Search results for Hydrogen Ion

782 hits were found for Hydrogen Ion

# Family MCID Name MIFTS Score
1
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.965
2
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.532
3
HLX001 Helix Syndrome 47 0.455
4
HRW001 Hair Whorl 36 0.451
5
P NRB001 Neuroblastoma 71 0.284
6
ISC004 Ischemia 60 0.280
7
CYS001 Cystic Fibrosis 80 0.223
8
HYP266 Hypoxia 56 0.222
9
MTB004 Metabolic Acidosis 50 0.221
10
ANX004 Anoxia 42 0.220
11
48X005 48,xyyy 39 0.204
12
MTH071 Methane Production 26 0.204
13
P DRR001 Diarrhea 57 0.200
14
P PHC003 Pheochromocytoma 71 0.198
15
ADR040 Adrenal Gland Pheochromocytoma 46 0.198
16
GLL048 Glial Tumor 45 0.195
17
P OVR082 Overgrowth Syndrome 50 0.195
18
P GLM045 Glioma 63 0.194
19
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.192
20
P KDN018 Kidney Disease 70 0.183
21
P CRD119 Cardiac Arrest 67 0.176
22
P ALZ034 Alzheimer Disease 88 0.173
23
LNG099 Lung Disease 61 0.169
24
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.168
25
P LTR001 Lateral Sclerosis 53 0.168
26
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.165
27
GLB015 Glioblastoma Multiforme 75 0.163
28
47X002 47,xyy 49 0.161
29
c HYP595 Hypertension, Essential 84 0.161
30
PRT037 Pertussis 65 0.160
31
BRN071 Brain Injury 49 0.160
32
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.157
33
CHL014 Cholera 55 0.156
34
P VSC007 Vascular Disease 63 0.153
35
IRR002 Irritable Bowel Syndrome 63 0.153
36
P PLM037 Pulmonary Hypertension 68 0.153
37
CLT003 Colitis 62 0.152
38
ALL026 Allergic Hypersensitivity Disease 64 0.151
39
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.148
40
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.148
41
P CTR002 Cataract 60 0.148
42
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.148
43
P LNG032 Lung Cancer 97 0.146
44
PLM010 Pulmonary Edema 55 0.144
45
P CLR023 Colorectal Cancer 98 0.142
46
TRM010 Traumatic Brain Injury 53 0.141
47
P PNC035 Pancreatic Cancer 84 0.139
48
ATH013 Atherosclerosis Susceptibility 66 0.138
49
HYP066 Hyperglycemia 61 0.138
50
HMC014 Homocysteinemia 53 0.137
51
P HPT023 Hepatocellular Carcinoma 100 0.136
52
BRN004 Brain Edema 55 0.135
53
CNG034 Congestive Heart Failure 70 0.134
54
OST159 Osteogenic Sarcoma 66 0.134
55
P PRS040 Prostate Cancer 97 0.134
56
P HRT032 Heart Disease 75 0.134
57
CRB004 Cerebral Artery Occlusion 44 0.133
58
P PRD008 Periodontitis 62 0.132
59
DNT012 Dental Caries 51 0.132
60
c ACT027 Acute Pancreatitis 59 0.132
61
PPL052 Papillomatosis, Confluent and Reticulated 34 0.129
62
P INF037 Inflammatory Bowel Disease 56 0.127
63
P LVR013 Liver Disease 68 0.127
64
OCL069 Ocular Motor Apraxia 51 0.125
65
TXC005 Toxic Shock Syndrome 61 0.125
66
DRM006 Dermatitis 61 0.124
67
c CHR684 Chronic Kidney Disease 66 0.124
68
BNR002 Bone Resorption Disease 48 0.123
69
P ENC018 Encephalopathy 61 0.123
70
c MGR028 Migraine with or Without Aura 1 69 0.123
71
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.121
72
MLN008 Melanoma 69 0.121
73
ULC004 Ulcerative Colitis 73 0.119
74
AGN016 Aging 56 0.118
75
SPN186 Spinal Cord Injury 60 0.117
76
IRN002 Iron Metabolism Disease 57 0.116
77
CYT002 Cytokine Deficiency 44 0.115
79
NNL006 Non-Alcoholic Steatohepatitis 51 0.114
80
c PRC016 Pre-Eclampsia 63 0.114
81
P GST044 Gastritis 55 0.114
82
HND015 Hand Skill, Relative 33 0.114
83
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.114
84
LVR012 Liver Cirrhosis 63 0.112
85
CRD223 Cardiac Arrhythmia 60 0.112
86
CNS004 Constipation 57 0.112
87
IMP005 Impotence 52 0.111
88
P MYC007 Myocardial Infarction 70 0.110
89
HYP005 Hypokalemia 55 0.109
90
DPH001 Diphtheria 60 0.108
91
OST012 Osteoarthritis 78 0.108
92
P NRP001 Neuropathy 56 0.108
93
P CHR345 Chronic Pain 50 0.108
94
PST092 Posttransplant Acute Limbic Encephalitis 29 0.107
95
FTT001 Fatty Liver Disease 61 0.107
96
HMN044 Human Immunodeficiency Virus Type 1 71 0.106
97
c MCR113 Microvascular Complications of Diabetes 3 52 0.105
98
c MCR120 Microvascular Complications of Diabetes 7 47 0.105
99
c MCR130 Microvascular Complications of Diabetes 6 41 0.105
100
c MCR133 Microvascular Complications of Diabetes 4 41 0.105
101
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.105
102
c SML038 Small Cell Cancer of the Lung 65 0.105
103
P LCT002 Lactose Intolerance 53 0.105
104
ATM095 Autoimmune Disease 61 0.105
105
SKN016 Skin Disease 63 0.104
106
END030 End Stage Renal Failure 58 0.102
107
P PNC044 Pancreatitis 61 0.102
108
P ADN016 Adenocarcinoma 64 0.102
109
BCT022 Bacterial Infectious Disease 56 0.102
110
P RSP003 Respiratory Failure 74 0.102
111
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.101
112
ANT024 Anthrax Disease 58 0.101
113
P PRN023 Prion Disease 57 0.101
114
ADN011 Adenoid Cystic Carcinoma 70 0.100
115
P PRD021 Periodic Paralysis 46 0.100
116
P HNT016 Huntington Disease 71 0.100
117
c ATR087 Atrial Standstill 1 74 0.100
118
DWN001 Down Syndrome 70 0.100
119
P HYP086 Hypothyroidism 68 0.099
120
MCS002 Mucositis 55 0.099
121
P LNG064 Lung Cancer Susceptibility 3 77 0.098
122
P BND020 Bone Disease 59 0.098
123
P PRK057 Parkinson Disease, Late-Onset 76 0.097
124
P BCL017 B-Cell Lymphoma 58 0.096
125
P HRP006 Herpes Simplex 65 0.096
126
IDP011 Idiopathic Interstitial Pneumonia 63 0.096
127
P PLM036 Pulmonary Fibrosis 61 0.096
128
HYP056 Hypoglycemia 66 0.095
129
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 22 0.095
130
P SZR006 Seizure Disorder 58 0.095
131
VSL002 Visual Epilepsy 58 0.095
132
HMS001 Hemosiderosis 54 0.095
133
P RRH023 Rare Hereditary Hemochromatosis 41 0.095
134
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.095
135
P MYC008 Myocarditis 59 0.094
136
P MSC005 Muscular Dystrophy 66 0.094
137
c SVR001 Severe Acute Respiratory Syndrome 55 0.093
138
P RHN004 Rhinitis 57 0.093
139
AST005 Asthma 77 0.093
140
c HPT073 Hepatitis C Virus 70 0.093
141
CNT047 Contact Dermatitis 57 0.092
142
P RNL007 Renal Tubular Acidosis 50 0.091
143
c ACT071 Acute Kidney Failure 59 0.090
144
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.089
145
SQM006 Squamous Cell Carcinoma 60 0.089
146
P MCR115 Microvascular Complications of Diabetes 5 66 0.089
147
CRB039 Cerebrovascular Disease 69 0.089
148
PPT005 Peptic Ulcer Disease 58 0.089
149
P PRP019 Peripheral Nervous System Disease 57 0.089
150
c HYP836 Hypercholesterolemia, Familial, 1 72 0.088
151
TTN003 Tetanus 64 0.088
152
PLY150 Polykaryocytosis Inducer 31 0.088
153
GST023 Gastric Ulcer 53 0.087
154
P CRN018 Coronary Artery Anomaly 63 0.087
155
ESP021 Esophageal Cancer 90 0.086
156
ALL003 Allergic Rhinitis 67 0.086
157
P GLM007 Glomerulonephritis 57 0.086
158
P INF038 Influenza 68 0.086
159
GNG013 Gingivitis 59 0.086
160
P HYP076 Hyperthyroidism 55 0.085
161
GST050 Gastrointestinal System Disease 56 0.085
162
P NRF023 Neurofibromatosis, Type Ii 76 0.084
163
P LYM031 Lymphocytic Leukemia 55 0.084
165
BCT002 Bacterial Vaginosis 52 0.084
166
P BPL003 Bipolar Disorder 56 0.084
167
P RCT021 Rectum Cancer 53 0.084
168
P AMY004 Amyloidosis 70 0.083
169
BRN024 Bronchitis 68 0.083
170
P MYP004 Myopathy 64 0.083
171
P ATX030 Ataxia-Telangiectasia 83 0.083
172
TLN003 Telangiectasis 51 0.083
173
P BRS047 Breast Cancer 96 0.083
174
P DDN001 Duodenal Ulcer 50 0.083
175
P MRC003 Mercury Poisoning 48 0.082
176
CRV035 Cervical Cancer 76 0.081
177
c DLT002 Dilated Cardiomyopathy 79 0.081
178
P LCT001 Lactic Acidosis 51 0.081
179
P ATR011 Atrial Fibrillation 66 0.081
180
P DBT009 Diabetes Mellitus 64 0.080
181
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.080
182
c MJR024 Major Affective Disorder 9 41 0.080
183
c MJR022 Major Affective Disorder 8 38 0.080
184
CYN003 Cyanide Poisoning 24 0.080
185
P FBR031 Febrile Seizures 51 0.080
186
P SKN015 Skin Carcinoma 67 0.080
187
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.079
188
OTT002 Otitis Media 71 0.079
189
URM002 Uremia 49 0.079
190
P CHR012 Chronic Granulomatous Disease 67 0.079
191
P DRM053 Dermatitis, Atopic 66 0.078
192
P FBR017 Fibrosarcoma 56 0.078
193
P MLG056 Malignant Hyperthermia 67 0.078
194
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.078
195
CHD004 Chudley-Mccullough Syndrome 44 0.078
196
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.078
197
DFC004 Deficiency Anemia 75 0.078
198
P INF032 Infertility 57 0.078
199
P MLN007 Male Infertility 56 0.078
200
PRT036 Peritonitis 65 0.078
201
P CYS018 Cystitis 59 0.078
202
P HYP069 Hyperparathyroidism 62 0.077
203
P CLC063 Celiac Disease 1 68 0.077
204
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.077
205
c ACT068 Acute Cystitis 63 0.077
206
OST003 Osteonecrosis 61 0.077
207
ALL010 Allergic Contact Dermatitis 55 0.077
208
SRC014 Sarcoma 65 0.077
209
P AST007 Astrocytoma 50 0.077
210
VCC001 Vaccinia 49 0.077
211
MLR004 Malaria 80 0.076
212
c MLG068 Malignant Glioma 45 0.076
213
P CRN300 Coronary Heart Disease 1 63 0.076
214
SPN035 Spindle Cell Sarcoma 51 0.075
215
P PLY014 Polycystic Kidney Disease 59 0.075
216
ALC007 Alcohol Dependence 66 0.074
217
GT001 Gout 63 0.073
218
ART140 Arteries, Anomalies of 53 0.073
219
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 59 0.073
220
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.073
221
P SLP006 Sleep Apnea 69 0.073
222
P LKM002 Leukemia 66 0.073
223
P INT068 Intestinal Disease 52 0.073
224
c LKM061 Leukemia, Acute Myeloid 83 0.073
225
P RTN016 Retinal Degeneration 53 0.073
226
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.073
227
HMP009 Haemophilus Influenzae 42 0.073
228
SFT003 Soft Tissue Sarcoma 56 0.073
229
STR067 Stroke, Ischemic 80 0.073
230
HRN029 Hearing Loss, Noise-Induced 37 0.073
231
P BLD134 Bladder Cancer 78 0.072
232
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.072
233
ERY051 Erythroleukemia, Familial 56 0.072
234
PNG002 Pain Agnosia 51 0.072
235
BRN028 Brain Cancer 73 0.071
236
DGN001 Degenerative Disc Disease 48 0.071
237
P OST002 Osteoporosis 73 0.071
238
MST005 Mastitis 53 0.071
239
STM007 Stomatitis 49 0.071
240
URT049 Urate Oxidase, Pseudogene 25 0.070
241
P NSP012 Nasopharyngeal Carcinoma 67 0.070
242
PLG002 Plague 57 0.070
243
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.070
244
HPT004 Hepatic Coma 43 0.069
245
ENT011 Enterocolitis 50 0.069
246
EYD002 Eye Disease 58 0.068
247
GLC003 Glucose Intolerance 54 0.068
248
ANX010 Anxiety 72 0.068
249
GST045 Gastroenteritis 59 0.068
250
KRT019 Keratitis, Hereditary 67 0.068
251
P HML002 Hemolytic Anemia 62 0.068
252
P RTN018 Retinal Disease 52 0.068
253
THY029 Thyroid Carcinoma 59 0.068
254
AVN001 Avian Influenza 56 0.068
255
HVY002 Heavy Metal Poisoning 22 0.068
256
LPD008 Lipid Metabolism Disorder 62 0.067
257
P PSR002 Psoriasis 62 0.067
258
PST011 Pustulosis of Palm and Sole 52 0.067
259
DPR016 Depression 63 0.067
260
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.067
261
SYN036 Syncope 45 0.067
262
P GST053 Gastric Cancer 83 0.066
263
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.066
264
GTR002 Goiter 52 0.066
265
ALL014 Allergic Encephalomyelitis 39 0.066
266
c GLL024 Gallbladder Disease 1 52 0.066
267
LWC001 Low Compliance Bladder 42 0.066
268
c ACT075 Acute Myocardial Infarction 56 0.066
269
c ACT134 Acute Liver Failure 51 0.066
270
INS024 Insulin-Like Growth Factor I 79 0.066
271
HPT019 Hepatic Encephalopathy 60 0.066
272
RTR008 Root Resorption 45 0.066
273
c PRD040 Periodontitis, Chronic 54 0.066
274
KRT009 Keratosis 53 0.065
275
P LYM118 Lymphoma 68 0.065
276
STN013 Stenotrophomonas Maltophilia Infection 25 0.065
277
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.065
278
P ESP024 Esophagitis 62 0.065
279
PLM033 Pulmonary Embolism 59 0.065
280
PLM001 Pulmonary Tuberculosis 70 0.064
281
ATX019 Ataxia with Vitamin E Deficiency 48 0.064
282
SCR011 Scrapie 38 0.064
283
PHN003 Phenylketonuria 75 0.064
284
MSC157 Muscular Dystrophy, Duchenne Type 71 0.064
285
P PRP029 Porphyria 62 0.064
286
P TRN020 Turner Syndrome 65 0.063
287
DYS073 Dysphagia 50 0.063
288
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.063
289
CLN015 Colon Adenocarcinoma 63 0.063
290
P CND004 Candidiasis 57 0.063
291
P ART021 Arteriosclerosis 54 0.063
292
P ECL001 Eclampsia 51 0.063
293
URT010 Ureteral Obstruction 46 0.062
294
HLC007 Helicobacter Pylori Infection 59 0.062
295
RTN003 Retinal Ischemia 50 0.062
296
c PCH010 Pachyonychia Congenita 3 43 0.062
297
c MNN043 Meningioma, Familial 74 0.062
298
MNN042 Meningioma, Radiation-Induced 62 0.062
299
SPN021 Spinal Meningioma 47 0.062
300
SCR001 Secretory Meningioma 37 0.062
301
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.062
302
CHR066 Chronic Fatigue Syndrome 61 0.062
303
P RTN008 Retinitis Pigmentosa 77 0.062
304
INS001 Insulinoma 60 0.062
305
STT001 Status Epilepticus 59 0.062
306
HYP060 Hyperinsulinism 54 0.062
307
OBS532 Obsolete: Ehlers-Danlos Syndrome, Fibronectinemic Type 15 0.062
308
SVR004 Severe Combined Immunodeficiency 73 0.061
309
RCK004 Rickets 69 0.061
310
PNC129 Pancreatic Adenocarcinoma 67 0.061
311
DBT010 Diabetic Neuropathy 55 0.061
312
P MTH007 Methemoglobinemia 46 0.061
313
MNT002 Mental Depression 57 0.061
314
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.061
315
VSC002 Vascular Dementia 57 0.060
316
PRP027 Peripheral Vascular Disease 71 0.060
317
P LKM062 Leukemia, Acute Lymphoblastic 68 0.060
318
ORL011 Oral Cancer 60 0.060
319
PRP080 Peripheral Artery Disease 53 0.060
320
OLV004 Oliver-Mcfarlane Syndrome 37 0.060
321
ADN018 Adenoma 58 0.060
322
P ALP008 Alopecia 56 0.060
323
P ART023 Arthropathy 62 0.060
324
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.060
325
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.060
326
BNG077 Benign Idiopathic Neonatal Seizures 26 0.059
327
P END044 Endometriosis 62 0.059
328
RTN023 Retinitis 46 0.059
329
PTT037 Pituitary Tumors 44 0.059
330
NRR001 Neuroretinitis 43 0.059
331
P MJR001 Major Depressive Disorder 68 0.059
332
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.058
333
LSH001 Leishmaniasis 63 0.058
334
P BNG032 Benign Mesothelioma 45 0.058
335
P KLZ004 Kala-Azar 1 41 0.058
336
P VSC011 Vasculitis 62 0.057
337
CHL123 Chlamydia 59 0.057
338
HYP025 Hyperphosphatemia 47 0.057
339
DMP001 Dumping Syndrome 44 0.057
340
P UVT001 Uveitis 57 0.057
341
CRD137 Cardiogenic Shock 48 0.057
342
P GLM040 Glioma Susceptibility 1 81 0.057
343
SCH014 Schistosomiasis 56 0.057
344
PPL022 Papilloma 54 0.057
345
KRT006 Keratoconjunctivitis 53 0.057
346
THY030 Thyroid Gland Disease 51 0.057
347
SQM002 Squamous Cell Papilloma 42 0.057
348
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.057
349
CRH001 Crohn's Disease 74 0.056
350
CRT072 Creutzfeldt-Jakob Disease 69 0.056
351
ANG054 Angina Pectoris 66 0.056
352
NRF026 Neurofibromatosis, Type Iv, of Riccardi 63 0.056
353
P SCK005 Sickle Cell Disease 50 0.056
354
ADL002 Adult Syndrome 69 0.056
355
HNS001 Hansen's Disease 34 0.056
356
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.056
357
THR024 Thrombosis 56 0.056
358
BCT004 Bacteriuria 48 0.056
359
RRS014 Rare Surgical Neurologic Disease 32 0.056
360
HYP014 Hyperuricemia 51 0.055
361
P TMP001 Temporal Lobe Epilepsy 50 0.055
362
PRR019 Perioral Myoclonia with Absences 28 0.055
363
P MLT020 Multiple Sclerosis 72 0.055
364
P OVR042 Ovarian Cancer 89 0.055
365
P ART022 Arthritis 70 0.055
366
OST017 Osteomyelitis 64 0.055
367
P PLY019 Polyneuropathy 56 0.055
368
MYL069 Myeloma, Multiple 85 0.054
369
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.054
370
GST092 Gastroesophageal Reflux 65 0.054
371
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.054
372
P ATS364 Autism 65 0.054
373
SPP010 Suppressor of Tumorigenicity 3 51 0.054
374
ORL015 Oral Squamous Cell Carcinoma 43 0.054
375
P DST107 Distal Renal Tubular Acidosis 41 0.054
376
P BRS044 Breast Adenocarcinoma 59 0.053
377
CRB090 Cerebral Hypoxia 43 0.053
378
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.053
379
P PNM007 Pneumonia 68 0.053
380
MYC005 Myocardial Stunning 46 0.053
381
CRT015 Carotid Artery Occlusion 44 0.053
382
CHL065 Cholangiocarcinoma 67 0.053
383
P BRN022 Bronchiectasis 59 0.053
384
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.053
385
INT079 Intrahepatic Cholangiocarcinoma 50 0.053
386
PLM031 Poliomyelitis 57 0.051
387
c RTN047 Retinitis Pigmentosa 18 44 0.051
388
P RHB003 Rhabdomyosarcoma 62 0.051
389
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.051
390
ACQ007 Acquired Immunodeficiency Syndrome 60 0.051
391
ALL006 Allergic Asthma 56 0.051
392
NPH003 Nephrocalcinosis 51 0.051
393
P RNV001 Renovascular Hypertension 49 0.051
394
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.051
395
P RHM011 Rheumatoid Arthritis 80 0.050
396
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.050
397
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.050
398
INT066 Interstitial Lung Disease 59 0.050
399
P INT070 Intestinal Obstruction 58 0.050
400
P HDC001 Headache 57 0.050
401
MTH009 Mouth Disease 56 0.050
402
WST005 West Nile Virus 55 0.050
403
RTN020 Retinal Vascular Disease 48 0.050
404
PRM329 Premature Aging 39 0.050
405
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.050
406
P SLM003 Salmonellosis 54 0.050
407
NRT004 Neuritis 53 0.050
408
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.050
409
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.050
410
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.050
411
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.050
412
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.050
413
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.050
414
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.050
415
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.050
416
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.050
417
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.050
418
LYM133 Lymphoma, Hodgkin, Classic 69 0.050
419
P THY023 Thymoma 65 0.050
420
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.050
421
c THY107 Thymoma, Familial 54 0.050
422
CLR109 Colorectal Adenocarcinoma 50 0.050
423
CHL004 Cholelithiasis 49 0.050
424
c HNT011 Huntington Disease-Like 3 38 0.050
425
CHR178 Chromosomal Triplication 35 0.049
426
LTH043 Lithium Transport 18 0.049
427
P MYL006 Myeloid Leukemia 60 0.048
428
PRS047 Prostatitis 56 0.048
429
P AVS003 Avascular Necrosis 42 0.048
430
OST151 Osteoporosis and Oculocutaneous Hypopigmentation Syndrome 23 0.048
431
c SYS001 Systemic Lupus Erythematosus 86 0.048
432
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.048
433
TRN015 Transient Cerebral Ischemia 62 0.048
434
P LPS004 Lupus Erythematosus 61 0.048
435
P CRD246 Cardiovascular System Disease 56 0.048
436
CHR100 Chronic Ulcer of Skin 53 0.048
437
P THY032 Thyroiditis 53 0.048
438
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.047
439
SCK003 Sickle Cell Anemia 72 0.047
440
P HYP061 Hypertrophic Cardiomyopathy 66 0.047
441
P DNG005 Dengue Virus 57 0.047
442
DMY004 Demyelinating Disease 52 0.047
443
DYS015 Dysentery 50 0.047
444
P FML011 Familial Adenomatous Polyposis 72 0.046
445
P DMN002 Dementia 67 0.046
446
CHG001 Chagas Disease 66 0.046
447
P MNC007 Monocytic Leukemia 54 0.046
448
OCL006 Ocular Hypertension 53 0.046
449
P SHR001 Short Bowel Syndrome 52 0.046
450
P CNJ013 Conjunctivitis 65 0.046
451
LNG031 Lung Benign Neoplasm 50 0.046
452
PRC003 Proctitis 47 0.046
453
ACT003 Acute Kidney Tubular Necrosis 45 0.046
454
c LKM071 Leukemia, Chronic Lymphocytic 79 0.045
455
END057 Endometrial Cancer 74 0.045
456
EWN003 Ewing Sarcoma 68 0.045
457
P MNN013 Meningitis 65 0.045
458
P NPH012 Nephrotic Syndrome 63 0.045
459
P MVM001 Movement Disease 61 0.045
460
ANR040 Aneurysm 58 0.045
461
P HMC002 Homocystinuria 54 0.045
462
P MSC003 Muscular Atrophy 52 0.045
463
P MYT002 Myotonic Dystrophy 49 0.045
464
P RRT020 Rare Tumor 41 0.045
465
ENM002 Enamel Erosion 27 0.045
466
IRN001 Iron Deficiency Anemia 58 0.045
467
MCP006 Mucoepidermoid Carcinoma 50 0.045
468
P INT143 Interstitial Cystitis 61 0.045
469
PRS045 Prostatic Hypertrophy 52 0.045
470
HRT011 Heart Septal Defect 50 0.045
471
NTR046 Neutrophil Migration 50 0.045
472
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.045
473
49X006 49, Xxxxy Syndrome 41 0.045
474
BLN006 Blind Loop Syndrome 37 0.045
475
P NRV007 Nervous System Disease 66 0.042
476
MSC007 Muscle Hypertrophy 63 0.042
477
URN010 Urinary Tract Obstruction 57 0.042
478
P GRV001 Graves' Disease 55 0.042
479
P OBS001 Obstructive Jaundice 48 0.042
480
SPL018 Splenomegaly 48 0.042
481
CHR074 Choriocarcinoma 46 0.042
482
c ATS307 Autosomal Recessive Cerebellar Ataxia 41 0.042
483
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 20 0.042
484
ACR006 Aceruloplasminemia 73 0.042
485
P SRC025 Sarcoidosis 1 70 0.042
486
P DYS154 Dystonia 65 0.042
487
P NTR004 Neutropenia 63 0.042
488
P ENC004 Encephalitis 61 0.042
489
P SLV026 Salivary Gland Carcinoma 60 0.042
490
P BNC003 Bone Cancer 57 0.042
491
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.042
492
GSG001 Gas Gangrene 50 0.042
493
CND006 Candida Glabrata 32 0.042
494
DDN004 Duodenogastric Reflux 32 0.042
495
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.042
496
ACR007 Acromegaly 71 0.042
497
P HYD006 Hydrocephalus 65 0.042
498
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 65 0.042
499
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.042
500
BRR014 Barrett Esophagus 64 0.042
501
NRM005 Neuromuscular Disease 63 0.042
502
P FRD001 Friedreich Ataxia 63 0.042
503
RTN017 Retinal Detachment 60 0.042
504
P SLP005 Sleep Disorder 59 0.042
505
BLR008 Bilirubin Metabolic Disorder 57 0.042
506
P EXN002 Exanthem 57 0.042
507
P MYP006 Myopia 55 0.042
508
CRV040 Cervix Carcinoma 50 0.042
509
PLC008 Placenta Disease 49 0.042
510
c HNT004 Huntington Disease-Like 2 49 0.042
511
EPT021 Epithelial Recurrent Erosion Dystrophy 37 0.042
512
c NRF024 Neurofibromatosis, Type I 71 0.041
513
NRF007 Neurofibroma 64 0.041
514
ACT119 Acute Promyelocytic Leukemia 63 0.041
515
NTR005 Nutritional Deficiency Disease 61 0.041
516
GLL018 Gallbladder Cancer 56 0.041
517
HPT022 Hepatoblastoma 56 0.041
518
c OPT053 Optic Atrophy 1 54 0.041
519
ACH005 Achalasia 50 0.041
520
P TCL004 T-Cell Leukemia 47 0.041
521
MXD026 Mixed Glioma 45 0.041
522
PCD001 Pica Disease 37 0.041
523
VLK001 Volkmann Contracture 32 0.041
524
CRN311 Coronary Ostial Stenosis or Atresia 20 0.041
525
IMM167 Immune Deficiency Disease 78 0.039
526
c PNS012 Paine Syndrome 61 0.039
527
P KDN017 Kidney Cancer 61 0.039
528
SPP011 Suppression of Tumorigenicity 12 59 0.039
529
c PRM005 Primary Hyperparathyroidism 58 0.039
530
PRP030 Purpura 55 0.039
531
HRT012 Heart Valve Disease 53 0.039
532
CHR073 Choreatic Disease 52 0.039
533
P HMP007 Hemophilia 51 0.039
534
P CHL066 Cholangitis 50 0.039
535
c BCT013 Bacterial Pneumonia 47 0.039
536
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 46 0.039
537
HDN002 Head Injury 45 0.039
538
KLD004 Keloid Disorder 40 0.039
539
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.039
540
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.039
541
P SCH015 Schizophrenia 75 0.038
542
P RTN024 Retinoblastoma 72 0.038
543
P CNR004 Cone-Rod Dystrophy 2 71 0.038
544
EMB004 Embryonal Carcinoma 57 0.038
545
c MST023 Mesothelioma, Malignant 57 0.038
546
RHM027 Rheumatic Disease 56 0.038
547
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.038
548
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.038
549
P DBT005 Diabetes Insipidus 55 0.038
550
CRY003 Cryptosporidiosis 54 0.038
551
CHK001 Chikungunya 53 0.038
552
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 53 0.038
553
c FML008 Familial Retinoblastoma 53 0.038
554
THY124 Thyroid Gland Papillary Carcinoma 52 0.038
555
VLV047 Volvulus of Midgut 50 0.038
556
P OPN001 Open-Angle Glaucoma 49 0.038
557
HMG002 Hemoglobinuria 49 0.038
558
P RNL015 Renal Hypertension 48 0.038
559
AST006 Astigmatism 47 0.038
560
ATN005 Autonomic Dysfunction 47 0.038
561
KWS001 Kwashiorkor 45 0.038
562
NWC001 Newcastle Disease 44 0.038
563
c RNL046 Renal Tubular Acidosis, Distal, Autosomal Dominant 34 0.038
564
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.038
565
P RNL115 Renal Tubular Acidosis, Proximal 31 0.038
566
WRN001 Werner Syndrome 69 0.037
567
ART016 Aortic Aneurysm 68 0.037
568
P MYC084 Mycobacterium Tuberculosis 1 68 0.037
569
SKN019 Skin Melanoma 67 0.037
570
c MCR129 Microvascular Complications of Diabetes 1 66 0.037
571
P HYP098 Hypereosinophilic Syndrome 66 0.037
572
c RHB024 Rhabdomyosarcoma 2 65 0.037
573
P MTR014 Motor Neuron Disease 64 0.037
574
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.037
575
HSH003 Hashimoto Thyroiditis 62 0.037
576
BRC012 Brucellosis 61 0.037
577
P VNT002 Ventricular Septal Defect 60 0.037
578
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.037
579
c MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.037
580
ILS001 Ileus 51 0.037
581
P ATR005 Atrophic Gastritis 50 0.037
582
PLR007 Pleural Empyema 49 0.037
583
c MCR112 Microvascular Complications of Diabetes 2 41 0.037
584
CNT057 Central Centrifugal Cicatricial Alopecia 36 0.037
585
PYR009 Pyridoxine Deficiency Anemia 34 0.037
586
RRD056 Rare Disease in Surgical Orthopedic 28 0.037
587
P FML340 Familial Episodic Pain Syndrome 27 0.037
588
c RNG015 Ring Chromosome 2 26 0.037
589
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.037
590
c RNG019 Ring Chromosome 3 21 0.037
591
P SYS005 Systemic Scleroderma 70 0.036
592
P FRG001 Fragile X Syndrome 68 0.036
593
c ATS007 Autism Spectrum Disorder 67 0.036
594
P PRP003 Porphyria Cutanea Tarda 67 0.036
595
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.036
596
c HMP029 Hemophilia a 65 0.036
597
ANR007 Anorexia Nervosa 63 0.036
598
P HYP750 Hypertriglyceridemia, Familial 61 0.036
599
RHM001 Rheumatic Fever 61 0.036
600
TRG002 Trigeminal Neuralgia 60 0.036
601
P HRD011 Hereditary Spherocytosis 60 0.036
602
CRV038 Cervical Squamous Cell Carcinoma 58 0.036
603
RBS001 Rabies 58 0.036
604
TRN018 Transitional Cell Carcinoma 56 0.036
605
FCT001 Factor Viii Deficiency 55 0.036
606
OCL022 Ocular Melanoma 53 0.036
607
PLS007 Plasmodium Falciparum Malaria 52 0.036
608
P CHN059 Chondrocalcinosis 51 0.036
609
c SVR005 Severe Pre-Eclampsia 49 0.036
610
P NGH001 Night Blindness 47 0.036
611
THY128 Thyroid Tumor 47 0.036
612
HST009 Histiocytoma 46 0.036
613
P HMR005 Hemorrhoid 46 0.036
614
MLG065 Malignant Fibroxanthoma 44 0.036
615
VGN019 Vaginal Discharge 44 0.036
616
c PRM038 Primary Agammaglobulinemia 43 0.036
617
PRS063 Paresthesia 43 0.036
618
P HYP265 Hypotonia 42 0.036
619
FBR003 Fibrous Histiocytoma 41 0.036
620
GLM044 Glomerular Disease 39 0.036
621
HYP001 Hypochromic Microcytic Anemia 38 0.036
622
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.036
623
MST020 Mast Cell Activation Syndrome 27 0.036
624
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.033
625
c EXD008 Exudative Vitreoretinopathy 1 69 0.033
626
BRK010 Burkitt Lymphoma 67 0.033
627
CLR108 Colorectal Adenoma 64 0.033
628
P GCH001 Gaucher's Disease 64 0.033
629
ART002 Arts Syndrome 63 0.033
630
IGR001 Ige Responsiveness, Atopic 59 0.033
631
P ALC033 Alcohol Use Disorder 58 0.033
632
THY122 Thyroid Gland Cancer 58 0.033
633
P OPT006 Optic Nerve Disease 57 0.033
634
DSS009 Disseminated Intravascular Coagulation 57 0.033
635
P OPT009 Optic Neuritis 56 0.033
636
ORL005 Oral Candidiasis 56 0.033
637
SLC006 Silicosis 56 0.033
638
INT007 Intermediate Coronary Syndrome 55 0.033
639
HMP005 Hemiplegia 54 0.033
640
PRC002 Paracoccidioidomycosis 53 0.033
641
P KRT007 Keratoconus 49 0.033
642
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 49 0.033
643
SXL003 Sexual Disorder 48 0.033
644
PPL002 Papillary Carcinoma 47 0.033
645
P CRC039 Coarctation of Aorta 47 0.033
646
LYM009 Lymphocytic Choriomeningitis 46 0.033
647
CYS019 Cystathioninuria 45 0.033
648
c MLG074 Malignant Mesenchymoma 39 0.033
649
MYC014 Mycobacterium Chelonae 32 0.033
650
THY006 Thymus Lymphoma 26 0.033
651
PRQ002 Paraquat Poisoning 25 0.033
652
c INH025 Inherited Prion Disease 18 0.033
653
c TBR025 Tuberous Sclerosis 1 76 0.032
654
P TBR001 Tuberous Sclerosis 70 0.032
655
LNG039 Lung Squamous Cell Carcinoma 65 0.032
656
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.032
657
c WLM018 Wilms Tumor 5 62 0.032
658
CHL068 Cholestasis 60 0.032
659
P BNG030 Benign Ependymoma 60 0.032
660
MCR013 Microphthalmia 60 0.032
661
CHL067 Cholecystitis 58 0.032
662
c DWL002 Dowling-Degos Disease 1 58 0.032
663
P SJG008 Sjogren Syndrome 56 0.032
664
VSC003 Visceral Leishmaniasis 55 0.032
665
P VNS003 Venous Insufficiency 55 0.032
666
AMN003 Amnestic Disorder 54 0.032
667
P LRY044 Larynx Cancer 54 0.032
668
CLR030 Clear Cell Renal Cell Carcinoma 53 0.032
669
MMM001 Mammary Paget's Disease 53 0.032
670
CLL010 Cellular Ependymoma 53 0.032
671
P RTN022 Retinal Vein Occlusion 52 0.032
672
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.032
673
BRN014 Bronchopneumonia 50 0.032
674
P OTS001 Otosclerosis 50 0.032
675
ENT004 Enthesopathy 48 0.032
676
P CLR019 Color Blindness 48 0.032
677
ART004 Aortic Atherosclerosis 48 0.032
678
CRN027 Corneal Neovascularization 47 0.032
679
CLS016 Clostridium Difficile Colitis 46 0.032
680
P VTR007 Vitreoretinopathy 46 0.032
681
SBC016 Subacute Delirium 44 0.032
682
c ATM099 Autoimmune Uveitis 44 0.032
683
P SPR086 Spermatogenic Failure 3 44 0.032
684
HYP457 Hypertrophic Scars 43 0.032
685
BNS007 Bone Sarcoma 42 0.032
686
STL007 Steel Syndrome 42 0.032
687
MNN028 Mononeuropathy of the Median Nerve, Mild 42 0.032
688
CLR033 Color Vision Deficiency 41 0.032
689
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.032
690
KLB003 Klebsiella Pneumonia 39 0.032
691
LCH001 Leech Infestation 36 0.032
692
c EPS028 Episodic Pain Syndrome, Familial, 3 27 0.032
693
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 27 0.032
694
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 19 0.032
695
c LKM063 Leukemia, Chronic Myeloid 71 0.027
696
MLT157 Multiple System Atrophy 1 70 0.027
697
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.027
698
c PRM196 Premature Ovarian Failure 1 68 0.027
699
c JVN010 Juvenile Rheumatoid Arthritis 67 0.027
700
P ASP006 Aspergillosis 66 0.027
701
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.027
702
CHY002 Chylomicron Retention Disease 64 0.027
703
CRB011 Cerebrotendinous Xanthomatosis 63 0.027
704
LYM017 Lyme Disease 63 0.027
705
c HPT003 Hepatitis a 63 0.027
706
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.027
707
BLL006 Bullous Pemphigoid 62 0.027
708
ALC006 Alcoholic Hepatitis 61 0.027
709
c ANM038 Anemia, Autoimmune Hemolytic 61 0.027
710
c HYP731 Hyperaldosteronism, Familial, Type I 60 0.027
711
APP008 Appendicitis 60 0.027
712
ETN001 Eating Disorder 59 0.027
713
P GLL022 Guillain-Barre Syndrome 59 0.027
714
PRT058 Pure Autonomic Failure 59 0.027
715
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.027
716
P URT039 Urticaria 58 0.027
717
P PLY041 Polymyositis 57 0.027
718
APH001 Aphthous Stomatitis 57 0.027
719
PHR003 Pharyngitis 56 0.027
720
ANS011 Anus Cancer 56 0.027
721
PNM008 Pneumothorax 56 0.027
722
P MTC069 Mitochondrial Disorders 56 0.027
723
P PLM034 Pulmonary Emphysema 56 0.027
724
c BCT007 Bacterial Meningitis 55 0.027
725
AND020 Androgen Insensitivity, Partial 55 0.027
726
P FTL001 Fetal Alcohol Syndrome 55 0.027
727
PRT038 Protein-Energy Malnutrition 54 0.027
728
P TCD001 Tic Disorder 54 0.027
729
P CYS039 Cystic Kidney Disease 54 0.027
730
P LNG035 Lung Large Cell Carcinoma 54 0.027
731
c CNT035 Central Nervous System Disease 54 0.027
732
P STS003 Sitosterolemia 53 0.027
733
P EPS030 Episodic Kinesigenic Dyskinesia 1 53 0.027
734
c HRM017 Hermansky-Pudlak Syndrome 2 53 0.027
735
c ATM024 Autoimmune Pancreatitis 53 0.027
736
TND005 Tendinitis 52 0.027
737
AZS001 Azoospermia 50 0.027
738
HYP081 Hypolipoproteinemia 50 0.027
739
HPT014 Hepatorenal Syndrome 50 0.027
740
IRD001 Iridocyclitis 50 0.027
741
HYP781 Hypoascorbemia 50 0.027
742
OPT003 Opiate Dependence 50 0.027
743
c VRL005 Viral Pneumonia 49 0.027
744
c CNT016 Central Retinal Vein Occlusion 49 0.027
745
XNT003 Xanthomatosis 49 0.027
746
BLD044 Bladder Disease 48 0.027
747
WTH001 Withdrawal Disorder 48 0.027
748
MTC005 Mitochondrial Metabolism Disease 48 0.027
749
VTM002 Vitamin B12 Deficiency 48 0.027
750
LSS003 Lassa Fever 48 0.027
751
SCH038 Schopf-Schulz-Passarge Syndrome 47 0.027
752
CRN017 Coronary Thrombosis 47 0.027
753
RYN005 Raynaud Phenomenon 46 0.027
754
KRT008 Keratopathy 46 0.027
755
EBL001 Ebola Hemorrhagic Fever 46 0.027
756
P CRV039 Cervicitis 45 0.027
757
URN003 Urinary Schistosomiasis 44 0.027
758
P BRB001 Beriberi 44 0.027
759
LRY022 Laryngoonychocutaneous Syndrome 44 0.027
760
TND004 Tendinopathy 44 0.027
761
DWR001 Dwarfism 44 0.027
762
P MYG005 Myoglobinuria 43 0.027
763
MND023 Mend Syndrome 43 0.027
764
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.027
765
P ECT005 Ectropion 41 0.027
766
SPS057 Spasticity 41 0.027
767
TNP004 Tn Polyagglutination Syndrome 40 0.027
770
CNT060 Central Serous Chorioretinopathy 38 0.027
771
SYS071 Systemic Autoimmune Disease 37 0.027
772
DNT008 Denture Stomatitis 35 0.027
773
PST010 Pasteurellosis 33 0.027
774
P VSC018 Visceral Steatosis 33 0.027
775
c HYP600 Hyperaldosteronism, Familial, Type Ii 32 0.027
776
NRD001 Neurodermatitis 32 0.027
777
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.027
778
EPL050 Epilepsy, Partial, with Pericentral Spikes 25 0.027
779
DRM046 Dermal Ridges-off-the-End 25 0.027
780
MCR330 Microphthalmia, Isolated, with Cataract 1 19 0.027
781
OBN001 Ouabain Resistance 18 0.027
782
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 17 0.027
Content
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