Search results for Chloride ion

981 hits were found for Chloride ion

# Family MCID Name MIFTS Score
1
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.874
2
CYS001 Cystic Fibrosis 84 0.468
3
HRW001 Hair Whorl 36 0.399
4
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.320
5
HLX001 Helix Syndrome 46 0.304
6
P DRR001 Diarrhea 55 0.285
7
P KDN018 Kidney Disease 73 0.262
8
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.258
9
MTB004 Metabolic Acidosis 48 0.255
10
48X005 48,xyyy 37 0.238
11
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.228
12
c HYP595 Hypertension, Essential 87 0.224
13
P NRB010 Neuroblastoma 1 66 0.223
14
HYP005 Hypokalemia 55 0.213
15
ALL026 Allergic Hypersensitivity Disease 65 0.212
16
MYT011 Myotonia 37 0.208
17
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.197
18
P GLM045 Glioma 64 0.194
19
GLL048 Glial Tumor 48 0.194
20
PRT037 Pertussis 66 0.191
21
c ACT071 Acute Kidney Failure 60 0.190
22
HYP266 Hypoxia 58 0.188
23
CHL014 Cholera 58 0.182
24
ANG020 Angiosarcoma 59 0.180
25
ANX004 Anoxia 44 0.179
26
ISC004 Ischemia 62 0.179
27
DRM006 Dermatitis 63 0.172
28
GLB002 Glioblastoma 74 0.171
29
GLB015 Glioblastoma Multiforme 60 0.171
30
LNG099 Lung Disease 62 0.170
31
CNG034 Congestive Heart Failure 69 0.169
32
P LNG028 Long Qt Syndrome 68 0.166
33
P HPT023 Hepatocellular Carcinoma 99 0.165
34
P HRT032 Heart Disease 78 0.156
35
CNG064 Congenital Chloride Diarrhea 33 0.156
36
CNT047 Contact Dermatitis 58 0.156
37
LWC001 Low Compliance Bladder 45 0.155
38
P CHR345 Chronic Pain 52 0.152
39
ATM095 Autoimmune Disease 62 0.152
40
P ALZ034 Alzheimer Disease 90 0.150
41
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.150
42
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.150
43
PPL052 Papillomatosis, Confluent and Reticulated 34 0.149
44
47X002 47,xyy 49 0.146
45
P MYT023 Myotonia Congenita 53 0.144
46
BNR002 Bone Resorption Disease 51 0.144
47
P CRD119 Cardiac Arrest 71 0.141
48
P PNC035 Pancreatic Cancer 86 0.139
49
P SZR006 Seizure Disorder 59 0.138
50
P LNG032 Lung Cancer 99 0.137
51
P ADN016 Adenocarcinoma 65 0.137
52
PNG002 Pain Agnosia 52 0.135
53
P PRS040 Prostate Cancer 97 0.135
54
VSL002 Visual Epilepsy 58 0.135
55
CYT002 Cytokine Deficiency 46 0.131
56
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.131
57
P LVR013 Liver Disease 71 0.131
58
OST159 Osteogenic Sarcoma 67 0.131
59
P PHC003 Pheochromocytoma 71 0.131
60
ADR040 Adrenal Gland Pheochromocytoma 51 0.131
61
LVR012 Liver Cirrhosis 67 0.130
62
c MGR028 Migraine with or Without Aura 1 70 0.130
63
PLM017 Pulmonary Alveolar Microlithiasis 54 0.130
64
P CRD132 Cardiac Conduction Defect 61 0.129
65
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.129
66
c CHR684 Chronic Kidney Disease 68 0.129
67
BRN071 Brain Injury 51 0.128
68
P CTR002 Cataract 62 0.127
69
DNT012 Dental Caries 52 0.125
70
c BRN108 Branchiootic Syndrome 1 62 0.125
71
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.123
72
OST012 Osteoarthritis 80 0.122
73
P PLY014 Polycystic Kidney Disease 61 0.122
74
P ENC018 Encephalopathy 64 0.122
75
SPN186 Spinal Cord Injury 63 0.121
76
ALL010 Allergic Contact Dermatitis 56 0.121
77
CNS004 Constipation 59 0.121
78
P EPL164 Epilepsy 73 0.121
79
PLM010 Pulmonary Edema 56 0.121
80
SCR003 Secretory Diarrhea 36 0.121
81
P BPL003 Bipolar Disorder 59 0.120
82
GNG013 Gingivitis 60 0.119
83
P CLR023 Colorectal Cancer 100 0.118
84
TRM010 Traumatic Brain Injury 54 0.118
85
P VSC007 Vascular Disease 65 0.118
86
P HYP069 Hyperparathyroidism 64 0.118
87
P PRD021 Periodic Paralysis 47 0.118
88
TTN003 Tetanus 62 0.117
89
CRD223 Cardiac Arrhythmia 61 0.116
90
BRN004 Brain Edema 57 0.116
91
c MJR024 Major Affective Disorder 9 42 0.116
92
c MJR022 Major Affective Disorder 8 39 0.116
93
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.115
94
IRN002 Iron Metabolism Disease 58 0.115
95
DFC004 Deficiency Anemia 77 0.115
96
P MRC003 Mercury Poisoning 47 0.115
97
P INF037 Inflammatory Bowel Disease 57 0.115
98
MLN008 Melanoma 68 0.113
99
ATS010 Autosomal Recessive Disease 49 0.113
100
OCL069 Ocular Motor Apraxia 53 0.113
101
P LTR001 Lateral Sclerosis 56 0.113
102
P PLM037 Pulmonary Hypertension 69 0.112
103
P MSC005 Muscular Dystrophy 68 0.112
104
HYP056 Hypoglycemia 68 0.109
105
P MYC007 Myocardial Infarction 74 0.109
106
END030 End Stage Renal Failure 60 0.109
107
HYP066 Hyperglycemia 63 0.109
108
ADN018 Adenoma 60 0.108
109
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.108
110
P BRT004 Bartter Disease 56 0.108
111
P HRP006 Herpes Simplex 66 0.107
112
P INF038 Influenza 69 0.107
113
P ATR011 Atrial Fibrillation 67 0.107
114
AST005 Asthma 80 0.105
115
BRN024 Bronchitis 70 0.105
116
TXC005 Toxic Shock Syndrome 63 0.105
117
P NRP001 Neuropathy 57 0.105
118
c ACT210 Acute Respiratory Distress Syndrome 59 0.105
119
c PNS012 Paine Syndrome 61 0.104
120
NPH003 Nephrocalcinosis 52 0.103
121
DPH001 Diphtheria 61 0.102
122
P NSP012 Nasopharyngeal Carcinoma 67 0.102
123
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.102
124
DWN001 Down Syndrome 70 0.102
125
CLT003 Colitis 63 0.102
126
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.101
127
PST092 Posttransplant Acute Limbic Encephalitis 29 0.101
128
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.100
129
BND020 Bone Disease 60 0.100
130
P GST044 Gastritis 58 0.100
131
P MYS003 Myasthenia Gravis 68 0.100
132
P TRN020 Turner Syndrome 66 0.100
133
P GLM007 Glomerulonephritis 58 0.098
134
P RNL007 Renal Tubular Acidosis 49 0.097
135
PPT005 Peptic Ulcer Disease 60 0.097
136
CRV035 Cervical Cancer 77 0.097
137
CRB004 Cerebral Artery Occlusion 38 0.097
138
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.096
139
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.096
140
c SML038 Small Cell Cancer of the Lung 67 0.095
141
P RHN004 Rhinitis 59 0.095
142
P GST053 Gastric Cancer 85 0.094
143
P DRM053 Dermatitis, Atopic 68 0.094
144
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.093
145
DPR016 Depression 64 0.092
146
P INF032 Infertility 60 0.092
147
VCC001 Vaccinia 50 0.092
148
P HYP086 Hypothyroidism 70 0.092
149
BRN028 Brain Cancer 75 0.092
150
P LNG064 Lung Cancer Susceptibility 3 79 0.091
151
P PRD008 Periodontitis 66 0.091
152
P OVR042 Ovarian Cancer 89 0.091
153
P HNT016 Huntington Disease 72 0.091
154
P BRS047 Breast Cancer 99 0.090
155
RCK004 Rickets 70 0.090
156
GTL001 Gitelman Syndrome 62 0.090
157
MCS002 Mucositis 56 0.090
158
STR067 Stroke, Ischemic 82 0.089
159
c HPT073 Hepatitis C Virus 74 0.089
160
P VSC011 Vasculitis 64 0.089
161
P AST007 Astrocytoma 52 0.088
162
ATH013 Atherosclerosis Susceptibility 68 0.088
163
SKN016 Skin Disease 64 0.088
164
BCT022 Bacterial Infectious Disease 57 0.088
165
P RSP003 Respiratory Failure 75 0.088
166
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.088
167
SQM006 Squamous Cell Carcinoma 60 0.088
168
c ACT068 Acute Cystitis 63 0.088
169
PLY150 Polykaryocytosis Inducer 31 0.087
170
ARG004 Argyria 28 0.087
171
c PRC016 Pre-Eclampsia 63 0.087
172
CRB039 Cerebrovascular Disease 71 0.087
173
PLG002 Plague 54 0.087
174
c HYP836 Hypercholesterolemia, Familial, 1 74 0.087
175
P CHN012 Chondrosarcoma 57 0.086
176
P CRN018 Coronary Artery Anomaly 67 0.086
177
ALC007 Alcohol Dependence 68 0.086
178
P MNN013 Meningitis 67 0.085
179
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.085
180
c ACT075 Acute Myocardial Infarction 59 0.084
181
HMS001 Hemosiderosis 54 0.084
182
LSH001 Leishmaniasis 64 0.084
183
P PSD003 Pseudohypoaldosteronism 45 0.084
184
P KLZ004 Kala-Azar 1 43 0.084
185
CRT084 Creatinine Clearance Quantitative Trait Locus 26 0.084
186
P OST002 Osteoporosis 79 0.083
187
ALL003 Allergic Rhinitis 69 0.083
189
SVR004 Severe Combined Immunodeficiency 74 0.083
190
AGN016 Aging 58 0.083
191
ANT024 Anthrax Disease 56 0.083
192
P DBT009 Diabetes Mellitus 66 0.083
193
P CRN300 Coronary Heart Disease 1 59 0.083
194
P FBR017 Fibrosarcoma 57 0.082
195
SYN036 Syncope 46 0.082
196
HPT004 Hepatic Coma 42 0.082
197
P MYP004 Myopathy 63 0.082
198
P INT070 Intestinal Obstruction 60 0.082
199
GST045 Gastroenteritis 60 0.082
200
P TRM003 Tremor 55 0.081
201
P EPS003 Episodic Ataxia 60 0.081
202
PHN003 Phenylketonuria 73 0.081
203
P RTN016 Retinal Degeneration 56 0.081
204
GTR002 Goiter 54 0.081
205
ALL014 Allergic Encephalomyelitis 40 0.081
206
SRC014 Sarcoma 67 0.081
207
P DNT020 Dent Disease 1 60 0.081
208
c ATR087 Atrial Standstill 1 76 0.080
209
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.080
210
IRR002 Irritable Bowel Syndrome 65 0.080
211
IDP011 Idiopathic Interstitial Pneumonia 65 0.079
212
SPN035 Spindle Cell Sarcoma 57 0.079
213
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.079
214
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.079
215
MDD011 Mood Disorder 62 0.079
216
P MLN007 Male Infertility 57 0.079
217
P MYT002 Myotonic Dystrophy 52 0.079
218
c SVR001 Severe Acute Respiratory Syndrome 56 0.078
219
ATX019 Ataxia with Vitamin E Deficiency 46 0.078
220
THR024 Thrombosis 58 0.078
221
OCL006 Ocular Hypertension 52 0.078
222
P PLM036 Pulmonary Fibrosis 66 0.078
223
MYT026 Myotonia Atrophica 25 0.077
224
P OST001 Osteopetrosis 70 0.077
225
P PRK057 Parkinson Disease, Late-Onset 77 0.077
226
P LYM031 Lymphocytic Leukemia 56 0.077
227
P DDN001 Duodenal Ulcer 50 0.077
228
c MCR120 Microvascular Complications of Diabetes 7 48 0.077
229
LYS002 Lysosomal Storage Disease 52 0.077
230
P SYS005 Systemic Scleroderma 68 0.077
231
P DBT005 Diabetes Insipidus 54 0.076
232
P OPN001 Open-Angle Glaucoma 50 0.076
233
P HYP076 Hyperthyroidism 55 0.076
234
PRT036 Peritonitis 66 0.076
235
MSC157 Muscular Dystrophy, Duchenne Type 70 0.076
236
c MCR113 Microvascular Complications of Diabetes 3 55 0.075
237
c MCR130 Microvascular Complications of Diabetes 6 42 0.075
238
c MCR133 Microvascular Complications of Diabetes 4 42 0.075
239
P BRS044 Breast Adenocarcinoma 59 0.075
240
PLM001 Pulmonary Tuberculosis 72 0.075
241
c ACT027 Acute Pancreatitis 60 0.075
242
c LKM061 Leukemia, Acute Myeloid 84 0.075
243
P TMP001 Temporal Lobe Epilepsy 53 0.075
244
HYP014 Hyperuricemia 52 0.075
245
URM002 Uremia 50 0.075
246
P BRN022 Bronchiectasis 60 0.074
247
c HPT001 Hepatitis C 62 0.074
248
ESP021 Esophageal Cancer 90 0.074
249
P RCT021 Rectum Cancer 54 0.074
250
ART140 Arteries, Anomalies of 60 0.074
251
P ECL001 Eclampsia 53 0.074
252
ULC004 Ulcerative Colitis 75 0.073
253
THY029 Thyroid Carcinoma 62 0.073
254
P BLD134 Bladder Cancer 79 0.073
255
P PRP019 Peripheral Nervous System Disease 64 0.073
256
P THL005 Thalassemia 62 0.073
257
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.073
258
FTT001 Fatty Liver Disease 63 0.073
259
ANX010 Anxiety 75 0.072
260
P PRP029 Porphyria 58 0.072
261
P BCL017 B-Cell Lymphoma 61 0.072
262
P HDC001 Headache 59 0.072
263
P MLG056 Malignant Hyperthermia 60 0.072
264
HPT019 Hepatic Encephalopathy 60 0.072
265
ERY051 Erythroleukemia, Familial 58 0.072
266
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.072
267
P AMY004 Amyloidosis 71 0.072
268
P RRH023 Rare Hereditary Hemochromatosis 41 0.072
269
HMN044 Human Immunodeficiency Virus Type 1 73 0.071
270
c SHR030 Short Qt Syndrome 47 0.071
271
KRT019 Keratitis, Hereditary 69 0.071
272
EYD002 Eye Disease 59 0.071
273
P INT068 Intestinal Disease 56 0.071
274
TRY001 Trypanosomiasis 50 0.071
275
P HYP370 Hypokalemic Periodic Paralysis, Type 1 62 0.071
276
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.071
277
ATR057 Atrioventricular Block 56 0.071
278
OVR082 Overgrowth Syndrome 51 0.071
279
c HPT016 Hepatitis B 63 0.071
280
PLM031 Poliomyelitis 58 0.071
281
P PNC044 Pancreatitis 61 0.070
282
STM007 Stomatitis 51 0.070
283
IMP005 Impotence 53 0.070
284
GST023 Gastric Ulcer 53 0.070
285
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 25 0.070
286
P PLY019 Polyneuropathy 55 0.070
287
ADL002 Adult Syndrome 62 0.070
288
RYN005 Raynaud Phenomenon 50 0.070
289
HVY002 Heavy Metal Poisoning 23 0.070
290
CTN007 Cutaneous Leishmaniasis 61 0.069
291
c MNN043 Meningioma, Familial 74 0.069
292
MNN042 Meningioma, Radiation-Induced 64 0.069
293
MNT002 Mental Depression 60 0.069
294
SPN021 Spinal Meningioma 40 0.069
295
LYM002 Lymphoplasmacyte-Rich Meningioma 40 0.069
296
SCR001 Secretory Meningioma 38 0.069
297
P MYC008 Myocarditis 60 0.069
298
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.069
299
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.069
300
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.069
301
ILS001 Ileus 51 0.069
302
P MCR115 Microvascular Complications of Diabetes 5 67 0.068
303
c SCN007 Secondary Hyperparathyroidism 52 0.068
304
P ART022 Arthritis 71 0.068
305
DSS012 Disseminated Infection with Mycobacterium Avium Complex 21 0.068
306
BCT004 Bacteriuria 48 0.068
307
c PRM005 Primary Hyperparathyroidism 60 0.068
308
BCT002 Bacterial Vaginosis 52 0.068
309
DYS073 Dysphagia 52 0.068
310
P CYS018 Cystitis 59 0.067
311
SFT003 Soft Tissue Sarcoma 57 0.067
312
IMM064 Immunodeficiency, Common Variable, 10 51 0.067
313
DBT010 Diabetic Neuropathy 56 0.067
314
STT001 Status Epilepticus 61 0.066
315
P MLT020 Multiple Sclerosis 73 0.066
316
P ALP008 Alopecia 58 0.066
317
TLN003 Telangiectasis 53 0.066
318
c RHB024 Rhabdomyosarcoma 2 64 0.066
319
P NRF023 Neurofibromatosis, Type Ii 77 0.066
320
P SNS001 Sensorineural Hearing Loss 62 0.066
321
P SKN015 Skin Carcinoma 67 0.065
322
PNC129 Pancreatic Adenocarcinoma 69 0.065
323
c PRS136 Prostate Cancer, Hereditary, 6 34 0.064
324
c PRS130 Prostate Cancer, Hereditary, 8 33 0.064
325
P NPH012 Nephrotic Syndrome 65 0.064
326
P DST107 Distal Renal Tubular Acidosis 45 0.064
327
P RHM011 Rheumatoid Arthritis 82 0.064
328
SCK003 Sickle Cell Anemia 74 0.064
329
P HML002 Hemolytic Anemia 64 0.064
330
c PRM038 Primary Agammaglobulinemia 45 0.064
331
c MLG068 Malignant Glioma 46 0.064
332
P RHB003 Rhabdomyosarcoma 62 0.064
333
P EPL140 Epilepsy, Idiopathic Generalized 62 0.064
334
ALL006 Allergic Asthma 56 0.064
335
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 47 0.064
336
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.063
337
P CNR004 Cone-Rod Dystrophy 2 72 0.062
338
SBC016 Subacute Delirium 43 0.062
339
P LCT001 Lactic Acidosis 52 0.062
340
P MYL006 Myeloid Leukemia 61 0.061
341
PTT037 Pituitary Tumors 47 0.061
342
GT001 Gout 63 0.061
343
c MCL013 Mucolipidosis Iv 60 0.061
344
HYP060 Hyperinsulinism 55 0.061
345
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.061
346
P BNG032 Benign Mesothelioma 47 0.061
347
DYS015 Dysentery 45 0.061
348
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.061
349
MYL069 Myeloma, Multiple 85 0.061
350
P LYM118 Lymphoma 70 0.061
351
NWC001 Newcastle Disease 45 0.060
352
HND015 Hand Skill, Relative 33 0.060
353
P NTR004 Neutropenia 64 0.060
354
NTR005 Nutritional Deficiency Disease 61 0.060
355
MLR004 Malaria 82 0.060
356
CHL123 Chlamydia 60 0.060
357
HYP025 Hyperphosphatemia 47 0.060
358
DMP001 Dumping Syndrome 44 0.060
359
INS024 Insulin-Like Growth Factor I 79 0.059
360
P LKM002 Leukemia 69 0.058
361
CHL065 Cholangiocarcinoma 68 0.058
362
ANG054 Angina Pectoris 66 0.058
363
MST005 Mastitis 55 0.058
364
GLC003 Glucose Intolerance 55 0.058
365
INT079 Intrahepatic Cholangiocarcinoma 54 0.058
366
P SCK005 Sickle Cell Disease 53 0.058
367
P PNM007 Pneumonia 71 0.058
368
P CNJ013 Conjunctivitis 67 0.058
369
TBR011 Tuberculous Meningitis 50 0.058
370
ACT003 Acute Kidney Tubular Necrosis 42 0.058
371
SPS057 Spasticity 38 0.058
372
GST050 Gastrointestinal System Disease 57 0.058
373
CHD004 Chudley-Mccullough Syndrome 44 0.058
374
MTH071 Methane Production 26 0.058
375
ORL011 Oral Cancer 62 0.058
376
P CND004 Candidiasis 61 0.058
377
ANR040 Aneurysm 60 0.058
378
P PYL005 Pyelonephritis 58 0.058
379
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.058
380
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.058
381
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.058
382
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.058
383
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.058
384
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.058
385
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.058
386
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.058
387
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.058
388
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.058
389
P RRT020 Rare Tumor 43 0.058
390
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.058
391
P ATX030 Ataxia-Telangiectasia 83 0.057
392
CHR066 Chronic Fatigue Syndrome 61 0.057
393
OST011 Osteomalacia 51 0.057
394
CHR178 Chromosomal Triplication 36 0.057
395
P THR014 Thrombocytopenia 67 0.057
396
KRT006 Keratoconjunctivitis 53 0.057
397
ENT011 Enterocolitis 51 0.057
398
c DLT002 Dilated Cardiomyopathy 81 0.057
399
P FBR031 Febrile Seizures 54 0.057
400
c SPN225 Spondyloarthropathy 1 74 0.057
401
VGN023 Vaginitis 54 0.057
402
KRT001 Keratoconjunctivitis Sicca 53 0.057
403
CLN015 Colon Adenocarcinoma 65 0.056
404
P ENC004 Encephalitis 64 0.056
405
P ART023 Arthropathy 61 0.056
406
IRN001 Iron Deficiency Anemia 59 0.056
407
YLL002 Yellow Fever 58 0.056
408
PTH003 Pathologic Nystagmus 53 0.056
409
P RTN018 Retinal Disease 53 0.056
410
c RTN047 Retinitis Pigmentosa 18 40 0.056
411
P KDN017 Kidney Cancer 60 0.055
412
P ART021 Arteriosclerosis 56 0.055
413
HDN002 Head Injury 47 0.055
414
ORL015 Oral Squamous Cell Carcinoma 44 0.055
415
AMN006 Aminoaciduria 39 0.055
416
DMY004 Demyelinating Disease 54 0.055
417
P PRD017 Periodic Paralyses 27 0.055
418
SPL018 Splenomegaly 48 0.055
419
CHL079 Children's Interstitial Lung Disease 27 0.055
420
OTT002 Otitis Media 71 0.055
421
OST003 Osteonecrosis 62 0.055
422
c LNG047 Long Qt Syndrome 2 57 0.055
423
P PSR002 Psoriasis 63 0.055
424
PPL022 Papilloma 56 0.055
425
PST011 Pustulosis of Palm and Sole 51 0.055
426
SQM002 Squamous Cell Papilloma 49 0.055
427
c BRT024 Bartter Syndrome Type 4 26 0.055
428
P DMN002 Dementia 68 0.054
429
GST092 Gastroesophageal Reflux 68 0.054
430
ANR007 Anorexia Nervosa 64 0.054
431
INT066 Interstitial Lung Disease 61 0.054
432
c PCH010 Pachyonychia Congenita 3 43 0.054
433
ADG002 Audiogenic Seizures 25 0.054
434
MNK001 Menkes Disease 62 0.054
435
END040 Endogenous Depression 55 0.054
436
HMP009 Haemophilus Influenzae 46 0.054
437
ACR006 Aceruloplasminemia 74 0.053
438
P SLP006 Sleep Apnea 71 0.053
439
P ATS364 Autism 68 0.053
440
P DYS154 Dystonia 65 0.053
441
PRS047 Prostatitis 57 0.053
442
CRD137 Cardiogenic Shock 50 0.053
443
HYP017 Hypophosphatemia 48 0.053
444
AVN001 Avian Influenza 56 0.053
445
CLF027 Cleft Palate, Isolated 67 0.053
446
P HYP750 Hypertriglyceridemia, Familial 62 0.053
447
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.053
448
VRC005 Varicose Veins 61 0.053
449
NRT004 Neuritis 52 0.053
450
RRS014 Rare Surgical Neurologic Disease 33 0.053
451
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.053
452
OST017 Osteomyelitis 65 0.053
453
MSL001 Measles 61 0.053
454
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.053
455
CRH001 Crohn's Disease 75 0.052
456
c FML001 Familial Atrial Fibrillation 67 0.052
457
MTH009 Mouth Disease 56 0.052
458
P URT039 Urticaria 61 0.051
459
c BRT053 Bartter Syndrome, Type 4a, Neonatal, with Sensorineural Deafness 34 0.051
460
INS001 Insulinoma 60 0.051
461
HYP052 Hyperkalemic Periodic Paralysis 59 0.051
462
MNR012 Meniere Disease 56 0.051
463
PRM057 Paramyotonia Congenita of Von Eulenburg 45 0.051
464
c GLL024 Gallbladder Disease 1 53 0.051
465
DGN001 Degenerative Disc Disease 49 0.051
466
P SCH015 Schizophrenia 76 0.050
467
MSC007 Muscle Hypertrophy 65 0.050
468
LKD001 Leukodystrophy 61 0.050
469
P HYP097 Hyperekplexia 61 0.050
470
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.050
471
P SJG008 Sjogren Syndrome 57 0.050
472
SNS003 Sensory Peripheral Neuropathy 56 0.050
473
LST001 Listeriosis 55 0.050
474
SPN051 Spondylitis 53 0.050
475
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.050
476
P RNL015 Renal Hypertension 47 0.050
477
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.050
478
INF009 Inflammatory Spondylopathy 29 0.050
479
PRP027 Peripheral Vascular Disease 72 0.050
480
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.050
481
CHR073 Choreatic Disease 52 0.050
482
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 45 0.050
483
P SRC025 Sarcoidosis 1 72 0.050
484
ERL001 Early Myoclonic Encephalopathy 60 0.050
485
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.050
486
P BNC003 Bone Cancer 56 0.050
487
c ACT134 Acute Liver Failure 53 0.050
488
DYS014 Dyspepsia 51 0.050
489
NRL016 Neural Tube Defects 83 0.049
490
P HYD006 Hydrocephalus 68 0.049
491
P EPL198 Epilepsy, Myoclonic Juvenile 62 0.049
492
P ESP024 Esophagitis 62 0.049
493
PLM033 Pulmonary Embolism 60 0.049
494
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 58 0.049
495
P HYP024 Hypoparathyroidism 56 0.049
496
c CNG216 Congenital Hydrocephalus 55 0.049
497
c GRV008 Graves Disease 1 55 0.049
498
BLL006 Bullous Pemphigoid 63 0.049
499
c MYT029 Myotonia Congenita, Autosomal Recessive 41 0.049
500
c MYT027 Myotonia Congenita, Autosomal Dominant 35 0.049
501
P END044 Endometriosis 63 0.049
502
RTR008 Root Resorption 44 0.049
503
HMG005 Hemoglobinopathy 57 0.048
504
SCR011 Scrapie 37 0.048
505
P FML187 Familial Hypertension 35 0.048
506
P EXN002 Exanthem 58 0.048
507
NNL006 Non-Alcoholic Steatohepatitis 53 0.048
508
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.048
509
ART016 Aortic Aneurysm 71 0.047
510
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.047
511
P INT143 Interstitial Cystitis 62 0.047
512
CHL068 Cholestasis 61 0.047
513
AZS001 Azoospermia 51 0.047
514
THR013 Thoracic Outlet Syndrome 49 0.047
515
ANR004 Anuria 47 0.047
516
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.047
517
49X002 49,xxxxy Syndrome 39 0.047
518
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.047
519
END057 Endometrial Cancer 74 0.047
520
LYM133 Lymphoma, Hodgkin, Classic 70 0.047
521
P LKM062 Leukemia, Acute Lymphoblastic 68 0.047
522
P MVM001 Movement Disease 63 0.047
523
P LPS002 Liposarcoma 62 0.047
524
P UVT001 Uveitis 58 0.047
525
PRP030 Purpura 56 0.047
526
c PRD040 Periodontitis, Chronic 56 0.047
527
SPP010 Suppressor of Tumorigenicity 3 54 0.047
528
P PNC025 Panic Disorder 53 0.047
529
P MSC003 Muscular Atrophy 52 0.047
530
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 27 0.047
531
IMM167 Immune Deficiency Disease 79 0.047
532
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.047
533
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.047
534
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.047
535
GRD007 Grade Iii Astrocytoma 59 0.047
536
P SLP005 Sleep Disorder 58 0.047
537
SCH014 Schistosomiasis 57 0.047
538
ENH001 Enhanced S-Cone Syndrome 56 0.047
539
P GLM044 Glomerular Disease 42 0.047
540
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.047
541
VGN019 Vaginal Discharge 35 0.047
542
P RTN008 Retinitis Pigmentosa 77 0.046
543
P HYP061 Hypertrophic Cardiomyopathy 68 0.046
544
P SCK002 Sick Sinus Syndrome 56 0.046
545
MST021 Meester-Loeys Syndrome 32 0.046
546
STN013 Stenotrophomonas Maltophilia Infection 26 0.046
547
NRT001 Neurotic Disorder 53 0.046
548
c INH020 Inherited Metabolic Disorder 51 0.046
549
CND006 Candida Glabrata 33 0.046
550
LPD008 Lipid Metabolism Disorder 64 0.045
551
CHL067 Cholecystitis 60 0.045
552
URN010 Urinary Tract Obstruction 59 0.045
553
RHM027 Rheumatic Disease 56 0.045
554
AMN003 Amnestic Disorder 55 0.045
555
P INS002 in Situ Carcinoma 55 0.045
556
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.045
557
ATN005 Autonomic Dysfunction 48 0.045
558
CRN019 Coronary Artery Vasospasm 48 0.045
559
c PSD092 Pseudohypoaldosteronism, Type Iie 45 0.045
560
CRT015 Carotid Artery Occlusion 44 0.045
561
INT052 Intestinal Volvulus 44 0.045
562
CLC006 Calcinosis 48 0.045
563
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.045
564
KRT008 Keratopathy 46 0.045
565
VGN020 Vaginal Disease 45 0.045
566
P HYP733 Hypercalciuria, Absorptive, 2 45 0.045
567
SYS071 Systemic Autoimmune Disease 38 0.045
568
P ART005 Arteriovenous Malformation 63 0.044
569
ACQ007 Acquired Immunodeficiency Syndrome 61 0.044
570
HMC014 Homocysteinemia 54 0.044
571
P MCL001 Mucolipidosis 46 0.044
572
RTN023 Retinitis 46 0.044
573
NRR001 Neuroretinitis 46 0.044
574
ACR007 Acromegaly 70 0.043
575
P CLC063 Celiac Disease 1 66 0.043
576
CHG001 Chagas Disease 66 0.043
577
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 63 0.043
578
RTN017 Retinal Detachment 62 0.043
579
FBR047 Fibromyalgia 60 0.043
580
BLR008 Bilirubin Metabolic Disorder 58 0.043
581
RTN003 Retinal Ischemia 52 0.043
582
THY128 Thyroid Tumor 49 0.043
583
c HNT004 Huntington Disease-Like 2 48 0.043
584
HST009 Histiocytoma 47 0.043
585
P HMR005 Hemorrhoid 47 0.043
586
MLG065 Malignant Fibroxanthoma 45 0.043
587
FBR003 Fibrous Histiocytoma 43 0.043
588
P HYP265 Hypotonia 43 0.043
589
GST040 Gastric Adenocarcinoma 67 0.043
590
P SCL018 Scoliosis 61 0.043
591
P RBL001 Rubella 56 0.043
592
HRT012 Heart Valve Disease 56 0.043
593
P CHL066 Cholangitis 53 0.043
594
c HNT011 Huntington Disease-Like 3 37 0.043
595
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 29 0.043
596
URT049 Urate Oxidase, Pseudogene 26 0.043
597
c VRL010 Viral Hepatitis 56 0.043
598
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.043
599
PHR003 Pharyngitis 56 0.043
600
PRS045 Prostatic Hypertrophy 55 0.043
601
P VTL001 Vitelliform Macular Dystrophy 43 0.043
602
P MYG005 Myoglobinuria 43 0.043
603
BST007 Best Vitelliform Macular Dystrophy 34 0.043
605
c BTT014 Beta-Thalassemia 73 0.042
606
HMR039 Hemorrhage, Intracerebral 59 0.042
607
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.042
608
KRT009 Keratosis 52 0.042
609
ONC002 Onchocerciasis 50 0.042
610
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.042
611
SCT005 Scott Syndrome 48 0.042
612
LCH001 Leech Infestation 40 0.042
613
CNT105 Central Core Disease of Muscle 61 0.041
614
P SLV026 Salivary Gland Carcinoma 58 0.041
615
P MTH008 Methylmalonic Acidemia 50 0.041
616
SLP001 Sleeping Sickness 47 0.041
617
c SYS001 Systemic Lupus Erythematosus 88 0.040
618
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.040
619
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 65 0.040
620
P LPS004 Lupus Erythematosus 62 0.040
621
PRT058 Pure Autonomic Failure 60 0.040
622
c HPT003 Hepatitis a 60 0.040
623
P SYP003 Syphilis 59 0.040
624
HYP081 Hypolipoproteinemia 51 0.040
625
BLD044 Bladder Disease 50 0.040
626
HYP781 Hypoascorbemia 48 0.040
627
PCD001 Pica Disease 33 0.040
628
EXN003 Exencephaly 32 0.040
629
c PNC108 Pancreatitis, Hereditary 70 0.039
630
c ATS007 Autism Spectrum Disorder 69 0.039
631
BRR014 Barrett Esophagus 67 0.039
632
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 64 0.039
633
P PRM002 Primary Hyperoxaluria 60 0.039
634
P HRD011 Hereditary Spherocytosis 59 0.039
635
RBS001 Rabies 57 0.039
636
HRY003 Hairy Cell Leukemia 57 0.039
637
RHM001 Rheumatic Fever 56 0.039
638
P SML001 Small Cell Carcinoma 55 0.039
639
MSC190 Muscular Disease 54 0.039
640
CMB003 Combined T Cell and B Cell Immunodeficiency 53 0.039
641
FDB001 Foodborne Botulism 53 0.039
642
P MNC007 Monocytic Leukemia 52 0.039
643
c SVR005 Severe Pre-Eclampsia 50 0.039
644
P NGH001 Night Blindness 48 0.039
645
PRS063 Paresthesia 46 0.039
646
IDP073 Idiopathic Hypercalciuria 43 0.039
647
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.039
648
HRD218 Hereditary Stomatocytosis 33 0.039
649
MTL005 Metal Allergy 32 0.039
650
c PSD093 Pseudohypoaldosteronism, Type Iid 30 0.039
651
P NRV007 Nervous System Disease 68 0.039
652
P ANG001 Angelman Syndrome 65 0.039
653
P CHR071 Charcot-Marie-Tooth Disease 65 0.039
654
P MYP006 Myopia 58 0.039
655
P LCH002 Lichen Planus 55 0.039
656
P LMB006 Limb-Girdle Muscular Dystrophy 55 0.039
657
P SLM003 Salmonellosis 54 0.039
658
LNG031 Lung Benign Neoplasm 52 0.039
659
HMN016 Hemangioendothelioma 41 0.039
660
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.039
661
c RNL046 Renal Tubular Acidosis, Distal, Autosomal Dominant 34 0.039
662
EWN003 Ewing Sarcoma 69 0.038
663
P THY023 Thymoma 64 0.038
664
P HMP007 Hemophilia 58 0.038
665
c THY107 Thymoma, Familial 55 0.038
666
P ACT105 Acute Mountain Sickness 53 0.038
667
STT041 Stuttering 53 0.038
668
c HPT007 Hepatitis E 53 0.038
669
PRP080 Peripheral Artery Disease 51 0.038
670
CHL004 Cholelithiasis 50 0.038
671
c BCT013 Bacterial Pneumonia 49 0.038
672
c FML036 Familial Periodic Paralysis 42 0.038
673
KLD004 Keloid Disorder 41 0.038
674
HRN029 Hearing Loss, Noise-Induced 38 0.038
675
ENM002 Enamel Erosion 28 0.038
676
OBS532 Obsolete: Ehlers-Danlos Syndrome, Fibronectinemic Type 15 0.038
677
CNN003 Conn's Syndrome 78 0.037
678
c EXD008 Exudative Vitreoretinopathy 1 69 0.037
679
c MCR129 Microvascular Complications of Diabetes 1 67 0.037
680
IGR001 Ige Responsiveness, Atopic 61 0.037
681
P OPT006 Optic Nerve Disease 59 0.037
682
DSS009 Disseminated Intravascular Coagulation 58 0.037
683
c FML035 Familial Hyperlipidemia 56 0.037
684
P PLM034 Pulmonary Emphysema 55 0.037
685
P OPT009 Optic Neuritis 55 0.037
686
URT010 Ureteral Obstruction 46 0.037
687
CHP002 Chops Syndrome 41 0.037
688
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.037
689
P RTN024 Retinoblastoma 74 0.035
690
P FCL005 Focal Segmental Glomerulosclerosis 63 0.035
691
c DWL002 Dowling-Degos Disease 1 59 0.035
692
c MST023 Mesothelioma, Malignant 59 0.035
693
P LRY044 Larynx Cancer 59 0.035
694
PRM236 Primary Biliary Cholangitis 57 0.035
695
P GRV001 Graves' Disease 57 0.035
696
FLR002 Filariasis 56 0.035
697
P PRM006 Primary Biliary Cirrhosis 54 0.035
698
DRR016 Diarrhea 2, with Microvillus Atrophy 54 0.035
699
CLR030 Clear Cell Renal Cell Carcinoma 54 0.035
700
FRZ001 Frozen Shoulder 53 0.035
701
MCL006 Macular Retinal Edema 52 0.035
702
P OBS001 Obstructive Jaundice 49 0.035
703
PRM020 Premenstrual Tension 48 0.035
704
VTR007 Vitreoretinopathy 48 0.035
705
CHR074 Choriocarcinoma 47 0.035
706
P MTH007 Methemoglobinemia 47 0.035
707
c FML008 Familial Retinoblastoma 46 0.035
708
ENT004 Enthesopathy 46 0.035
709
P CRN025 Corneal Dystrophy 45 0.035
710
VSD002 Vas Deferens, Congenital Bilateral Aplasia of 45 0.035
711
P SDR002 Siderosis 42 0.035
712
FNG016 Fungal Keratitis 42 0.035
713
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.035
714
P HRD086 Hereditary Hypophosphatemic Rickets 41 0.035
715
KLB003 Klebsiella Pneumonia 36 0.035
716
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 26 0.035
717
P FML011 Familial Adenomatous Polyposis 73 0.034
718
P FRG001 Fragile X Syndrome 69 0.034
719
P MPL001 Maple Syrup Urine Disease 68 0.034
720
P PRP003 Porphyria Cutanea Tarda 66 0.034
721
NRM005 Neuromuscular Disease 62 0.034
722
HLC007 Helicobacter Pylori Infection 61 0.034
723
SPP011 Suppression of Tumorigenicity 12 61 0.034
724
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 60 0.034
725
WST005 West Nile Virus 56 0.034
726
FCT001 Factor Viii Deficiency 54 0.034
727
THY030 Thyroid Gland Disease 53 0.034
728
CLR109 Colorectal Adenocarcinoma 51 0.034
729
P SHR001 Short Bowel Syndrome 50 0.034
730
c ACT078 Acute Porphyria 49 0.034
731
P JVN007 Juvenile Absence Epilepsy 47 0.034
732
MYT030 Myotonia, Potassium-Aggravated 45 0.034
733
ISL099 Isolated Methylmalonic Acidemia 30 0.034
734
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.034
735
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.034
736
P HYP098 Hypereosinophilic Syndrome 67 0.034
737
BRC012 Brucellosis 62 0.034
738
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.034
739
P FCS002 Fucosidosis 58 0.034
740
P ALC033 Alcohol Use Disorder 58 0.034
741
PNM008 Pneumothorax 56 0.034
742
c BNG091 Benign Chronic Pemphigus 56 0.034
743
P SBS003 Substance Abuse 56 0.034
744
P CYS039 Cystic Kidney Disease 55 0.034
745
P THY032 Thyroiditis 52 0.034
746
P RNL017 Renal Oncocytoma 52 0.034
747
c MGL009 Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 51 0.034
748
c INF145 Infantile Liver Failure Syndrome 1 50 0.034
749
PPT001 Peptic Esophagitis 47 0.034
750
CCC002 Coccidiosis 46 0.034
751
ART031 Aortic Coarctation 45 0.034
752
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.034
753
c MCR112 Microvascular Complications of Diabetes 2 42 0.034
754
P BRB001 Beriberi 41 0.034
755
STT004 Steatorrhea 39 0.034
756
DNT008 Denture Stomatitis 38 0.034
757
JMP002 Jumping Frenchmen of Maine 23 0.034
758
NND001 Nondystrophic Myotonia 20 0.034
759
P RTT002 Rett Syndrome 81 0.030
760
P CHR012 Chronic Granulomatous Disease 69 0.030
761
PSY004 Psychotic Disorder 68 0.030
762
P GLM040 Glioma Susceptibility 1 68 0.030
763
c BSL007 Basal Cell Carcinoma 68 0.030
764
P FRD012 Friedreich Ataxia 1 65 0.030
765
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.030
766
MCR013 Microphthalmia 62 0.030
767
c PRG042 Progressive Familial Heart Block, Type Ia 62 0.030
768
LSC001 Lesch-Nyhan Syndrome 61 0.030
769
CRV038 Cervical Squamous Cell Carcinoma 58 0.030
770
EMB004 Embryonal Carcinoma 57 0.030
771
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.030
772
GLS001 Gliosarcoma 56 0.030
773
P PTT014 Pitt-Hopkins Syndrome 55 0.030
774
P VNS003 Venous Insufficiency 55 0.030
775
ESP023 Esophageal Disease 55 0.030
776
VSC003 Visceral Leishmaniasis 55 0.030
777
HMT018 Hematopoietic Stem Cell Transplantation 54 0.030
778
AST006 Astigmatism 53 0.030
779
NPH018 Nephrogenic Systemic Fibrosis 51 0.030
780
LRN003 Learning Disability 51 0.030
781
FLR001 Filarial Elephantiasis 51 0.030
782
P THY054 Thyrotoxic Periodic Paralysis 51 0.030
783
CRY003 Cryptosporidiosis 50 0.030
784
HMG002 Hemoglobinuria 49 0.030
785
c PRG126 Progressive Familial Heart Block 49 0.030
786
CRN027 Corneal Neovascularization 48 0.030
787
c CHR431 Chronic Venous Insufficiency 48 0.030
788
CCN002 Cocaine Abuse 48 0.030
789
CLS016 Clostridium Difficile Colitis 48 0.030
790
BRN014 Bronchopneumonia 47 0.030
791
VTM033 Vitamin K Deficiency Bleeding 47 0.030
792
MYC005 Myocardial Stunning 45 0.030
793
FBR054 Fibroma 45 0.030
794
c SRC023 Sarcoidosis 2 43 0.030
795
STL007 Steel Syndrome 42 0.030
796
c FML294 Familial Short Qt Syndrome 41 0.030
797
c SPR086 Spermatogenic Failure 3 41 0.030
798
MNN028 Mononeuropathy of the Median Nerve, Mild 41 0.030
799
PLR006 Pleural Cancer 40 0.030
800
OVR093 Overhydrated Hereditary Stomatocytosis 40 0.030
801
c EPL133 Epilepsy, Juvenile Absence 1 40 0.030
802
DSS010 Dissociative Disorder 35 0.030
803
BLR004 Biliary Dyskinesia 33 0.030
804
ISL119 Isolated Optic Neuritis 31 0.030
805
PRX097 Paroxysmal Dystonia 31 0.030
806
c THY083 Thyrotoxic Periodic Paralysis 2 30 0.030
807
c PRG019 Paragangliomas 2 30 0.030
808
c FML159 Familial Periodic Paralyses 17 0.030
809
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.030
810
P MYC084 Mycobacterium Tuberculosis 1 69 0.030
811
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.030
812
ACT119 Acute Promyelocytic Leukemia 63 0.030
813
P MCH002 Machado-Joseph Disease 61 0.030
814
VTR013 Vitreoretinopathy, Neovascular Inflammatory 61 0.030
815
c ACT073 Acute Leukemia 59 0.030
816
P LDD007 Liddle Syndrome 1 58 0.030
817
P HYP726 Hypercalcemia, Infantile, 1 58 0.030
818
INT007 Intermediate Coronary Syndrome 58 0.030
819
VSC002 Vascular Dementia 57 0.030
820
ORL005 Oral Candidiasis 56 0.030
821
c BCT007 Bacterial Meningitis 56 0.030
822
P ALP106 Alport Syndrome 1, X-Linked 55 0.030
823
CRC006 Carcinoid Syndrome 55 0.030
824
CHR100 Chronic Ulcer of Skin 53 0.030
825
P PTT006 Pituitary Adenoma 53 0.030
826
STR008 Strongyloidiasis 53 0.030
827
FML063 Familial Glucocorticoid Deficiency 51 0.030
828
ACH005 Achalasia 50 0.030
829
HPT014 Hepatorenal Syndrome 49 0.030
830
MTN003 Motion Sickness 48 0.030
831
P TCL004 T-Cell Leukemia 48 0.030
832
TTR011 Tetraploidy 47 0.030
833
WTH001 Withdrawal Disorder 47 0.030
834
c VRL012 Viral Meningitis 47 0.030
835
ANH002 Anhidrosis 47 0.030
836
P EPT020 Epithelioid Hemangioendothelioma 45 0.030
837
DWR001 Dwarfism 45 0.030
838
TND005 Tendinitis 45 0.030
839
CRB090 Cerebral Hypoxia 45 0.030
840
CRN017 Coronary Thrombosis 45 0.030
841
IDP033 Idiopathic Edema 44 0.030
842
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 44 0.030
843
TND004 Tendinopathy 44 0.030
844
BRS064 Bursitis 42 0.030
845
P CRV039 Cervicitis 42 0.030
846
PLY100 Polyploidy 41 0.030
848
BLN006 Blind Loop Syndrome 40 0.030
849
c OVR114 Ovarian Cancer 1 39 0.030
850
HYP264 Hypertonia 39 0.030
851
c ACT004 Acute Diarrhea 38 0.030
852
c ELL005 Elliptocytosis 2 35 0.030
853
c LKM005 Leukemia, T-Cell, Chronic 35 0.030
854
c ELL006 Elliptocytosis 3 34 0.030
855
c HYP600 Hyperaldosteronism, Familial, Type Ii 32 0.030
856
ANP008 Anaplastic Oligoastrocytoma 31 0.030
857
RRD056 Rare Disease in Surgical Orthopedic 29 0.030
858
NRM009 Normokalemic Periodic Paralysis 28 0.030
859
CYN003 Cyanide Poisoning 24 0.030
860
ETH012 Ethylene Glycol Poisoning 22 0.030
861
OBN001 Ouabain Resistance 19 0.030
862
c LKM063 Leukemia, Chronic Myeloid 74 0.025
863
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.025
864
ADR007 Adrenoleukodystrophy 72 0.025
865
MLT157 Multiple System Atrophy 1 71 0.025
866
P ORT004 Orthostatic Intolerance 68 0.025
867
P ASP006 Aspergillosis 67 0.025
868
ACR008 Acrocallosal Syndrome 66 0.025
869
MLD001 Melioidosis 66 0.025
870
P ALP004 Alport Syndrome 66 0.025
871
P MTR014 Motor Neuron Disease 66 0.025
872
WLF001 Wolff-Parkinson-White Syndrome 65 0.025
873
CLR108 Colorectal Adenoma 64 0.025
874
LYM017 Lyme Disease 64 0.025
875
P VNW001 Von Willebrand's Disease 64 0.025
876
HSH003 Hashimoto Thyroiditis 63 0.025
877
OVR029 Ovarian Hyperstimulation Syndrome 63 0.025
878
CHY002 Chylomicron Retention Disease 63 0.025
879
BRS099 Breast Ductal Carcinoma 63 0.025
880
MRK001 Merkel Cell Carcinoma 62 0.025
881
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 62 0.025
882
P ANP001 Anaplastic Large Cell Lymphoma 62 0.025
883
GRG001 Greig Cephalopolysyndactyly Syndrome 61 0.025
884
APP008 Appendicitis 61 0.025
885
P TXP001 Toxoplasmosis 61 0.025
886
c LPM012 Lipomatosis, Multiple 60 0.025
887
ALC006 Alcoholic Hepatitis 60 0.025
888
P GLY013 Glycogen Storage Disease 59 0.025
889
ECT006 Ectodermal Dysplasia 58 0.025
890
c HYP731 Hyperaldosteronism, Familial, Type I 57 0.025
891
DCT002 Ductal Carcinoma in Situ 57 0.025
892
P PLY041 Polymyositis 57 0.025
893
FCL014 Focal Epilepsy 56 0.025
894
PRT038 Protein-Energy Malnutrition 56 0.025
895
HPT046 Hepatic Veno-Occlusive Disease 56 0.025
896
c MSC170 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2 56 0.025
897
VTM027 Vitamin D-Dependent Rickets, Type 2a 56 0.025
898
c MYP132 Myopathy, Congenital 55 0.025
899
SLC006 Silicosis 55 0.025
900
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 55 0.025
901
HMP005 Hemiplegia 55 0.025
902
ORL004 Oral Submucous Fibrosis 55 0.025
903
TCK001 Tick-Borne Encephalitis 53 0.025
904
CYS036 Cystinosis, Nephropathic 53 0.025
905
HRT011 Heart Septal Defect 52 0.025
906
ASP003 Aseptic Meningitis 51 0.025
907
CRY005 Cryptococcosis 51 0.025
908
P ANL018 Analbuminemia 51 0.025
909
ANK001 Ankylosis 51 0.025
910
ALP077 Alpha-Methylacetoacetic Aciduria 51 0.025
911
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 51 0.025
912
P KRT007 Keratoconus 51 0.025
913
P AGG001 Aggressive Periodontitis 50 0.025
914
P ALL008 Allergic Bronchopulmonary Aspergillosis 50 0.025
915
MNN009 Meningoencephalitis 50 0.025
916
SXL003 Sexual Disorder 49 0.025
917
P RNV001 Renovascular Hypertension 49 0.025
918
CRC014 Carcinoid Tumors, Intestinal 49 0.025
919
LPD009 Lipid Storage Disease 49 0.025
920
c ANT034 Anterior Uveitis 48 0.025
921
P TRT019 Torticollis 48 0.025
922
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 48 0.025
923
KRT002 Keratomalacia 47 0.025
924
MCR191 Microscopic Colitis 47 0.025
925
P ENC008 Encephalocele 47 0.025
926
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 47 0.025
927
NDL007 Nodular Goiter 46 0.025
928
HRN026 Hernia, Hiatus 46 0.025
929
BST008 Bestrophinopathy, Autosomal Recessive 46 0.025
930
URN003 Urinary Schistosomiasis 45 0.025
931
c ACT076 Acute Myocarditis 45 0.025
932
CRV043 Cervical Dystonia 45 0.025
933
c LRG001 Large Cell Carcinoma 45 0.025
934
TNG009 Tongue Squamous Cell Carcinoma 44 0.025
935
AMB001 Amebiasis 44 0.025
936
URT001 Urethritis 44 0.025
937
PLR007 Pleural Empyema 44 0.025
938
DRG024 Drug Allergy 43 0.025
939
MCR011 Microinvasive Gastric Cancer 43 0.025
940
ISC015 Ischemic Colitis 43 0.025
941
c MLG079 Malignant Pleural Mesothelioma 43 0.025
942
P PRT026 Parotitis 43 0.025
943
PHY002 Physical Disorder 42 0.025
944
DBT007 Diabetic Cataract 42 0.025
945
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.025
946
P DCR003 Dacryoadenitis 42 0.025
947
SCR015 Scarlet Fever 41 0.025
948
PLM005 Pleomorphic Lipoma 41 0.025
949
P ANT061 Antenatal Bartter Syndrome 40 0.025
951
IDP070 Idiopathic Scoliosis 39 0.025
952
LYM042 Lymphocytic Colitis 39 0.025
953
CRT055 Creatine Deficiency Syndromes 39 0.025
954
RTC003 Root Caries 37 0.025
955
BKS003 Beukes Hip Dysplasia 37 0.025
956
P MXL015 Maxillary Sinusitis 37 0.025
957
MXD026 Mixed Glioma 36 0.025
958
c CHR020 Chronic Interstitial Cystitis 36 0.025
959
HNS001 Hansen's Disease 35 0.025
960
ACL001 Acalculous Cholecystitis 35 0.025
961
CRY019 Cryohydrocytosis 34 0.025
962
P VSC018 Visceral Steatosis 34 0.025
963
TXC020 Toxic Oil Syndrome 34 0.025
964
VRS002 Virus-Associated Trichodysplasia Spinulosa 33 0.025
965
PLC006 Placental Choriocarcinoma 33 0.025
966
MYC014 Mycobacterium Chelonae 32 0.025
967
ISC001 Ischemic Neuropathy 32 0.025
968
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.025
969
TBL029 Tubulin, Beta 29 0.025
970
DNT010 Dentin Caries 27 0.025
971
c RNG015 Ring Chromosome 2 27 0.025
972
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 0.025
973
c MYP127 Myopia 2, Autosomal Dominant 24 0.025
974
CRC034 Carcinoma Showing Thymus-Like Differentiation 23 0.025
975
FTL005 Fetal Adenoma 21 0.025
976
NPH026 Nephrotic Syndrome, Idiopathic, Steroid-Resistant 20 0.025
977
PST047 Post-Traumatic Epilepsy 20 0.025
978
SPN092 Spinal Shock 19 0.025
979
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 18 0.025
980
CNN008 Cinnamon Odor, Pleasantness of 14 0.025
981
P ISL045 Isolated Focal Cortical Dysplasia Type I 12 0.025
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