Search results for s-adenosylmethionine

616 hits were found for s-adenosylmethionine

# Family MCID Name MIFTS Score
1
HMC014 Homocysteinemia 52 12.230
2
NNL005 Non-Alcoholic Fatty Liver Disease 63 11.633
3
P LVR013 Liver Disease 69 10.762
4
FTT001 Fatty Liver Disease 62 10.598
5
CHL068 Cholestasis 61 8.628
6
NNL006 Non-Alcoholic Steatohepatitis 54 7.789
7
P ALC033 Alcohol Use Disorder 61 7.435
8
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 7.331
9
P HMC002 Homocystinuria 53 7.295
10
ALC007 Alcohol Dependence 66 6.614
11
SLP001 Sleeping Sickness 56 6.422
12
VTM002 Vitamin B12 Deficiency 48 5.967
13
P MJR001 Major Depressive Disorder 68 5.878
14
MNT002 Mental Depression 57 5.878
15
TRY001 Trypanosomiasis 50 5.875
16
DPR016 Depression 65 5.745
17
LVR012 Liver Cirrhosis 63 5.727
18
HYP003 Hypermethioninemia 51 5.630
19
CHL045 Choline Deficiency Disease 39 5.563
20
P VSC007 Vascular Disease 63 5.242
21
NRL016 Neural Tube Defects 81 5.190
22
P NRB001 Neuroblastoma 66 5.130
23
P HPT021 Hepatitis 69 5.050
24
VCC001 Vaccinia 47 4.936
25
MTH011 Methionine Adenosyltransferase Deficiency 18 4.748
26
OST012 Osteoarthritis 77 4.541
27
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 4.541
28
MTH074 Methionine Adenosyltransferase I/iii Deficiency 42 4.511
29
P HPT023 Hepatocellular Carcinoma 96 4.502
30
c CHR684 Chronic Kidney Disease 69 4.481
31
P INT099 Intrahepatic Cholestasis of Pregnancy 62 4.300
32
FBR047 Fibromyalgia 58 4.283
33
HYP241 Hypermethioninemia Due to Adenosine Kinase Deficiency 37 4.260
34
P ALZ034 Alzheimer Disease 87 4.205
35
ALC006 Alcoholic Hepatitis 61 4.023
36
P KDN018 Kidney Disease 72 4.017
37
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 50 3.897
38
PNM001 Pneumocystosis 61 3.846
39
ALC009 Alcoholic Liver Cirrhosis 54 3.833
40
P GST053 Gastric Cancer 83 3.770
41
MLD018 Mild Cognitive Impairment 48 3.756
42
STM007 Stomatitis 54 3.711
43
P BRS047 Breast Cancer 98 3.566
44
P FBR017 Fibrosarcoma 56 3.451
45
P PRK039 Parkinsonism 55 3.379
46
P HYP265 Hypotonia 42 3.367
47
P PRK057 Parkinson Disease, Late-Onset 80 3.356
48
P LKM062 Leukemia, Acute Lymphoblastic 69 3.280
49
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 48 3.280
50
VLV047 Volvulus of Midgut 52 3.260
51
MDD011 Mood Disorder 62 3.257
52
ULC004 Ulcerative Colitis 74 3.190
53
P KLZ004 Kala-Azar 1 41 3.190
54
LSH001 Leishmaniasis 64 3.190
55
ART002 Arts Syndrome 66 3.152
56
CHG001 Chagas Disease 66 3.152
57
HYP814 Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency 34 3.095
58
CHL014 Cholera 62 3.095
59
HYP266 Hypoxia 57 3.095
60
PYR009 Pyridoxine Deficiency Anemia 35 3.010
61
P NRP001 Neuropathy 60 2.996
62
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 2.951
63
GLY015 Glycine N-Methyltransferase Deficiency 40 2.940
64
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 2.891
65
P ADN016 Adenocarcinoma 63 2.891
66
c HPT003 Hepatitis a 63 2.872
67
P PNM007 Pneumonia 67 2.865
68
P INF037 Inflammatory Bowel Disease 53 2.850
69
c SCN036 Secondary Progressive Multiple Sclerosis 55 2.850
70
P PNC044 Pancreatitis 61 2.850
71
HPT004 Hepatic Coma 43 2.780
72
RPD005 Rapidly Involuting Congenital Hemangioma 46 2.780
73
CYS001 Cystic Fibrosis 78 2.755
74
PRM236 Primary Biliary Cholangitis 60 2.755
75
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 2.747
76
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 2.659
77
c BCT013 Bacterial Pneumonia 48 2.659
78
HPT019 Hepatic Encephalopathy 59 2.659
79
P ART021 Arteriosclerosis 54 2.659
80
P CHR345 Chronic Pain 50 2.659
81
P MYC084 Mycobacterium Tuberculosis 1 68 2.656
82
ACT098 Acute Erythroid Leukemia 55 2.656
83
P PRS040 Prostate Cancer 95 2.656
84
CRH001 Crohn's Disease 80 2.656
85
P DYS154 Dystonia 64 2.645
86
47X002 47,xyy 48 2.645
87
c HPT016 Hepatitis B 62 2.645
88
HLX001 Helix Syndrome 48 2.551
89
ALL029 Allergic Disease 59 2.551
90
c MCR130 Microvascular Complications of Diabetes 6 41 2.529
91
c MCR120 Microvascular Complications of Diabetes 7 47 2.529
92
c MCR113 Microvascular Complications of Diabetes 3 52 2.529
93
c MCR133 Microvascular Complications of Diabetes 4 41 2.529
94
P PRP019 Peripheral Nervous System Disease 58 2.529
95
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.493
96
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.493
97
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.493
98
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 2.493
99
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 2.493
100
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.493
101
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 2.493
102
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.493
103
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 2.493
104
OST159 Osteogenic Sarcoma 66 2.482
105
ISC004 Ischemia 61 2.482
106
P TRM003 Tremor 48 2.448
107
DMY004 Demyelinating Disease 50 2.439
108
c ACT134 Acute Liver Failure 59 2.384
109
c CHL134 Cholestasis, Benign Recurrent Intrahepatic, 1 55 2.384
110
P MLN008 Melanoma 76 2.384
111
HYP014 Hyperuricemia 51 2.384
112
DWN001 Down Syndrome 70 2.369
113
ATH013 Atherosclerosis Susceptibility 63 2.319
114
MLR004 Malaria 80 2.319
115
HMN047 Human Cytomegalovirus Infection 57 2.319
116
c BRN108 Branchiootic Syndrome 1 62 2.319
117
c PCH010 Pachyonychia Congenita 3 43 2.319
118
c HYP836 Hypercholesterolemia, Familial, 1 73 2.319
119
SVR001 Severe Acute Respiratory Syndrome 67 2.319
120
c HPT001 Hepatitis C 62 2.319
121
c ACT027 Acute Pancreatitis 60 2.289
122
P VSC018 Visceral Steatosis 32 2.283
123
HMN044 Human Immunodeficiency Virus Type 1 78 2.221
124
SVR004 Severe Combined Immunodeficiency 72 2.221
125
FRN006 Frontotemporal Dementia 68 2.189
126
P PHC003 Pheochromocytoma 69 2.189
127
EPD015 Epidemic Typhus 44 2.189
128
c MJR022 Major Affective Disorder 8 38 2.189
129
c MJR024 Major Affective Disorder 9 41 2.189
130
ADR040 Adrenal Gland Pheochromocytoma 46 2.189
131
CRY014 Cryptococcal Meningitis 48 2.189
132
P BPL003 Bipolar Disorder 56 2.189
133
END086 End Stage Renal Disease 52 2.189
134
PSY004 Psychotic Disorder 66 2.189
135
c INH020 Inherited Metabolic Disorder 48 2.189
136
P ENC018 Encephalopathy 62 2.189
137
PYR016 Pyridoxine Deficiency 29 2.189
138
ART140 Arteries, Anomalies of 53 2.044
139
P BLD134 Bladder Cancer 79 2.044
140
P LKM071 Leukemia, Chronic Lymphocytic 75 2.044
141
LPP008 Lipoprotein Quantitative Trait Locus 65 2.044
142
SYN089 Syndromic X-Linked Intellectual Disability Snyder Type 35 2.044
143
VSC003 Visceral Leishmaniasis 55 2.044
144
ADN001 Adenosine Deaminase Deficiency 59 2.044
145
P GST044 Gastritis 55 2.044
146
OVR059 Ovary Adenocarcinoma 49 2.044
147
c PRC016 Pre-Eclampsia 65 2.044
148
P SBS003 Substance Abuse 54 2.044
149
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 34 2.044
150
P ATS364 Autism 69 1.934
151
AGN016 Aging 54 1.934
152
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 1.882
153
P LNG032 Lung Cancer 98 1.881
154
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 49 1.881
155
P CLR023 Colorectal Cancer 100 1.881
156
P EXN002 Exanthem 58 1.881
157
CLR108 Colorectal Adenoma 64 1.881
158
IMM167 Immune Deficiency Disease 78 1.881
159
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 1.881
160
c HPT073 Hepatitis C Virus 71 1.881
161
ADN018 Adenoma 59 1.881
162
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.881
163
CHL123 Chlamydia 58 1.881
164
IRR002 Irritable Bowel Syndrome 65 1.881
165
MSL001 Measles 61 1.881
166
HYP066 Hyperglycemia 61 1.835
167
P PNC035 Pancreatic Cancer 86 1.773
168
CLR109 Colorectal Adenocarcinoma 50 1.773
169
GLB002 Glioblastoma 67 1.730
170
DPH001 Diphtheria 59 1.730
171
48X005 48,xyyy 39 1.730
172
SRT004 Serotonin Syndrome 54 1.686
173
P RTT002 Rett Syndrome 79 1.686
174
c GLL024 Gallbladder Disease 1 52 1.686
175
LSC001 Lesch-Nyhan Syndrome 62 1.686
176
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 1.686
177
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 1.686
178
RSP019 Respiratory Distress Syndrome in Premature Infants 52 1.686
179
P HYP750 Hypertriglyceridemia, Familial 62 1.686
180
ESP021 Esophageal Cancer 83 1.686
181
MLY001 Molybdenum Cofactor Deficiency 40 1.686
182
TRM010 Traumatic Brain Injury 51 1.686
183
P HRP006 Herpes Simplex 65 1.686
184
P DBT009 Diabetes Mellitus 67 1.686
185
P HML002 Hemolytic Anemia 62 1.686
186
DBT010 Diabetic Neuropathy 54 1.686
187
ACQ007 Acquired Immunodeficiency Syndrome 59 1.686
188
P SNS001 Sensorineural Hearing Loss 59 1.686
189
GT001 Gout 64 1.686
190
NWB001 Newborn Respiratory Distress Syndrome 56 1.686
191
MNN009 Meningoencephalitis 48 1.686
192
IRN002 Iron Metabolism Disease 57 1.686
193
SPL018 Splenomegaly 49 1.686
194
CHR121 Charcot-Marie-Tooth Neuropathy X Type 5 17 1.686
195
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 1.618
196
c ATS007 Autism Spectrum Disorder 72 1.618
197
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.618
198
HYP060 Hyperinsulinism 54 1.618
199
END040 Endogenous Depression 55 1.525
200
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 1.498
201
CLT003 Colitis 63 1.498
202
c SCK017 Sick Sinus Syndrome 1 34 1.498
203
URM002 Uremia 47 1.498
204
MGL001 Megaloblastic Anemia 58 1.498
205
CHR178 Chromosomal Triplication 34 1.498
206
c HMC039 Hemochromatosis, Type 1 73 1.433
207
DSR074 Disorder of Purine Metabolism 23 1.433
208
SPS016 Spasmodic Dysphonia 31 1.433
209
c SCL052 Scleroderma, Familial Progressive 61 1.433
210
c MTC063 Mitochondrial Dna Depletion Syndrome 3 51 1.433
211
P AST005 Asthma 76 1.433
212
c PLM164 Pulmonary Hypertension, Primary, 1 76 1.433
213
c MGR028 Migraine with or Without Aura 1 64 1.433
214
P PLM037 Pulmonary Hypertension 72 1.433
215
SPS134 Spasmodic Dystonia 29 1.433
216
c CHR711 Chronic Asthma 41 1.433
217
URL001 Urolithiasis 46 1.433
218
HMM004 Hamamy Syndrome 39 1.433
219
ADN022 Adenylosuccinase Deficiency 44 1.433
220
P GLL020 Gallbladder Disease 56 1.433
221
ASP008 Aspiration Pneumonitis 42 1.433
222
CRN036 Craniopharyngioma 64 1.433
223
TRC003 Trichomoniasis 53 1.433
224
ADR005 Adrenal Carcinoma 62 1.433
225
SPN035 Spindle Cell Sarcoma 54 1.433
226
TRN015 Transient Cerebral Ischemia 63 1.433
227
LRY018 Laryngeal Squamous Cell Carcinoma 44 1.433
228
TXC005 Toxic Shock Syndrome 62 1.433
229
SRC014 Sarcoma 65 1.433
230
P MCR010 Microcephaly 60 1.433
231
BRN024 Bronchitis 67 1.433
232
P GLL018 Gallbladder Cancer 53 1.433
233
LST001 Listeriosis 59 1.433
234
P URT039 Urticaria 58 1.433
235
P HRD011 Hereditary Spherocytosis 64 1.433
236
P BNC003 Bone Cancer 58 1.433
237
CRB090 Cerebral Hypoxia 42 1.433
238
UTR043 Uterine Sarcoma 40 1.433
239
PRM243 Primary Bone Cancer 22 1.433
240
c LKM061 Leukemia, Acute Myeloid 83 1.368
241
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 50 1.368
242
P MYP004 Myopathy 67 1.368
243
P PLL002 Pellagra 46 1.368
244
P NTR004 Neutropenia 63 1.368
245
CRB039 Cerebrovascular Disease 66 1.368
246
LPD008 Lipid Metabolism Disorder 62 1.368
247
HYP056 Hypoglycemia 65 1.368
248
PRN011 Pernicious Anemia 53 1.223
249
THR024 Thrombosis 56 1.223
250
P RTN024 Retinoblastoma 73 1.223
251
CHL065 Cholangiocarcinoma 58 1.223
252
P CYS018 Cystitis 59 1.223
253
SKN016 Skin Disease 63 1.223
254
P DNG005 Dengue Virus 56 1.223
255
P CHR071 Charcot-Marie-Tooth Disease 64 1.223
256
P LKM002 Leukemia 67 1.223
257
TTH006 Tooth Disease 51 1.223
258
INT079 Intrahepatic Cholangiocarcinoma 51 1.223
259
P INF032 Infertility 57 1.223
260
PLC008 Placenta Disease 49 1.223
261
VSC002 Vascular Dementia 60 1.223
262
HMP009 Haemophilus Influenzae 41 1.223
263
c CHR408 Charcot-Marie-Tooth Disease, X-Linked Recessive, 5 43 1.060
264
P RHM011 Rheumatoid Arthritis 82 1.060
265
P MLT020 Multiple Sclerosis 79 1.060
266
c AMY091 Amyotrophic Lateral Sclerosis 1 88 1.060
267
PRP027 Peripheral Vascular Disease 71 1.060
268
ATS010 Autosomal Recessive Disease 42 1.060
269
CRB150 Cerebral Creatine Deficiency Syndrome 2 54 1.060
270
DFC004 Deficiency Anemia 74 1.060
271
P URN019 Urinary Tract Infection 49 1.060
272
c SCH085 Schizophrenia 2 27 1.060
273
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.060
274
EWN003 Ewing Sarcoma 70 1.060
275
OCL069 Ocular Motor Apraxia 57 1.060
276
P BCL017 B-Cell Lymphoma 59 1.060
277
NTR005 Nutritional Deficiency Disease 61 1.060
278
P MYL006 Myeloid Leukemia 61 1.060
279
P MVM001 Movement Disease 61 1.060
280
YLL002 Yellow Fever 61 1.060
281
P OPT006 Optic Nerve Disease 58 1.060
282
PLS011 Plasmacytoma 56 1.060
283
PPT005 Peptic Ulcer Disease 58 1.060
284
P LNG064 Lung Cancer Susceptibility 3 70 1.060
285
P LTR001 Lateral Sclerosis 58 1.060
286
TRN018 Transitional Cell Carcinoma 56 1.060
287
SPT005 Spotted Fever 49 1.060
288
ADJ001 Adjustment Disorder 47 1.060
289
GST050 Gastrointestinal System Disease 55 1.060
290
P THR015 Thrombophilia 51 1.060
291
CRT055 Creatine Deficiency Syndromes 37 1.060
292
DFN002 Dfnx1 Nonsyndromic Hearing Loss and Deafness 8 1.060
293
CYT002 Cytokine Deficiency 43 1.060
294
LYM019 Lymphosarcoma 46 1.060
295
NRT001 Neurotic Disorder 56 0.913
296
ANX004 Anoxia 40 0.865
297
VNZ002 Venezuelan Equine Encephalitis 46 0.865
298
ACT181 Acute Motor Axonal Neuropathy 22 0.865
299
P CRN300 Coronary Heart Disease 1 73 0.865
300
NCL008 Nuclear Ribonucleic Acid 15 0.865
301
PRS129 Prostatic Hyperplasia, Benign 49 0.865
302
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.865
303
INS024 Insulin-Like Growth Factor I 78 0.865
304
ANN002 Anencephaly 57 0.865
305
P OVR042 Ovarian Cancer 88 0.865
306
ATM095 Autoimmune Disease 61 0.865
307
P ATX030 Ataxia-Telangiectasia 80 0.865
308
BWN001 Bowen-Conradi Syndrome 53 0.865
310
PLY023 Polycystic Liver Disease 60 0.865
311
CHK001 Chikungunya 60 0.865
312
SBJ001 Subjective Cognitive Decline 30 0.865
313
P FTL001 Fetal Alcohol Syndrome 55 0.865
314
c THY056 Thyroid Dyshormonogenesis 3 31 0.865
315
ARM002 Aromatic L-Amino Acid Decarboxylase Deficiency 56 0.865
316
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.865
317
c TBR025 Tuberous Sclerosis 1 84 0.865
318
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.865
319
c TYP009 Type 2 Diabetes Mellitus 92 0.865
320
CRB204 Cerebellar, Ocular, Craniofacial, and Genital Syndrome 28 0.865
321
PRT037 Pertussis 65 0.865
322
P LPS004 Lupus Erythematosus 61 0.865
323
P MSC003 Muscular Atrophy 52 0.865
324
P CNT005 Central Nervous System Lymphoma 52 0.865
325
CRC021 Carcinosarcoma 64 0.865
326
P TYR004 Tyrosinemia 50 0.865
327
P ATR005 Atrophic Gastritis 50 0.865
328
PST092 Posttransplant Acute Limbic Encephalitis 28 0.865
329
P MSC005 Muscular Dystrophy 67 0.865
330
PRS047 Prostatitis 58 0.865
331
P THR014 Thrombocytopenia 66 0.865
332
P OLG002 Oligodendroglioma 66 0.865
333
P PLM036 Pulmonary Fibrosis 66 0.865
334
LYM027 Lymphopenia 56 0.865
335
LNG099 Lung Disease 62 0.865
336
AML001 Amelanotic Melanoma 37 0.865
337
P PRD008 Periodontitis 64 0.865
338
TLN003 Telangiectasis 51 0.865
339
PLC002 Plica Syndrome 35 0.865
340
LWC001 Low Compliance Bladder 45 0.865
341
PRS021 Prostatic Adenoma 43 0.865
342
P HYP086 Hypothyroidism 69 0.865
343
CCC002 Coccidiosis 50 0.865
344
P TBR001 Tuberous Sclerosis 69 0.865
345
P ECL001 Eclampsia 52 0.865
346
P INT143 Interstitial Cystitis 60 0.865
347
PRS045 Prostatic Hypertrophy 53 0.865
348
KRT002 Keratomalacia 55 0.865
349
c HPT007 Hepatitis E 51 0.865
350
P HYP076 Hyperthyroidism 53 0.865
351
PRP030 Purpura 54 0.865
352
SYN007 Synovitis 55 0.865
353
P ADL010 Adult Respiratory Distress Syndrome 71 0.865
354
P CRD246 Cardiovascular System Disease 56 0.865
355
P DRR001 Diarrhea 55 0.865
356
P ENC004 Encephalitis 61 0.865
357
ORL011 Oral Cancer 60 0.865
358
c XLN110 X-Linked Charcot-Marie-Tooth Disease 31 0.865
359
EXN003 Exencephaly 30 0.865
360
DWR001 Dwarfism 44 0.865
361
PNF002 Painful Legs and Moving Toes Syndrome 14 0.865
362
PRM226 Primary Central Nervous System Lymphoma 47 0.865
363
P NNS032 Non-Syndromic X-Linked Intellectual Disability 46 0.821
364
P CNG436 Congenital Disorder of Deglycosylation 51 0.821
365
PLM001 Pulmonary Tuberculosis 69 0.821
366
P ART023 Arthropathy 61 0.821
367
c NNS082 Non-Syndromic X-Linked Intellectual Disability 9 17 0.821
368
SNL007 Senile Cataract 40 0.821
369
PTH003 Pathologic Nystagmus 52 0.821
370
LYS003 Lysinuric Protein Intolerance 57 0.612
371
c TYP008 Type 1 Diabetes Mellitus 70 0.612
372
PST021 Postpartum Depression 50 0.612
373
c BCT007 Bacterial Meningitis 55 0.612
374
P DBT005 Diabetes Insipidus 54 0.612
375
HST016 Histiocytic Sarcoma 39 0.612
376
NNS045 Non-Specific Syndromic Intellectual Disability 42 0.612
377
PLY100 Polyploidy 36 0.612
378
PNM013 Pneumococcal Meningitis 43 0.612
379
P THL005 Thalassemia 56 0.612
380
RDT013 Radiation Proctitis 48 0.612
381
P OVR082 Overgrowth Syndrome 49 0.612
382
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.612
383
P NSP012 Nasopharyngeal Carcinoma 61 0.612
384
c MGR022 Migraine with or Without Aura 3 17 0.612
385
c OTP006 Otopalatodigital Syndrome, Type I 60 0.612
386
SPP011 Suppression of Tumorigenicity 12 61 0.612
387
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.612
388
CRB151 Cerebral Creatine Deficiency Syndrome 1 50 0.612
389
P FRG001 Fragile X Syndrome 70 0.612
390
P LPR021 Leprosy 3 71 0.612
391
ALP077 Alpha-Methylacetoacetic Aciduria 52 0.612
392
c ANM038 Anemia, Autoimmune Hemolytic 64 0.612
393
c AML061 Amelogenesis Imperfecta, Type Ie 36 0.612
394
P RTN008 Retinitis Pigmentosa 80 0.612
395
c LSS005 Lissencephaly 1 57 0.612
396
MSC157 Muscular Dystrophy, Duchenne Type 79 0.612
397
END057 Endometrial Cancer 72 0.612
398
P SCH015 Schizophrenia 74 0.612
399
P LFR001 Li-Fraumeni Syndrome 73 0.612
400
OBS002 Obsessive-Compulsive Disorder 68 0.612
401
c SYS001 Systemic Lupus Erythematosus 87 0.612
402
PRX015 Paroxysmal Extreme Pain Disorder 56 0.612
403
PLY150 Polykaryocytosis Inducer 29 0.612
404
c ATR087 Atrial Standstill 1 74 0.612
405
BRK010 Burkitt Lymphoma 66 0.612
406
c THR092 Thrombophilia Due to Thrombin Defect 74 0.612
407
CYS019 Cystathioninuria 46 0.612
408
HYP774 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome 54 0.612
409
c LKM063 Leukemia, Chronic Myeloid 71 0.612
410
SPC010 Speech and Communication Disorders 48 0.612
411
P ADL017 Adult T-Cell Leukemia 56 0.612
412
P ANP001 Anaplastic Large Cell Lymphoma 61 0.612
413
MTB004 Metabolic Acidosis 48 0.612
414
CRB148 Cerebral Creatine Deficiency Syndrome 3 39 0.612
415
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.612
416
MYL009 Myelodysplastic Syndrome 67 0.612
417
DFF005 Diffuse Large B-Cell Lymphoma 54 0.612
418
BTN004 Biotin Deficiency 45 0.612
419
HYP346 Hypotrichosis and Recurrent Skin Vesicles 29 0.612
420
MSC007 Muscle Hypertrophy 64 0.612
421
THY121 Thyroid Gland Anaplastic Carcinoma 67 0.612
422
P KRT014 Keratosis Follicularis Spinulosa Decalvans 31 0.612
423
P PLY014 Polycystic Kidney Disease 69 0.612
424
MYL020 Myelomeningocele 51 0.612
425
PHY002 Physical Disorder 41 0.612
426
P LYM118 Lymphoma 67 0.612
427
CRH005 Crohn's Colitis 53 0.612
428
c RTN041 Retinitis Pigmentosa 11 42 0.612
429
NRL018 Neural Tube Defects, Folate-Sensitive 45 0.612
430
CHR103 Charge Syndrome 66 0.612
431
P CHN012 Chondrosarcoma 57 0.612
432
CRN264 Craniosynostosis with Fibular Aplasia 29 0.612
433
FCT007 Factor Vii Deficiency 64 0.612
434
VSC053 Visceral Steatosis, Congenital 34 0.612
435
TRD006 Tardive Dyskinesia 53 0.612
436
c TYR012 Tyrosinemia, Type I 61 0.612
437
WLS001 Wilson Disease 70 0.612
438
LGH007 Leigh Syndrome 70 0.612
439
P STS008 Sotos Syndrome 1 60 0.612
440
c DPH024 Diaphragmatic Hernia, Congenital 64 0.612
441
P CTR177 Citrullinemia, Type Ii, Adult-Onset 55 0.612
442
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 0.612
443
VLT001 Vulto-Van Silfhout-De Vries Syndrome 41 0.612
444
CRP030 Corpus Callosum, Agenesis of, with Facial Anomalies and Cerebellar Ataxia 37 0.612
445
c MGR040 Migraine with or Without Aura 12 16 0.612
446
ACT119 Acute Promyelocytic Leukemia 62 0.612
448
WST005 West Nile Virus 57 0.612
449
CFF002 Coffin-Lowry Syndrome 60 0.612
450
MLY008 Molybdenum Cofactor Deficiency, Complementation Group a 47 0.612
451
c SPS148 Spastic Paraplegia 31, Autosomal Dominant 47 0.612
452
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 68 0.612
453
c AMY089 Amyotrophic Lateral Sclerosis 7 28 0.612
454
LGN006 Legionnaire Disease 52 0.612
455
c SPS111 Spastic Paraplegia 27, Autosomal Recessive 28 0.612
456
c LFR007 Li-Fraumeni Syndrome 2 46 0.612
457
BLM001 Bloom Syndrome 65 0.612
458
HMC042 Homocystinuria-Megaloblastic Anemia, Cble Complementation Type 33 0.612
459
c HYD064 Hydrocephalus, Congenital, 1 51 0.612
460
MYL069 Myeloma, Multiple 77 0.612
461
ORT008 Orotic Aciduria 57 0.612
462
PLY158 Polyglucosan Body Neuropathy, Adult Form 39 0.612
463
c PNC106 Pancreatic Agenesis 1 51 0.612
464
P SPP010 Suppressor of Tumorigenicity 3 51 0.612
465
DGR001 Digeorge Syndrome 62 0.612
466
c SML038 Small Cell Cancer of the Lung 69 0.612
467
DRR014 Darier-White Disease 59 0.612
468
c FBR084 Fibromatosis, Gingival, 1 49 0.612
469
P HNT016 Huntington Disease 73 0.612
470
P MDL005 Medulloblastoma 75 0.612
471
P GLM040 Glioma Susceptibility 1 71 0.612
472
P MYC007 Myocardial Infarction 70 0.612
473
ADN024 Adenine Phosphoribosyltransferase Deficiency 53 0.612
474
CMB072 Combined Oxidative Phosphorylation Deficiency 28 23 0.612
475
MTC163 Mitochondrial Complex I Deficiency, Nuclear Type 16 23 0.612
476
DSS032 Disease by Infectious Agent 55 0.612
477
NRR001 Neuroretinitis 42 0.612
478
BCT022 Bacterial Infectious Disease 56 0.612
479
GLC003 Glucose Intolerance 54 0.612
480
ARG004 Argyria 26 0.612
482
PRM329 Premature Aging 36 0.612
483
THY029 Thyroid Carcinoma 51 0.612
484
P ISL078 Isolated Ectopia Lentis 58 0.612
485
MDD018 Middle East Respiratory Syndrome 44 0.612
486
P GNG025 Gingival Fibromatosis 47 0.612
487
ZKF001 Zika Fever 52 0.612
488
c ACT073 Acute Leukemia 58 0.612
489
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.612
490
P FML355 Familial Intrahepatic Cholestasis 42 0.612
491
CWP001 Cowpox 45 0.612
492
P AMY004 Amyloidosis 70 0.612
493
BRN004 Brain Edema 54 0.612
494
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 67 0.612
495
CRN030 Coronary Stenosis 50 0.612
496
RTN023 Retinitis 46 0.612
497
CRV002 Cervix Uteri Carcinoma in Situ 47 0.612
498
PRP007 Priapism 47 0.612
499
P PSR002 Psoriasis 63 0.612
500
AMB001 Amebiasis 57 0.612
501
CHC001 Chickenpox 57 0.612
502
P CHL066 Cholangitis 52 0.612
503
HPT022 Hepatoblastoma 54 0.612
504
CLL010 Cellular Ependymoma 57 0.612
505
CHR066 Chronic Fatigue Syndrome 60 0.612
506
GLL048 Glial Tumor 52 0.612
507
SYN036 Syncope 45 0.612
508
P RRH023 Rare Hereditary Hemochromatosis 54 0.612
509
MNG007 Manganese Poisoning 28 0.612
510
PNC129 Pancreatic Adenocarcinoma 65 0.612
511
c VRL010 Viral Hepatitis 53 0.612
512
MNK002 Monkeypox 41 0.612
513
TRT001 Teratocarcinoma 42 0.612
514
P SKN015 Skin Carcinoma 71 0.612
515
P PNC025 Panic Disorder 52 0.612
516
OVR063 Overnutrition 42 0.612
517
PST011 Pustulosis of Palm and Sole 52 0.612
518
ANT024 Anthrax Disease 58 0.612
519
P ART022 Arthritis 71 0.612
520
P BNG030 Benign Ependymoma 51 0.612
521
P CCK001 Cockayne Syndrome 68 0.612
522
P NGH001 Night Blindness 52 0.612
523
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 0.612
524
P MMP001 Mumps 57 0.612
525
DNG001 Dengue Shock Syndrome 40 0.612
526
CHL004 Cholelithiasis 49 0.612
527
OST011 Osteomalacia 52 0.612
528
P DMN002 Dementia 66 0.612
529
HMS001 Hemosiderosis 48 0.612
530
DNG003 Dengue Disease 65 0.612
531
P HYP061 Hypertrophic Cardiomyopathy 69 0.612
532
DNG002 Dengue Hemorrhagic Fever 60 0.612
533
PNC001 Pancytopenia 53 0.612
534
CRT013 Carotid Stenosis 51 0.612
535
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.612
536
P HMN010 Hemangioma 62 0.612
537
BLR008 Bilirubin Metabolic Disorder 57 0.612
538
P BRB001 Beriberi 44 0.612
539
SNS003 Sensory Peripheral Neuropathy 52 0.612
540
P DDN001 Duodenal Ulcer 53 0.612
541
c ATM011 Autoimmune Hepatitis 63 0.612
542
KRT009 Keratosis 53 0.612
543
CLN015 Colon Adenocarcinoma 65 0.612
544
MLG169 Malignant Astrocytoma 57 0.612
545
P GLY013 Glycogen Storage Disease 60 0.612
546
P HRT032 Heart Disease 81 0.612
547
HPT014 Hepatorenal Syndrome 49 0.612
548
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.612
549
PRT013 Portal Hypertension 59 0.612
550
P RSP003 Respiratory Failure 74 0.612
551
LYM017 Lyme Disease 62 0.612
552
QFV001 Q Fever 62 0.612
553
P PLY011 Polycystic Ovary Syndrome 57 0.612
554
MXD026 Mixed Glioma 45 0.612
555
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.612
556
P EPL003 Epulis 30 0.612
557
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.612
558
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.612
559
PRM020 Premenstrual Tension 39 0.612
560
EMB004 Embryonal Carcinoma 56 0.612
561
GNG013 Gingivitis 59 0.612
562
PRC003 Proctitis 49 0.612
563
P KDN017 Kidney Cancer 61 0.612
564
GST045 Gastroenteritis 58 0.612
565
GNR003 Generalized Atherosclerosis 43 0.612
566
WRN003 Wernicke Encephalopathy 46 0.612
567
PNC034 Pancreas Disease 50 0.612
568
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.612
569
P OBS001 Obstructive Jaundice 48 0.612
570
P PLY019 Polyneuropathy 52 0.612
571
c ATS204 Autosomal Recessive Non-Syndromic Intellectual Disability 48 0.612
572
P PRP029 Porphyria 60 0.612
573
KLB003 Klebsiella Pneumonia 50 0.612
574
P EHL001 Ehlers-Danlos Syndrome 58 0.612
575
GNR004 Generalized Anxiety Disorder 55 0.612
576
SQM006 Squamous Cell Carcinoma 60 0.612
577
RLP003 Relapsing Fever 49 0.612
578
c SVR005 Severe Pre-Eclampsia 50 0.612
579
HLL004 Hellp Syndrome 53 0.612
580
P INS002 in Situ Carcinoma 53 0.612
581
P MNN013 Meningitis 65 0.612
582
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 17 0.612
583
NCL011 Nuclear Gene-Encoded Leigh Syndrome Spectrum 21 0.612
584
P MYC008 Myocarditis 59 0.612
585
P TXP001 Toxoplasmosis 60 0.612
586
KDN013 Kidney Hypertrophy 34 0.612
587
HNS001 Hansen's Disease 32 0.612
588
c LKM005 Leukemia, T-Cell, Chronic 34 0.612
589
MYL080 Myalgic Encephalomyelitis/chronic Fatigue Syndrome 29 0.612
590
c RNG019 Ring Chromosome 3 19 0.612
591
SFT003 Soft Tissue Sarcoma 57 0.612
592
P RGD004 Rigid Spine Muscular Dystrophy 22 0.612
593
DSR002 Disorders of Intracellular Cobalamin Metabolism 29 0.612
594
P MTC069 Mitochondrial Disorders 57 0.612
595
P CRB088 Cerebral Atrophy 33 0.612
596
PTT037 Pituitary Tumors 44 0.612
597
BCK006 Back Pain 47 0.612
598
MYT011 Myotonia 39 0.612
599
BRN071 Brain Injury 50 0.612
600
P MYC033 Myoclonus 47 0.612
601
CRL001 Cerulean Cataract 26 0.612
602
CRV045 Cervical Intraepithelial Neoplasia 39 0.612
603
PRN029 Parainfluenza Virus Type 3 32 0.612
604
DHY008 Dihydroxyadeninuria 24 0.612
605
HVY002 Heavy Metal Poisoning 22 0.612
606
MTH046 Methylmalonic Acidemia Without Homocystinuria 39 0.612
607
OVR094 Ovarian Epithelial Cancer 39 0.612
608
ALL014 Allergic Encephalomyelitis 34 0.612
609
DSS012 Disseminated Infection with Mycobacterium Avium Complex 19 0.612
610
FBR019 Fibromatosis 42 0.612
611
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.612
612
LRG010 L-Arginine:glycine Amidinotransferase Deficiency 17 0.612
613
NDL013 Nodular Regenerative Hyperplasia 46 0.612
614
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.612
615
PRT058 Pure Autonomic Failure 58 0.612
616
GLM045 Glioma 63 0.612
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