Search results for Glutathione

1357 hits were found for Glutathione

# Family MCID Name MIFTS Score
1
GLT007 Glutathione Synthetase Deficiency 47 8.109
2
GLT036 Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia Due to 18 6.845
3
GLT039 Glutathione Peroxidase Deficiency 34 5.233
4
HML010 Hemolytic Anemia Due to Glutathione Reductase Deficiency 19 5.130
5
HYD063 Hydroxyacyl Glutathione Hydrolase Deficiency 12 3.924
6
GLT034 Glutathione Transferase Activity Toward Trans-Stilbene Oxide 4 3.222
7
c HML057 Hemolytic Anemia Due to Hexose Monophosphate Shunt and Glutathione Metabolism Anomalies 5 2.298
8
P CTR002 Cataract 60 0.236
9
P CLR023 Colorectal Cancer 99 0.222
10
P LNG032 Lung Cancer 98 0.222
11
P BLD134 Bladder Cancer 79 0.212
12
P OVR042 Ovarian Cancer 88 0.210
13
P LVR013 Liver Disease 68 0.203
14
P BRS047 Breast Cancer 97 0.201
15
P NRB001 Neuroblastoma 72 0.187
16
SQM006 Squamous Cell Carcinoma 60 0.177
17
P HPT023 Hepatocellular Carcinoma 100 0.175
18
P HML002 Hemolytic Anemia 63 0.175
19
P ADN016 Adenocarcinoma 64 0.173
20
P GLM045 Glioma 63 0.173
21
LNG099 Lung Disease 60 0.170
22
GLL048 Glial Tumor 45 0.170
23
LVR012 Liver Cirrhosis 62 0.168
24
SCH014 Schistosomiasis 57 0.164
25
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.163
26
CYS001 Cystic Fibrosis 81 0.161
27
P GST053 Gastric Cancer 83 0.159
28
48X005 48,xyyy 39 0.157
29
P PRS040 Prostate Cancer 97 0.151
30
DFC004 Deficiency Anemia 70 0.151
31
HYP066 Hyperglycemia 61 0.150
32
c PRC016 Pre-Eclampsia 63 0.148
33
P MYL006 Myeloid Leukemia 60 0.148
34
HYP266 Hypoxia 57 0.148
35
ISC004 Ischemia 58 0.145
36
P KDN018 Kidney Disease 72 0.144
37
P LKM002 Leukemia 68 0.144
38
HLX001 Helix Syndrome 47 0.144
39
P PRK057 Parkinson Disease, Late-Onset 78 0.141
40
47X002 47,xyy 49 0.138
41
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.137
42
P INF032 Infertility 57 0.135
43
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.129
44
P ALZ034 Alzheimer Disease 88 0.129
45
GLB015 Glioblastoma Multiforme 75 0.129
46
ORL011 Oral Cancer 60 0.129
47
P LTR001 Lateral Sclerosis 54 0.129
48
PPL052 Papillomatosis, Confluent and Reticulated 33 0.129
49
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.128
50
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.128
51
CHL068 Cholestasis 61 0.126
52
FTT001 Fatty Liver Disease 61 0.125
53
P LKM062 Leukemia, Acute Lymphoblastic 69 0.123
54
ADN018 Adenoma 59 0.123
55
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.123
56
AST005 Asthma 76 0.122
57
P VSC007 Vascular Disease 63 0.122
58
c SML038 Small Cell Cancer of the Lung 65 0.120
59
P MLN007 Male Infertility 55 0.120
60
c LKM061 Leukemia, Acute Myeloid 84 0.117
61
AGN016 Aging 56 0.117
62
RBF001 Riboflavin Deficiency 49 0.117
63
ESP021 Esophageal Cancer 90 0.113
64
P LNG064 Lung Cancer Susceptibility 3 78 0.113
65
P ALC033 Alcohol Use Disorder 58 0.113
66
c CHR684 Chronic Kidney Disease 70 0.112
67
ANX004 Anoxia 40 0.112
68
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.110
69
P END044 Endometriosis 63 0.108
70
CRV035 Cervical Cancer 76 0.106
71
P ATS364 Autism 70 0.106
72
P BPL003 Bipolar Disorder 56 0.106
73
TRN018 Transitional Cell Carcinoma 56 0.106
74
c MJR024 Major Affective Disorder 9 41 0.106
75
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.106
76
c MJR022 Major Affective Disorder 8 38 0.106
77
P MSC005 Muscular Dystrophy 66 0.104
78
P NRP001 Neuropathy 56 0.104
79
P INF037 Inflammatory Bowel Disease 54 0.104
80
c MCR130 Microvascular Complications of Diabetes 6 41 0.104
81
c MCR113 Microvascular Complications of Diabetes 3 52 0.102
82
P AST007 Astrocytoma 51 0.102
83
c MCR120 Microvascular Complications of Diabetes 7 47 0.102
84
c MCR133 Microvascular Complications of Diabetes 4 41 0.102
85
OVR094 Ovarian Epithelial Cancer 38 0.102
86
P SCH015 Schizophrenia 74 0.101
87
P MLN008 Melanoma 69 0.101
88
OST159 Osteogenic Sarcoma 66 0.101
89
P SKN015 Skin Carcinoma 66 0.101
90
IRN002 Iron Metabolism Disease 57 0.101
91
MTB004 Metabolic Acidosis 50 0.101
92
ORL015 Oral Squamous Cell Carcinoma 43 0.101
93
CHR178 Chromosomal Triplication 35 0.101
94
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.099
95
DWN001 Down Syndrome 70 0.099
96
P LRY044 Larynx Cancer 55 0.099
97
MLR004 Malaria 81 0.097
98
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.097
99
VLV047 Volvulus of Midgut 49 0.097
100
CYT002 Cytokine Deficiency 42 0.097
101
P PHC003 Pheochromocytoma 71 0.095
102
CLN015 Colon Adenocarcinoma 65 0.095
103
P PSR002 Psoriasis 62 0.095
104
P PNC044 Pancreatitis 61 0.095
105
c ACT027 Acute Pancreatitis 60 0.095
106
ERY051 Erythroleukemia, Familial 56 0.095
107
PST011 Pustulosis of Palm and Sole 52 0.095
108
ADR040 Adrenal Gland Pheochromocytoma 46 0.095
109
SNL007 Senile Cataract 42 0.095
110
c LNG109 Lung Cancer Susceptibility 1 27 0.095
111
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.092
112
P HNT016 Huntington Disease 72 0.092
113
ATH013 Atherosclerosis Susceptibility 65 0.092
114
LPP008 Lipoprotein Quantitative Trait Locus 62 0.092
115
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.092
116
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.092
117
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.092
118
P HYP086 Hypothyroidism 69 0.090
119
P CRN300 Coronary Heart Disease 1 63 0.090
120
ATM095 Autoimmune Disease 62 0.090
121
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.090
122
P THL005 Thalassemia 60 0.090
123
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.090
124
HMS001 Hemosiderosis 54 0.090
125
ART140 Arteries, Anomalies of 52 0.090
126
P RRH023 Rare Hereditary Hemochromatosis 41 0.090
127
MYL009 Myelodysplastic Syndrome 70 0.088
128
CLT003 Colitis 62 0.088
129
DRM006 Dermatitis 61 0.088
130
P BCL017 B-Cell Lymphoma 58 0.088
131
BLR008 Bilirubin Metabolic Disorder 57 0.088
133
SCK003 Sickle Cell Anemia 74 0.086
134
HMN044 Human Immunodeficiency Virus Type 1 71 0.086
135
c BSL007 Basal Cell Carcinoma 68 0.086
136
P PLM036 Pulmonary Fibrosis 65 0.086
137
P DBT009 Diabetes Mellitus 64 0.086
138
P PRD008 Periodontitis 64 0.086
139
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.086
140
c ACT071 Acute Kidney Failure 60 0.086
141
P ECL001 Eclampsia 50 0.086
142
c PCH010 Pachyonychia Congenita 3 44 0.086
143
P RHM011 Rheumatoid Arthritis 80 0.084
144
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.084
145
c LKM063 Leukemia, Chronic Myeloid 72 0.084
146
ALC007 Alcohol Dependence 66 0.084
147
HYP056 Hypoglycemia 66 0.084
148
BRR014 Barrett Esophagus 65 0.084
149
ACT119 Acute Promyelocytic Leukemia 63 0.084
150
ALL026 Allergic Hypersensitivity Disease 62 0.084
151
P OPN001 Open-Angle Glaucoma 49 0.084
152
IMM167 Immune Deficiency Disease 78 0.081
153
P MLT020 Multiple Sclerosis 72 0.081
154
DPR016 Depression 63 0.081
155
P BRS044 Breast Adenocarcinoma 59 0.081
156
P FBR017 Fibrosarcoma 56 0.081
157
P HYP076 Hyperthyroidism 55 0.081
158
c VRL010 Viral Hepatitis 52 0.081
159
KRT002 Keratomalacia 47 0.081
160
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.081
161
MYL069 Myeloma, Multiple 85 0.079
162
END057 Endometrial Cancer 74 0.079
163
c HPT073 Hepatitis C Virus 72 0.079
164
P HPT021 Hepatitis 67 0.079
165
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.079
166
P NTR004 Neutropenia 63 0.079
167
HLC007 Helicobacter Pylori Infection 59 0.079
168
c ACT075 Acute Myocardial Infarction 57 0.079
169
P SZR006 Seizure Disorder 56 0.079
170
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.079
171
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 49 0.079
172
HVY002 Heavy Metal Poisoning 22 0.079
173
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.076
174
c HYP595 Hypertension, Essential 84 0.076
175
P PNC035 Pancreatic Cancer 84 0.076
176
c BTT014 Beta-Thalassemia 74 0.076
177
c MNN043 Meningioma, Familial 74 0.076
178
ULC004 Ulcerative Colitis 73 0.076
179
c ATM011 Autoimmune Hepatitis 63 0.076
180
c GLC092 Glaucoma, Primary Open Angle 62 0.076
181
MNN042 Meningioma, Radiation-Induced 62 0.076
182
ALL006 Allergic Asthma 56 0.076
183
PPL022 Papilloma 54 0.076
184
HMC014 Homocysteinemia 53 0.076
185
P SPP010 Suppressor of Tumorigenicity 3 51 0.076
186
END086 End Stage Renal Disease 51 0.076
187
SPN021 Spinal Meningioma 50 0.076
188
SQM002 Squamous Cell Papilloma 46 0.076
189
CRB004 Cerebral Artery Occlusion 45 0.076
190
SCR001 Secretory Meningioma 41 0.076
191
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.076
192
P LKM071 Leukemia, Chronic Lymphocytic 79 0.074
193
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.074
194
P APL001 Aplastic Anemia 74 0.074
195
P MYC007 Myocardial Infarction 70 0.074
196
GST040 Gastric Adenocarcinoma 70 0.074
197
P LYM118 Lymphoma 68 0.074
198
CHL065 Cholangiocarcinoma 68 0.074
199
TXC005 Toxic Shock Syndrome 62 0.074
200
P KDN017 Kidney Cancer 60 0.074
201
ACQ007 Acquired Immunodeficiency Syndrome 60 0.074
202
THY029 Thyroid Carcinoma 59 0.074
203
VSL002 Visual Epilepsy 59 0.074
204
MNT002 Mental Depression 58 0.074
205
P PRP019 Peripheral Nervous System Disease 58 0.074
206
BRN056 Bronchopulmonary Dysplasia 57 0.074
207
P TRM003 Tremor 54 0.074
208
NNL006 Non-Alcoholic Steatohepatitis 54 0.074
210
INT079 Intrahepatic Cholangiocarcinoma 51 0.074
211
P SCK005 Sickle Cell Disease 50 0.074
212
URM002 Uremia 49 0.074
213
c MLG068 Malignant Glioma 46 0.074
214
P NSP012 Nasopharyngeal Carcinoma 66 0.071
215
P MCR115 Microvascular Complications of Diabetes 5 66 0.071
216
CLR108 Colorectal Adenoma 64 0.071
217
LSH001 Leishmaniasis 63 0.071
218
c HPT001 Hepatitis C 62 0.071
219
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.071
220
c ACT073 Acute Leukemia 58 0.071
221
HPT046 Hepatic Veno-Occlusive Disease 56 0.071
222
FLR002 Filariasis 55 0.071
223
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.071
224
P LCT001 Lactic Acidosis 51 0.071
225
ATS010 Autosomal Recessive Disease 48 0.071
226
P MRC003 Mercury Poisoning 48 0.071
227
HMP009 Haemophilus Influenzae 43 0.071
228
P KLZ004 Kala-Azar 1 41 0.071
229
LKP003 Leukoplakia 39 0.071
230
5XP001 5-Oxoprolinase Deficiency 31 0.071
231
PST092 Posttransplant Acute Limbic Encephalitis 29 0.071
232
c SYS001 Systemic Lupus Erythematosus 86 0.068
233
CRH001 Crohn's Disease 74 0.068
234
SVR004 Severe Combined Immunodeficiency 73 0.068
235
SKN016 Skin Disease 63 0.068
236
P ENC018 Encephalopathy 61 0.068
237
IGR001 Ige Responsiveness, Atopic 59 0.068
238
PLM010 Pulmonary Edema 54 0.068
239
DBT010 Diabetic Neuropathy 54 0.068
240
PRS045 Prostatic Hypertrophy 53 0.068
241
P SML001 Small Cell Carcinoma 52 0.068
242
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.068
243
FSC002 Fascioliasis 42 0.068
244
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.068
245
STR067 Stroke, Ischemic 81 0.065
246
P HRT032 Heart Disease 75 0.065
247
PHN003 Phenylketonuria 75 0.065
248
LPD008 Lipid Metabolism Disorder 62 0.065
249
P PRM006 Primary Biliary Cirrhosis 62 0.065
250
ALC006 Alcoholic Hepatitis 61 0.065
251
PPT005 Peptic Ulcer Disease 59 0.065
252
CNT047 Contact Dermatitis 58 0.065
253
c ACT134 Acute Liver Failure 56 0.065
254
HPT022 Hepatoblastoma 56 0.065
255
P ART021 Arteriosclerosis 54 0.065
256
c PRD040 Periodontitis, Chronic 53 0.065
257
PRS021 Prostatic Adenoma 51 0.065
258
KSH001 Keshan Disease 34 0.065
259
c HYP836 Hypercholesterolemia, Familial, 1 73 0.062
260
LYM133 Lymphoma, Hodgkin, Classic 69 0.062
261
P PNM007 Pneumonia 68 0.062
262
P MJR001 Major Depressive Disorder 68 0.062
263
GST092 Gastroesophageal Reflux 67 0.062
264
SRC014 Sarcoma 65 0.062
265
P PRP029 Porphyria 62 0.062
266
NTR005 Nutritional Deficiency Disease 62 0.062
267
IRN001 Iron Deficiency Anemia 59 0.062
268
CYS010 Cystinosis 59 0.062
269
DSS008 Disease of Mental Health 58 0.062
270
BCT022 Bacterial Infectious Disease 56 0.062
271
P GST044 Gastritis 56 0.062
272
P INS002 in Situ Carcinoma 53 0.062
273
TRM010 Traumatic Brain Injury 51 0.062
274
VRC001 Varicocele 49 0.062
275
P BNG032 Benign Mesothelioma 46 0.062
276
ORL012 Oral Leukoplakia 39 0.062
277
GLT014 Glutathionuria 39 0.062
278
HRN029 Hearing Loss, Noise-Induced 37 0.062
279
P MDL005 Medulloblastoma 77 0.059
280
BRN028 Brain Cancer 74 0.059
281
MSC157 Muscular Dystrophy, Duchenne Type 72 0.059
282
PSY004 Psychotic Disorder 67 0.059
283
c ATS007 Autism Spectrum Disorder 67 0.059
284
CHG001 Chagas Disease 66 0.059
285
P DRM053 Dermatitis, Atopic 66 0.059
286
c DWL002 Dowling-Degos Disease 1 58 0.059
287
P GLM007 Glomerulonephritis 57 0.059
288
BRN004 Brain Edema 56 0.059
289
DFF005 Diffuse Large B-Cell Lymphoma 55 0.059
290
HYP060 Hyperinsulinism 54 0.059
291
SPN035 Spindle Cell Sarcoma 53 0.059
292
ALC009 Alcoholic Liver Cirrhosis 53 0.059
293
P DDN001 Duodenal Ulcer 52 0.059
294
PRS129 Prostatic Hyperplasia, Benign 49 0.059
295
BRN071 Brain Injury 49 0.059
296
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.059
297
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.059
298
c LKM005 Leukemia, T-Cell, Chronic 34 0.059
299
P ATX030 Ataxia-Telangiectasia 82 0.056
300
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.056
301
CNG034 Congestive Heart Failure 69 0.056
302
ANG054 Angina Pectoris 66 0.056
303
P MTR014 Motor Neuron Disease 65 0.056
304
TBC004 Tobacco Addiction 64 0.056
305
P RHB003 Rhabdomyosarcoma 63 0.056
306
c HPT003 Hepatitis a 62 0.056
307
MDD011 Mood Disorder 62 0.056
308
BLD131 Bladder Urothelial Carcinoma 62 0.056
309
SPN186 Spinal Cord Injury 60 0.056
310
INS001 Insulinoma 60 0.056
311
c HPT016 Hepatitis B 59 0.056
312
P CYS018 Cystitis 59 0.056
313
P TYR004 Tyrosinemia 58 0.056
314
P CND004 Candidiasis 58 0.056
315
P RHN004 Rhinitis 57 0.056
316
ALL010 Allergic Contact Dermatitis 56 0.056
317
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.056
318
EMB004 Embryonal Carcinoma 56 0.056
319
FLR001 Filarial Elephantiasis 55 0.056
320
PRT038 Protein-Energy Malnutrition 54 0.056
321
P RCT021 Rectum Cancer 52 0.056
322
TLN003 Telangiectasis 52 0.056
323
P TRT010 Teratoma 52 0.056
324
CLR109 Colorectal Adenocarcinoma 51 0.056
325
P HRD144 Hereditary Mixed Polyposis Syndrome 51 0.056
326
HYP781 Hypoascorbemia 51 0.056
327
AZS001 Azoospermia 50 0.056
328
P KRT007 Keratoconus 50 0.056
329
INT017 Intestinal Schistosomiasis 48 0.056
330
SPL018 Splenomegaly 48 0.056
331
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.056
332
KWS001 Kwashiorkor 44 0.056
333
CRV045 Cervical Intraepithelial Neoplasia 39 0.056
334
GMM011 Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia Due to 25 0.056
335
NRL016 Neural Tube Defects 82 0.052
336
c DLT002 Dilated Cardiomyopathy 79 0.052
337
OST012 Osteoarthritis 78 0.052
338
c ATR087 Atrial Standstill 1 75 0.052
339
P GRF003 Graft-Versus-Host Disease 72 0.052
340
PLM001 Pulmonary Tuberculosis 69 0.052
341
BRN024 Bronchitis 68 0.052
342
ALL003 Allergic Rhinitis 67 0.052
343
P CHR012 Chronic Granulomatous Disease 67 0.052
344
c DBT099 Diabetes Mellitus, Type I 65 0.052
345
GT001 Gout 64 0.052
346
TRN015 Transient Cerebral Ischemia 63 0.052
347
P TRC086 Trichohepatoenteric Syndrome 1 62 0.052
348
P LPS004 Lupus Erythematosus 61 0.052
349
P NPH012 Nephrotic Syndrome 60 0.052
350
P MYC008 Myocarditis 59 0.052
351
PRN019 Perinatal Necrotizing Enterocolitis 59 0.052
352
P ADL017 Adult T-Cell Leukemia 56 0.052
353
CYS005 Cysticercosis 53 0.052
354
GST023 Gastric Ulcer 53 0.052
355
P MSC003 Muscular Atrophy 52 0.052
356
ONC002 Onchocerciasis 52 0.052
357
ENT011 Enterocolitis 51 0.052
358
BLR001 Biliary Atresia 50 0.052
359
c INH020 Inherited Metabolic Disorder 47 0.052
360
ILC002 Ileocolitis 43 0.052
361
DBT007 Diabetic Cataract 38 0.052
362
ALL014 Allergic Encephalomyelitis 38 0.052
363
HRW001 Hair Whorl 36 0.052
364
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.052
365
P GLM040 Glioma Susceptibility 1 81 0.048
366
ANX010 Anxiety 73 0.048
367
P MPL001 Maple Syrup Urine Disease 69 0.048
368
P MYC084 Mycobacterium Tuberculosis 1 68 0.048
369
P CRD119 Cardiac Arrest 67 0.048
370
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.048
371
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.048
372
ANR007 Anorexia Nervosa 63 0.048
373
c SCL052 Scleroderma, Familial Progressive 61 0.048
374
CHR066 Chronic Fatigue Syndrome 61 0.048
375
GRD007 Grade Iii Astrocytoma 59 0.048
376
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.048
377
P GLL018 Gallbladder Cancer 57 0.048
378
P MTC069 Mitochondrial Disorders 56 0.048
379
HMG005 Hemoglobinopathy 56 0.048
380
MCS002 Mucositis 56 0.048
381
INT007 Intermediate Coronary Syndrome 55 0.048
382
TRD006 Tardive Dyskinesia 54 0.048
383
GLC003 Glucose Intolerance 54 0.048
384
HLL004 Hellp Syndrome 54 0.048
385
TRC023 Trichinosis 53 0.048
386
MST005 Mastitis 53 0.048
387
P INT068 Intestinal Disease 53 0.048
388
P RTN018 Retinal Disease 53 0.048
389
SRS001 Serous Cystadenocarcinoma 52 0.048
390
P INT099 Intrahepatic Cholestasis of Pregnancy 51 0.048
391
SCH012 Schizoaffective Disorder 50 0.048
392
TRY001 Trypanosomiasis 50 0.048
393
HMG002 Hemoglobinuria 50 0.048
394
c CNG027 Congenital Hemolytic Anemia 50 0.048
395
ASB001 Asbestosis 47 0.048
396
TST014 Testicular Cancer 46 0.048
397
CRT015 Carotid Artery Occlusion 45 0.048
398
MST004 Mast Cell Neoplasm 42 0.048
399
EXT007 Extracutaneous Mastocytoma 38 0.048
400
CNG017 Congenital Nonspherocytic Hemolytic Anemia 35 0.048
401
ARG004 Argyria 27 0.048
402
ASB003 Asbestos Intoxication 26 0.048
403
c NRF023 Neurofibromatosis, Type Ii 80 0.044
404
P RTN008 Retinitis Pigmentosa 79 0.044
405
P RSP003 Respiratory Failure 74 0.044
406
OTT002 Otitis Media 72 0.044
407
c EXD008 Exudative Vitreoretinopathy 1 71 0.044
408
WLS001 Wilson Disease 71 0.044
409
P MYP004 Myopathy 70 0.044
410
P ART022 Arthritis 69 0.044
411
P LPR021 Leprosy 3 69 0.044
412
P SYS005 Systemic Scleroderma 68 0.044
413
PNC129 Pancreatic Adenocarcinoma 68 0.044
414
CRB039 Cerebrovascular Disease 67 0.044
415
P HYP098 Hypereosinophilic Syndrome 67 0.044
416
c RHB024 Rhabdomyosarcoma 2 67 0.044
417
P CLC063 Celiac Disease 1 66 0.044
418
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.044
419
P DMN002 Dementia 66 0.044
420
P MNN013 Meningitis 66 0.044
421
LNG039 Lung Squamous Cell Carcinoma 66 0.044
422
KRT019 Keratitis, Hereditary 65 0.044
423
PRT037 Pertussis 65 0.044
424
P HRP006 Herpes Simplex 65 0.044
425
c WLM013 Wilms Tumor 1 65 0.044
426
P ADL010 Adult Respiratory Distress Syndrome 65 0.044
427
P CHR071 Charcot-Marie-Tooth Disease 65 0.044
428
P FRD001 Friedreich Ataxia 64 0.044
429
LYM017 Lyme Disease 64 0.044
430
P VSC011 Vasculitis 62 0.044
431
YLL002 Yellow Fever 61 0.044
432
HPT019 Hepatic Encephalopathy 60 0.044
433
P SNS001 Sensorineural Hearing Loss 60 0.044
434
STT001 Status Epilepticus 60 0.044
435
P OPT006 Optic Nerve Disease 60 0.044
436
SPP011 Suppression of Tumorigenicity 12 59 0.044
437
CHL014 Cholera 59 0.044
438
EYD002 Eye Disease 58 0.044
439
P CRD246 Cardiovascular System Disease 57 0.044
440
P PLY018 Polycythemia 56 0.044
441
P PLY011 Polycystic Ovary Syndrome 56 0.044
442
GST050 Gastrointestinal System Disease 56 0.044
443
P PNM006 Pneumoconiosis 56 0.044
444
ORP003 Oropharynx Cancer 55 0.044
445
P DRR001 Diarrhea 55 0.044
446
P DRM007 Dermatitis Herpetiformis 55 0.044
447
P ALP008 Alopecia 54 0.044
448
THR013 Thoracic Outlet Syndrome 54 0.044
449
SLP001 Sleeping Sickness 54 0.044
450
CLR030 Clear Cell Renal Cell Carcinoma 53 0.044
451
P HMC002 Homocystinuria 53 0.044
452
NNT012 Neonatal Jaundice 53 0.044
453
TXC002 Toxic Encephalopathy 53 0.044
454
OVR059 Ovary Adenocarcinoma 53 0.044
455
PLS007 Plasmodium Falciparum Malaria 52 0.044
456
KRT009 Keratosis 51 0.044
457
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.044
458
P CHL066 Cholangitis 51 0.044
459
c SVR005 Severe Pre-Eclampsia 50 0.044
460
VTM002 Vitamin B12 Deficiency 48 0.044
461
ANT018 Anthracosis 48 0.044
462
LYM019 Lymphosarcoma 46 0.044
463
P MTH007 Methemoglobinemia 46 0.044
464
HPT004 Hepatic Coma 45 0.044
465
c SPR009 Sporadic Breast Cancer 45 0.044
466
c SPR086 Spermatogenic Failure 3 44 0.044
467
OPS001 Opisthorchiasis 41 0.044
468
c DRM040 Dermatitis Herpetiformis, Familial 35 0.044
469
ACT149 Acetaminophen Metabolism 35 0.044
470
HNS001 Hansen's Disease 34 0.044
471
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.044
472
PRS131 Prostate Cancer/brain Cancer Susceptibility 25 0.044
473
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.039
474
P RTN024 Retinoblastoma 73 0.039
475
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.039
476
P FML011 Familial Adenomatous Polyposis 72 0.039
477
P EPL164 Epilepsy 71 0.039
478
MLT157 Multiple System Atrophy 1 70 0.039
479
c PNC108 Pancreatitis, Hereditary 70 0.039
480
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.039
481
ABT001 Abetalipoproteinemia 69 0.039
482
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.039
483
MLD001 Melioidosis 68 0.039
484
P PLM037 Pulmonary Hypertension 67 0.039
485
c MCR129 Microvascular Complications of Diabetes 1 66 0.039
486
TTN003 Tetanus 65 0.039
487
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.039
488
PRT036 Peritonitis 64 0.039
489
P PLY014 Polycystic Kidney Disease 62 0.039
490
P HYP750 Hypertriglyceridemia, Familial 62 0.039
491
P ESP024 Esophagitis 62 0.039
492
BLL006 Bullous Pemphigoid 62 0.039
493
GNG013 Gingivitis 59 0.039
494
CHL067 Cholecystitis 57 0.039
495
P EXN002 Exanthem 57 0.039
496
P PRN023 Prion Disease 57 0.039
497
c MST023 Mesothelioma, Malignant 57 0.039
498
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.039
499
TNS005 Tonsillitis 57 0.039
500
VSC002 Vascular Dementia 57 0.039
501
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.039
502
HYP005 Hypokalemia 55 0.039
503
ORL004 Oral Submucous Fibrosis 55 0.039
504
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.039
505
FND002 Fundus Dystrophy 55 0.039
506
VSC003 Visceral Leishmaniasis 55 0.039
507
c BCT007 Bacterial Meningitis 55 0.039
508
P RNL017 Renal Oncocytoma 53 0.039
509
P ACT008 Actinic Keratosis 53 0.039
510
P PNC025 Panic Disorder 53 0.039
511
c FML008 Familial Retinoblastoma 53 0.039
512
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.039
513
IMP005 Impotence 52 0.039
514
P THY032 Thyroiditis 52 0.039
515
PPT001 Peptic Esophagitis 52 0.039
516
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.039
517
c INH030 Inherited Retinal Disorder 51 0.039
518
OCL069 Ocular Motor Apraxia 51 0.039
519
CYS014 Cystadenocarcinoma 51 0.039
520
LNG031 Lung Benign Neoplasm 51 0.039
521
SCB001 Scabies 50 0.039
522
P FNC004 Fanconi Syndrome 50 0.039
523
P OBS001 Obstructive Jaundice 50 0.039
524
IRR003 Irritant Dermatitis 49 0.039
525
P BRS053 Breast Fibroadenoma 49 0.039
526
BNR002 Bone Resorption Disease 48 0.039
527
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.039
528
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.039
529
RTN023 Retinitis 46 0.039
530
TTH006 Tooth Disease 46 0.039
531
c GLC111 Galactosemia Ii 46 0.039
532
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.039
533
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.039
534
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.039
535
URT010 Ureteral Obstruction 45 0.039
536
HMR023 Hemorrhagic Cystitis 45 0.039
537
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.039
538
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.039
539
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.039
540
SMN007 Seminoma 43 0.039
541
SDD008 Sudden Sensorineural Hearing Loss 43 0.039
543
ATX019 Ataxia with Vitamin E Deficiency 42 0.039
544
NRR001 Neuroretinitis 42 0.039
545
P RRT020 Rare Tumor 41 0.039
546
c MCR112 Microvascular Complications of Diabetes 2 41 0.039
547
P FNC034 Fanconi Renotubular Syndrome 2 40 0.039
548
c PRG020 Paragangliomas 3 39 0.039
549
BRR002 Barrett's Adenocarcinoma 36 0.039
550
MTG002 Mutagen Sensitivity 35 0.039
551
PRM329 Premature Aging 35 0.039
552
P CMP072 Camptodactyly Syndrome, Guadalajara, Type I 34 0.039
553
MNG007 Manganese Poisoning 29 0.039
554
c MGR022 Migraine with or Without Aura 3 17 0.039
555
INS024 Insulin-Like Growth Factor I 79 0.034
556
c SPN225 Spondyloarthropathy 1 73 0.034
557
c THR092 Thrombophilia Due to Thrombin Defect 73 0.034
558
P SRC025 Sarcoidosis 1 70 0.034
559
MYL005 Myelofibrosis 70 0.034
560
LGH007 Leigh Syndrome 70 0.034
561
WRN001 Werner Syndrome 69 0.034
562
PLY001 Polycythemia Vera 69 0.034
563
P SLP006 Sleep Apnea 69 0.034
564
ART016 Aortic Aneurysm 69 0.034
565
P ANG001 Angelman Syndrome 69 0.034
566
OBS002 Obsessive-Compulsive Disorder 68 0.034
567
P OLG002 Oligodendroglioma 67 0.034
568
BRK010 Burkitt Lymphoma 67 0.034
569
P TRN020 Turner Syndrome 67 0.034
570
P MLG056 Malignant Hyperthermia 67 0.034
571
c TYR012 Tyrosinemia, Type I 66 0.034
572
GLN010 Glanzmann Thrombasthenia 66 0.034
573
P NRV007 Nervous System Disease 66 0.034
574
P THY023 Thymoma 65 0.034
575
NRM005 Neuromuscular Disease 64 0.034
576
CLF027 Cleft Palate, Isolated 64 0.034
577
P GLC113 Galactosemia I 64 0.034
578
P GCH001 Gaucher's Disease 63 0.034
579
P ANR048 Aniridia 1 63 0.034
580
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.034
581
BRS099 Breast Ductal Carcinoma 62 0.034
582
P TXP001 Toxoplasmosis 60 0.034
583
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.034
584
INT066 Interstitial Lung Disease 60 0.034
585
ACN002 Acanthosis Nigricans 60 0.034
586
PRT013 Portal Hypertension 59 0.034
587
P DNG005 Dengue Virus 59 0.034
588
BRS051 Breast Disease 58 0.034
589
CNS004 Constipation 58 0.034
590
LYM027 Lymphopenia 58 0.034
591
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 0.034
592
P UVT001 Uveitis 57 0.034
593
c CHL119 Cholangitis, Primary Sclerosing 57 0.034
594
P HDC001 Headache 57 0.034
595
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.034
596
CMM005 Common Cold 57 0.034
597
P FTL001 Fetal Alcohol Syndrome 57 0.034
598
CYT008 Cytomegalovirus Infection 57 0.034
599
P PLY019 Polyneuropathy 56 0.034
600
MCL006 Macular Retinal Edema 55 0.034
601
NPH009 Nephrolithiasis 55 0.034
602
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.034
603
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.034
604
P SBS003 Substance Abuse 55 0.034
605
MYM001 Myoma 54 0.034
606
PNC001 Pancytopenia 54 0.034
607
P RTN016 Retinal Degeneration 53 0.034
608
CLF001 Cleft Lip 53 0.034
609
DNT012 Dental Caries 53 0.034
610
P HMG032 Hemoglobin H Disease 52 0.034
611
THY030 Thyroid Gland Disease 52 0.034
612
c THY107 Thymoma, Familial 52 0.034
613
CRV040 Cervix Carcinoma 51 0.034
614
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.034
615
ACT017 Acute Chest Syndrome 51 0.034
616
CRN030 Coronary Stenosis 50 0.034
617
NTR046 Neutrophil Migration 50 0.034
618
c LRG001 Large Cell Carcinoma 50 0.034
619
LPR001 Lepromatous Leprosy 50 0.034
620
P ATR005 Atrophic Gastritis 50 0.034
621
CHL004 Cholelithiasis 49 0.034
622
P SCL009 Sclerosing Cholangitis 48 0.034
623
IGG001 Iga Glomerulonephritis 48 0.034
624
DRG003 Drug Dependence 47 0.034
625
PPL002 Papillary Carcinoma 47 0.034
626
THY128 Thyroid Tumor 47 0.034
627
P BLR006 Biliary Tract Disease 47 0.034
628
RNL077 Renal Fibrosis 47 0.034
629
GST071 Gastrointestinal Carcinoma 47 0.034
630
CHR074 Choriocarcinoma 47 0.034
631
RTN020 Retinal Vascular Disease 46 0.034
632
ALB002 Albinism 46 0.034
633
c GRN049 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I 46 0.034
634
OLG001 Oligospermia 45 0.034
635
ATN004 Autonomic Neuropathy 45 0.034
636
TBR006 Tuberculoid Leprosy 44 0.034
637
GRN017 Granulocytopenia 44 0.034
638
CLN003 Clonorchiasis 44 0.034
639
DMP001 Dumping Syndrome 44 0.034
640
CVD001 Covid-19 44 0.034
641
P CRN024 Corneal Disease 44 0.034
642
CLN044 Colon Adenoma 44 0.034
643
PLY068 Polysubstance Abuse 43 0.034
644
DRG002 Drug-Induced Hepatitis 43 0.034
645
MRS001 Marasmus 42 0.034
646
c CHR576 Chronic Beryllium Disease 42 0.034
647
IDP091 Idiopathic Nephrotic Syndrome 42 0.034
648
THR035 Thrombasthenia 40 0.034
649
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.034
650
ALC005 Alcoholic Pancreatitis 40 0.034
651
PRM020 Premenstrual Tension 40 0.034
652
P BRY005 Beryllium Disease 40 0.034
653
EXT006 Extrahepatic Cholestasis 39 0.034
654
CHL045 Choline Deficiency Disease 39 0.034
655
c OVR114 Ovarian Cancer 1 38 0.034
656
SMT002 Smooth Muscle Tumor 38 0.034
657
SYS071 Systemic Autoimmune Disease 37 0.034
658
ATX010 Ataxia Neuropathy Spectrum 34 0.034
659
DXR001 Doxorubicin Induced Cardiomyopathy 33 0.034
660
ACT064 Acute Necrotizing Encephalitis 33 0.034
661
CND006 Candida Glabrata 32 0.034
662
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.034
663
PRC051 Paracetamol Poisoning 30 0.034
664
TCK004 Tick Infestation 28 0.034
665
BRD005 Borderline Leprosy 27 0.034
666
BLD137 Blood Group--Ahonen 16 0.034
667
P RTT002 Rett Syndrome 80 0.028
668
c TBR025 Tuberous Sclerosis 1 77 0.028
669
KPS004 Kaposi Sarcoma 75 0.028
670
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.028
671
ADR007 Adrenoleukodystrophy 75 0.028
672
LPT014 Leptin Deficiency or Dysfunction 74 0.028
673
c HMC039 Hemochromatosis, Type 1 74 0.028
674
P CNR004 Cone-Rod Dystrophy 2 73 0.028
675
P FML018 Familial Mediterranean Fever 73 0.028
676
P AMY004 Amyloidosis 70 0.028
677
c GCH015 Gaucher Disease, Type I 70 0.028
678
P TTR001 Tetralogy of Fallot 70 0.028
679
ADL002 Adult Syndrome 70 0.028
680
P TBR001 Tuberous Sclerosis 70 0.028
681
P DMN001 Diamond-Blackfan Anemia 69 0.028
682
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.028
683
CRB037 Cerebral Palsy 69 0.028
684
MNT001 Mantle Cell Lymphoma 69 0.028
685
SKN019 Skin Melanoma 68 0.028
686
P INF038 Influenza 68 0.028
687
P FLL037 Follicular Lymphoma 67 0.028
688
P PRP003 Porphyria Cutanea Tarda 67 0.028
689
FLL027 Fallopian Tube Carcinoma 67 0.028
690
P BLD062 Bile Duct Cancer 67 0.028
691
c MGR028 Migraine with or Without Aura 1 67 0.028
692
MYC006 Mycosis Fungoides 66 0.028
693
ART001 Arterial Tortuosity Syndrome 66 0.028
694
P CNJ013 Conjunctivitis 65 0.028
695
PRP001 Propionic Acidemia 65 0.028
696
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.028
697
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.028
698
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.028
699
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.028
700
c JVN010 Juvenile Rheumatoid Arthritis 64 0.028
701
BRC012 Brucellosis 64 0.028
702
PLM031 Poliomyelitis 64 0.028
703
P LMY004 Leiomyosarcoma 63 0.028
704
c OPT053 Optic Atrophy 1 63 0.028
705
c ALP101 Alpha-Thalassemia 62 0.028
706
P ART023 Arthropathy 62 0.028
707
LSC001 Lesch-Nyhan Syndrome 62 0.028
708
CRC021 Carcinosarcoma 62 0.028
709
MSL001 Measles 62 0.028
710
INT002 Intermittent Claudication 61 0.028
711
P ENC004 Encephalitis 61 0.028
712
c WLM018 Wilms Tumor 5 61 0.028
713
GST033 Gestational Diabetes 61 0.028
714
VRL011 Viral Infectious Disease 61 0.028
715
DPH001 Diphtheria 60 0.028
716
P ATR010 Atrial Heart Septal Defect 60 0.028
717
RHM001 Rheumatic Fever 60 0.028
718
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.028
719
ETN001 Eating Disorder 60 0.028
720
P HRD011 Hereditary Spherocytosis 60 0.028
721
c PRK089 Parkinson Disease 2, Autosomal Recessive Juvenile 59 0.028
722
P BRN022 Bronchiectasis 59 0.028
723
CHL123 Chlamydia 59 0.028
724
P LYM033 Lymphoproliferative Syndrome 59 0.028
725
DBN001 Dubin-Johnson Syndrome 59 0.028
726
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.028
727
GST045 Gastroenteritis 59 0.028
728
ANR040 Aneurysm 59 0.028
729
P SYP003 Syphilis 58 0.028
730
P ANP001 Anaplastic Large Cell Lymphoma 58 0.028
731
GLB001 Gilbert Syndrome 58 0.028
732
c SPN301 Spinocerebellar Ataxia 2 58 0.028
733
CRV038 Cervical Squamous Cell Carcinoma 58 0.028
734
P PLY041 Polymyositis 57 0.028
735
THY122 Thyroid Gland Cancer 57 0.028
736
THR024 Thrombosis 57 0.028
737
CHR177 Chromophobe Renal Cell Carcinoma 57 0.028
738
JPN002 Japanese Encephalitis 57 0.028
739
P PYL005 Pyelonephritis 56 0.028
740
PLS011 Plasmacytoma 56 0.028
741
ADN027 Adenomyosis 56 0.028
742
GNR004 Generalized Anxiety Disorder 56 0.028
743
GRS011 Gerstmann-Straussler Disease 56 0.028
744
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.028
745
P PLM034 Pulmonary Emphysema 55 0.028
746
P ANT006 Antiphospholipid Syndrome 55 0.028
747
P MYP006 Myopia 55 0.028
748
P ALP106 Alport Syndrome 1, X-Linked 55 0.028
749
END040 Endogenous Depression 55 0.028
750
HRY003 Hairy Cell Leukemia 55 0.028
751
BRN015 Bronchiolo-Alveolar Adenocarcinoma 54 0.028
752
P PMP001 Pemphigus 54 0.028
753
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.028
754
SNS003 Sensory Peripheral Neuropathy 54 0.028
755
PRC002 Paracoccidioidomycosis 54 0.028
756
CRH005 Crohn's Colitis 53 0.028
757
ECH003 Echinococcosis 53 0.028
758
GTR002 Goiter 53 0.028
759
c HPT007 Hepatitis E 53 0.028
760
FML037 Female Breast Cancer 52 0.028
761
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 52 0.028
762
PRV004 Periventricular Leukomalacia 52 0.028
763
LMY002 Leiomyoma 52 0.028
764
PNG002 Pain Agnosia 51 0.028
765
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.028
766
PLS006 Plasmodium Vivax Malaria 51 0.028
767
ASP003 Aseptic Meningitis 51 0.028
768
P HRD012 Hereditary Elliptocytosis 51 0.028
769
c ACT078 Acute Porphyria 51 0.028
770
LNT004 Lentigines 50 0.028
771
PLR008 Pleurisy 50 0.028
772
c HNT004 Huntington Disease-Like 2 50 0.028
773
RTN003 Retinal Ischemia 50 0.028
774
HPT014 Hepatorenal Syndrome 50 0.028
775
CHL122 Cholesteatoma of Middle Ear 50 0.028
776
c INF145 Infantile Liver Failure Syndrome 1 50 0.028
777
P TMP001 Temporal Lobe Epilepsy 50 0.028
778
PLC008 Placenta Disease 50 0.028
779
PRN009 Paranoid Schizophrenia 50 0.028
780
P MTH008 Methylmalonic Acidemia 50 0.028
781
ILT001 Ileitis 50 0.028
782
HRT011 Heart Septal Defect 50 0.028
783
ONC007 Oncocytoma 49 0.028
784
ENT004 Enthesopathy 49 0.028
785
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.028
786
c BPL002 Bipolar I Disorder 49 0.028
787
VCC001 Vaccinia 49 0.028
788
CHL061 Childhood Leukemia 48 0.028
789
CCN001 Cocaine Dependence 48 0.028
790
END062 Endometrial Hyperplasia 48 0.028
791
GLC106 Glucocorticoid Resistance, Generalized 48 0.028
792
MCR018 Microcytic Anemia 47 0.028
793
CLF056 Cleft Lip with or Without Cleft Palate 47 0.028
794
NRN001 Neuroendocrine Carcinoma 47 0.028
795
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.028
796
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.028
797
P OVR046 Ovarian Cyst 47 0.028
798
ASP004 Asphyxia Neonatorum 46 0.028
799
MYC005 Myocardial Stunning 46 0.028
800
P BRB001 Beriberi 46 0.028
801
CHD004 Chudley-Mccullough Syndrome 46 0.028
802
P MYC033 Myoclonus 46 0.028
803
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.028
804
AGR002 Agoraphobia 45 0.028
805
P SBR004 Seborrheic Dermatitis 45 0.028
806
c CHR517 Charcot-Marie-Tooth Disease, Type 4a 45 0.028
807
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.028
808
P CHR345 Chronic Pain 44 0.028
809
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.028
810
P MTC004 Mitochondrial Encephalomyopathy 44 0.028
811
P SDR002 Siderosis 44 0.028
812
P END039 Endodermal Sinus Tumor 44 0.028
813
P PRL003 Proliferative Glomerulonephritis 44 0.028
814
PRT035 Peritoneum Cancer 44 0.028
815
c PRM038 Primary Agammaglobulinemia 44 0.028
816
MTR010 Mature Teratoma 44 0.028
817
ADR041 Adrenal Cortical Adenoma 43 0.028
818
P PHR004 Pharynx Cancer 43 0.028
819
RDC006 Red Cell Aplasia 43 0.028
820
P CND005 Cone Dystrophy 43 0.028
821
P CRN026 Corneal Edema 43 0.028
822
STL007 Steel Syndrome 43 0.028
823
EPT021 Epithelial Recurrent Erosion Dystrophy 42 0.028
824
EXC002 Exocrine Pancreatic Insufficiency 42 0.028
825
c MLG079 Malignant Pleural Mesothelioma 42 0.028
826
c HMG001 Hemoglobin C Disease 40 0.028
827
MLT001 Multiple Chemical Sensitivity 40 0.028
828
HNZ004 Heinz Body Anemias 39 0.028
829
SKN020 Skin Papilloma 39 0.028
830
FRM003 Farmer's Lung 39 0.028
831
HYP141 Hyperphenylalaninemia 39 0.028
832
SCR011 Scrapie 39 0.028
833
ADR022 Adrenomyeloneuropathy 38 0.028
834
OVR047 Ovarian Cystadenocarcinoma 38 0.028
835
KSH004 Kashin-Beck Disease 38 0.028
836
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.028
837
c CHR020 Chronic Interstitial Cystitis 37 0.028
838
NRW001 Norwegian Scabies 37 0.028
839
P HRD217 Hereditary Optic Neuropathy 36 0.028
840
PRS011 Persian Gulf Syndrome 36 0.028
842
OLG022 Oligoasthenoteratozoospermia 36 0.028
843
SPR020 Superficial Mycosis 35 0.028
844
OLG006 Oligoastrocytoma 35 0.028
845
INT040 Intrinsic Asthma 34 0.028
846
CLC008 Colchicine Resistance 34 0.028
848
CRB132 Cerebral Sinovenous Thrombosis 33 0.028
849
BWN006 Bowen's Disease 32 0.028
850
HRD218 Hereditary Stomatocytosis 32 0.028
851
c BLD140 Blood Group, I System 32 0.028
852
WHT017 Wheat Allergy 32 0.028
853
BLD047 Bladder Squamous Cell Carcinoma 31 0.028
854
PLY150 Polykaryocytosis Inducer 31 0.028
855
c ALC016 Alcohol Sensitivity, Acute 31 0.028
856
FNT004 Fainting 30 0.028
857
MTY003 Mutyh Polyposis 30 0.028
858
PYR016 Pyridoxine Deficiency 30 0.028
859
MYC088 Mycobacterium Avium Complex Infections 29 0.028
860
FTL007 Fetal Hydantoin Syndrome 29 0.028
861
ISL099 Isolated Methylmalonic Acidemia 29 0.028
862
GLT040 Glutamate-Cysteine Ligase Deficiency 29 0.028
863
MTR001 Mature Cataract 28 0.028
864
MYL080 Myalgic Encephalomyelitis/chronic Fatigue Syndrome 27 0.028
865
TRN002 Transitional Meningioma 25 0.028
866
ANT078 Antipyrine Metabolism 24 0.028
867
ACT133 Acetylation, Slow 23 0.028
868
HML018 Homologous Wasting Disease 22 0.028
869
AND005 Androgen Insensitivity Syndrome, Mild 19 0.028
870
PHC015 Phacoanaphylactic Uveitis 19 0.028
871
c PGT006 Paget Disease of Bone 4 17 0.028
872
PRX092 Peroxidase, Salivary 9 0.028
873
CNN003 Conn's Syndrome 79 0.020
874
MRF001 Marfan Syndrome 77 0.020
875
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.020
876
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.020
877
BSL036 Basal Cell Nevus Syndrome 73 0.020
878
PRP027 Peripheral Vascular Disease 71 0.020
879
ADN011 Adenoid Cystic Carcinoma 70 0.020
880
PTZ001 Peutz-Jeghers Syndrome 70 0.020
881
P HYP061 Hypertrophic Cardiomyopathy 70 0.020
882
P ASP006 Aspergillosis 69 0.020
883
SVR097 Severe Cutaneous Adverse Reaction 69 0.020
884
EWN003 Ewing Sarcoma 69 0.020
885
MST024 Mastocytosis, Cutaneous 69 0.020
886
CMM004 Common Variable Immunodeficiency 68 0.020
887
P MYS003 Myasthenia Gravis 68 0.020
888
RCK004 Rickets 68 0.020
889
P THR014 Thrombocytopenia 67 0.020
890
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.020
891
GLL008 Gilles De La Tourette Syndrome 66 0.020
892
CHD001 Chediak-Higashi Syndrome 66 0.020
893
c FML021 Familial Hypercholesterolemia 66 0.020
894
P HYD006 Hydrocephalus 66 0.020
895
KHL003 Kohlschutter-Tonz Syndrome 65 0.020
896
GTL001 Gitelman Syndrome 65 0.020
897
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.020
898
MSM014 Mismatch Repair Cancer Syndrome 65 0.020
899
c ART101 Aortic Valve Disease 2 65 0.020
900
P PRS038 Personality Disorder 65 0.020
901
MNK001 Menkes Disease 64 0.020
902
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.020
903
P HRM001 Hermansky-Pudlak Syndrome 64 0.020
904
NRF007 Neurofibroma 64 0.020
905
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 64 0.020
906
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.020
907
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.020
908
c CNG006 Congenital Hypothyroidism 64 0.020
909
MSC007 Muscle Hypertrophy 64 0.020
910
CYS013 Cystinuria 63 0.020
911
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.020
912
TYP007 Typhoid Fever 63 0.020
913
PLG002 Plague 63 0.020
914
c MLG084 Malignant Fibrous Histiocytoma 63 0.020
915
END041 Endometrial Adenocarcinoma 63 0.020
916
HMT002 Hematologic Cancer 62 0.020
917
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.020
918
c FNC043 Fanconi Anemia, Complementation Group E 62 0.020
919
c BRN108 Branchiootic Syndrome 1 62 0.020
920
c SVR001 Severe Acute Respiratory Syndrome 62 0.020
921
HYD038 Hydrops Fetalis, Nonimmune 62 0.020
922
GLY010 Glycine Encephalopathy 62 0.020
923
ESP020 Esophageal Atresia 62 0.020
924
PSR001 Psoriatic Arthritis 61 0.020
926
OST003 Osteonecrosis 61 0.020
927
RCT015 Reactive Arthritis 61 0.020
928
SDD001 Sudden Infant Death Syndrome 61 0.020
929
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.020
930
SZR001 Sezary's Disease 60 0.020
931
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 60 0.020
932
P TST021 Testicular Germ Cell Tumor 60 0.020
933
P BNG030 Benign Ependymoma 60 0.020
934
P VNT002 Ventricular Septal Defect 60 0.020
935
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.020
936
CRD223 Cardiac Arrhythmia 60 0.020
937
P ALP009 Alopecia Areata 60 0.020
938
c WLF013 Wolfram Syndrome 1 60 0.020
939
P WLF004 Wolfram Syndrome 60 0.020
940
LBR030 Leber Optic Atrophy 60 0.020
941
c HYP731 Hyperaldosteronism, Familial, Type I 60 0.020
942
P PTN014 Patent Ductus Arteriosus 1 60 0.020
943
P EMR001 Emery-Dreifuss Muscular Dystrophy 60 0.020
944
P OCL002 Oculocutaneous Albinism 60 0.020
945
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 60 0.020
946
P GLY013 Glycogen Storage Disease 60 0.020
947
P RBL001 Rubella 59 0.020
948
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.020
949
P BND020 Bone Disease 59 0.020
950
P SLP005 Sleep Disorder 59 0.020
951
SRC027 Sarcoma, Synovial 58 0.020
952
CRY005 Cryptococcosis 58 0.020
953
ALK013 Alkaptonuria 58 0.020
954
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.020
955
PST028 Post-Traumatic Stress Disorder 58 0.020
956
c XRD022 Xeroderma Pigmentosum, Complementation Group D 58 0.020
957
FBR047 Fibromyalgia 58 0.020
958
CMP010 Complex Regional Pain Syndrome 58 0.020
959
c BNG091 Benign Chronic Pemphigus 58 0.020
960
CCC001 Coccidioidomycosis 58 0.020
961
ERY003 Erythema Multiforme 58 0.020
962
NWB001 Newborn Respiratory Distress Syndrome 58 0.020
963
EXT034 Extrinsic Allergic Alveolitis 58 0.020
964
LNG108 Langerhans Cell Histiocytosis 58 0.020
965
PMP006 Pemphigus Vulgaris, Familial 57 0.020
966
P PLV020 Pelvic Organ Prolapse 57 0.020
967
c CHR417 Chronic Graft Versus Host Disease 57 0.020
968
BLM002 Bulimia Nervosa 57 0.020
969
MCR013 Microphthalmia 57 0.020
970
c ANM036 Anemia, Sideroblastic, 1 57 0.020
971
MNR012 Meniere Disease 57 0.020
972
CHK001 Chikungunya 57 0.020
973
DSS009 Disseminated Intravascular Coagulation 57 0.020
974
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.020
975
APH001 Aphthous Stomatitis 57 0.020
976
P END033 Endocarditis 57 0.020
977
P FCL005 Focal Segmental Glomerulosclerosis 57 0.020
978
P MYS005 Myositis 56 0.020
979
TCK001 Tick-Borne Encephalitis 56 0.020
980
EXF001 Exfoliation Syndrome 56 0.020
981
c ESS001 Essential Tremor 56 0.020
982
SFT003 Soft Tissue Sarcoma 56 0.020
983
SCH003 Schizophreniform Disorder 56 0.020
984
PRS047 Prostatitis 56 0.020
985
ANS011 Anus Cancer 56 0.020
986
OVR012 Ovarian Serous Cystadenocarcinoma 56 0.020
987
MTH009 Mouth Disease 56 0.020
988
P NRF002 Neurofibromatosis 56 0.020
989
SLC006 Silicosis 56 0.020
990
c ERY071 Erythrocytosis, Familial, 2, Autosomal Recessive 55 0.020
991
MCN007 Meconium Aspiration Syndrome 55 0.020
992
LMB062 Limb Ischemia 55 0.020
993
P GRV001 Graves' Disease 55 0.020
994
P PTT006 Pituitary Adenoma 55 0.020
995
CHR100 Chronic Ulcer of Skin 55 0.020
996
P VNS003 Venous Insufficiency 55 0.020
997
c ATM024 Autoimmune Pancreatitis 55 0.020
998
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 0.020
999
HMP005 Hemiplegia 55 0.020
1000
PRP030 Purpura 54 0.020
1001
RSC001 Rosacea 54 0.020
1002
BRN014 Bronchopneumonia 54 0.020
1003
CLL010 Cellular Ependymoma 54 0.020
1004
WST005 West Nile Virus 54 0.020
1005
GST009 Gastroschisis 53 0.020
1006
MMM001 Mammary Paget's Disease 53 0.020
1007
P EPD016 Epidermolysis Bullosa 53 0.020
1008
RHM028 Rheumatic Heart Disease 53 0.020
1009
c CNR007 Cone-Rod Dystrophy 6 53 0.020
1010
P MNC007 Monocytic Leukemia 53 0.020
1011
PRP036 Peripheral T-Cell Lymphoma 53 0.020
1012
ENC055 Encephalopathy, Ethylmalonic 53 0.020
1013
P ORL007 Oral Cavity Cancer 53 0.020
1014
P SHR001 Short Bowel Syndrome 53 0.020
1015
P GRS003 Griscelli Syndrome 53 0.020
1016
P CTN003 Cutaneous Lupus Erythematosus 53 0.020
1017
NRT001 Neurotic Disorder 53 0.020
1018
END002 Endometrioid Ovary Carcinoma 53 0.020
1019
PRN011 Pernicious Anemia 53 0.020
1020
P LMB006 Limb-Girdle Muscular Dystrophy 53 0.020
1021
PRP080 Peripheral Artery Disease 53 0.020
1022
c GLL024 Gallbladder Disease 1 53 0.020
1023
c CNT035 Central Nervous System Disease 52 0.020
1024
CHR073 Choreatic Disease 52 0.020
1025
OST011 Osteomalacia 52 0.020
1026
P PRG013 Paraganglioma 52 0.020
1027
ESP023 Esophageal Disease 52 0.020
1028
PLM014 Pleomorphic Adenoma 52 0.020
1029
PRP016 Paraplegia 52 0.020
1030
P D2H002 D-2-Hydroxyglutaric Aciduria 1 52 0.020
1031
MRG003 Marginal Zone B-Cell Lymphoma 52 0.020
1032
DYS015 Dysentery 52 0.020
1033
P ACT105 Acute Mountain Sickness 52 0.020
1034
P PRV002 Periventricular Nodular Heterotopia 52 0.020
1035
DFF036 Differentiated Thyroid Carcinoma 52 0.020
1036
P MGR003 Migraine with Aura 52 0.020
1037
c ACT135 Acute Graft Versus Host Disease 52 0.020
1038
THR004 Thrombocytosis 51 0.020
1039
TRC010 Trichotillomania 51 0.020
1040
UNV001 Unverricht-Lundborg Syndrome 51 0.020
1041
FDL002 Food Allergy 51 0.020
1042
PLS009 Plasma Cell Neoplasm 51 0.020
1043
c PNC106 Pancreatic Agenesis 1 51 0.020
1044
MGL001 Megaloblastic Anemia 51 0.020
1045
CYS036 Cystinosis, Nephropathic 51 0.020
1046
CCC002 Coccidiosis 51 0.020
1047
NRM004 Neuroma 51 0.020
1048
ACH005 Achalasia 51 0.020
1049
HND002 Hand, Foot and Mouth Disease 51 0.020
1050
P RNL007 Renal Tubular Acidosis 51 0.020
1051
TLR001 Tularemia 51 0.020
1052
HYP081 Hypolipoproteinemia 51 0.020
1053
P MMB011 Membranous Nephropathy 50 0.020
1054
P OVR082 Overgrowth Syndrome 50 0.020
1055
P PRS049 Persistent Mullerian Duct Syndrome 50 0.020
1056
STM007 Stomatitis 50 0.020
1057
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.020
1058
MCP006 Mucoepidermoid Carcinoma 50 0.020
1059
MLL001 Molluscum Contagiosum 50 0.020
1060
P AGG001 Aggressive Periodontitis 50 0.020
1061
TRP002 Tropical Spastic Paraparesis 50 0.020
1062
CLR003 Clear Cell Adenocarcinoma 50 0.020
1063
OCL022 Ocular Melanoma 50 0.020
1064
DYS073 Dysphagia 50 0.020
1065
RNL078 Renal Dysplasia 50 0.020
1066
c INF023 Inflammatory Breast Carcinoma 50 0.020
1067
HYP080 Hypogonadism 50 0.020
1068
DBT004 Diabetic Polyneuropathy 49 0.020
1069
c CHR418 Chronic Leukemia 49 0.020
1070
VRR004 Verrucous Carcinoma 49 0.020
1071
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.020
1072
MCN001 Mucinous Adenocarcinoma 49 0.020
1073
PLY024 Polymicrogyria 49 0.020
1074
AMB002 Amblyopia 49 0.020
1075
P END046 Endometritis 49 0.020
1076
SPN028 Spondyloepimetaphyseal Dysplasia, Strudwick Type 49 0.020
1077
GST049 Gastrointestinal System Cancer 49 0.020
1078
P CRV031 Cervical Adenocarcinoma 49 0.020
1079
MTC005 Mitochondrial Metabolism Disease