Search results for Zinc chloride

1150 hits were found for Zinc chloride

# Family MCID Name MIFTS Score
1
P DRR001 Diarrhea 57 0.446
2
CYS001 Cystic Fibrosis 80 0.373
3
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.261
4
IRN002 Iron Metabolism Disease 57 0.260
5
P KDN018 Kidney Disease 70 0.247
6
DRM006 Dermatitis 61 0.239
7
48X005 48,xyyy 39 0.226
8
LVR012 Liver Cirrhosis 63 0.223
9
DFC004 Deficiency Anemia 75 0.219
10
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.203
11
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.202
12
ALL026 Allergic Hypersensitivity Disease 64 0.200
13
HLX001 Helix Syndrome 47 0.199
14
HYP005 Hypokalemia 55 0.196
15
P LVR013 Liver Disease 68 0.193
16
c ACT071 Acute Kidney Failure 59 0.190
17
c HYP595 Hypertension, Essential 84 0.184
18
CNT047 Contact Dermatitis 57 0.177
19
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.176
20
P HPT023 Hepatocellular Carcinoma 100 0.173
21
MTB004 Metabolic Acidosis 50 0.173
22
HRW001 Hair Whorl 36 0.167
23
P NRB001 Neuroblastoma 71 0.166
24
GNG013 Gingivitis 59 0.165
25
NTR005 Nutritional Deficiency Disease 61 0.164
26
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.164
27
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.163
28
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.162
29
ISC004 Ischemia 60 0.161
30
P LTR001 Lateral Sclerosis 53 0.161
31
CNG034 Congestive Heart Failure 70 0.159
32
MYT011 Myotonia 35 0.159
33
P SZR006 Seizure Disorder 58 0.157
34
CMM005 Common Cold 56 0.156
35
P ALZ034 Alzheimer Disease 88 0.156
36
BNR002 Bone Resorption Disease 48 0.155
37
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.154
38
P ALP008 Alopecia 56 0.154
39
c CHR684 Chronic Kidney Disease 66 0.154
40
CYT002 Cytokine Deficiency 44 0.153
41
HYP066 Hyperglycemia 61 0.153
42
VSL002 Visual Epilepsy 58 0.153
43
P PNM007 Pneumonia 68 0.153
44
P HRT032 Heart Disease 75 0.152
45
HYP266 Hypoxia 56 0.151
46
P DBT009 Diabetes Mellitus 64 0.151
47
CHL079 Children's Interstitial Lung Disease 27 0.150
48
ATM095 Autoimmune Disease 61 0.150
49
P NRF023 Neurofibromatosis, Type Ii 76 0.148
50
ATS010 Autosomal Recessive Disease 48 0.147
51
CHL014 Cholera 55 0.147
53
P PRS040 Prostate Cancer 97 0.145
54
P GLM045 Glioma 63 0.144
55
GLL048 Glial Tumor 45 0.143
56
DWN001 Down Syndrome 70 0.142
57
PPL052 Papillomatosis, Confluent and Reticulated 34 0.142
58
P ENC018 Encephalopathy 61 0.142
59
IRN001 Iron Deficiency Anemia 58 0.141
60
LNG099 Lung Disease 61 0.138
61
c ACT004 Acute Diarrhea 39 0.137
62
P HRP006 Herpes Simplex 65 0.136
63
LWC001 Low Compliance Bladder 42 0.135
64
BRN071 Brain Injury 49 0.134
65
P CLR023 Colorectal Cancer 98 0.132
66
LSH001 Leishmaniasis 63 0.132
67
P KLZ004 Kala-Azar 1 41 0.132
68
P MYC007 Myocardial Infarction 70 0.131
69
ADN018 Adenoma 58 0.129
70
P PSR002 Psoriasis 62 0.129
71
PST011 Pustulosis of Palm and Sole 52 0.129
72
P VSC007 Vascular Disease 63 0.129
73
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.127
74
P INF032 Infertility 57 0.126
75
PRT037 Pertussis 65 0.126
76
TRM010 Traumatic Brain Injury 53 0.125
77
47X002 47,xyy 49 0.125
78
P HYP086 Hypothyroidism 68 0.125
79
P OST002 Osteoporosis 73 0.124
80
P THL005 Thalassemia 60 0.124
81
KRT002 Keratomalacia 48 0.122
82
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.122
83
P MRC003 Mercury Poisoning 48 0.122
84
HMN044 Human Immunodeficiency Virus Type 1 71 0.122
85
ALC007 Alcohol Dependence 66 0.122
86
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.121
87
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.121
88
ALL010 Allergic Contact Dermatitis 55 0.121
89
P ADN016 Adenocarcinoma 64 0.121
90
P CTR002 Cataract 60 0.121
91
GLB015 Glioblastoma Multiforme 75 0.121
92
RCK004 Rickets 69 0.121
93
CRH001 Crohn's Disease 74 0.121
94
END030 End Stage Renal Failure 58 0.120
95
c PRC016 Pre-Eclampsia 63 0.120
96
SKN016 Skin Disease 63 0.120
97
HYP080 Hypogonadism 50 0.119
98
INS024 Insulin-Like Growth Factor I 79 0.119
99
P SCK005 Sickle Cell Disease 50 0.119
100
HYP064 Hypogonadotropism 40 0.118
101
PNG002 Pain Agnosia 51 0.118
102
P BRS047 Breast Cancer 96 0.118
103
HYP056 Hypoglycemia 66 0.118
104
HPT004 Hepatic Coma 43 0.117
105
GST045 Gastroenteritis 59 0.117
106
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.116
107
P NRP001 Neuropathy 56 0.116
108
P INF037 Inflammatory Bowel Disease 56 0.116
109
P PRD008 Periodontitis 62 0.116
110
P GST053 Gastric Cancer 83 0.116
111
c ACT075 Acute Myocardial Infarction 56 0.115
112
DNT012 Dental Caries 51 0.115
113
SPN186 Spinal Cord Injury 60 0.115
114
P MLN007 Male Infertility 56 0.113
115
c PCH010 Pachyonychia Congenita 3 43 0.113
116
P PNC035 Pancreatic Cancer 84 0.113
117
CNS004 Constipation 57 0.113
118
P LKM002 Leukemia 66 0.113
119
HPT019 Hepatic Encephalopathy 60 0.113
120
AST005 Asthma 77 0.113
121
P BCL017 B-Cell Lymphoma 58 0.112
122
OST159 Osteogenic Sarcoma 66 0.111
123
CLT003 Colitis 62 0.110
124
CTN007 Cutaneous Leishmaniasis 61 0.110
125
P OVR042 Ovarian Cancer 89 0.110
126
P NSP012 Nasopharyngeal Carcinoma 67 0.110
127
TTN003 Tetanus 64 0.109
128
P CRD119 Cardiac Arrest 67 0.109
129
ATX019 Ataxia with Vitamin E Deficiency 48 0.109
130
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.109
131
IMM167 Immune Deficiency Disease 78 0.109
132
TXC005 Toxic Shock Syndrome 61 0.108
133
SCK003 Sickle Cell Anemia 72 0.107
134
ATH013 Atherosclerosis Susceptibility 66 0.107
135
FTT001 Fatty Liver Disease 61 0.107
136
PPT005 Peptic Ulcer Disease 58 0.107
137
PLM001 Pulmonary Tuberculosis 70 0.107
138
P CRN018 Coronary Artery Anomaly 63 0.106
139
P DRM053 Dermatitis, Atopic 66 0.106
140
DPR016 Depression 63 0.105
141
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.105
142
ANR007 Anorexia Nervosa 63 0.105
143
P RHN004 Rhinitis 57 0.105
144
P BPL003 Bipolar Disorder 56 0.105
145
c MJR024 Major Affective Disorder 9 41 0.105
146
c MJR022 Major Affective Disorder 8 38 0.105
147
ESP021 Esophageal Cancer 90 0.105
148
EYD002 Eye Disease 58 0.104
149
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.103
150
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.103
151
P PNC044 Pancreatitis 61 0.103
152
OST012 Osteoarthritis 78 0.102
153
AGN016 Aging 56 0.102
154
CRV035 Cervical Cancer 76 0.101
155
c MCR120 Microvascular Complications of Diabetes 7 47 0.101
156
PLM010 Pulmonary Edema 55 0.100
157
P GLM007 Glomerulonephritis 57 0.100
158
DRR008 Diarrhea 1, Secretory Chloride, Congenital 51 0.100
159
SCR003 Secretory Diarrhea 36 0.100
160
P MNN013 Meningitis 65 0.099
161
P NTR004 Neutropenia 63 0.099
162
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.099
163
P EXN002 Exanthem 57 0.099
164
P HYP069 Hyperparathyroidism 62 0.098
165
URM002 Uremia 49 0.098
166
DYS015 Dysentery 50 0.098
167
c MCR113 Microvascular Complications of Diabetes 3 52 0.098
168
c MCR130 Microvascular Complications of Diabetes 6 41 0.098
169
c MCR133 Microvascular Complications of Diabetes 4 41 0.098
170
GST023 Gastric Ulcer 53 0.098
171
NRL016 Neural Tube Defects 82 0.098
172
P CRN300 Coronary Heart Disease 1 63 0.097
173
P LNG032 Lung Cancer 97 0.097
174
BRN024 Bronchitis 68 0.097
175
BCT022 Bacterial Infectious Disease 56 0.097
176
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.097
177
P GST044 Gastritis 55 0.097
178
c PNS012 Paine Syndrome 61 0.096
179
BRN004 Brain Edema 55 0.096
180
MDD011 Mood Disorder 62 0.096
181
P TRM003 Tremor 53 0.095
182
P LYM031 Lymphocytic Leukemia 55 0.094
183
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.094
184
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.094
185
c BTT014 Beta-Thalassemia 72 0.094
186
P EPL164 Epilepsy 71 0.094
187
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 53 0.094
188
c BRN108 Branchiootic Syndrome 1 61 0.093
189
HMS001 Hemosiderosis 54 0.093
190
NPH003 Nephrocalcinosis 51 0.093
191
ADL002 Adult Syndrome 69 0.093
192
P PHC003 Pheochromocytoma 71 0.093
193
ADR040 Adrenal Gland Pheochromocytoma 46 0.093
194
P ATS364 Autism 65 0.093
195
STM007 Stomatitis 49 0.093
196
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.092
197
PRS045 Prostatic Hypertrophy 52 0.092
198
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.092
199
THR024 Thrombosis 56 0.092
200
P RTN024 Retinoblastoma 72 0.092
201
c FML008 Familial Retinoblastoma 53 0.092
202
P NPH012 Nephrotic Syndrome 63 0.091
203
P MYT002 Myotonic Dystrophy 49 0.091
204
OCL069 Ocular Motor Apraxia 51 0.091
205
c LKM061 Leukemia, Acute Myeloid 83 0.091
206
SQM006 Squamous Cell Carcinoma 60 0.091
207
STR067 Stroke, Ischemic 80 0.091
208
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.091
209
c ACT027 Acute Pancreatitis 59 0.090
210
CRB004 Cerebral Artery Occlusion 44 0.090
211
ART140 Arteries, Anomalies of 53 0.089
212
P SKN015 Skin Carcinoma 67 0.089
213
PST092 Posttransplant Acute Limbic Encephalitis 29 0.089
214
P RHM011 Rheumatoid Arthritis 80 0.089
215
c HYP836 Hypercholesterolemia, Familial, 1 72 0.088
216
c HPT016 Hepatitis B 59 0.088
217
GTR002 Goiter 52 0.088
218
c ACT068 Acute Cystitis 63 0.088
219
P HYP076 Hyperthyroidism 55 0.088
220
ULC004 Ulcerative Colitis 73 0.087
221
INS001 Insulinoma 60 0.087
222
HVY002 Heavy Metal Poisoning 22 0.087
223
P CRD246 Cardiovascular System Disease 56 0.087
224
P BND020 Bone Disease 59 0.086
225
ANX004 Anoxia 42 0.086
226
PRS047 Prostatitis 56 0.086
227
CRB039 Cerebrovascular Disease 69 0.086
228
P SYS005 Systemic Scleroderma 70 0.086
229
P MYL006 Myeloid Leukemia 60 0.086
230
P PRP019 Peripheral Nervous System Disease 57 0.085
231
P PLY014 Polycystic Kidney Disease 59 0.085
232
P INT070 Intestinal Obstruction 58 0.085
233
NWC001 Newcastle Disease 44 0.085
234
PRT038 Protein-Energy Malnutrition 54 0.084
235
PRS021 Prostatic Adenoma 51 0.084
236
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.084
237
MLN008 Melanoma 69 0.084
238
PRT036 Peritonitis 65 0.084
239
PRS129 Prostatic Hyperplasia, Benign 49 0.083
240
CHL068 Cholestasis 60 0.083
241
GLC003 Glucose Intolerance 54 0.083
242
P MSC005 Muscular Dystrophy 66 0.083
243
P TRN020 Turner Syndrome 65 0.082
244
MYL069 Myeloma, Multiple 85 0.082
245
P LNG064 Lung Cancer Susceptibility 3 77 0.082
246
c RHB024 Rhabdomyosarcoma 2 65 0.082
247
ORL011 Oral Cancer 60 0.082
248
P ECL001 Eclampsia 51 0.082
249
P PLM037 Pulmonary Hypertension 68 0.082
250
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.081
251
SVR004 Severe Combined Immunodeficiency 73 0.081
252
MNT002 Mental Depression 57 0.081
253
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.081
254
P ART022 Arthritis 70 0.081
255
P DMN002 Dementia 67 0.081
256
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 59 0.081
257
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.081
258
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.081
259
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.081
260
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.081
261
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.081
262
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.081
263
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.081
264
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.081
265
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.081
266
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.081
267
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.081
268
PRT013 Portal Hypertension 60 0.080
269
MLR004 Malaria 80 0.080
270
P RRH023 Rare Hereditary Hemochromatosis 41 0.080
271
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.080
272
c PRM038 Primary Agammaglobulinemia 43 0.080
273
P ALP009 Alopecia Areata 60 0.080
274
P INT068 Intestinal Disease 52 0.080
275
PPL022 Papilloma 54 0.080
276
ACT119 Acute Promyelocytic Leukemia 63 0.080
277
ANX010 Anxiety 72 0.079
278
P RTN016 Retinal Degeneration 53 0.079
279
c HPT001 Hepatitis C 63 0.079
280
P RSP003 Respiratory Failure 74 0.079
281
BLR008 Bilirubin Metabolic Disorder 57 0.079
282
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.079
283
c ATS007 Autism Spectrum Disorder 67 0.079
284
ILS001 Ileus 51 0.078
285
P CHR345 Chronic Pain 50 0.078
286
c ATR087 Atrial Standstill 1 74 0.078
287
ARG004 Argyria 28 0.078
288
HYP781 Hypoascorbemia 50 0.078
289
MCS002 Mucositis 55 0.078
290
P VSC011 Vasculitis 62 0.078
291
P MYS003 Myasthenia Gravis 68 0.077
292
KRT009 Keratosis 53 0.077
293
P BLD134 Bladder Cancer 78 0.077
294
P OST001 Osteopetrosis 71 0.077
295
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.077
296
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.077
297
PCD001 Pica Disease 37 0.077
298
THY029 Thyroid Carcinoma 59 0.076
299
AZS001 Azoospermia 50 0.076
300
PLY150 Polykaryocytosis Inducer 31 0.076
301
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.076
302
ACQ007 Acquired Immunodeficiency Syndrome 60 0.076
303
P OVR082 Overgrowth Syndrome 50 0.076
304
SQM002 Squamous Cell Papilloma 42 0.076
305
BRN028 Brain Cancer 73 0.076
306
P HPT021 Hepatitis 67 0.076
307
GST050 Gastrointestinal System Disease 56 0.076
308
MST005 Mastitis 53 0.076
309
ORL015 Oral Squamous Cell Carcinoma 43 0.075
310
VCC001 Vaccinia 49 0.075
311
ENT011 Enterocolitis 50 0.075
312
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.075
313
P OPN001 Open-Angle Glaucoma 49 0.075
314
IDP011 Idiopathic Interstitial Pneumonia 63 0.075
315
BRN002 Bronchiolitis 59 0.075
316
c VRL010 Viral Hepatitis 51 0.074
317
P HNT016 Huntington Disease 71 0.074
318
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.074
319
CLN015 Colon Adenocarcinoma 63 0.074
320
P CLC063 Celiac Disease 1 68 0.074
321
RYN005 Raynaud Phenomenon 46 0.074
322
CLF027 Cleft Palate, Isolated 64 0.074
323
P FBR017 Fibrosarcoma 56 0.074
324
P PLM036 Pulmonary Fibrosis 61 0.073
325
ACR062 Acroosteolysis 35 0.073
326
ALL014 Allergic Encephalomyelitis 39 0.073
327
P HML002 Hemolytic Anemia 62 0.073
328
ALL003 Allergic Rhinitis 67 0.073
329
DWR001 Dwarfism 44 0.073
330
OCL006 Ocular Hypertension 53 0.072
331
P BRS044 Breast Adenocarcinoma 59 0.072
332
P MLT020 Multiple Sclerosis 72 0.072
333
LPD008 Lipid Metabolism Disorder 62 0.072
334
HYP060 Hyperinsulinism 54 0.072
335
P MYC008 Myocarditis 59 0.071
336
P LKM062 Leukemia, Acute Lymphoblastic 68 0.071
337
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.071
338
P PLY019 Polyneuropathy 56 0.071
339
P DDN001 Duodenal Ulcer 50 0.071
340
P ADL010 Adult Respiratory Distress Syndrome 63 0.071
341
STT001 Status Epilepticus 59 0.071
342
P CND004 Candidiasis 57 0.071
343
GLS018 Glass Syndrome 53 0.071
344
P PRK057 Parkinson Disease, Late-Onset 76 0.071
345
P SCH015 Schizophrenia 75 0.071
346
ART016 Aortic Aneurysm 68 0.071
347
P HYP750 Hypertriglyceridemia, Familial 61 0.071
348
DPH001 Diphtheria 60 0.071
349
BRN056 Bronchopulmonary Dysplasia 57 0.071
350
P DBT005 Diabetes Insipidus 55 0.071
351
IMP005 Impotence 52 0.070
352
P ALC033 Alcohol Use Disorder 58 0.070
353
CHR178 Chromosomal Triplication 35 0.070
354
P HDC001 Headache 57 0.070
355
GST092 Gastroesophageal Reflux 65 0.070
356
P TMP001 Temporal Lobe Epilepsy 50 0.070
357
P LYM118 Lymphoma 68 0.070
358
P AST007 Astrocytoma 50 0.069
359
ACT003 Acute Kidney Tubular Necrosis 45 0.069
360
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.069
361
P CNR004 Cone-Rod Dystrophy 2 71 0.069
362
P PNM006 Pneumoconiosis 55 0.069
363
ANT018 Anthracosis 48 0.069
364
P LPR021 Leprosy 3 67 0.069
365
HNS001 Hansen's Disease 34 0.069
366
P MCR115 Microvascular Complications of Diabetes 5 66 0.068
367
P ART021 Arteriosclerosis 54 0.067
368
TLN003 Telangiectasis 51 0.067
369
SRC014 Sarcoma 65 0.067
370
KRT019 Keratitis, Hereditary 67 0.067
371
c PRM005 Primary Hyperparathyroidism 58 0.067
372
SPL018 Splenomegaly 48 0.067
373
ALC009 Alcoholic Liver Cirrhosis 53 0.067
374
P MYP004 Myopathy 64 0.067
375
SBC016 Subacute Delirium 44 0.066
376
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.066
377
SCH014 Schistosomiasis 56 0.066
378
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.066
379
P KDN017 Kidney Cancer 61 0.066
380
SPN035 Spindle Cell Sarcoma 51 0.065
381
P NGH001 Night Blindness 47 0.065
382
P RNL007 Renal Tubular Acidosis 50 0.065
383
P BRN022 Bronchiectasis 59 0.065
384
PLM031 Poliomyelitis 57 0.065
385
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.065
386
c SML038 Small Cell Cancer of the Lung 65 0.065
387
P THR014 Thrombocytopenia 68 0.064
388
PHR003 Pharyngitis 56 0.064
389
MSL001 Measles 61 0.064
390
P THY032 Thyroiditis 53 0.064
391
SPP010 Suppressor of Tumorigenicity 3 51 0.064
392
OLG001 Oligospermia 45 0.064
393
DRY001 Dry Eye Syndrome 47 0.063
394
SPS057 Spasticity 41 0.063
395
PNC129 Pancreatic Adenocarcinoma 67 0.063
396
c ALP101 Alpha-Thalassemia 62 0.063
397
c SPN225 Spondyloarthropathy 1 73 0.063
398
P URT039 Urticaria 58 0.063
399
c HPT003 Hepatitis a 63 0.063
400
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.063
401
CCC002 Coccidiosis 50 0.063
402
c HPT073 Hepatitis C Virus 70 0.063
403
HMP009 Haemophilus Influenzae 42 0.063
404
IRR003 Irritant Dermatitis 47 0.063
405
PHN003 Phenylketonuria 75 0.062
406
ANG054 Angina Pectoris 66 0.062
407
BCT004 Bacteriuria 48 0.062
408
P OPT006 Optic Nerve Disease 57 0.062
409
P CNJ013 Conjunctivitis 65 0.062
410
TRY001 Trypanosomiasis 50 0.062
411
c PRS136 Prostate Cancer, Hereditary, 6 33 0.062
412
c PRS130 Prostate Cancer, Hereditary, 8 32 0.062
413
P LPS004 Lupus Erythematosus 61 0.061
414
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.061
415
c GRV008 Graves Disease 1 55 0.061
416
P AMY004 Amyloidosis 70 0.061
417
BLL006 Bullous Pemphigoid 62 0.061
418
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.061
419
P PYL005 Pyelonephritis 56 0.061
420
HYP014 Hyperuricemia 51 0.061
421
P SBR004 Seborrheic Dermatitis 45 0.061
422
PTT037 Pituitary Tumors 44 0.061
423
P MNC007 Monocytic Leukemia 54 0.060
424
P HYP098 Hypereosinophilic Syndrome 66 0.060
425
CHG001 Chagas Disease 66 0.060
426
c FNC043 Fanconi Anemia, Complementation Group E 62 0.060
427
GST020 Gastric Antral Vascular Ectasia 41 0.060
428
P SNS001 Sensorineural Hearing Loss 61 0.059
429
VRC005 Varicose Veins 60 0.059
430
49X006 49, Xxxxy Syndrome 41 0.059
431
P RHB003 Rhabdomyosarcoma 62 0.059
432
P SJG008 Sjogren Syndrome 56 0.059
433
ANT024 Anthrax Disease 58 0.059
434
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.059
435
HDN002 Head Injury 45 0.059
436
PRP027 Peripheral Vascular Disease 71 0.059
437
P DYS154 Dystonia 65 0.059
438
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.059
439
P ESP024 Esophagitis 62 0.059
440
P PRP029 Porphyria 62 0.058
441
c ACT134 Acute Liver Failure 51 0.058
442
c THR092 Thrombophilia Due to Thrombin Defect 73 0.058
443
ERY051 Erythroleukemia, Familial 56 0.058
444
P BNG032 Benign Mesothelioma 45 0.058
445
P ATR011 Atrial Fibrillation 66 0.058
446
P CYS018 Cystitis 59 0.058
447
P SPR086 Spermatogenic Failure 3 44 0.058
448
P TCL004 T-Cell Leukemia 47 0.057
449
LYM133 Lymphoma, Hodgkin, Classic 69 0.057
450
PRN019 Perinatal Necrotizing Enterocolitis 54 0.057
451
P LCH002 Lichen Planus 54 0.057
452
c PRD040 Periodontitis, Chronic 54 0.057
453
OST011 Osteomalacia 52 0.057
454
P SLP006 Sleep Apnea 69 0.057
455
NWB001 Newborn Respiratory Distress Syndrome 58 0.057
456
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.057
457
c SCN007 Secondary Hyperparathyroidism 50 0.057
458
P INF038 Influenza 68 0.057
459
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 22 0.057
460
ALL006 Allergic Asthma 56 0.057
461
MLC004 Mulchandani-Bhoj-Conlin Syndrome 32 0.057
462
SXL003 Sexual Disorder 48 0.056
463
GT001 Gout 63 0.056
464
P INS002 in Situ Carcinoma 52 0.056
465
CRT015 Carotid Artery Occlusion 44 0.056
466
MTH071 Methane Production 26 0.056
467
P MYC084 Mycobacterium Tuberculosis 1 68 0.056
468
P ATX030 Ataxia-Telangiectasia 83 0.055
469
c SYS001 Systemic Lupus Erythematosus 86 0.055
470
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.055
471
P RTN018 Retinal Disease 52 0.055
472
P RTN008 Retinitis Pigmentosa 77 0.055
473
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.055
474
c WLM013 Wilms Tumor 1 65 0.055
475
RTN023 Retinitis 46 0.055
476
GRD001 Giardiasis 45 0.055
477
NRR001 Neuroretinitis 43 0.055
478
CRD132 Cardiac Conduction Defect 59 0.055
479
P FNC004 Fanconi Syndrome 50 0.055
480
KRT001 Keratoconjunctivitis Sicca 50 0.055
481
c DWL002 Dowling-Degos Disease 1 58 0.054
482
MTH009 Mouth Disease 56 0.054
483
MSC007 Muscle Hypertrophy 63 0.054
484
P TRC086 Trichohepatoenteric Syndrome 1 59 0.054
485
ANR040 Aneurysm 58 0.054
486
PLG002 Plague 57 0.054
487
DYS073 Dysphagia 50 0.054
488
EXN003 Exencephaly 31 0.054
489
BCT002 Bacterial Vaginosis 52 0.054
490
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.054
491
NRT004 Neuritis 53 0.054
492
THR013 Thoracic Outlet Syndrome 53 0.054
493
RRS014 Rare Surgical Neurologic Disease 32 0.054
494
ALC006 Alcoholic Hepatitis 61 0.054
495
P EHL001 Ehlers-Danlos Syndrome 57 0.054
496
END057 Endometrial Cancer 74 0.053
497
c SVR001 Severe Acute Respiratory Syndrome 55 0.053
498
P MYP006 Myopia 55 0.053
499
P MSC003 Muscular Atrophy 52 0.053
500
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.053
501
DCB001 Decubitus Ulcer 60 0.053
502
c ACT073 Acute Leukemia 58 0.053
503
P GRV001 Graves' Disease 55 0.053
504
EMB004 Embryonal Carcinoma 57 0.052
505
c MGR028 Migraine with or Without Aura 1 69 0.052
506
LYS002 Lysosomal Storage Disease 52 0.052
507
CRD223 Cardiac Arrhythmia 60 0.052
508
DRM011 Dermatophytosis 52 0.052
509
NNL006 Non-Alcoholic Steatohepatitis 51 0.052
510
RHM027 Rheumatic Disease 56 0.052
511
AMN003 Amnestic Disorder 54 0.052
512
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.052
513
P HRS035 Hirschsprung Disease 1 65 0.052
514
CHR066 Chronic Fatigue Syndrome 61 0.052
515
VRL011 Viral Infectious Disease 61 0.052
516
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.052
517
c MLG068 Malignant Glioma 45 0.052
518
LST001 Listeriosis 54 0.051
519
SKN019 Skin Melanoma 67 0.051
520
FDB001 Foodborne Botulism 56 0.051
521
CHR100 Chronic Ulcer of Skin 53 0.051
522
c EXD008 Exudative Vitreoretinopathy 1 69 0.051
523
P HYP265 Hypotonia 42 0.051
524
OTT002 Otitis Media 71 0.051
525
P MTR014 Motor Neuron Disease 64 0.051
526
THY030 Thyroid Gland Disease 51 0.051
527
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.051
528
ATR057 Atrioventricular Block 55 0.050
529
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.050
530
MNG007 Manganese Poisoning 29 0.050
531
c ATS347 Autosomal Dominant Polycystic Kidney Disease 59 0.050
532
VGN023 Vaginitis 55 0.050
533
MCN017 Meconium Ileus 52 0.050
534
RTN017 Retinal Detachment 60 0.050
535
P SBS003 Substance Abuse 54 0.050
536
P SLM003 Salmonellosis 54 0.050
537
PNC001 Pancytopenia 54 0.050
538
RTN003 Retinal Ischemia 50 0.050
539
DMP001 Dumping Syndrome 44 0.050
540
EXC002 Exocrine Pancreatic Insufficiency 41 0.050
541
BRR014 Barrett Esophagus 64 0.050
542
P END044 Endometriosis 62 0.050
543
P SCL018 Scoliosis 60 0.050
544
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 57 0.050
545
RTR008 Root Resorption 45 0.050
546
ORL013 Oral Lichen Planus 45 0.050
547
P FBR031 Febrile Seizures 51 0.049
548
P GRF003 Graft-Versus-Host Disease 71 0.049
549
c MCL013 Mucolipidosis Iv 64 0.049
550
IRR002 Irritable Bowel Syndrome 63 0.049
551
P ART023 Arthropathy 62 0.049
552
P ENC004 Encephalitis 61 0.049
553
PLM033 Pulmonary Embolism 59 0.049
554
VLV047 Volvulus of Midgut 50 0.049
555
CHL065 Cholangiocarcinoma 67 0.049
556
INT079 Intrahepatic Cholangiocarcinoma 50 0.049
557
MSC157 Muscular Dystrophy, Duchenne Type 71 0.049
558
c MCR129 Microvascular Complications of Diabetes 1 66 0.049
559
P ANR048 Aniridia 1 63 0.049
560
PLS009 Plasma Cell Neoplasm 51 0.049
561
MYL020 Myelomeningocele 51 0.048
562
ECT026 Ectopic Pregnancy 49 0.048
563
c MYT029 Myotonia Congenita, Autosomal Recessive 41 0.048
564
c SCL052 Scleroderma, Familial Progressive 62 0.048
565
P HYP097 Hyperekplexia 61 0.048
566
P EPD016 Epidermolysis Bullosa 53 0.048
567
CLC006 Calcinosis 48 0.048
568
SYS071 Systemic Autoimmune Disease 37 0.048
569
ADG002 Audiogenic Seizures 26 0.048
570
MYL009 Myelodysplastic Syndrome 70 0.048
571
P ASP006 Aspergillosis 66 0.048
572
ANG005 Anogenital Venereal Wart 56 0.048
573
HMG005 Hemoglobinopathy 55 0.048
574
P SHR001 Short Bowel Syndrome 52 0.048
575
LPT014 Leptin Deficiency or Dysfunction 73 0.048
576
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.048
577
TBC004 Tobacco Addiction 64 0.048
578
P PRM006 Primary Biliary Cirrhosis 61 0.048
579
VSC002 Vascular Dementia 57 0.048
580
P LRY044 Larynx Cancer 54 0.048
581
PRM020 Premenstrual Tension 39 0.048
582
OVR094 Ovarian Epithelial Cancer 38 0.048
583
ANP008 Anaplastic Oligoastrocytoma 30 0.048
584
P AGM001 Agammaglobulinemia 65 0.048
585
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.048
586
ATN011 Autoinflammation with Infantile Enterocolitis 43 0.048
587
c CHR682 Chronic Bilirubin Encephalopathy 38 0.048
588
P HYD006 Hydrocephalus 65 0.046
589
P SYP003 Syphilis 59 0.046
590
CHL067 Cholecystitis 58 0.046
591
P HYP024 Hypoparathyroidism 55 0.046
592
HYP081 Hypolipoproteinemia 50 0.046
593
CRD137 Cardiogenic Shock 48 0.046
594
ATN005 Autonomic Dysfunction 47 0.046
595
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.046
596
ACR006 Aceruloplasminemia 73 0.046
597
c INF071 Inflammatory Bowel Disease 1 68 0.046
598
CRB037 Cerebral Palsy 68 0.046
599
ACN002 Acanthosis Nigricans 60 0.046
600
DBT010 Diabetic Neuropathy 55 0.046
601
HLC007 Helicobacter Pylori Infection 59 0.046
602
ORL004 Oral Submucous Fibrosis 55 0.046
603
CLR109 Colorectal Adenocarcinoma 50 0.046
604
P INT143 Interstitial Cystitis 61 0.046
605
KRT006 Keratoconjunctivitis 53 0.046
606
c SVR005 Severe Pre-Eclampsia 49 0.046
607
FLL008 Folliculitis 46 0.046
608
c FML001 Familial Atrial Fibrillation 66 0.046
609
CMM004 Common Variable Immunodeficiency 67 0.045
610
c MYT021 Myotonic Dystrophy 1 66 0.045
611
P LPS002 Liposarcoma 65 0.045
612
CHL123 Chlamydia 59 0.045
613
CMR002 Coumarin Resistance 56 0.045
614
PRP030 Purpura 55 0.045
615
DMY004 Demyelinating Disease 52 0.045
616
c PSR017 Psoriasis 2 52 0.045
617
TRC003 Trichomoniasis 52 0.045
618
LNG031 Lung Benign Neoplasm 50 0.045
619
INT067 Interstitial Nephritis 46 0.045
620
CYN002 Cyanosis, Transient Neonatal 45 0.045
621
c MCR112 Microvascular Complications of Diabetes 2 41 0.045
622
BRS051 Breast Disease 58 0.044
623
GRW007 Growth Hormone Deficiency 43 0.044
624
SPN051 Spondylitis 52 0.044
625
P RNL015 Renal Hypertension 48 0.044
626
KRT008 Keratopathy 46 0.044
627
BCK006 Back Pain 42 0.044
628
P RRT020 Rare Tumor 41 0.044
629
INF009 Inflammatory Spondylopathy 32 0.044
630
TYP007 Typhoid Fever 63 0.044
631
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.044
632
DRR016 Diarrhea 2, with Microvillus Atrophy 57 0.044
633
RSP019 Respiratory Distress Syndrome in Premature Infants 57 0.044
634
P CHN012 Chondrosarcoma 56 0.044
635
P SDR002 Siderosis 44 0.044
636
CNN003 Conn's Syndrome 79 0.043
637
P APL001 Aplastic Anemia 74 0.043
638
YLL002 Yellow Fever 60 0.043
639
DSS009 Disseminated Intravascular Coagulation 57 0.043
640
c FML035 Familial Hyperlipidemia 55 0.043
641
CHR073 Choreatic Disease 52 0.043
642
TXC002 Toxic Encephalopathy 52 0.043
644
PRN014 Paronychia 49 0.043
645
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.043
646
URT010 Ureteral Obstruction 46 0.043
647
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 46 0.043
648
TRP009 Triple X Syndrome 42 0.043
649
ATX010 Ataxia Neuropathy Spectrum 38 0.043
650
ACT064 Acute Necrotizing Encephalitis 32 0.043
651
OSM001 Osmotic Diarrhea 32 0.043
652
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.043
653
BLD137 Blood Group--Ahonen 19 0.043
654
PRT058 Pure Autonomic Failure 59 0.043
656
ATM052 Autoimmune Disease 1 37 0.043
657
CHR177 Chromophobe Renal Cell Carcinoma 56 0.043
658
CRT017 Cartilage Disease 54 0.043
659
CRH005 Crohn's Colitis 52 0.043
660
c PSR023 Psoriasis 1 49 0.043
661
WTH001 Withdrawal Disorder 48 0.043
662
LYM019 Lymphosarcoma 47 0.043
663
TST014 Testicular Cancer 46 0.043
664
c PSR028 Psoriasis 7 39 0.043
665
c PSR032 Psoriasis 11 38 0.043
666
c PSR018 Psoriasis 13 38 0.043
667
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.043
668
c DLT002 Dilated Cardiomyopathy 79 0.043
669
c BSL007 Basal Cell Carcinoma 68 0.043
670
CLR108 Colorectal Adenoma 64 0.043
671
DSS008 Disease of Mental Health 57 0.043
672
VSC003 Visceral Leishmaniasis 55 0.043
673
CLF001 Cleft Lip 53 0.043
674
PLP001 Pulpitis 48 0.043
675
KPS004 Kaposi Sarcoma 75 0.041
676
GST040 Gastric Adenocarcinoma 70 0.041
677
c PNC108 Pancreatitis, Hereditary 69 0.041
678
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 65 0.041
679
P ICH004 Ichthyosis 54 0.041
680
CMB003 Combined T Cell and B Cell Immunodeficiency 52 0.041
681
HPT014 Hepatorenal Syndrome 50 0.041
682
c INH020 Inherited Metabolic Disorder 46 0.041
683
CRB090 Cerebral Hypoxia 43 0.041
684
KND001 Kindler Syndrome 63 0.041
685
PRP016 Paraplegia 53 0.041
686
PYL006 Pyloric Stenosis 48 0.041
687
AMN006 Aminoaciduria 38 0.041
688
KHL003 Kohlschutter-Tonz Syndrome 64 0.041
689
CRY005 Cryptococcosis 58 0.041
690
GNT003 Genital Herpes 54 0.041
691
LMY002 Leiomyoma 50 0.041
692
P KRT007 Keratoconus 49 0.041
693
BRN009 Burning Mouth Syndrome 49 0.041
694
TRT001 Teratocarcinoma 46 0.041
695
HND015 Hand Skill, Relative 33 0.041
696
ACR007 Acromegaly 71 0.040
697
P SRC025 Sarcoidosis 1 70 0.040
698
P ANG001 Angelman Syndrome 67 0.040
699
c MCL062 Mucolipidosis Ii Alpha/beta 66 0.040
700
OST017 Osteomyelitis 64 0.040
701
BRC012 Brucellosis 61 0.040
702
HYD002 Hydronephrosis 59 0.040
703
PNM008 Pneumothorax 56 0.040
704
P ANG015 Angioedema 54 0.040
705
c CRS016 Crisponi/cold-Induced Sweating Syndrome 1 53 0.040
706
P MMB011 Membranous Nephropathy 50 0.040
707
c INF145 Infantile Liver Failure Syndrome 1 50 0.040
708
RFR010 Refractory Anemia 48 0.040
709
HYP025 Hyperphosphatemia 47 0.040
710
KRT013 Keratolytic Winter Erythema 46 0.040
711
P HMR005 Hemorrhoid 46 0.040
712
TST015 Testicular Disease 43 0.040
713
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.040
714
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.040
715
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.040
716
P SLP005 Sleep Disorder 59 0.040
717
IGR001 Ige Responsiveness, Atopic 59 0.040
718
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 57 0.040
719
HMR039 Hemorrhage, Intracerebral 57 0.040
720
P OPT009 Optic Neuritis 56 0.040
721
ALB002 Albinism 46 0.040
722
CHP002 Chops Syndrome 42 0.040
723
MNK001 Menkes Disease 64 0.039
724
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.039
725
c MST023 Mesothelioma, Malignant 57 0.039
726
TNS005 Tonsillitis 57 0.039
727
SFT003 Soft Tissue Sarcoma 56 0.039
728
ORL005 Oral Candidiasis 56 0.039
729
END040 Endogenous Depression 54 0.039
730
KHN001 Kuhnt-Junius Degeneration 48 0.039
732
KLB003 Klebsiella Pneumonia 39 0.039
733
MTL005 Metal Allergy 38 0.039
734
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.039
735
URT049 Urate Oxidase, Pseudogene 25 0.039
736
URN010 Urinary Tract Obstruction 57 0.039
737
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.039
738
PTH003 Pathologic Nystagmus 51 0.039
739
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 42 0.039
740
P FNC026 Fanconi Renotubular Syndrome 1 36 0.039
741
P RTT002 Rett Syndrome 80 0.038
742
c LKM063 Leukemia, Chronic Myeloid 71 0.038
743
P TXP001 Toxoplasmosis 60 0.038
744
P ECT006 Ectodermal Dysplasia 59 0.038
745
PLS011 Plasmacytoma 56 0.038
746
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.038
747
ANL018 Analbuminemia 54 0.038
748
c PNC106 Pancreatic Agenesis 1 50 0.038
749
AMB001 Amebiasis 49 0.038
750
SLP001 Sleeping Sickness 48 0.038
751
MCR018 Microcytic Anemia 47 0.038
752
PNC034 Pancreas Disease 46 0.038
753
LKP003 Leukoplakia 39 0.038
754
OBS532 Obsolete: Ehlers-Danlos Syndrome, Fibronectinemic Type 15 0.038
755
c MNN043 Meningioma, Familial 74 0.037
756
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.037
757
AND002 Androgen Insensitivity Syndrome 66 0.037
758
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.037
759
P CHR071 Charcot-Marie-Tooth Disease 64 0.037
760
P NRN021 Neuronal Ceroid Lipofuscinosis 63 0.037
761
MNN042 Meningioma, Radiation-Induced 62 0.037
762
c ATM011 Autoimmune Hepatitis 62 0.037
763
P MVM001 Movement Disease 61 0.037
764
HRP004 Herpes Zoster 60 0.037
765
CRY035 Cryptorchidism, Unilateral or Bilateral 59 0.037
766
c BNG091 Benign Chronic Pemphigus 59 0.037
767
FBR047 Fibromyalgia 59 0.037
768
P AXN002 Axenfeld-Rieger Syndrome 58 0.037
769
GLL018 Gallbladder Cancer 56 0.037
770
BRN012 Bronchiolitis Obliterans 56 0.037
771
P PNC025 Panic Disorder 53 0.037
772
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 52 0.037
773
P LCT001 Lactic Acidosis 51 0.037
774
c HNT004 Huntington Disease-Like 2 49 0.037
775
RYN001 Raynaud Disease 49 0.037
776
SPN021 Spinal Meningioma 47 0.037
777
MCC002 Mucocutaneous Leishmaniasis 47 0.037
778
CHR074 Choriocarcinoma 46 0.037
779
ORC001 Orchitis 45 0.037
780
c HYP272 Hypercholesterolemia, Familial, 3 43 0.037
781
RDN001 Reading Disorder 40 0.037
782
ALC005 Alcoholic Pancreatitis 39 0.037
783
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.037
784
SCR001 Secretory Meningioma 37 0.037
785
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.037
786
ALR002 Al-Raqad Syndrome 34 0.037
787
P GLM040 Glioma Susceptibility 1 81 0.036
788
THY111 Thyroid Carcinoma, Familial Medullary 67 0.036
789
CNN005 Connective Tissue Disease 66 0.036
790
P GLY013 Glycogen Storage Disease 59 0.036
791
SPP011 Suppression of Tumorigenicity 12 59 0.036
792
P BNC003 Bone Cancer 57 0.036
793
AMN001 Amenorrhea 54 0.036
794
HMC014 Homocysteinemia 53 0.036
795
PPT001 Peptic Esophagitis 51 0.036
796
P PST059 Pustular Psoriasis 38 0.036
797
c PRG020 Paragangliomas 3 38 0.036
798
LWC002 Lowe Oculocerebrorenal Syndrome 66 0.036
799
APN008 Apnea, Obstructive Sleep 65 0.036
800
RHM001 Rheumatic Fever 61 0.036
801
ING001 Inguinal Hernia 60 0.036
802
P RBL001 Rubella 58 0.036
803
INT007 Intermediate Coronary Syndrome 55 0.036
804
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 53 0.036
805
NRT001 Neurotic Disorder 52 0.036
806
SPS003 Spastic Diplegia 50 0.036
807
c VRL012 Viral Meningitis 48 0.036
808
PPL001 Papillary Adenoma 45 0.036
809
SMN007 Seminoma 44 0.036
810
SPR126 Superior Semicircular Canal Dehiscence 40 0.036
811
PLY100 Polyploidy 40 0.036
812
ENT001 Enterocele 39 0.036
813
P CRB088 Cerebral Atrophy 38 0.036
814
c HMG029 Hemoglobin Se Disease 38 0.036
815
P CRB059 Cerebellar Degeneration 37 0.036
816
CND006 Candida Glabrata 32 0.036
817
RSP007 Respiratory Distress Syndrome, Infant 30 0.036
818
MYL005 Myelofibrosis 67 0.036
819
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.036
820
P PLM034 Pulmonary Emphysema 56 0.036
821
SYN007 Synovitis 55 0.036
822
TRD006 Tardive Dyskinesia 55 0.036
823
P PLY018 Polycythemia 55 0.036
824
ONC002 Onchocerciasis 51 0.036
825
CRN019 Coronary Artery Vasospasm 46 0.036
826
CHD004 Chudley-Mccullough Syndrome 44 0.036
827
LCH001 Leech Infestation 36 0.036
828
ENT003 Enterobiasis 33 0.036
829
c INF002 Inflammatory Diarrhea 33 0.036
830
EWN003 Ewing Sarcoma 68 0.034
831
PSY004 Psychotic Disorder 67 0.034
832
P HYP061 Hypertrophic Cardiomyopathy 66 0.034
833
PRP001 Propionic Acidemia 66 0.034
834
HSH003 Hashimoto Thyroiditis 62 0.034
835
P PRD006 Prader-Willi Syndrome 59 0.034
836
BLM002 Bulimia Nervosa 57 0.034
837
SLC006 Silicosis 56 0.034
838
P PMP001 Pemphigus 55 0.034
839
P DRM007 Dermatitis Herpetiformis 54 0.034
840
MYM001 Myoma 53 0.034
841
P XRD029 Xeroderma Pigmentosum, Complementation Group a 53 0.034
842
P RCT021 Rectum Cancer 53 0.034
843
OST016 Osteochondrosis 53 0.034
844
c HPT007 Hepatitis E 52 0.034
845
P ACT008 Actinic Keratosis 52 0.034
846
P HMP007 Hemophilia 51 0.034
847
THY125 Thyroid Gland Medullary Carcinoma 51 0.034
848
P HYP040 Hypospadias 51 0.034
849
BRN014 Bronchopneumonia 50 0.034
850
PLR007 Pleural Empyema 49 0.034
851
c BCT013 Bacterial Pneumonia 47 0.034
852
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.034
853
ORL012 Oral Leukoplakia 39 0.034
854
IDP070 Idiopathic Scoliosis 37 0.034
855
c CHR020 Chronic Interstitial Cystitis 37 0.034
856
HRN029 Hearing Loss, Noise-Induced 37 0.034
857
c DRM040 Dermatitis Herpetiformis, Familial 35 0.034
858
RTC003 Root Caries 33 0.034
859
CYT018 Cytochrome P450 2d6 Variant 27 0.034
860
CRP001 Carpal Tunnel Syndrome 67 0.033
861
ART001 Arterial Tortuosity Syndrome 66 0.033
862
c ART101 Aortic Valve Disease 2 63 0.033
863
PPL049 Papillon-Lefevre Syndrome 63 0.033
864
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.033
865
P HYP726 Hypercalcemia, Infantile, 1 57 0.033
866
CYT008 Cytomegalovirus Infection 56 0.033
867
MCL006 Macular Retinal Edema 55 0.033
868
c BCT007 Bacterial Meningitis 55 0.033
869
P ALP106 Alport Syndrome 1, X-Linked 55 0.033
870
P PTT006 Pituitary Adenoma 54 0.033
871
P SML001 Small Cell Carcinoma 52 0.033
872
TND005 Tendinitis 52 0.033
873
VLV011 Vulvovaginal Candidiasis 51 0.033
874
P CHL066 Cholangitis 50 0.033
875
ENT004 Enthesopathy 48 0.033
876
P OBS001 Obstructive Jaundice 48 0.033
877
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 46 0.033
878
ATN004 Autonomic Neuropathy 44 0.033
879
TND004 Tendinopathy 44 0.033
880
IDP033 Idiopathic Edema 43 0.033
881
PRS063 Paresthesia 43 0.033
882
MYF002 Myofascial Pain Syndrome 42 0.033
883
FNG016 Fungal Keratitis 40 0.033
884
GLC008 Glucose Metabolism Disease 40 0.033
885
MST004 Mast Cell Neoplasm 38 0.033
886
EXT007 Extracutaneous Mastocytoma 38 0.033
887
c HNT011 Huntington Disease-Like 3 38 0.033
888
P PRC031 Preeclampsia/eclampsia 1 37 0.033
889
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 33 0.033
890
MTY003 Mutyh Polyposis 29 0.033
891
CYN003 Cyanide Poisoning 24 0.033
892
OBS524 Obsolete: Benign Exophthalmos Syndrome 15 0.033
893
P NRV007 Nervous System Disease 66 0.032
894
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.032
895
P UVT001 Uveitis 57 0.032
896
P CYS039 Cystic Kidney Disease 54 0.032
897
ASP007 Aspiration Pneumonia 48 0.032
898
LNG015 Lingual-Facial-Buccal Dyskinesia 47 0.032
899
P BRB001 Beriberi 44 0.032
900
c HMG001 Hemoglobin C Disease 40 0.032
901
SWL001 Swallowing Disorders 38 0.032
902
c CHR098 Chronic Pyelonephritis 35 0.032
903
DNT008 Denture Stomatitis 35 0.032
904
BNT001 Banti's Syndrome 21 0.032
905
MLT157 Multiple System Atrophy 1 70 0.031
906
FCT007 Factor Vii Deficiency 66 0.031
907
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 66 0.031
908
CHY002 Chylomicron Retention Disease 64 0.031
909
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.031
910
NRM005 Neuromuscular Disease 63 0.031
911
P FRD001 Friedreich Ataxia 63 0.031
912
BRS099 Breast Ductal Carcinoma 62 0.031
913
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.031
914
BRG013 Buerger Disease 57 0.031
915
P MLT074 Multiple Endocrine Neoplasia 55 0.031
916
FCT001 Factor Viii Deficiency 55 0.031
917
PRP080 Peripheral Artery Disease 53 0.031
918
EXP004 Exophthalmos 52 0.031
919
THR004 Thrombocytosis 51 0.031
920
PLR008 Pleurisy 51 0.031
921
c ACT078 Acute Porphyria 49 0.031
922
CHL004 Cholelithiasis 49 0.031
923
c LRG001 Large Cell Carcinoma 49 0.031
924
VTM033 Vitamin K Deficiency Bleeding 48 0.031
925
CRN027 Corneal Neovascularization 47 0.031
926
LPT006 Leptin Receptor Deficiency 47 0.031
927
P PRS049 Persistent Mullerian Duct Syndrome 47 0.031
928
P END084 Endocrine System Disease 44 0.031
929
c CRV002 Cervix Uteri Carcinoma in Situ 44 0.031
930
c PRS128 Persistent Mullerian Duct Syndrome, Types I and Ii 44 0.031
931
FBR054 Fibroma 44 0.031
932
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.031
933
DBT007 Diabetic Cataract 39 0.031
934
CRV045 Cervical Intraepithelial Neoplasia 39 0.031
935
DSS010 Dissociative Disorder 38 0.031
936
ENM002 Enamel Erosion 27 0.031
937
STN013 Stenotrophomonas Maltophilia Infection 25 0.031
938
P TMP003 Temporal Arteritis 67 0.028
939
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.028
940
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 58 0.028
941
RBS001 Rabies 58 0.028
942
c MYT020 Myotonic Dystrophy 2 57 0.028
943
P STR020 Strabismus 56 0.028
944
P MYS005 Myositis 56 0.028
945
HRY003 Hairy Cell Leukemia 55 0.028
946
CRC006 Carcinoid Syndrome 55 0.028
947
P RST001 Restless Legs Syndrome 54 0.028
948
ESP002 Esophageal Varix 51 0.028
949
FML063 Familial Glucocorticoid Deficiency 51 0.028
950
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 50 0.028
951
END021 Endomyocardial Fibrosis 48 0.028
952
TTR011 Tetraploidy 47 0.028
953
P CRC039 Coarctation of Aorta 47 0.028
954
TNP001 Tinea Pedis 47 0.028
955
P VTR007 Vitreoretinopathy 46 0.028
956
P CRN025 Corneal Dystrophy 45 0.028
957
PST053 Postherpetic Neuralgia 42 0.028
958
P LTH003 Lethal Congenital Contracture Syndrome 42 0.028
959
ART008 Arteriosclerosis Obliterans 40 0.028
960
MCH006 Mechanical Strabismus 39 0.028
961
c OVR114 Ovarian Cancer 1 38 0.028
962
HYP264 Hypertonia 38 0.028
963
KDN013 Kidney Hypertrophy 34 0.028
964
c RST012 Restless Legs Syndrome 1 34 0.028
965
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.028
966
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 27 0.028
967
P FML011 Familial Adenomatous Polyposis 72 0.027
968
c MLT160 Multiple Endocrine Neoplasia, Type Iia 69 0.027
969
P MPL001 Maple Syrup Urine Disease 69 0.027
970
P OCL013 Oculodentodigital Dysplasia 69 0.027
971
P FRG001 Fragile X Syndrome 68 0.027
972
P CHR012 Chronic Granulomatous Disease 67 0.027
973
P PRP003 Porphyria Cutanea Tarda 67 0.027
974
GRG001 Greig Cephalopolysyndactyly Syndrome 67 0.027
975
MLD001 Melioidosis 67 0.027
976
P THY023 Thymoma 65 0.027
977
P PRS038 Personality Disorder 65 0.027
978
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.027
979
PLL001 Pallister-Hall Syndrome 64 0.027
980
LYM017 Lyme Disease 63 0.027
981
OVR029 Ovarian Hyperstimulation Syndrome 63 0.027
982
OST003 Osteonecrosis 61 0.027
983
MCR013 Microphthalmia 60 0.027
984
c LPM012 Lipomatosis, Multiple 59 0.027
985
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.027
986
CRV038 Cervical Squamous Cell Carcinoma 58 0.027
987
ERY029 Erythermalgia, Primary 58 0.027
988
RNL024 Renal Glucosuria 57 0.027
989
c ADL017 Adult T-Cell Leukemia 57 0.027
990
PTT009 Pituitary Gland Disease 54 0.027
991
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 53 0.027
992
HRT012 Heart Valve Disease 53 0.027
993
ECH003 Echinococcosis 53 0.027
994
c HYP768 Hyperlipoproteinemia, Type I 52 0.027
995
PRN011 Pernicious Anemia 52 0.027
996
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 52 0.027
997
URC002 Urea Cycle Disorder 51 0.027
998
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 51 0.027
999
PRT029 Parathyroid Adenoma 50 0.027
1000
DBT004 Diabetic Polyneuropathy 50 0.027
1001
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.027
1002
OPT003 Opiate Dependence 50 0.027
1003
NPH010 Nephrosclerosis 49 0.027
1004
LRN003 Learning Disability 49 0.027
1005
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 49 0.027
1006
SKN013 Skin Benign Neoplasm 49 0.027
1007
HMG002 Hemoglobinuria 49 0.027
1008
CRP032 Corpus Callosum, Agenesis of 49 0.027
1009
QDR001 Quadriplegia 48 0.027
1010
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.027
1011
PLC007 Placental Abruption 48 0.027
1012
P ENC008 Encephalocele 47 0.027
1013
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.027
1014
P MCL001 Mucolipidosis 47 0.027
1015
P PRC019 Precocious Puberty 47 0.027
1016
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 46 0.027
1017
P PRD037 Periodontal Ehlers-Danlos Syndrome 46 0.027
1018
MXD026 Mixed Glioma 45 0.027
1019
CRV043 Cervical Dystonia 45 0.027
1020
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.027
1021
SPP008 Suppurative Otitis Media 45 0.027
1022
c CLR017 Clear Cell Sarcoma 44 0.027
1023
VLV044 Vulvar Intraepithelial Neoplasia 44 0.027
1024
TNG009 Tongue Squamous Cell Carcinoma 44 0.027
1025
OVR063 Overnutrition 43 0.027
1026
P STR092 Striatal Degeneration, Autosomal Dominant 2 43 0.027
1027
PHY002 Physical Disorder 42 0.027
1028
MNN028 Mononeuropathy of the Median Nerve, Mild 42 0.027
1029
MRP001 Morphine Dependence 41 0.027
1030
P PRG092 Pregnancy Loss, Recurrent 1 40 0.027
1031
KLD004 Keloid Disorder 40 0.027
1032
NND010 Nondisjunction 34 0.027
1033
FNT004 Fainting 31 0.027
1034
TBL029 Tubulin, Beta 28 0.027
1035
c RNG015 Ring Chromosome 2 26 0.027
1036
EPL050 Epilepsy, Partial, with Pericentral Spikes 25 0.027
1037
c ART115 Aortic Valve Disease 1 75 0.023
1038
ADR007 Adrenoleukodystrophy 74 0.023
1039
P TTR001 Tetralogy of Fallot 69 0.023
1040
P PRM011 Primary Ciliary Dyskinesia 69 0.023
1041
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 67 0.023
1042
ACH004 Achondroplasia 66 0.023
1043
P ACR001 Aicardi-Goutieres Syndrome 65 0.023
1044
MGK001 Megakaryocytic Leukemia 64 0.023
1045
CYS013 Cystinuria 62 0.023
1046
c GLY060 Glycogen Storage Disease Ia 61 0.023
1047
P ANP001 Anaplastic Large Cell Lymphoma 61 0.023
1048
LBR030 Leber Optic Atrophy 60 0.023
1049
CNV004 Canavan Disease 60 0.023
1050
PNM010 Pneumothorax, Primary Spontaneous 60 0.023
1051
P PTT014 Pitt-Hopkins Syndrome 60 0.023
1052
APP008 Appendicitis 60 0.023
1053
MXD005 Mixed Connective Tissue Disease 59 0.023
1054
DCT002 Ductal Carcinoma in Situ 59 0.023
1055
c PTT056 Pituitary Adenoma 1, Multiple Types 58 0.023
1056
P SHR029 Short Syndrome 57 0.023
1057
c ESS001 Essential Tremor 56 0.023
1058
WLF002 Wolf-Hirschhorn Syndrome 56 0.023
1059
ICH001 Ichthyosis Vulgaris 55 0.023
1060
VTM027 Vitamin D-Dependent Rickets, Type 2a 55 0.023
1061
P VNS003 Venous Insufficiency 55 0.023
1062
WST005 West Nile Virus 55 0.023
1063
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.023
1064
GLS001 Gliosarcoma 54 0.023
1065
c OPT053 Optic Atrophy 1 54 0.023
1066
c THY107 Thymoma, Familial 54 0.023
1067
GST037 Gastroparesis 53 0.023
1068
HMT008 Hematuria, Benign Familial 53 0.023
1069
P ALL008 Allergic Bronchopulmonary Aspergillosis 53 0.023
1070
c GLL024 Gallbladder Disease 1 52 0.023
1071
c ACR116 Aicardi-Goutieres Syndrome 1 51 0.023
1072
OVR059 Ovary Adenocarcinoma 51 0.023
1073
P MTH008 Methylmalonic Acidemia 51 0.023
1074
SCB001 Scabies 51 0.023
1075
HRT011 Heart Septal Defect 50 0.023
1076
c BRS049 Breast Carcinoma in Situ 50 0.023
1077
BRX001 Bruxism 50 0.023
1078