Search results for Glutathione

618 hits were found for Glutathione

# Family MCID Name MIFTS Score
1
GLT007 Glutathione Synthetase Deficiency 47 8.667
2
GLT036 Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia Due to 17 6.158
3
GLT039 Glutathione Peroxidase Deficiency 36 4.802
4
HML010 Hemolytic Anemia Due to Glutathione Reductase Deficiency 4 3.297
5
HYD063 Hydroxyacyl Glutathione Hydrolase Deficiency 11 3.284
6
GLT034 Glutathione Transferase Activity Toward Trans-Stilbene Oxide 3 3.284
7
P LNG032 Lung Cancer 99 0.319
8
P BRS047 Breast Cancer 100 0.301
9
P LKM002 Leukemia 75 0.248
10
P HPT021 Hepatitis 75 0.245
11
PRS047 Prostatitis 59 0.236
12
AGN016 Aging 65 0.216
13
P CLR023 Colorectal Cancer 98 0.212
14
P PRS040 Prostate Cancer 88 0.209
15
END072 Endotheliitis 46 0.207
16
GST053 Gastric Cancer 84 0.205
17
c BLD140 Blood Group, I System 37 0.203
18
P BLD134 Bladder Cancer 78 0.201
19
SQM006 Squamous Cell Carcinoma 74 0.191
20
AST005 Asthma 83 0.176
21
P CTR002 Cataract 60 0.172
22
P OVR042 Ovarian Cancer 82 0.170
23
P HPT023 Hepatocellular Carcinoma 94 0.167
24
NRN002 Neuronitis 43 0.167
25
P ESP024 Esophagitis 64 0.165
26
P ADN016 Adenocarcinoma 71 0.160
27
c SML038 Small Cell Cancer of the Lung 67 0.160
28
P INF032 Infertility 59 0.160
29
P DBT009 Diabetes Mellitus 72 0.158
30
MLN008 Melanoma 72 0.145
31
P LYM118 Lymphoma 71 0.145
32
P SCH015 Schizophrenia 71 0.139
33
P MYL006 Myeloid Leukemia 69 0.137
34
P RHM011 Rheumatoid Arthritis 91 0.128
35
P ART022 Arthritis 77 0.128
36
P LVR013 Liver Disease 76 0.128
37
P NRB001 Neuroblastoma 73 0.128
38
CYS001 Cystic Fibrosis 85 0.125
39
ISC004 Ischemia 66 0.125
40
CRB009 Cerebritis 41 0.125
41
P END044 Endometriosis 71 0.121
42
P PNC044 Pancreatitis 64 0.121
43
P ALZ034 Alzheimer Disease 95 0.118
44
P GLM045 Glioma 61 0.118
45
P CRV039 Cervicitis 49 0.118
46
MLR004 Malaria 86 0.115
47
P PRK057 Parkinson Disease, Late-Onset 78 0.115
48
P LYM026 Lymphoblastic Leukemia 66 0.111
49
c LKM061 Leukemia, Acute Myeloid 81 0.108
50
P HML002 Hemolytic Anemia 62 0.108
51
P LRY019 Laryngitis 57 0.108
52
P MYC084 Mycobacterium Tuberculosis 1 69 0.104
53
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.104
54
P THY032 Thyroiditis 56 0.104
55
ART140 Arteries, Anomalies of 51 0.104
56
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.104
57
P CRN018 Coronary Artery Anomaly 69 0.100
58
ORL011 Oral Cancer 60 0.100
59
P MYC007 Myocardial Infarction 81 0.097
60
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.097
61
GLB002 Glioblastoma 74 0.097
62
ORL015 Oral Squamous Cell Carcinoma 59 0.097
63
c OVR114 Ovarian Cancer 1 54 0.097
64
SNL007 Senile Cataract 41 0.097
65
ESP021 Esophageal Cancer 79 0.092
66
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.092
67
P NRP001 Neuropathy 63 0.092
68
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 62 0.092
69
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.092
70
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.092
71
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.092
72
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.092
73
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.092
74
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.092
75
LKP003 Leukoplakia 42 0.092
76
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.092
77
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.092
78
MYL009 Myelodysplastic Syndrome 75 0.088
79
P ENC018 Encephalopathy 58 0.088
80
MLN007 Male Infertility 53 0.088
81
ORL012 Oral Leukoplakia 45 0.088
82
BSL008 Basal Ganglia Disease 44 0.088
83
MVM001 Movement Disease 40 0.088
84
P MLT020 Multiple Sclerosis 85 0.084
85
c HPT001 Hepatitis C 73 0.084
86
P CRV035 Cervical Cancer 72 0.084
87
P THL005 Thalassemia 65 0.084
88
c LNG109 Lung Cancer Susceptibility 1 23 0.084
89
P HRT032 Heart Disease 80 0.079
90
P ATS364 Autism 70 0.079
91
P KDN018 Kidney Disease 69 0.079
92
c BSL007 Basal Cell Carcinoma 66 0.079
93
PNC034 Pancreas Disease 59 0.079
94
RTN023 Retinitis 52 0.079
95
c BSL024 Basal Cell Carcinoma 1 42 0.079
96
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.074
97
c LKM063 Leukemia, Chronic Myeloid 80 0.074
98
c MCL042 Macular Degeneration, Age-Related, 1 79 0.074
99
PSY004 Psychotic Disorder 72 0.074
100
c BTT014 Beta-Thalassemia 70 0.074
101
c HPT016 Hepatitis B 68 0.074
102
P PRD008 Periodontitis 67 0.074
103
P AST007 Astrocytoma 66 0.074
104
ADN018 Adenoma 63 0.074
105
CHL068 Cholestasis 60 0.074
106
P LTR001 Lateral Sclerosis 58 0.074
107
P INF037 Inflammatory Bowel Disease 52 0.074
108
c MTR002 Mitral Valve Insufficiency 46 0.074
109
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.074
110
5XP001 5-Oxoprolinase Deficiency 25 0.074
111
P PNC035 Pancreatic Cancer 89 0.068
112
c SYS001 Systemic Lupus Erythematosus 86 0.068
113
c HYP595 Hypertension, Essential 78 0.068
114
APL001 Aplastic Anemia 74 0.068
115
LVR012 Liver Cirrhosis 73 0.068
116
THY028 Thyroid Cancer 72 0.068
117
c CHR089 Chronic Kidney Failure 72 0.068
118
VSC007 Vascular Disease 71 0.068
119
P LPS004 Lupus Erythematosus 69 0.068
120
GLB015 Glioblastoma Multiforme 68 0.068
121
c PRC016 Pre-Eclampsia 65 0.068
122
HYP066 Hyperglycemia 64 0.068
123
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.068
124
FTT001 Fatty Liver Disease 62 0.068
125
P ECL001 Eclampsia 57 0.068
126
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 48 0.068
127
NSP002 Nasopharyngitis 46 0.068
128
GLC008 Glucose Metabolism Disease 38 0.068
129
c LKM071 Leukemia, Chronic Lymphocytic 75 0.062
130
SCK003 Sickle Cell Anemia 73 0.062
131
P NSP012 Nasopharyngeal Carcinoma 71 0.062
132
DRM006 Dermatitis 67 0.062
133
c CNT035 Central Nervous System Disease 65 0.062
134
HYP266 Hypoxia 61 0.062
135
c ACT073 Acute Leukemia 61 0.062
136
c GLC092 Glaucoma, Primary Open Angle 58 0.062
137
TRN018 Transitional Cell Carcinoma 58 0.062
138
VRC001 Varicocele 52 0.062
139
P OPN001 Open-Angle Glaucoma 51 0.062
140
ANX004 Anoxia 49 0.062
141
FXF002 Fox-Fordyce Disease 40 0.062
142
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 40 0.062
143
c LKM004 Leukemia, B-Cell, Chronic 37 0.062
144
c LKM056 Leukemia, Chronic Lymphocytic 2 35 0.062
145
P RNG031 Ring Chromosome Y Syndrome 29 0.062
146
LKT001 Leukotriene C4 Synthase Deficiency 24 0.062
147
GLT014 Glutathionuria 21 0.062
148
GMM011 Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia Due to 20 0.062
149
SQM013 Squamous Cell Carcinoma, Head and Neck 79 0.056
150
P NRV007 Nervous System Disease 75 0.056
151
PLM001 Pulmonary Tuberculosis 72 0.056
152
BRN028 Brain Cancer 72 0.056
153
P BCL006 B-Cell Lymphomas 70 0.056
154
GLL018 Gallbladder Cancer 67 0.056
155
LNG099 Lung Disease 67 0.056
156
ATM095 Autoimmune Disease 66 0.056
157
c MLG068 Malignant Glioma 66 0.056
158
ACQ007 Acquired Immunodeficiency Syndrome 65 0.056
159
P PSR002 Psoriasis 65 0.056
160
MDD011 Mood Disorder 64 0.056
161
DFF005 Diffuse Large B-Cell Lymphoma 64 0.056
162
PRD007 Periodontal Disease 64 0.056
163
c ACT075 Acute Myocardial Infarction 64 0.056
164
c ATM011 Autoimmune Hepatitis 63 0.056
165
CLT003 Colitis 63 0.056
166
ALC006 Alcoholic Hepatitis 62 0.056
167
MTR014 Motor Neuron Disease 62 0.056
168
P RHN004 Rhinitis 62 0.056
169
P INT001 Intrahepatic Cholestasis 62 0.056
170
c ACT027 Acute Pancreatitis 61 0.056
171
P BPL003 Bipolar Disorder 61 0.056
172
NRM005 Neuromuscular Disease 60 0.056
173
CLR108 Colorectal Adenoma 60 0.056
174
PLS007 Plasmodium Falciparum Malaria 59 0.056
175
P CRN300 Coronary Heart Disease 1 57 0.056
176
BRN106 Burns 57 0.056
177
c MCR113 Microvascular Complications of Diabetes 3 55 0.056
178
TXC002 Toxic Encephalopathy 55 0.056
179
CLR109 Colorectal Adenocarcinoma 54 0.056
180
ALC009 Alcoholic Liver Cirrhosis 53 0.056
181
P TCL004 T-Cell Leukemia 50 0.056
182
MTB004 Metabolic Acidosis 49 0.056
183
PST011 Pustulosis of Palm and Sole 47 0.056
184
AZS001 Azoospermia 47 0.056
185
BLR008 Bilirubin Metabolic Disorder 45 0.056
186
BRN080 Brain Ischemia 45 0.056
187
c MCR130 Microvascular Complications of Diabetes 6 42 0.056
188
DBT007 Diabetic Cataract 38 0.056
189
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.056
190
c MCR120 Microvascular Complications of Diabetes 7 34 0.056
191
c MCR133 Microvascular Complications of Diabetes 4 32 0.056
192
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.056
193
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.048
194
P ATX030 Ataxia-Telangiectasia 80 0.048
195
LYM133 Lymphoma, Hodgkin, Classic 78 0.048
196
P MDL005 Medulloblastoma 76 0.048
197
c HPT073 Hepatitis C Virus 73 0.048
198
P PNM007 Pneumonia 70 0.048
199
c MNN043 Meningioma, Familial 69 0.048
200
P CHR012 Chronic Granulomatous Disease 69 0.048
201
P DRM053 Dermatitis, Atopic 68 0.048
202
ALL003 Allergic Rhinitis 68 0.048
203
DMN002 Dementia 68 0.048
204
MTH009 Mouth Disease 64 0.048
205
c ADL017 Adult T-Cell Leukemia 63 0.048
206
P ALC004 Alcohol Abuse 63 0.048
207
SCH014 Schistosomiasis 62 0.048
208
THR024 Thrombosis 61 0.048
209
P ACT074 Acute Lymphocytic Leukemia 61 0.048
210
MCS002 Mucositis 61 0.048
211
P PLY018 Polycythemia 60 0.048
212
SNS001 Sensorineural Hearing Loss 59 0.048
213
TRD006 Tardive Dyskinesia 59 0.048
214
PHR003 Pharyngitis 59 0.048
215
P LPR021 Leprosy 3 59 0.048
216
P SML001 Small Cell Carcinoma 58 0.048
217
HMT018 Hematopoietic Stem Cell Transplantation 58 0.048
218
P LRY044 Larynx Cancer 57 0.048
219
P PNC025 Panic Disorder 57 0.048
220
NNL002 Nonalcoholic Steatohepatitis 56 0.048
221
P PRM006 Primary Biliary Cirrhosis 55 0.048
222
P PNM006 Pneumoconiosis 55 0.048
223
TST014 Testicular Cancer 54 0.048
224
SCK005 Sickle Cell Disease 54 0.048
225
CLN015 Colon Adenocarcinoma 53 0.048
226
P GLM040 Glioma Susceptibility 1 51 0.048
227
GNG011 Gingival Disease 50 0.048
228
c PRD040 Periodontitis, Chronic 49 0.048
229
P RNL017 Renal Oncocytoma 49 0.048
230
THR035 Thrombasthenia 46 0.048
231
SQM022 Squamous Cell Carcinoma of the Larynx 45 0.048
232
FSC002 Fascioliasis 45 0.048
233
ASB001 Asbestosis 45 0.048
234
BRR002 Barrett's Adenocarcinoma 43 0.048
235
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.048
236
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.048
237
EXT006 Extrahepatic Cholestasis 39 0.048
238
OLG001 Oligospermia 39 0.048
239
c BLR024 Biliary Cirrhosis, Primary, 1 35 0.048
240
c INF145 Infantile Liver Failure Syndrome 1 33 0.048
241
P STR035 Streptococcal Group a Invasive Disease 28 0.048
242
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 27 0.048
243
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.048
244
ASB003 Asbestos Intoxication 19 0.048
245
CTR009 Cataract Congenital Dominant Non Nuclear 16 0.048
246
MYL069 Myeloma, Multiple 86 0.039
247
P INF038 Influenza 77 0.039
248
PLY001 Polycythemia Vera 75 0.039
249
ANX010 Anxiety 72 0.039
250
P MNN013 Meningitis 71 0.039
251
HMN044 Human Immunodeficiency Virus Type 1 71 0.039
252
DWN001 Down Syndrome 70 0.039
253
CNN003 Conn's Syndrome 70 0.039
254
P TST021 Testicular Germ Cell Tumor 70 0.039
255
CHL065 Cholangiocarcinoma 70 0.039
256
P EPL164 Epilepsy 70 0.039
257
P DMN001 Diamond-Blackfan Anemia 70 0.039
258
P DBT085 Diabetes Mellitus, Insulin-Dependent 69 0.039
259
P ANR048 Aniridia 1 68 0.039
260
SRC014 Sarcoma 68 0.039
261
P CHR071 Charcot-Marie-Tooth Disease 67 0.039
262
CHR066 Chronic Fatigue Syndrome 67 0.039
263
P CNJ013 Conjunctivitis 67 0.039
264
PRT036 Peritonitis 67 0.039
265
P MPL001 Maple Syrup Urine Disease 66 0.039
266
c EXD008 Exudative Vitreoretinopathy 1 65 0.039
267
P PLY011 Polycystic Ovary Syndrome 65 0.039
268
P CLC063 Celiac Disease 1 65 0.039
269
GLC006 Galactosemia 64 0.039
270
CNT047 Contact Dermatitis 64 0.039
271
HLC007 Helicobacter Pylori Infection 64 0.039
272
RSP006 Respiratory System Disease 63 0.039
273
PNC033 Pancreas Adenocarcinoma 63 0.039
274
P PRP029 Porphyria 62 0.039
275
FLL027 Fallopian Tube Carcinoma 62 0.039
276
P EXN002 Exanthem 62 0.039
277
MRB003 Morbid Obesity 61 0.039
278
BRN056 Bronchopulmonary Dysplasia 61 0.039
279
c THR092 Thrombophilia Due to Thrombin Defect 61 0.039
280
ALL006 Allergic Asthma 60 0.039
281
MNT002 Mental Depression 60 0.039
282
c SCL052 Scleroderma, Familial Progressive 60 0.039
283
P MLG056 Malignant Hyperthermia 60 0.039
284
P PLY014 Polycystic Kidney Disease 60 0.039
285
P NPH012 Nephrotic Syndrome 60 0.039
286
HRY003 Hairy Cell Leukemia 60 0.039
287
HPT019 Hepatic Encephalopathy 59 0.039
288
CHR177 Chromophobe Renal Cell Carcinoma 59 0.039
289
TRN015 Transient Cerebral Ischemia 58 0.039
290
FLR002 Filariasis 58 0.039
291
P OVR049 Ovarian Disease 58 0.039
292
ADN027 Adenomyosis 57 0.039
293
IMM136 Immune System Disease 57 0.039
294
DBN001 Dubin-Johnson Syndrome 56 0.039
295
IGR001 Ige Responsiveness, Atopic 56 0.039
296
P MYP006 Myopia 56 0.039
297
CYS010 Cystinosis 55 0.039
298
NRT004 Neuritis 55 0.039
299
MGR028 Migraine with or Without Aura 1 55 0.039
300
TTH006 Tooth Disease 54 0.039
301
PYR041 Pyruvate Kinase Deficiency of Red Cells 54 0.039
302
ASP003 Aseptic Meningitis 54 0.039
303
PRP019 Peripheral Nervous System Disease 53 0.039
304
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.039
305
HMG005 Hemoglobinopathy 53 0.039
306
HLL004 Hellp Syndrome 53 0.039
307
PRT038 Protein-Energy Malnutrition 52 0.039
308
c PNS012 Paine Syndrome 52 0.039
309
NSD001 Nose Disease 51 0.039
310
SCB001 Scabies 50 0.039
311
P MRC003 Mercury Poisoning 50 0.039
312
HMS001 Hemosiderosis 50 0.039
313
THR013 Thoracic Outlet Syndrome 50 0.039
314
PLL012 Pollen Allergy 48 0.039
315
GRS011 Gerstmann-Straussler Disease 48 0.039
316
P TYR004 Tyrosinemia 48 0.039
317
c ACT078 Acute Porphyria 48 0.039
318
PRS129 Prostatic Hyperplasia, Benign 47 0.039
319
c SPR009 Sporadic Breast Cancer 47 0.039
320
SDD008 Sudden Sensorineural Hearing Loss 46 0.039
321
NRR001 Neuroretinitis 46 0.039
322
ALB002 Albinism 45 0.039
323
c CHR020 Chronic Interstitial Cystitis 44 0.039
324
c WLM011 Wilms Tumor 6 44 0.039
325
KWS001 Kwashiorkor 43 0.039
326
PRT035 Peritoneum Cancer 42 0.039
327
CND005 Cone Dystrophy 42 0.039
328
GST071 Gastrointestinal Carcinoma 40 0.039
329
SMT002 Smooth Muscle Tumor 39 0.039
330
HNZ004 Heinz Body Anemias 38 0.039
331
CND006 Candida Glabrata 38 0.039
332
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.039
333
FLR001 Filarial Elephantiasis 37 0.039
334
P GRM010 Germ Cells Tumors 37 0.039
335
PGM003 Pigmentation Disease 36 0.039
336
FLL029 Fallopian Tube Disease 35 0.039
337
KSH001 Keshan Disease 33 0.039
338
ARB001 Ariboflavinosis 32 0.039
339
GND003 Gonadal Disease 32 0.039
340
ALP072 Alpha-Fetoprotein Deficiency 32 0.039
341
c CTR119 Cataract 32, Multiple Types 32 0.039
342
c TST046 Testicular Germ Cell Tumor 1 26 0.039
343
PRS011 Persian Gulf Syndrome 26 0.039
344
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 24 0.039
345
CRC034 Carcinoma Showing Thymus-Like Differentiation 24 0.039
346
TRN002 Transitional Meningioma 23 0.039
347
ANT078 Antipyrine Metabolism 22 0.039
348
ANR038 Anorexia Nervosa 1 21 0.039
349
PLY150 Polykaryocytosis Inducer 20 0.039
350
HRN018 Hearing Loss, Cisplatin-Induced 19 0.039
351
BLD137 Blood Group--Ahonen 17 0.039
352
OST012 Osteoarthritis 88 0.028
353
P RTT002 Rett Syndrome 82 0.028
354
P HYP607 Hypercholesterolemia, Familial 81 0.028
355
CRH001 Crohn's Disease 80 0.028
356
ULC004 Ulcerative Colitis 80 0.028
357
NRL016 Neural Tube Defects 79 0.028
358
P DLT002 Dilated Cardiomyopathy 76 0.028
359
END057 Endometrial Cancer 76 0.028
360
PHN003 Phenylketonuria 73 0.028
361
P FML018 Familial Mediterranean Fever 73 0.028
362
MLD001 Melioidosis 73 0.028
363
P PHC003 Pheochromocytoma 72 0.028
364
ADR007 Adrenoleukodystrophy 72 0.028
365
P FML011 Familial Adenomatous Polyposis 71 0.028
366
c HMC039 Hemochromatosis, Type 1 71 0.028
367
BRC012 Brucellosis 71 0.028
368
BRK010 Burkitt Lymphoma 71 0.028
369
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.028
370
P MYP004 Myopathy 69 0.028
371
P AMY004 Amyloidosis 69 0.028
372
P ATR011 Atrial Fibrillation 68 0.028
373
CRB039 Cerebrovascular Disease 68 0.028
374
c PRM196 Premature Ovarian Failure 1 68 0.028
375
PNC041 Pancreatic Ductal Adenocarcinoma 67 0.028
376
P ADL010 Adult Respiratory Distress Syndrome 67 0.028
377
BRN024 Bronchitis 67 0.028
378
SPN186 Spinal Cord Injury 67 0.028
379
P KDN017 Kidney Cancer 66 0.028
380
P MCR115 Microvascular Complications of Diabetes 5 66 0.028
381
VSC011 Vasculitis 66 0.028
382
GST050 Gastrointestinal System Disease 66 0.028
383
CHL123 Chlamydia 64 0.028
384
GLL008 Gilles De La Tourette Syndrome 64 0.028
385
P ALP009 Alopecia Areata 64 0.028
386
GNG013 Gingivitis 64 0.028
387
PLM031 Poliomyelitis 64 0.028
388
P LNG064 Lung Cancer Susceptibility 3 64 0.028
389
ACT119 Acute Promyelocytic Leukemia 64 0.028
390
c HPT003 Hepatitis a 63 0.028
391
P PLV020 Pelvic Organ Prolapse 63 0.028
392
P ART021 Arteriosclerosis 62 0.028
393
P HRM001 Hermansky-Pudlak Syndrome 62 0.028
394
P HYP086 Hypothyroidism 62 0.028
395
DFC004 Deficiency Anemia 62 0.028
396
LSC001 Lesch-Nyhan Syndrome 62 0.028
397
c MCR129 Microvascular Complications of Diabetes 1 62 0.028
398
VTR013 Vitreoretinopathy, Neovascular Inflammatory 61 0.028
399
SDD001 Sudden Infant Death Syndrome 61 0.028
400
ETN001 Eating Disorder 61 0.028
401
INT002 Intermittent Claudication 61 0.028
402
P WLF004 Wolfram Syndrome 61 0.028
403
TXC005 Toxic Shock Syndrome 61 0.028
404
CLF027 Cleft Palate, Isolated 61 0.028
405
P FBR017 Fibrosarcoma 61 0.028
406
TNS005 Tonsillitis 61 0.028
407
P RBL001 Rubella 61 0.028
408
c PNC108 Pancreatitis, Hereditary 60 0.028
409
P NTR004 Neutropenia 60 0.028
410
c ALP101 Alpha-Thalassemia 60 0.028
411
P DRR001 Diarrhea 60 0.028
412
ALL010 Allergic Contact Dermatitis 60 0.028
413
GST040 Gastric Adenocarcinoma 60 0.028
414
c CHL119 Cholangitis, Primary Sclerosing 60 0.028
415
LNG039 Lung Squamous Cell Carcinoma 60 0.028
416
P FCL005 Focal Segmental Glomerulosclerosis 60 0.028
417
DBT010 Diabetic Neuropathy 60 0.028
418
c VRL010 Viral Hepatitis 59 0.028
419
c ALZ049 Alzheimer Disease 2 59 0.028
420
SLP005 Sleep Disorder 59 0.028
421
PRC002 Paracoccidioidomycosis 59 0.028
422
END030 End Stage Renal Failure 59 0.028
423
END041 Endometrial Adenocarcinoma 59 0.028
424
LPD008 Lipid Metabolism Disorder 59 0.028
425
c FCL025 Focal Segmental Glomerulosclerosis 1 59 0.028
426
VGN023 Vaginitis 59 0.028
427
EMB004 Embryonal Carcinoma 59 0.028
428
RLP002 Relapsing-Remitting Multiple Sclerosis 59 0.028
429
SRC027 Sarcoma, Synovial 58 0.028
430
c ESS001 Essential Tremor 58 0.028
431
SFT003 Soft Tissue Sarcoma 58 0.028
432
LMY002 Leiomyoma 58 0.028
433
PPL022 Papilloma 58 0.028
434
P FRD012 Friedreich Ataxia 1 58 0.028
435
VSC002 Vascular Dementia 58 0.028
436
DMY004 Demyelinating Disease 58 0.028
437
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 58 0.028
438
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.028
439
LYM019 Lymphosarcoma 58 0.028
440
P BRS044 Breast Adenocarcinoma 58 0.028
441
URN009 Urinary System Disease 58 0.028
442
CLR003 Clear Cell Adenocarcinoma 57 0.028
443
c HPT007 Hepatitis E 57 0.028
444
NPH009 Nephrolithiasis 57 0.028
445
LBR002 Leber Hereditary Optic Neuropathy 57 0.028
446
P ALP008 Alopecia 56 0.028
447
ORL004 Oral Submucous Fibrosis 56 0.028
448
HYP060 Hyperinsulinism 56 0.028
449
P RTN016 Retinal Degeneration 56 0.028
450
P ACT008 Actinic Keratosis 56 0.028
451
PLS006 Plasmodium Vivax Malaria 56 0.028
452
P HYP076 Hyperthyroidism 56 0.028
453
P SPN301 Spinocerebellar Ataxia 2 56 0.028
454
MTH078 Methylmalonic Aciduria, Cblb Type 56 0.028
455
IRN001 Iron Deficiency Anemia 55 0.028
456
CLR030 Clear Cell Renal Cell Carcinoma 55 0.028
457
AMN001 Amenorrhea 55 0.028
458
SRS001 Serous Cystadenocarcinoma 55 0.028
459
SPP010 Suppressor of Tumorigenicity 3 55 0.028
460
TBC004 Tobacco Addiction 55 0.028
461
BLR006 Biliary Tract Disease 55 0.028
462
P TRC086 Trichohepatoenteric Syndrome 1 54 0.028
463
c MLG079 Malignant Pleural Mesothelioma 54 0.028
464
P FNC004 Fanconi Syndrome 54 0.028
465
CLF001 Cleft Lip 54 0.028
466
P TRM003 Tremor 54 0.028
467
ESP020 Esophageal Atresia 54 0.028
468
c ACT071 Acute Kidney Failure 54 0.028
469
SPN041 Spinal Cord Disease 54 0.028
470
P HMG032 Hemoglobin H Disease 53 0.028
471
OVR063 Overnutrition 53 0.028
472
c CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 53 0.028
473
P SCL009 Sclerosing Cholangitis 53 0.028
474
MSC033 Muscle Disorders 53 0.028
475
KRT009 Keratosis 53 0.028
476
OPT006 Optic Nerve Disease 53 0.028
477
P TRT010 Teratoma 53 0.028
478
ACT103 Acute Lymphoblastic Leukemia, Childhood 53 0.028
479
c BLM008 Bulimia Nervosa 2 53 0.028
480
ONC002 Onchocerciasis 53 0.028
481
P OVR046 Ovarian Cyst 52 0.028
482
OST011 Osteomalacia 52 0.028
483
URM002 Uremia 52 0.028
484
P CHL066 Cholangitis 52 0.028
485
c SCN036 Secondary Progressive Multiple Sclerosis 52 0.028
486
P MGL001 Megaloblastic Anemia 52 0.028
487
c ACT134 Acute Liver Failure 52 0.028
488
PLR008 Pleurisy 52 0.028
489
c BNG091 Benign Chronic Pemphigus 52 0.028
490
MYL001 Myelitis 52 0.028
491
P CHR345 Chronic Pain 52 0.028
492
OCL006 Ocular Hypertension 51 0.028
493
MCL006 Macular Retinal Edema 51 0.028
494
MCP006 Mucoepidermoid Carcinoma 51 0.028
495
TRS021 Triosephosphate Isomerase Deficiency 51 0.028
496
NNT012 Neonatal Jaundice 51 0.028
497
PPL002 Papillary Carcinoma 51 0.028
498
P END046 Endometritis 51 0.028
499
CYS014 Cystadenocarcinoma 51 0.028
500
ELS001 Eales Disease 50 0.028
501
HYD012 Hydrops Fetalis 50 0.028
502
P HMC002 Homocystinuria 50 0.028
503
c BPL002 Bipolar I Disorder 50 0.028
504
MGC001 Megacolon 50 0.028
505
c WLM018 Wilms Tumor 5 49 0.028
506
LRN003 Learning Disability 49 0.028
507
DFF036 Differentiated Thyroid Carcinoma 49 0.028
508
P KRT007 Keratoconus 49 0.028
509
URT010 Ureteral Obstruction 49 0.028
510
ONC007 Oncocytoma 48 0.028
511
c ERY048 Erythrocytosis, Familial, 2 48 0.028
512
ISC002 Ischemic Optic Neuropathy 48 0.028
513
GLC009 Glucosephosphate Dehydrogenase Deficiency 48 0.028
514
P ATS308 Autosomal Dominant Cerebellar Ataxia 47 0.028
515
MYC005 Myocardial Stunning 47 0.028
516
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.028
517
ALP093 Alpha-Thalassemia/mental Retardation Syndrome, Chromosome 16-Related 47 0.028
518
MGR001 Migraine Without Aura 47 0.028
519
OVR012 Ovarian Serous Cystadenocarcinoma 47 0.028
520
HYD038 Hydrops Fetalis, Nonimmune 47 0.028
521
c CNG027 Congenital Hemolytic Anemia 46 0.028
522
P MTH007 Methemoglobinemia 46 0.028
523
P D2H002 D-2-Hydroxyglutaric Aciduria 1 46 0.028
524
TRC010 Trichotillomania 46 0.028
525
VTM002 Vitamin B12 Deficiency 46 0.028
526
ATN004 Autonomic Neuropathy 46 0.028
527
P PHR004 Pharynx Cancer 46 0.028
528
CLN044 Colon Adenoma 45 0.028
529
P OVR106 Ovarian Clear Cell Carcinoma 45 0.028
530
P PRT026 Parotitis 45 0.028
531
IRN002 Iron Metabolism Disease 45 0.028
532
c PRK092 Parkinson Disease 6, Autosomal Recessive Early-Onset 44 0.028
533
P PRV002 Periventricular Nodular Heterotopia 44 0.028
534
c CHR095 Chronic Progressive External Ophthalmoplegia 44 0.028
535
DNT001 Dental Fluorosis 44 0.028
536
TTR005 Tetrahydrobiopterin Deficiency 44 0.028
537
OST062 Osteoarthritis with Mild Chondrodysplasia 43 0.028
538
P BRY005 Beryllium Disease 43 0.028
539
MCR018 Microcytic Anemia 43 0.028
540
CRV045 Cervical Intraepithelial Neoplasia 43 0.028
541
ILC002 Ileocolitis 43 0.028
542
c CHR576 Chronic Beryllium Disease 42 0.028
543
CRT015 Carotid Artery Occlusion 42 0.028
544
SPN050 Spinocerebellar Degeneration 41 0.028
545
OCL022 Ocular Melanoma 41 0.028
546
FRM003 Farmer's Lung 41 0.028
547
MTG002 Mutagen Sensitivity 41 0.028
548
SPP011 Suppression of Tumorigenicity 12 41 0.028
549
P HRD012 Hereditary Elliptocytosis 41 0.028
550
EGG001 Egg Allergy 41 0.028
551
DRG002 Drug-Induced Hepatitis 41 0.028
552
P ORF002 Orofacial Cleft 41 0.028
553
MYC033 Myoclonus 40 0.028
554
WLL004 Wallerian Degeneration 40 0.028
555
c PRG011 Progressive Myoclonus Epilepsy 40 0.028
556
c PSR017 Psoriasis 2 40 0.028
557
CRV002 Cervix Uteri Carcinoma in Situ 40 0.028
558
DXR001 Doxorubicin Induced Cardiomyopathy 40 0.028
559
SCR011 Scrapie 40 0.028
560
GLC084 Glaucoma, Normal Tension 39 0.028
561
MSC004 Muscle Tissue Disease 39 0.028
562
PST020 Postpoliomyelitis Syndrome 39 0.028
563
ALC005 Alcoholic Pancreatitis 39 0.028
564
c GLL024 Gallbladder Disease 1 39 0.028
565
c PSR018 Psoriasis 13 39 0.028
566
OPS001 Opisthorchiasis 39 0.028
567
MTH064 Methemoglobinemia, Beta-Globin Type 38 0.028
568
AMN002 Amino Acid Metabolic Disorder 38 0.028
569
c MLG147 Malignant Hyperthermia 1 38 0.028
570
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 38 0.028
571
OVR034 Ovarian Clear Cell Adenocarcinoma 38 0.028
572
INT040 Intrinsic Asthma 38 0.028
573
ORG002 Organic Acidemia 38 0.028
574
KSH004 Kashin-Beck Disease 37 0.028
575
PYR016 Pyridoxine Deficiency 37 0.028
576
c PSR028 Psoriasis 7 37 0.028
577
RBS002 Rubeosis Iridis 37 0.028
578
TXC020 Toxic Oil Syndrome 37 0.028
579
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 36 0.028
580
c PNC106 Pancreatic Agenesis 1 36 0.028
581
PLY024 Polymicrogyria 36 0.028
582
P MYC026 Myoclonus Epilepsy 35 0.028
583
LWT001 Low Tension Glaucoma 35 0.028
584
MLD002 Mild Pre-Eclampsia 35 0.028
585
OVR109 Ovarian Germ Cell Teratoma 35 0.028
586
c PSR032 Psoriasis 11 35 0.028
587
BWN006 Bowen's Disease 35 0.028
588
HYP001 Hypochromic Microcytic Anemia 34 0.028
589
SKN020 Skin Papilloma 34 0.028
590
P SMK004 Smoking As a Quantitative Trait Locus 3 34 0.028
591
P ATS366 Autism X-Linked 2 34 0.028
592
c BSL011 Basal Cell Carcinoma, Multiple 34 0.028
593
c SKN012 Skin Carcinoma in Situ 33 0.028
594
GST039 Gastroduodenitis 33 0.028
595
IMM039 Immune Hydrops Fetalis 33 0.028
596
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 33 0.028
597
PLY110 Polymicrogyria, Bilateral Temporooccipital 32 0.028
598
SYN089 Syndromic X-Linked Intellectual Disability Snyder Type 32 0.028
599
ART110 Arteritic Anterior Ischemic Optic Neuropathy 31 0.028
600
ATM052 Autoimmune Disease 1 30 0.028
601
MYC015 Mycobacterium Fortuitum 30 0.028
602
c MCR112 Microvascular Complications of Diabetes 2 30 0.028
603
CNG017 Congenital Nonspherocytic Hemolytic Anemia 30 0.028
604
HWK001 Hawkinsinuria 29 0.028
605
IMM002 Immature Cataract 28 0.028
606
c DBT054 Diabetes Mellitus, Insulin-Dependent, 24 28 0.028
607
c TYP035 Type 1 Diabetes Mellitus 11 28 0.028
608
PRQ002 Paraquat Poisoning 27 0.028
609
c TYP033 Type 1 Diabetes Mellitus 7 26 0.028
610
GLC081 Glucose Phosphate Isomerase Deficiency 26 0.028
611
c ALZ062 Alzheimer Disease 19 26 0.028
612
STT003 Steatitis 22 0.028
613
c DMN020 Diamond-Blackfan Anemia 8 20 0.028
614
MNG007 Manganese Poisoning 18 0.028
615
6PH001 6-Phosphogluconate Dehydrogenase Deficiency 18 0.028
616
INB001 Inborn Amino Acid Metabolism Disorder 16 0.028
617
AMN012 Aminoacidopathies 15 0.028
618
ATR076 Atrophic Muscular Disease 6 0.028
Content
Loading form....