Search results for Calcium

2819 hits were found for Calcium

# Family MCID Name MIFTS Score
1
c CHN022 Chondrocalcinosis 2 35 8.354
2
NPH091 Nephrolithiasis, Calcium Oxalate 54 7.104
3
IMM066 Immunodeficiency 9 25 5.887
4
IMM065 Immunodeficiency 10 29 5.883
5
FML307 Familial Calcium Pyrophosphate Deposition 36 5.294
6
NPH009 Nephrolithiasis 58 3.447
7
P CHN059 Chondrocalcinosis 48 3.131
8
c BLD126 Bleeding Disorder, Platelet-Type, 18 20 2.938
9
c AML006 Amelogenesis Imperfecta Hypoplastic Type, Ig 22 2.095
10
CMB055 Combined Immunodeficiency Due to Crac Channel Dysfunction 14 2.077
11
P HYP069 Hyperparathyroidism 59 0.244
12
P OST002 Osteoporosis 74 0.239
13
P CLR023 Colorectal Cancer 99 0.211
14
GST049 Gastrointestinal System Cancer 62 0.208
15
GST071 Gastrointestinal Carcinoma 45 0.208
16
P ADN016 Adenocarcinoma 70 0.190
17
c LRG017 Large Intestine Cancer 63 0.189
18
P INT068 Intestinal Disease 62 0.185
19
INT253 Intestinal Benign Neoplasm 57 0.185
20
BND020 Bone Disease 64 0.184
21
RCT017 Rectal Disease 43 0.183
22
CLN019 Colonic Disease 62 0.182
23
P KDN018 Kidney Disease 71 0.170
24
RCK004 Rickets 66 0.164
25
c SCN007 Secondary Hyperparathyroidism 55 0.163
26
BNR002 Bone Resorption Disease 54 0.163
27
P RCT021 Rectum Cancer 58 0.159
28
c PRM005 Primary Hyperparathyroidism 60 0.154
29
ISC004 Ischemia 67 0.153
30
c HYP595 Hypertension, Essential 81 0.150
31
P LKM002 Leukemia 72 0.150
32
P HYP024 Hypoparathyroidism 55 0.145
33
c CHR089 Chronic Kidney Failure 73 0.142
34
P BRS047 Breast Cancer 100 0.142
35
P LYM118 Lymphoma 69 0.141
36
CLC006 Calcinosis 53 0.132
37
P MLG056 Malignant Hyperthermia 60 0.130
38
LYM024 Lymphatic System Disease 54 0.129
39
P LYM033 Lymphoproliferative Syndrome 63 0.129
40
LYM019 Lymphosarcoma 53 0.129
41
P HYP073 Hypersensitivity Reaction Type Iv Disease 50 0.128
42
CLN015 Colon Adenocarcinoma 57 0.126
43
RCT020 Rectum Adenocarcinoma 40 0.125
44
P ALZ034 Alzheimer Disease 87 0.125
45
HYP025 Hyperphosphatemia 49 0.125
46
P HRT032 Heart Disease 76 0.123
47
P CRN018 Coronary Artery Anomaly 75 0.123
48
ANG054 Angina Pectoris 69 0.123
49
P MYC007 Myocardial Infarction 78 0.121
50
P ART022 Arthritis 77 0.121
52
P PRS040 Prostate Cancer 93 0.120
53
P LYM031 Lymphocytic Leukemia 61 0.120
54
URN009 Urinary System Disease 59 0.119
55
P DBT009 Diabetes Mellitus 67 0.118
56
P CRN300 Coronary Heart Disease 1 61 0.117
57
BNF002 Bone Fracture 48 0.117
58
P LKM062 Leukemia, Acute Lymphoblastic 68 0.116
59
ART140 Arteries, Anomalies of 66 0.116
60
LYM040 Lymphoblastic Lymphoma 57 0.114
61
c ACT074 Acute Lymphocytic Leukemia 63 0.113
62
IMM136 Immune System Disease 57 0.113
63
VSC007 Vascular Disease 72 0.112
64
IDP073 Idiopathic Hypercalciuria 48 0.112
65
INS001 Insulinoma 64 0.112
66
LYM067 Lymphoid Leukemia 47 0.111
67
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 29 0.110
68
c PRC016 Pre-Eclampsia 61 0.109
69
ISC006 Ischemic Heart Disease 72 0.108
70
P ART021 Arteriosclerosis 61 0.108
71
LMB002 Lambert-Eaton Myasthenic Syndrome 58 0.108
72
P OVR042 Ovarian Cancer 83 0.105
73
ALL026 Allergic Hypersensitivity Disease 68 0.105
74
P HYP802 Hypocalcemia, Autosomal Dominant 1 66 0.105
75
END030 End Stage Renal Failure 60 0.105
76
BRK010 Burkitt Lymphoma 69 0.101
77
ACQ007 Acquired Immunodeficiency Syndrome 66 0.101
78
ADN018 Adenoma 64 0.101
79
HMN014 Human Immunodeficiency Virus Infectious Disease 62 0.101
80
P LNG032 Lung Cancer 99 0.100
81
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 92 0.100
82
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 63 0.100
83
P FML068 Familial Hypocalciuric Hypercalcemia 50 0.098
84
MYL069 Myeloma, Multiple 85 0.098
85
LYM133 Lymphoma, Hodgkin, Classic 72 0.097
86
c GLL024 Gallbladder Disease 1 45 0.097
87
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.097
88
HYP266 Hypoxia 63 0.096
89
P ECL001 Eclampsia 58 0.095
90
SPS003 Spastic Diplegia 55 0.095
91
c PRS136 Prostate Cancer, Hereditary, 6 40 0.095
92
c PRS130 Prostate Cancer, Hereditary, 8 37 0.095
93
ESP021 Esophageal Cancer 82 0.094
94
GST053 Gastric Cancer 78 0.094
95
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 40 0.094
96
P ART023 Arthropathy 68 0.094
97
URM002 Uremia 53 0.094
98
CLN045 Colonic Benign Neoplasm 48 0.094
99
P RHM011 Rheumatoid Arthritis 81 0.093
100
P EPL164 Epilepsy 72 0.093
101
AGN016 Aging 63 0.093
102
c BNM029 Bone Mineral Density Quantitative Trait Locus 15 46 0.093
103
P PRD008 Periodontitis 66 0.091
104
JNT002 Joint Disorders 64 0.091
105
TTH006 Tooth Disease 54 0.091
106
CNG034 Congestive Heart Failure 70 0.090
107
P NRP001 Neuropathy 63 0.090
108
ISL119 Isolated Optic Neuritis 34 0.090
109
THY028 Thyroid Cancer 72 0.089
110
P ATR011 Atrial Fibrillation 69 0.089
111
OST011 Osteomalacia 52 0.089
112
NTR005 Nutritional Deficiency Disease 59 0.088
113
P PNC044 Pancreatitis 62 0.087
114
ACT103 Acute Lymphoblastic Leukemia, Childhood 55 0.087
115
DNT012 Dental Caries 52 0.087
116
NPH003 Nephrocalcinosis 50 0.087
117
P PNC035 Pancreatic Cancer 82 0.086
118
LPD008 Lipid Metabolism Disorder 65 0.086
119
END035 Endocrine Gland Cancer 57 0.086
120
P GLM045 Glioma 55 0.085
121
CYS001 Cystic Fibrosis 82 0.084
122
OST017 Osteomyelitis 64 0.083
123
P DRR001 Diarrhea 58 0.083
124
GST050 Gastrointestinal System Disease 67 0.082
125
HYP060 Hyperinsulinism 57 0.082
126
P MSC005 Muscular Dystrophy 66 0.081
127
CLR108 Colorectal Adenoma 64 0.081
128
BRR014 Barrett Esophagus 70 0.080
129
GT001 Gout 62 0.080
130
PNC034 Pancreas Disease 59 0.079
131
c PNC106 Pancreatic Agenesis 1 51 0.079
132
PRT030 Parathyroid Gland Disease 50 0.079
133
LYM143 Lymphoma, Non-Hodgkin, Familial 73 0.078
134
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.078
135
P PSD015 Pseudohypoparathyroidism 51 0.078
136
RTR008 Root Resorption 46 0.078
137
P INF032 Infertility 60 0.077
138
P SCH015 Schizophrenia 73 0.076
139
DPR016 Depression 72 0.076
140
STM006 Stomach Disease 55 0.076
141
OST012 Osteoarthritis 80 0.075
142
P LVR013 Liver Disease 76 0.075
143
ESP023 Esophageal Disease 59 0.075
144
c ADL052 Adult Acute Lymphocytic Leukemia 45 0.075
145
SKN016 Skin Disease 68 0.074
146
RNL011 Renal Osteodystrophy 49 0.074
147
FSH001 Fish-Eye Disease 50 0.073
148
P HPT023 Hepatocellular Carcinoma 96 0.072
149
CRB039 Cerebrovascular Disease 70 0.072
150
P AST007 Astrocytoma 52 0.072
151
SKN027 Skin Conditions 51 0.072
152
TRP008 Tropical Calcific Pancreatitis 50 0.072
153
P ENC018 Encephalopathy 65 0.071
154
FXF002 Fox-Fordyce Disease 40 0.071
155
OST097 Osteoporotic Fracture 36 0.071
156
P MLT020 Multiple Sclerosis 75 0.070
157
SRC014 Sarcoma 70 0.070
158
THR024 Thrombosis 64 0.070
159
GND003 Gonadal Disease 49 0.070
160
c AMY091 Amyotrophic Lateral Sclerosis 1 90 0.069
161
P PLM037 Pulmonary Hypertension 77 0.069
162
PNC033 Pancreas Adenocarcinoma 67 0.069
163
PRD007 Periodontal Disease 66 0.069
164
MLN008 Melanoma 63 0.069
165
P CRD132 Cardiac Conduction Defect 63 0.069
166
ZLL002 Zollinger-Ellison Syndrome 58 0.069
167
PRM020 Premenstrual Tension 53 0.069
168
MTB004 Metabolic Acidosis 50 0.069
169
P HMP006 Hemiplegic Migraine 49 0.069
170
P LTR001 Lateral Sclerosis 60 0.068
171
c SML038 Small Cell Cancer of the Lung 68 0.067
172
ATM095 Autoimmune Disease 68 0.067
173
GST040 Gastric Adenocarcinoma 66 0.067
174
c ACT027 Acute Pancreatitis 59 0.067
175
c HYP752 Hypocalciuric Hypercalcemia, Familial, Type I 46 0.067
176
P MSC007 Muscle Hypertrophy 64 0.066
177
ATH013 Atherosclerosis Susceptibility 60 0.066
178
RTC009 Reticulum Cell Sarcoma 55 0.066
179
GNG012 Gingival Overgrowth 53 0.066
180
PLM017 Pulmonary Alveolar Microlithiasis 52 0.066
181
RTC005 Reticulosarcoma 48 0.066
182
INT038 Interdigitating Dendritic Cell Sarcoma 43 0.066
183
PHS001 Phosphorus Metabolism Disease 40 0.066
184
STR067 Stroke, Ischemic 82 0.064
185
P DLT002 Dilated Cardiomyopathy 75 0.064
186
P PNM007 Pneumonia 72 0.064
187
PRT037 Pertussis 70 0.064
188
THY111 Thyroid Carcinoma, Familial Medullary 70 0.064
189
CNN005 Connective Tissue Disease 67 0.064
190
P PRP019 Peripheral Nervous System Disease 66 0.064
191
RHM027 Rheumatic Disease 65 0.064
192
HYP056 Hypoglycemia 64 0.064
193
P OVR049 Ovarian Disease 63 0.064
194
P HYP061 Hypertrophic Cardiomyopathy 59 0.064
195
PLC008 Placenta Disease 59 0.064
196
HMT018 Hematopoietic Stem Cell Transplantation 59 0.064
197
CRN030 Coronary Stenosis 52 0.064
198
c ATR087 Atrial Standstill 1 70 0.063
199
DMN002 Dementia 69 0.063
200
BRS051 Breast Disease 66 0.063
201
OST159 Osteogenic Sarcoma 66 0.063
202
P CRD119 Cardiac Arrest 66 0.063
203
GLC003 Glucose Intolerance 59 0.063
204
SQM006 Squamous Cell Carcinoma 58 0.063
205
BRN080 Brain Ischemia 43 0.063
206
c SYS001 Systemic Lupus Erythematosus 88 0.062
207
AST005 Asthma 81 0.062
208
P PHC003 Pheochromocytoma 72 0.062
209
P LPS004 Lupus Erythematosus 69 0.062
210
P HYP086 Hypothyroidism 66 0.062
211
MSC157 Muscular Dystrophy, Duchenne Type 65 0.062
212
MTH009 Mouth Disease 64 0.062
213
MYC005 Myocardial Stunning 47 0.062
214
P HYP776 Hyperparathyroidism, Neonatal Severe 42 0.062
215
INS024 Insulin-Like Growth Factor I 82 0.061
216
GLB002 Glioblastoma 74 0.061
217
P PLY011 Polycystic Ovary Syndrome 64 0.061
218
P BNC003 Bone Cancer 62 0.061
219
P CTR002 Cataract 59 0.061
220
CNS004 Constipation 58 0.061
221
BRN071 Brain Injury 55 0.061
222
P ATS308 Autosomal Dominant Cerebellar Ataxia 55 0.061
223
MLR006 Male Reproductive Organ Cancer 49 0.061
224
HMN044 Human Immunodeficiency Virus Type 1 75 0.059
225
P MYL006 Myeloid Leukemia 67 0.059
226
HYP066 Hyperglycemia 64 0.059
227
ERY003 Erythema Multiforme 62 0.059
228
P EXN002 Exanthem 62 0.059
229
P TRC086 Trichohepatoenteric Syndrome 1 60 0.059
230
P PRM002 Primary Hyperoxaluria 58 0.059
231
c MCR113 Microvascular Complications of Diabetes 3 58 0.059
232
c ACT075 Acute Myocardial Infarction 57 0.059
233
GLC008 Glucose Metabolism Disease 53 0.059
234
CLC001 Calciphylaxis 52 0.059
235
c FML023 Familial Hemiplegic Migraine 50 0.059
236
c MCR120 Microvascular Complications of Diabetes 7 46 0.059
237
c MCR130 Microvascular Complications of Diabetes 6 43 0.059
238
c MCR133 Microvascular Complications of Diabetes 4 43 0.059
239
INT323 Intraocular Pressure Quantitative Trait Locus 38 0.059
240
c TRC078 Trichohepatoenteric Syndrome 2 35 0.059
241
P BPL003 Bipolar Disorder 61 0.058
242
DFF005 Diffuse Large B-Cell Lymphoma 58 0.058
243
P RNL007 Renal Tubular Acidosis 51 0.058
244
PRP017 Periapical Periodontitis 48 0.058
245
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 34 0.058
246
CRH001 Crohn's Disease 79 0.057
247
P HPT021 Hepatitis 73 0.057
248
P HNT016 Huntington Disease 73 0.057
249
P PLY014 Polycystic Kidney Disease 62 0.057
250
MCS002 Mucositis 60 0.057
251
SFT003 Soft Tissue Sarcoma 59 0.057
252
c MLG074 Malignant Mesenchymoma 54 0.057
253
P CLL015 Collagen Disease 52 0.057
254
c BDY007 Body Mass Index Quantitative Trait Locus 1 48 0.057
255
c PLM164 Pulmonary Hypertension, Primary, 1 70 0.055
256
P ATS364 Autism 67 0.055
257
P PSR002 Psoriasis 67 0.055
258
PRT010 Parathyroid Carcinoma 64 0.055
259
STT001 Status Epilepticus 60 0.055
260
BRN106 Burns 59 0.055
261
TXC002 Toxic Encephalopathy 57 0.055
262
NTR046 Neutrophil Migration 56 0.055
263
MCN001 Mucinous Adenocarcinoma 54 0.055
264
CYS014 Cystadenocarcinoma 53 0.055
265
PRS042 Prostate Disease 47 0.055
266
GLC086 Glucocorticoid-Induced Osteoporosis 46 0.055
267
P HRD086 Hereditary Hypophosphatemic Rickets 45 0.055
268
ESP025 Esophagus Adenocarcinoma 43 0.055
269
APP009 Appendix Adenocarcinoma 43 0.055
270
ATX038 Ataxia and Polyneuropathy, Adult-Onset 42 0.055
271
DNT014 Dental Pulp Disease 41 0.055
272
SCK003 Sickle Cell Anemia 74 0.054
273
PRP027 Peripheral Vascular Disease 72 0.054
274
LVR012 Liver Cirrhosis 67 0.054
275
P ENC004 Encephalitis 66 0.054
276
P LNG028 Long Qt Syndrome 66 0.054
277
SPN186 Spinal Cord Injury 66 0.054
278
GST045 Gastroenteritis 65 0.054
279
P BCL006 B-Cell Lymphomas 64 0.054
280
c ADL017 Adult T-Cell Leukemia 62 0.054
281
HDC001 Headache 62 0.054
282
c ACT073 Acute Leukemia 62 0.054
283
WVR001 Weaver Syndrome 60 0.054
284
TRN015 Transient Cerebral Ischemia 59 0.054
285
NRT004 Neuritis 58 0.054
286
PNM001 Pneumocystosis 58 0.054
287
MMM001 Mammary Paget's Disease 56 0.054
288
P TCL004 T-Cell Leukemia 53 0.054
289
P SCL057 Scoliosis, Isolated 1 45 0.054
290
BCL008 B-Cell Childhood Acute Lymphoblastic Leukemia 35 0.054
291
ENM002 Enamel Erosion 29 0.054
292
DSS008 Disease of Mental Health 71 0.053
293
LPT014 Leptin Deficiency or Dysfunction 70 0.053
294
DRM006 Dermatitis 69 0.053
295
FTT001 Fatty Liver Disease 66 0.053
296
P MYP004 Myopathy 64 0.053
297
OVR029 Ovarian Hyperstimulation Syndrome 64 0.053
298
RNL114 Renal Cell Carcinoma, Nonpapillary 63 0.053
299
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 61 0.053
300
NRM005 Neuromuscular Disease 61 0.053
301
P HYP370 Hypokalemic Periodic Paralysis, Type 1 60 0.053
302
P MSC033 Muscle Disorders 57 0.053
303
P INF037 Inflammatory Bowel Disease 56 0.053
304
CRD223 Cardiac Arrhythmia 55 0.053
305
CYS039 Cystic Kidney Disease 55 0.053
306
PLS025 Plasmablastic Lymphoma 53 0.053
307
P DDN001 Duodenal Ulcer 51 0.053
308
HYP017 Hypophosphatemia 49 0.053
309
P FML187 Familial Hypertension 42 0.053
310
LYM048 Lymphoma, Large-Cell, Immunoblastic 34 0.053
311
BLD165 Blood Group, Colton System 34 0.053
312
CRY024 Crystal Arthropathies 27 0.053
313
RPD005 Rapidly Involuting Congenital Hemangioma 25 0.053
314
P HYP607 Hypercholesterolemia, Familial 81 0.051
315
P MCR115 Microvascular Complications of Diabetes 5 70 0.051
316
GST092 Gastroesophageal Reflux 66 0.051
317
P THL005 Thalassemia 65 0.051
318
CHL065 Cholangiocarcinoma 64 0.051
319
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 60 0.051
320
P HYP076 Hyperthyroidism 55 0.051
321
P MYT002 Myotonic Dystrophy 52 0.051
322
GRN017 Granulocytopenia 51 0.051
323
WTH001 Withdrawal Disorder 50 0.051
324
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 49 0.051
325
c PRC031 Preeclampsia/eclampsia 1 41 0.051
326
SPN125 Spondyloenchondrodysplasia 31 0.051
327
MYT026 Myotonia Atrophica 28 0.051
328
c LKM061 Leukemia, Acute Myeloid 81 0.050
329
c LKM071 Leukemia, Chronic Lymphocytic 78 0.050
330
c LKM063 Leukemia, Chronic Myeloid 73 0.050
331
ANX010 Anxiety 73 0.050
332
MNT002 Mental Depression 65 0.050
333
P THR014 Thrombocytopenia 64 0.050
334
BCT022 Bacterial Infectious Disease 62 0.050
335
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 62 0.050
336
DBT010 Diabetic Neuropathy 60 0.050
337
P PGT001 Paget's Disease of Bone 59 0.050
338
EWN002 Ewing's Family of Tumors 57 0.050
339
LNG031 Lung Benign Neoplasm 56 0.050
340
OBS082 Obstructive Nephropathy 52 0.050
341
c MTR002 Mitral Valve Insufficiency 50 0.050
342
CNN004 Connective Tissue Cancer 45 0.050
343
GST012 Gastroesophageal Junction Adenocarcinoma 42 0.050
344
c LKM004 Leukemia, B-Cell, Chronic 38 0.050
345
ACT118 Acute Non Lymphoblastic Leukemia 32 0.050
346
NTR027 Neutrophil Actin Dysfunction 32 0.050
347
P SRC025 Sarcoidosis 1 76 0.048
348
MRF001 Marfan Syndrome 75 0.048
349
P NRV007 Nervous System Disease 71 0.048
350
DWN001 Down Syndrome 71 0.048
351
ART016 Aortic Aneurysm 71 0.048
352
ACR007 Acromegaly 70 0.048
353
VRL011 Viral Infectious Disease 68 0.048
354
THR100 Thrombocytopenic Purpura, Autoimmune 67 0.048
355
OST003 Osteonecrosis 67 0.048
356
c ACT210 Acute Respiratory Distress Syndrome 66 0.048
357
P NTR004 Neutropenia 60 0.048
358
PTT009 Pituitary Gland Disease 59 0.048
359
P SCL018 Scoliosis 58 0.048
360
TRM010 Traumatic Brain Injury 56 0.048
361
HYP005 Hypokalemia 55 0.048
362
c OVR114 Ovarian Cancer 1 51 0.048
363
P NRB010 Neuroblastoma 1 51 0.048
364
THY030 Thyroid Gland Disease 50 0.048
365
ADR040 Adrenal Gland Pheochromocytoma 49 0.048
366
c CHR579 Chiari Malformation Type Ii 49 0.048
367
c CRN243 Carney Complex, Type 1 45 0.048
368
TND005 Tendinitis 45 0.048
369
BNS001 Bone Osteosarcoma 39 0.048
370
HDG004 Hodgkin's Granuloma 30 0.048
371
HDG006 Hodgkin's Paragranuloma 22 0.048
372
TCL018 T-Cell Childhood Acute Lymphocytic Leukemia 21 0.048
373
CRN167 Caronte 19 0.048
374
ETH012 Ethylene Glycol Poisoning 18 0.048
375
RCT006 Rectum Mucinous Adenocarcinoma 15 0.048
376
P INF038 Influenza 75 0.046
377
PLM129 Pulmonary Disease, Chronic Obstructive 75 0.046
378
MNT001 Mantle Cell Lymphoma 73 0.046
379
ACR006 Aceruloplasminemia 73 0.046
380
MYL009 Myelodysplastic Syndrome 70 0.046
381
LNG099 Lung Disease 70 0.046
382
ACH004 Achondroplasia 68 0.046
383
c SCL052 Scleroderma, Familial Progressive 67 0.046
384
P NRV006 Nervous System Cancer 60 0.046
385
CHL014 Cholera 60 0.046
386
P ANP001 Anaplastic Large Cell Lymphoma 60 0.046
387
CHL068 Cholestasis 60 0.046
388
TRD006 Tardive Dyskinesia 60 0.046
389
c PRD040 Periodontitis, Chronic 59 0.046
390
RTN018 Retinal Disease 58 0.046
391
PRP080 Peripheral Artery Disease 56 0.046
392
BLR006 Biliary Tract Disease 52 0.046
393
PLP001 Pulpitis 50 0.046
394
CRB004 Cerebral Artery Occlusion 47 0.046
395
GST030 Gastrinoma 43 0.046
396
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 41 0.046
397
IDP070 Idiopathic Scoliosis 40 0.046
398
LYM049 Lymphoma, Small Cleaved-Cell, Diffuse 37 0.046
399
CLN002 Colon Mucinous Adenocarcinoma 32 0.046
400
SML025 Small Non-Cleaved Cell Lymphoma 25 0.046
401
RCT013 Rectum Signet Ring Adenocarcinoma 17 0.046
402
LRG015 Large Intestine Adenoma 17 0.046
403
c JVN010 Juvenile Rheumatoid Arthritis 70 0.045
404
BRT054 Brittle Bone Disorder 70 0.045
405
c THR092 Thrombophilia Due to Thrombin Defect 69 0.045
406
TTN003 Tetanus 66 0.045
407
P TXP001 Toxoplasmosis 66 0.045
408
c CNT035 Central Nervous System Disease 65 0.045
409
INT002 Intermittent Claudication 64 0.045
410
PPT005 Peptic Ulcer Disease 63 0.045
411
c ART101 Aortic Valve Disease 2 63 0.045
412
HYP020 Hyperprolactinemia 63 0.045
413
P SZR006 Seizure Disorder 61 0.045
414
P HMR003 Hemorrhagic Disease 59 0.045
415
P TRM003 Tremor 55 0.045
416
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 55 0.045
417
PRT029 Parathyroid Adenoma 52 0.045
418
P BLD051 Blood Coagulation Disease 52 0.045
419
PRD004 Prediabetes Syndrome 51 0.045
420
c SPN309 Spinocerebellar Ataxia 6 49 0.045
421
CHR074 Choriocarcinoma 49 0.045
422
P LCT002 Lactose Intolerance 47 0.045
423
RST023 Resting Heart Rate, Variation in 44 0.045
424
STT004 Steatorrhea 43 0.045
425
VSC008 Vascular Hemostatic Disease 43 0.045
426
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 38 0.045
427
DNT006 Dental Pulp Necrosis 34 0.045
428
MYT011 Myotonia 34 0.045
430
MNS002 Mini Stroke 25 0.045
431
HRN028 Horns in Sheep 24 0.045
432
P RTN008 Retinitis Pigmentosa 80 0.043
433
P GRF003 Graft-Versus-Host Disease 71 0.043
434
P BLD134 Bladder Cancer 70 0.043
435
P TTR001 Tetralogy of Fallot 70 0.043
436
CNN003 Conn's Syndrome 70 0.043
437
c HPT016 Hepatitis B 70 0.043
438
P PSD087 Pseudoxanthoma Elasticum 68 0.043
439
P FLL037 Follicular Lymphoma 67 0.043
440
c ART138 Aortic Aneurysm, Familial Abdominal, 1 66 0.043
441
GLB015 Glioblastoma Multiforme 64 0.043
442
IRR002 Irritable Bowel Syndrome 64 0.043
443
RSP006 Respiratory System Disease 64 0.043
444
P BLD062 Bile Duct Cancer 64 0.043
445
MYL031 Myeloproliferative Neoplasm 64 0.043
446
P NPH012 Nephrotic Syndrome 63 0.043
447
P GLL020 Gallbladder Disease 62 0.043
448
c FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.043
449
P EPS003 Episodic Ataxia 59 0.043
450
P CHL002 Childhood Absence Epilepsy 59 0.043
451
GLM004 Gliomatosis Cerebri 58 0.043
452
P RTN016 Retinal Degeneration 56 0.043
453
NRN004 Neuroendocrine Tumor 56 0.043
454
PRS036 Parasitic Protozoa Infectious Disease 52 0.043
455
P SLL003 Salla Disease 52 0.043
456
P BLD036 Bile Duct Disease 51 0.043
457
INT007 Intermediate Coronary Syndrome 50 0.043
458
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 48 0.043
459
BRN041 Bornholm Eye Disease 45 0.043
460
PRS063 Paresthesia 45 0.043
461
OVR094 Ovarian Epithelial Cancer 41 0.043
462
c MGR032 Migraine, Familial Hemiplegic, 1 40 0.043
463
c PGT007 Paget Disease of Bone 3 39 0.043
464
DNT007 Dentin Sensitivity 39 0.043
465
HML018 Homologous Wasting Disease 24 0.043
466
NRL016 Neural Tube Defects 79 0.041
467
BRN028 Brain Cancer 72 0.041
468
c JVN004 Juvenile Myelomonocytic Leukemia 70 0.041
469
ALC007 Alcohol Dependence 69 0.041
470
ANR007 Anorexia Nervosa 68 0.041
471
CLT003 Colitis 65 0.041
472
P CHR285 Chronic Myelomonocytic Leukemia 64 0.041
473
PLM033 Pulmonary Embolism 64 0.041
474
P OST001 Osteopetrosis 63 0.041
475
ANT024 Anthrax Disease 61 0.041
476
c VSC019 Vesicoureteral Reflux 1 58 0.041
477
P CNT005 Central Nervous System Lymphoma 57 0.041
478
c ACT068 Acute Cystitis 56 0.041
479
P NNL004 Nonalcoholic Fatty Liver Disease 56 0.041
480
SNS003 Sensory Peripheral Neuropathy 56 0.041
481
P MSC003 Muscular Atrophy 56 0.041
482
GLL018 Gallbladder Cancer 55 0.041
483
THR004 Thrombocytosis 55 0.041
484
PRP016 Paraplegia 54 0.041
485
HPR003 Heparin-Induced Thrombocytopenia 53 0.041
486
c PRM226 Primary Central Nervous System Lymphoma 52 0.041
487
c PNC128 Pain - Chronic 49 0.041
488
PRT035 Peritoneum Cancer 47 0.041
489
c HYP794 Hyperoxaluria, Primary, Type I 45 0.041
490
OST004 Osteitis Fibrosa 45 0.041
491
P RNL045 Renal Tubular Acidosis, Distal 45 0.041
492
BLD054 Blood Protein Disease 43 0.041
493
CRB085 Cerebral Hemorrhage 42 0.041
494
P CRB059 Cerebellar Degeneration 40 0.041
495
c BST008 Bestrophinopathy, Autosomal Recessive 33 0.041
497
P RTT002 Rett Syndrome 82 0.039
498
PLY001 Polycythemia Vera 75 0.039
499
MYL005 Myelofibrosis 69 0.039
500
P SYS005 Systemic Scleroderma 67 0.039
501
P DRM010 Dermatomyositis 65 0.039
502
P ADL010 Adult Respiratory Distress Syndrome 64 0.039
503
P RHN004 Rhinitis 64 0.039
504
HMT002 Hematologic Cancer 64 0.039
505
GST033 Gestational Diabetes 63 0.039
506
GTL001 Gitelman Syndrome 62 0.039
507
HMR039 Hemorrhage, Intracerebral 62 0.039
508
P BRG001 Brugada Syndrome 61 0.039
509
CCC001 Coccidioidomycosis 61 0.039
510
EMB004 Embryonal Carcinoma 59 0.039
511
NWB001 Newborn Respiratory Distress Syndrome 59 0.039
512
P DNT020 Dent Disease 1 59 0.039
513
PLM010 Pulmonary Edema 59 0.039
514
P KDN017 Kidney Cancer 59 0.039
515
ILT001 Ileitis 59 0.039
516
GST023 Gastric Ulcer 58 0.039
517
c ACT020 Acute T Cell Leukemia 57 0.039
518
SCK005 Sickle Cell Disease 57 0.039
519
P PMP001 Pemphigus 56 0.039
520
P VNS003 Venous Insufficiency 54 0.039
521
SPN041 Spinal Cord Disease 54 0.039
522
ACT058 Active Peptic Ulcer Disease 53 0.039
523
MSC190 Muscular Disease 53 0.039
524
P LCT001 Lactic Acidosis 52 0.039
525
HYD002 Hydronephrosis 52 0.039
526
HMS001 Hemosiderosis 52 0.039
527
P RNV001 Renovascular Hypertension 52 0.039
528
CRN019 Coronary Artery Vasospasm 50 0.039
529
c CHR431 Chronic Venous Insufficiency 50 0.039
530
KRT008 Keratopathy 48 0.039
531
EPD070 Epidermoid Cysts 48 0.039
532
NRR001 Neuroretinitis 47 0.039
533
MRG013 Mirage Syndrome 45 0.039
534
P JVN024 Juvenile Hereditary Hemochromatosis 44 0.039
535
BRN039 Bronchial Neoplasm 43 0.039
536
c PLY105 Polycystic Ovary Syndrome 1 42 0.039
537
P CHR084 Chromosomal Disease 42 0.039
538
BNG018 Benign Paroxysmal Positional Nystagmus 40 0.039
539
c APL023 Aplasia Cutis Congenita, Nonsyndromic 40 0.039
540
MSC004 Muscle Tissue Disease 39 0.039
541
RSP007 Respiratory Distress Syndrome, Infant 37 0.039
542
P VRT013 Vertigo, Benign Recurrent 37 0.039
543
GRM010 Germ Cells Tumors 35 0.039
544
c LKM005 Leukemia, T-Cell, Chronic 31 0.039
545
P LNG064 Lung Cancer Susceptibility 3 79 0.037
546
c SPN225 Spondyloarthropathy 1 75 0.037
547
c HMC039 Hemochromatosis, Type 1 74 0.037
548
c BTT014 Beta-Thalassemia 72 0.037
549
P RTN024 Retinoblastoma 72 0.037
550
CRP001 Carpal Tunnel Syndrome 71 0.037
551
BRC012 Brucellosis 70 0.037
552
P SLP006 Sleep Apnea 70 0.037
553
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 69 0.037
554
c MGR028 Migraine with or Without Aura 1 69 0.037
555
PRT036 Peritonitis 66 0.037
556
VRC005 Varicose Veins 66 0.037
557
P END044 Endometriosis 65 0.037
558
MDD011 Mood Disorder 65 0.037
559
INT066 Interstitial Lung Disease 65 0.037
560
P AMY004 Amyloidosis 64 0.037
561
WLL001 Williams-Beuren Syndrome 63 0.037
562
GNG013 Gingivitis 63 0.037
563
P MYS005 Myositis 61 0.037
564
P GLM007 Glomerulonephritis 61 0.037
565
CRH005 Crohn's Colitis 61 0.037
566
P GRV001 Graves' Disease 61 0.037
567
P SJG008 Sjogren Syndrome 60 0.037
568
P SML001 Small Cell Carcinoma 60 0.037
569
IRN002 Iron Metabolism Disease 60 0.037
570
c INF071 Inflammatory Bowel Disease 1 60 0.037
571
c PRG042 Progressive Familial Heart Block, Type Ia 59 0.037
572
P CYS018 Cystitis 58 0.037
573
MRG003 Marginal Zone B-Cell Lymphoma 58 0.037
574
P ANG015 Angioedema 57 0.037
575
c GRV008 Graves Disease 1 57 0.037
576
P MLT074 Multiple Endocrine Neoplasia 56 0.037
577
P DBT005 Diabetes Insipidus 55 0.037
578
TST014 Testicular Cancer 54 0.037
579
GTR002 Goiter 54 0.037
580
LMB062 Limb Ischemia 54 0.037
581
PNC041 Pancreatic Ductal Adenocarcinoma 54 0.037
582
ATR057 Atrioventricular Block 54 0.037
583
STM007 Stomatitis 53 0.037
584
OVR063 Overnutrition 53 0.037
585
CRT013 Carotid Stenosis 53 0.037
586
P OVR046 Ovarian Cyst 52 0.037
587
CHL061 Childhood Leukemia 52 0.037
588
KLD001 Keloids 51 0.037
589
MTR003 Mitral Valve Stenosis 51 0.037
590
SPL004 Splenic Marginal Zone Lymphoma 50 0.037
591
CCC002 Coccidiosis 50 0.037
592
GRW007 Growth Hormone Deficiency 49 0.037
593
BNN003 Bone Inflammation Disease 48 0.037
594
MMM006 Mammographic Density 47 0.037
595
c MLG068 Malignant Glioma 47 0.037
596
PRP056 Porphyria, Acute Hepatic 47 0.037
597
SPN369 Spinal Disease 47 0.037
598
SYS003 Systolic Heart Failure 46 0.037
599
NDL024 Nodal Marginal Zone Lymphoma 43 0.037
600
MLG086 Malignant Hyperthermia Susceptibility 41 0.037
601
SCR035 Sacral Agenesis with Vertebral Anomalies 41 0.037
602
PRM050 Primary Orthostatic Tremor 33 0.037
603
CRC034 Carcinoma Showing Thymus-Like Differentiation 28 0.037
604
MLR004 Malaria 84 0.035
605
KPS004 Kaposi Sarcoma 77 0.035
606
PHN003 Phenylketonuria 74 0.035
607
P DBT085 Diabetes Mellitus, Insulin-Dependent 73 0.035
608
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.035
609
CMM004 Common Variable Immunodeficiency 71 0.035
610
P DRM053 Dermatitis, Atopic 71 0.035
611
ALL003 Allergic Rhinitis 70 0.035
612
BRN024 Bronchitis 70 0.035
613
P ESS003 Essential Thrombocythemia 69 0.035
614
LSH001 Leishmaniasis 69 0.035
615
P INT143 Interstitial Cystitis 66 0.035
616
P VSC011 Vasculitis 66 0.035
617
P SKN015 Skin Carcinoma 65 0.035
618
P THY023 Thymoma 63 0.035
619
P UVT001 Uveitis 62 0.035
620
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 61 0.035
621
P EPL140 Epilepsy, Idiopathic Generalized 61 0.035
622
P CMR001 Camurati-Engelmann Disease 61 0.035
623
HRY003 Hairy Cell Leukemia 60 0.035
624
P PNS012 Paine Syndrome 60 0.035
625
c INS002 in Situ Carcinoma 60 0.035
626
c SVR001 Severe Acute Respiratory Syndrome 60 0.035
627
PRP030 Purpura 60 0.035
628
P PLY018 Polycythemia 60 0.035
629
CFF002 Coffin-Lowry Syndrome 59 0.035
630
c ACT135 Acute Graft Versus Host Disease 58 0.035
631
c EPS035 Episodic Ataxia, Type 2 57 0.035
632
P TMR018 Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 56 0.035
633
VTM027 Vitamin D-Dependent Rickets, Type 2a 56 0.035
634
P CTN015 Cutaneous T Cell Lymphoma 56 0.035
635
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 55 0.035
636
CLR109 Colorectal Adenocarcinoma 54 0.035
637
MYL004 Myelodysplastic Myeloproliferative Cancer 54 0.035
638
PNG002 Pain Agnosia 54 0.035
639
ENT011 Enterocolitis 54 0.035
640
P INN002 Inner Ear Disease 54 0.035
641
P BRT004 Bartter Disease 53 0.035
642
HYP080 Hypogonadism 53 0.035
643
TST015 Testicular Disease 52 0.035
644
P SHR001 Short Bowel Syndrome 52 0.035
645
TMT001 Timothy Syndrome 52 0.035
646
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.035
647
ADT003 Auditory System Disease 52 0.035
648
KRT002 Keratomalacia 51 0.035
649
CHL004 Cholelithiasis 51 0.035
650
c BPL002 Bipolar I Disorder 49 0.035
651
P ART018 Aortic Valve Insufficiency 49 0.035
652
MLK006 Milk Allergy 48 0.035
653
P ART084 Arteriovenous Fistula 48 0.035
654
HRT007 Heart Cancer 47 0.035
655
BLR013 Biliary Tract Cancer 47 0.035
656
VST004 Vestibular Disease 45 0.035
657
CRB086 Cerebral Aneurysms 45 0.035
658
MCC013 Mucocutaneous Ulceration, Chronic 45 0.035
659
P MJR007 Major Affective Disorder 1 45 0.035
660
FML075 Familial Isolated Hyperparathyroidism 45 0.035
661
HRT008 Heart Conduction Disease 44 0.035
662
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 43 0.035
663
HYP064 Hypogonadotropism 42 0.035
664
CHL149 Childhood Acute Myeloid Leukemia 42 0.035
665
c HYP608 Hypocalciuric Hypercalcemia, Familial, Type Iii 40 0.035
666
P LBY004 Labyrinthitis 40 0.035
667
c MJR023 Major Affective Disorder 7 39 0.035
668
CYT002 Cytokine Deficiency 39 0.035
669
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 38 0.035
670
P HYP733 Hypercalciuria, Absorptive, 2 37 0.035
671
c MJR022 Major Affective Disorder 8 36 0.035
672
c MJR024 Major Affective Disorder 9 36 0.035
674
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 31 0.035
675
CRN288 Corneal Dystrophy, Band-Shaped 31 0.035
676
ENM001 Enamel Caries 30 0.035
677
TRD008 Triiodothyronine Receptor Auxiliary Protein 27 0.035
678
c HYP831 Hyperparathyroidism, Transient Neonatal 20 0.035
679
P MDL005 Medulloblastoma 76 0.033
680
PLM001 Pulmonary Tuberculosis 74 0.033
681
WRN001 Werner Syndrome 73 0.033
682
MYC006 Mycosis Fungoides 73 0.033
683
CRB037 Cerebral Palsy 71 0.033
684
P FRN006 Frontotemporal Dementia 69 0.033
685
P ALC004 Alcohol Abuse 68 0.033
686
END057 Endometrial Cancer 68 0.033
687
c ATS007 Autism Spectrum Disorder 67 0.033
688
c HPT003 Hepatitis a 66 0.033
689
FBR047 Fibromyalgia 66 0.033
690
SZR001 Sezary's Disease 66 0.033
691
LWC002 Lowe Oculocerebrorenal Syndrome 66 0.033
692
P LYN001 Lynch Syndrome 66 0.033
693
P DYS154 Dystonia 65 0.033
694
P HML002 Hemolytic Anemia 64 0.033
695
P ANR048 Aniridia 1 64 0.033
696
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 64 0.033
697
P GLM040 Glioma Susceptibility 1 63 0.033
698
c PNC108 Pancreatitis, Hereditary 62 0.033
699
PLS011 Plasmacytoma 62 0.033
700
RHM001 Rheumatic Fever 61 0.033
701
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.033
702
P FBR017 Fibrosarcoma 61 0.033
703
P SBS003 Substance Abuse 60 0.033
704
URT039 Urticaria 60 0.033
705
P LRY044 Larynx Cancer 60 0.033
706
DMY004 Demyelinating Disease 60 0.033
707
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 60 0.033
708
DBT062 Diabetic Foot Ulcers 58 0.033
709
IGG001 Iga Glomerulonephritis 58 0.033
710
HRT012 Heart Valve Disease 58 0.033
711
DSS009 Disseminated Intravascular Coagulation 58 0.033
712
P PLY041 Polymyositis 58 0.033
713
CRT016 Carotid Artery Disease 58 0.033
714
OST016 Osteochondrosis 58 0.033
715
VSC002 Vascular Dementia 57 0.033
716
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 57 0.033
717
IMP005 Impotence 56 0.033
718
MYM001 Myoma 56 0.033
719
ANK001 Ankylosis 56 0.033
720
AMN001 Amenorrhea 55 0.033
721
c SVR005 Severe Pre-Eclampsia 55 0.033
722
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.033
723
PRS021 Prostatic Adenoma 55 0.033
724
SPN051 Spondylitis 55 0.033
725
THR016 Thrombophlebitis 54 0.033
726
PRS129 Prostatic Hyperplasia, Benign 53 0.033
727
MCL006 Macular Retinal Edema 53 0.033
728
P MLN007 Male Infertility 52 0.033
729
HDN002 Head Injury 52 0.033
730
P CMP008 Compartment Syndrome 52 0.033
731
c RTN162 Retinitis Pigmentosa 2 51 0.033
732
P NGH001 Night Blindness 50 0.033
733
ACN001 Acinar Cell Carcinoma 49 0.033
734
GNG011 Gingival Disease 49 0.033
735
HYP789 Hypophosphatemic Rickets with Hypercalciuria, Hereditary 49 0.033
736
VND001 Vein Disease 49 0.033
737
P RNL015 Renal Hypertension 49 0.033
738
SYN036 Syncope 49 0.033
739
URT010 Ureteral Obstruction 49 0.033
740
DYS073 Dysphagia 48 0.033
741
DBT008 Diabetic Angiopathy 48 0.033
742
RYN001 Raynaud Disease 48 0.033
743
DFF003 Diffuse Scleroderma 46 0.033
744
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.033
745
THR035 Thrombasthenia 46 0.033
746
GST105 Gastroesophageal Adenocarcinoma 45 0.033
747
P CLS010 Cluster Headache 45 0.033
748
LFT001 Left Bundle Branch Hemiblock 44 0.033
749
P TST026 Testicular Germ Cell Cancer 44 0.033
750
ACT003 Acute Kidney Tubular Necrosis 44 0.033
751
SLT001 Solitary Osseous Plasmacytoma 44 0.033
753
P HYP265 Hypotonia 43 0.033
754
c HYP057 Hypervitaminosis D 43 0.033
755
MST004 Mast Cell Neoplasm 42 0.033
756
EXT007 Extracutaneous Mastocytoma 41 0.033
757
CHR178 Chromosomal Triplication 41 0.033
758
EXC002 Exocrine Pancreatic Insufficiency 41 0.033
759
c HYP753 Hypocalciuric Hypercalcemia, Familial, Type Ii 40 0.033
760
ATX010 Ataxia Neuropathy Spectrum 39 0.033
761
CLC004 Calcific Tendinitis 38 0.033
762
c TST017 Testicular Malignant Germ Cell Cancer 38 0.033
763
CRD220 Cardiac Valvular Defect, Developmental 36 0.033
764
ESP027 Esophagus Squamous Cell Carcinoma 35 0.033
765
PRN032 Paraneoplastic Cerebellar Degeneration 35 0.033
766
PNC015 Pancreatic Acinar Cell Adenocarcinoma 34 0.033
767
HRW001 Hair Whorl 33 0.033
768
IDP085 Idiopathic Infantile Hypercalcemia 28 0.033
769
BRN055 Bronchogenic Cyst 27 0.033
770
c RTN181 Retinitis Pigmentosa 2, X-Linked 21 0.033
771
CRV035 Cervical Cancer 76 0.030
772
P PRK057 Parkinson Disease, Late-Onset 76 0.030
773
P WSK001 Wiskott-Aldrich Syndrome 76 0.030
774
P NRF023 Neurofibromatosis, Type Ii 75 0.030
775
PSY004 Psychotic Disorder 74 0.030
776
c HPT073 Hepatitis C Virus 72 0.030
777
P RSP003 Respiratory Failure 72 0.030
778
P HRP006 Herpes Simplex 71 0.030
779
P CLC063 Celiac Disease 1 71 0.030
780
c HPT001 Hepatitis C 69 0.030
781
OBS002 Obsessive-Compulsive Disorder 68 0.030
782
c PRM196 Premature Ovarian Failure 1 68 0.030
783
GLN010 Glanzmann Thrombasthenia 67 0.030
784
P MJR001 Major Depressive Disorder 67 0.030
785
SKN019 Skin Melanoma 67 0.030
786
DFC004 Deficiency Anemia 66 0.030
787
P GCH001 Gaucher's Disease 66 0.030
788
ART005 Arteriovenous Malformation 66 0.030
789
P NSP012 Nasopharyngeal Carcinoma 65 0.030
790
P SNS014 Sinusitis 65 0.030
791
ETN001 Eating Disorder 65 0.030
792
CNT047 Contact Dermatitis 64 0.030
793
CYS013 Cystinuria 64 0.030
794
P TST021 Testicular Germ Cell Tumor 63 0.030
795
HRP004 Herpes Zoster 63 0.030
796
PRM236 Primary Biliary Cholangitis 63 0.030
797
P EPN002 Ependymoma 62 0.030
798
TRN018 Transitional Cell Carcinoma 62 0.030
799
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 62 0.030
800
MSC152 Muscular Dystrophy, Becker Type 62 0.030
801
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 62 0.030
802
SPN027 Spinal Stenosis 61 0.030
803
RSC001 Rosacea 61 0.030
804
P PTN014 Patent Ductus Arteriosus 1 61 0.030
805
SPT004 Septic Arthritis 61 0.030
806
P PRT013 Portal Hypertension 61 0.030
807
P GST044 Gastritis 60 0.030
808
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.030
809
P ESP024 Esophagitis 60 0.030
810
P UTR058 Uterine Anomalies 60 0.030
811
BRN056 Bronchopulmonary Dysplasia 60 0.030
812
CLL003 Cellulitis 60 0.030
813
OPT006 Optic Nerve Disease 60 0.030
814
SLP005 Sleep Disorder 60 0.030
815
CNT061 Conotruncal Heart Malformations 60 0.030
816
INT030 Intracranial Aneurysm 59 0.030
817
c THY109 Thyroid Cancer, Nonmedullary, 1 59 0.030
818
PLG002 Plague 59 0.030
819
P MYC008 Myocarditis 59 0.030
820
P SPN301 Spinocerebellar Ataxia 2 59 0.030
821
CHL028 Childhood Type Dermatomyositis 59 0.030
822
c ESS001 Essential Tremor 59 0.030
823
BRN004 Brain Edema 59 0.030
824
P HYP750 Hypertriglyceridemia, Familial 58 0.030
825
RLP002 Relapsing-Remitting Multiple Sclerosis 58 0.030
826
CHL067 Cholecystitis 58 0.030
827
PRN019 Perinatal Necrotizing Enterocolitis 58 0.030
828
P TMP001 Temporal Lobe Epilepsy 58 0.030
829
DCT002 Ductal Carcinoma in Situ 58 0.030
830
PRM042 Primary Effusion Lymphoma 58 0.030
831
GLS001 Gliosarcoma 57 0.030
832
HLL004 Hellp Syndrome 57 0.030
833
PRS047 Prostatitis 56 0.030
834
MCN017 Meconium Ileus 56 0.030
835
c PRM012 Primary Polycythemia 56 0.030
836
PST021 Postpartum Depression 56 0.030
837
P ALP008 Alopecia 56 0.030
838
c OST164 Osteoporosis, Juvenile 56 0.030
839
TLN003 Telangiectasis 56 0.030
840
GNT002 Giant Cell Glioblastoma 56 0.030
841
P OPT009 Optic Neuritis 55 0.030
842
RDC002 Radiculopathy 55 0.030
843
c BNG091 Benign Chronic Pemphigus 54 0.030
844
c ACT071 Acute Kidney Failure 54 0.030
845
P PRM006 Primary Biliary Cirrhosis 54 0.030
846
P PTT006 Pituitary Adenoma 54 0.030
847
MCR004 Macroglobulinemia 54 0.030
848
ERY017 Erythema Elevatum Diutinum 54 0.030
849
c BNG030 Benign Ependymoma 53 0.030
850
P OBS001 Obstructive Jaundice 53 0.030
851
FRZ001 Frozen Shoulder 53 0.030
852
BSC001 Buschke-Ollendorff Syndrome 53 0.030
853
P MTC069 Mitochondrial Disorders 53 0.030
854
CHN016 Cohen Syndrome 53 0.030
855
SXL003 Sexual Disorder 53 0.030
856
PLR008 Pleurisy 53 0.030
857
CRT049 Critical Limb Ischemia 53 0.030
858
P SML016 Small Intestine Cancer 53 0.030
859
c CNG027 Congenital Hemolytic Anemia 53 0.030
860
LKC003 Leukocyte Disease 52 0.030
861
INT067 Interstitial Nephritis 52 0.030
862
P PRC019 Precocious Puberty 52 0.030
863
P FNC004 Fanconi Syndrome 52 0.030
864
P PLG001 Pelger-Huet Anomaly 52 0.030
865
RYN005 Raynaud Phenomenon 52 0.030
866
PST095 Post-Thrombotic Syndrome 51 0.030
867
SMT003 Somatostatinoma 51 0.030
868
DRG003 Drug Dependence 51 0.030
869
PRT018 Portal Vein Thrombosis 50 0.030
870
ACT088 Acute Insulin Response 50 0.030
871
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.030
872
c PRG126 Progressive Familial Heart Block 50 0.030
873
c THY107 Thymoma, Familial 50 0.030
874
NWC001 Newcastle Disease 50 0.030
875
PRL017 Prolymphocytic Leukemia 49 0.030
876
PGM003 Pigmentation Disease 49 0.030
877
DNT001 Dental Fluorosis 48 0.030
878
c HMC010 Hemochromatosis, Type 3 47 0.030
879
P HYP058 Hypervitaminosis a 47 0.030
880
DCB001 Decubitus Ulcer 47 0.030
881
PMP004 Pemphigus Foliaceus 46 0.030
882
DBT002 Diabetic Autonomic Neuropathy 46 0.030
883
HYP085 Hypothalamic Disease 46 0.030
884
DST006 Diastolic Heart Failure 46 0.030
885
SML008 Small Intestine Lymphoma 46 0.030
886
P HRT035 Heart Block, Congenital 45 0.030
887
PPT001 Peptic Esophagitis 45 0.030
888
NPH010 Nephrosclerosis 45 0.030
889
HMP001 Hemopericardium 45 0.030
890
CRB008 Cerebral Atherosclerosis 44 0.030
891
BRS064 Bursitis 44 0.030
892
MNN017 Mononeuropathy 44 0.030
893
HYP082 Hypopharynx Cancer 43 0.030
894
BCL014 B-Cell Growth Factor 43 0.030
895
SPR008 Supratentorial Primitive Neuroectodermal Tumor 43 0.030
896
CLN044 Colon Adenoma 43 0.030
897
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 43 0.030
898
DYS011 Dyskinesia of Esophagus 42 0.030
899
CRD137 Cardiogenic Shock 42 0.030
900
BWN003 Bowenoid Papulosis 42 0.030
901
OVR112 Ovarian Germ Cell Cancer 42 0.030
902
P LRG016 Large Intestine Adenocarcinoma 42 0.030
903
HYP070 Hyperpituitarism 42 0.030
904
GNT050 Genitourinary Tract Anomalies 40 0.030
905
LWT001 Low Tension Glaucoma 40 0.030
906
HYD003 Hydrarthrosis 40 0.030
907
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 40 0.030
908
P HYP599 Hypoparathyroidism, Familial Isolated 40 0.030
909
EXC003 Excessive Tearing 38 0.030
910
c HYP602 Hyperoxaluria, Primary, Type Ii 38 0.030
911
c BLR024 Biliary Cirrhosis, Primary, 1 38 0.030
912
CRD245 Cardiac-Urogenital Syndrome 38 0.030
913
P VSC018 Visceral Steatosis 37 0.030
914
c HYP534 Hypomagnesemia 3, Renal 37 0.030
915
SWL001 Swallowing Disorders 36 0.030
916
c BSL038 Basal Ganglia Calcification, Idiopathic, 1 36 0.030
917
FNT004 Fainting 36 0.030
918
EXT025 Extragonadal Germ Cell Cancer 35 0.030
919
c TST046 Testicular Germ Cell Tumor 1 35 0.030
920
URN022 Urinary Tract Infections, Recurrent 34 0.030
921
MSC012 Muscular Dystrophy, Duchenne and Becker Type 33 0.030
922
PPL052 Papillomatosis, Confluent and Reticulated 33 0.030
923
SNG003 Single Ventricular Heart 31 0.030
924
ENP001 Enophthalmos 30 0.030
925
RDN004 Radin Blood Group Antigen 28 0.030
926
MTH071 Methane Production 27 0.030
927
CHR476 Chronic Angina 27 0.030
928
DNT010 Dentin Caries 26 0.030
929
DGS002 Degos 'en Cocarde' Erythrokeratoderma 25 0.030
930
PRR001 Periarthritis 25 0.030
931
HYP705 Hyperadrenalism 23 0.030
932
GLC025 Galactorrhoea-Hyperprolactinaemia 23 0.030
934
INT074 Intracranial Arteriosclerosis 16 0.030
935
EWN003 Ewing Sarcoma 74 0.028
936
MLT157 Multiple System Atrophy 1 72 0.028
937
MLD001 Melioidosis 72 0.028
938
CHG001 Chagas Disease 72 0.028
939
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.028
940
P FML011 Familial Adenomatous Polyposis 71 0.028
941
P MNN013 Meningitis 69 0.028
942
P WLD002 Waldenstrom Macroglobulinemia 69 0.028
943
c WLM013 Wilms Tumor 1 68 0.028
944
APN008 Apnea, Obstructive Sleep 68 0.028
945
CTN007 Cutaneous Leishmaniasis 68 0.028
946
P HYP098 Hypereosinophilic Syndrome 67 0.028
947
HSH003 Hashimoto Thyroiditis 67 0.028
948
GLL008 Gilles De La Tourette Syndrome 67 0.028
949
MVM001 Movement Disease 67 0.028
950
CHL123 Chlamydia 66 0.028
951
c HMP004 Hemophilia B 66 0.028
952
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 66 0.028
953
P CNJ013 Conjunctivitis 65 0.028
954
BLL006 Bullous Pemphigoid 64 0.028
955
P ANG001 Angelman Syndrome 64 0.028
956
c WLM018 Wilms Tumor 5 64 0.028
957
FLL027 Fallopian Tube Carcinoma 64 0.028
958
c CNR004 Cone-Rod Dystrophy 2 63 0.028
959
APH001 Aphthous Stomatitis 63 0.028
960
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 63 0.028
961
CMP010 Complex Regional Pain Syndrome 63 0.028
962
DPH001 Diphtheria 63 0.028
963
ALC006 Alcoholic Hepatitis 62 0.028
964
KRT001 Keratoconjunctivitis Sicca 62 0.028
965
P GLY013 Glycogen Storage Disease 61 0.028
966
HNC001 Henoch-Schoenlein Purpura 61 0.028
967
CRY035 Cryptorchidism, Unilateral or Bilateral 61 0.028
968
GRD007 Grade Iii Astrocytoma 61 0.028
969
P HST010 Histiocytosis 60 0.028
970
SPP010 Suppressor of Tumorigenicity 3 60 0.028
971
ORP003 Oropharynx Cancer 60 0.028
972
HPT019 Hepatic Encephalopathy 60 0.028
973
c VRL010 Viral Hepatitis 60 0.028
974
P SPN052 Spondyloarthropathy 59 0.028
975
P RST001 Restless Legs Syndrome 59 0.028
976
END040 Endogenous Depression 59 0.028
977
SYN007 Synovitis 59 0.028
978
c MYT020 Myotonic Dystrophy 2 58 0.028
979
LMY002 Leiomyoma 58 0.028
980
BLD044 Bladder Disease 57 0.028
981
P RHB003 Rhabdomyosarcoma 57 0.028
982
INT075 Intracranial Hypertension 57 0.028
983
P PLY019 Polyneuropathy 57 0.028
984
LYS002 Lysosomal Storage Disease 56 0.028
985
ART017 Aortic Disease 56 0.028
986
BLD053 Blood Platelet Disease 56 0.028
987
CRC006 Carcinoid Syndrome 56 0.028
988
P THR015 Thrombophilia 56 0.028
989
c ALM001 Al Amyloidosis 55 0.028
990
P INT070 Intestinal Obstruction 55 0.028
991
INT079 Intrahepatic Cholangiocarcinoma 55 0.028
992
HYP014 Hyperuricemia 55 0.028
993
OPT003 Opiate Dependence 55 0.028
994
PSD014 Pseudopseudohypoparathyroidism 55 0.028
995
P MCR010 Microcephaly 55 0.028
996
P PMP005 Pemphigus Vulgaris 54 0.028
997
P LPC002 Lip Cancer 54 0.028
998
P HMR005 Hemorrhoid 54 0.028
999
P RTN022 Retinal Vein Occlusion 54 0.028
1000
NNL002 Nonalcoholic Steatohepatitis 54 0.028
1001
c LBR014 Leber Congenital Amaurosis 4 54 0.028
1002
HMG005 Hemoglobinopathy 54 0.028
1003
P PRC012 Pericardial Effusion 53 0.028
1004
P CNG010 Congenital Stationary Night Blindness 53 0.028
1005
CHR563 Chronic Eosinophilic Leukemia 53 0.028
1006
P OPN001 Open-Angle Glaucoma 53 0.028
1007
DRY001 Dry Eye Syndrome 53 0.028
1008
ISL003 Isolated Growth Hormone Deficiency 52 0.028
1009
LPD009 Lipid Storage Disease 52 0.028
1010
SNS008 Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis 52 0.028
1011
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 52 0.028
1012
P BRN035 Brain Stem Glioma 52 0.028
1013
CLS016 Clostridium Difficile Colitis 52 0.028
1014
NSD001 Nose Disease 52 0.028
1015
P PTY003 Pityriasis Rubra Pilaris 51 0.028
1016
LRY017 Laryngeal Disease 51 0.028
1017
RNL077 Renal Fibrosis 51 0.028
1018
P CHL066 Cholangitis 51 0.028
1019
CRC014 Carcinoid Tumors, Intestinal 51 0.028
1020
ISL001 Islet Cell Tumor 51 0.028
1021
EXT010 Extramedullary Plasmacytoma 51 0.028
1022
ACT011 Acute Contagious Conjunctivitis 51 0.028
1023
PTH003 Pathologic Nystagmus 50 0.028
1024
CHR073 Choreatic Disease 50 0.028
1025
GLC036 Glucagonoma 50 0.028
1026
SPH010 Sphingolipidosis 50 0.028
1027
CHL018 Childhood Medulloblastoma 50 0.028
1028
LRG008 Large Granular Lymphocyte Leukemia 49 0.028
1029
HYP006 Hypertensive Heart Disease 49 0.028
1030
NTR003 Natural Killer Cell Leukemia 49 0.028
1031
MST002 Mast-Cell Leukemia 49 0.028
1032
PRV004 Periventricular Leukomalacia 49 0.028
1033
PRN014 Paronychia 49 0.028
1034
c PSR017 Psoriasis 2 49 0.028
1035
SXD002 Sex Development Disorder 49 0.028
1036
HYP457 Hypertrophic Scars 48 0.028
1037
HYP741 Hyperparathyroidism 2 with Jaw Tumors 48 0.028
1038
RTN023 Retinitis 48 0.028
1039
PTT037 Pituitary Tumors 48 0.028
1040
TCL002 T-Cell Large Granular Lymphocyte Leukemia 47 0.028
1041
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 47 0.028
1042
P BRB001 Beriberi 46 0.028
1043
APP010 Appendix Cancer 46 0.028
1044
MDL009 Medullary Sponge Kidney 46 0.028
1045
SKL017 Skeletal Dysplasias 46 0.028
1046
RGH001 Right Bundle Branch Block 46 0.028
1047
ATN004 Autonomic Neuropathy 46 0.028
1048
PST053 Postherpetic Neuralgia 45 0.028
1049
ART004 Aortic Atherosclerosis 45 0.028
1050
HPT004 Hepatic Coma 45 0.028
1051
CRN024 Corneal Disease 45 0.028
1052
SGN002 Signet Ring Cell Adenocarcinoma 45 0.028
1053
GRM004 Germinoma 45 0.028
1054
PRM175 Primary Familial Brain Calcification 44 0.028
1055
FDL002 Food Allergy 44 0.028
1056
PHT003 Phototoxic Dermatitis 44 0.028
1057
HYP030 Hypoactive Sexual Desire Disorder 44 0.028
1058
SPS057 Spasticity 44 0.028
1059
c PSR028 Psoriasis 7 43 0.028
1060
c PSR032 Psoriasis 11 43 0.028
1061
c SRC023 Sarcoidosis 2 43 0.028
1062
LCR008 Lacrimal Apparatus Disease 43 0.028
1063
P OCY003 Oocyte Maturation Defect 1 42 0.028
1064
c PSR018 Psoriasis 13 42 0.028
1065
MTR007 Motor Peripheral Neuropathy 41 0.028
1066
c PMP006 Pemphigus Vulgaris, Familial 41 0.028
1067
TRT001 Teratocarcinoma 41 0.028
1068
LKM006 Leukomalacia 41 0.028
1069
PRN039 Paraneoplastic Syndromes 40 0.028
1070
HLX001 Helix Syndrome 40 0.028
1071
c CHR020 Chronic Interstitial Cystitis 39 0.028
1072
URT014 Ureterolithiasis 39 0.028
1073
PDT014 Pediatric Ependymoma 38 0.028
1074
CHR286 Chronic Neutrophilic Leukemia 38 0.028
1075
P VTM026 Vitamin D Hydroxylation-Deficient Rickets, Type 1a 37 0.028
1076
OLC001 Olecranon Bursitis 36 0.028
1077
P BCL013 B-Cell Adult Acute Lymphocytic Leukemia 35 0.028
1078
CNT018 Central Nervous System Leukemia 35 0.028
1079
TTH007 Tooth Erosion 34 0.028
1080
RFR002 Refractory Hairy Cell Leukemia 34 0.028
1081
c HYP603 Hyperoxaluria, Primary, Type Iii 33 0.028
1082
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 32 0.028
1083
P PRX010 Paroxysmal Ventricular Fibrillation 32 0.028
1084
RNL001 Renal Artery Obstruction 31 0.028
1085
c ANR047 Aniridia 2 31 0.028
1086
HYP827 Hypomagnesemia 5, Renal, with or Without Ocular Involvement 29 0.028
1087
P STR035 Streptococcal Group a Invasive Disease 29 0.028
1088
FNC005 Functional Colonic Disease 29 0.028
1089
PDT040 Pediatric Hypertension 29 0.028
1090