Search results for Calcium

3524 hits were found for Calcium

# Family MCID Name MIFTS Score
1
c CHN022 Chondrocalcinosis 2 41 8.286
2
NPH091 Nephrolithiasis, Calcium Oxalate 60 7.842
3
FML307 Familial Calcium Pyrophosphate Deposition 40 6.024
4
IMM066 Immunodeficiency 9 30 5.049
5
IMM065 Immunodeficiency 10 33 4.606
6
P CHN059 Chondrocalcinosis 52 3.222
7
c BLD126 Bleeding Disorder, Platelet-Type, 18 39 2.910
8
c AML006 Amelogenesis Imperfecta Hypoplastic Type, Ig 18 2.080
9
CMB055 Combined Immunodeficiency Due to Crac Channel Dysfunction 17 2.080
10
c NRL030 Neurological Muscular Channelopathy Due to a Genetic Calcium Channel Defect 3 2.080
11
c NRL036 Neurological Channelopathy of the Central Nervous System Due to a Genetic Calcium Channel Defect 2 2.080
12
P HYP069 Hyperparathyroidism 63 0.462
13
P OST002 Osteoporosis 74 0.387
14
NPH009 Nephrolithiasis 55 0.371
15
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.370
16
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.370
17
BNR002 Bone Resorption Disease 48 0.362
18
RCK004 Rickets 68 0.354
19
PRT037 Pertussis 65 0.330
20
URL001 Urolithiasis 45 0.322
21
c HYP595 Hypertension, Essential 84 0.307
22
P KDN018 Kidney Disease 72 0.297
23
c SCN007 Secondary Hyperparathyroidism 51 0.290
24
c PRM005 Primary Hyperparathyroidism 58 0.264
25
P CLR023 Colorectal Cancer 99 0.242
26
P NRB001 Neuroblastoma 72 0.240
27
P BND020 Bone Disease 59 0.238
28
c CHR684 Chronic Kidney Disease 70 0.230
29
P HYP024 Hypoparathyroidism 56 0.215
30
LPP008 Lipoprotein Quantitative Trait Locus 62 0.212
31
ANG054 Angina Pectoris 66 0.212
32
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.210
33
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.209
34
HYP025 Hyperphosphatemia 48 0.205
35
CNG034 Congestive Heart Failure 69 0.201
36
ART140 Arteries, Anomalies of 52 0.195
37
HLX001 Helix Syndrome 47 0.195
38
ISC004 Ischemia 58 0.188
39
P CRN300 Coronary Heart Disease 1 63 0.187
40
c PRC016 Pre-Eclampsia 63 0.186
41
ATH013 Atherosclerosis Susceptibility 65 0.185
42
END086 End Stage Renal Disease 51 0.183
43
P HRT032 Heart Disease 75 0.181
44
ADN018 Adenoma 59 0.181
45
48X005 48,xyyy 39 0.178
46
P ADN016 Adenocarcinoma 64 0.172
47
HYP266 Hypoxia 57 0.170
48
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.162
49
P MSC005 Muscular Dystrophy 66 0.161
50
IDP073 Idiopathic Hypercalciuria 43 0.161
51
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.159
52
OST011 Osteomalacia 52 0.159
53
ANX004 Anoxia 40 0.158
54
P GLM045 Glioma 63 0.156
55
CHL014 Cholera 59 0.156
56
P ALZ034 Alzheimer Disease 88 0.155
57
GLL048 Glial Tumor 45 0.155
58
P VSC007 Vascular Disease 63 0.153
59
INS001 Insulinoma 60 0.152
60
P RCT021 Rectum Cancer 52 0.151
61
DNT012 Dental Caries 53 0.151
62
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.149
63
OST159 Osteogenic Sarcoma 66 0.149
64
P LTR001 Lateral Sclerosis 54 0.149
65
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.149
66
P MLG056 Malignant Hyperthermia 67 0.146
67
ALL026 Allergic Hypersensitivity Disease 62 0.145
68
c MGR028 Migraine with or Without Aura 1 67 0.143
69
NPH003 Nephrocalcinosis 51 0.143
70
P PRD008 Periodontitis 64 0.143
71
P FML068 Familial Hypocalciuric Hypercalcemia 54 0.140
72
P PHC003 Pheochromocytoma 71 0.140
73
ADR040 Adrenal Gland Pheochromocytoma 46 0.139
74
c ATR087 Atrial Standstill 1 75 0.138
75
MTB004 Metabolic Acidosis 50 0.138
76
LPD008 Lipid Metabolism Disorder 62 0.137
77
P MYC007 Myocardial Infarction 70 0.136
78
CLC006 Calcinosis 48 0.136
79
TTN003 Tetanus 65 0.135
80
GT001 Gout 64 0.135
81
47X002 47,xyy 49 0.135
82
P HYP726 Hypercalcemia, Infantile, 1 58 0.135
83
HYP056 Hypoglycemia 66 0.133
84
AGN016 Aging 56 0.133
85
HYP017 Hypophosphatemia 50 0.133
86
P CRD119 Cardiac Arrest 67 0.131
87
c GLL024 Gallbladder Disease 1 53 0.130
88
OST017 Osteomyelitis 64 0.130
89
P ART023 Arthropathy 62 0.128
90
CYS001 Cystic Fibrosis 81 0.128
91
P ECL001 Eclampsia 50 0.128
92
c HYP836 Hypercholesterolemia, Familial, 1 73 0.127
93
MSC157 Muscular Dystrophy, Duchenne Type 72 0.127
94
c ACT027 Acute Pancreatitis 60 0.127
95
URM002 Uremia 49 0.127
96
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.126
97
c DLT002 Dilated Cardiomyopathy 79 0.125
98
P HYP076 Hyperthyroidism 55 0.125
99
P PLM037 Pulmonary Hypertension 67 0.123
100
c RHB024 Rhabdomyosarcoma 2 67 0.123
101
LMB002 Lambert-Eaton Myasthenic Syndrome 53 0.123
102
P LYM118 Lymphoma 68 0.122
103
c ACT071 Acute Kidney Failure 60 0.121
104
P SRC025 Sarcoidosis 1 70 0.121
105
INT007 Intermediate Coronary Syndrome 55 0.121
106
RNL011 Renal Osteodystrophy 50 0.120
107
HRW001 Hair Whorl 36 0.120
108
P PRS040 Prostate Cancer 97 0.120
109
P MYP004 Myopathy 70 0.120
110
CLN015 Colon Adenocarcinoma 65 0.119
111
P HYP061 Hypertrophic Cardiomyopathy 70 0.118
112
P NRP001 Neuropathy 56 0.118
113
c MCR120 Microvascular Complications of Diabetes 7 47 0.117
114
LYM019 Lymphosarcoma 46 0.117
115
P LKM002 Leukemia 68 0.117
116
P HYP086 Hypothyroidism 69 0.116
117
P DRR001 Diarrhea 55 0.116
118
c MCR113 Microvascular Complications of Diabetes 3 52 0.116
119
PPL052 Papillomatosis, Confluent and Reticulated 33 0.116
120
P SZR006 Seizure Disorder 56 0.116
121
P ART021 Arteriosclerosis 54 0.116
122
c MCR130 Microvascular Complications of Diabetes 6 41 0.116
123
c MCR133 Microvascular Complications of Diabetes 4 41 0.116
124
P BRS047 Breast Cancer 97 0.115
125
OST012 Osteoarthritis 78 0.114
126
VSL002 Visual Epilepsy 59 0.114
127
CRN030 Coronary Stenosis 50 0.114
128
DWN001 Down Syndrome 70 0.112
129
P ATR011 Atrial Fibrillation 66 0.112
130
HYP066 Hyperglycemia 61 0.111
131
CLR108 Colorectal Adenoma 64 0.110
132
CRD132 Cardiac Conduction Defect 58 0.110
133
HYP060 Hyperinsulinism 54 0.110
134
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.109
135
CNS004 Constipation 58 0.108
136
HMN044 Human Immunodeficiency Virus Type 1 71 0.108
137
P PNC044 Pancreatitis 61 0.108
138
HYP005 Hypokalemia 55 0.108
139
P LKM062 Leukemia, Acute Lymphoblastic 69 0.107
140
ATM095 Autoimmune Disease 62 0.107
141
P BPL003 Bipolar Disorder 56 0.107
142
P CHR345 Chronic Pain 44 0.107
143
c MJR024 Major Affective Disorder 9 41 0.106
144
c MJR022 Major Affective Disorder 8 38 0.106
145
P DBT009 Diabetes Mellitus 64 0.106
146
THY029 Thyroid Carcinoma 59 0.106
147
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.105
148
P MCR115 Microvascular Complications of Diabetes 5 66 0.105
149
P CRD246 Cardiovascular System Disease 57 0.104
150
PLY150 Polykaryocytosis Inducer 31 0.104
151
P CTR002 Cataract 60 0.103
152
c ACT075 Acute Myocardial Infarction 57 0.102
153
RTR008 Root Resorption 45 0.102
154
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.101
155
P PLY014 Polycystic Kidney Disease 62 0.101
156
INS024 Insulin-Like Growth Factor I 79 0.100
157
ATR057 Atrioventricular Block 55 0.100
158
CRB004 Cerebral Artery Occlusion 45 0.100
159
TRM010 Traumatic Brain Injury 51 0.099
160
IRN002 Iron Metabolism Disease 57 0.098
161
GLB015 Glioblastoma Multiforme 75 0.097
162
CRD223 Cardiac Arrhythmia 60 0.097
163
PRT029 Parathyroid Adenoma 50 0.097
164
P HYP733 Hypercalciuria, Absorptive, 2 45 0.096
165
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.095
166
CRB039 Cerebrovascular Disease 67 0.095
167
PNG002 Pain Agnosia 51 0.095
168
P OVR082 Overgrowth Syndrome 50 0.095
169
BRN071 Brain Injury 49 0.095
170
CYT002 Cytokine Deficiency 42 0.095
171
P PNC035 Pancreatic Cancer 84 0.095
172
PTT037 Pituitary Tumors 44 0.095
173
P HNT016 Huntington Disease 72 0.094
174
P LVR013 Liver Disease 68 0.094
175
LVR012 Liver Cirrhosis 62 0.094
176
STT001 Status Epilepticus 60 0.094
177
LYM040 Lymphoblastic Lymphoma 54 0.094
178
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.094
179
DPR016 Depression 63 0.093
180
SPN186 Spinal Cord Injury 60 0.093
181
P PRP019 Peripheral Nervous System Disease 58 0.093
182
IMM167 Immune Deficiency Disease 78 0.092
183
P ENC018 Encephalopathy 61 0.092
184
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.092
185
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.092
186
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.092
187
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.092
188
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.092
189
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.092
190
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.092
191
P PSR002 Psoriasis 62 0.092
192
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.092
193
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.092
194
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.092
195
P OVR042 Ovarian Cancer 88 0.091
196
ALC007 Alcohol Dependence 66 0.091
197
STR067 Stroke, Ischemic 81 0.090
198
P GST053 Gastric Cancer 83 0.089
199
ACQ007 Acquired Immunodeficiency Syndrome 60 0.089
200
P AST007 Astrocytoma 51 0.089
201
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 0.088
202
P RNL007 Renal Tubular Acidosis 51 0.088
203
NTR005 Nutritional Deficiency Disease 62 0.087
204
P EPL164 Epilepsy 71 0.087
205
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.087
206
P FML023 Familial Hemiplegic Migraine 53 0.087
207
P PSD015 Pseudohypoparathyroidism 56 0.086
208
P HYP776 Hyperparathyroidism, Neonatal Severe 47 0.086
209
P LNG032 Lung Cancer 98 0.085
210
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.085
211
MYL069 Myeloma, Multiple 85 0.085
212
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.085
213
SKN016 Skin Disease 63 0.085
214
PST011 Pustulosis of Palm and Sole 52 0.085
215
P TRN020 Turner Syndrome 67 0.084
216
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.084
217
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.084
218
GTR002 Goiter 53 0.084
219
P DDN001 Duodenal Ulcer 52 0.084
220
RYN005 Raynaud Phenomenon 47 0.084
221
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.084
222
ADL002 Adult Syndrome 70 0.083
223
c ATS007 Autism Spectrum Disorder 67 0.083
224
P NPH012 Nephrotic Syndrome 60 0.083
225
PPT005 Peptic Ulcer Disease 59 0.083
226
P LCT002 Lactose Intolerance 53 0.083
227
TXC005 Toxic Shock Syndrome 62 0.082
228
FTT001 Fatty Liver Disease 61 0.082
229
P TRM003 Tremor 54 0.082
230
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.082
231
MMM001 Mammary Paget's Disease 53 0.082
232
PRP027 Peripheral Vascular Disease 71 0.081
233
P PRM002 Primary Hyperoxaluria 62 0.081
234
MYC005 Myocardial Stunning 46 0.081
235
ATX019 Ataxia with Vitamin E Deficiency 42 0.080
236
LNG099 Lung Disease 60 0.079
237
CLN045 Colonic Benign Neoplasm 46 0.079
238
OST003 Osteonecrosis 61 0.078
239
P BCL017 B-Cell Lymphoma 58 0.078
240
P ART022 Arthritis 69 0.078
241
c ACT068 Acute Cystitis 63 0.078
242
MNT002 Mental Depression 58 0.078
243
HMS001 Hemosiderosis 54 0.078
244
P FML187 Familial Hypertension 37 0.078
245
ESP021 Esophageal Cancer 90 0.077
246
THY111 Thyroid Carcinoma, Familial Medullary 67 0.077
247
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.077
248
P GLM007 Glomerulonephritis 57 0.077
249
AST005 Asthma 76 0.076
250
P LNG028 Long Qt Syndrome 66 0.076
251
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.076
252
P RHM011 Rheumatoid Arthritis 80 0.075
253
P DMN002 Dementia 66 0.075
254
P INF037 Inflammatory Bowel Disease 54 0.075
255
GNG012 Gingival Overgrowth 51 0.075
256
P RRH023 Rare Hereditary Hemochromatosis 41 0.075
257
c BRN108 Branchiootic Syndrome 1 62 0.074
258
P EPS003 Episodic Ataxia 59 0.074
259
P INF032 Infertility 57 0.074
260
GLC003 Glucose Intolerance 54 0.074
261
THY125 Thyroid Gland Medullary Carcinoma 50 0.074
262
P PRD021 Periodic Paralysis 45 0.074
263
P HPT023 Hepatocellular Carcinoma 100 0.074
264
HYP014 Hyperuricemia 52 0.074
265
DNT006 Dental Pulp Necrosis 41 0.074
266
P ATS364 Autism 70 0.073
267
c SML038 Small Cell Cancer of the Lung 65 0.073
268
IRR002 Irritable Bowel Syndrome 65 0.073
269
P THL005 Thalassemia 60 0.073
270
ZLL002 Zollinger-Ellison Syndrome 55 0.073
271
WTH001 Withdrawal Disorder 48 0.073
272
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.072
273
c THR092 Thrombophilia Due to Thrombin Defect 73 0.072
274
DFC004 Deficiency Anemia 70 0.072
275
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.072
276
LYM133 Lymphoma, Hodgkin, Classic 69 0.072
277
TRN015 Transient Cerebral Ischemia 63 0.072
278
DRM006 Dermatitis 61 0.072
279
P TMP001 Temporal Lobe Epilepsy 50 0.072
280
PLP001 Pulpitis 49 0.072
281
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.072
282
PRM020 Premenstrual Tension 40 0.072
283
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.072
284
c SYS001 Systemic Lupus Erythematosus 86 0.071
285
c EPS035 Episodic Ataxia, Type 2 63 0.071
286
CHL068 Cholestasis 61 0.071
287
P MYL006 Myeloid Leukemia 60 0.071
288
P MLN007 Male Infertility 55 0.071
289
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.070
290
ACR007 Acromegaly 71 0.070
291
PLM001 Pulmonary Tuberculosis 69 0.070
292
SQM006 Squamous Cell Carcinoma 60 0.070
293
GLS018 Glass Syndrome 57 0.070
294
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.070
295
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.070
296
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.070
297
c LKM061 Leukemia, Acute Myeloid 84 0.069
298
P PNM007 Pneumonia 68 0.069
299
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.069
300
P TXP001 Toxoplasmosis 60 0.069
301
P PLY011 Polycystic Ovary Syndrome 56 0.069
302
c GRV008 Graves Disease 1 56 0.069
303
MCS002 Mucositis 56 0.069
304
BNN003 Bone Inflammation Disease 48 0.069
305
c PRM038 Primary Agammaglobulinemia 44 0.069
306
c LKM005 Leukemia, T-Cell, Chronic 34 0.069
307
P HDC001 Headache 57 0.068
308
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.068
309
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.068
310
P MLN008 Melanoma 69 0.068
311
PNC129 Pancreatic Adenocarcinoma 68 0.068
312
PRT036 Peritonitis 64 0.068
313
P SPN309 Spinocerebellar Ataxia 6 59 0.068
314
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.068
315
P LPS004 Lupus Erythematosus 61 0.067
316
SYN007 Synovitis 54 0.067
317
P CYS039 Cystic Kidney Disease 54 0.067
318
DBT010 Diabetic Neuropathy 54 0.067
319
c HYP752 Hypocalciuric Hypercalcemia, Familial, Type I 45 0.067
320
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.067
321
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.067
322
PLC002 Plica Syndrome 36 0.067
323
CRH001 Crohn's Disease 74 0.066
324
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.066
325
c SCL052 Scleroderma, Familial Progressive 61 0.066
326
PLM033 Pulmonary Embolism 59 0.066
327
P MSC003 Muscular Atrophy 52 0.066
328
SCN001 Secondary Hyperparathyroidism of Renal Origin 27 0.066
329
TND005 Tendinitis 54 0.065
330
OCL069 Ocular Motor Apraxia 51 0.065
331
P MYT002 Myotonic Dystrophy 49 0.065
332
SVR004 Severe Combined Immunodeficiency 73 0.064
333
ART016 Aortic Aneurysm 69 0.064
334
PRT010 Parathyroid Carcinoma 67 0.064
335
BCT022 Bacterial Infectious Disease 56 0.064
336
IMP005 Impotence 52 0.064
337
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.064
338
P BLD134 Bladder Cancer 79 0.063
339
SCK003 Sickle Cell Anemia 74 0.063
340
LPT014 Leptin Deficiency or Dysfunction 74 0.063
341
GST092 Gastroesophageal Reflux 67 0.063
342
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.063
343
MDD011 Mood Disorder 62 0.063
344
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.063
345
ANK001 Ankylosis 51 0.063
346
P RNL015 Renal Hypertension 47 0.063
347
CHL079 Children's Interstitial Lung Disease 26 0.063
348
P PRK057 Parkinson Disease, Late-Onset 78 0.062
349
MRF001 Marfan Syndrome 77 0.062
350
NRM005 Neuromuscular Disease 64 0.062
351
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.062
352
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.062
353
TMT001 Timothy Syndrome 61 0.062
354
P MLT074 Multiple Endocrine Neoplasia 56 0.062
355
CRN019 Coronary Artery Vasospasm 46 0.062
356
OST004 Osteitis Fibrosa 41 0.062
357
MLR004 Malaria 81 0.061
358
P SCH015 Schizophrenia 74 0.061
359
c HMC039 Hemochromatosis, Type 1 74 0.061
360
BRT054 Brittle Bone Disorder 72 0.061
361
P MYS003 Myasthenia Gravis 68 0.061
362
P MJR001 Major Depressive Disorder 68 0.061
363
P DRM053 Dermatitis, Atopic 66 0.061
364
MSC007 Muscle Hypertrophy 64 0.061
365
ANR040 Aneurysm 59 0.061
366
P RHN004 Rhinitis 57 0.061
367
P RTN016 Retinal Degeneration 53 0.061
368
P BRT004 Bartter Disease 52 0.061
369
CLR109 Colorectal Adenocarcinoma 51 0.061
370
NTR046 Neutrophil Migration 50 0.061
371
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.061
372
RST023 Resting Heart Rate, Variation in 41 0.061
373
ENM002 Enamel Erosion 26 0.061
374
CRY024 Crystal Arthropathies 20 0.061
375
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 19 0.061
376
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.060
377
P SYS005 Systemic Scleroderma 68 0.060
378
P HRP006 Herpes Simplex 65 0.060
379
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.060
380
P HYP750 Hypertriglyceridemia, Familial 62 0.060
381
P SCL018 Scoliosis 60 0.060
382
c PRD040 Periodontitis, Chronic 53 0.060
383
P LCT001 Lactic Acidosis 51 0.060
384
CLC001 Calciphylaxis 51 0.060
385
P RNV001 Renovascular Hypertension 48 0.060
386
SYN036 Syncope 45 0.060
387
ALL014 Allergic Encephalomyelitis 38 0.060
388
ANX010 Anxiety 73 0.059
389
P DYS154 Dystonia 65 0.059
390
P PGT001 Paget's Disease of Bone 58 0.059
391
P EXN002 Exanthem 57 0.059
392
VSC002 Vascular Dementia 57 0.059
393
P GRV001 Graves' Disease 55 0.059
394
STM007 Stomatitis 50 0.059
395
P CRB059 Cerebellar Degeneration 37 0.059
396
P LNG064 Lung Cancer Susceptibility 3 78 0.058
397
P OST001 Osteopetrosis 70 0.058
398
P THR014 Thrombocytopenia 67 0.058
399
P NTR004 Neutropenia 63 0.058
400
P ADL017 Adult T-Cell Leukemia 56 0.058
401
PLM010 Pulmonary Edema 54 0.058
402
P SCK005 Sickle Cell Disease 50 0.058
403
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.058
404
P LKM071 Leukemia, Chronic Lymphocytic 79 0.057
405
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.057
406
CMM004 Common Variable Immunodeficiency 68 0.057
407
BRN024 Bronchitis 68 0.057
408
BRK010 Burkitt Lymphoma 67 0.057
409
P ENC004 Encephalitis 61 0.057
410
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.057
411
THR024 Thrombosis 57 0.057
412
SCH014 Schistosomiasis 57 0.057
413
ERY051 Erythroleukemia, Familial 56 0.057
414
BRN004 Brain Edema 56 0.057
415
PRP016 Paraplegia 52 0.057
416
c SVR005 Severe Pre-Eclampsia 50 0.057
417
P DST107 Distal Renal Tubular Acidosis 42 0.057
418
MLG086 Malignant Hyperthermia Susceptibility 39 0.057
419
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.057
420
P CNR004 Cone-Rod Dystrophy 2 73 0.055
421
c FML021 Familial Hypercholesterolemia 66 0.055
422
P SKN015 Skin Carcinoma 66 0.055
423
BRR014 Barrett Esophagus 65 0.055
424
HYD002 Hydronephrosis 60 0.055
425
P PYL005 Pyelonephritis 56 0.055
426
P ALP008 Alopecia 54 0.055
427
c HYP864 Hypoparathyroidism, Familial Isolated, 1 48 0.055
428
49X006 49, Xxxxy Syndrome 41 0.055
429
MYT011 Myotonia 34 0.055
430
P RSP003 Respiratory Failure 74 0.054
431
CHL065 Cholangiocarcinoma 68 0.054
432
CNN005 Connective Tissue Disease 68 0.054
433
c HYP794 Hyperoxaluria, Primary, Type I 63 0.054
434
PRT013 Portal Hypertension 59 0.054
435
P ALC033 Alcohol Use Disorder 58 0.054
436
P NGH001 Night Blindness 48 0.054
437
c DRR009 Diarrhea 6 46 0.054
438
GNG003 Gingival Recession 44 0.054
439
P LTH003 Lethal Congenital Contracture Syndrome 40 0.054
441
ETH012 Ethylene Glycol Poisoning 26 0.054
442
c LKM063 Leukemia, Chronic Myeloid 72 0.053
443
c ART101 Aortic Valve Disease 2 65 0.053
444
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.053
445
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.053
446
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.053
447
ALL006 Allergic Asthma 56 0.053
448
GST050 Gastrointestinal System Disease 56 0.053
449
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.053
450
THY030 Thyroid Gland Disease 52 0.053
451
PTH003 Pathologic Nystagmus 52 0.053
452
ENT004 Enthesopathy 49 0.053
453
CHL004 Cholelithiasis 49 0.053
454
CRD137 Cardiogenic Shock 47 0.053
455
GST030 Gastrinoma 45 0.053
456
CRT015 Carotid Artery Occlusion 45 0.053
457
P MLT020 Multiple Sclerosis 72 0.052
458
P BRG001 Brugada Syndrome 71 0.052
459
SRC014 Sarcoma 65 0.052
460
P DRM010 Dermatomyositis 61 0.052
461
c ACT073 Acute Leukemia 58 0.052
462
P CNG010 Congenital Stationary Night Blindness 54 0.052
463
SPN035 Spindle Cell Sarcoma 53 0.052
464
INT079 Intrahepatic Cholangiocarcinoma 51 0.052
465
c PCH010 Pachyonychia Congenita 3 44 0.052
466
c CHR682 Chronic Bilirubin Encephalopathy 39 0.052
468
c NRF023 Neurofibromatosis, Type Ii 80 0.051
469
END057 Endometrial Cancer 74 0.051
470
P GRF003 Graft-Versus-Host Disease 72 0.051
471
P MTR014 Motor Neuron Disease 65 0.051
472
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.051
473
CLT003 Colitis 62 0.051
474
P CHL002 Childhood Absence Epilepsy 61 0.051
475
P MYC008 Myocarditis 59 0.051
476
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.051
477
c BNG091 Benign Chronic Pemphigus 58 0.051
478
P GST044 Gastritis 56 0.051
479
P VNS003 Venous Insufficiency 55 0.051
480
c XNT010 Xanthinuria, Type I 53 0.051
481
PRP080 Peripheral Artery Disease 53 0.051
482
c HYP243 Hyperparathyroidism 1 51 0.051
483
ENT011 Enterocolitis 51 0.051
484
P OPN001 Open-Angle Glaucoma 49 0.051
485
RTN023 Retinitis 46 0.051
486
PPL001 Papillary Adenoma 44 0.051
487
c HYP272 Hypercholesterolemia, Familial, 3 44 0.051
488
NRR001 Neuroretinitis 42 0.051
489
PST092 Posttransplant Acute Limbic Encephalitis 29 0.051
490
NRL016 Neural Tube Defects 82 0.050
491
P RTN024 Retinoblastoma 73 0.050
492
P SLP006 Sleep Apnea 69 0.050
493
c MCR129 Microvascular Complications of Diabetes 1 66 0.050
494
CHG001 Chagas Disease 66 0.050
495
HYP020 Hyperprolactinemia 64 0.050
496
CNT105 Central Core Disease of Muscle 60 0.050
497
c HPT016 Hepatitis B 59 0.050
498
GNG013 Gingivitis 59 0.050
499
BLR008 Bilirubin Metabolic Disorder 57 0.050
500
P MYS005 Myositis 56 0.050
501
P FBR017 Fibrosarcoma 56 0.050
502
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.050
503
P PMP001 Pemphigus 54 0.050
504
P RTN018 Retinal Disease 53 0.050
505
ACT003 Acute Kidney Tubular Necrosis 45 0.050
506
P TRC031 Trichorhinophalangeal Syndrome 40 0.050
507
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.048
508
P AMY004 Amyloidosis 70 0.048
509
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.048
510
FCT007 Factor Vii Deficiency 67 0.048
511
ALL003 Allergic Rhinitis 67 0.048
512
P CLC063 Celiac Disease 1 66 0.048
513
c FML001 Familial Atrial Fibrillation 65 0.048
514
OVR029 Ovarian Hyperstimulation Syndrome 64 0.048
515
LSH001 Leishmaniasis 63 0.048
516
ANR007 Anorexia Nervosa 63 0.048
517
c SVR001 Severe Acute Respiratory Syndrome 62 0.048
518
PNM001 Pneumocystosis 59 0.048
519
TRD006 Tardive Dyskinesia 54 0.048
520
SNS003 Sensory Peripheral Neuropathy 54 0.048
521
MST005 Mastitis 53 0.048
522
TXC002 Toxic Encephalopathy 53 0.048
523
c FML008 Familial Retinoblastoma 53 0.048
524
PRS021 Prostatic Adenoma 51 0.048
525
HYP081 Hypolipoproteinemia 51 0.048
526
HYP080 Hypogonadism 50 0.048
527
SYS003 Systolic Heart Failure 49 0.048
528
c CHR431 Chronic Venous Insufficiency 49 0.048
529
PRS129 Prostatic Hyperplasia, Benign 49 0.048
530
CRB090 Cerebral Hypoxia 44 0.048
531
P HYP265 Hypotonia 43 0.048
532
IDP070 Idiopathic Scoliosis 42 0.048
533
P KLZ004 Kala-Azar 1 41 0.048
534
c PRS136 Prostate Cancer, Hereditary, 6 33 0.048
535
c PRS130 Prostate Cancer, Hereditary, 8 32 0.048
536
PRR001 Periarthritis 32 0.048
537
P GLM040 Glioma Susceptibility 1 81 0.047
538
ULC004 Ulcerative Colitis 73 0.047
539
c DBT099 Diabetes Mellitus, Type I 65 0.047
540
TBC004 Tobacco Addiction 64 0.047
541
P END044 Endometriosis 63 0.047
542
P VSC011 Vasculitis 62 0.047
543
P HYP035 Hypophosphatasia 61 0.047
544
GST033 Gestational Diabetes 61 0.047
545
P ANP001 Anaplastic Large Cell Lymphoma 58 0.047
546
c FML035 Familial Hyperlipidemia 55 0.047
547
AMN001 Amenorrhea 54 0.047
548
PRS045 Prostatic Hypertrophy 53 0.047
549
FRZ001 Frozen Shoulder 53 0.047
550
GST023 Gastric Ulcer 53 0.047
551
CRT013 Carotid Stenosis 50 0.047
552
PLS025 Plasmablastic Lymphoma 47 0.047
553
SBC016 Subacute Delirium 44 0.047
554
LWC001 Low Compliance Bladder 43 0.047
555
c CTR132 Cataract 3, Multiple Types 41 0.047
556
c MCR112 Microvascular Complications of Diabetes 2 41 0.047
557
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.047
558
c PNS012 Paine Syndrome 61 0.046
559
P PLY019 Polyneuropathy 56 0.046
560
P SCK002 Sick Sinus Syndrome 55 0.046
561
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.046
562
DYS073 Dysphagia 50 0.046
563
MCN001 Mucinous Adenocarcinoma 49 0.046
564
HYP006 Hypertensive Heart Disease 49 0.046
565
HDN002 Head Injury 46 0.046
566
APP009 Appendix Adenocarcinoma 44 0.046
567
c HYP057 Hypervitaminosis D 42 0.046
568
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.046
569
PRN032 Paraneoplastic Cerebellar Degeneration 28 0.046
570
VLK001 Volkmann Contracture 25 0.046
571
c SPN225 Spondyloarthropathy 1 73 0.044
572
GST040 Gastric Adenocarcinoma 70 0.044
573
c PNC108 Pancreatitis, Hereditary 70 0.044
574
P LPR021 Leprosy 3 69 0.044
575
P THY023 Thymoma 65 0.044
576
c JVN010 Juvenile Rheumatoid Arthritis 64 0.044
577
PLM031 Poliomyelitis 64 0.044
578
c FNC043 Fanconi Anemia, Complementation Group E 62 0.044
579
P DNT020 Dent Disease 1 62 0.044
580
P BRS044 Breast Adenocarcinoma 59 0.044
581
GST045 Gastroenteritis 59 0.044
582
SPT004 Septic Arthritis 58 0.044
583
CHL067 Cholecystitis 57 0.044
584
SFT003 Soft Tissue Sarcoma 56 0.044
585
AMN003 Amnestic Disorder 54 0.044
586
c THY107 Thymoma, Familial 52 0.044
587
TLN003 Telangiectasis 52 0.044
588
c MGR032 Migraine, Familial Hemiplegic, 1 51 0.044
589
ACH005 Achalasia 51 0.044
590
P MTR003 Mitral Valve Stenosis 50 0.044
591
NPH010 Nephrosclerosis 50 0.044
592
VTM033 Vitamin K Deficiency Bleeding 48 0.044
593
c MLG069 Malignant Hypertension 47 0.044
594
CHR074 Choriocarcinoma 47 0.044
595
c MLG068 Malignant Glioma 46 0.044
596
PRT030 Parathyroid Gland Disease 45 0.044
597
SPS057 Spasticity 45 0.044
598
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.044
599
BCK006 Back Pain 42 0.044
600
P SCL057 Scoliosis, Isolated 1 41 0.044
601
PHS001 Phosphorus Metabolism Disease 40 0.044
602
HNS001 Hansen's Disease 34 0.044
603
CLC004 Calcific Tendinitis 30 0.044
604
ENM001 Enamel Caries 28 0.044
605
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.043
606
P RTN008 Retinitis Pigmentosa 79 0.043
607
c MNN043 Meningioma, Familial 74 0.043
608
CRB037 Cerebral Palsy 69 0.043
609
P PLM036 Pulmonary Fibrosis 65 0.043
610
PLG002 Plague 63 0.043
611
P EPL140 Epilepsy, Idiopathic Generalized 62 0.043
612
MNN042 Meningioma, Radiation-Induced 62 0.043
613
WLL001 Williams-Beuren Syndrome 60 0.043
614
P SNS001 Sensorineural Hearing Loss 60 0.043
615
VRC005 Varicose Veins 60 0.043
616
SPN027 Spinal Stenosis 59 0.043
617
P CYS018 Cystitis 59 0.043
618
EYD002 Eye Disease 58 0.043
619
DSS009 Disseminated Intravascular Coagulation 57 0.043
620
P CHN012 Chondrosarcoma 56 0.043
621
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.043
622
NRN004 Neuroendocrine Tumor 55 0.043
623
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.043
624
END040 Endogenous Depression 55 0.043
625
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.043
626
OST016 Osteochondrosis 53 0.043
627
HRT012 Heart Valve Disease 53 0.043
628
HMC014 Homocysteinemia 53 0.043
629
GSG001 Gas Gangrene 53 0.043
630
P PNC025 Panic Disorder 53 0.043
631
P MGR003 Migraine with Aura 52 0.043
632
LNG031 Lung Benign Neoplasm 51 0.043
633
SPN021 Spinal Meningioma 50 0.043
634
RYN001 Raynaud Disease 48 0.043
635
BRS064 Bursitis 48 0.043
636
c MTR002 Mitral Valve Insufficiency 48 0.043
637
KRT002 Keratomalacia 47 0.043
638
ATN005 Autonomic Dysfunction 46 0.043
639
DST006 Diastolic Heart Failure 45 0.043
640
P SPR041 Spermatogenic Failure 6 44 0.043
641
TRP009 Triple X Syndrome 42 0.043
642
SCR001 Secretory Meningioma 41 0.043
643
c SPR043 Spermatogenic Failure 9 41 0.043
644
P MLG074 Malignant Mesenchymoma 40 0.043
645
MDL009 Medullary Sponge Kidney 40 0.043
646
OVR094 Ovarian Epithelial Cancer 38 0.043
647
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.043
648
CHR178 Chromosomal Triplication 35 0.043
649
P ASP006 Aspergillosis 69 0.042
650
MNT001 Mantle Cell Lymphoma 69 0.042
651
P NRV007 Nervous System Disease 66 0.042
652
P PSD087 Pseudoxanthoma Elasticum 65 0.042
653
P KDN017 Kidney Cancer 60 0.042
654
ANT024 Anthrax Disease 58 0.042
655
FBR047 Fibromyalgia 58 0.042
656
CNT047 Contact Dermatitis 58 0.042
657
BRS051 Breast Disease 58 0.042
658
P BNC003 Bone Cancer 58 0.042
659
BRD001 Brody Myopathy 57 0.042
660
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.042
661
EMB004 Embryonal Carcinoma 56 0.042
662
LMB062 Limb Ischemia 55 0.042
663
URN010 Urinary Tract Obstruction 55 0.042
664
P SHR001 Short Bowel Syndrome 53 0.042
665
P LMB006 Limb-Girdle Muscular Dystrophy 53 0.042
666
P SML001 Small Cell Carcinoma 52 0.042
667
SPN051 Spondylitis 51 0.042
668
P HMP007 Hemophilia 51 0.042
669
FDL002 Food Allergy 51 0.042
670
PLS009 Plasma Cell Neoplasm 51 0.042
671
CYS014 Cystadenocarcinoma 51 0.042
672
P FNC004 Fanconi Syndrome 50 0.042
673
P ART018 Aortic Valve Insufficiency 49 0.042
674
CCN002 Cocaine Abuse 49 0.042
675
KRT008 Keratopathy 47 0.042
676
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.042
677
URT010 Ureteral Obstruction 45 0.042
678
HPT004 Hepatic Coma 45 0.042
679
GRN017 Granulocytopenia 44 0.042
680
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.042
681
GST020 Gastric Antral Vascular Ectasia 41 0.042
682
THR035 Thrombasthenia 40 0.042
683
MCN008 Mucinous Cystadenocarcinoma 40 0.042
684
P FNC034 Fanconi Renotubular Syndrome 2 40 0.042
685
HYP540 Hypertension, Diastolic 40 0.042
686
c CHL157 Childhood B-Cell Acute Lymphoblastic Leukemia 33 0.042
687
IDP085 Idiopathic Infantile Hypercalcemia 28 0.042
688
BRN028 Brain Cancer 74 0.040
689
c BTT014 Beta-Thalassemia 74 0.040
690
c HPT073 Hepatitis C Virus 72 0.040
691
c INF071 Inflammatory Bowel Disease 1 67 0.040
692
CRP001 Carpal Tunnel Syndrome 67 0.040
693
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.040
694
KHL003 Kohlschutter-Tonz Syndrome 65 0.040
695
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.040
696
P GCH001 Gaucher's Disease 63 0.040
697
P HML002 Hemolytic Anemia 63 0.040
698
P MVM001 Movement Disease 63 0.040
699
P ESP024 Esophagitis 62 0.040
700
BLL006 Bullous Pemphigoid 62 0.040
701
P PRM006 Primary Biliary Cirrhosis 62 0.040
702
P TMR018 Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 61 0.040
703
DPH001 Diphtheria 60 0.040
704
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.040
705
P OPT006 Optic Nerve Disease 60 0.040
706
PRN019 Perinatal Necrotizing Enterocolitis 59 0.040
707
P SYP003 Syphilis 58 0.040
708
P URT039 Urticaria 58 0.040
709
P GLL018 Gallbladder Cancer 57 0.040
710
c VSC019 Vesicoureteral Reflux 1 57 0.040
711
P MYP006 Myopia 55 0.040
712
P MNC007 Monocytic Leukemia 53 0.040
713
P INT068 Intestinal Disease 53 0.040
714
P BSL038 Basal Ganglia Calcification, Idiopathic, 1 52 0.040
715
ILS001 Ileus 51 0.040
716
RGH001 Right Bundle Branch Block 48 0.040
717
INT067 Interstitial Nephritis 48 0.040
718
DGN001 Degenerative Disc Disease 48 0.040
719
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.040
720
RTN020 Retinal Vascular Disease 46 0.040
721
GRW007 Growth Hormone Deficiency 46 0.040
722
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.040
723
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.040
724
OST115 Osteonecrosis of the Jaw 40 0.040
725
KLD004 Keloid Disorder 40 0.040
726
WLL004 Wallerian Degeneration 39 0.040
727
INF009 Inflammatory Spondylopathy 31 0.040
728
CRV035 Cervical Cancer 76 0.038
729
MYL009 Myelodysplastic Syndrome 70 0.038
730
c GCH015 Gaucher Disease, Type I 70 0.038
731
P FRG001 Fragile X Syndrome 70 0.038
732
P MYC084 Mycobacterium Tuberculosis 1 68 0.038
733
P FRN006 Frontotemporal Dementia 68 0.038
734
P FLL037 Follicular Lymphoma 67 0.038
735
GTL001 Gitelman Syndrome 65 0.038
736
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.038
737
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.038
738
PSR001 Psoriatic Arthritis 61 0.038
739
VRL011 Viral Infectious Disease 61 0.038
740
c JVN061 Juvenile Arthritis 60 0.038
741
HPT019 Hepatic Encephalopathy 60 0.038
742
P SLP005 Sleep Disorder 59 0.038
743
P CND004 Candidiasis 58 0.038
744
PMP006 Pemphigus Vulgaris, Familial 57 0.038
745
CHR100 Chronic Ulcer of Skin 55 0.038
746
PRP030 Purpura 54 0.038
747
NNL006 Non-Alcoholic Steatohepatitis 54 0.038
748
DMY004 Demyelinating Disease 52 0.038
749
RDC002 Radiculopathy 50 0.038
750
AZS001 Azoospermia 50 0.038
751
c FLL041 Follicular Lymphoma 1 49 0.038
752
DRG003 Drug Dependence 47 0.038
753
RNL077 Renal Fibrosis 47 0.038
754
DNT001 Dental Fluorosis 43 0.038
755
CRB086 Cerebral Aneurysms 40 0.038
756
P PRC031 Preeclampsia/eclampsia 1 38 0.038
757
c PLY105 Polycystic Ovary Syndrome 1 38 0.038
758
PRN039 Paraneoplastic Syndromes 38 0.038
759
BNG018 Benign Paroxysmal Positional Nystagmus 37 0.038
760
ARG004 Argyria 27 0.038
761
c LNG052 Long Qt Syndrome 8 27 0.038
762
MTH071 Methane Production 26 0.038
763
XLN012 X-Linked Congenital Stationary Night Blindness 26 0.038
764
P FML011 Familial Adenomatous Polyposis 72 0.037
765
MYL005 Myelofibrosis 70 0.037
766
EWN003 Ewing Sarcoma 69 0.037
767
c HMP004 Hemophilia B 68 0.037
768
P HYP098 Hypereosinophilic Syndrome 67 0.037
769
P BLD062 Bile Duct Cancer 67 0.037
770
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 63 0.037
771
CYS013 Cystinuria 63 0.037
772
c GLC092 Glaucoma, Primary Open Angle 62 0.037
773
MSL001 Measles 62 0.037
774
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 60 0.037
775
RHM001 Rheumatic Fever 60 0.037
776
ORL011 Oral Cancer 60 0.037
777
PRT058 Pure Autonomic Failure 59 0.037
778
IRN001 Iron Deficiency Anemia 59 0.037
779
P PRN023 Prion Disease 57 0.037
780
P ANG015 Angioedema 57 0.037
781
c ESS001 Essential Tremor 56 0.037
782
VTM027 Vitamin D-Dependent Rickets, Type 2a 56 0.037
783
P NRF002 Neurofibromatosis 56 0.037
784
PPL022 Papilloma 54 0.037
785
P INS002 in Situ Carcinoma 53 0.037
786
OCL006 Ocular Hypertension 53 0.037
787
P CNT005 Central Nervous System Lymphoma 53 0.037
788
NNT012 Neonatal Jaundice 53 0.037
789
P THY032 Thyroiditis 52 0.037
790
P TRT010 Teratoma 52 0.037
791
PLM017 Pulmonary Alveolar Microlithiasis 50 0.037
792
GST049 Gastrointestinal System Cancer 49 0.037
793
c BPL002 Bipolar I Disorder 49 0.037
794
VCC001 Vaccinia 49 0.037
795
IGG001 Iga Glomerulonephritis 48 0.037
796
c PRM226 Primary Central Nervous System Lymphoma 48 0.037
797
MLK006 Milk Allergy 48 0.037
798
GST071 Gastrointestinal Carcinoma 47 0.037
799
CNT033 Central Nervous System Cancer 47 0.037
800
ASP004 Asphyxia Neonatorum 46 0.037
801
BCK003 Background Diabetic Retinopathy 46 0.037
802
P HMR005 Hemorrhoid 46 0.037
803
SQM002 Squamous Cell Papilloma 46 0.037
804
TRT001 Teratocarcinoma 45 0.037
805
NWC001 Newcastle Disease 45 0.037
807
TST015 Testicular Disease 43 0.037
808
MST004 Mast Cell Neoplasm 42 0.037
810
c HYP753 Hypocalciuric Hypercalcemia, Familial, Type Ii 42 0.037
811
P CLS010 Cluster Headache 42 0.037
812
c HYP608 Hypocalciuric Hypercalcemia, Familial, Type Iii 41 0.037
813
PRS063 Paresthesia 41 0.037
814
ALD013 Aldosterone-Producing Adenoma 39 0.037
815
MNR003 Mineral Metabolism Disease 39 0.037
816
EXT007 Extracutaneous Mastocytoma 38 0.037
817
CRN288 Corneal Dystrophy, Band-Shaped 38 0.037
818
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.037
819
GLM044 Glomerular Disease 37 0.037
820
P DNT007 Dentin Sensitivity 36 0.037
821
MNG007 Manganese Poisoning 29 0.037
822
P MDL005 Medulloblastoma 77 0.035
823
P CHR012 Chronic Granulomatous Disease 67 0.035
824
GLN010 Glanzmann Thrombasthenia 66 0.035
825
c PSD108 Pseudohypoparathyroidism, Type Ia 66 0.035
826
c MCL013 Mucolipidosis Iv 66 0.035
827
P ART005 Arteriovenous Malformation 65 0.035
828
PPL049 Papillon-Lefevre Syndrome 65 0.035
829
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 62 0.035
830
ERL001 Early Myoclonic Encephalopathy 62 0.035
831
c HPT001 Hepatitis C 62 0.035
832
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.035
833
INT066 Interstitial Lung Disease 60 0.035
834
END081 Endosteal Hyperostosis, Autosomal Dominant 60 0.035
835
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.035
836
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.035
837
P MTR012 Mitral Valve Disease 58 0.035
838
P MTC069 Mitochondrial Disorders 56 0.035
839
PRS047 Prostatitis 56 0.035
840
ISL001 Islet Cell Tumor 56 0.035
841
DFF005 Diffuse Large B-Cell Lymphoma 55 0.035
842
P PTT006 Pituitary Adenoma 55 0.035
843
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.035
844
FCL014 Focal Epilepsy 54 0.035
845
HLL004 Hellp Syndrome 54 0.035
846
HYP741 Hyperparathyroidism 2 with Jaw Tumors 53 0.035
847
INT075 Intracranial Hypertension 53 0.035
848
ACR041 Acromelic Frontonasal Dysostosis 52 0.035
849
ART074 Aortic Dissection 52 0.035
850
BHR001 Behr Syndrome 51 0.035
851
SCH012 Schizoaffective Disorder 50 0.035
852
c HYP603 Hyperoxaluria, Primary, Type Iii 50 0.035
853
TRY001 Trypanosomiasis 50 0.035
854
OPT003 Opiate Dependence 50 0.035
855
LFT001 Left Bundle Branch Hemiblock 49 0.035
856
SNT005 Sinoatrial Node Disease 49 0.035
857
SCT005 Scott Syndrome 49 0.035
858
ATS010 Autosomal Recessive Disease 48 0.035
859
PRP017 Periapical Periodontitis 46 0.035
860
P BNG032 Benign Mesothelioma 46 0.035
861
GST012 Gastroesophageal Junction Adenocarcinoma 46 0.035
862
ASP026 Asplenia, Isolated Congenital 44 0.035
863
CVD001 Covid-19 44 0.035
864
MMM006 Mammographic Density 41 0.035
865
RDN001 Reading Disorder 40 0.035
866
P CHL156 Childhood T-Cell Acute Lymphoblastic Leukemia 38 0.035
867
c HNT011 Huntington Disease-Like 3 38 0.035
868
HRN029 Hearing Loss, Noise-Induced 37 0.035
869
SCR003 Secretory Diarrhea 37 0.035
870
ENP001 Enophthalmos 35 0.035
871
RTC003 Root Caries 33 0.035
872
CYT018 Cytochrome P450 2d6 Variant 27 0.035
873
HVY002 Heavy Metal Poisoning 22 0.035
874
P RTT002 Rett Syndrome 80 0.033
875
CNN003 Conn's Syndrome 79 0.033
876
P TBR001 Tuberous Sclerosis 70 0.033
877
ACR008 Acrocallosal Syndrome 69 0.033
878
ODN023 Odontochondrodysplasia 68 0.033
879
OBS002 Obsessive-Compulsive Disorder 68 0.033
880
SKN019 Skin Melanoma 68 0.033
881
P INF038 Influenza 68 0.033
882
P HPT021 Hepatitis 67 0.033
883
P HYD006 Hydrocephalus 66 0.033
884
MYL031 Myeloproliferative Neoplasm 66 0.033
885
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 0.033
886
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.033
887
P ADL010 Adult Respiratory Distress Syndrome 65 0.033
888
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.033
889
DGR001 Digeorge Syndrome 64 0.033
890
P RHB003 Rhabdomyosarcoma 63 0.033
891
MSC152 Muscular Dystrophy, Becker Type 63 0.033
892
c ALP101 Alpha-Thalassemia 62 0.033
893
P SJG008 Sjogren Syndrome 61 0.033
894
ING001 Inguinal Hernia 60 0.033
895
ETN001 Eating Disorder 60 0.033
896
P GLY013 Glycogen Storage Disease 60 0.033
897
P MCR010 Microcephaly 59 0.033
898
CHL123 Chlamydia 59 0.033
899
P NMN002 Niemann-Pick Disease 59 0.033
900
P GLL022 Guillain-Barre Syndrome 59 0.033
901
INC002 Inclusion Body Myositis 58 0.033
902
CHL028 Childhood Type Dermatomyositis 58 0.033
903
c DWL002 Dowling-Degos Disease 1 58 0.033
904
LYM027 Lymphopenia 58 0.033
905
P UVT001 Uveitis 57 0.033
906
P GLL020 Gallbladder Disease 57 0.033
907
THY122 Thyroid Gland Cancer 57 0.033
908
TRP006 Tarp Syndrome 57 0.033
909
P FCL005 Focal Segmental Glomerulosclerosis 57 0.033
910
HMR039 Hemorrhage, Intracerebral 57 0.033
911
CMR002 Coumarin Resistance 56 0.033
912
TRN018 Transitional Cell Carcinoma 56 0.033
913
P SBS003 Substance Abuse 55 0.033
914
P SLM003 Salmonellosis 55 0.033
915
CRT017 Cartilage Disease 54 0.033
916
PRT038 Protein-Energy Malnutrition 54 0.033
917
SLP001 Sleeping Sickness 54 0.033
918
CLL003 Cellulitis 54 0.033
919
CRH005 Crohn's Colitis 53 0.033
920
P PTS002 Ptosis 53 0.033
921
LYS002 Lysosomal Storage Disease 52 0.033
922
c VRL010 Viral Hepatitis 52 0.033
923
DYS015 Dysentery 52 0.033
924
c HYP602 Hyperoxaluria, Primary, Type Ii 51 0.033
925
SPN019 Spondylolisthesis 51 0.033
926
HYP789 Hypophosphatemic Rickets with Hypercalciuria, Hereditary 51 0.033
927
LRN003 Learning Disability 49 0.033
928
QDR001 Quadriplegia 48 0.033
929
HYP043 Hyperandrogenism 48 0.033
930
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.033
931
FBR009 Fibrous Dysplasia 48 0.033
932
PLC007 Placental Abruption 48 0.033
933
SXL003 Sexual Disorder 47 0.033
934
PRD004 Prediabetes Syndrome 47 0.033
935
NDL007 Nodular Goiter 47 0.033
936
RTC005 Reticulosarcoma 47 0.033
937
P HRT035 Heart Block, Congenital 46 0.033
938
P BRB001 Beriberi 46 0.033
939
ATN004 Autonomic Neuropathy 45 0.033
940
URT014 Ureterolithiasis 44 0.033
941
CHN010 Chondroma 43 0.033
942
BNM001 Bone Marrow Cancer 43 0.033
943
c SRC023 Sarcoidosis 2 43 0.033
944
P MJR007 Major Affective Disorder 1 43 0.033
945
P AVS003 Avascular Necrosis 42 0.033
946
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.033
947
AMN006 Aminoaciduria 38 0.033
948
c CHR098 Chronic Pyelonephritis 38 0.033
949
END028 Endemic Goiter 37 0.033
950
BCL014 B-Cell Growth Factor 35 0.033
951
PYR009 Pyridoxine Deficiency Anemia 34 0.033
952
c CHR064 Chronic Monocytic Leukemia 33 0.033
953
c ATM068 Autoimmune Hypoparathyroidism 32 0.033
954
DNT010 Dentin Caries 32 0.033
955
CLN002 Colon Mucinous Adenocarcinoma 28 0.033
956
MST020 Mast Cell Activation Syndrome 26 0.033
957
HML018 Homologous Wasting Disease 22 0.033
958
P ATX030 Ataxia-Telangiectasia 82 0.031
959
KPS004 Kaposi Sarcoma 75 0.031
960
PHN003 Phenylketonuria 75 0.031
961
c ART115 Aortic Valve Disease 1 75 0.031
962
OTT002 Otitis Media 72 0.031
963
MLT157 Multiple System Atrophy 1 70 0.031
964
P OCL013 Oculodentodigital Dysplasia 69 0.031
965
c NMN015 Niemann-Pick Disease, Type C1 68 0.031
966
P NSP012 Nasopharyngeal Carcinoma 66 0.031
967
MSM014 Mismatch Repair Cancer Syndrome 65 0.031
968
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.031
969
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.031
970
INT002 Intermittent Claudication 61 0.031
971
P HMN010 Hemangioma 61 0.031
972
TRG002 Trigeminal Neuralgia 60 0.031
973
P WLF004 Wolfram Syndrome 60 0.031
974
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.031
975
DRR014 Darier-White Disease 60 0.031
976
P CNT004 Centronuclear Myopathy 59 0.031
977
P DNG005 Dengue Virus 59 0.031
978
c SPN301 Spinocerebellar Ataxia 2 58 0.031
979
PST028 Post-Traumatic Stress Disorder 58 0.031
980
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.031
981
BRN056 Bronchopulmonary Dysplasia 57 0.031
982
P PLY041 Polymyositis 57 0.031
983
P END033 Endocarditis 57 0.031
984
P FTL001 Fetal Alcohol Syndrome 57 0.031
985
P PLY018 Polycythemia 56 0.031
986
c ACT134 Acute Liver Failure 56 0.031
987
MTH009 Mouth Disease 56 0.031
988
INT030 Intracranial Aneurysm 56 0.031
989
P MYT023 Myotonia Congenita 56 0.031
990
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.031
991
VSC003 Visceral Leishmaniasis 55 0.031
992
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 0.031
993
MYM001 Myoma 54 0.031
994
NRT001 Neurotic Disorder 53 0.031
995
P MYP087 Myopathy, Tubular Aggregate, 1 53 0.031
996
CHR073 Choreatic Disease 52 0.031
997
SMT003 Somatostatinoma 52 0.031
998
c ACT135 Acute Graft Versus Host Disease 52 0.031
999
THR004 Thrombocytosis 51 0.031
1000
P SPP010 Suppressor of Tumorigenicity 3 51 0.031
1001
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.031
1002
RYS001 Reye Syndrome 51 0.031
1003
c HNT004 Huntington Disease-Like 2 50 0.031
1004
PST021 Postpartum Depression 50 0.031
1005
PLC008 Placenta Disease 50 0.031
1006
HYP068 Hyperostosis 48 0.031
1007
P FML362 Familial Isolated Hypoparathyroidism 47 0.031
1008
P CLL015 Collagen Disease 47 0.031
1009
c INH020 Inherited Metabolic Disorder 47 0.031
1010
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.031
1011
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.031
1012
P VTR007 Vitreoretinopathy 46 0.031
1013
SPN020 Spondylosis 46 0.031
1014
EXS001 Exostosis 46 0.031
1015
P MYC033 Myoclonus 46 0.031
1016
CNT017 Central Nervous System Origin Vertigo 45 0.031
1017
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.031
1018
DMP001 Dumping Syndrome 44 0.031
1019
SPN369 Spinal Disease 43 0.031
1020
PMP004 Pemphigus Foliaceus 43 0.031
1021
URM005 Uremic Pruritus 42 0.031
1022
MRP001 Morphine Dependence 41 0.031
1023
c ACT004 Acute Diarrhea 39 0.031
1024
SCR011 Scrapie 39 0.031
1025
HYP264 Hypertonia 38 0.031
1026
FRS012 First-Degree Atrioventricular Block 38 0.031
1027
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.031
1028
PRM329 Premature Aging 35 0.031
1029
CNC014 Cancer-Associated Retinopathy 34 0.031
1030
P BCL013 B-Cell Adult Acute Lymphocytic Leukemia 32 0.031
1031
P SPN202 Spinocerebellar Ataxia, X-Linked 1 32 0.031
1032
c CHR013 Chronic Apical Periodontitis 31 0.031
1033
BRN055 Bronchogenic Cyst 27 0.031
1034
ADG002 Audiogenic Seizures 25 0.031
1035
c HYP831 Hyperparathyroidism, Transient Neonatal 24 0.031
1036
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 20 0.031
1037
P LYN001 Lynch Syndrome 77 0.029
1038
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.029
1039
P ANG001 Angelman Syndrome 69 0.029
1040
P TMP003 Temporal Arteritis 68 0.029
1041
PSY004 Psychotic Disorder 67 0.029
1042
P MNN013 Meningitis 66 0.029
1043
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.029
1044
P CNJ013 Conjunctivitis 65 0.029
1045
KRT019 Keratitis, Hereditary 65 0.029
1046
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.029
1047
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.029
1048
P FRD001 Friedreich Ataxia 64 0.029
1049
INT146 Intervertebral Disc Disease 63 0.029
1050
c OPT053 Optic Atrophy 1 63 0.029
1051
HMT002 Hematologic Cancer 62 0.029
1052
c HPT003 Hepatitis a 62 0.029
1053
CRC021 Carcinosarcoma 62 0.029
1054
P PRP029 Porphyria 62 0.029
1055
P INT143 Interstitial Cystitis 61 0.029
1056
ALC006 Alcoholic Hepatitis 61 0.029
1057
HRP004 Herpes Zoster 60 0.029
1058
P PTN014 Patent Ductus Arteriosus 1 60 0.029
1059
PSD012 Pseudoachondroplasia 58 0.029
1060
P INT070 Intestinal Obstruction 58 0.029
1061
P MLT007 Multiple Epiphyseal Dysplasia 58 0.029
1062
ERY003 Erythema Multiforme 58 0.029
1063
DSS008 Disease of Mental Health 58 0.029
1064
MNR012 Meniere Disease 57 0.029
1065
HMT008 Hematuria, Benign Familial 56 0.029
1066
GNR004 Generalized Anxiety Disorder 56 0.029
1067
P PNM006 Pneumoconiosis 56 0.029
1068
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.029
1069
c BCT007 Bacterial Meningitis 55 0.029
1070
P ANT006 Antiphospholipid Syndrome 55 0.029
1071
ACT058 Active Peptic Ulcer Disease 55 0.029
1072
P DBT005 Diabetes Insipidus 55 0.029
1073
HMP005 Hemiplegia 55 0.029
1074
HRY003 Hairy Cell Leukemia 55 0.029
1075
c OST164 Osteoporosis, Juvenile 53 0.029
1076
c