
29
MTH074 Methionine Adenosyltransferase I/iii Deficiency 43 2.599
30
OST012 Osteoarthritis 77 2.561
31
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 36 2.551
32
P HPT023 Hepatocellular Carcinoma 95 2.518
33
PNM001 Pneumocystosis 60 2.469
34
P PNM007 Pneumonia 64 2.469
35
P ALZ034 Alzheimer Disease 87 2.465
36
VCC001 Vaccinia 49 2.464
37
FBR047 Fibromyalgia 57 2.446
38
c HPT003 Hepatitis a 63 2.413
39
P PRK039 Parkinsonism 55 2.352
40
P GST053 Gastric Cancer 82 2.318
41
ALC006 Alcoholic Hepatitis 61 2.304
42
P VSC018 Visceral Steatosis 32 2.284
43
P VSC007 Vascular Disease 62 2.126
44
P KDN018 Kidney Disease 71 2.069
45
c CHR684 Chronic Kidney Disease 73 2.051
46
VLV047 Volvulus of Midgut 55 2.045
47
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 2.035
48
STM007 Stomatitis 52 1.993
49
P TRM003 Tremor 50 1.988
50
PYR009 Pyridoxine Deficiency Anemia 35 1.983
51
P FBR017 Fibrosarcoma 55 1.928
52
NRL016 Neural Tube Defects 80 1.911
53
P PRK057 Parkinson Disease, Late-Onset 79 1.904
54
MDD011 Mood Disorder 61 1.904
55
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.882
56
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 1.882
57
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.882
58
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 1.882
59
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 1.882
60
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.882
61
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 1.882
62
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 1.882
63
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.882
64
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.882
65
ART002 Arts Syndrome 66 1.853
66
CHG001 Chagas Disease 65 1.853
67
MLD018 Mild Cognitive Impairment 48 1.826
68
P BRS047 Breast Cancer 97 1.763
69
c HPT016 Hepatitis B 62 1.763
70
ISC004 Ischemia 61 1.727
71
P DYS154 Dystonia 64 1.727
72
P HYP265 Hypotonia 42 1.711
73
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 48 1.690
74
P LKM062 Leukemia, Acute Lymphoblastic 69 1.690
75
OST159 Osteogenic Sarcoma 66 1.686
76
P KLZ004 Kala-Azar 1 41 1.667
77
LSH001 Leishmaniasis 63 1.667
78
HYP814 Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency 34 1.644
79
CHL014 Cholera 62 1.644
80
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.619
81
P NRP001 Neuropathy 59 1.619
82
HYP266 Hypoxia 56 1.619
83
P ADN016 Adenocarcinoma 63 1.593
84
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.565
85
HPT004 Hepatic Coma 43 1.565
86
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 1.535
87
HPT019 Hepatic Encephalopathy 59 1.535
88
P ART021 Arteriosclerosis 53 1.535
89
c BCT013 Bacterial Pneumonia 47 1.535
90
P CHR345 Chronic Pain 50 1.535
91
c MCR133 Microvascular Complications of Diabetes 4 41 1.502
92
c MCR113 Microvascular Complications of Diabetes 3 52 1.502
93
c MCR130 Microvascular Complications of Diabetes 6 41 1.502
94
c MCR120 Microvascular Complications of Diabetes 7 47 1.502
95
P PRP019 Peripheral Nervous System Disease 57 1.502
96
c CHL134 Cholestasis, Benign Recurrent Intrahepatic, 1 55 1.466
97
HYP014 Hyperuricemia 51 1.466
98
P MLN008 Melanoma 75 1.466
99
c ACT134 Acute Liver Failure 57 1.466
100
HMN044 Human Immunodeficiency Virus Type 1 76 1.425
101
SVR004 Severe Combined Immunodeficiency 70 1.425
102
47X002 47,xyy 47 1.425
103
ULC004 Ulcerative Colitis 74 1.412
104
AGN016 Aging 53 1.371
105
GLY015 Glycine N-Methyltransferase Deficiency 40 1.350
106
c SCN036 Secondary Progressive Multiple Sclerosis 55 1.327
107
P PNC035 Pancreatic Cancer 87 1.313
108
CLR109 Colorectal Adenocarcinoma 50 1.313
109
P INF037 Inflammatory Bowel Disease 53 1.304
110
CYS001 Cystic Fibrosis 77 1.304
111
P PNC044 Pancreatitis 61 1.304
112
PRM236 Primary Biliary Cholangitis 62 1.304
113
ACT098 Acute Erythroid Leukemia 55 1.279
114
HLX001 Helix Syndrome 47 1.253
115
P MYC084 Mycobacterium Tuberculosis 1 68 1.253
116
ALL029 Allergic Disease 61 1.253
117
CRH001 Crohn's Disease 80 1.253
118
P PRS040 Prostate Cancer 95 1.225
119
SVR001 Severe Acute Respiratory Syndrome 68 1.225
120
DMY004 Demyelinating Disease 50 1.225
121
MLR004 Malaria 77 1.195
122
ATH013 Atherosclerosis Susceptibility 63 1.195
123
c BRN108 Branchiootic Syndrome 1 63 1.195
124
c PCH010 Pachyonychia Congenita 3 43 1.195
125
c HYP836 Hypercholesterolemia, Familial, 1 73 1.195
126
HMN047 Human Cytomegalovirus Infection 59 1.195
127
LPD008 Lipid Metabolism Disorder 61 1.195
128
c HPT001 Hepatitis C 61 1.195
129
P ENC018 Encephalopathy 62 1.195
130
c MJR022 Major Affective Disorder 8 37 1.162
131
c MJR024 Major Affective Disorder 9 40 1.162
132
FRN006 Frontotemporal Dementia 68 1.162
133
P PHC003 Pheochromocytoma 70 1.162
134
EPD015 Epidemic Typhus 44 1.162
135
ADR040 Adrenal Gland Pheochromocytoma 45 1.162
136
CRY014 Cryptococcal Meningitis 48 1.162
137
P BPL003 Bipolar Disorder 56 1.162
138
PSY004 Psychotic Disorder 66 1.162
139
c PRC016 Pre-Eclampsia 64 1.162
140
c INH020 Inherited Metabolic Disorder 47 1.162
141
END086 End Stage Renal Disease 54 1.162
142
PYR016 Pyridoxine Deficiency 29 1.162
143
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.126
144
LPP008 Lipoprotein Quantitative Trait Locus 65 1.126
145
IMM167 Immune Deficiency Disease 76 1.126
146
P LKM071 Leukemia, Chronic Lymphocytic 74 1.126
147
SYN089 Syndromic X-Linked Intellectual Disability Snyder Type 37 1.126
148
P GST044 Gastritis 55 1.126
149
P SBS003 Substance Abuse 54 1.126
150
ADN001 Adenosine Deaminase Deficiency 59 1.126
151
OVR059 Ovary Adenocarcinoma 49 1.126
152
VSC003 Visceral Leishmaniasis 54 1.126
153
DFC004 Deficiency Anemia 74 1.085
154
P BLD134 Bladder Cancer 79 1.085
155
P CLR023 Colorectal Cancer 100 1.085
156
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 48 1.085
157
c HPT073 Hepatitis C Virus 70 1.085
158
P EXN002 Exanthem 58 1.085
159
P LNG032 Lung Cancer 98 1.085
160
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 1.085
161
CHL123 Chlamydia 58 1.085
162
CLR108 Colorectal Adenoma 63 1.085
163
ADN018 Adenoma 58 1.085
164
MSL001 Measles 61 1.085
165
IRR002 Irritable Bowel Syndrome 64 1.085
166
END040 Endogenous Depression 54 1.065
167
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.037
168
P RTT002 Rett Syndrome 79 1.037
169
LSC001 Lesch-Nyhan Syndrome 62 1.037
170
RSP019 Respiratory Distress Syndrome in Premature Infants 52 1.037
171
P HYP750 Hypertriglyceridemia, Familial 61 1.037
172
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 1.037
173
c GLL024 Gallbladder Disease 1 53 1.037
174
ESP021 Esophageal Cancer 84 1.037
175
P SNS001 Sensorineural Hearing Loss 60 1.037
176
MLY001 Molybdenum Cofactor Deficiency 40 1.037
177
IRN002 Iron Metabolism Disease 56 1.037
178
MNN009 Meningoencephalitis 47 1.037
179
NWB001 Newborn Respiratory Distress Syndrome 56 1.037
180
GT001 Gout 63 1.037
181
P HML002 Hemolytic Anemia 62 1.037
182
ACQ007 Acquired Immunodeficiency Syndrome 58 1.037
183
CHR121 Charcot-Marie-Tooth Neuropathy X Type 5 17 1.037
184
P DBT009 Diabetes Mellitus 67 1.037
185
DBT010 Diabetic Neuropathy 54 1.037
186
P HRP006 Herpes Simplex 65 1.037
187
TRM010 Traumatic Brain Injury 50 1.037
188
SRT004 Serotonin Syndrome 54 1.037
189
SPL018 Splenomegaly 47 1.037
190
HMM004 Hamamy Syndrome 39 0.973
191
P GLL020 Gallbladder Disease 57 0.973
192
c MGR028 Migraine with or Without Aura 1 63 0.973
193
c SCL052 Scleroderma, Familial Progressive 60 0.973
194
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.973
195
c MTC063 Mitochondrial Dna Depletion Syndrome 3 51 0.973
196
P PLM037 Pulmonary Hypertension 69 0.973
197
c HMC039 Hemochromatosis, Type 1 73 0.973
198
P AST005 Asthma 75 0.973
199
ADN022 Adenylosuccinase Deficiency 44 0.973
200
c CHR711 Chronic Asthma 41 0.973
201
P BNC003 Bone Cancer 58 0.973
202
TRC003 Trichomoniasis 53 0.973
203
SPS134 Spasmodic Dystonia 28 0.973
204
P GLL018 Gallbladder Cancer 59 0.973
205
ASP008 Aspiration Pneumonitis 43 0.973
206
TRN015 Transient Cerebral Ischemia 62 0.973
207
SPN035 Spindle Cell Sarcoma 51 0.973
208
CRN036 Craniopharyngioma 63 0.973
209
ADR005 Adrenal Carcinoma 58 0.973
210
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.973
211
LST001 Listeriosis 59 0.973
212
P HRD011 Hereditary Spherocytosis 63 0.973
213
URL001 Urolithiasis 45 0.973
214
P MCR010 Microcephaly 59 0.973
215
TXC005 Toxic Shock Syndrome 61 0.973
216
P URT039 Urticaria 57 0.973
217
SRC014 Sarcoma 64 0.973
218
BRN024 Bronchitis 67 0.973
219
PRM243 Primary Bone Cancer 22 0.973
220
UTR043 Uterine Sarcoma 40 0.973
221
SPS016 Spasmodic Dysphonia 32 0.973
222
CRB090 Cerebral Hypoxia 42 0.973
223
DSR074 Disorder of Purine Metabolism 24 0.973
224
NRT001 Neurotic Disorder 56 0.912
225
P NNS032 Non-Syndromic X-Linked Intellectual Disability 46 0.821
226
P CNG436 Congenital Disorder of Deglycosylation 51 0.821
227
PLM001 Pulmonary Tuberculosis 69 0.821
228
P ART023 Arthropathy 59 0.821
229
c NNS082 Non-Syndromic X-Linked Intellectual Disability 9 17 0.821
230
SNL007 Senile Cataract 40 0.821
231
PTH003 Pathologic Nystagmus 52 0.821
232
DWN001 Down Syndrome 70 0.591
233
c ACT027 Acute Pancreatitis 60 0.571
234
P ATS364 Autism 72 0.506
235
HYP066 Hyperglycemia 60 0.483
236
c ATS007 Autism Spectrum Disorder 71 0.432
237
DPH001 Diphtheria 59 0.432
238
GLB002 Glioblastoma 67 0.432
239
48X005 48,xyyy 39 0.432
240
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.404
241
HYP060 Hyperinsulinism 53 0.404
242
CLT003 Colitis 63 0.374
243
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.374
244
c SCK017 Sick Sinus Syndrome 1 34 0.374
245
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.374
246
MGL001 Megaloblastic Anemia 59 0.374
247
URM002 Uremia 47 0.374
248
CHR178 Chromosomal Triplication 33 0.374
249
c LKM061 Leukemia, Acute Myeloid 83 0.341
250
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 50 0.341
251
P MYP004 Myopathy 67 0.341
252
P NTR004 Neutropenia 62 0.341
253
CRB039 Cerebrovascular Disease 65 0.341
254
P PLL002 Pellagra 46 0.341
255
HYP056 Hypoglycemia 65 0.341
256
PRN011 Pernicious Anemia 52 0.305
257
P RTN024 Retinoblastoma 72 0.305
258
P DNG005 Dengue Virus 55 0.305
259
CHL065 Cholangiocarcinoma 57 0.305
260
THR024 Thrombosis 56 0.305
261
TTH006 Tooth Disease 51 0.305
262
P CYS018 Cystitis 58 0.305
263
P LKM002 Leukemia 65 0.305
264
INT079 Intrahepatic Cholangiocarcinoma 51 0.305
265
P CHR071 Charcot-Marie-Tooth Disease 64 0.305
266
P INF032 Infertility 60 0.305
267
SKN016 Skin Disease 63 0.305
268
PLC008 Placenta Disease 48 0.305
269
VSC002 Vascular Dementia 59 0.305
270
HMP009 Haemophilus Influenzae 41 0.305
271
P RHM011 Rheumatoid Arthritis 81 0.264
272
ART140 Arteries, Anomalies of 52 0.264
273
OCL069 Ocular Motor Apraxia 57 0.264
274
c CHR408 Charcot-Marie-Tooth Disease, X-Linked Recessive, 5 43 0.264
275
P MLT020 Multiple Sclerosis 79 0.264
276
c SCH085 Schizophrenia 2 27 0.264
277
PRP027 Peripheral Vascular Disease 71 0.264
278
ATS010 Autosomal Recessive Disease 42 0.264
279
EWN003 Ewing Sarcoma 69 0.264
280
CRB150 Cerebral Creatine Deficiency Syndrome 2 54 0.264
281
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.264
282
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.264
283
P LNG064 Lung Cancer Susceptibility 3 69 0.264
284
TRN018 Transitional Cell Carcinoma 56 0.264
285
P THR015 Thrombophilia 51 0.264
286
P MVM001 Movement Disease 61 0.264
287
ADJ001 Adjustment Disorder 46 0.264
288
NTR005 Nutritional Deficiency Disease 60 0.264
289
P LTR001 Lateral Sclerosis 57 0.264
290
P URN019 Urinary Tract Infection 48 0.264
291
P OPT006 Optic Nerve Disease 57 0.264
292
PLS011 Plasmacytoma 56 0.264
293
SPT005 Spotted Fever 49 0.264
294
P MYL006 Myeloid Leukemia 60 0.264
295
CRT055 Creatine Deficiency Syndromes 38 0.264
296
YLL002 Yellow Fever 61 0.264
297
P BCL017 B-Cell Lymphoma 57 0.264
298
PPT005 Peptic Ulcer Disease 58 0.264
299
CYT002 Cytokine Deficiency 43 0.264
300
LYM019 Lymphosarcoma 46 0.264
301
GST050 Gastrointestinal System Disease 55 0.264
302
DFN002 Dfnx1 Nonsyndromic Hearing Loss and Deafness 8 0.264
303
P CRN300 Coronary Heart Disease 1 73 0.216
304
ARM002 Aromatic L-Amino Acid Decarboxylase Deficiency 55 0.216
305
PLY023 Polycystic Liver Disease 62 0.216
306
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.216
307
P OVR042 Ovarian Cancer 88 0.216
308
NCL008 Nuclear Ribonucleic Acid 15 0.216
309
INS024 Insulin-Like Growth Factor I 77 0.216
310
CRB204 Cerebellar, Ocular, Craniofacial, and Genital Syndrome 27 0.216
312
ANN002 Anencephaly 57 0.216
313
P ATX030 Ataxia-Telangiectasia 80 0.216
314
BWN001 Bowen-Conradi Syndrome 54 0.216
315
c TBR025 Tuberous Sclerosis 1 84 0.216
316
c THY056 Thyroid Dyshormonogenesis 3 32 0.216
317
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.216
318
ATM095 Autoimmune Disease 61 0.216
319
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.216
320
PRS129 Prostatic Hyperplasia, Benign 48 0.216
321
P FTL001 Fetal Alcohol Syndrome 55 0.216
322
CHK001 Chikungunya 60 0.216
323
SBJ001 Subjective Cognitive Decline 29 0.216
324
P OLG002 Oligodendroglioma 66 0.216
325
P CNT005 Central Nervous System Lymphoma 51 0.216
326
PRP030 Purpura 54 0.216
327
CCC002 Coccidiosis 50 0.216
328
P TBR001 Tuberous Sclerosis 69 0.216
329
P DRR001 Diarrhea 55 0.216
330
P ECL001 Eclampsia 52 0.216
331
LYM027 Lymphopenia 56 0.216
332
P INT143 Interstitial Cystitis 59 0.216
333
P HYP086 Hypothyroidism 68 0.216
334
SYN007 Synovitis 54 0.216
335
CRC021 Carcinosarcoma 62 0.216
336
AML001 Amelanotic Melanoma 37 0.216
337
PRS021 Prostatic Adenoma 43 0.216
338
P PLM036 Pulmonary Fibrosis 65 0.216
339
TRT001 Teratocarcinoma 41 0.216
340
PLC002 Plica Syndrome 35 0.216
341
P ADL010 Adult Respiratory Distress Syndrome 70 0.216
342
PRS045 Prostatic Hypertrophy 53 0.216
343
KRT002 Keratomalacia 54 0.216
344
LWC001 Low Compliance Bladder 44 0.216
345
P THR014 Thrombocytopenia 66 0.216
346
PRS047 Prostatitis 57 0.216
347
P CRD246 Cardiovascular System Disease 55 0.216
348
PRT037 Pertussis 49 0.216
349
TLN003 Telangiectasis 51 0.216
350
c HPT007 Hepatitis E 50 0.216
351
P TYR004 Tyrosinemia 49 0.216
352
P ATR005 Atrophic Gastritis 50 0.216
353
VNZ002 Venezuelan Equine Encephalitis 45 0.216
354
P ENC004 Encephalitis 61 0.216
355
P MSC003 Muscular Atrophy 52 0.216
356
P PRD008 Periodontitis 63 0.216
357
LNG099 Lung Disease 62 0.216
358
P LPS004 Lupus Erythematosus 61 0.216
359
P HYP076 Hyperthyroidism 53 0.216
360
PRM226 Primary Central Nervous System Lymphoma 47 0.216
361
c XLN110 X-Linked Charcot-Marie-Tooth Disease 33 0.216
362
P MSC005 Muscular Dystrophy 66 0.216
363
ORL011 Oral Cancer 60 0.216
364
ANX004 Anoxia 40 0.216
365
PNF002 Painful Legs and Moving Toes Syndrome 14 0.216
366
ACT181 Acute Motor Axonal Neuropathy 25 0.216
367
DWR001 Dwarfism 44 0.216
368
EXN003 Exencephaly 30 0.216
369
PST092 Posttransplant Acute Limbic Encephalitis 29 0.216
370
P OVR082 Overgrowth Syndrome 41 0.216
371
MYL020 Myelomeningocele 51 0.153
372
ACT119 Acute Promyelocytic Leukemia 62 0.153
373
MTC163 Mitochondrial Complex I Deficiency, Nuclear Type 16 23 0.153
374
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 0.153
375
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.153
376
c MGR022 Migraine with or Without Aura 3 16 0.153
377
CRH005 Crohn's Colitis 53 0.153
378
MYL009 Myelodysplastic Syndrome 67 0.153
379
MTB004 Metabolic Acidosis 48 0.153
380
c SPS111 Spastic Paraplegia 27, Autosomal Recessive 28 0.153
381
c HNT011 Huntington Disease-Like 3 33 0.153
382
P LYM118 Lymphoma 66 0.153
383
c ATS204 Autosomal Recessive Non-Syndromic Intellectual Disability 47 0.153
384
DNG001 Dengue Shock Syndrome 40 0.153
385
P SCH015 Schizophrenia 74 0.153
386
c WLM013 Wilms Tumor 1 65 0.153
387
CYS019 Cystathioninuria 46 0.153
388
ALP077 Alpha-Methylacetoacetic Aciduria 52 0.153
389
c ANM038 Anemia, Autoimmune Hemolytic 63 0.153
390
c SYS001 Systemic Lupus Erythematosus 85 0.153
391
OBS002 Obsessive-Compulsive Disorder 67 0.153
392
P MDL005 Medulloblastoma 75 0.153
393
PRX015 Paroxysmal Extreme Pain Disorder 56 0.153
394
DRR014 Darier-White Disease 58 0.153
395
c TYP009 Type 2 Diabetes Mellitus 91 0.153
396
c FBR084 Fibromatosis, Gingival, 1 51 0.153
397
c SML038 Small Cell Cancer of the Lung 68 0.153
398
c GLY007 Glycogen Storage Disease Iv 58 0.153
399
c HYD064 Hydrocephalus, Congenital, 1 51 0.153
400
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.153
401
LGH007 Leigh Syndrome 70 0.153
402
PLY150 Polykaryocytosis Inducer 29 0.153
403
EPT021 Epithelial Recurrent Erosion Dystrophy 45 0.153
404
MLY008 Molybdenum Cofactor Deficiency, Complementation Group a 47 0.153
405
DGR001 Digeorge Syndrome 62 0.153
406
MSC157 Muscular Dystrophy, Duchenne Type 78 0.153
407
c OTP006 Otopalatodigital Syndrome, Type I 59 0.153
408
PLY158 Polyglucosan Body Neuropathy, Adult Form 39 0.153
409
c TYR012 Tyrosinemia, Type I 61 0.153
410
CFF002 Coffin-Lowry Syndrome 59 0.153
411
SPP011 Suppression of Tumorigenicity 12 61 0.153
412
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.153
413
NRL018 Neural Tube Defects, Folate-Sensitive 46 0.153
414
P CTR177 Citrullinemia, Type Ii, Adult-Onset 56 0.153
415
TRD006 Tardive Dyskinesia 53 0.153
416
WLS001 Wilson Disease 70 0.153
417
c AML061 Amelogenesis Imperfecta, Type Ie 37 0.153
418
P NSP012 Nasopharyngeal Carcinoma 60 0.153
419
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.153
420
SPC010 Speech and Communication Disorders 47 0.153
421
DSS032 Disease by Infectious Agent 55 0.153
422
CMB072 Combined Oxidative Phosphorylation Deficiency 28 23 0.153
423
CRP030 Corpus Callosum, Agenesis of, with Facial Anomalies and Cerebellar Ataxia 37 0.153
424
CRB148 Cerebral Creatine Deficiency Syndrome 3 40 0.153
425
MSC007 Muscle Hypertrophy 64 0.153
426
c PNC106 Pancreatic Agenesis 1 51 0.153
427
CRB151 Cerebral Creatine Deficiency Syndrome 1 50 0.153
428
P SPP010 Suppressor of Tumorigenicity 3 50 0.153
429
CHR103 Charge Syndrome 65 0.153
430
P CHN012 Chondrosarcoma 56 0.153
431
CRN264 Craniosynostosis with Fibular Aplasia 29 0.153
432
LYS003 Lysinuric Protein Intolerance 57 0.153
433
BLM001 Bloom Syndrome 65 0.153
434
c TYP008 Type 1 Diabetes Mellitus 77 0.153
435
c DPH024 Diaphragmatic Hernia, Congenital 63 0.153
436
P STS008 Sotos Syndrome 1 62 0.153
437
HMC042 Homocystinuria-Megaloblastic Anemia, Cble Complementation Type 34 0.153
438
HYP774 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome 54 0.153
439
P LPR021 Leprosy 3 71 0.153
440
MYL069 Myeloma, Multiple 76 0.153
441
P RTN008 Retinitis Pigmentosa 79 0.153
442
P FRG001 Fragile X Syndrome 70 0.153
443
c THR092 Thrombophilia Due to Thrombin Defect 74 0.153
445
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.153
446
P MYC007 Myocardial Infarction 69 0.153
447
c LSS005 Lissencephaly 1 57 0.153
448
c AMY089 Amyotrophic Lateral Sclerosis 7 27 0.153
449
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.153
450
VLT001 Vulto-Van Silfhout-De Vries Syndrome 41 0.153
451
c LKM063 Leukemia, Chronic Myeloid 70 0.153
452
LGN006 Legionnaire Disease 52 0.153
453
c LFR007 Li-Fraumeni Syndrome 2 45 0.153
454
ADN024 Adenine Phosphoribosyltransferase Deficiency 53 0.153
455
c SPS148 Spastic Paraplegia 31, Autosomal Dominant 49 0.153
456
c ATR087 Atrial Standstill 1 74 0.153
457
BRK010 Burkitt Lymphoma 65 0.153
458
P HNT016 Huntington Disease 73 0.153
459
P GLM040 Glioma Susceptibility 1 70 0.153
460
P LFR001 Li-Fraumeni Syndrome 73 0.153
461
VSC053 Visceral Steatosis, Congenital 35 0.153
462
FCT007 Factor Vii Deficiency 64 0.153
463
ORT008 Orotic Aciduria 56 0.153
464
WST005 West Nile Virus 55 0.153
465
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 68 0.153
466
c MGR040 Migraine with or Without Aura 12 16 0.153
467
END057 Endometrial Cancer 76 0.153
468
c RTN041 Retinitis Pigmentosa 11 43 0.153
469
P ADL017 Adult T-Cell Leukemia 53 0.153
470
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.153
471
P ANP001 Anaplastic Large Cell Lymphoma 59 0.153
472
DFF005 Diffuse Large B-Cell Lymphoma 55 0.153
473
BTN004 Biotin Deficiency 44 0.153
474
PHY002 Physical Disorder 40 0.153
475
P GNG025 Gingival Fibromatosis 48 0.153
476
ZKF001 Zika Fever 51 0.153
477
P MMP001 Mumps 56 0.153
478
P RSP003 Respiratory Failure 73 0.153
479
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.153
480
P PLY014 Polycystic Kidney Disease 71 0.153
481
DBT081 Diabetic Encephalopathy 36 0.153
482
QFV001 Q Fever 61 0.153
483
P DDN001 Duodenal Ulcer 52 0.153
484
PNC001 Pancytopenia 52 0.153
485
GNR003 Generalized Atherosclerosis 42 0.153
486
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.153
487
CLN015 Colon Adenocarcinoma 64 0.153
488
c ATM011 Autoimmune Hepatitis 62 0.153
489
MLG169 Malignant Astrocytoma 57 0.153
490
PRC003 Proctitis 49 0.153
491
MNK002 Monkeypox 41 0.153
492
BLR008 Bilirubin Metabolic Disorder 57 0.153
493
P HMN010 Hemangioma 61 0.153
494
P GLY013 Glycogen Storage Disease 59 0.153
495
WRN003 Wernicke Encephalopathy 45 0.153
496
SQM006 Squamous Cell Carcinoma 59 0.153
497
P BRB001 Beriberi 44 0.153
498
KRT009 Keratosis 52 0.153
499
HMS001 Hemosiderosis 48 0.153
500
BCT022 Bacterial Infectious Disease 55 0.153
501
P ISL078 Isolated Ectopia Lentis 58 0.153
502
P BNG030 Benign Ependymoma 51 0.153
503
BRN004 Brain Edema 54 0.153
504
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.153
505
CLL010 Cellular Ependymoma 58 0.153
506
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 67 0.153
507
MXD026 Mixed Glioma 45 0.153
508
OVR063 Overnutrition 42 0.153
509
P EPL003 Epulis 30 0.153
510
GST045 Gastroenteritis 58 0.153
511
P PLY011 Polycystic Ovary Syndrome 57 0.153
512
LYM017 Lyme Disease 63 0.153
513
HPT014 Hepatorenal Syndrome 49 0.153
514
MDD018 Middle East Respiratory Syndrome 44 0.153
515
c VRL010 Viral Hepatitis 52 0.153
516
P OBS001 Obstructive Jaundice 49 0.153
517
NRR001 Neuroretinitis 42 0.153
518
KLB003 Klebsiella Pneumonia 49 0.153
519
P PRP029 Porphyria 60 0.153
520
P EHL001 Ehlers-Danlos Syndrome 57 0.153
521
P PLY019 Polyneuropathy 52 0.153
522
PNC034 Pancreas Disease 49 0.153
523
P KDN017 Kidney Cancer 60 0.153
524
PST011 Pustulosis of Palm and Sole 52 0.153
525
PNC129 Pancreatic Adenocarcinoma 64 0.153
526
SNS003 Sensory Peripheral Neuropathy 51 0.153
527
GNG013 Gingivitis 59 0.153
528
EMB004 Embryonal Carcinoma 55 0.153
529
P SKN015 Skin Carcinoma 71 0.153
530
P CCK001 Cockayne Syndrome 67 0.153
531
CRN030 Coronary Stenosis 50 0.153
532
P HYP061 Hypertrophic Cardiomyopathy 68 0.153
533
OST011 Osteomalacia 52 0.153
534
GLC003 Glucose Intolerance 53 0.153
535
PRT013 Portal Hypertension 59 0.153
536
c ACT073 Acute Leukemia 59 0.153
537
BBN001 Bubonic Plague 40 0.153
538
CRT013 Carotid Stenosis 51 0.153
539
P KRT014 Keratosis Follicularis Spinulosa Decalvans 31 0.153
540
GNR004 Generalized Anxiety Disorder 54 0.153
541
P DMN002 Dementia 65 0.153
542
CHL004 Cholelithiasis 48 0.153
543
DNG003 Dengue Disease 65 0.153
544
DNG002 Dengue Hemorrhagic Fever 59 0.153
545
RLP003 Relapsing Fever 50 0.153
546
c SVR005 Severe Pre-Eclampsia 49 0.153
547
HLL004 Hellp Syndrome 53 0.153
548
P ART022 Arthritis 70 0.153
549
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.153
550
P PNC025 Panic Disorder 52 0.153
551
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.153
552
RTN023 Retinitis 45 0.153
553
PLG002 Plague 58 0.153
554
HPT022 Hepatoblastoma 54 0.153
555
ANT024 Anthrax Disease 57 0.153
556
PRM020 Premenstrual Tension 39 0.153
557
PRP007 Priapism 46 0.153
558
P PSR002 Psoriasis 63 0.153
559
AMB001 Amebiasis 56 0.153
560
CWP001 Cowpox 44 0.153
561
CRV002 Cervix Uteri Carcinoma in Situ 48 0.153
562
P MYC008 Myocarditis 59 0.153
563
CHR066 Chronic Fatigue Syndrome 59 0.153
564
P NGH001 Night Blindness 52 0.153
565
GLM045 Glioma 62 0.153
566
HNS001 Hansen's Disease 32 0.153
567
MYL080 Myalgic Encephalomyelitis/chronic Fatigue Syndrome 32 0.153
568
NDL013 Nodular Regenerative Hyperplasia 46 0.153
569
P CHL066 Cholangitis 51 0.153
570
PST021 Postpartum Depression 50 0.153
571
KDN013 Kidney Hypertrophy 33 0.153
572
CHC001 Chickenpox 56 0.153
573
P INS002 in Situ Carcinoma 52 0.153
574
P TXP001 Toxoplasmosis 59 0.153
575
DSR002 Disorders of Intracellular Cobalamin Metabolism 30 0.153
576
P MTC069 Mitochondrial Disorders 57 0.153
577
ALL014 Allergic Encephalomyelitis 34 0.153
578
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.153
579
FBR019 Fibromatosis 44 0.153
580
LRG010 L-Arginine:glycine Amidinotransferase Deficiency 18 0.153
581
c LKM005 Leukemia, T-Cell, Chronic 33 0.153
582
PRT058 Pure Autonomic Failure 58 0.153
583
P THL005 Thalassemia 56 0.153
584
PTT037 Pituitary Tumors 44 0.153
585
P DBT005 Diabetes Insipidus 54 0.153
586
c BCT007 Bacterial Meningitis 55 0.153
587
P MNN013 Meningitis 65 0.153
588
c RNG019 Ring Chromosome 3 19 0.153
589
P RGD004 Rigid Spine Muscular Dystrophy 21 0.153
590
P AMY004 Amyloidosis 69 0.153
591
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.153
592
CRL001 Cerulean Cataract 26 0.153
593
CRV045 Cervical Intraepithelial Neoplasia 38 0.153
594
OVR094 Ovarian Epithelial Cancer 39 0.153
595
PRN029 Parainfluenza Virus Type 3 32 0.153
596
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.153
597
DHY008 Dihydroxyadeninuria 24 0.153
598
DSS012 Disseminated Infection with Mycobacterium Avium Complex 18 0.153
599
HVY002 Heavy Metal Poisoning 22 0.153
600
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 24 0.153
601
NCL011 Nuclear Gene-Encoded Leigh Syndrome Spectrum 21 0.153
602
SYN036 Syncope 44 0.153
603
P RRH023 Rare Hereditary Hemochromatosis 52 0.153
604
P FML355 Familial Intrahepatic Cholestasis 38 0.153
605
PNM013 Pneumococcal Meningitis 43 0.153
607
PLY100 Polyploidy 36 0.153
608
SFT003 Soft Tissue Sarcoma 43 0.153
609
MNG007 Manganese Poisoning 28 0.153
610
ARG004 Argyria 26 0.153
611
HST016 Histiocytic Sarcoma 38 0.153
612
NNS045 Non-Specific Syndromic Intellectual Disability 41 0.153
613
c HMN021 Human T-Cell Leukemia Virus Type 1 46 0.153
614
MTH046 Methylmalonic Acidemia Without Homocystinuria 39 0.153
615
BRN071 Brain Injury 50 0.153
616
P MYC033 Myoclonus 46 0.153
617
MYT011 Myotonia 37 0.153
618
GLY078 Glycogen Storage Disease Due to Glycogen Branching Enzyme Deficiency 38 0.153
619
P CRB088 Cerebral Atrophy 32 0.153
620
GLL048 Glial Tumor 51 0.153
621
RDT013 Radiation Proctitis 47 0.153
622
PRM329 Premature Aging 36 0.153
623
THY029 Thyroid Carcinoma 55 0.153
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