Search results for Water

2290 hits were found for Water

# Family MCID Name MIFTS Score
1
ELS006 Elsahy-Waters Syndrome 35 4.199
2
WTR002 Water-Clear Cell Adenoma 18 3.663
3
P EPL074 Epilepsy, Hot Water, 1 17 3.659
4
c EPL075 Epilepsy, Hot Water, 2 8 3.616
5
CLR003 Clear Cell Adenocarcinoma 50 3.594
6
HYP693 Hyperparathyroidism, Primary, Caused by Water Clear Cell Hyperplasia 25 2.130
7
HTW001 Hot Water Reflex Epilepsy 3 2.105
8
BLC004 Blackwater Fever 32 2.097
9
EXC003 Excessive Tearing 33 2.075
10
IMM002 Immature Cataract 25 2.075
11
HML049 Hemolytic Anemia, Lethal Congenital Nonspherocytic, with Genital and Other Abnormalities 17 2.075
12
P DRR001 Diarrhea 57 0.412
13
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.350
14
DNT012 Dental Caries 51 0.344
15
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.318
16
CHL014 Cholera 55 0.309
17
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.287
18
GST045 Gastroenteritis 59 0.284
19
P DBT005 Diabetes Insipidus 55 0.270
20
HRW001 Hair Whorl 36 0.258
21
PLM010 Pulmonary Edema 55 0.251
22
HLX001 Helix Syndrome 47 0.247
23
48X005 48,xyyy 39 0.238
24
PPL052 Papillomatosis, Confluent and Reticulated 34 0.238
25
SCH014 Schistosomiasis 56 0.237
26
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.236
27
DNT001 Dental Fluorosis 43 0.234
28
c HPT003 Hepatitis a 63 0.227
29
P KDN018 Kidney Disease 70 0.225
30
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.219
31
DRM006 Dermatitis 61 0.212
32
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.208
33
LGN006 Legionnaire Disease 50 0.207
34
TYP007 Typhoid Fever 63 0.202
35
LVR012 Liver Cirrhosis 63 0.201
36
ADN018 Adenoma 58 0.197
37
CRY003 Cryptosporidiosis 54 0.196
38
CNG034 Congestive Heart Failure 70 0.188
39
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.188
40
P BLD134 Bladder Cancer 78 0.187
41
LGN002 Legionellosis 61 0.185
42
BRN004 Brain Edema 55 0.184
43
47X002 47,xyy 49 0.177
44
P DRM053 Dermatitis, Atopic 66 0.174
45
DYS015 Dysentery 50 0.172
46
P MTH007 Methemoglobinemia 46 0.167
47
GTR002 Goiter 52 0.161
48
P CLR023 Colorectal Cancer 98 0.161
49
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.159
50
ANX004 Anoxia 42 0.158
51
OCL069 Ocular Motor Apraxia 51 0.153
52
P HRT032 Heart Disease 75 0.152
53
c HYP595 Hypertension, Essential 84 0.151
54
SKN016 Skin Disease 63 0.149
55
P LVR013 Liver Disease 68 0.146
56
c CHR684 Chronic Kidney Disease 66 0.142
57
PNG002 Pain Agnosia 51 0.140
58
P HYP086 Hypothyroidism 68 0.139
59
PLM031 Poliomyelitis 57 0.139
60
CNS004 Constipation 57 0.138
61
P GST053 Gastric Cancer 83 0.134
62
P CTR002 Cataract 60 0.134
63
DMP001 Dumping Syndrome 44 0.134
64
P SZR006 Seizure Disorder 58 0.133
65
GRD001 Giardiasis 45 0.133
66
c ACT071 Acute Kidney Failure 59 0.132
67
VSL002 Visual Epilepsy 58 0.132
68
P GST044 Gastritis 55 0.130
69
MTH071 Methane Production 26 0.130
70
LPT001 Leptospirosis 66 0.128
71
AVN001 Avian Influenza 56 0.128
72
P HPT023 Hepatocellular Carcinoma 100 0.127
73
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.126
74
NNL006 Non-Alcoholic Steatohepatitis 51 0.126
75
P PSR002 Psoriasis 62 0.125
76
PST011 Pustulosis of Palm and Sole 52 0.124
77
P NPH012 Nephrotic Syndrome 63 0.123
78
P SLM003 Salmonellosis 54 0.123
79
PST092 Posttransplant Acute Limbic Encephalitis 29 0.123
80
AGN016 Aging 56 0.122
81
c HPT007 Hepatitis E 52 0.122
82
ALL026 Allergic Hypersensitivity Disease 64 0.121
83
P DBT009 Diabetes Mellitus 64 0.117
84
HYP066 Hyperglycemia 61 0.117
85
HYP005 Hypokalemia 55 0.117
86
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.116
87
P EPL164 Epilepsy 71 0.116
88
GST050 Gastrointestinal System Disease 56 0.116
89
P SKN015 Skin Carcinoma 67 0.115
90
P ENC018 Encephalopathy 61 0.115
91
PRS045 Prostatic Hypertrophy 52 0.115
92
DYS073 Dysphagia 50 0.115
93
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.115
94
P RSP003 Respiratory Failure 74 0.114
95
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.114
96
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.114
97
PRS021 Prostatic Adenoma 51 0.114
98
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.114
99
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.114
100
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.114
101
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.114
102
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.114
103
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.114
104
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.114
105
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.114
106
SPN186 Spinal Cord Injury 60 0.113
107
PRS129 Prostatic Hyperplasia, Benign 49 0.113
108
OST012 Osteoarthritis 78 0.112
109
LNG099 Lung Disease 61 0.112
110
BCK006 Back Pain 42 0.111
111
P ALZ034 Alzheimer Disease 88 0.110
112
CYS001 Cystic Fibrosis 80 0.110
113
P RCT021 Rectum Cancer 53 0.110
114
BRN071 Brain Injury 49 0.110
115
CNT047 Contact Dermatitis 57 0.108
116
MTB004 Metabolic Acidosis 50 0.108
117
ANP008 Anaplastic Oligoastrocytoma 30 0.108
118
P HYD006 Hydrocephalus 65 0.107
119
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.107
120
PPT005 Peptic Ulcer Disease 58 0.107
121
TRM010 Traumatic Brain Injury 53 0.107
122
MNN009 Meningoencephalitis 49 0.107
123
PPL001 Papillary Adenoma 45 0.107
124
PRM004 Primary Amebic Meningoencephalitis 31 0.107
125
P VSC007 Vascular Disease 63 0.105
126
TXC005 Toxic Shock Syndrome 61 0.105
127
GST023 Gastric Ulcer 53 0.105
128
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.104
129
KRT019 Keratitis, Hereditary 67 0.104
130
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.104
131
P RHN004 Rhinitis 57 0.104
132
P PYL005 Pyelonephritis 56 0.104
133
CRB039 Cerebrovascular Disease 69 0.103
134
BRN024 Bronchitis 68 0.103
135
PRT036 Peritonitis 65 0.103
136
KRT009 Keratosis 53 0.103
137
HYP266 Hypoxia 56 0.102
138
P PLY014 Polycystic Kidney Disease 59 0.101
139
ISC004 Ischemia 60 0.100
140
P PRD008 Periodontitis 62 0.099
141
P DDN001 Duodenal Ulcer 50 0.099
142
CRB004 Cerebral Artery Occlusion 44 0.099
143
STN013 Stenotrophomonas Maltophilia Infection 25 0.099
144
P GLM045 Glioma 63 0.097
145
P LYM025 Lymphedema 53 0.097
146
NWC001 Newcastle Disease 44 0.097
147
FTT001 Fatty Liver Disease 61 0.096
148
END030 End Stage Renal Failure 58 0.096
149
P OVR082 Overgrowth Syndrome 50 0.096
150
ESP021 Esophageal Cancer 90 0.095
151
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.095
152
P CRD119 Cardiac Arrest 67 0.095
153
GLL048 Glial Tumor 45 0.095
154
DFC004 Deficiency Anemia 75 0.094
155
c PRC016 Pre-Eclampsia 63 0.094
156
P ADL010 Adult Respiratory Distress Syndrome 63 0.094
157
IRN002 Iron Metabolism Disease 57 0.094
158
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 27 0.094
159
MLR004 Malaria 80 0.093
160
P INF038 Influenza 68 0.093
161
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.093
162
CHL067 Cholecystitis 58 0.093
163
c VRL010 Viral Hepatitis 51 0.093
164
CYT002 Cytokine Deficiency 44 0.093
165
PLY150 Polykaryocytosis Inducer 31 0.093
166
TRC008 Trachoma 53 0.091
167
URM002 Uremia 49 0.091
168
INT017 Intestinal Schistosomiasis 47 0.091
169
NRL016 Neural Tube Defects 82 0.090
170
P KDN017 Kidney Cancer 61 0.090
171
PTH003 Pathologic Nystagmus 51 0.090
172
RFL002 Reflex Epilepsy 38 0.090
173
MYC016 Mycobacterium Gordonae 21 0.090
174
AMN003 Amnestic Disorder 54 0.089
175
P INT068 Intestinal Disease 52 0.089
176
TLR001 Tularemia 49 0.089
177
INP001 Inappropriate Adh Syndrome 49 0.089
178
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.089
179
DPS001 Dipsogenic Diabetes Insipidus 23 0.089
180
ADL002 Adult Syndrome 69 0.088
181
c RHB024 Rhabdomyosarcoma 2 65 0.088
182
NTR005 Nutritional Deficiency Disease 61 0.088
183
c ATS347 Autosomal Dominant Polycystic Kidney Disease 59 0.086
184
P HDC001 Headache 57 0.086
185
BNR002 Bone Resorption Disease 48 0.086
186
CMP002 Campylobacteriosis 46 0.086
187
END028 Endemic Goiter 37 0.086
188
CHL079 Children's Interstitial Lung Disease 27 0.086
189
P CRN300 Coronary Heart Disease 1 63 0.085
190
P GLM007 Glomerulonephritis 57 0.085
191
SHG001 Shigellosis 55 0.085
192
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.084
193
ALC007 Alcohol Dependence 66 0.084
194
GST092 Gastroesophageal Reflux 65 0.084
195
LPD008 Lipid Metabolism Disorder 62 0.084
196
c PNS012 Paine Syndrome 61 0.084
197
P EXN002 Exanthem 57 0.084
198
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.084
199
P LTR001 Lateral Sclerosis 53 0.084
200
P ECL001 Eclampsia 51 0.084
201
P BRS047 Breast Cancer 96 0.082
202
P PNC035 Pancreatic Cancer 84 0.082
203
HYP056 Hypoglycemia 66 0.082
204
ATH013 Atherosclerosis Susceptibility 66 0.082
205
IRR002 Irritable Bowel Syndrome 63 0.082
206
CLT003 Colitis 62 0.082
207
BRC012 Brucellosis 61 0.082
208
P TXP001 Toxoplasmosis 60 0.082
209
P HYP076 Hyperthyroidism 55 0.082
210
P OPN001 Open-Angle Glaucoma 49 0.082
211
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.081
212
ALL003 Allergic Rhinitis 67 0.081
213
P ADN016 Adenocarcinoma 64 0.081
214
P INT070 Intestinal Obstruction 58 0.081
215
BCT022 Bacterial Infectious Disease 56 0.081
216
P INF037 Inflammatory Bowel Disease 56 0.081
217
STR067 Stroke, Ischemic 80 0.080
218
HMN044 Human Immunodeficiency Virus Type 1 71 0.080
219
PRT058 Pure Autonomic Failure 59 0.080
220
RHM027 Rheumatic Disease 56 0.080
221
c CHR098 Chronic Pyelonephritis 35 0.080
222
DWN001 Down Syndrome 70 0.078
223
P PLM037 Pulmonary Hypertension 68 0.078
224
FBR047 Fibromyalgia 59 0.078
225
MST005 Mastitis 53 0.078
226
PRP027 Peripheral Vascular Disease 71 0.077
227
P PNM007 Pneumonia 68 0.077
228
P HPT021 Hepatitis 67 0.077
229
OST159 Osteogenic Sarcoma 66 0.077
230
P NTR004 Neutropenia 63 0.077
231
c GLC092 Glaucoma, Primary Open Angle 62 0.077
232
ACQ007 Acquired Immunodeficiency Syndrome 60 0.077
233
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.077
234
ENT011 Enterocolitis 50 0.077
235
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.077
236
PLM001 Pulmonary Tuberculosis 70 0.075
237
MLD001 Melioidosis 67 0.075
238
P HYP069 Hyperparathyroidism 62 0.075
239
P ENC004 Encephalitis 61 0.075
240
GNG013 Gingivitis 59 0.075
241
HLC007 Helicobacter Pylori Infection 59 0.075
242
P URT039 Urticaria 58 0.075
243
PPL022 Papilloma 54 0.075
244
HDN002 Head Injury 45 0.075
245
SQM002 Squamous Cell Papilloma 42 0.075
246
P NRF023 Neurofibromatosis, Type Ii 76 0.074
247
P OST002 Osteoporosis 73 0.074
248
ULC004 Ulcerative Colitis 73 0.074
249
P MYC007 Myocardial Infarction 70 0.074
250
P MSC005 Muscular Dystrophy 66 0.074
251
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.074
252
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.074
253
SYN036 Syncope 45 0.074
254
c ACT004 Acute Diarrhea 39 0.074
255
HVY002 Heavy Metal Poisoning 22 0.074
256
P OVR042 Ovarian Cancer 89 0.072
257
P NRB001 Neuroblastoma 71 0.072
258
P CNJ013 Conjunctivitis 65 0.072
259
P TRN020 Turner Syndrome 65 0.072
260
P NRM001 Neuromyelitis Optica 60 0.072
261
CHL123 Chlamydia 59 0.072
262
IGR001 Ige Responsiveness, Atopic 59 0.072
263
EXT034 Extrinsic Allergic Alveolitis 58 0.072
264
PLG002 Plague 57 0.072
265
c SVR001 Severe Acute Respiratory Syndrome 55 0.072
266
IMP005 Impotence 52 0.072
267
ENT004 Enthesopathy 48 0.072
268
ATX019 Ataxia with Vitamin E Deficiency 48 0.072
269
IRR003 Irritant Dermatitis 47 0.072
270
CHD004 Chudley-Mccullough Syndrome 44 0.072
271
RRS014 Rare Surgical Neurologic Disease 32 0.072
272
BNG077 Benign Idiopathic Neonatal Seizures 26 0.072
273
GT001 Gout 63 0.071
274
DPR016 Depression 63 0.071
275
P CRN018 Coronary Artery Anomaly 63 0.071
276
c ACT068 Acute Cystitis 63 0.071
277
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.071
278
P END044 Endometriosis 62 0.071
279
P BND020 Bone Disease 59 0.071
280
P INF032 Infertility 57 0.071
281
c ACT075 Acute Myocardial Infarction 56 0.071
282
P ART021 Arteriosclerosis 54 0.071
283
CHR100 Chronic Ulcer of Skin 53 0.071
284
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.071
285
CYN002 Cyanosis, Transient Neonatal 45 0.071
286
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.071
287
CRH001 Crohn's Disease 74 0.069
288
c MGR028 Migraine with or Without Aura 1 69 0.069
289
LSH001 Leishmaniasis 63 0.069
290
ANR007 Anorexia Nervosa 63 0.069
291
c MCR113 Microvascular Complications of Diabetes 3 52 0.069
292
P CHR345 Chronic Pain 50 0.069
293
P KLZ004 Kala-Azar 1 41 0.069
295
MST021 Meester-Loeys Syndrome 33 0.069
296
HND015 Hand Skill, Relative 33 0.069
297
MYC015 Mycobacterium Fortuitum 31 0.069
298
IMM167 Immune Deficiency Disease 78 0.067
299
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.067
300
CLN015 Colon Adenocarcinoma 63 0.067
301
P CYS018 Cystitis 59 0.067
302
PNM008 Pneumothorax 56 0.067
303
ECH003 Echinococcosis 53 0.067
304
c MCR120 Microvascular Complications of Diabetes 7 47 0.067
305
SBC016 Subacute Delirium 44 0.067
306
c MCR130 Microvascular Complications of Diabetes 6 41 0.067
307
c MCR133 Microvascular Complications of Diabetes 4 41 0.067
308
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.067
309
c HYP836 Hypercholesterolemia, Familial, 1 72 0.066
310
P LKM002 Leukemia 66 0.066
311
DPH001 Diphtheria 60 0.066
312
STT001 Status Epilepticus 59 0.066
313
HYD002 Hydronephrosis 59 0.066
314
NWB001 Newborn Respiratory Distress Syndrome 58 0.066
315
P BPL003 Bipolar Disorder 56 0.066
316
P HYP083 Hypopituitarism 53 0.066
317
ART140 Arteries, Anomalies of 53 0.066
318
P RNL015 Renal Hypertension 48 0.066
319
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.066
320
c MJR024 Major Affective Disorder 9 41 0.066
321
c MJR022 Major Affective Disorder 8 38 0.066
322
STC004 Stachybotrys Chartarum 34 0.066
323
MYC014 Mycobacterium Chelonae 32 0.066
324
GLB015 Glioblastoma Multiforme 75 0.064
325
P AMY004 Amyloidosis 70 0.064
326
P HRP006 Herpes Simplex 65 0.064
327
PRT013 Portal Hypertension 60 0.064
328
THY029 Thyroid Carcinoma 59 0.064
329
BRN056 Bronchopulmonary Dysplasia 57 0.064
330
P NRP001 Neuropathy 56 0.064
331
ALL010 Allergic Contact Dermatitis 55 0.064
332
STM007 Stomatitis 49 0.064
333
c PCH010 Pachyonychia Congenita 3 43 0.064
334
SCR035 Sacral Agenesis with Vertebral Anomalies 38 0.064
335
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.064
336
MYX011 Myxozoa 17 0.064
337
P LNG032 Lung Cancer 97 0.062
338
INS024 Insulin-Like Growth Factor I 79 0.062
339
P LNG064 Lung Cancer Susceptibility 3 77 0.062
340
AST005 Asthma 77 0.062
341
P MLT020 Multiple Sclerosis 72 0.062
342
P MNN013 Meningitis 65 0.062
343
P ATS364 Autism 65 0.062
344
TTN003 Tetanus 64 0.062
345
ATM095 Autoimmune Disease 61 0.062
346
CHL068 Cholestasis 60 0.062
347
MTH009 Mouth Disease 56 0.062
348
P LYM031 Lymphocytic Leukemia 55 0.062
349
OCL006 Ocular Hypertension 53 0.062
350
GLS018 Glass Syndrome 53 0.062
351
P AST007 Astrocytoma 50 0.062
352
VCC001 Vaccinia 49 0.062
353
RST023 Resting Heart Rate, Variation in 41 0.062
354
FSC002 Fascioliasis 41 0.062
355
DRC001 Dracunculiasis 36 0.062
356
DPH003 Diphyllobothriasis 30 0.062
357
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 22 0.062
358
P SCH015 Schizophrenia 75 0.060
359
ANX010 Anxiety 72 0.060
360
P HYP098 Hypereosinophilic Syndrome 66 0.060
361
OST017 Osteomyelitis 64 0.060
362
c FNC043 Fanconi Anemia, Complementation Group E 62 0.060
363
P PNC044 Pancreatitis 61 0.060
364
RTN017 Retinal Detachment 60 0.060
365
c PRM005 Primary Hyperparathyroidism 58 0.060
366
P CND004 Candidiasis 57 0.060
367
MNT002 Mental Depression 57 0.060
368
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.060
369
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.060
370
NRG002 Neurogenic Bladder 54 0.060
371
P TRM003 Tremor 53 0.060
372
CCC002 Coccidiosis 50 0.060
373
ACN019 Acanthamoeba Keratitis 31 0.060
374
URT052 Urticaria, Aquagenic 21 0.060
375
P PRS040 Prostate Cancer 97 0.058
376
P DMN002 Dementia 67 0.058
377
P LPR021 Leprosy 3 67 0.058
378
SDD001 Sudden Infant Death Syndrome 61 0.058
379
DCB001 Decubitus Ulcer 60 0.058
380
P PTN014 Patent Ductus Arteriosus 1 60 0.058
381
c ACT027 Acute Pancreatitis 59 0.058
382
P ALC033 Alcohol Use Disorder 58 0.058
383
PTT041 Pituitary Stalk Interruption Syndrome 50 0.058
384
HPT014 Hepatorenal Syndrome 50 0.058
385
P TMP001 Temporal Lobe Epilepsy 50 0.058
386
c LRG017 Large Intestine Cancer 47 0.058
387
EPD015 Epidemic Typhus 46 0.058
388
P BNG032 Benign Mesothelioma 45 0.058
389
P OTT001 Otitis Externa 39 0.058
390
SCR003 Secretory Diarrhea 36 0.058
391
HNS001 Hansen's Disease 34 0.058
392
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.058
393
ARG004 Argyria 28 0.058
394
c ATR087 Atrial Standstill 1 74 0.056
395
P ART022 Arthritis 70 0.056
396
P ASP006 Aspergillosis 66 0.056
397
PRT037 Pertussis 65 0.056
398
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.056
399
CLF027 Cleft Palate, Isolated 64 0.056
400
ART002 Arts Syndrome 63 0.056
401
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.056
402
P HML002 Hemolytic Anemia 62 0.056
403
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.056
404
c DNG003 Dengue Disease 59 0.056
405
IRN001 Iron Deficiency Anemia 58 0.056
406
c DWL002 Dowling-Degos Disease 1 58 0.056
407
URN010 Urinary Tract Obstruction 57 0.056
408
P DNG005 Dengue Virus 57 0.056
409
P FBR017 Fibrosarcoma 56 0.056
410
FDB001 Foodborne Botulism 56 0.056
411
WST005 West Nile Virus 55 0.056
412
PRN019 Perinatal Necrotizing Enterocolitis 54 0.056
413
HYP060 Hyperinsulinism 54 0.056
414
GLC003 Glucose Intolerance 54 0.056
415
HMS001 Hemosiderosis 54 0.056
416
P HML001 Hemolytic-Uremic Syndrome 52 0.056
417
P ACT105 Acute Mountain Sickness 52 0.056
418
ILS001 Ileus 51 0.056
419
ASP007 Aspiration Pneumonia 48 0.056
420
SCH038 Schopf-Schulz-Passarge Syndrome 47 0.056
421
ANR004 Anuria 46 0.056
422
P HMR005 Hemorrhoid 46 0.056
423
LWC001 Low Compliance Bladder 42 0.056
424
MYC017 Mycobacterium Kansasii 37 0.056
425
LCH001 Leech Infestation 36 0.056
426
SVR004 Severe Combined Immunodeficiency 73 0.054
427
MSC157 Muscular Dystrophy, Duchenne Type 71 0.054
428
OTT002 Otitis Media 71 0.054
429
P SLP006 Sleep Apnea 69 0.054
430
P THR014 Thrombocytopenia 68 0.054
431
P NSP012 Nasopharyngeal Carcinoma 67 0.054
432
ANG054 Angina Pectoris 66 0.054
433
HPT019 Hepatic Encephalopathy 60 0.054
434
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.054
435
TRG002 Trigeminal Neuralgia 60 0.054
436
CMM005 Common Cold 56 0.054
437
INT075 Intracranial Hypertension 53 0.054
438
PRT029 Parathyroid Adenoma 50 0.054
439
P RNV001 Renovascular Hypertension 49 0.054
440
BCT004 Bacteriuria 48 0.054
441
BBS001 Babesiosis 48 0.054
442
P MRC003 Mercury Poisoning 48 0.054
443
URN003 Urinary Schistosomiasis 44 0.054
444
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.054
445
ALL014 Allergic Encephalomyelitis 39 0.054
446
PRR015 Preauricular Fistulae, Congenital 21 0.054
447
BRN028 Brain Cancer 73 0.052
448
P LYM118 Lymphoma 68 0.052
449
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.052
450
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.052
451
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.052
452
NRM005 Neuromuscular Disease 63 0.052
453
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.052
454
EYD002 Eye Disease 58 0.052
455
P BCL017 B-Cell Lymphoma 58 0.052
456
DSS008 Disease of Mental Health 57 0.052
457
P PRP019 Peripheral Nervous System Disease 57 0.052
458
ALL006 Allergic Asthma 56 0.052
459
ANN002 Anencephaly 55 0.052
460
VSC003 Visceral Leishmaniasis 55 0.052
461
STV003 Stuve-Wiedemann Syndrome 53 0.052
462
OST011 Osteomalacia 52 0.052
463
PRS034 Parasitic Helminthiasis Infectious Disease 49 0.052
464
HMG002 Hemoglobinuria 49 0.052
465
ATN005 Autonomic Dysfunction 47 0.052
466
URT010 Ureteral Obstruction 46 0.052
467
HPT004 Hepatic Coma 43 0.052
468
MYL069 Myeloma, Multiple 85 0.050
469
c DLT002 Dilated Cardiomyopathy 79 0.050
470
P SYS005 Systemic Scleroderma 70 0.050
471
MDD011 Mood Disorder 62 0.050
472
YLL002 Yellow Fever 60 0.050
473
ORL011 Oral Cancer 60 0.050
474
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.050
475
RSP019 Respiratory Distress Syndrome in Premature Infants 57 0.050
476
EPT010 Epithelial-Myoepithelial Carcinoma 53 0.050
477
DMY004 Demyelinating Disease 52 0.050
478
SPP010 Suppressor of Tumorigenicity 3 51 0.050
479
ACH005 Achalasia 50 0.050
480
AMB001 Amebiasis 49 0.050
481
PYL006 Pyloric Stenosis 48 0.050
482
BRL010 Buruli Ulcer 45 0.050
483
MYX004 Myxedema 44 0.050
484
P BRB001 Beriberi 44 0.050
485
PRM020 Premenstrual Tension 39 0.050
486
LRY004 Laryngotracheitis 31 0.050
487
CRC001 Cercarial Dermatitis 26 0.050
488
MYC021 Mycobacterium Xenopi 25 0.050
489
CLR014 Clear Cell Adenoma 24 0.050
490
OBS532 Obsolete: Ehlers-Danlos Syndrome, Fibronectinemic Type 15 0.050
491
P RHM011 Rheumatoid Arthritis 80 0.048
492
SCK003 Sickle Cell Anemia 72 0.048
493
MLT157 Multiple System Atrophy 1 70 0.048
494
CHL065 Cholangiocarcinoma 67 0.048
495
CLR108 Colorectal Adenoma 64 0.048
496
P ESP024 Esophagitis 62 0.048
497
P HYP750 Hypertriglyceridemia, Familial 61 0.048
498
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.048
499
P SYP003 Syphilis 59 0.048
500
P BRS044 Breast Adenocarcinoma 59 0.048
501
ANT024 Anthrax Disease 58 0.048
502
P CRD246 Cardiovascular System Disease 56 0.048
503
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.048
504
P PLY019 Polyneuropathy 56 0.048
505
P BRT004 Bartter Disease 55 0.048
506
c GRV008 Graves Disease 1 55 0.048
507
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.048
508
P VNS003 Venous Insufficiency 55 0.048
509
P SHR001 Short Bowel Syndrome 52 0.048
510
c GLL024 Gallbladder Disease 1 52 0.048
511
P LCT001 Lactic Acidosis 51 0.048
512
PLR008 Pleurisy 51 0.048
513
c ACT134 Acute Liver Failure 51 0.048
514
THY030 Thyroid Gland Disease 51 0.048
515
CLR109 Colorectal Adenocarcinoma 50 0.048
516
INT079 Intrahepatic Cholangiocarcinoma 50 0.048
517
VLV047 Volvulus of Midgut 50 0.048
518
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.048
519
CHL004 Cholelithiasis 49 0.048
520
QDR001 Quadriplegia 48 0.048
521
HYP025 Hyperphosphatemia 47 0.048
522
ARC002 Arachnoiditis 42 0.048
523
SPN354 Spinal Arachnoiditis 36 0.048
524
PNT001 Pontiac Fever 30 0.048
525
ACT181 Acute Motor Axonal Neuropathy 26 0.048
526
EXR008 Exercise-Induced Malignant Hyperthermia 21 0.048
527
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.048
528
AQG001 Aquagenic Pruritus 19 0.048
529
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.045
530
P PRK057 Parkinson Disease, Late-Onset 76 0.045
531
c BSL007 Basal Cell Carcinoma 68 0.045
532
P MYC084 Mycobacterium Tuberculosis 1 68 0.045
533
SRC014 Sarcoma 65 0.045
534
c CNG006 Congenital Hypothyroidism 65 0.045
535
P ORT004 Orthostatic Intolerance 63 0.045
536
P VSC011 Vasculitis 62 0.045
537
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.045
538
APP008 Appendicitis 60 0.045
539
P BRN022 Bronchiectasis 59 0.045
540
ANR040 Aneurysm 58 0.045
541
PHR003 Pharyngitis 56 0.045
542
P ALP008 Alopecia 56 0.045
543
P MLN007 Male Infertility 56 0.045
544
P NRM002 Normal Pressure Hydrocephalus 56 0.045
545
MCS002 Mucositis 55 0.045
546
P PLY018 Polycythemia 55 0.045
547
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.045
548
P MYP006 Myopia 55 0.045
549
P PTT006 Pituitary Adenoma 54 0.045
550
CHK001 Chikungunya 53 0.045
551
NRT004 Neuritis 53 0.045
552
c LTN004 Late-Onset Retinal Degeneration 52 0.045
553
P INS002 in Situ Carcinoma 52 0.045
554
FML063 Familial Glucocorticoid Deficiency 51 0.045
555
P HYP040 Hypospadias 51 0.045
556
SCB001 Scabies 51 0.045
557
SPN035 Spindle Cell Sarcoma 51 0.045
558
P MTR003 Mitral Valve Stenosis 50 0.045
559
P OTS001 Otosclerosis 50 0.045
560
ASC010 Ascaris Lumbricoides Infection 49 0.045
561
c CHR431 Chronic Venous Insufficiency 49 0.045
562
AST006 Astigmatism 47 0.045
563
RYN005 Raynaud Phenomenon 46 0.045
564
EXS001 Exostosis 46 0.045
565
ATN004 Autonomic Neuropathy 44 0.045
566
c RTN047 Retinitis Pigmentosa 18 44 0.045
567
IDP033 Idiopathic Edema 43 0.045
568
CHP002 Chops Syndrome 42 0.045
569
MYF002 Myofascial Pain Syndrome 42 0.045
570
P HYP265 Hypotonia 42 0.045
571
RDN001 Reading Disorder 40 0.045
572
PLY100 Polyploidy 40 0.045
573
TRP004 Tropical Sprue 39 0.045
574
SCR011 Scrapie 38 0.045
575
NPH013 Nephrogenic Syndrome of Inappropriate Antidiuresis 36 0.045
576
ASC001 Ascaridiasis 35 0.045
577
GRN004 Granulomatous Amebic Encephalitis 29 0.045
578
c SYS001 Systemic Lupus Erythematosus 86 0.043
579
PHN003 Phenylketonuria 75 0.043
580
P SRC025 Sarcoidosis 1 70 0.043
581
RCK004 Rickets 69 0.043
582
LYM133 Lymphoma, Hodgkin, Classic 69 0.043
583
P CLC063 Celiac Disease 1 68 0.043
584
CRB037 Cerebral Palsy 68 0.043
585
PSY004 Psychotic Disorder 67 0.043
586
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.043
587
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.043
588
CHG001 Chagas Disease 66 0.043
589
P MTR014 Motor Neuron Disease 64 0.043
590
TBC004 Tobacco Addiction 64 0.043
591
MSC007 Muscle Hypertrophy 63 0.043
592
P INT143 Interstitial Cystitis 61 0.043
593
PST028 Post-Traumatic Stress Disorder 58 0.043
594
RBS001 Rabies 58 0.043
595
LYM027 Lymphopenia 57 0.043
596
P END033 Endocarditis 57 0.043
597
BLR008 Bilirubin Metabolic Disorder 57 0.043
598
HPT022 Hepatoblastoma 56 0.043
599
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.043
600
P SBS003 Substance Abuse 54 0.043
601
P ICH004 Ichthyosis 54 0.043
602
c PRD040 Periodontitis, Chronic 54 0.043
603
GST009 Gastroschisis 54 0.043
604
PRP016 Paraplegia 53 0.043
605
P FBR031 Febrile Seizures 51 0.043
606
CYS008 Cystic Echinococcosis 50 0.043
607
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.043
608
ACT084 Acute Stress Disorder 48 0.043
609
c PRM093 Premature Ovarian Failure 7 47 0.043
610
CNT025 Central Pontine Myelinolysis 45 0.043
611
KWS001 Kwashiorkor 45 0.043
612
c PRM038 Primary Agammaglobulinemia 43 0.043
613
SNL007 Senile Cataract 42 0.043
614
P RRH023 Rare Hereditary Hemochromatosis 41 0.043
615
OPS001 Opisthorchiasis 40 0.043
616
P CRN026 Corneal Edema 40 0.043
617
SWL001 Swallowing Disorders 38 0.043
618
ABD010 Abdominal Wall Defect 35 0.043
619
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.043
620
OSM001 Osmotic Diarrhea 32 0.043
621
RSP007 Respiratory Distress Syndrome, Infant 30 0.043
622
c MNN043 Meningioma, Familial 74 0.040
623
LPT014 Leptin Deficiency or Dysfunction 73 0.040
624
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.040
625
c LKM063 Leukemia, Chronic Myeloid 71 0.040
626
P LKM062 Leukemia, Acute Lymphoblastic 68 0.040
627
c ATS007 Autism Spectrum Disorder 67 0.040
628
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.040
629
CRN036 Craniopharyngioma 65 0.040
630
P LNG028 Long Qt Syndrome 65 0.040
631
KWS002 Kawasaki Disease 64 0.040
632
P MYP004 Myopathy 64 0.040
633
IDP011 Idiopathic Interstitial Pneumonia 63 0.040
634
MNN042 Meningioma, Radiation-Induced 62 0.040
635
P PLM036 Pulmonary Fibrosis 61 0.040
636
P VNT002 Ventricular Septal Defect 60 0.040
637
DBT087 Diabetes Insipidus, Neurohypophyseal 59 0.040
638
LYM021 Lymphadenitis 58 0.040
639
P UVT001 Uveitis 57 0.040
640
VSC002 Vascular Dementia 57 0.040
641
PRS047 Prostatitis 56 0.040
642
TRN018 Transitional Cell Carcinoma 56 0.040
643
PRT038 Protein-Energy Malnutrition 54 0.040
644
JPN002 Japanese Encephalitis 54 0.040
645
LST001 Listeriosis 54 0.040
646
GST037 Gastroparesis 53 0.040
647
HYP014 Hyperuricemia 51 0.040
648
MYL020 Myelomeningocele 51 0.040
649
HRT011 Heart Septal Defect 50 0.040
650
CHL061 Childhood Leukemia 50 0.040
651
HYP781 Hypoascorbemia 50 0.040
652
BHR001 Behr Syndrome 49 0.040
653
CLN045 Colonic Benign Neoplasm 49 0.040
654
URT001 Urethritis 48 0.040
655
P CMP008 Compartment Syndrome 48 0.040
656
MCR020 Microsporidiosis 48 0.040
657
P OBS001 Obstructive Jaundice 48 0.040
658
SPL018 Splenomegaly 48 0.040
659
SPN021 Spinal Meningioma 47 0.040
660
MCR018 Microcytic Anemia 47 0.040
661
P PRD021 Periodic Paralysis 46 0.040
662
c DRM054 Dermatitis, Atopic, 2 45 0.040
663
CRT015 Carotid Artery Occlusion 44 0.040
664
HPT067 Hepatocellular Adenoma 43 0.040
665
PRS063 Paresthesia 43 0.040
666
MCL003 Macular Holes 42 0.040
667
KLB003 Klebsiella Pneumonia 39 0.040
668
SCR001 Secretory Meningioma 37 0.040
669
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.040
670
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.040
671
CND006 Candida Glabrata 32 0.040
672
GST039 Gastroduodenitis 32 0.040
673
c NRM008 Neuromyelitis Optica Spectrum Disorder 31 0.040
674
CRC034 Carcinoma Showing Thymus-Like Differentiation 23 0.040
675
GST019 Gastrointestinal Stromal Tumor 76 0.037
676
CRV035 Cervical Cancer 76 0.037
677
c THR092 Thrombophilia Due to Thrombin Defect 73 0.037
678
P FML011 Familial Adenomatous Polyposis 72 0.037
679
ACR007 Acromegaly 71 0.037
680
WLS001 Wilson Disease 70 0.037
681
GST040 Gastric Adenocarcinoma 70 0.037
682
PLY001 Polycythemia Vera 69 0.037
683
SKN019 Skin Melanoma 67 0.037
684
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.037
685
HYP020 Hyperprolactinemia 64 0.037
686
PTT046 Pituitary Hormone Deficiency, Combined, 2 63 0.037
687
P ART023 Arthropathy 62 0.037
688
P HMN010 Hemangioma 61 0.037
689
c BRN108 Branchiootic Syndrome 1 61 0.037
690
P LPS004 Lupus Erythematosus 61 0.037
691
MSL001 Measles 61 0.037
692
P MYC008 Myocarditis 59 0.037
693
BRN002 Bronchiolitis 59 0.037
694
PLM033 Pulmonary Embolism 59 0.037
695
ANG020 Angiosarcoma 58 0.037
696
QFV001 Q Fever 58 0.037
697
THR024 Thrombosis 56 0.037
698
SYN007 Synovitis 55 0.037
699
HMP005 Hemiplegia 54 0.037
700
P CYS039 Cystic Kidney Disease 54 0.037
701
MYM001 Myoma 53 0.037
702
CLF001 Cleft Lip 53 0.037
703
PRP080 Peripheral Artery Disease 53 0.037
704
SBC001 Subacute Sclerosing Panencephalitis 52 0.037
705
EXP004 Exophthalmos 52 0.037
706
TND005 Tendinitis 52 0.037
707
ASP003 Aseptic Meningitis 51 0.037
708
P SCK005 Sickle Cell Disease 50 0.037
709
OPT003 Opiate Dependence 50 0.037
710
KRT002 Keratomalacia 48 0.037
711
PRD004 Prediabetes Syndrome 47 0.037
712
P END046 Endometritis 47 0.037
713
CLN019 Colonic Disease 46 0.037
714
ALB002 Albinism 46 0.037
715
KRT008 Keratopathy 46 0.037
716
FLL008 Folliculitis 46 0.037
717
ACT003 Acute Kidney Tubular Necrosis 45 0.037
718
RTR001 Retrograde Amnesia 45 0.037
719
DVR002 Diverticulitis 44 0.037
720
RFR003 Refractive Error 44 0.037
721
DWR001 Dwarfism 44 0.037
722
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 43 0.037
723
URT037 Urethral Stricture 43 0.037
724
GRW007 Growth Hormone Deficiency 43 0.037
725
MYC013 Mycobacterium Abscessus 42 0.037
726
KLD004 Keloid Disorder 40 0.037
727
ANS003 Anisakiasis 39 0.037
728
WLL004 Wallerian Degeneration 39 0.037
729
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 38 0.037
730
P MXL015 Maxillary Sinusitis 37 0.037
731
WHP002 Whiplash 36 0.037
732
SRC011 Sarcocystosis 30 0.037
733
CYC002 Cyclosporiasis 27 0.037
734
THL004 Theileriasis 27 0.037
735
CGT001 Ciguatera Fish Poisoning 21 0.037
736
PRT021 Parathyroid Transitional Clear Cell Adenoma 17 0.037
737
MGB001 Megabladder, Congenital 15 0.037
739
P GLM040 Glioma Susceptibility 1 81 0.034
740
P PHC003 Pheochromocytoma 71 0.034
741
P CNR004 Cone-Rod Dystrophy 2 71 0.034
742
MLN008 Melanoma 69 0.034
743
P MJR001 Major Depressive Disorder 68 0.034
744
CRP001 Carpal Tunnel Syndrome 67 0.034
745
c JVN010 Juvenile Rheumatoid Arthritis 67 0.034
746
P ANG001 Angelman Syndrome 67 0.034
747
P ATR011 Atrial Fibrillation 66 0.034
748
OVR029 Ovarian Hyperstimulation Syndrome 63 0.034
749
TRN015 Transient Cerebral Ischemia 62 0.034
750
INT002 Intermittent Claudication 61 0.034
751
OST003 Osteonecrosis 61 0.034
752
ING001 Inguinal Hernia 60 0.034
753
INS001 Insulinoma 60 0.034
754
SQM006 Squamous Cell Carcinoma 60 0.034
755
PNM010 Pneumothorax, Primary Spontaneous 60 0.034
756
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.034
757
P GLL022 Guillain-Barre Syndrome 59 0.034
758
P TRC086 Trichohepatoenteric Syndrome 1 59 0.034
759
P PLV020 Pelvic Organ Prolapse 59 0.034
760
MNR012 Meniere Disease 57 0.034
761
P BNC003 Bone Cancer 57 0.034
762
GST033 Gestational Diabetes 57 0.034
763
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 57 0.034
764
c MST023 Mesothelioma, Malignant 57 0.034
765
TNS005 Tonsillitis 57 0.034
766
ERY051 Erythroleukemia, Familial 56 0.034
767
P MYS005 Myositis 56 0.034
768
ZLL002 Zollinger-Ellison Syndrome 55 0.034
769
RSC001 Rosacea 55 0.034
770
CRC006 Carcinoid Syndrome 55 0.034
771
VGN023 Vaginitis 55 0.034
772
CLL003 Cellulitis 54 0.034
773
FCL014 Focal Epilepsy 54 0.034
774
PRC013 Pericarditis 54 0.034
775
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 53 0.034
776
RHM028 Rheumatic Heart Disease 53 0.034
777
INT051 Intussusception 53 0.034
778
NPH003 Nephrocalcinosis 51 0.034
779
TLN003 Telangiectasis 51 0.034
780
MYL001 Myelitis 51 0.034
781
PPT001 Peptic Esophagitis 51 0.034
782
PLM017 Pulmonary Alveolar Microlithiasis 50 0.034
783
TRY001 Trypanosomiasis 50 0.034
784
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.034
785
FDL002 Food Allergy 49 0.034
786
PLC008 Placenta Disease 49 0.034
787
SLP001 Sleeping Sickness 48 0.034
788
ANT018 Anthracosis 48 0.034
789
STM006 Stomach Disease 48 0.034
790
HRD005 Hard Palate Cancer 46 0.034
791
INT067 Interstitial Nephritis 46 0.034
792
PLY012 Polyhydramnios 46 0.034
793
TST014 Testicular Cancer 46 0.034
794
ADR040 Adrenal Gland Pheochromocytoma 46 0.034
795
KRT013 Keratolytic Winter Erythema 46 0.034
796
P BLR006 Biliary Tract Disease 46 0.034
797
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.034
798
P SBR004 Seborrheic Dermatitis 45 0.034
799
P OVR046 Ovarian Cyst 45 0.034
800
PTT037 Pituitary Tumors 44 0.034
801
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.034
802
TND004 Tendinopathy 44 0.034
803
PNM013 Pneumococcal Meningitis 43 0.034
804
TNS014 Tenosynovitis 43 0.034
805
ORL015 Oral Squamous Cell Carcinoma 43 0.034
806
IRT001 Iritis 43 0.034
807
MCR011 Microinvasive Gastric Cancer 43 0.034
808
TRP009 Triple X Syndrome 42 0.034
809
PRS036 Parasitic Protozoa Infectious Disease 42 0.034
810
GST020 Gastric Antral Vascular Ectasia 41 0.034
811
49X006 49, Xxxxy Syndrome 41 0.034
812
CRB086 Cerebral Aneurysms 40 0.034
813
VLL006 Villous Adenoma 38 0.034
814
CVT001 Cavitary Optic Disc Anomalies 38 0.034
815
FSR001 Fusariosis 38 0.034
816
KSH004 Kashin-Beck Disease 38 0.034
817
OLV004 Oliver-Mcfarlane Syndrome 37 0.034
818
SHW001 Shwartzman Phenomenon 36 0.034
819
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.034
820
NRD001 Neurodermatitis 32 0.034
821
PRL013 Paralytic Poliomyelitis 31 0.034
822
RRD056 Rare Disease in Surgical Orthopedic 28 0.034
823
ENM002 Enamel Erosion 27 0.034
824
P SLP004 Salpingo-Oophoritis 24 0.034
825
AQG004 Aquagenic Syringeal Acrokeratoderma 17 0.034
826
c LKM061 Leukemia, Acute Myeloid 83 0.030
827
c LKM071 Leukemia, Chronic Lymphocytic 79 0.030
828
P MDL005 Medulloblastoma 77 0.030
829
c SPN225 Spondyloarthropathy 1 73 0.030
830
P RTN024 Retinoblastoma 72 0.030
831
c EXD008 Exudative Vitreoretinopathy 1 69 0.030
832
CRT072 Creutzfeldt-Jakob Disease 69 0.030
833
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.030
834
OBS002 Obsessive-Compulsive Disorder 68 0.030
835
P FLL037 Follicular Lymphoma 66 0.030
836
P NRV007 Nervous System Disease 66 0.030
837
c MCL013 Mucolipidosis Iv 64 0.030
838
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 63 0.030
839
LYM017 Lyme Disease 63 0.030
840
NRF026 Neurofibromatosis, Type Iv, of Riccardi 63 0.030
841
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.030
842
CHR066 Chronic Fatigue Syndrome 61 0.030
843
CRC021 Carcinosarcoma 61 0.030
844
VRL011 Viral Infectious Disease 61 0.030
845
MCR013 Microphthalmia 60 0.030
846
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.030
847
ETN001 Eating Disorder 59 0.030
848
P SLP005 Sleep Disorder 59 0.030
849
INT066 Interstitial Lung Disease 59 0.030
850
END081 Endosteal Hyperostosis, Autosomal Dominant 59 0.030
851
c HPT016 Hepatitis B 59 0.030
852
SPN027 Spinal Stenosis 59 0.030
853
CRD132 Cardiac Conduction Defect 59 0.030
854
P OPT009 Optic Neuritis 56 0.030
855
ORL005 Oral Candidiasis 56 0.030
856
SML019 Smallpox 56 0.030
857
SLC006 Silicosis 56 0.030
858
P PLM034 Pulmonary Emphysema 56 0.030
859
P PNM006 Pneumoconiosis 55 0.030
860
PRP030 Purpura 55 0.030
861
MCL006 Macular Retinal Edema 55 0.030
862
NRL004 Neuroleptic Malignant Syndrome 55 0.030
863
c BCT007 Bacterial Meningitis 55 0.030
864
ACT058 Active Peptic Ulcer Disease 55 0.030
865
FLR002 Filariasis 55 0.030
866
INT007 Intermediate Coronary Syndrome 55 0.030
867
TNG003 Tongue Cancer 55 0.030
868
DBT010 Diabetic Neuropathy 55 0.030
869
P FML068 Familial Hypocalciuric Hypercalcemia 54 0.030
870
PTT009 Pituitary Gland Disease 54 0.030
871
CYS005 Cysticercosis 54 0.030
872
P RTN016 Retinal Degeneration 53 0.030
873
KRT006 Keratoconjunctivitis 53 0.030
874
OST016 Osteochondrosis 53 0.030
875
c FML008 Familial Retinoblastoma 53 0.030
876
P LCT002 Lactose Intolerance 53 0.030
877
NNT012 Neonatal Jaundice 53 0.030
878
P PNC025 Panic Disorder 53 0.030
879
SPN051 Spondylitis 52 0.030
880
MCN017 Meconium Ileus 52 0.030
881
P END047 Endophthalmitis 52 0.030
882
P MSC003 Muscular Atrophy 52 0.030
883
MTN003 Motion Sickness 52 0.030
884
P TRT010 Teratoma 51 0.030
885
c PRM108 Primary Progressive Multiple Sclerosis 51 0.030
886
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 50 0.030
887
c INF145 Infantile Liver Failure Syndrome 1 50 0.030
888
HYP080 Hypogonadism 50 0.030
889
HYP748 Hypertelorism 50 0.030
890
CRV040 Cervix Carcinoma 50 0.030
891
RSP006 Respiratory System Disease 50 0.030
892
P RNL007 Renal Tubular Acidosis 50 0.030
893
ALV002 Alveolar Echinococcosis 50 0.030
894
PLR007 Pleural Empyema 49 0.030
895
PLM029 Palmoplantar Keratosis 47 0.030
896
WRN003 Wernicke Encephalopathy 47 0.030
897
TNP001 Tinea Pedis 47 0.030
898
LYM019 Lymphosarcoma 47 0.030
899
P HYP733 Hypercalciuria, Absorptive, 2 46 0.030
900
P TRN034 Transverse Myelitis 46 0.030
901
P PRD037 Periodontal Ehlers-Danlos Syndrome 46 0.030
902
OPD001 Opioid Abuse 45 0.030
903
HRN026 Hernia, Hiatus 45 0.030
904
P PLL002 Pellagra 45 0.030
905
CLN044 Colon Adenoma 42 0.030
906
HMP009 Haemophilus Influenzae 42 0.030
907
ASP008 Aspiration Pneumonitis 42 0.030
908
DYS011 Dyskinesia of Esophagus 42 0.030
909
SPS057 Spasticity 41 0.030
910
HYP064 Hypogonadotropism 40 0.030
911
ART103 Arthrogryposis, Mental Retardation, and Seizures 40 0.030
912
HYP001 Hypochromic Microcytic Anemia 38 0.030
913
PLM156 Palmoplantar Carcinoma, Multiple Self-Healing 38 0.030
914
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.030
915
PNC016 Pancreatic Cholera 38 0.030
916
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 37 0.030
917
AKL001 Au-Kline Syndrome 37 0.030
918
BLR004 Biliary Dyskinesia 37 0.030
919
HRN029 Hearing Loss, Noise-Induced 37 0.030
920
SZR028 Seizures, Scoliosis, and Macrocephaly/microcephaly Syndrome 36 0.030
921
ACL001 Acalculous Cholecystitis 35 0.030
922
PYR009 Pyridoxine Deficiency Anemia 34 0.030
923
c ACQ047 Acquired Methemoglobinemia 34 0.030
924
AMN014 Aminopterin Syndrome Sine Aminopterin 33 0.030
925
BWN006 Bowen's Disease 32 0.030
926
MLC004 Mulchandani-Bhoj-Conlin Syndrome 32 0.030
927
MTG001 Metagonimiasis 32 0.030
928
INF009 Inflammatory Spondylopathy 32 0.030
929
HYP346 Hypotrichosis and Recurrent Skin Vesicles 29 0.030
930
OCC001 Occupational Dermatitis 29 0.030
932
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.030
933
CYT018 Cytochrome P450 2d6 Variant 27 0.030
934
ACR039 Acromegaloid Hypertrichosis Syndrome 27 0.030
935
DST016 Distomatosis 26 0.030
936
AMB007 Amoebic Keratitis 20 0.030
937
P ATX030 Ataxia-Telangiectasia 83 0.026
938
CNN003 Conn's Syndrome 79 0.026
939
KPS004 Kaposi Sarcoma 75 0.026
940
P HNT016 Huntington Disease 71 0.026
941
MYL009 Myelodysplastic Syndrome 70 0.026
942
c FML021 Familial Hypercholesterolemia 68 0.026
943
PNC129 Pancreatic Adenocarcinoma 67 0.026
944
THY111 Thyroid Carcinoma, Familial Medullary 67 0.026
945
MNT001 Mantle Cell Lymphoma 66 0.026
946
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 65 0.026
947
APN008 Apnea, Obstructive Sleep 65 0.026
948
BRR014 Barrett Esophagus 64 0.026
949
PPL049 Papillon-Lefevre Syndrome 63 0.026
950
P LMY004 Leiomyosarcoma 62 0.026
951
P RHB003 Rhabdomyosarcoma 62 0.026
952
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.026
954
P PRP029 Porphyria 62 0.026
955
CTN007 Cutaneous Leishmaniasis 61 0.026
956
BLD131 Bladder Urothelial Carcinoma 61 0.026
957
P MVM001 Movement Disease 61 0.026
958
CNV004 Canavan Disease 60 0.026
959
VRC005 Varicose Veins 60 0.026
960
P ATR010 Atrial Heart Septal Defect 60 0.026
961
CRD223 Cardiac Arrhythmia 60 0.026
962
P MYL006 Myeloid Leukemia 60 0.026
963
CHC001 Chickenpox 60 0.026
964
DNG002 Dengue Hemorrhagic Fever 60 0.026
965
c VSC019 Vesicoureteral Reflux 1 59 0.026
966
CRY035 Cryptorchidism, Unilateral or Bilateral 59 0.026
967
CMP010 Complex Regional Pain Syndrome 58 0.026
968
THY122 Thyroid Gland Cancer 58 0.026
969
BRS051 Breast Disease 58 0.026
970
P OPT006 Optic Nerve Disease 57 0.026
971
BLM002 Bulimia Nervosa 57 0.026
972
P PRN023 Prion Disease 57 0.026
973
P SJG008 Sjogren Syndrome 56 0.026
974
PLS011 Plasmacytoma 56 0.026
975
PTN001 Patent Foramen Ovale 56 0.026
976
P PLY011 Polycystic Ovary Syndrome 56 0.026
977
P GRV001 Graves' Disease 55 0.026
978
ATR057 Atrioventricular Block 55 0.026
979
LMB062 Limb Ischemia 55 0.026
980
PLV003 Pelvic Inflammatory Disease 55 0.026
981
CPL003 Capillary Leak Syndrome 55 0.026
982
P FTL001 Fetal Alcohol Syndrome 55 0.026
983
PRT002 Paratyphoid Fever 55 0.026
984
EXF001 Exfoliation Syndrome 54 0.026
985
GLS001 Gliosarcoma 54 0.026
986
SNS003 Sensory Peripheral Neuropathy 53 0.026
987
HMC014 Homocysteinemia 53 0.026
988
P THY032 Thyroiditis 53 0.026
989
P RTN018 Retinal Disease 52 0.026
990
CRH005 Crohn's Colitis 52 0.026
991
MCN007 Meconium Aspiration Syndrome 52 0.026
992
CMB003 Combined T Cell and B Cell Immunodeficiency 52 0.026
993
DRM011 Dermatophytosis 52 0.026
994
P SML001 Small Cell Carcinoma 52 0.026
995
P ACT008 Actinic Keratosis 52 0.026
996
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.026
997
ANK001 Ankylosis 52 0.026
998
MCR141 Mucormycosis 51 0.026
999
THY125 Thyroid Gland Medullary Carcinoma 51 0.026
1000
ONC002 Onchocerciasis 51 0.026
1001
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.026
1002
P PRC012 Pericardial Effusion 51 0.026
1003
P FNC004 Fanconi Syndrome 50 0.026
1004
BRN014 Bronchopneumonia 50 0.026
1005
LMY002 Leiomyoma 50 0.026
1006
P CHL066 Cholangitis 50 0.026
1007
CRT013 Carotid Stenosis 50 0.026
1008
c XNT010 Xanthinuria, Type I 50 0.026
1009
ILT001 Ileitis 50 0.026
1010
CRN030 Coronary Stenosis 50 0.026
1011
KRT001 Keratoconjunctivitis Sicca 50 0.026
1012
STT002 Status Asthmaticus 49 0.026
1013
HYP017 Hypophosphatemia 49 0.026
1014
HYP006 Hypertensive Heart Disease 49 0.026
1015
P MYT002 Myotonic Dystrophy 49 0.026
1016
RNL011 Renal Osteodystrophy 49 0.026
1017
LRN003 Learning Disability 49 0.026
1018
P HYP058 Hypervitaminosis a 49 0.026
1019
c INV001 Invasive Aspergillosis 48 0.026
1020
PLP001 Pulpitis 48 0.026
1021
WTH001 Withdrawal Disorder 48 0.026
1022
VTM002 Vitamin B12 Deficiency 48 0.026
1023
SXL003 Sexual Disorder 48 0.026
1024
P BRS053 Breast Fibroadenoma 48 0.026
1025
SYM002 Sympathetic Ophthalmia 48 0.026
1026
ERY004 Erysipelas 48 0.026
1027
FCL012 Facial Paralysis 48 0.026
1028
BNN003 Bone Inflammation Disease 48 0.026
1029
RCT017 Rectal Disease 48 0.026
1030
DGN001 Degenerative Disc Disease 48 0.026
1031
LPD004 Lipoid Nephrosis 47 0.026
1032
DRY001 Dry Eye Syndrome 47 0.026
1033
PPL002 Papillary Carcinoma 47 0.026
1034
c BCT013 Bacterial Pneumonia 47 0.026
1035
RNL077 Renal Fibrosis 47 0.026
1036
P VTR007 Vitreoretinopathy 46 0.026
1037
RCT020 Rectum Adenocarcinoma 46 0.026
1038
P PRP056 Porphyria, Acute Hepatic 46 0.026
1039
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.026
1040
HMP001 Hemopericardium 46 0.026
1041
ANH002 Anhidrosis 46 0.026
1042
MGC001 Megacolon 46 0.026
1043
SPN020 Spondylosis 46 0.026
1044
MYC005 Myocardial Stunning 46 0.026
1045
HYD005 Hydrocele 46 0.026
1046
c CHR048 Chronic Rhinitis 46 0.026
1047
ACT055 Actinomycosis 45 0.026
1048
P CRV039 Cervicitis 45 0.026
1049
GST030 Gastrinoma 45 0.026
1050
c MLG068 Malignant Glioma 45 0.026
1051
OBS004 Obstructive Hydrocephalus 45 0.026
1052
DNB001 Danubian Endemic Familial Nephropathy 45 0.026
1053
P PSD003 Pseudohypoaldosteronism 45 0.026
1054
ATN011 Autoinflammation with Infantile Enterocolitis 43 0.026
1055
P MYG005 Myoglobinuria 43 0.026
1056
P ORF002 Orofacial Cleft 43 0.026
1057
MGS001 Megaesophagus 43 0.026
1058
ACH015 Achalasia, Familial Esophageal 43 0.026
1059
CTS002 Cat-Scratch Disease 42 0.026
1060
P HYP009 Hypertrophic Pyloric Stenosis 42 0.026
1061
c ATS307 Autosomal Recessive Cerebellar Ataxia 41 0.026
1062
MCR017 Macrocytic Anemia 41 0.026
1063
P STN012 Sting-Associated Vasculopathy, Infantile-Onset 41 0.026
1064
P RRT020 Rare Tumor 41 0.026
1065
SCR015 Scarlet Fever 40 0.026
1066
LKP003 Leukoplakia 39 0.026
1067
P DYS021 Dysautonomia 39 0.026
1068
OST115 Osteonecrosis of the Jaw 39 0.026
1069
MST004 Mast Cell Neoplasm 38 0.026
1070
PRM024 Primary Angle-Closure Glaucoma 38 0.026
1071
EXT007 Extracutaneous Mastocytoma 38 0.026
1072
c PRG020 Paragangliomas 3 38 0.026
1073
P SLP003 Salpingitis 37 0.026
1074
PRS025 Presbyopia 37 0.026
1075
P PRC031 Preeclampsia/eclampsia 1 37 0.026
1076
ANT019 Anterograde Amnesia 37 0.026
1077
HYP189 Hypoadrenalism 37 0.026
1078
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 36 0.026
1079
HRM002 Hermaphroditism 36 0.026
1080
MYT011 Myotonia 35 0.026
1082
SCK001 Sick Building Syndrome 35 0.026
1083
DNT008 Denture Stomatitis 35 0.026
1084
FXD003 Fixed Drug Eruption 35 0.026
1085
STL001 St. Louis Encephalitis 35 0.026
1086
MTN002 Mite Infestation 34 0.026
1087
ATY012 Atypical Mycobacteriosis, Familial 34 0.026
1088
KDN013 Kidney Hypertrophy 34 0.026
1089
CLD011 Cold Urticaria 34 0.026
1090
RTC003 Root Caries 33 0.026
1091
PLR005 Pleuropneumonia 32 0.026
1092
P MYP105 Myopathy, Myosin Storage, Autosomal Dominant 31 0.026
1093
ACT228 Acute Radiation Syndrome 29 0.026
1094
MNG007 Manganese Poisoning 29 0.026
1095
MTR001 Mature Cataract 28 0.026
1096
c STN011 Sting-Associated Vasculopathy with Onset in Infancy 28 0.026
1097
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 28 0.026
1098
ACT162 Acute Sensory Ataxic Neuropathy 26 0.026
1099
c RNG015 Ring Chromosome 2 26 0.026
1100
ADG002 Audiogenic Seizures 26 0.026
1101
<