Search results for Zinc chloride

1203 hits were found for Zinc chloride

# Family MCID Name MIFTS Score
1
P DRR001 Diarrhea 55 0.434
2
CYS001 Cystic Fibrosis 81 0.357
3
IRN002 Iron Metabolism Disease 57 0.250
4
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.250
5
P KDN018 Kidney Disease 72 0.239
6
DRM006 Dermatitis 61 0.230
7
48X005 48,xyyy 39 0.218
8
LVR012 Liver Cirrhosis 62 0.216
9
DFC004 Deficiency Anemia 70 0.213
10
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.198
11
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.194
12
HYP005 Hypokalemia 55 0.192
13
HLX001 Helix Syndrome 47 0.189
14
P LVR013 Liver Disease 68 0.188
15
c ACT071 Acute Kidney Failure 60 0.184
16
ALL026 Allergic Hypersensitivity Disease 62 0.183
17
c HYP595 Hypertension, Essential 84 0.179
18
CNT047 Contact Dermatitis 58 0.171
19
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.169
20
MTB004 Metabolic Acidosis 50 0.168
21
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.166
22
P HPT023 Hepatocellular Carcinoma 100 0.165
23
P ANP001 Anaplastic Large Cell Lymphoma 58 0.162
24
HRW001 Hair Whorl 36 0.162
25
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.161
26
NTR005 Nutritional Deficiency Disease 62 0.160
27
P LTR001 Lateral Sclerosis 54 0.159
28
GNG013 Gingivitis 59 0.159
29
P NRB001 Neuroblastoma 72 0.158
30
CMM005 Common Cold 57 0.157
31
CNG034 Congestive Heart Failure 69 0.157
32
ISC004 Ischemia 58 0.155
33
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.154
34
MYT011 Myotonia 34 0.154
35
P ALZ034 Alzheimer Disease 88 0.153
36
BNR002 Bone Resorption Disease 48 0.150
37
P PNM007 Pneumonia 68 0.150
38
P ALP008 Alopecia 54 0.150
39
P SZR006 Seizure Disorder 56 0.150
40
CYT002 Cytokine Deficiency 42 0.150
41
P DBT009 Diabetes Mellitus 64 0.149
42
P HRT032 Heart Disease 75 0.149
43
c CHR684 Chronic Kidney Disease 70 0.148
44
ATM095 Autoimmune Disease 62 0.148
45
VSL002 Visual Epilepsy 59 0.146
46
HYP266 Hypoxia 57 0.146
47
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.145
48
HYP066 Hyperglycemia 61 0.145
49
ATS010 Autosomal Recessive Disease 48 0.145
50
CHL079 Children's Interstitial Lung Disease 26 0.144
51
c NRF023 Neurofibromatosis, Type Ii 80 0.144
52
CHL014 Cholera 59 0.142
53
DWN001 Down Syndrome 70 0.142
54
c DRR009 Diarrhea 6 46 0.141
56
P GLM045 Glioma 63 0.139
57
GLL048 Glial Tumor 45 0.139
58
PPL052 Papillomatosis, Confluent and Reticulated 33 0.138
59
P PRS040 Prostate Cancer 97 0.138
60
P ENC018 Encephalopathy 61 0.138
61
IRN001 Iron Deficiency Anemia 59 0.136
62
LNG099 Lung Disease 60 0.134
63
P HRP006 Herpes Simplex 65 0.134
64
c ACT004 Acute Diarrhea 39 0.132
65
P MYC007 Myocardial Infarction 70 0.131
66
P CLR023 Colorectal Cancer 99 0.131
67
LSH001 Leishmaniasis 63 0.128
68
P KLZ004 Kala-Azar 1 41 0.128
69
LWC001 Low Compliance Bladder 43 0.125
70
NPH009 Nephrolithiasis 55 0.125
71
P PSR002 Psoriasis 62 0.124
72
PST011 Pustulosis of Palm and Sole 52 0.124
73
47X002 47,xyy 49 0.124
74
P VSC007 Vascular Disease 63 0.124
75
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.124
76
ADN018 Adenoma 59 0.123
77
BRN071 Brain Injury 49 0.123
78
P INF032 Infertility 57 0.121
79
PRT037 Pertussis 65 0.121
80
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.121
81
P THL005 Thalassemia 60 0.120
82
P HYP086 Hypothyroidism 69 0.120
83
P OST002 Osteoporosis 74 0.120
84
RCK004 Rickets 68 0.120
85
KRT002 Keratomalacia 47 0.119
86
P ADN016 Adenocarcinoma 64 0.119
87
HMN044 Human Immunodeficiency Virus Type 1 71 0.119
88
TRM010 Traumatic Brain Injury 51 0.118
89
ALL010 Allergic Contact Dermatitis 56 0.118
90
ALC007 Alcohol Dependence 66 0.117
91
P MRC003 Mercury Poisoning 48 0.117
92
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.117
93
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.117
94
P SCK005 Sickle Cell Disease 50 0.116
95
c PRC016 Pre-Eclampsia 63 0.116
96
P CTR002 Cataract 60 0.116
97
HYP080 Hypogonadism 50 0.116
98
INS024 Insulin-Like Growth Factor I 79 0.116
99
PNG002 Pain Agnosia 51 0.116
100
SKN016 Skin Disease 63 0.116
101
P BRS047 Breast Cancer 97 0.115
102
GLB015 Glioblastoma Multiforme 75 0.115
103
CRH001 Crohn's Disease 74 0.115
104
HYP056 Hypoglycemia 66 0.115
105
P LKM002 Leukemia 68 0.115
106
HPT004 Hepatic Coma 45 0.114
107
P PRD008 Periodontitis 64 0.113
108
GST045 Gastroenteritis 59 0.113
109
c ACT075 Acute Myocardial Infarction 57 0.113
110
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.112
111
DNT012 Dental Caries 53 0.112
112
END086 End Stage Renal Disease 51 0.112
113
SPN186 Spinal Cord Injury 60 0.112
114
P GST053 Gastric Cancer 83 0.110
115
HPT019 Hepatic Encephalopathy 60 0.110
116
P MLN007 Male Infertility 55 0.110
117
P OVR042 Ovarian Cancer 88 0.110
118
c PCH010 Pachyonychia Congenita 3 44 0.110
119
P BCL017 B-Cell Lymphoma 58 0.110
120
P NRP001 Neuropathy 56 0.110
121
P INF037 Inflammatory Bowel Disease 54 0.109
122
P PNC035 Pancreatic Cancer 84 0.109
123
CNS004 Constipation 58 0.109
124
OST159 Osteogenic Sarcoma 66 0.108
125
AST005 Asthma 76 0.108
126
P CRD119 Cardiac Arrest 67 0.108
127
TXC005 Toxic Shock Syndrome 62 0.107
128
P NSP012 Nasopharyngeal Carcinoma 66 0.107
129
FTT001 Fatty Liver Disease 61 0.106
130
CTN007 Cutaneous Leishmaniasis 62 0.106
131
SCK003 Sickle Cell Anemia 74 0.106
132
TTN003 Tetanus 65 0.105
133
ATX019 Ataxia with Vitamin E Deficiency 42 0.105
134
P BPL003 Bipolar Disorder 56 0.104
135
c MJR024 Major Affective Disorder 9 41 0.104
136
c MJR022 Major Affective Disorder 8 38 0.104
137
CLT003 Colitis 62 0.104
138
IMM167 Immune Deficiency Disease 78 0.104
139
ANR007 Anorexia Nervosa 63 0.104
140
ESP021 Esophageal Cancer 90 0.104
141
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.104
142
ATH013 Atherosclerosis Susceptibility 65 0.103
143
PPT005 Peptic Ulcer Disease 59 0.103
144
EYD002 Eye Disease 58 0.103
145
DPR016 Depression 63 0.103
146
LPP008 Lipoprotein Quantitative Trait Locus 62 0.102
147
PLM001 Pulmonary Tuberculosis 69 0.102
148
P DRM053 Dermatitis, Atopic 66 0.102
149
P RHN004 Rhinitis 57 0.101
150
DRR008 Diarrhea 1, Secretory Chloride, Congenital 51 0.101
151
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.100
152
OST012 Osteoarthritis 78 0.099
153
P PNC044 Pancreatitis 61 0.098
154
P CRN300 Coronary Heart Disease 1 63 0.098
155
CRV035 Cervical Cancer 76 0.098
156
PLM010 Pulmonary Edema 54 0.098
157
AGN016 Aging 56 0.098
158
P LNG032 Lung Cancer 98 0.098
159
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.097
160
P GLM007 Glomerulonephritis 57 0.097
161
BCT022 Bacterial Infectious Disease 56 0.096
162
SCR003 Secretory Diarrhea 37 0.096
163
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.096
164
P MNN013 Meningitis 66 0.096
165
DYS015 Dysentery 52 0.096
166
MDD011 Mood Disorder 62 0.096
167
P EXN002 Exanthem 57 0.095
168
URM002 Uremia 49 0.095
169
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.095
170
c MCR120 Microvascular Complications of Diabetes 7 47 0.095
171
GST023 Gastric Ulcer 53 0.094
172
NRL016 Neural Tube Defects 82 0.094
173
BRN004 Brain Edema 56 0.094
174
BRN024 Bronchitis 68 0.093
175
STM007 Stomatitis 50 0.093
176
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.093
177
P HYP069 Hyperparathyroidism 63 0.093
178
P GST044 Gastritis 56 0.093
179
c ACT027 Acute Pancreatitis 60 0.093
180
c BRN108 Branchiootic Syndrome 1 62 0.093
181
ADL002 Adult Syndrome 70 0.092
182
P NTR004 Neutropenia 63 0.092
183
c MCR113 Microvascular Complications of Diabetes 3 52 0.092
184
c MCR130 Microvascular Complications of Diabetes 6 41 0.092
185
c MCR133 Microvascular Complications of Diabetes 4 41 0.092
186
P TRM003 Tremor 54 0.092
187
c BTT014 Beta-Thalassemia 74 0.092
188
URL001 Urolithiasis 45 0.092
189
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.092
190
c PNS012 Paine Syndrome 61 0.092
191
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.092
192
P ATS364 Autism 70 0.091
193
c LKM061 Leukemia, Acute Myeloid 84 0.091
194
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.091
195
HMS001 Hemosiderosis 54 0.091
196
SQM006 Squamous Cell Carcinoma 60 0.090
197
NPH003 Nephrocalcinosis 51 0.090
198
P RTN024 Retinoblastoma 73 0.090
199
c FML008 Familial Retinoblastoma 53 0.090
200
P EPL164 Epilepsy 71 0.089
201
PRS045 Prostatic Hypertrophy 53 0.089
202
P MYL006 Myeloid Leukemia 60 0.089
203
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.089
204
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.089
205
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.088
206
P NPH012 Nephrotic Syndrome 60 0.088
207
P PHC003 Pheochromocytoma 71 0.088
208
ADR040 Adrenal Gland Pheochromocytoma 46 0.088
209
P SKN015 Skin Carcinoma 66 0.088
210
OCL069 Ocular Motor Apraxia 51 0.088
211
THR024 Thrombosis 57 0.088
212
c SVR001 Severe Acute Respiratory Syndrome 62 0.087
213
CRB004 Cerebral Artery Occlusion 45 0.087
214
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.086
215
c ACT068 Acute Cystitis 63 0.086
216
P MYT002 Myotonic Dystrophy 49 0.086
217
ULC004 Ulcerative Colitis 73 0.086
218
P CHR345 Chronic Pain 44 0.086
219
c HPT016 Hepatitis B 59 0.086
220
P BND020 Bone Disease 59 0.086
221
PST092 Posttransplant Acute Limbic Encephalitis 29 0.086
222
P TRN020 Turner Syndrome 67 0.085
223
c HYP836 Hypercholesterolemia, Familial, 1 73 0.085
224
CVD001 Covid-19 44 0.085
225
GTR002 Goiter 53 0.085
226
c DBT099 Diabetes Mellitus, Type I 65 0.085
227
MNT002 Mental Depression 58 0.085
228
INS001 Insulinoma 60 0.084
229
ART140 Arteries, Anomalies of 52 0.084
230
STR067 Stroke, Ischemic 81 0.084
231
HVY002 Heavy Metal Poisoning 22 0.084
232
P PLY014 Polycystic Kidney Disease 62 0.084
233
PRS047 Prostatitis 56 0.084
234
P HYP076 Hyperthyroidism 55 0.084
235
ANX010 Anxiety 73 0.083
236
P PRP019 Peripheral Nervous System Disease 58 0.083
237
GLC003 Glucose Intolerance 54 0.083
238
ANX004 Anoxia 40 0.083
239
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.083
240
P SYS005 Systemic Scleroderma 68 0.083
241
P MLN008 Melanoma 69 0.082
242
P CRD246 Cardiovascular System Disease 57 0.082
243
P INT070 Intestinal Obstruction 58 0.082
244
NWC001 Newcastle Disease 45 0.082
245
PRT038 Protein-Energy Malnutrition 54 0.082
246
P LNG064 Lung Cancer Susceptibility 3 78 0.082
247
PRS021 Prostatic Adenoma 51 0.081
248
P DMN002 Dementia 66 0.081
249
ORL011 Oral Cancer 60 0.081
250
P RHM011 Rheumatoid Arthritis 80 0.081
251
c PRM038 Primary Agammaglobulinemia 44 0.081
252
PRS129 Prostatic Hyperplasia, Benign 49 0.080
253
CHL068 Cholestasis 61 0.080
254
P ART022 Arthritis 69 0.080
255
P MSC005 Muscular Dystrophy 66 0.080
256
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.079
257
MYL069 Myeloma, Multiple 85 0.079
258
PRT036 Peritonitis 64 0.079
259
MLR004 Malaria 81 0.079
260
MCS002 Mucositis 56 0.079
261
P RRH023 Rare Hereditary Hemochromatosis 41 0.079
262
P ECL001 Eclampsia 50 0.079
263
SVR004 Severe Combined Immunodeficiency 73 0.078
264
HYP781 Hypoascorbemia 51 0.078
265
BLR008 Bilirubin Metabolic Disorder 57 0.078
266
c ATS007 Autism Spectrum Disorder 67 0.078
267
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.078
268
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.078
269
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.078
270
P RSP003 Respiratory Failure 74 0.077
271
PRT013 Portal Hypertension 59 0.077
272
P ALP009 Alopecia Areata 60 0.077
273
P INT068 Intestinal Disease 53 0.077
274
PPL022 Papilloma 54 0.077
275
P PLM037 Pulmonary Hypertension 67 0.077
276
ACT119 Acute Promyelocytic Leukemia 63 0.077
277
c RHB024 Rhabdomyosarcoma 2 67 0.077
278
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.077
279
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.077
280
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.077
281
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.077
282
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.077
283
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.077
284
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.077
285
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.077
286
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.077
287
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.077
288
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.077
289
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.076
290
ILS001 Ileus 51 0.076
291
c HPT001 Hepatitis C 62 0.075
292
MST005 Mastitis 53 0.075
293
ARG004 Argyria 27 0.075
294
c ATR087 Atrial Standstill 1 75 0.075
295
GST050 Gastrointestinal System Disease 56 0.075
296
P RTN016 Retinal Degeneration 53 0.075
297
ENT011 Enterocolitis 51 0.074
298
P OVR082 Overgrowth Syndrome 50 0.074
299
KRT009 Keratosis 51 0.074
300
BRN028 Brain Cancer 74 0.074
301
P HPT021 Hepatitis 67 0.074
302
P LKM062 Leukemia, Acute Lymphoblastic 69 0.074
303
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.074
304
P MYS003 Myasthenia Gravis 68 0.074
305
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.074
306
PCD001 Pica Disease 41 0.074
307
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.074
308
P OST001 Osteopetrosis 70 0.074
309
P ADL010 Adult Respiratory Distress Syndrome 65 0.074
310
THY029 Thyroid Carcinoma 59 0.074
311
PLY150 Polykaryocytosis Inducer 31 0.074
312
ACQ007 Acquired Immunodeficiency Syndrome 60 0.074
313
ALL014 Allergic Encephalomyelitis 38 0.074
314
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.073
315
SQM002 Squamous Cell Papilloma 46 0.073
316
P HML002 Hemolytic Anemia 63 0.073
317
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.073
318
ORL015 Oral Squamous Cell Carcinoma 43 0.073
319
VCC001 Vaccinia 49 0.072
320
AZS001 Azoospermia 50 0.072
321
P OPN001 Open-Angle Glaucoma 49 0.072
322
BRN002 Bronchiolitis 59 0.072
323
LPD008 Lipid Metabolism Disorder 62 0.072
324
P HNT016 Huntington Disease 72 0.072
325
P DBT005 Diabetes Insipidus 55 0.071
326
CRB039 Cerebrovascular Disease 67 0.071
327
P CLC063 Celiac Disease 1 66 0.071
328
P BLD134 Bladder Cancer 79 0.071
329
CLF027 Cleft Palate, Isolated 64 0.071
330
P FBR017 Fibrosarcoma 56 0.071
331
P VSC011 Vasculitis 62 0.071
332
OCL006 Ocular Hypertension 53 0.071
333
RYN005 Raynaud Phenomenon 47 0.071
334
P MYC008 Myocarditis 59 0.071
335
c VRL010 Viral Hepatitis 52 0.070
336
P PLM036 Pulmonary Fibrosis 65 0.070
337
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.070
338
DWR001 Dwarfism 44 0.070
339
ACR062 Acroosteolysis 35 0.070
340
GLS018 Glass Syndrome 57 0.070
341
ALL003 Allergic Rhinitis 67 0.070
342
BRN056 Bronchopulmonary Dysplasia 57 0.070
343
P CNR004 Cone-Rod Dystrophy 2 73 0.070
344
P ALC033 Alcohol Use Disorder 58 0.070
345
P PRK057 Parkinson Disease, Late-Onset 78 0.070
346
P BRS044 Breast Adenocarcinoma 59 0.070
347
HYP060 Hyperinsulinism 54 0.069
348
P MLT020 Multiple Sclerosis 72 0.069
349
STT001 Status Epilepticus 60 0.069
350
P CND004 Candidiasis 58 0.069
351
CLN015 Colon Adenocarcinoma 65 0.069
352
P DDN001 Duodenal Ulcer 52 0.069
353
SPL018 Splenomegaly 48 0.069
354
P LYM118 Lymphoma 68 0.068
355
DPH001 Diphtheria 60 0.068
356
CHR178 Chromosomal Triplication 35 0.068
357
P MYP004 Myopathy 70 0.067
358
ART016 Aortic Aneurysm 69 0.067
359
GST092 Gastroesophageal Reflux 67 0.067
360
P TMP001 Temporal Lobe Epilepsy 50 0.067
361
P PLY019 Polyneuropathy 56 0.067
362
P AST007 Astrocytoma 51 0.067
363
ACT003 Acute Kidney Tubular Necrosis 45 0.067
364
IMP005 Impotence 52 0.067
365
P SCH015 Schizophrenia 74 0.066
366
SRC014 Sarcoma 65 0.066
367
P HYP750 Hypertriglyceridemia, Familial 62 0.066
368
P LPR021 Leprosy 3 69 0.066
369
HNS001 Hansen's Disease 34 0.066
370
P PNM006 Pneumoconiosis 56 0.066
371
ANT018 Anthracosis 48 0.066
372
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.066
373
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.065
374
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.065
375
SCH014 Schistosomiasis 57 0.065
376
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.065
377
P ART021 Arteriosclerosis 54 0.065
378
TLN003 Telangiectasis 52 0.065
379
SPN035 Spindle Cell Sarcoma 53 0.065
380
KRT019 Keratitis, Hereditary 65 0.065
381
ALC009 Alcoholic Liver Cirrhosis 53 0.064
382
P HDC001 Headache 57 0.064
383
P NGH001 Night Blindness 48 0.064
384
P RNL007 Renal Tubular Acidosis 51 0.064
385
P THR014 Thrombocytopenia 67 0.064
386
SBC016 Subacute Delirium 44 0.064
387
c SML038 Small Cell Cancer of the Lung 65 0.064
388
P KDN017 Kidney Cancer 60 0.063
389
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.063
390
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.063
391
P THY032 Thyroiditis 52 0.063
392
c SPN225 Spondyloarthropathy 1 73 0.063
393
ANG054 Angina Pectoris 66 0.063
394
PLM031 Poliomyelitis 64 0.063
395
P TRC086 Trichohepatoenteric Syndrome 1 62 0.063
396
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.063
397
GST020 Gastric Antral Vascular Ectasia 41 0.063
398
P BRN022 Bronchiectasis 59 0.063
399
c PRM005 Primary Hyperparathyroidism 58 0.062
400
TRY001 Trypanosomiasis 50 0.062
401
c PRS136 Prostate Cancer, Hereditary, 6 33 0.062
402
c PRS130 Prostate Cancer, Hereditary, 8 32 0.062
403
P MCR115 Microvascular Complications of Diabetes 5 66 0.062
404
PHR003 Pharyngitis 57 0.062
405
MSL001 Measles 62 0.062
406
P SPP010 Suppressor of Tumorigenicity 3 51 0.062
407
CCC002 Coccidiosis 51 0.062
408
c HPT073 Hepatitis C Virus 72 0.062
409
DRY001 Dry Eye Syndrome 47 0.061
410
PNC129 Pancreatic Adenocarcinoma 68 0.061
411
c ALP101 Alpha-Thalassemia 62 0.061
412
SPS057 Spasticity 45 0.061
413
P URT039 Urticaria 58 0.061
414
c HPT003 Hepatitis a 62 0.061
415
NWB001 Newborn Respiratory Distress Syndrome 58 0.061
416
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.061
417
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.061
418
P AMY004 Amyloidosis 70 0.061
419
OLG001 Oligospermia 45 0.061
420
HMP009 Haemophilus Influenzae 43 0.061
421
IRR003 Irritant Dermatitis 49 0.060
422
PHN003 Phenylketonuria 75 0.060
423
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.060
424
BCT004 Bacteriuria 49 0.060
425
P OPT006 Optic Nerve Disease 60 0.060
426
P CNJ013 Conjunctivitis 65 0.059
427
P LPS004 Lupus Erythematosus 61 0.059
428
c GRV008 Graves Disease 1 56 0.059
429
P HYP098 Hypereosinophilic Syndrome 67 0.059
430
CHG001 Chagas Disease 66 0.059
431
P LCH002 Lichen Planus 53 0.059
432
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.059
433
c LKM005 Leukemia, T-Cell, Chronic 34 0.059
434
P SBR004 Seborrheic Dermatitis 45 0.059
435
BLL006 Bullous Pemphigoid 62 0.059
436
ALL006 Allergic Asthma 56 0.059
437
c FNC043 Fanconi Anemia, Complementation Group E 62 0.059
438
P PYL005 Pyelonephritis 56 0.059
439
HYP014 Hyperuricemia 52 0.059
440
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.059
441
PTT037 Pituitary Tumors 44 0.058
442
P DYS154 Dystonia 65 0.058
443
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.058
444
P ESP024 Esophagitis 62 0.058
445
c CHR682 Chronic Bilirubin Encephalopathy 39 0.058
446
P MNC007 Monocytic Leukemia 53 0.058
447
GT001 Gout 64 0.058
448
ERY051 Erythroleukemia, Familial 56 0.058
449
DYS073 Dysphagia 50 0.058
450
P RHB003 Rhabdomyosarcoma 63 0.057
451
P SJG008 Sjogren Syndrome 61 0.057
452
P SNS001 Sensorineural Hearing Loss 60 0.057
453
VRC005 Varicose Veins 60 0.057
454
49X006 49, Xxxxy Syndrome 41 0.057
455
c ACT073 Acute Leukemia 58 0.057
456
ANT024 Anthrax Disease 58 0.057
457
HDN002 Head Injury 46 0.057
458
PRP027 Peripheral Vascular Disease 71 0.056
459
VRL011 Viral Infectious Disease 61 0.056
460
P PRP029 Porphyria 62 0.056
461
c ACT134 Acute Liver Failure 56 0.056
462
P BNG032 Benign Mesothelioma 46 0.056
463
MDD018 Middle East Respiratory Syndrome 43 0.056
464
P ATR011 Atrial Fibrillation 66 0.056
465
P CYS018 Cystitis 59 0.056
466
c SPR086 Spermatogenic Failure 3 44 0.056
467
P MYC084 Mycobacterium Tuberculosis 1 68 0.055
468
c DWL002 Dowling-Degos Disease 1 58 0.055
469
LYM133 Lymphoma, Hodgkin, Classic 69 0.055
470
PRN019 Perinatal Necrotizing Enterocolitis 59 0.055
471
c PRD040 Periodontitis, Chronic 53 0.055
472
OST011 Osteomalacia 52 0.055
473
c MLG068 Malignant Glioma 46 0.055
474
c SCN007 Secondary Hyperparathyroidism 51 0.055
475
P INF038 Influenza 68 0.055
476
DRM011 Dermatophytosis 52 0.055
477
CRD223 Cardiac Arrhythmia 60 0.054
478
THR013 Thoracic Outlet Syndrome 54 0.054
479
MLC004 Mulchandani-Bhoj-Conlin Syndrome 44 0.054
480
c WLM013 Wilms Tumor 1 65 0.054
481
P EHL001 Ehlers-Danlos Syndrome 58 0.054
482
SXL003 Sexual Disorder 47 0.054
483
c MGR028 Migraine with or Without Aura 1 67 0.054
484
LYS002 Lysosomal Storage Disease 52 0.054
485
P INS002 in Situ Carcinoma 53 0.054
486
CRT015 Carotid Artery Occlusion 45 0.054
487
MTH071 Methane Production 26 0.054
488
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.054
489
SKN019 Skin Melanoma 68 0.053
490
P MYP006 Myopia 55 0.053
491
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.053
492
P RTN008 Retinitis Pigmentosa 79 0.053
493
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.053
494
RTN023 Retinitis 46 0.053
495
GRD001 Giardiasis 45 0.053
496
NRR001 Neuroretinitis 42 0.053
497
c SYS001 Systemic Lupus Erythematosus 86 0.053
498
END057 Endometrial Cancer 74 0.053
499
P SLP006 Sleep Apnea 69 0.053
500
P RTN018 Retinal Disease 53 0.053
501
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.053
502
DCB001 Decubitus Ulcer 61 0.053
503
CHR100 Chronic Ulcer of Skin 55 0.053
504
ORL013 Oral Lichen Planus 45 0.053
505
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.052
506
P FNC004 Fanconi Syndrome 50 0.052
507
KRT001 Keratoconjunctivitis Sicca 49 0.052
508
ANR040 Aneurysm 59 0.052
509
MTH009 Mouth Disease 56 0.052
510
AMN003 Amnestic Disorder 54 0.052
511
PLG002 Plague 63 0.052
512
EXN003 Exencephaly 31 0.052
513
c THR092 Thrombophilia Due to Thrombin Defect 73 0.052
514
BCT002 Bacterial Vaginosis 53 0.052
515
MSC007 Muscle Hypertrophy 64 0.052
516
NRT004 Neuritis 52 0.052
517
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.052
518
P ANR048 Aniridia 1 63 0.051
519
MYL009 Myelodysplastic Syndrome 70 0.051
520
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.051
521
ALC006 Alcoholic Hepatitis 61 0.050
522
EMB004 Embryonal Carcinoma 56 0.050
523
VLV047 Volvulus of Midgut 49 0.050
524
P ATX030 Ataxia-Telangiectasia 82 0.050
525
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.050
526
CHR066 Chronic Fatigue Syndrome 61 0.050
527
P MSC003 Muscular Atrophy 52 0.050
528
P ENC004 Encephalitis 61 0.050
529
PLM033 Pulmonary Embolism 59 0.050
530
LST001 Listeriosis 56 0.050
531
BRR014 Barrett Esophagus 65 0.049
532
FDB001 Foodborne Botulism 55 0.049
533
P GRV001 Graves' Disease 55 0.049
534
c EXD008 Exudative Vitreoretinopathy 1 71 0.049
535
ACN002 Acanthosis Nigricans 60 0.049
536
c FML035 Familial Hyperlipidemia 55 0.049
537
PLS009 Plasma Cell Neoplasm 51 0.049
538
P HYP265 Hypotonia 43 0.049
539
OTT002 Otitis Media 72 0.049
540
P MTR014 Motor Neuron Disease 65 0.049
541
THY030 Thyroid Gland Disease 52 0.049
542
CLC006 Calcinosis 48 0.048
543
MNG007 Manganese Poisoning 29 0.048
544
VGN023 Vaginitis 54 0.048
545
MCN017 Meconium Ileus 52 0.048
546
P FNC034 Fanconi Renotubular Syndrome 2 40 0.048
547
LPT014 Leptin Deficiency or Dysfunction 74 0.048
548
P HRS035 Hirschsprung Disease 1 65 0.048
549
RTN017 Retinal Detachment 61 0.048
550
P SBS003 Substance Abuse 55 0.048
551
P SLM003 Salmonellosis 55 0.048
552
PNC001 Pancytopenia 54 0.048
553
RTN003 Retinal Ischemia 50 0.048
554
DMP001 Dumping Syndrome 44 0.048
555
EXC002 Exocrine Pancreatic Insufficiency 42 0.048
556
P END044 Endometriosis 63 0.048
557
P SCL018 Scoliosis 60 0.048
558
RTR008 Root Resorption 45 0.048
559
PRM020 Premenstrual Tension 40 0.048
560
P FBR031 Febrile Seizures 53 0.048
561
P GRF003 Graft-Versus-Host Disease 72 0.047
562
c MCL013 Mucolipidosis Iv 66 0.047
563
IRR002 Irritable Bowel Syndrome 65 0.047
564
P ART023 Arthropathy 62 0.047
565
ATN005 Autonomic Dysfunction 46 0.047
566
CHL065 Cholangiocarcinoma 68 0.047
567
INT079 Intrahepatic Cholangiocarcinoma 51 0.047
568
MSC157 Muscular Dystrophy, Duchenne Type 72 0.047
569
ATX010 Ataxia Neuropathy Spectrum 34 0.047
570
ACT064 Acute Necrotizing Encephalitis 33 0.047
571
BLD137 Blood Group--Ahonen 16 0.047
572
P HYP097 Hyperekplexia 61 0.046
573
c SCL052 Scleroderma, Familial Progressive 61 0.046
574
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.046
575
ATR057 Atrioventricular Block 55 0.046
576
SNS003 Sensory Peripheral Neuropathy 54 0.046
577
P EPD016 Epidermolysis Bullosa 53 0.046
578
SYS071 Systemic Autoimmune Disease 37 0.046
579
ADG002 Audiogenic Seizures 25 0.046
580
CRD132 Cardiac Conduction Defect 58 0.046
581
MYL020 Myelomeningocele 51 0.046
582
ECT026 Ectopic Pregnancy 50 0.046
583
c MYT029 Myotonia Congenita, Autosomal Recessive 41 0.046
584
P ASP006 Aspergillosis 69 0.046
585
HMG005 Hemoglobinopathy 56 0.046
586
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 0.046
587
P SHR001 Short Bowel Syndrome 53 0.046
588
c DLT002 Dilated Cardiomyopathy 79 0.046
589
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.046
590
c BSL007 Basal Cell Carcinoma 68 0.046
591
P PRM006 Primary Biliary Cirrhosis 62 0.046
592
VSC002 Vascular Dementia 57 0.046
593
P LRY044 Larynx Cancer 55 0.046
594
OVR094 Ovarian Epithelial Cancer 38 0.046
595
ANP008 Anaplastic Oligoastrocytoma 30 0.046
596
P AGM001 Agammaglobulinemia 65 0.046
597
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.046
598
CRH005 Crohn's Colitis 53 0.046
599
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.046
600
P HYD006 Hydrocephalus 66 0.045
601
P SYP003 Syphilis 58 0.045
602
CHL067 Cholecystitis 57 0.045
603
HYP081 Hypolipoproteinemia 51 0.045
604
CRD137 Cardiogenic Shock 47 0.045
605
ATM052 Autoimmune Disease 1 37 0.045
606
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.045
607
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.045
608
CRB037 Cerebral Palsy 69 0.045
609
c INF071 Inflammatory Bowel Disease 1 67 0.045
610
P HYP024 Hypoparathyroidism 56 0.045
611
DBT010 Diabetic Neuropathy 54 0.045
612
TRP009 Triple X Syndrome 42 0.045
613
HLC007 Helicobacter Pylori Infection 59 0.044
614
ORL004 Oral Submucous Fibrosis 55 0.044
615
CLR109 Colorectal Adenocarcinoma 51 0.044
616
GLS007 Glossitis 47 0.044
617
PND002 Pendred Syndrome 65 0.044
618
P INT143 Interstitial Cystitis 61 0.044
619
KRT006 Keratoconjunctivitis 53 0.044
620
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.044
621
c SVR005 Severe Pre-Eclampsia 50 0.044
622
FLL008 Folliculitis 46 0.044
623
c FML001 Familial Atrial Fibrillation 65 0.044
624
CMM004 Common Variable Immunodeficiency 68 0.044
625
c MCR129 Microvascular Complications of Diabetes 1 66 0.044
626
P LPS002 Liposarcoma 65 0.044
627
BRC012 Brucellosis 64 0.044
628
CHL123 Chlamydia 59 0.044
629
AYM001 Ayme-Gripp Syndrome 57 0.044
630
CMR002 Coumarin Resistance 56 0.044
631
PRP030 Purpura 54 0.044
632
NNL006 Non-Alcoholic Steatohepatitis 54 0.044
633
TRC003 Trichomoniasis 53 0.044
634
c PSR017 Psoriasis 2 53 0.044
635
DMY004 Demyelinating Disease 52 0.044
636
LNG031 Lung Benign Neoplasm 51 0.044
637
INT067 Interstitial Nephritis 48 0.044
638
KRT013 Keratolytic Winter Erythema 46 0.044
639
CYN002 Cyanosis, Transient Neonatal 45 0.044
640
BRS051 Breast Disease 58 0.043
641
P KRT007 Keratoconus 50 0.043
642
GRW007 Growth Hormone Deficiency 46 0.043
643
TYP007 Typhoid Fever 63 0.042
644
DRR016 Diarrhea 2, with Microvillus Atrophy 60 0.042
645
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.042
646
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.042
647
P CHN012 Chondrosarcoma 56 0.042
648
ANL018 Analbuminemia 54 0.042
649
P SDR002 Siderosis 44 0.042
650
CRN322 Coronavirus Infectious Disease 40 0.042
651
P EPL140 Epilepsy, Idiopathic Generalized 62 0.042
652
INT066 Interstitial Lung Disease 60 0.042
653
SPN051 Spondylitis 51 0.042
654
P RNL015 Renal Hypertension 47 0.042
655
KRT008 Keratopathy 47 0.042
656
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.042
657
BCK006 Back Pain 42 0.042
658
P RRT020 Rare Tumor 41 0.042
659
INF009 Inflammatory Spondylopathy 31 0.042
660
CNN003 Conn's Syndrome 79 0.042
661
P APL001 Aplastic Anemia 74 0.042
662
YLL002 Yellow Fever 61 0.042
663
DSS009 Disseminated Intravascular Coagulation 57 0.042
664
TXC002 Toxic Encephalopathy 53 0.042
665
CHR073 Choreatic Disease 52 0.042
667
PRN014 Paronychia 49 0.042
668
HYP025 Hyperphosphatemia 48 0.042
669
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.042
670
P HMR005 Hemorrhoid 46 0.042
671
URT010 Ureteral Obstruction 45 0.042
672
OSM001 Osmotic Diarrhea 32 0.042
673
PRT058 Pure Autonomic Failure 59 0.041
675
P ANG001 Angelman Syndrome 69 0.041
676
c MYT021 Myotonic Dystrophy 1 69 0.041
677
CHR177 Chromophobe Renal Cell Carcinoma 57 0.041
678
END040 Endogenous Depression 55 0.041
679
CRT017 Cartilage Disease 54 0.041
680
c PSR023 Psoriasis 1 52 0.041
681
MGL001 Megaloblastic Anemia 51 0.041
682
WTH001 Withdrawal Disorder 48 0.041
683
c PSR032 Psoriasis 11 47 0.041
684
LYM019 Lymphosarcoma 46 0.041
685
TST014 Testicular Cancer 46 0.041
686
c PSR028 Psoriasis 7 42 0.041
687
c PSR018 Psoriasis 13 41 0.041
688
CND006 Candida Glabrata 32 0.041
689
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.041
690
P MDL005 Medulloblastoma 77 0.041
691
TBC004 Tobacco Addiction 64 0.041
692
CLR108 Colorectal Adenoma 64 0.041
693
DSS008 Disease of Mental Health 58 0.041
694
VSC003 Visceral Leishmaniasis 55 0.041
695
CLF001 Cleft Lip 53 0.041
696
PLP001 Pulpitis 49 0.041
697
KPS004 Kaposi Sarcoma 75 0.040
698
GST040 Gastric Adenocarcinoma 70 0.040
699
c PNC108 Pancreatitis, Hereditary 70 0.040
700
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.040
701
MNK001 Menkes Disease 64 0.040
702
P ICH004 Ichthyosis 54 0.040
703
HPT014 Hepatorenal Syndrome 50 0.040
704
c INH020 Inherited Metabolic Disorder 47 0.040
705
CRB090 Cerebral Hypoxia 44 0.040
706
SPR126 Superior Semicircular Canal Dehiscence 40 0.040
707
c HMG029 Hemoglobin Se Disease 39 0.040
708
PRP016 Paraplegia 52 0.040
709
PYL006 Pyloric Stenosis 48 0.040
710
AMN006 Aminoaciduria 38 0.040
711
c LKM063 Leukemia, Chronic Myeloid 72 0.039
712
KHL003 Kohlschutter-Tonz Syndrome 65 0.039
713
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.039
714
CRY005 Cryptococcosis 58 0.039
715
GNT003 Genital Herpes 54 0.039
716
LMY002 Leiomyoma 52 0.039
717
BRN009 Burning Mouth Syndrome 50 0.039
718
TRT001 Teratocarcinoma 45 0.039
719
HND015 Hand Skill, Relative 33 0.039
720
ACR007 Acromegaly 71 0.039
721
P SRC025 Sarcoidosis 1 70 0.039
722
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.039
723
AND002 Androgen Insensitivity Syndrome 66 0.039
724
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.039
725
OST017 Osteomyelitis 64 0.039
726
HYD002 Hydronephrosis 60 0.039
727
P AXN002 Axenfeld-Rieger Syndrome 59 0.039
728
FBR047 Fibromyalgia 58 0.039
729
P GLL018 Gallbladder Cancer 57 0.039
730
P ANG015 Angioedema 57 0.039
731
PNM008 Pneumothorax 56 0.039
732
NRT001 Neurotic Disorder 53 0.039
733
c CRS016 Crisponi/cold-Induced Sweating Syndrome 1 52 0.039
734
P MMB011 Membranous Nephropathy 50 0.039
735
RFR010 Refractory Anemia 48 0.039
736
TST015 Testicular Disease 43 0.039
737
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.039
738
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.039
739
RDN001 Reading Disorder 40 0.039
740
ALR002 Al-Raqad Syndrome 33 0.039
741
P OCL013 Oculodentodigital Dysplasia 69 0.039
742
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.039
743
c MLG084 Malignant Fibrous Histiocytoma 63 0.039
744
P SLP005 Sleep Disorder 59 0.039
745
P OPT009 Optic Neuritis 57 0.039
746
HMR039 Hemorrhage, Intracerebral 57 0.039
747
ALB002 Albinism 46 0.039
748
CHP002 Chops Syndrome 44 0.039
749
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.038
750
c MST023 Mesothelioma, Malignant 57 0.038
751
TNS005 Tonsillitis 57 0.038
752
SFT003 Soft Tissue Sarcoma 56 0.038
753
ORL005 Oral Candidiasis 56 0.038
754
KHN001 Kuhnt-Junius Degeneration 47 0.038
755
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.038
757
MTL005 Metal Allergy 41 0.038
758
KLB003 Klebsiella Pneumonia 41 0.038
759
c MCR112 Microvascular Complications of Diabetes 2 41 0.038
760
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.038
761
URT049 Urate Oxidase, Pseudogene 25 0.038
762
P GLM040 Glioma Susceptibility 1 81 0.037
763
P RTT002 Rett Syndrome 80 0.037
764
P ECT006 Ectodermal Dysplasia 62 0.037
765
P TXP001 Toxoplasmosis 60 0.037
766
PLS011 Plasmacytoma 56 0.037
767
AMB001 Amebiasis 55 0.037
768
SLP001 Sleeping Sickness 54 0.037
769
c PNC106 Pancreatic Agenesis 1 51 0.037
770
PNC034 Pancreas Disease 48 0.037
771
VTM002 Vitamin B12 Deficiency 48 0.037
772
MCR018 Microcytic Anemia 47 0.037
773
LKP003 Leukoplakia 39 0.037
774
KND001 Kindler Syndrome 64 0.037
775
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.037
776
URN010 Urinary Tract Obstruction 55 0.037
777
PTH003 Pathologic Nystagmus 52 0.037
778
CRN019 Coronary Artery Vasospasm 46 0.037
779
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.037
780
c FNC026 Fanconi Renotubular Syndrome 1 39 0.037
781
c MNN043 Meningioma, Familial 74 0.035
782
P CHR071 Charcot-Marie-Tooth Disease 65 0.035
783
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.035
784
P MVM001 Movement Disease 63 0.035
785
c ATM011 Autoimmune Hepatitis 63 0.035
786
MNN042 Meningioma, Radiation-Induced 62 0.035
787
HRP004 Herpes Zoster 60 0.035
788
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.035
789
c BNG091 Benign Chronic Pemphigus 58 0.035
790
SPT004 Septic Arthritis 58 0.035
791
BRN012 Bronchiolitis Obliterans 55 0.035
792
P CYS039 Cystic Kidney Disease 54 0.035
793
P PNC025 Panic Disorder 53 0.035
794
P LCT001 Lactic Acidosis 51 0.035
795
c HNT004 Huntington Disease-Like 2 50 0.035
796
SPN021 Spinal Meningioma 50 0.035
797
c INF145 Infantile Liver Failure Syndrome 1 50 0.035
798
RYN001 Raynaud Disease 48 0.035
799
MCC002 Mucocutaneous Leishmaniasis 47 0.035
800
CHR074 Choriocarcinoma 47 0.035
801
ORC001 Orchitis 46 0.035
802
c HYP272 Hypercholesterolemia, Familial, 3 44 0.035
803
SCR001 Secretory Meningioma 41 0.035
804
ALC005 Alcoholic Pancreatitis 40 0.035
805
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.035
806
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.035
807
EWN003 Ewing Sarcoma 69 0.035
808
CNN005 Connective Tissue Disease 68 0.035
809
THY111 Thyroid Carcinoma, Familial Medullary 67 0.035
810
TRN015 Transient Cerebral Ischemia 63 0.035
811
HSH003 Hashimoto Thyroiditis 62 0.035
812
P GLY013 Glycogen Storage Disease 60 0.035
813
SPP011 Suppression of Tumorigenicity 12 59 0.035
814
P BNC003 Bone Cancer 58 0.035
815
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.035
816
AMN001 Amenorrhea 54 0.035
817
HMC014 Homocysteinemia 53 0.035
818
PPT001 Peptic Esophagitis 52 0.035
819
c PRG020 Paragangliomas 3 39 0.035
820
P PST059 Pustular Psoriasis 37 0.035
821
RTC003 Root Caries 33 0.035
822
ART001 Arterial Tortuosity Syndrome 66 0.035
823
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.035
824
NRM005 Neuromuscular Disease 64 0.035
825
RHM001 Rheumatic Fever 60 0.035
826
ING001 Inguinal Hernia 60 0.035
827
P RBL001 Rubella 59 0.035
828
P ALP106 Alport Syndrome 1, X-Linked 55 0.035
829
SPS003 Spastic Diplegia 51 0.035
830
P CHL066 Cholangitis 51 0.035
831
c VRL012 Viral Meningitis 48 0.035
832
PPL001 Papillary Adenoma 44 0.035
833
SMN007 Seminoma 43 0.035
834
P MJR007 Major Affective Disorder 1 43 0.035
835
PLY100 Polyploidy 40 0.035
836
ENT001 Enterocele 39 0.035
837
c OVR114 Ovarian Cancer 1 38 0.035
838
P CRB088 Cerebral Atrophy 37 0.035
839
P CRB059 Cerebellar Degeneration 37 0.035
840
c MJR003 Major Affective Disorder 6 33 0.035
841
c MJR006 Major Affective Disorder 5 33 0.035
842
RSP007 Respiratory Distress Syndrome, Infant 30 0.035
843
MTY003 Mutyh Polyposis 30 0.035
844
MYL005 Myelofibrosis 70 0.034
845
P HMN010 Hemangioma 61 0.034
846
IGR001 Ige Responsiveness, Atopic 59 0.034
847
P PLY018 Polycythemia 56 0.034
848
P PLM034 Pulmonary Emphysema 55 0.034
849
SYN007 Synovitis 54 0.034
850
TRD006 Tardive Dyskinesia 54 0.034
851
ONC002 Onchocerciasis 52 0.034
852
CHD004 Chudley-Mccullough Syndrome 46 0.034
853
ENT003 Enterobiasis 38 0.034
854
GLM044 Glomerular Disease 37 0.034
855
PLC002 Plica Syndrome 36 0.034
856
LCH001 Leech Infestation 35 0.034
857
c INF002 Inflammatory Diarrhea 34 0.034
858
PSY004 Psychotic Disorder 67 0.033
859
PRP001 Propionic Acidemia 65 0.033
860
P PRD006 Prader-Willi Syndrome 59 0.033
861
BLM002 Bulimia Nervosa 57 0.033
862
SLC006 Silicosis 56 0.033
863
P DRM007 Dermatitis Herpetiformis 55 0.033
864
P PMP001 Pemphigus 54 0.033
865
BRN014 Bronchopneumonia 54 0.033
866
MYM001 Myoma 54 0.033
867
P LCT002 Lactose Intolerance 53 0.033
868
OST016 Osteochondrosis 53 0.033
869
P ACT008 Actinic Keratosis 53 0.033
870
c HPT007 Hepatitis E 53 0.033
871
P HMP007 Hemophilia 51 0.033
872
P HYP040 Hypospadias 51 0.033
873
PLR007 Pleural Empyema 50 0.033
874
THY125 Thyroid Gland Medullary Carcinoma 50 0.033
875
c BCT013 Bacterial Pneumonia 48 0.033
876
IDP070 Idiopathic Scoliosis 42 0.033
877
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.033
878
ORL012 Oral Leukoplakia 39 0.033
879
c CHR020 Chronic Interstitial Cystitis 37 0.033
880
HRN029 Hearing Loss, Noise-Induced 37 0.033
881
c DRM040 Dermatitis Herpetiformis, Familial 35 0.033
882
ENC065 Encephalitis/encephalopathy, Mild, with Reversible Myelin Vacuolization 33 0.033
883
CYT018 Cytochrome P450 2d6 Variant 27 0.033
884
STN013 Stenotrophomonas Maltophilia Infection 25 0.033
885
CRP001 Carpal Tunnel Syndrome 67 0.031
886
PPL049 Papillon-Lefevre Syndrome 65 0.031
887
APN008 Apnea, Obstructive Sleep 64 0.031
888
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.031
889
CYT008 Cytomegalovirus Infection 57 0.031
890
P ADL017 Adult T-Cell Leukemia 56 0.031
891
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 55 0.031
892
MCL006 Macular Retinal Edema 55 0.031
893
c BCT007 Bacterial Meningitis 55 0.031
894
INT007 Intermediate Coronary Syndrome 55 0.031
895
TND005 Tendinitis 54 0.031
896
PRN011 Pernicious Anemia 53 0.031
897
P SML001 Small Cell Carcinoma 52 0.031
898
SKN013 Skin Benign Neoplasm 51 0.031
899
P OBS001 Obstructive Jaundice 50 0.031
900
ENT004 Enthesopathy 49 0.031
901
VLV011 Vulvovaginal Candidiasis 49 0.031
902
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.031
903
IDP033 Idiopathic Edema 44 0.031
904
TND004 Tendinopathy 43 0.031
905
MST004 Mast Cell Neoplasm 42 0.031
906
MYF002 Myofascial Pain Syndrome 42 0.031
907
PRS063 Paresthesia 41 0.031
908
FNG016 Fungal Keratitis 40 0.031
909
GLC008 Glucose Metabolism Disease 40 0.031
910
EXT007 Extracutaneous Mastocytoma 38 0.031
911
P PRC031 Preeclampsia/eclampsia 1 38 0.031
912
c HNT011 Huntington Disease-Like 3 38 0.031
913
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.031
914
c MJR008 Major Affective Disorder 2 35 0.031
915
c MJR023 Major Affective Disorder 7 33 0.031
916
c MJR004 Major Affective Disorder 4 28 0.031
917
CYN003 Cyanide Poisoning 24 0.031
918
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.031
919
P NRV007 Nervous System Disease 66 0.031
920
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.031
921
IDP011 Idiopathic Interstitial Pneumonia 59 0.031
922
P UVT001 Uveitis 57 0.031
923
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.031
924
ESP002 Esophageal Varix 51 0.031
925
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.031
926
ASP007 Aspiration Pneumonia 48 0.031
927
P BRB001 Beriberi 46 0.031
928
c HMG001 Hemoglobin C Disease 40 0.031
929
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.031
930
HYP264 Hypertonia 38 0.031
931
SWL001 Swallowing Disorders 38 0.031
932
c CHR098 Chronic Pyelonephritis 38 0.031
933
DNT008 Denture Stomatitis 35 0.031
934
BNT001 Banti's Syndrome 21 0.031
935
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 68 0.030
936
FCT007 Factor Vii Deficiency 67 0.030
937
CHY002 Chylomicron Retention Disease 65 0.030
938
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.030
939
BRS099 Breast Ductal Carcinoma 62 0.030
940
ERY003 Erythema Multiforme 58 0.030
941
BRG013 Buerger Disease 58 0.030
942
P MLT074 Multiple Endocrine Neoplasia 56 0.030
943
HRT012 Heart Valve Disease 53 0.030
944
PRP080 Peripheral Artery Disease 53 0.030
945
EXP004 Exophthalmos 52 0.030
946
P RCT021 Rectum Cancer 52 0.030
947
THR004 Thrombocytosis 51 0.030
948
c ACT078 Acute Porphyria 51 0.030
949
PLR008 Pleurisy 50 0.030
950
P PRS049 Persistent Mullerian Duct Syndrome 50 0.030
951
c LRG001 Large Cell Carcinoma 50 0.030
952
CHL004 Cholelithiasis 49 0.030
953
VTM033 Vitamin K Deficiency Bleeding 48 0.030
954
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.030
955
P END084 Endocrine System Disease 45 0.030
956
FBR054 Fibroma 44 0.030
957
CRV043 Cervical Dystonia 42 0.030
958
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.030
959
CRV045 Cervical Intraepithelial Neoplasia 39 0.030
960
DSS010 Dissociative Disorder 39 0.030
961
DBT007 Diabetic Cataract 38 0.030
962
ESP025 Esophagus Adenocarcinoma 38 0.030
963
ENM002 Enamel Erosion 26 0.030
964
P TMP003 Temporal Arteritis 68 0.027
965
P ART005 Arteriovenous Malformation 65 0.027
966
c ART101 Aortic Valve Disease 2 65 0.027
967
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.027
968
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.027
969
MSS001 Masa Syndrome 62 0.027
970
RBS001 Rabies 58 0.027
971
FML063 Familial Glucocorticoid Deficiency 58 0.027
972
c CHL119 Cholangitis, Primary Sclerosing 57 0.027
973
P FCL005 Focal Segmental Glomerulosclerosis 57 0.027
974
P MYS005 Myositis 56 0.027
975
P PTT006 Pituitary Adenoma 55 0.027
976
P STR020 Strabismus 55 0.027
977
CRC006 Carcinoid Syndrome 55 0.027
978
HRY003 Hairy Cell Leukemia 55 0.027
979
P RST001 Restless Legs Syndrome 54 0.027
980
CLR030 Clear Cell Renal Cell Carcinoma 53 0.027
981
FNG017 Fungal Infectious Disease 53 0.027
982
P CRN025 Corneal Dystrophy 49 0.027
983
P CRV039 Cervicitis 49 0.027
984
END021 Endomyocardial Fibrosis 49 0.027
985
P SCL009 Sclerosing Cholangitis 48 0.027
986
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 47 0.027
987
TTR011 Tetraploidy 47 0.027
988
STM006 Stomach Disease 47 0.027
989
P CRC039 Coarctation of Aorta 47 0.027
990
P VTR007 Vitreoretinopathy 46 0.027
991
c ACT076 Acute Myocarditis 46 0.027
992
TNP001 Tinea Pedis 46 0.027
993
MCH006 Mechanical Strabismus 42 0.027
994
PST053 Postherpetic Neuralgia 40 0.027
995
P LTH003 Lethal Congenital Contracture Syndrome 40 0.027
996
ART008 Arteriosclerosis Obliterans 40 0.027
997
BLN006 Blind Loop Syndrome 37 0.027
998
c RST012 Restless Legs Syndrome 1 34 0.027
999
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.027
1000
KDN013 Kidney Hypertrophy 32 0.027
1001
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.027
1002
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 26 0.027
1003
P FML011 Familial Adenomatous Polyposis 72 0.027
1004
MLT157 Multiple System Atrophy 1 70 0.027
1005
P FRG001 Fragile X Syndrome 70 0.027
1006
c MLT160 Multiple Endocrine Neoplasia, Type Iia 70 0.027
1007
P MPL001 Maple Syrup Urine Disease 69 0.027
1008
MLD001 Melioidosis 68 0.027
1009
P CHR012 Chronic Granulomatous Disease 67 0.027
1010
P PRP003 Porphyria Cutanea Tarda 67 0.027
1011
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.027
1012
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.027
1013
P PRS038 Personality Disorder 65 0.027
1014
P THY023 Thymoma 65 0.027
1015
PLL001 Pallister-Hall Syndrome 64 0.027
1016
OVR029 Ovarian Hyperstimulation Syndrome 64 0.027
1017
LYM017 Lyme Disease 64 0.027
1018
P SHR029 Short Syndrome 63 0.027
1019
P ACR001 Aicardi-Goutieres Syndrome 62 0.027
1020
OST003 Osteonecrosis 61 0.027
1021
c LPM012 Lipomatosis, Multiple 60 0.027
1022
END081 Endosteal Hyperostosis, Autosomal Dominant 60 0.027
1023
RNL024 Renal Glucosuria 58 0.027
1024
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.027
1025
ERY029 Erythermalgia, Primary 58 0.027
1026
CRV038 Cervical Squamous Cell Carcinoma 58 0.027
1027
MCR013 Microphthalmia 57 0.027
1028
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.027
1029
PTT009 Pituitary Gland Disease 54 0.027
1030
ECH003 Echinococcosis 53 0.027
1031
P LRY019 Laryngitis 52 0.027
1032
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.027
1033
FCT001 Factor Viii Deficiency 51 0.027
1034
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 51 0.027
1035
URC002 Urea Cycle Disorder 51 0.027
1036
PRT029 Parathyroid Adenoma 50 0.027
1037
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.027
1038
HMG002 Hemoglobinuria 50 0.027
1039
NPH010 Nephrosclerosis 50 0.027
1040
OPT003 Opiate Dependence 50 0.027
1041
CRP032 Corpus Callosum, Agenesis of 49 0.027
1042
DDN006 Duodenitis 49 0.027
1043
LRN003 Learning Disability 49 0.027
1044
QDR001 Quadriplegia 48 0.027
1045
DFN270 Deafness, Dystonia, and Cerebral Hypomyelination 48 0.027
1046
P MCL001 Mucolipidosis 48 0.027
1047
PLC007 Placental Abruption 48 0.027
1048
PRD004 Prediabetes Syndrome 47 0.027
1049
CRN027 Corneal Neovascularization 47 0.027
1050
P ENC008 Encephalocele 47 0.027
1051
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.027
1052
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.027
1053
MXD026 Mixed Glioma 45 0.027
1054
SPP008 Suppurative Otitis Media 45 0.027
1055
c CLR017 Clear Cell Sarcoma 45 0.027
1056
TNG009 Tongue Squamous Cell Carcinoma 44 0.027
1057
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.027
1058
HPT082 Hepatic Adenomas, Familial 44 0.027
1059
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.027
1060
PHY002 Physical Disorder 42 0.027
1061
MRP001 Morphine Dependence 41 0.027
1062
KLD004 Keloid Disorder 40 0.027
1063
ADP007 Adie Pupil 39 0.027
1064
SCL001 Scalp Dermatosis 38 0.027
1065
NND010 Nondisjunction 34 0.027
1066
TBL029 Tubulin, Beta 28 0.027
1067
HNM002 Hinman Syndrome 27 0.027
1068
c RNG015 Ring Chromosome 2 26 0.027
1069
EPL050 Epilepsy, Partial, with Pericentral Spikes 25 0.027
1070
c ART115 Aortic Valve Disease 1 75 0.022
1071
ADR007 Adrenoleukodystrophy 75 0.022
1072
P TTR001 Tetralogy of Fallot 70 0.022
1073
P PRM011 Primary Ciliary Dyskinesia 69 0.022
1074
c HYP768 Hyperlipoproteinemia, Type I 67 0.022
1075
ACH004 Achondroplasia 66 0.022
1076
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 64 0.022
1077
P FRD001 Friedreich Ataxia 64 0.022
1078