Search results for Chloride ion

989 hits were found for Chloride ion

# Family MCID Name MIFTS Score
1
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.851
2
CYS001 Cystic Fibrosis 81 0.437
3
HRW001 Hair Whorl 36 0.390
4
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.321
5
HLX001 Helix Syndrome 47 0.292
6
P DRR001 Diarrhea 55 0.279
7
P KDN018 Kidney Disease 72 0.253
8
MTB004 Metabolic Acidosis 50 0.249
9
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.224
10
48X005 48,xyyy 39 0.223
11
P ANP001 Anaplastic Large Cell Lymphoma 58 0.220
12
c HYP595 Hypertension, Essential 84 0.216
13
P NRB001 Neuroblastoma 72 0.213
14
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.209
15
HYP005 Hypokalemia 55 0.209
16
MYT011 Myotonia 34 0.201
17
ALL026 Allergic Hypersensitivity Disease 62 0.199
18
PRT037 Pertussis 65 0.185
19
P GLM045 Glioma 63 0.184
20
GLL048 Glial Tumor 45 0.183
21
c ACT071 Acute Kidney Failure 60 0.183
22
HYP266 Hypoxia 57 0.179
23
ANG020 Angiosarcoma 64 0.179
24
CHL014 Cholera 59 0.177
25
ANX004 Anoxia 40 0.173
26
CNG034 Congestive Heart Failure 69 0.170
27
P HPT023 Hepatocellular Carcinoma 100 0.166
28
DRM006 Dermatitis 61 0.164
29
P LNG028 Long Qt Syndrome 66 0.163
30
ISC004 Ischemia 58 0.162
31
LNG099 Lung Disease 60 0.161
32
GLB015 Glioblastoma Multiforme 75 0.160
33
P HRT032 Heart Disease 75 0.154
34
CNG064 Congenital Chloride Diarrhea 32 0.154
35
CNT047 Contact Dermatitis 58 0.153
36
LWC001 Low Compliance Bladder 43 0.149
37
ATM095 Autoimmune Disease 62 0.148
38
P ALZ034 Alzheimer Disease 88 0.147
39
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.147
40
PPL052 Papillomatosis, Confluent and Reticulated 33 0.146
41
47X002 47,xyy 49 0.144
42
NPH009 Nephrolithiasis 55 0.143
43
P CHR345 Chronic Pain 44 0.142
44
P MYT023 Myotonia Congenita 56 0.140
45
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.139
46
BNR002 Bone Resorption Disease 48 0.139
47
P CRD119 Cardiac Arrest 67 0.137
48
P PNC035 Pancreatic Cancer 84 0.136
49
P ADN016 Adenocarcinoma 64 0.136
50
P LNG032 Lung Cancer 98 0.135
51
PNG002 Pain Agnosia 51 0.133
52
P SZR006 Seizure Disorder 56 0.133
53
VSL002 Visual Epilepsy 59 0.130
54
OST159 Osteogenic Sarcoma 66 0.129
55
CYT002 Cytokine Deficiency 42 0.129
56
c CHR684 Chronic Kidney Disease 70 0.128
57
P LVR013 Liver Disease 68 0.127
58
DNT012 Dental Caries 53 0.127
59
LVR012 Liver Cirrhosis 62 0.126
60
CRD132 Cardiac Conduction Defect 58 0.125
61
P PHC003 Pheochromocytoma 71 0.125
62
ADR040 Adrenal Gland Pheochromocytoma 46 0.125
63
P PRS040 Prostate Cancer 97 0.124
64
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.124
65
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.124
66
P BPL003 Bipolar Disorder 56 0.124
67
c MGR028 Migraine with or Without Aura 1 67 0.123
68
CRD223 Cardiac Arrhythmia 60 0.122
69
c BRN108 Branchiootic Syndrome 1 62 0.122
70
c MJR024 Major Affective Disorder 9 41 0.120
71
c MJR022 Major Affective Disorder 8 38 0.120
72
ALL010 Allergic Contact Dermatitis 56 0.119
73
SCR003 Secretory Diarrhea 37 0.119
74
SPN186 Spinal Cord Injury 60 0.118
75
P PLY014 Polycystic Kidney Disease 62 0.118
76
URL001 Urolithiasis 45 0.117
77
CNS004 Constipation 58 0.116
78
PLM010 Pulmonary Edema 54 0.116
79
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.116
80
P CTR002 Cataract 60 0.116
81
BRN071 Brain Injury 49 0.115
82
P ENC018 Encephalopathy 61 0.115
83
P EPL164 Epilepsy 71 0.115
84
GNG013 Gingivitis 59 0.115
85
P CLR023 Colorectal Cancer 99 0.114
86
P LTR001 Lateral Sclerosis 54 0.114
87
ATS010 Autosomal Recessive Disease 48 0.114
88
BRN004 Brain Edema 56 0.113
89
P VSC007 Vascular Disease 63 0.113
90
P HYP069 Hyperparathyroidism 63 0.113
91
OST012 Osteoarthritis 78 0.113
92
TTN003 Tetanus 65 0.113
93
P PRD021 Periodic Paralysis 45 0.111
94
IRN002 Iron Metabolism Disease 57 0.111
95
P MYC007 Myocardial Infarction 70 0.111
96
P MRC003 Mercury Poisoning 48 0.110
97
OCL069 Ocular Motor Apraxia 51 0.110
98
P HRP006 Herpes Simplex 65 0.109
99
DFC004 Deficiency Anemia 70 0.108
100
P MSC005 Muscular Dystrophy 66 0.108
101
TRM010 Traumatic Brain Injury 51 0.107
102
BRN024 Bronchitis 68 0.107
103
P NSP012 Nasopharyngeal Carcinoma 66 0.107
104
TXC005 Toxic Shock Syndrome 62 0.106
105
PST092 Posttransplant Acute Limbic Encephalitis 29 0.106
106
HYP056 Hypoglycemia 66 0.105
107
AST005 Asthma 76 0.105
108
P PLM037 Pulmonary Hypertension 67 0.105
109
P BRT004 Bartter Disease 52 0.104
110
P MLN008 Melanoma 69 0.104
111
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.104
112
HYP066 Hyperglycemia 61 0.103
113
ADN018 Adenoma 59 0.103
114
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.103
115
P ATR011 Atrial Fibrillation 66 0.101
116
DPH001 Diphtheria 60 0.101
117
NPH003 Nephrocalcinosis 51 0.100
118
P TRN020 Turner Syndrome 67 0.099
119
P INF037 Inflammatory Bowel Disease 54 0.099
120
END086 End Stage Renal Disease 51 0.099
121
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.098
122
P GST044 Gastritis 56 0.098
123
P BND020 Bone Disease 59 0.098
124
P NRP001 Neuropathy 56 0.098
125
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.098
126
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.097
127
P GLM007 Glomerulonephritis 57 0.097
128
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.096
129
CLT003 Colitis 62 0.096
130
CRV035 Cervical Cancer 76 0.096
131
CRB004 Cerebral Artery Occlusion 45 0.096
132
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.096
133
P MYS003 Myasthenia Gravis 68 0.096
134
P RNL007 Renal Tubular Acidosis 51 0.095
135
c PNS012 Paine Syndrome 61 0.094
136
DWN001 Down Syndrome 70 0.093
137
PPT005 Peptic Ulcer Disease 59 0.093
138
c SVR001 Severe Acute Respiratory Syndrome 62 0.093
139
P PRD008 Periodontitis 64 0.092
140
RCK004 Rickets 68 0.092
141
MCS002 Mucositis 56 0.092
142
P HYP086 Hypothyroidism 69 0.092
143
BRN028 Brain Cancer 74 0.091
144
P RHN004 Rhinitis 57 0.091
145
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.091
146
P RSP003 Respiratory Failure 74 0.090
147
P DRM053 Dermatitis, Atopic 66 0.090
148
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.090
149
P LNG064 Lung Cancer Susceptibility 3 78 0.089
150
P GST053 Gastric Cancer 83 0.089
151
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.089
152
c SML038 Small Cell Cancer of the Lung 65 0.089
153
P CHN012 Chondrosarcoma 56 0.089
154
ATH013 Atherosclerosis Susceptibility 65 0.088
155
VCC001 Vaccinia 49 0.088
156
BCT022 Bacterial Infectious Disease 56 0.088
157
P INF038 Influenza 68 0.088
158
c PRC016 Pre-Eclampsia 63 0.088
159
c ACT068 Acute Cystitis 63 0.088
160
P HNT016 Huntington Disease 72 0.088
161
DPR016 Depression 63 0.088
162
P OVR042 Ovarian Cancer 88 0.088
163
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.088
164
c ACT075 Acute Myocardial Infarction 57 0.088
165
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.087
166
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.087
167
PLG002 Plague 63 0.086
168
P BRS047 Breast Cancer 97 0.086
169
PLY150 Polykaryocytosis Inducer 31 0.086
170
GTL001 Gitelman Syndrome 65 0.085
171
P AST007 Astrocytoma 51 0.085
172
SKN016 Skin Disease 63 0.085
173
STR067 Stroke, Ischemic 81 0.084
174
c HPT073 Hepatitis C Virus 72 0.084
175
MDD018 Middle East Respiratory Syndrome 43 0.084
176
SQM006 Squamous Cell Carcinoma 60 0.084
177
ARG004 Argyria 27 0.084
178
c HYP836 Hypercholesterolemia, Familial, 1 73 0.083
179
MDD011 Mood Disorder 62 0.083
180
HMS001 Hemosiderosis 54 0.083
181
ALC007 Alcohol Dependence 66 0.083
182
LSH001 Leishmaniasis 63 0.082
183
P PSD003 Pseudohypoaldosteronism 44 0.082
184
P KLZ004 Kala-Azar 1 41 0.082
185
P MNN013 Meningitis 66 0.082
186
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.082
187
P INF032 Infertility 57 0.082
188
ALL003 Allergic Rhinitis 67 0.081
189
SRC014 Sarcoma 65 0.081
190
THR024 Thrombosis 57 0.080
192
SVR004 Severe Combined Immunodeficiency 73 0.080
193
ANT024 Anthrax Disease 58 0.080
194
P TRM003 Tremor 54 0.080
195
LPP008 Lipoprotein Quantitative Trait Locus 62 0.080
196
P VSC011 Vasculitis 62 0.080
197
P FBR017 Fibrosarcoma 56 0.079
198
SPN035 Spindle Cell Sarcoma 53 0.079
199
P OST001 Osteopetrosis 70 0.079
200
HPT004 Hepatic Coma 45 0.079
201
P MYP004 Myopathy 70 0.079
202
P INT070 Intestinal Obstruction 58 0.079
203
GST045 Gastroenteritis 59 0.079
204
P EPS003 Episodic Ataxia 59 0.078
205
PHN003 Phenylketonuria 75 0.078
206
GTR002 Goiter 53 0.078
207
ALL014 Allergic Encephalomyelitis 38 0.078
208
P MLN007 Male Infertility 55 0.078
209
P PRK057 Parkinson Disease, Late-Onset 78 0.078
210
P DBT009 Diabetes Mellitus 64 0.078
211
c ACT027 Acute Pancreatitis 60 0.078
212
P DNT020 Dent Disease 1 62 0.077
213
c ATR087 Atrial Standstill 1 75 0.077
214
SYN036 Syncope 45 0.077
215
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.077
216
IRR002 Irritable Bowel Syndrome 65 0.077
217
P DBT005 Diabetes Insipidus 55 0.077
218
P CRN300 Coronary Heart Disease 1 63 0.077
219
OCL006 Ocular Hypertension 53 0.076
220
P RTN016 Retinal Degeneration 53 0.076
221
c LKM061 Leukemia, Acute Myeloid 84 0.076
222
AGN016 Aging 56 0.076
223
P OST002 Osteoporosis 74 0.076
224
P MYT002 Myotonic Dystrophy 49 0.076
225
FTT001 Fatty Liver Disease 61 0.076
226
KRT019 Keratitis, Hereditary 65 0.076
227
P PLM036 Pulmonary Fibrosis 65 0.075
228
P BRN022 Bronchiectasis 59 0.074
229
P OVR082 Overgrowth Syndrome 50 0.074
230
P THL005 Thalassemia 60 0.074
231
THY029 Thyroid Carcinoma 59 0.074
232
P DDN001 Duodenal Ulcer 52 0.074
233
LYS002 Lysosomal Storage Disease 52 0.074
234
P SYS005 Systemic Scleroderma 68 0.074
235
P BCL017 B-Cell Lymphoma 58 0.074
236
P RCT021 Rectum Cancer 52 0.074
237
P OPN001 Open-Angle Glaucoma 49 0.074
238
P HYP076 Hyperthyroidism 55 0.073
239
P ECL001 Eclampsia 50 0.073
240
EYD002 Eye Disease 58 0.073
241
MSC157 Muscular Dystrophy, Duchenne Type 72 0.073
242
c MCR120 Microvascular Complications of Diabetes 7 47 0.072
243
MNT002 Mental Depression 58 0.072
244
P BRS044 Breast Adenocarcinoma 59 0.072
245
HYP014 Hyperuricemia 52 0.072
246
P TMP001 Temporal Lobe Epilepsy 50 0.072
247
URM002 Uremia 49 0.072
248
PLM001 Pulmonary Tuberculosis 69 0.072
249
ATX019 Ataxia with Vitamin E Deficiency 42 0.072
250
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.072
251
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.072
252
c HPT001 Hepatitis C 62 0.071
253
ESP021 Esophageal Cancer 90 0.071
254
ADL002 Adult Syndrome 70 0.071
255
c MCR113 Microvascular Complications of Diabetes 3 52 0.071
256
c MCR130 Microvascular Complications of Diabetes 6 41 0.071
257
c MCR133 Microvascular Complications of Diabetes 4 41 0.071
258
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.071
259
HVY002 Heavy Metal Poisoning 22 0.071
260
P RRH023 Rare Hereditary Hemochromatosis 41 0.071
261
ALL006 Allergic Asthma 56 0.070
262
P PRP019 Peripheral Nervous System Disease 58 0.070
263
GST050 Gastrointestinal System Disease 56 0.070
264
P PRP029 Porphyria 62 0.070
265
HMN044 Human Immunodeficiency Virus Type 1 71 0.070
266
P MLG056 Malignant Hyperthermia 67 0.070
267
ANX010 Anxiety 73 0.069
268
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.069
269
HPT019 Hepatic Encephalopathy 60 0.069
270
ERY051 Erythroleukemia, Familial 56 0.069
271
DYS073 Dysphagia 50 0.069
272
PRT036 Peritonitis 64 0.068
273
c SHR030 Short Qt Syndrome 46 0.068
274
c MNN043 Meningioma, Familial 74 0.068
275
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.068
276
MNN042 Meningioma, Radiation-Induced 62 0.068
277
SPN021 Spinal Meningioma 50 0.068
278
SCR001 Secretory Meningioma 41 0.068
279
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.068
280
CTN007 Cutaneous Leishmaniasis 62 0.068
281
P MYC008 Myocarditis 59 0.068
282
P INT068 Intestinal Disease 53 0.068
283
TRY001 Trypanosomiasis 50 0.068
284
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.068
285
PLM031 Poliomyelitis 64 0.068
286
c HPT016 Hepatitis B 59 0.068
287
P PNC044 Pancreatitis 61 0.068
288
STM007 Stomatitis 50 0.068
289
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.068
290
GST023 Gastric Ulcer 53 0.068
291
TLN003 Telangiectasis 52 0.068
292
P AMY004 Amyloidosis 70 0.068
293
SFT003 Soft Tissue Sarcoma 56 0.068
294
P PLY019 Polyneuropathy 56 0.067
295
IMP005 Impotence 52 0.067
296
RYN005 Raynaud Phenomenon 47 0.067
297
CRB039 Cerebrovascular Disease 67 0.067
298
P HDC001 Headache 57 0.067
299
c PRM038 Primary Agammaglobulinemia 44 0.067
300
P SKN015 Skin Carcinoma 66 0.066
301
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.066
302
c MLG068 Malignant Glioma 46 0.066
303
ATR057 Atrioventricular Block 55 0.066
304
c SCN007 Secondary Hyperparathyroidism 51 0.066
305
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.066
306
ILS001 Ileus 51 0.066
307
ULC004 Ulcerative Colitis 73 0.066
308
P MYL006 Myeloid Leukemia 60 0.066
309
ART140 Arteries, Anomalies of 52 0.066
310
P MLT020 Multiple Sclerosis 72 0.066
311
BCT004 Bacteriuria 49 0.066
312
c PRM005 Primary Hyperparathyroidism 58 0.065
313
BCT002 Bacterial Vaginosis 53 0.065
314
P CYS018 Cystitis 59 0.065
315
PNC129 Pancreatic Adenocarcinoma 68 0.064
316
DBT010 Diabetic Neuropathy 54 0.064
317
STT001 Status Epilepticus 60 0.064
318
P MCR115 Microvascular Complications of Diabetes 5 66 0.064
319
P HML002 Hemolytic Anemia 63 0.064
320
P ALP008 Alopecia 54 0.064
321
P DST107 Distal Renal Tubular Acidosis 42 0.064
322
c NRF023 Neurofibromatosis, Type Ii 80 0.063
323
P SNS001 Sensorineural Hearing Loss 60 0.063
324
P LCT001 Lactic Acidosis 51 0.063
325
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.063
326
P PNM007 Pneumonia 68 0.062
327
c PRS136 Prostate Cancer, Hereditary, 6 33 0.062
328
c PRS130 Prostate Cancer, Hereditary, 8 32 0.062
329
P NPH012 Nephrotic Syndrome 60 0.062
330
SCK003 Sickle Cell Anemia 74 0.061
331
P RHB003 Rhabdomyosarcoma 63 0.061
332
P EPL140 Epilepsy, Idiopathic Generalized 62 0.061
333
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 56 0.061
334
P CNR004 Cone-Rod Dystrophy 2 73 0.061
335
P NTR004 Neutropenia 63 0.061
336
P CRD246 Cardiovascular System Disease 57 0.061
337
HYP025 Hyperphosphatemia 48 0.061
338
c RHB024 Rhabdomyosarcoma 2 67 0.060
339
P THR014 Thrombocytopenia 67 0.060
340
NWC001 Newcastle Disease 45 0.060
341
SBC016 Subacute Delirium 44 0.060
342
c DLT002 Dilated Cardiomyopathy 79 0.059
343
P ATX030 Ataxia-Telangiectasia 82 0.059
344
NTR005 Nutritional Deficiency Disease 62 0.059
345
INS024 Insulin-Like Growth Factor I 79 0.059
346
P ART022 Arthritis 69 0.059
347
PTT037 Pituitary Tumors 44 0.059
348
c MCL013 Mucolipidosis Iv 66 0.059
349
GT001 Gout 64 0.059
350
HYP060 Hyperinsulinism 54 0.059
351
DYS015 Dysentery 52 0.059
352
PTH003 Pathologic Nystagmus 52 0.059
353
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.059
354
P BNG032 Benign Mesothelioma 46 0.059
355
MTH071 Methane Production 26 0.059
356
P LKM002 Leukemia 68 0.059
357
ANG054 Angina Pectoris 66 0.059
358
GLC003 Glucose Intolerance 54 0.059
359
P SCK005 Sickle Cell Disease 50 0.059
360
CVD001 Covid-19 44 0.059
361
P RRT020 Rare Tumor 41 0.059
362
MYL069 Myeloma, Multiple 85 0.058
363
P PSR002 Psoriasis 62 0.058
364
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.058
365
PST011 Pustulosis of Palm and Sole 52 0.058
366
P BLD134 Bladder Cancer 79 0.058
367
P RTN018 Retinal Disease 53 0.058
368
CHD004 Chudley-Mccullough Syndrome 46 0.058
369
HND015 Hand Skill, Relative 33 0.058
370
P CNJ013 Conjunctivitis 65 0.058
371
SPL018 Splenomegaly 48 0.058
372
ACT003 Acute Kidney Tubular Necrosis 45 0.058
373
P SCH015 Schizophrenia 74 0.058
374
ORL011 Oral Cancer 60 0.058
375
SPS057 Spasticity 45 0.058
376
MLR004 Malaria 81 0.058
377
CHR066 Chronic Fatigue Syndrome 61 0.057
378
CHL123 Chlamydia 59 0.057
379
DMY004 Demyelinating Disease 52 0.057
380
DMP001 Dumping Syndrome 44 0.057
381
PPL022 Papilloma 54 0.057
382
ENT011 Enterocolitis 51 0.057
383
SQM002 Squamous Cell Papilloma 46 0.057
384
P ENC004 Encephalitis 61 0.056
385
P FBR031 Febrile Seizures 53 0.056
386
CHL065 Cholangiocarcinoma 68 0.056
387
MST005 Mastitis 53 0.056
388
INT079 Intrahepatic Cholangiocarcinoma 51 0.056
389
TBR011 Tuberculous Meningitis 48 0.056
390
IRN001 Iron Deficiency Anemia 59 0.056
391
INT066 Interstitial Lung Disease 60 0.056
392
P CND004 Candidiasis 58 0.056
393
P PYL005 Pyelonephritis 56 0.056
394
ORL015 Oral Squamous Cell Carcinoma 43 0.056
395
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.056
396
END040 Endogenous Depression 55 0.055
397
OST011 Osteomalacia 52 0.055
398
P FML187 Familial Hypertension 37 0.055
399
CHR178 Chromosomal Triplication 35 0.055
400
P DMN002 Dementia 66 0.055
401
P HYP750 Hypertriglyceridemia, Familial 62 0.055
402
P LKD001 Leukodystrophy 59 0.055
403
KRT006 Keratoconjunctivitis 53 0.055
404
c SPN225 Spondyloarthropathy 1 73 0.054
405
VGN023 Vaginitis 54 0.054
406
KRT001 Keratoconjunctivitis Sicca 49 0.054
407
P ART023 Arthropathy 62 0.054
408
CLN015 Colon Adenocarcinoma 65 0.054
409
YLL002 Yellow Fever 61 0.054
410
MNK001 Menkes Disease 64 0.054
411
c RTN047 Retinitis Pigmentosa 18 42 0.054
412
P KDN017 Kidney Cancer 60 0.053
413
ANR040 Aneurysm 59 0.053
414
P EXN002 Exanthem 57 0.053
415
MTH009 Mouth Disease 56 0.053
416
P ART021 Arteriosclerosis 54 0.053
417
HDN002 Head Injury 46 0.053
418
AMN006 Aminoaciduria 38 0.053
419
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.053
420
OST017 Osteomyelitis 64 0.053
421
PRM057 Paramyotonia Congenita of Von Eulenburg 58 0.053
422
P PRD017 Periodic Paralyses 25 0.053
423
OTT002 Otitis Media 72 0.053
424
c LNG047 Long Qt Syndrome 2 58 0.053
425
c BRT024 Bartter Syndrome Type 4 20 0.053
426
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.052
427
GST092 Gastroesophageal Reflux 67 0.052
428
ANR007 Anorexia Nervosa 63 0.052
429
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.052
430
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.052
431
c PCH010 Pachyonychia Congenita 3 44 0.052
432
ADG002 Audiogenic Seizures 25 0.052
433
INS001 Insulinoma 60 0.052
434
HMP009 Haemophilus Influenzae 43 0.052
435
P SLP006 Sleep Apnea 69 0.051
436
P DYS154 Dystonia 65 0.051
437
PRS047 Prostatitis 56 0.051
438
CHR073 Choreatic Disease 52 0.051
439
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.051
440
P HYD006 Hydrocephalus 66 0.051
441
HYP017 Hypophosphatemia 50 0.051
442
CRD137 Cardiogenic Shock 47 0.051
443
OST003 Osteonecrosis 61 0.051
444
AVN001 Avian Influenza 59 0.051
445
DGN001 Degenerative Disc Disease 48 0.051
446
MSL001 Measles 62 0.051
447
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.051
448
CLF027 Cleft Palate, Isolated 64 0.051
449
MSC007 Muscle Hypertrophy 64 0.051
450
CHL068 Cholestasis 61 0.051
451
VRC005 Varicose Veins 60 0.051
452
c FML001 Familial Atrial Fibrillation 65 0.050
453
P URT039 Urticaria 58 0.049
454
P BRT053 Bartter Syndrome, Type 4a, Neonatal, with Sensorineural Deafness 46 0.049
455
CHL079 Children's Interstitial Lung Disease 26 0.049
456
P LYM118 Lymphoma 68 0.049
457
P END044 Endometriosis 63 0.049
458
HYP052 Hyperkalemic Periodic Paralysis 61 0.049
459
MNR012 Meniere Disease 57 0.049
460
HMG005 Hemoglobinopathy 56 0.049
461
c GLL024 Gallbladder Disease 1 53 0.049
462
P HYP097 Hyperekplexia 61 0.048
463
P SJG008 Sjogren Syndrome 61 0.048
464
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.048
465
LST001 Listeriosis 56 0.048
466
SNS003 Sensory Peripheral Neuropathy 54 0.048
467
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.048
468
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.048
469
SPN051 Spondylitis 51 0.048
470
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.048
471
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.048
472
P RNL015 Renal Hypertension 47 0.048
473
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.048
474
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.048
475
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.048
476
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.048
477
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.048
478
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.048
479
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.048
480
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.048
481
INF009 Inflammatory Spondylopathy 31 0.048
482
IMM167 Immune Deficiency Disease 78 0.048
483
END057 Endometrial Cancer 74 0.048
484
PRP027 Peripheral Vascular Disease 71 0.048
485
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.048
486
GLM044 Glomerular Disease 37 0.048
487
P SRC025 Sarcoidosis 1 70 0.048
488
ERL001 Early Myoclonic Encephalopathy 62 0.048
489
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.048
490
c ACT134 Acute Liver Failure 56 0.048
491
c PRD040 Periodontitis, Chronic 53 0.048
492
NRT001 Neurotic Disorder 53 0.048
493
P SPP010 Suppressor of Tumorigenicity 3 51 0.048
494
CND006 Candida Glabrata 32 0.048
495
NRL016 Neural Tube Defects 82 0.048
496
CRH001 Crohn's Disease 74 0.048
497
c DBT099 Diabetes Mellitus, Type I 65 0.048
498
P EPL198 Epilepsy, Myoclonic Juvenile 62 0.048
499
PLM033 Pulmonary Embolism 59 0.048
500
c GRV008 Graves Disease 1 56 0.048
501
P INS002 in Situ Carcinoma 53 0.048
502
BLL006 Bullous Pemphigoid 62 0.047
503
c MYT029 Myotonia Congenita, Autosomal Recessive 41 0.047
504
c MYT027 Myotonia Congenita, Autosomal Dominant 34 0.047
505
P ART005 Arteriovenous Malformation 65 0.047
506
P SCL018 Scoliosis 60 0.047
507
RTR008 Root Resorption 45 0.047
508
P MJR007 Major Affective Disorder 1 43 0.047
509
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.047
510
SCR011 Scrapie 39 0.047
511
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.046
512
AMN003 Amnestic Disorder 54 0.046
513
VLV047 Volvulus of Midgut 49 0.046
514
P INT143 Interstitial Cystitis 61 0.045
515
NRT004 Neuritis 52 0.045
516
AZS001 Azoospermia 50 0.045
517
CLC006 Calcinosis 48 0.045
518
ANR004 Anuria 46 0.045
519
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.045
520
49X006 49, Xxxxy Syndrome 41 0.045
521
P ATS364 Autism 70 0.045
522
LYM133 Lymphoma, Hodgkin, Classic 69 0.045
523
P LKM062 Leukemia, Acute Lymphoblastic 69 0.045
524
P LPS002 Liposarcoma 65 0.045
525
P MVM001 Movement Disease 63 0.045
526
FBR047 Fibromyalgia 58 0.045
527
P UVT001 Uveitis 57 0.045
528
P MYP006 Myopia 55 0.045
529
PRP030 Purpura 54 0.045
530
P PNC025 Panic Disorder 53 0.045
531
P MSC003 Muscular Atrophy 52 0.045
532
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.045
533
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.045
534
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.045
535
c MLG084 Malignant Fibrous Histiocytoma 63 0.045
536
P ESP024 Esophagitis 62 0.045
537
P SLP005 Sleep Disorder 59 0.045
538
GRD007 Grade Iii Astrocytoma 59 0.045
539
SCH014 Schistosomiasis 57 0.045
540
P HYP024 Hypoparathyroidism 56 0.045
541
P HMR005 Hemorrhoid 46 0.045
542
VGN019 Vaginal Discharge 46 0.045
543
P HYP265 Hypotonia 43 0.045
544
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.045
545
P RTN008 Retinitis Pigmentosa 79 0.044
546
MST021 Meester-Loeys Syndrome 35 0.044
547
STN013 Stenotrophomonas Maltophilia Infection 25 0.044
548
c INH020 Inherited Metabolic Disorder 47 0.044
549
c MJR003 Major Affective Disorder 6 33 0.044
550
c MJR006 Major Affective Disorder 5 33 0.044
551
c BTT014 Beta-Thalassemia 74 0.044
552
LPD008 Lipid Metabolism Disorder 62 0.044
553
CHL067 Cholecystitis 57 0.044
554
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.044
555
URN010 Urinary Tract Obstruction 55 0.044
556
ATN005 Autonomic Dysfunction 46 0.044
557
CRN019 Coronary Artery Vasospasm 46 0.044
558
CRT015 Carotid Artery Occlusion 45 0.044
559
c PSD092 Pseudohypoaldosteronism, Type Iie 39 0.044
560
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.044
561
ART016 Aortic Aneurysm 69 0.043
562
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.043
563
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.043
564
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.043
565
GLS018 Glass Syndrome 57 0.043
566
KRT008 Keratopathy 47 0.043
567
P HYP733 Hypercalciuria, Absorptive, 2 45 0.043
568
SYS071 Systemic Autoimmune Disease 37 0.043
569
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.043
570
P CNG001 Congenital Myasthenic Syndrome 66 0.042
571
ACQ007 Acquired Immunodeficiency Syndrome 60 0.042
572
HMC014 Homocysteinemia 53 0.042
573
P MCL001 Mucolipidosis 48 0.042
574
RTN023 Retinitis 46 0.042
575
NRR001 Neuroretinitis 42 0.042
576
P RHM011 Rheumatoid Arthritis 80 0.042
577
ACR007 Acromegaly 71 0.042
578
P CLC063 Celiac Disease 1 66 0.042
579
CHG001 Chagas Disease 66 0.042
580
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.042
581
RTN017 Retinal Detachment 61 0.042
582
BLR008 Bilirubin Metabolic Disorder 57 0.042
583
c HNT004 Huntington Disease-Like 2 50 0.042
584
RTN003 Retinal Ischemia 50 0.042
585
THY128 Thyroid Tumor 47 0.042
586
P FBR003 Fibrous Histiocytoma 44 0.042
587
GST040 Gastric Adenocarcinoma 70 0.041
588
P RBL001 Rubella 59 0.041
589
P CHL066 Cholangitis 51 0.041
590
c HNT011 Huntington Disease-Like 3 38 0.041
591
URT049 Urate Oxidase, Pseudogene 25 0.041
592
PHR003 Pharyngitis 57 0.041
593
PRS045 Prostatic Hypertrophy 53 0.041
594
PRP016 Paraplegia 52 0.041
595
c VRL010 Viral Hepatitis 52 0.041
596
VGN020 Vaginal Disease 49 0.041
597
P MYG005 Myoglobinuria 44 0.041
598
P VTL001 Vitelliform Macular Dystrophy 42 0.041
599
BST007 Best Vitelliform Macular Dystrophy 34 0.041
601
VRL011 Viral Infectious Disease 61 0.041
602
HMR039 Hemorrhage, Intracerebral 57 0.041
603
ONC002 Onchocerciasis 52 0.041
604
KRT009 Keratosis 51 0.041
605
SCT005 Scott Syndrome 49 0.041
606
LCH001 Leech Infestation 35 0.041
607
CNT105 Central Core Disease of Muscle 60 0.039
608
SPP011 Suppression of Tumorigenicity 12 59 0.039
609
P BNC003 Bone Cancer 58 0.039
610
P SLV026 Salivary Gland Carcinoma 57 0.039
611
SLP001 Sleeping Sickness 54 0.039
612
CLR109 Colorectal Adenocarcinoma 51 0.039
613
P MTH008 Methylmalonic Acidemia 50 0.039
614
DDN004 Duodenogastric Reflux 33 0.039
615
c HPT003 Hepatitis a 62 0.039
616
P LPS004 Lupus Erythematosus 61 0.039
617
PRT058 Pure Autonomic Failure 59 0.039
618
P SYP003 Syphilis 58 0.039
619
HYP781 Hypoascorbemia 51 0.039
620
HYP081 Hypolipoproteinemia 51 0.039
621
BLD044 Bladder Disease 48 0.039
622
PCD001 Pica Disease 41 0.039
623
EXN003 Exencephaly 31 0.039
624
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.039
625
c PNC108 Pancreatitis, Hereditary 70 0.038
626
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.038
627
c ATS007 Autism Spectrum Disorder 67 0.038
628
BRR014 Barrett Esophagus 65 0.038
629
NRM005 Neuromuscular Disease 64 0.038
630
P PRM002 Primary Hyperoxaluria 62 0.038
631
RHM001 Rheumatic Fever 60 0.038
632
P HRD011 Hereditary Spherocytosis 60 0.038
633
RBS001 Rabies 58 0.038
634
FDB001 Foodborne Botulism 55 0.038
635
HRY003 Hairy Cell Leukemia 55 0.038
636
P MNC007 Monocytic Leukemia 53 0.038
637
P SML001 Small Cell Carcinoma 52 0.038
638
c SVR005 Severe Pre-Eclampsia 50 0.038
639
P OBS001 Obstructive Jaundice 50 0.038
640
P NGH001 Night Blindness 48 0.038
641
IDP073 Idiopathic Hypercalciuria 43 0.038
642
MTL005 Metal Allergy 41 0.038
643
PRS063 Paresthesia 41 0.038
644
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.038
645
c MJR008 Major Affective Disorder 2 35 0.038
646
c MJR023 Major Affective Disorder 7 33 0.038
647
HRD218 Hereditary Stomatocytosis 32 0.038
648
c PSD093 Pseudohypoaldosteronism, Type Iid 31 0.038
649
c MJR004 Major Affective Disorder 4 28 0.038
650
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 26 0.038
651
P ANG001 Angelman Syndrome 69 0.038
652
P NRV007 Nervous System Disease 66 0.038
653
P CHR071 Charcot-Marie-Tooth Disease 65 0.038
654
P SBS003 Substance Abuse 55 0.038
655
P SLM003 Salmonellosis 55 0.038
656
NNL006 Non-Alcoholic Steatohepatitis 54 0.038
657
P LCH002 Lichen Planus 53 0.038
658
P LMB006 Limb-Girdle Muscular Dystrophy 53 0.038
659
LNG031 Lung Benign Neoplasm 51 0.038
660
CHR074 Choriocarcinoma 47 0.038
661
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.038
662
HMN016 Hemangioendothelioma 34 0.038
663
P FRG001 Fragile X Syndrome 70 0.036
664
EWN003 Ewing Sarcoma 69 0.036
665
P THY023 Thymoma 65 0.036
666
HRT012 Heart Valve Disease 53 0.036
667
c HPT007 Hepatitis E 53 0.036
668
PRP080 Peripheral Artery Disease 53 0.036
669
STT041 Stuttering 52 0.036
670
THY030 Thyroid Gland Disease 52 0.036
671
c THY107 Thymoma, Familial 52 0.036
672
P ACT105 Acute Mountain Sickness 52 0.036
673
P HMP007 Hemophilia 51 0.036
674
CHL004 Cholelithiasis 49 0.036
675
c BCT013 Bacterial Pneumonia 48 0.036
676
c FML036 Familial Periodic Paralysis 44 0.036
677
KLD004 Keloid Disorder 40 0.036
678
HRN029 Hearing Loss, Noise-Induced 37 0.036
679
ENM002 Enamel Erosion 26 0.036
680
c SYS001 Systemic Lupus Erythematosus 86 0.036
681
CNN003 Conn's Syndrome 79 0.036
682
c EXD008 Exudative Vitreoretinopathy 1 71 0.036
683
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.036
684
P OPT006 Optic Nerve Disease 60 0.036
685
IGR001 Ige Responsiveness, Atopic 59 0.036
686
DSS009 Disseminated Intravascular Coagulation 57 0.036
687
c FML035 Familial Hyperlipidemia 55 0.036
688
P PLM034 Pulmonary Emphysema 55 0.036
689
PLS009 Plasma Cell Neoplasm 51 0.036
690
ALB002 Albinism 46 0.036
691
URT010 Ureteral Obstruction 45 0.036
692
CHP002 Chops Syndrome 44 0.036
693
P RTN024 Retinoblastoma 73 0.034
694
c BSL007 Basal Cell Carcinoma 68 0.034
695
P PRM006 Primary Biliary Cirrhosis 62 0.034
696
DRR016 Diarrhea 2, with Microvillus Atrophy 60 0.034
697
c DWL002 Dowling-Degos Disease 1 58 0.034
698
c MST023 Mesothelioma, Malignant 57 0.034
699
P FCL005 Focal Segmental Glomerulosclerosis 57 0.034
700
MCL006 Macular Retinal Edema 55 0.034
701
P GRV001 Graves' Disease 55 0.034
702
CHR100 Chronic Ulcer of Skin 55 0.034
703
FLR002 Filariasis 55 0.034
704
P LRY044 Larynx Cancer 55 0.034
705
CLR030 Clear Cell Renal Cell Carcinoma 53 0.034
706
FRZ001 Frozen Shoulder 53 0.034
707
c FML008 Familial Retinoblastoma 53 0.034
708
ESP023 Esophageal Disease 52 0.034
709
P CRN025 Corneal Dystrophy 49 0.034
710
ENT004 Enthesopathy 49 0.034
711
P VTR007 Vitreoretinopathy 46 0.034
712
P MTH007 Methemoglobinemia 46 0.034
713
VSD002 Vas Deferens, Congenital Bilateral Aplasia of 45 0.034
714
P SDR002 Siderosis 44 0.034
715
KLB003 Klebsiella Pneumonia 41 0.034
716
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.034
717
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.034
718
FNG016 Fungal Keratitis 40 0.034
719
PRM020 Premenstrual Tension 40 0.034
720
BLR004 Biliary Dyskinesia 38 0.034
721
ANP008 Anaplastic Oligoastrocytoma 30 0.034
722
P GLM040 Glioma Susceptibility 1 81 0.033
723
P FML011 Familial Adenomatous Polyposis 72 0.033
724
P MPL001 Maple Syrup Urine Disease 69 0.033
725
P PRP003 Porphyria Cutanea Tarda 67 0.033
726
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 65 0.033
727
HLC007 Helicobacter Pylori Infection 59 0.033
728
CRV038 Cervical Squamous Cell Carcinoma 58 0.033
729
WST005 West Nile Virus 54 0.033
730
P SHR001 Short Bowel Syndrome 53 0.033
731
c ACT078 Acute Porphyria 51 0.033
732
P JVN007 Juvenile Absence Epilepsy 47 0.033
733
MYT030 Myotonia, Potassium-Aggravated 45 0.033
734
STL007 Steel Syndrome 43 0.033
735
DSS010 Dissociative Disorder 39 0.033
736
ISL099 Isolated Methylmalonic Acidemia 29 0.033
737
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.033
738
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.033
739
SKN019 Skin Melanoma 68 0.033
740
P HYP098 Hypereosinophilic Syndrome 67 0.033
741
c MCR129 Microvascular Complications of Diabetes 1 66 0.033
742
BRC012 Brucellosis 64 0.033
743
FCS002 Fucosidosis 61 0.033
744
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.033
745
c BNG091 Benign Chronic Pemphigus 58 0.033
746
P ALC033 Alcohol Use Disorder 58 0.033
747
P GLL018 Gallbladder Cancer 57 0.033
748
PNM008 Pneumothorax 56 0.033
749
P CYS039 Cystic Kidney Disease 54 0.033
750
CRH005 Crohn's Colitis 53 0.033
751
P RNL017 Renal Oncocytoma 53 0.033
752
P THY032 Thyroiditis 52 0.033
753
CCC002 Coccidiosis 51 0.033
754
c INF145 Infantile Liver Failure Syndrome 1 50 0.033
755
c MGL009 Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 50 0.033
756
WTH001 Withdrawal Disorder 48 0.033
757
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.033
758
P BRB001 Beriberi 46 0.033
759
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.033
760
HYP264 Hypertonia 38 0.033
761
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.033
762
DNT008 Denture Stomatitis 35 0.033
763
c LKM005 Leukemia, T-Cell, Chronic 34 0.033
764
JMP002 Jumping Frenchmen of Maine 22 0.033
765
NND001 Nondystrophic Myotonia 20 0.033
766
P RTT002 Rett Syndrome 80 0.029
767
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.029
768
P CHR012 Chronic Granulomatous Disease 67 0.029
769
PSY004 Psychotic Disorder 67 0.029
770
P FRD001 Friedreich Ataxia 64 0.029
771
P PTT014 Pitt-Hopkins Syndrome 63 0.029
772
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.029
773
LSC001 Lesch-Nyhan Syndrome 62 0.029
774
DCT002 Ductal Carcinoma in Situ 59 0.029
775
MCR013 Microphthalmia 57 0.029
776
CHK001 Chikungunya 57 0.029
777
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.029
778
SBC001 Subacute Sclerosing Panencephalitis 56 0.029
779
EMB004 Embryonal Carcinoma 56 0.029
780
FLR001 Filarial Elephantiasis 55 0.029
781
c PRG126 Progressive Familial Heart Block 55 0.029
782
VSC003 Visceral Leishmaniasis 55 0.029
783
P VNS003 Venous Insufficiency 55 0.029
784
GLS001 Gliosarcoma 54 0.029
785
CRY003 Cryptosporidiosis 54 0.029
786
BRN014 Bronchopneumonia 54 0.029
787
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.029
788
NPH018 Nephrogenic Systemic Fibrosis 50 0.029
789
HMG002 Hemoglobinuria 50 0.029
790
c CHR431 Chronic Venous Insufficiency 49 0.029
791
CCN002 Cocaine Abuse 49 0.029
792
LRN003 Learning Disability 49 0.029
793
VTM033 Vitamin K Deficiency Bleeding 48 0.029
794
CLS016 Clostridium Difficile Colitis 48 0.029
795
CRN027 Corneal Neovascularization 47 0.029
796
AST006 Astigmatism 47 0.029
797
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.029
798
P THY054 Thyrotoxic Periodic Paralysis 46 0.029
799
MYC005 Myocardial Stunning 46 0.029
800
TNG009 Tongue Squamous Cell Carcinoma 44 0.029
801
c SPR086 Spermatogenic Failure 3 44 0.029
802
FBR054 Fibroma 44 0.029
803
c EPL133 Epilepsy, Juvenile Absence 1 43 0.029
804
OVR093 Overhydrated Hereditary Stomatocytosis 43 0.029
805
c SRC023 Sarcoidosis 2 43 0.029
806
IDP070 Idiopathic Scoliosis 42 0.029
807
c FML294 Familial Short Qt Syndrome 41 0.029
808
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.029
809
PLR006 Pleural Cancer 38 0.029
810
PRX097 Paroxysmal Dystonia 32 0.029
811
c THY083 Thyrotoxic Periodic Paralysis 2 31 0.029
812
c PRG019 Paragangliomas 2 31 0.029
813
c FML159 Familial Periodic Paralyses 16 0.029
814
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.029
815
MYL009 Myelodysplastic Syndrome 70 0.029
816
P MYC084 Mycobacterium Tuberculosis 1 68 0.029
817
ACT119 Acute Promyelocytic Leukemia 63 0.029
818
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.029
819
P MCH002 Machado-Joseph Disease 62 0.029
820
P LDD007 Liddle Syndrome 1 59 0.029
821
c ACT073 Acute Leukemia 58 0.029
822
FML063 Familial Glucocorticoid Deficiency 58 0.029
823
VSC002 Vascular Dementia 57 0.029
824
HPT046 Hepatic Veno-Occlusive Disease 56 0.029
825
ORL005 Oral Candidiasis 56 0.029
826
c BCT007 Bacterial Meningitis 55 0.029
827
P PTT006 Pituitary Adenoma 55 0.029
828
CRC006 Carcinoid Syndrome 55 0.029
829
P ALP106 Alport Syndrome 1, X-Linked 55 0.029
830
INT007 Intermediate Coronary Syndrome 55 0.029
831
TND005 Tendinitis 54 0.029
832
ANL018 Analbuminemia 54 0.029
833
MTN003 Motion Sickness 53 0.029
834
RYS001 Reye Syndrome 51 0.029
835
STR008 Strongyloidiasis 51 0.029
836
INT071 Intestinal Perforation 51 0.029
837
HPT014 Hepatorenal Syndrome 50 0.029
838
P CRV039 Cervicitis 49 0.029
839
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.029
840
BRS064 Bursitis 48 0.029
841
c VRL012 Viral Meningitis 48 0.029
842
ANH002 Anhidrosis 47 0.029
843
CRN017 Coronary Thrombosis 47 0.029
844
TTR011 Tetraploidy 47 0.029
845
P CRC039 Coarctation of Aorta 47 0.029
846
c ACT076 Acute Myocarditis 46 0.029
847
DWR001 Dwarfism 44 0.029
848
IDP033 Idiopathic Edema 44 0.029
849
CRB090 Cerebral Hypoxia 44 0.029
850
TND004 Tendinopathy 43 0.029
851
P EPT020 Epithelioid Hemangioendothelioma 43 0.029
853
c MCR112 Microvascular Complications of Diabetes 2 41 0.029
854
CRN322 Coronavirus Infectious Disease 40 0.029
855
PLY100 Polyploidy 40 0.029
856
c ACT004 Acute Diarrhea 39 0.029
857
c OVR114 Ovarian Cancer 1 38 0.029
858
c ELL005 Elliptocytosis 2 38 0.029
859
BLN006 Blind Loop Syndrome 37 0.029
860
c RNL046 Renal Tubular Acidosis, Distal, Autosomal Dominant 37 0.029
861
c ELL006 Elliptocytosis 3 36 0.029
862
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.029
863
c HYP600 Hyperaldosteronism, Familial, Type Ii 32 0.029
864
NRM009 Normokalemic Periodic Paralysis 28 0.029
865
ETH012 Ethylene Glycol Poisoning 26 0.029
866
CYN003 Cyanide Poisoning 24 0.029
867
c RRH015 Rare Hemorrhagic Disorder 23 0.029
868
OBN001 Ouabain Resistance 18 0.029
869
ADR007 Adrenoleukodystrophy 75 0.024
870
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.024
871
MLT157 Multiple System Atrophy 1 70 0.024
872
P ASP006 Aspergillosis 69 0.024
873
ACR008 Acrocallosal Syndrome 69 0.024
874
P ALP004 Alport Syndrome 68 0.024
875
MLD001 Melioidosis 68 0.024
876
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.024
877
P VNW001 Von Willebrand's Disease 65 0.024
878
P MTR014 Motor Neuron Disease 65 0.024
879
CHY002 Chylomicron Retention Disease 65 0.024
880
MRK001 Merkel Cell Carcinoma 65 0.024
881
OVR029 Ovarian Hyperstimulation Syndrome 64 0.024
882
CLR108 Colorectal Adenoma 64 0.024
883
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.024
884
LYM017 Lyme Disease 64 0.024
885
TRN015 Transient Cerebral Ischemia 63 0.024
886
c OPT053 Optic Atrophy 1 63 0.024
887
P ECT006 Ectodermal Dysplasia 62 0.024
888
P ORT004 Orthostatic Intolerance 62 0.024
889
HSH003 Hashimoto Thyroiditis 62 0.024
890
BRS099 Breast Ductal Carcinoma 62 0.024
891
ALC006 Alcoholic Hepatitis 61 0.024
892
APP008 Appendicitis 61 0.024
893
c LPM012 Lipomatosis, Multiple 60 0.024
894
P TXP001 Toxoplasmosis 60 0.024
895
c MSC170 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2 60 0.024
896
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 60 0.024
897
c HYP731 Hyperaldosteronism, Familial, Type I 60 0.024
898
P GLY013 Glycogen Storage Disease 60 0.024
899
CRY005 Cryptococcosis 58 0.024
900
P HYP726 Hypercalcemia, Infantile, 1 58 0.024
901
P PLY041 Polymyositis 57 0.024
902
TCK001 Tick-Borne Encephalitis 56 0.024
903
VTM027 Vitamin D-Dependent Rickets, Type 2a 56 0.024
904
SLC006 Silicosis 56 0.024
905
ORL004 Oral Submucous Fibrosis 55 0.024
906
AMB001 Amebiasis 55 0.024
907
ALP077 Alpha-Methylacetoacetic Aciduria 55 0.024
908
c MYP132 Myopathy, Congenital 55 0.024
909
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 0.024
910
HMP005 Hemiplegia 55 0.024
911
FCL014 Focal Epilepsy 54 0.024
912
PRT038 Protein-Energy Malnutrition 54 0.024
913
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.024
914
P LCT002 Lactose Intolerance 53 0.024
915
P ALL008 Allergic Bronchopulmonary Aspergillosis 53 0.024
916
IRD001 Iridocyclitis 53 0.024
917
c NMN014 Niemann-Pick Disease, Type C2 51 0.024
918
ANK001 Ankylosis 51 0.024
919
CYS036 Cystinosis, Nephropathic 51 0.024
920
ACH005 Achalasia 51 0.024
921
ASP003 Aseptic Meningitis 51 0.024
922
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.024
923
PLR007 Pleural Empyema 50 0.024
924
P AGG001 Aggressive Periodontitis 50 0.024
925
P KRT007 Keratoconus 50 0.024
926
c LRG001 Large Cell Carcinoma 50 0.024
927
HRT011 Heart Septal Defect 50 0.024
928
OPT003 Opiate Dependence 50 0.024
929
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 49 0.024
930
URT001 Urethritis 49 0.024
931
BLD053 Blood Platelet Disease 49 0.024
932
MNN009 Meningoencephalitis 49 0.024
933
P RNV001 Renovascular Hypertension 48 0.024
934
P TRT019 Torticollis 48 0.024
935
VTM002 Vitamin B12 Deficiency 48 0.024
936
SXL003 Sexual Disorder 47 0.024
937
HRN026 Hernia, Hiatus 47 0.024
938
MCR018 Microcytic Anemia 47 0.024
939
CRC014 Carcinoid Tumors, Intestinal 47 0.024
940
PPL002 Papillary Carcinoma 47 0.024
941
NDL007 Nodular Goiter 47 0.024
942
KRT002 Keratomalacia 47 0.024
943
P ENC008 Encephalocele 47 0.024
944
BST008 Bestrophinopathy, Autosomal Recessive 46 0.024
945
URN003 Urinary Schistosomiasis 46 0.024
946
MXD026 Mixed Glioma 45 0.024
947
P DCR003 Dacryoadenitis 45 0.024
948
ISC015 Ischemic Colitis 44 0.024
949
MCR011 Microinvasive Gastric Cancer 43 0.024
950
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.024
951
PHY002 Physical Disorder 42 0.024
952
CRV043 Cervical Dystonia 42 0.024
953
P PRT026 Parotitis 42 0.024
954
c MLG079 Malignant Pleural Mesothelioma 42 0.024
955
LYM042 Lymphocytic Colitis 41 0.024
956
BKS003 Beukes Hip Dysplasia 41 0.024
957
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.024
958
PLM005 Pleomorphic Lipoma 40 0.024
959
SCR015 Scarlet Fever 39 0.024
961
DBT007 Diabetic Cataract 38 0.024
962
CRT055 Creatine Deficiency Syndromes 38 0.024
963
P ANT061 Antenatal Bartter Syndrome 37 0.024
964
c CHR020 Chronic Interstitial Cystitis 37 0.024
965
PLC006 Placental Choriocarcinoma 36 0.024
966
P MXL015 Maxillary Sinusitis 36 0.024
967
ACL001 Acalculous Cholecystitis 35 0.024
968
CRY019 Cryohydrocytosis 34 0.024
969
HNS001 Hansen's Disease 34 0.024
970
RTC003 Root Caries 33 0.024
971
P VSC018 Visceral Steatosis 33 0.024
972
TXC020 Toxic Oil Syndrome 33 0.024
973
HPT081 Hepatic Infarction 33 0.024
974
DNT010 Dentin Caries 32 0.024
975
MYC014 Mycobacterium Chelonae 31 0.024
976
GST007 Gastric Dilatation 31 0.024
977
ISL119 Isolated Optic Neuritis 30 0.024
978
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.024
979
c MYP127 Myopia 2, Autosomal Dominant 28 0.024
980
TBL029 Tubulin, Beta 28 0.024
981
c RNG015 Ring Chromosome 2 26 0.024
982
EPL050 Epilepsy, Partial, with Pericentral Spikes 25 0.024
983
CRC034 Carcinoma Showing Thymus-Like Differentiation 23 0.024
984
PST047 Post-Traumatic Epilepsy 22 0.024
985
FTL005 Fetal Adenoma 20 0.024
986
SPN092 Spinal Shock 19 0.024
987
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 17 0.024
988
CNN008 Cinnamon Odor, Pleasantness of 14 0.024
989
P ISL045 Isolated Focal Cortical Dysplasia Type I 11 0.024
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