Search results for calcium

2287 hits were found for calcium

# Family MCID Name MIFTS Score
1
c CHN022 Chondrocalcinosis 2 32 8.381
2
NPH091 Nephrolithiasis, Calcium Oxalate 51 6.009
3
FML307 Familial Calcium Pyrophosphate Deposition 27 5.168
4
IMM065 Immunodeficiency 10 27 5.091
5
IMM066 Immunodeficiency 9 23 5.091
6
NPH009 Nephrolithiasis 57 3.245
7
P CHN059 Chondrocalcinosis 47 3.012
8
c BLD126 Bleeding Disorder, Platelet-Type, 18 18 2.936
9
c AML006 Amelogenesis Imperfecta Hypoplastic Type, Ig 15 2.097
10
CMB055 Combined Immunodeficiency Due to Crac Channel Dysfunction 15 2.076
11
NRN002 Neuronitis 43 0.333
12
c BLD140 Blood Group, I System 37 0.248
13
P CLR023 Colorectal Cancer 98 0.227
14
P INT068 Intestinal Disease 65 0.214
15
P ADN016 Adenocarcinoma 71 0.209
16
RCT017 Rectal Disease 38 0.206
17
CLN019 Colonic Disease 55 0.205
18
P OST002 Osteoporosis 75 0.200
19
END072 Endotheliitis 46 0.192
20
P HYP069 Hyperparathyroidism 58 0.183
21
P KDN018 Kidney Disease 69 0.171
22
P LKM002 Leukemia 75 0.158
23
P LYM118 Lymphoma 71 0.153
24
LYM019 Lymphosarcoma 58 0.144
25
c CHR089 Chronic Kidney Failure 72 0.144
26
LYM024 Lymphatic System Disease 45 0.144
27
P PNC044 Pancreatitis 64 0.142
28
P HYP726 Hypercalcemia, Infantile, 1 57 0.142
29
RCT020 Rectum Adenocarcinoma 25 0.142
30
CLN015 Colon Adenocarcinoma 53 0.141
31
ISC004 Ischemia 66 0.140
32
P BRS047 Breast Cancer 100 0.139
33
HYP025 Hyperphosphatemia 48 0.137
34
URN009 Urinary System Disease 58 0.134
35
P NRB001 Neuroblastoma 73 0.130
36
AGN016 Aging 65 0.128
37
P LYM026 Lymphoblastic Leukemia 66 0.127
38
BNF002 Bone Fracture 56 0.127
39
IMM136 Immune System Disease 57 0.125
40
P ACT074 Acute Lymphocytic Leukemia 61 0.123
41
P HYP024 Hypoparathyroidism 55 0.123
42
LYM067 Lymphoid Leukemia 43 0.123
43
c LKM062 Leukemia, Acute Lymphoblastic 64 0.122
44
P PRS040 Prostate Cancer 88 0.120
45
c PRM005 Primary Hyperparathyroidism 59 0.120
46
c HYP595 Hypertension, Essential 78 0.118
47
P HRT032 Heart Disease 80 0.117
48
RCK004 Rickets 63 0.117
49
VSC007 Vascular Disease 71 0.114
50
ADN018 Adenoma 63 0.113
51
P ALZ034 Alzheimer Disease 95 0.112
52
CLC006 Calcinosis 51 0.112
53
LMB002 Lambert-Eaton Myasthenic Syndrome 58 0.111
54
ACQ007 Acquired Immunodeficiency Syndrome 65 0.110
55
P ART022 Arthritis 77 0.108
56
P DBT009 Diabetes Mellitus 72 0.108
57
P CRN018 Coronary Artery Anomaly 69 0.107
58
P CRN300 Coronary Heart Disease 1 57 0.107
59
SCN001 Secondary Hyperparathyroidism of Renal Origin 40 0.107
60
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.107
61
PRS047 Prostatitis 59 0.106
62
SPS003 Spastic Diplegia 55 0.104
63
P HYP802 Hypocalcemia, Autosomal Dominant 1 64 0.104
64
END030 End Stage Renal Failure 59 0.104
65
P LNG032 Lung Cancer 99 0.103
66
ISC006 Ischemic Heart Disease 73 0.100
67
P ART021 Arteriosclerosis 62 0.100
68
ACT103 Acute Lymphoblastic Leukemia, Childhood 53 0.100
69
GST053 Gastric Cancer 84 0.099
70
GST050 Gastrointestinal System Disease 66 0.099
71
ART140 Arteries, Anomalies of 51 0.099
72
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.098
73
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.098
74
RCT018 Rectal Neoplasm 53 0.097
75
P FML068 Familial Hypocalciuric Hypercalcemia 49 0.097
76
P PNC035 Pancreatic Cancer 89 0.096
77
TTH006 Tooth Disease 54 0.096
78
P GLM045 Glioma 61 0.095
79
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.095
80
P HYP733 Hypercalciuria, Absorptive, 2 37 0.095
81
INS001 Insulinoma 66 0.092
82
P EPL164 Epilepsy 70 0.091
83
NPH003 Nephrocalcinosis 49 0.091
84
P HPT021 Hepatitis 75 0.090
85
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.089
86
PRT030 Parathyroid Gland Disease 50 0.089
87
SKN016 Skin Disease 68 0.088
88
PNC034 Pancreas Disease 59 0.088
89
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.088
90
P MYC007 Myocardial Infarction 81 0.087
91
LPD008 Lipid Metabolism Disorder 59 0.087
92
RTN023 Retinitis 52 0.087
93
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.086
94
HYP266 Hypoxia 61 0.086
95
P THY032 Thyroiditis 56 0.086
96
SKN027 Skin Conditions 48 0.086
97
CRB009 Cerebritis 41 0.086
98
P MLG056 Malignant Hyperthermia 60 0.085
99
ESP023 Esophageal Disease 58 0.085
100
STM006 Stomach Disease 52 0.085
101
ESP021 Esophageal Cancer 79 0.083
102
ANG054 Angina Pectoris 53 0.083
103
P RHM011 Rheumatoid Arthritis 91 0.082
104
P INF032 Infertility 59 0.081
105
P PSD015 Pseudohypoparathyroidism 50 0.081
106
FXF002 Fox-Fordyce Disease 40 0.081
107
GNG013 Gingivitis 64 0.080
108
BRR014 Barrett Esophagus 64 0.080
109
CLR108 Colorectal Adenoma 60 0.080
110
P ART106 Arterial Calcification, Generalized, of Infancy, 1 36 0.078
111
P SCH015 Schizophrenia 71 0.077
112
P ATR011 Atrial Fibrillation 68 0.077
113
DNT012 Dental Caries 50 0.077
114
P ART023 Arthropathy 68 0.076
115
MGR028 Migraine with or Without Aura 1 55 0.076
116
CYS001 Cystic Fibrosis 85 0.075
117
c PRC016 Pre-Eclampsia 65 0.075
118
PNC033 Pancreas Adenocarcinoma 63 0.075
119
GST040 Gastric Adenocarcinoma 60 0.075
120
GND003 Gonadal Disease 32 0.075
121
P PNM007 Pneumonia 70 0.073
122
HYP060 Hyperinsulinism 56 0.073
123
RTC009 Reticulum Cell Sarcoma 51 0.073
124
RTC005 Reticulosarcoma 49 0.073
125
P HMP006 Hemiplegic Migraine 49 0.073
126
INT038 Interdigitating Dendritic Cell Sarcoma 46 0.073
127
GLC008 Glucose Metabolism Disease 38 0.073
128
PHS001 Phosphorus Metabolism Disease 34 0.073
129
P LVR013 Liver Disease 76 0.072
130
BRK010 Burkitt Lymphoma 71 0.072
131
LNG099 Lung Disease 67 0.072
132
ATM095 Autoimmune Disease 66 0.072
133
P NRP001 Neuropathy 63 0.072
134
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.072
135
P ECL001 Eclampsia 57 0.072
136
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.072
137
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.072
138
c SML038 Small Cell Cancer of the Lung 67 0.070
139
BRS051 Breast Disease 67 0.070
140
CNN005 Connective Tissue Disease 65 0.070
141
P DRR001 Diarrhea 60 0.070
142
LYM040 Lymphoblastic Lymphoma 58 0.070
143
P PRD008 Periodontitis 67 0.069
144
PLC008 Placenta Disease 48 0.069
145
MYC005 Myocardial Stunning 47 0.069
146
RHM027 Rheumatic Disease 62 0.068
147
HMT018 Hematopoietic Stem Cell Transplantation 58 0.068
148
IDP073 Idiopathic Hypercalciuria 46 0.068
149
OST097 Osteoporotic Fracture 41 0.068
150
c CTR119 Cataract 32, Multiple Types 32 0.068
151
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.066
152
SQM006 Squamous Cell Carcinoma 74 0.066
153
CNG034 Congestive Heart Failure 74 0.066
154
P MSC005 Muscular Dystrophy 66 0.066
155
JNT002 Joint Disorders 60 0.066
156
P LTR001 Lateral Sclerosis 58 0.066
157
CLC001 Calciphylaxis 53 0.066
158
RNL011 Renal Osteodystrophy 49 0.066
159
P MLT020 Multiple Sclerosis 85 0.065
160
AST005 Asthma 83 0.065
161
SRC014 Sarcoma 68 0.065
162
DFF005 Diffuse Large B-Cell Lymphoma 64 0.065
163
MTH009 Mouth Disease 64 0.065
164
THR024 Thrombosis 61 0.065
165
ANR040 Aneurysm 61 0.065
166
BNC003 Bone Cancer 59 0.065
167
P OVR049 Ovarian Disease 58 0.065
168
P CLL015 Collagen Disease 53 0.065
169
c FML023 Familial Hemiplegic Migraine 51 0.065
170
ENT004 Enthesopathy 38 0.065
171
MLN008 Melanoma 72 0.063
172
P BCL006 B-Cell Lymphomas 70 0.063
173
MCS002 Mucositis 61 0.063
174
P ATS308 Autosomal Dominant Cerebellar Ataxia 47 0.063
175
MYL069 Myeloma, Multiple 86 0.061
176
P OVR042 Ovarian Cancer 82 0.061
177
GLB002 Glioblastoma 74 0.061
178
P MYL006 Myeloid Leukemia 69 0.061
179
VRL011 Viral Infectious Disease 64 0.061
180
PRS042 Prostate Disease 56 0.061
181
MCN001 Mucinous Adenocarcinoma 54 0.061
182
CYS014 Cystadenocarcinoma 51 0.061
183
ESP025 Esophagus Adenocarcinoma 42 0.061
184
ENM002 Enamel Erosion 28 0.061
185
P HPT023 Hepatocellular Carcinoma 94 0.060
186
LYM133 Lymphoma, Hodgkin, Classic 78 0.060
187
P MYP004 Myopathy 69 0.060
188
DMN002 Dementia 68 0.060
189
CRD119 Cardiac Arrest 63 0.060
190
P EXN002 Exanthem 62 0.060
191
GT001 Gout 60 0.060
192
ALL026 Allergic Hypersensitivity Disease 59 0.060
193
P ENC018 Encephalopathy 58 0.060
194
GNG012 Gingival Overgrowth 52 0.060
195
BCL008 B-Cell Childhood Acute Lymphoblastic Leukemia 30 0.060
196
P DLT002 Dilated Cardiomyopathy 76 0.058
197
PRT037 Pertussis 70 0.058
198
CRB039 Cerebrovascular Disease 68 0.058
199
P AST007 Astrocytoma 66 0.058
200
P PSR002 Psoriasis 65 0.058
201
WVR001 Weaver Syndrome 61 0.058
202
P BPL003 Bipolar Disorder 61 0.058
203
P HYP370 Hypokalemic Periodic Paralysis, Type 1 59 0.058
204
SFT003 Soft Tissue Sarcoma 58 0.058
205
PNM001 Pneumocystosis 55 0.058
206
TXC002 Toxic Encephalopathy 55 0.058
207
OST011 Osteomalacia 52 0.058
208
PLS025 Plasmablastic Lymphoma 51 0.058
209
c MLG074 Malignant Mesenchymoma 51 0.058
210
RTR008 Root Resorption 44 0.058
211
P PRC031 Preeclampsia/eclampsia 1 41 0.058
212
DNT014 Dental Pulp Disease 39 0.058
213
LYM048 Lymphoma, Large-Cell, Immunoblastic 31 0.058
214
HMN044 Human Immunodeficiency Virus Type 1 71 0.056
215
GST045 Gastroenteritis 65 0.056
216
P HYP061 Hypertrophic Cardiomyopathy 65 0.056
217
PRD007 Periodontal Disease 64 0.056
218
MNT002 Mental Depression 60 0.056
219
NRM005 Neuromuscular Disease 60 0.056
220
HRY003 Hairy Cell Leukemia 60 0.056
221
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.056
222
CNS004 Constipation 57 0.056
223
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 54 0.056
224
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.056
225
P INF037 Inflammatory Bowel Disease 52 0.056
226
PRT029 Parathyroid Adenoma 50 0.056
227
ANX004 Anoxia 49 0.056
228
GST030 Gastrinoma 44 0.056
229
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 36 0.056
230
c CRN243 Carney Complex, Type 1 35 0.056
231
OST012 Osteoarthritis 88 0.055
232
c LKM063 Leukemia, Chronic Myeloid 80 0.055
233
P NRV007 Nervous System Disease 75 0.055
234
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.055
235
CHL065 Cholangiocarcinoma 70 0.055
236
PRT036 Peritonitis 67 0.055
237
HYP066 Hyperglycemia 64 0.055
238
c ADL017 Adult T-Cell Leukemia 63 0.055
239
PTT009 Pituitary Gland Disease 56 0.055
240
P MYP006 Myopia 56 0.055
241
P PRM002 Primary Hyperoxaluria 53 0.055
242
URM002 Uremia 52 0.055
243
P TCL004 T-Cell Leukemia 50 0.055
244
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.055
245
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.055
246
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.055
247
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.055
248
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.055
249
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.055
250
BRN080 Brain Ischemia 45 0.055
251
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.055
252
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.055
253
MLG086 Malignant Hyperthermia Susceptibility 38 0.055
254
GST012 Gastroesophageal Junction Adenocarcinoma 36 0.055
255
P RNG031 Ring Chromosome Y Syndrome 29 0.055
256
HDG004 Hodgkin's Granuloma 28 0.055
257
HDG006 Hodgkin's Paragranuloma 21 0.055
258
TCL018 T-Cell Childhood Acute Lymphocytic Leukemia 20 0.055
259
CRH001 Crohn's Disease 80 0.053
260
MNT001 Mantle Cell Lymphoma 76 0.053
261
c LKM071 Leukemia, Chronic Lymphocytic 75 0.053
262
OST159 Osteogenic Sarcoma 70 0.053
263
c ACT075 Acute Myocardial Infarction 64 0.053
264
P CTR002 Cataract 60 0.053
265
GLC003 Glucose Intolerance 58 0.053
266
BRN071 Brain Injury 54 0.053
267
P CRD132 Cardiac Conduction Defect 53 0.053
268
CRD223 Cardiac Arrhythmia 52 0.053
269
TMR011 Tumoral Calcinosis, Hyperphosphatemic, Familial 50 0.053
270
GNG011 Gingival Disease 50 0.053
271
EWN002 Ewing's Family of Tumors 49 0.053
272
c LKM004 Leukemia, B-Cell, Chronic 37 0.053
273
P CNN004 Connective Tissue Cancer 35 0.053
274
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 28 0.053
275
ETH012 Ethylene Glycol Poisoning 21 0.053
276
RCT006 Rectum Mucinous Adenocarcinoma 6 0.053
277
LVR012 Liver Cirrhosis 73 0.051
278
P ATS364 Autism 70 0.051
279
P LPS004 Lupus Erythematosus 69 0.051
280
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.051
281
PRT010 Parathyroid Carcinoma 64 0.051
282
RSP006 Respiratory System Disease 63 0.051
283
NRV006 Nervous System Cancer 61 0.051
284
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 61 0.051
285
P PLY014 Polycystic Kidney Disease 60 0.051
286
P ANP001 Anaplastic Large Cell Lymphoma 60 0.051
287
NRT004 Neuritis 55 0.051
288
P TRC086 Trichohepatoenteric Syndrome 1 54 0.051
289
MSC033 Muscle Disorders 53 0.051
290
DDN006 Duodenitis 46 0.051
291
HYP017 Hypophosphatemia 45 0.051
292
LYM049 Lymphoma, Small Cleaved-Cell, Diffuse 36 0.051
293
CLN002 Colon Mucinous Adenocarcinoma 31 0.051
294
SML025 Small Non-Cleaved Cell Lymphoma 25 0.051
295
LRG015 Large Intestine Adenoma 16 0.051
296
RCT013 Rectum Signet Ring Adenocarcinoma 8 0.051
297
INS024 Insulin-Like Growth Factor I 83 0.049
298
c LKM061 Leukemia, Acute Myeloid 81 0.049
299
P PLM037 Pulmonary Hypertension 79 0.049
300
MRF001 Marfan Syndrome 75 0.049
301
ANX010 Anxiety 72 0.049
302
ART016 Aortic Aneurysm 70 0.049
303
c CNT035 Central Nervous System Disease 65 0.049
304
c ART101 Aortic Valve Disease 2 65 0.049
305
OVR029 Ovarian Hyperstimulation Syndrome 64 0.049
306
P LNG028 Long Qt Syndrome 63 0.049
307
TRN015 Transient Cerebral Ischemia 58 0.049
308
P EPS003 Episodic Ataxia 57 0.049
309
P HYP076 Hyperthyroidism 56 0.049
310
BLR006 Biliary Tract Disease 55 0.049
311
CRN030 Coronary Stenosis 52 0.049
312
PLP001 Pulpitis 50 0.049
313
P BLD051 Blood Coagulation Disease 38 0.049
314
BNS001 Bone Osteosarcoma 38 0.049
315
c TRC078 Trichohepatoenteric Syndrome 2 34 0.049
316
ACT118 Acute Non Lymphoblastic Leukemia 32 0.049
317
CRY024 Crystal Arthropathies 26 0.049
318
c SYS001 Systemic Lupus Erythematosus 86 0.047
319
STR067 Stroke, Ischemic 84 0.047
320
P HYP607 Hypercholesterolemia, Familial 81 0.047
321
P FLL037 Follicular Lymphoma 76 0.047
322
MYL009 Myelodysplastic Syndrome 75 0.047
323
P GRF003 Graft-Versus-Host Disease 72 0.047
324
BRN028 Brain Cancer 72 0.047
325
c JVN010 Juvenile Rheumatoid Arthritis 71 0.047
326
ACR007 Acromegaly 70 0.047
327
SPN186 Spinal Cord Injury 67 0.047
328
ACR006 Aceruloplasminemia 65 0.047
329
P THR014 Thrombocytopenia 65 0.047
330
MYL031 Myeloproliferative Neoplasm 64 0.047
331
OST017 Osteomyelitis 64 0.047
332
GST092 Gastroesophageal Reflux 64 0.047
333
P HMR003 Hemorrhagic Disease 61 0.047
334
c THR092 Thrombophilia Due to Thrombin Defect 61 0.047
335
c OVR114 Ovarian Cancer 1 54 0.047
336
PRP019 Peripheral Nervous System Disease 53 0.047
337
PLS009 Plasma Cell Neoplasm 51 0.047
338
MTB004 Metabolic Acidosis 49 0.047
339
P LCT002 Lactose Intolerance 48 0.047
340
STT004 Steatorrhea 41 0.047
341
PRP056 Porphyria, Acute Hepatic 41 0.047
342
HML018 Homologous Wasting Disease 18 0.047
343
P INF038 Influenza 77 0.045
344
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.045
345
P PLY011 Polycystic Ovary Syndrome 65 0.045
346
P GLL020 Gallbladder Disease 64 0.045
347
HYP020 Hyperprolactinemia 64 0.045
348
HMT002 Hematologic Cancer 64 0.045
349
HYP056 Hypoglycemia 62 0.045
350
PGT001 Paget's Disease of Bone 60 0.045
351
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.045
352
BRN106 Burns 57 0.045
353
P CNT005 Central Nervous System Lymphoma 57 0.045
354
BLR007 Biliary Tract Neoplasm 53 0.045
355
BLD036 Bile Duct Disease 52 0.045
356
P RNL007 Renal Tubular Acidosis 51 0.045
357
c PRM226 Primary Central Nervous System Lymphoma 51 0.045
358
CRB085 Cerebral Hemorrhage 47 0.045
359
NRR001 Neuroretinitis 46 0.045
360
PRD004 Prediabetes Syndrome 46 0.045
361
OST004 Osteitis Fibrosa 45 0.045
362
MRG013 Mirage Syndrome 44 0.045
363
ACT058 Active Peptic Ulcer Disease 43 0.045
364
c CHR579 Chiari Malformation Type Ii 42 0.045
365
TND005 Tendinitis 42 0.045
366
c HYP794 Hyperoxaluria, Primary, Type I 41 0.045
367
P CRB059 Cerebellar Degeneration 40 0.045
368
DNT007 Dentin Sensitivity 40 0.045
369
MSC004 Muscle Tissue Disease 39 0.045
370
c CTR122 Cataract 5, Multiple Types 38 0.045
371
VSC008 Vascular Hemostatic Disease 36 0.045
372
c LKM005 Leukemia, T-Cell, Chronic 25 0.045
373
P PHC003 Pheochromocytoma 72 0.042
374
PRP027 Peripheral Vascular Disease 71 0.042
375
BRC012 Brucellosis 71 0.042
376
c JVN004 Juvenile Myelomonocytic Leukemia 70 0.042
377
GLL018 Gallbladder Cancer 67 0.042
378
P KDN017 Kidney Cancer 66 0.042
379
P MCR115 Microvascular Complications of Diabetes 5 66 0.042
380
P ENC004 Encephalitis 66 0.042
381
P THL005 Thalassemia 65 0.042
382
P CHR285 Chronic Myelomonocytic Leukemia 63 0.042
383
CLT003 Colitis 63 0.042
384
P HYP086 Hypothyroidism 62 0.042
385
GTL001 Gitelman Syndrome 62 0.042
386
BLD034 Bile Duct Carcinoma 60 0.042
387
P GST049 Gastrointestinal System Cancer 60 0.042
388
DBT010 Diabetic Neuropathy 60 0.042
389
c ATR087 Atrial Standstill 1 59 0.042
390
NRN004 Neuroendocrine Tumor 58 0.042
391
HMR039 Hemorrhage, Intracerebral 57 0.042
392
ZLL002 Zollinger-Ellison Syndrome 57 0.042
393
RTN018 Retinal Disease 56 0.042
394
TRM010 Traumatic Brain Injury 54 0.042
395
SCK005 Sickle Cell Disease 54 0.042
396
c INF071 Inflammatory Bowel Disease 1 54 0.042
397
ILT001 Ileitis 52 0.042
398
PRM020 Premenstrual Tension 49 0.042
399
OST062 Osteoarthritis with Mild Chondrodysplasia 43 0.042
400
MYT011 Myotonia 41 0.042
401
P BRN120 Bronchus Cancer 39 0.042
402
c HYP752 Hypocalciuric Hypercalcemia, Familial, Type I 38 0.042
403
P GRM010 Germ Cells Tumors 37 0.042
404
MNG003 Mungan Syndrome 34 0.042
405
DNT006 Dental Pulp Necrosis 29 0.042
406
CRC034 Carcinoma Showing Thymus-Like Differentiation 24 0.042
407
NRL016 Neural Tube Defects 79 0.040
408
P BLD134 Bladder Cancer 78 0.040
409
MSC157 Muscular Dystrophy, Duchenne Type 74 0.040
410
c HPT016 Hepatitis B 68 0.040
411
P PSD087 Pseudoxanthoma Elasticum 67 0.040
412
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 67 0.040
413
P TXP001 Toxoplasmosis 65 0.040
414
P MYS005 Myositis 63 0.040
415
IRR002 Irritable Bowel Syndrome 63 0.040
416
MRB003 Morbid Obesity 61 0.040
417
P GLM007 Glomerulonephritis 61 0.040
418
P NTR004 Neutropenia 60 0.040
419
P NPH012 Nephrotic Syndrome 60 0.040
420
CCC001 Coccidioidomycosis 60 0.040
421
P SML001 Small Cell Carcinoma 58 0.040
422
MRG003 Marginal Zone B-Cell Lymphoma 56 0.040
423
P CHL002 Childhood Absence Epilepsy 56 0.040
424
THR004 Thrombocytosis 55 0.040
425
SPN041 Spinal Cord Disease 54 0.040
426
OVR063 Overnutrition 53 0.040
427
STM007 Stomatitis 52 0.040
428
CCC002 Coccidiosis 52 0.040
429
SPL004 Splenic Marginal Zone Lymphoma 52 0.040
430
P CHR345 Chronic Pain 52 0.040
431
HMS001 Hemosiderosis 50 0.040
432
CHR074 Choriocarcinoma 49 0.040
433
c ACT020 Acute T Cell Leukemia 48 0.040
434
c SPN309 Spinocerebellar Ataxia 6 48 0.040
435
BCK006 Back Pain 46 0.040
436
EPD070 Epidermoid Cysts 46 0.040
437
PRN037 Prinzmetal's Variant Angina 44 0.040
438
PHC013 Phaeochromocytoma 44 0.040
439
PRT035 Peritoneum Cancer 42 0.040
440
NDL020 Nodal Marginal Zone B-Cell Lymphoma 38 0.040
441
c PLY105 Polycystic Ovary Syndrome 1 30 0.040
442
P MYL005 Myelofibrosis 75 0.037
443
SCK003 Sickle Cell Anemia 73 0.037
444
P END044 Endometriosis 71 0.037
445
CMM004 Common Variable Immunodeficiency 71 0.037
446
P AMY004 Amyloidosis 69 0.037
447
GLB015 Glioblastoma Multiforme 68 0.037
448
c MLG068 Malignant Glioma 66 0.037
449
P ESP024 Esophagitis 64 0.037
450
WLL001 Williams-Beuren Syndrome 63 0.037
451
P RHN004 Rhinitis 62 0.037
452
c ACT027 Acute Pancreatitis 61 0.037
453
VSC002 Vascular Dementia 58 0.037
454
DMY004 Demyelinating Disease 58 0.037
455
c ACT135 Acute Graft Versus Host Disease 57 0.037
456
P PTT006 Pituitary Adenoma 57 0.037
457
P CTN015 Cutaneous T Cell Lymphoma 56 0.037
458
P UTR058 Uterine Anomalies 55 0.037
459
c MCR113 Microvascular Complications of Diabetes 3 55 0.037
460
P PMP001 Pemphigus 55 0.037
461
INT007 Intermediate Coronary Syndrome 55 0.037
462
TST014 Testicular Cancer 54 0.037
463
P TRM003 Tremor 54 0.037
464
c VSC019 Vesicoureteral Reflux 1 54 0.037
465
P VNS003 Venous Insufficiency 53 0.037
466
HYP005 Hypokalemia 53 0.037
467
P DDN001 Duodenal Ulcer 53 0.037
468
P OVR046 Ovarian Cyst 52 0.037
469
INN002 Inner Ear Disease 52 0.037
470
THY030 Thyroid Gland Disease 51 0.037
471
P CRV039 Cervicitis 49 0.037
472
c PRD040 Periodontitis, Chronic 49 0.037
473
P GNT008 Giant Cell Tumor 49 0.037
474
HYP789 Hypophosphatemic Rickets with Hypercalciuria, Hereditary 49 0.037
475
GRN017 Granulocytopenia 49 0.037
476
c BRN108 Branchiootic Syndrome 1 47 0.037
477
c CHR431 Chronic Venous Insufficiency 47 0.037
478
P ATX024 Ataxia-Oculomotor Apraxia 3 47 0.037
479
HRT007 Heart Cancer 46 0.037
480
THR035 Thrombasthenia 46 0.037
481
ANG046 Angioimmunoblastic T-Cell Lymphoma 46 0.037
482
HRT012 Heart Valve Disease 45 0.037
483
VST004 Vestibular Disease 45 0.037
484
MYL004 Myelodysplastic Myeloproliferative Cancer 45 0.037
485
SYS003 Systolic Heart Failure 44 0.037
486
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 44 0.037
487
TST015 Testicular Disease 43 0.037
488
SPN369 Spinal Disease 42 0.037
489
GLC086 Glucocorticoid-Induced Osteoporosis 42 0.037
490
RST023 Resting Heart Rate, Variation in 42 0.037
491
c MCR130 Microvascular Complications of Diabetes 6 42 0.037
492
P LBY004 Labyrinthitis 41 0.037
493
c HYP753 Hypocalciuric Hypercalcemia, Familial, Type Ii 38 0.037
494
c HYP311 Hyperparathyroidism 3 37 0.037
495
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.037
496
c MCR120 Microvascular Complications of Diabetes 7 34 0.037
497
c MCR133 Microvascular Complications of Diabetes 4 32 0.037
498
P SCL057 Scoliosis, Isolated 1 28 0.037
499
MNS002 Mini Stroke 23 0.037
500
RFR001 Refractory Plasma Cell Neoplasm 19 0.037
501
MYC006 Mycosis Fungoides 73 0.035
502
c HPT073 Hepatitis C Virus 73 0.035
503
c HPT001 Hepatitis C 73 0.035
504
P ESS003 Essential Thrombocythemia 71 0.035
505
DWN001 Down Syndrome 70 0.035
506
P DBT085 Diabetes Mellitus, Insulin-Dependent 69 0.035
507
P MYC084 Mycobacterium Tuberculosis 1 69 0.035
508
PNC041 Pancreatic Ductal Adenocarcinoma 67 0.035
509
P SYS005 Systemic Scleroderma 67 0.035
510
BRT054 Brittle Bone Disorder 67 0.035
511
VSC011 Vasculitis 66 0.035
512
P SLP006 Sleep Apnea 65 0.035
513
MDD011 Mood Disorder 64 0.035
514
c HPT003 Hepatitis a 63 0.035
515
OST003 Osteonecrosis 63 0.035
516
LWC002 Lowe Oculocerebrorenal Syndrome 62 0.035
517
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 62 0.035
518
PLM033 Pulmonary Embolism 62 0.035
519
P CMR001 Camurati-Engelmann Disease 62 0.035
520
P GRV001 Graves' Disease 62 0.035
521
FTT001 Fatty Liver Disease 62 0.035
522
P BRG001 Brugada Syndrome 61 0.035
523
c ACT073 Acute Leukemia 61 0.035
524
HRP004 Herpes Zoster 61 0.035
525
c SCL052 Scleroderma, Familial Progressive 60 0.035
526
CHL068 Cholestasis 60 0.035
527
PLS011 Plasmacytoma 60 0.035
528
SLP005 Sleep Disorder 59 0.035
529
SZR001 Sezary's Disease 58 0.035
530
CRT016 Carotid Artery Disease 58 0.035
531
P ALP008 Alopecia 56 0.035
532
c MYT020 Myotonic Dystrophy 2 56 0.035
533
MYM001 Myoma 56 0.035
534
P DNT020 Dent Disease 1 55 0.035
535
HDC001 Headache 55 0.035
536
AMN001 Amenorrhea 55 0.035
537
P SZR006 Seizure Disorder 55 0.035
538
P FNC004 Fanconi Syndrome 54 0.035
539
P DBT005 Diabetes Insipidus 54 0.035
540
ISL001 Islet Cell Tumor 54 0.035
541
c ACT071 Acute Kidney Failure 54 0.035
542
PRP080 Peripheral Artery Disease 54 0.035
543
CLR109 Colorectal Adenocarcinoma 54 0.035
544
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.035
545
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 53 0.035
546
THR016 Thrombophlebitis 53 0.035
547
c PNS012 Paine Syndrome 52 0.035
548
GRW007 Growth Hormone Deficiency 52 0.035
549
CRT013 Carotid Stenosis 52 0.035
550
ACN001 Acinar Cell Carcinoma 52 0.035
551
c BNG091 Benign Chronic Pemphigus 52 0.035
552
PRL017 Prolymphocytic Leukemia 51 0.035
553
CHN070 Cohen-Gibson Syndrome 51 0.035
554
P NGH001 Night Blindness 51 0.035
555
CHL061 Childhood Leukemia 50 0.035
556
PTT037 Pituitary Tumors 49 0.035
557
PLM017 Pulmonary Alveolar Microlithiasis 48 0.035
558
P RNV001 Renovascular Hypertension 48 0.035
559
DBT008 Diabetic Angiopathy 48 0.035
560
P HYP058 Hypervitaminosis a 48 0.035
561
VND001 Vein Disease 48 0.035
562
HDN002 Head Injury 48 0.035
563
DST006 Diastolic Heart Failure 47 0.035
564
VTM027 Vitamin D-Dependent Rickets, Type 2a 46 0.035
565
c MTR002 Mitral Valve Insufficiency 46 0.035
566
CRD137 Cardiogenic Shock 45 0.035
567
P HRT035 Heart Block, Congenital 45 0.035
568
EXC002 Exocrine Pancreatic Insufficiency 45 0.035
569
P TST026 Testicular Germ Cell Cancer 44 0.035
570
BRS064 Bursitis 42 0.035
571
P RNL045 Renal Tubular Acidosis, Distal 42 0.035
572
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.035
573
PNG002 Pain Agnosia 41 0.035
574
P CHR084 Chromosomal Disease 40 0.035
575
P HYP265 Hypotonia 40 0.035
576
PPT001 Peptic Esophagitis 40 0.035
577
P HYP599 Hypoparathyroidism, Familial Isolated 39 0.035
578
HYP776 Hyperparathyroidism, Neonatal Severe 39 0.035
579
P VSC018 Visceral Steatosis 38 0.035
580
CLC004 Calcific Tendinitis 38 0.035
581
c HYP602 Hyperoxaluria, Primary, Type Ii 37 0.035
582
PNC015 Pancreatic Acinar Cell Adenocarcinoma 35 0.035
583
PRN032 Paraneoplastic Cerebellar Degeneration 33 0.035
584
MNT310 Mental Retardation, X-Linked, Syndromic, Snyder-Robinson Type 32 0.035
585
BNG018 Benign Paroxysmal Positional Nystagmus 32 0.035
586
P VRT013 Vertigo, Benign Recurrent 31 0.035
587
ENM001 Enamel Caries 30 0.035
588
IDP085 Idiopathic Infantile Hypercalcemia 26 0.035
589
ACN026 Acinar Cell Carcinoma of Pancreas 25 0.035
590
MLR004 Malaria 86 0.032
591
P RTT002 Rett Syndrome 82 0.032
592
P MDL005 Medulloblastoma 76 0.032
593
P WSK001 Wiskott-Aldrich Syndrome 76 0.032
594
PLY001 Polycythemia Vera 75 0.032
595
PHN003 Phenylketonuria 73 0.032
596
MLD001 Melioidosis 73 0.032
597
PLM001 Pulmonary Tuberculosis 72 0.032
598
PSY004 Psychotic Disorder 72 0.032
599
THY028 Thyroid Cancer 72 0.032
600
LSH001 Leishmaniasis 71 0.032
601
P LYN001 Lynch Syndrome 71 0.032
602
c HMC039 Hemochromatosis, Type 1 71 0.032
603
P MNN013 Meningitis 71 0.032
604
P RSP003 Respiratory Failure 71 0.032
605
CNN003 Conn's Syndrome 70 0.032
606
P TST021 Testicular Germ Cell Tumor 70 0.032
607
c BTT014 Beta-Thalassemia 70 0.032
608
CRB037 Cerebral Palsy 70 0.032
609
P MJR001 Major Depressive Disorder 70 0.032
610
c MNN043 Meningioma, Familial 69 0.032
611
ALL003 Allergic Rhinitis 68 0.032
612
P ANR048 Aniridia 1 68 0.032
613
c ATS007 Autism Spectrum Disorder 68 0.032
614
APN008 Apnea, Obstructive Sleep 67 0.032
615
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.032
616
P CNJ013 Conjunctivitis 67 0.032
617
DRM006 Dermatitis 67 0.032
618
GLN010 Glanzmann Thrombasthenia 66 0.032
619
P WLD002 Waldenstrom Macroglobulinemia 65 0.032
620
VRC005 Varicose Veins 64 0.032
621
CRP001 Carpal Tunnel Syndrome 64 0.032
622
P SRC025 Sarcoidosis 1 63 0.032
623
P SNS014 Sinusitis 62 0.032
624
ALC006 Alcoholic Hepatitis 62 0.032
625
P GLY013 Glycogen Storage Disease 61 0.032
626
GLS001 Gliosarcoma 61 0.032
627
c PNC108 Pancreatitis, Hereditary 60 0.032
628
STT001 Status Epilepticus 60 0.032
629
P PLY018 Polycythemia 60 0.032
630
ERY003 Erythema Multiforme 60 0.032
631
DBT062 Diabetic Foot Ulcers 59 0.032
632
URT039 Urticaria 59 0.032
633
RLP002 Relapsing-Remitting Multiple Sclerosis 59 0.032
634
P INT030 Intracranial Aneurysm 58 0.032
635
P PLY019 Polyneuropathy 58 0.032
636
P MYC008 Myocarditis 58 0.032
637
P EPL140 Epilepsy, Idiopathic Generalized 58 0.032
638
ART017 Aortic Disease 57 0.032
639
GST023 Gastric Ulcer 57 0.032
640
P ANG015 Angioedema 57 0.032
641
c PRG042 Progressive Familial Heart Block, Type Ia 57 0.032
642
PLM010 Pulmonary Edema 57 0.032
643
P LRY019 Laryngitis 57 0.032
644
NNL002 Nonalcoholic Steatohepatitis 56 0.032
645
P SCL018 Scoliosis 56 0.032
646
P CNG010 Congenital Stationary Night Blindness 56 0.032
647
PRN019 Perinatal Necrotizing Enterocolitis 56 0.032
648
P RTN016 Retinal Degeneration 56 0.032
649
GNT002 Giant Cell Glioblastoma 56 0.032
650
P SPN301 Spinocerebellar Ataxia 2 56 0.032
651
PLG002 Plague 55 0.032
652
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.032
653
P HYP750 Hypertriglyceridemia, Familial 55 0.032
654
P PRM006 Primary Biliary Cirrhosis 55 0.032
655
PST021 Postpartum Depression 54 0.032
656
IMP005 Impotence 54 0.032
657
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 54 0.032
658
SMT003 Somatostatinoma 54 0.032
659
c OST164 Osteoporosis, Juvenile 54 0.032
660
MCR004 Macroglobulinemia 54 0.032
661
P EPN002 Ependymoma 53 0.032
662
c SVR005 Severe Pre-Eclampsia 53 0.032
663
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 53 0.032
664
HMG005 Hemoglobinopathy 53 0.032
665
PRP016 Paraplegia 53 0.032
666
HLL004 Hellp Syndrome 53 0.032
667
c PRM012 Primary Polycythemia 53 0.032
668
c BLM008 Bulimia Nervosa 2 53 0.032
669
PST095 Post-Thrombotic Syndrome 52 0.032
670
ENT011 Enterocolitis 52 0.032
671
ATR057 Atrioventricular Block 52 0.032
672
P SML016 Small Intestine Cancer 52 0.032
673
ATN005 Autonomic Dysfunction 51 0.032
674
DRG003 Drug Dependence 51 0.032
675
KLD001 Keloids 50 0.032
676
P MYT002 Myotonic Dystrophy 50 0.032
677
PRT018 Portal Vein Thrombosis 50 0.032
678
LYM012 Lymphoplasmacytic Lymphoma 50 0.032
679
c BPL002 Bipolar I Disorder 50 0.032
680
SNS003 Sensory Peripheral Neuropathy 48 0.032
681
c BSL038 Basal Ganglia Calcification, Idiopathic, 1 47 0.032
682
PST011 Pustulosis of Palm and Sole 47 0.032
683
P RNL015 Renal Hypertension 46 0.032
684
HYP085 Hypothalamic Disease 46 0.032
685
BNN003 Bone Inflammation Disease 46 0.032
686
BLD053 Blood Platelet Disease 45 0.032
687
CLN044 Colon Adenoma 45 0.032
688
ESP027 Esophagus Squamous Cell Carcinoma 45 0.032
689
SML008 Small Intestine Lymphoma 45 0.032
690
SXL003 Sexual Disorder 45 0.032
691
SPR008 Supratentorial Primitive Neuroectodermal Tumor 44 0.032
692
DFF003 Diffuse Scleroderma 44 0.032
693
c CHR020 Chronic Interstitial Cystitis 44 0.032
694
KRT008 Keratopathy 44 0.032
695
HYP070 Hyperpituitarism 43 0.032
696
IDP070 Idiopathic Scoliosis 42 0.032
697
MNN017 Mononeuropathy 42 0.032
698
c HMC010 Hemochromatosis, Type 3 42 0.032
699
CRN019 Coronary Artery Vasospasm 42 0.032
700
SPS057 Spasticity 41 0.032
701
GNT050 Genitourinary Tract Anomalies 41 0.032
702
c HYP608 Hypocalciuric Hypercalcemia, Familial, Type Iii 37 0.032
703
LRG016 Large Intestine Adenocarcinoma 37 0.032
704
c HYP534 Hypomagnesemia 3, Renal 37 0.032
705
PGM003 Pigmentation Disease 36 0.032
706
OLC001 Olecranon Bursitis 35 0.032
707
c BLR024 Biliary Cirrhosis, Primary, 1 35 0.032
708
LKC003 Leukocyte Disease 34 0.032
709
HRW001 Hair Whorl 31 0.032
710
ENP001 Enophthalmos 29 0.032
711
CRN288 Corneal Dystrophy, Band-Shaped 29 0.032
712
BRN055 Bronchogenic Cyst 28 0.032
713
PRR001 Periarthritis 27 0.032
714
HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 27 0.032
715
EXT025 Extragonadal Germ Cell Cancer 25 0.032
716
LYM126 Lymphoma Aids Related 21 0.032
717
MXD001 Mixed Cerebral Palsy 20 0.032
718
P AST055 Asthma-Related Traits 1 18 0.032
719
ULC004 Ulcerative Colitis 80 0.028
720
c MCL042 Macular Degeneration, Age-Related, 1 79 0.028
721
P PRK057 Parkinson Disease, Late-Onset 78 0.028
722
P RTN024 Retinoblastoma 76 0.028
723
KWS002 Kawasaki Disease 72 0.028
724
P NSP012 Nasopharyngeal Carcinoma 71 0.028
725
P HRP006 Herpes Simplex 70 0.028
726
WRN001 Werner Syndrome 70 0.028
727
P TTR001 Tetralogy of Fallot 70 0.028
728
c WLM013 Wilms Tumor 1 69 0.028
729
c PRM196 Premature Ovarian Failure 1 68 0.028
730
P ADL010 Adult Respiratory Distress Syndrome 67 0.028
731
BRN024 Bronchitis 67 0.028
732
HSH003 Hashimoto Thyroiditis 67 0.028
733
LPD012 Lipoid Congenital Adrenal Hyperplasia 66 0.028
734
CTN007 Cutaneous Leishmaniasis 66 0.028
735
P CLC063 Celiac Disease 1 65 0.028
736
P DRM010 Dermatomyositis 65 0.028
737
MLT157 Multiple System Atrophy 1 65 0.028
738
TTN003 Tetanus 65 0.028
739
ART005 Arteriovenous Malformation 64 0.028
740
P ALP009 Alopecia Areata 64 0.028
741
CYS013 Cystinuria 64 0.028
742
MSC152 Muscular Dystrophy, Becker Type 64 0.028
743
KRT001 Keratoconjunctivitis Sicca 63 0.028
744
c ACT210 Acute Respiratory Distress Syndrome 63 0.028
745
CRN036 Craniopharyngioma 63 0.028
746
THY111 Thyroid Carcinoma, Familial Medullary 63 0.028
747
SKN019 Skin Melanoma 63 0.028
748
FLL027 Fallopian Tube Carcinoma 62 0.028
749
SYN007 Synovitis 61 0.028
750
ETN001 Eating Disorder 61 0.028
751
INT002 Intermittent Claudication 61 0.028
752
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.028
753
P HMP007 Hemophilia 61 0.028
754
P FBR017 Fibrosarcoma 61 0.028
755
P GST044 Gastritis 61 0.028
756
P RHB003 Rhabdomyosarcoma 61 0.028
757
P SPN052 Spondyloarthropathy 61 0.028
758
PRM042 Primary Effusion Lymphoma 61 0.028
759
PPT005 Peptic Ulcer Disease 60 0.028
760
P HST010 Histiocytosis 60 0.028
761
SPN027 Spinal Stenosis 60 0.028
762
c VRL010 Viral Hepatitis 59 0.028
763
PST028 Post-Traumatic Stress Disorder 59 0.028
764
c PCH015 Pachyonychia Congenita 1 59 0.028
765
P HYP724 Hyperlipoproteinemia, Type Iii 59 0.028
766
RHM001 Rheumatic Fever 59 0.028
767
c LYN004 Lynch Syndrome I 59 0.028
768
c BCT007 Bacterial Meningitis 59 0.028
769
CRC006 Carcinoid Syndrome 59 0.028
770
c ESS001 Essential Tremor 58 0.028
771
LMY002 Leiomyoma 58 0.028
772
BRN038 Bronchial Disease 58 0.028
773
P THR015 Thrombophilia 58 0.028
774
RSC001 Rosacea 58 0.028
775
P SJG008 Sjogren Syndrome 58 0.028
776
IMM158 Immune Suppression 57 0.028
777
P CYS018 Cystitis 57 0.028
778
ISL003 Isolated Growth Hormone Deficiency 57 0.028
779
CNT105 Central Core Disease of Muscle 57 0.028
780
NWB001 Newborn Respiratory Distress Syndrome 56 0.028
781
c ALM001 Al Amyloidosis 56 0.028
782
LYS002 Lysosomal Storage Disease 56 0.028
783
DCT002 Ductal Carcinoma in Situ 56 0.028
784
GRD007 Grade Iii Astrocytoma 56 0.028
785
DSS009 Disseminated Intravascular Coagulation 56 0.028
786
CRT049 Critical Limb Ischemia 56 0.028
787
P MSC003 Muscular Atrophy 55 0.028
788
RDC002 Radiculopathy 55 0.028
789
FDL002 Food Allergy 55 0.028
790
P MLT074 Multiple Endocrine Neoplasia 55 0.028
791
HMZ003 Homozygous Familial Hypercholesterolemia 54 0.028
792
ERY017 Erythema Elevatum Diutinum 54 0.028
793
c EPS035 Episodic Ataxia, Type 2 54 0.028
794
P THY054 Thyrotoxic Periodic Paralysis 54 0.028
795
ADR013 Adrenal Gland Hyperfunction 54 0.028
796
HYP080 Hypogonadism 54 0.028
797
GTR002 Goiter 53 0.028
798
P RTN022 Retinal Vein Occlusion 53 0.028
799
LPD009 Lipid Storage Disease 53 0.028
800
PRV004 Periventricular Leukomalacia 53 0.028
801
c PSD066 Pseudohypoparathyroidism, Type Ib 52 0.028
802
EXT010 Extramedullary Plasmacytoma 52 0.028
803
GLC036 Glucagonoma 52 0.028
804
LMB062 Limb Ischemia 52 0.028
805
TMT001 Timothy Syndrome 52 0.028
806
OST016 Osteochondrosis 52 0.028
807
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 52 0.028
808
P PRC019 Precocious Puberty 52 0.028
809
DRY001 Dry Eye Syndrome 51 0.028
810
MCL006 Macular Retinal Edema 51 0.028
811
MST002 Mast-Cell Leukemia 51 0.028
812
ADR012 Adrenal Gland Disease 51 0.028
813
NSD001 Nose Disease 51 0.028
814
CHL018 Childhood Medulloblastoma 51 0.028
815
CHR563 Chronic Eosinophilic Leukemia 51 0.028
816
P LCT001 Lactic Acidosis 51 0.028
817
P HMR005 Hemorrhoid 51 0.028
818
CHL004 Cholelithiasis 51 0.028
819
ORP003 Oropharynx Cancer 51 0.028
820
HYP043 Hyperandrogenism 50 0.028
821
c RTN162 Retinitis Pigmentosa 2 50 0.028
822
IDP024 Idiopathic Inflammatory Myopathy 49 0.028
823
c WLM018 Wilms Tumor 5 49 0.028
824
MTC069 Mitochondrial Disorders 49 0.028
825
LRG008 Large Granular Lymphocyte Leukemia 49 0.028
826
c MLG069 Malignant Hypertension 49 0.028
827
HYP741 Hyperparathyroidism 2 with Jaw Tumors 49 0.028
828
CHR286 Chronic Neutrophilic Leukemia 49 0.028
829
RYN001 Raynaud Disease 48 0.028
830
HYP457 Hypertrophic Scars 48 0.028
831
ART004 Aortic Atherosclerosis 48 0.028
832
TCL002 T-Cell Large Granular Lymphocyte Leukemia 48 0.028
833
P CLS010 Cluster Headache 47 0.028
834
DYS073 Dysphagia 47 0.028
835
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.028
836
CRN024 Corneal Disease 47 0.028
837
HYP082 Hypopharynx Cancer 47 0.028
838
P ART084 Arteriovenous Fistula 46 0.028
839
MLK006 Milk Allergy 46 0.028
840
LKM006 Leukomalacia 46 0.028
841
OVR094 Ovarian Epithelial Cancer 46 0.028
842
CRC014 Carcinoid Tumors, Intestinal 46 0.028
843
MCL027 Macular Dystrophy, Dominant Cystoid 45 0.028
844
DMP001 Dumping Syndrome 45 0.028
845
PST053 Postherpetic Neuralgia 44 0.028
846
BNG036 Bone Giant Cell Tumor 44 0.028
847
SQM023 Squamous Cell Carcinoma of the Oropharynx 44 0.028
848
DNT001 Dental Fluorosis 44 0.028
849
ACT088 Acute Insulin Response 43 0.028
850
LCR008 Lacrimal Apparatus Disease 43 0.028
851
URM005 Uremic Pruritus 43 0.028
852
P BRN035 Brain Stem Glioma 42 0.028
853
CWM001 Cow Milk Allergy 42 0.028
854
CLP006 Clopidogrel Resistance 42 0.028
855
OVR112 Ovarian Germ Cell Cancer 42 0.028
856
CRB086 Cerebral Aneurysms 42 0.028
857
c HYP057 Hypervitaminosis D 40 0.028
858
APP010 Appendix Cancer 40 0.028
859
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.028
860
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 39 0.028
861
SLT001 Solitary Osseous Plasmacytoma 39 0.028
862
DYS011 Dyskinesia of Esophagus 39 0.028
863
PNC053 Pancreatic Islet Cell Tumors 39 0.028
864
URT014 Ureterolithiasis 38 0.028
865
GLS018 Glass Syndrome 38 0.028
866
LRY017 Laryngeal Disease 38 0.028
867
DLT018 Dilution, Pigmentary 37 0.028
868
PYR016 Pyridoxine Deficiency 37 0.028
869
SXD001 Sex Differentiation Disease 37 0.028
870
URT020 Ureterocele 37 0.028
871
SWL001 Swallowing Disorders 36 0.028
872
PDT014 Pediatric Ependymoma 36 0.028
873
TTH007 Tooth Erosion 36 0.028
874
MSC012 Muscular Dystrophy, Duchenne and Becker Type 35 0.028
875
P BCL013 B-Cell Adult Acute Lymphocytic Leukemia 35 0.028
876
PRN039 Paraneoplastic Syndromes 35 0.028
877
RHM035 Rheumatic Fever-Related Antigen 34 0.028
878
ACR110 Acrodysostosis 1 with or Without Hormone Resistance 33 0.028
879
ANG066 Angel-Shaped Phalangoepiphyseal Dysplasia 33 0.028
880
c MGR032 Migraine, Familial Hemiplegic, 1 32 0.028
881
RFR002 Refractory Hairy Cell Leukemia 32 0.028
882
RNL001 Renal Artery Obstruction 31 0.028
883
P KLZ004 Kala-Azar 1 31 0.028
884
c HYP603 Hyperoxaluria, Primary, Type Iii 30 0.028
885
c ATM068 Autoimmune Hypoparathyroidism 30 0.028
886
ENC014 Enchondroma 30 0.028
887
URN022 Urinary Tract Infections, Recurrent 29 0.028
888
RSP007 Respiratory Distress Syndrome, Infant 28 0.028
889
c ANR047 Aniridia 2 28 0.028
890
P PRX010 Paroxysmal Ventricular Fibrillation 28 0.028
891
P STR035 Streptococcal Group a Invasive Disease 28 0.028
892
DNT010 Dentin Caries 27 0.028
893
HYP213 Hypomelanotic Disorder 25 0.028
894
FNC005 Functional Colonic Disease 24 0.028
895
ULC005 Ulcer of Lower Limbs 23 0.028
896
GLC025 Galactorrhoea-Hyperprolactinaemia 21 0.028
897
PNL011 Pineal Region Germinoma 20 0.028
898
HDG009 Hodgkin Lymphoma, Childhood 20 0.028
899
LYM053 Lymphomatous Thyroiditis 19 0.028
900
c HYP302 Hypomagnesemia 4, Renal 18 0.028
901
CLS052 Classic Hairy Cell Leukemia 16 0.028
902
SPR039 Supratentorial Primitive Neuroectodermal Tumors, Childhood 14 0.028
903
VSC009 Vascular Skin Disease 10 0.028
904
P RTN008 Retinitis Pigmentosa 81 0.024
905
GST019 Gastrointestinal Stromal Tumor 74 0.024
906
PLM134 Pulmonary Fibrosis, Idiopathic 73 0.024
907
P CRV035 Cervical Cancer 72 0.024
908
NRF026 Neurofibromatosis, Type Iv, of Riccardi 72 0.024
909
c MLT156 Multiple Endocrine Neoplasia, Type I 70 0.024
910
FRN006 Frontotemporal Dementia 70 0.024
911
CNT061 Conotruncal Heart Malformations 70 0.024
912
APR006 Apert Syndrome 69 0.024
913
P NRF023 Neurofibromatosis, Type Ii 69 0.024
914
c HMP029 Hemophilia a 69 0.024
915
P DRM053 Dermatitis, Atopic 68 0.024
916
P PLM036 Pulmonary Fibrosis 68 0.024
917
c MYT021 Myotonic Dystrophy 1 68 0.024
918
P NMN002 Niemann-Pick Disease 68 0.024
919
P CHR071 Charcot-Marie-Tooth Disease 67 0.024
920
P MCL013 Mucolipidosis Iv 67 0.024
921
OTT002 Otitis Media 67 0.024
922
P ATT013 Attention Deficit-Hyperactivity Disorder 67 0.024
923
c LCL006 Localized Scleroderma 66 0.024
924
P HYP098 Hypereosinophilic Syndrome 65 0.024
925
c CHR417 Chronic Graft Versus Host Disease 65 0.024
926
ALC007 Alcohol Dependence 65 0.024
927
CHL123 Chlamydia 64 0.024
928
VLC001 Velocardiofacial Syndrome 64 0.024
929
LNG108 Langerhans Cell Histiocytosis 63 0.024
930
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 63 0.024
931
P INT143 Interstitial Cystitis 63 0.024
932
P ALC004 Alcohol Abuse 63 0.024
933
GST033 Gestational Diabetes 62 0.024
934
P GCH001 Gaucher's Disease 62 0.024
935
P HML002 Hemolytic Anemia 62 0.024
936
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 62 0.024
937
PRP030 Purpura 61 0.024
938
P DYS154 Dystonia 61 0.024
939
P UVT001 Uveitis 61 0.024
940
P HMN010 Hemangioma 61 0.024
941
LMY014 Leiomyoma, Uterine 61 0.024
942
BRN056 Bronchopulmonary Dysplasia 61 0.024
943
PLM070 Pulmonic Stenosis 61 0.024
944
ALL006 Allergic Asthma 60 0.024
945
LYS012 Lysosomal Acid Lipase Deficiency 60 0.024
946
TRG002 Trigeminal Neuralgia 60 0.024
947
P HMR012 Hemorrhagic Fever 60 0.024
948
c MCP004 Mucopolysaccharidosis Iv 60 0.024
949
ATH013 Atherosclerosis Susceptibility 59 0.024
950
P ORL007 Oral Cavity Cancer 59 0.024
951
P PRT013 Portal Hypertension 59 0.024
952
P ANT006 Antiphospholipid Syndrome 59 0.024
953
c HRD002 Hereditary Angioedema 59 0.024
954
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 59 0.024
955
TRD006 Tardive Dyskinesia 59 0.024
956
P PLM034 Pulmonary Emphysema 59 0.024
957
CHR177 Chromophobe Renal Cell Carcinoma 59 0.024
958
ING001 Inguinal Hernia 59 0.024
959
P LMY004 Leiomyosarcoma 59 0.024
960
PHR003 Pharyngitis 59 0.024
961
P OLG002 Oligodendroglioma 59 0.024
962
ICH054 Ichthyosis, X-Linked 59 0.024
963
P USH001 Usher Syndrome 59 0.024
964
P HYP035 Hypophosphatasia 58 0.024
965
P FRD012 Friedreich Ataxia 1 58 0.024
966
CMP010 Complex Regional Pain Syndrome 58 0.024
967
CFF002 Coffin-Lowry Syndrome 58 0.024
968
c CRD093 Cardiomyopathy, Dilated, 1a 58 0.024
969
TRN018 Transitional Cell Carcinoma 58 0.024
970
P HYP614 Hyperlipidemia, Familial Combined 57 0.024
971
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 57 0.024
972
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 57 0.024
973
P LRY044 Larynx Cancer 57 0.024
974
P SBS003 Substance Abuse 57 0.024
975
HYP810 Hypereosinophilic Syndrome, Idiopathic 57 0.024
976
P LPD010 Lipodystrophy 57 0.024
977
BRN004 Brain Edema 57 0.024
978
P MCR010 Microcephaly 57 0.024
979
c GCH015 Gaucher Disease, Type I 57 0.024
980
ATY005 Atypical Teratoid Rhabdoid Tumor 57 0.024
981
CYT008 Cytomegalovirus Infection 57 0.024
982
HYP052 Hyperkalemic Periodic Paralysis 57 0.024
983
CHL014 Cholera 56 0.024
984
P PMP005 Pemphigus Vulgaris 56 0.024
985
FCL014 Focal Epilepsy 56 0.024
986
c INS002 in Situ Carcinoma 56 0.024
987
ANK001 Ankylosis 56 0.024
988
PSD014 Pseudopseudohypoparathyroidism 56 0.024
989
BLD044 Bladder Disease 55 0.024
990
SMT006 Somatoform Disorder 55 0.024
991
c BRS049 Breast Carcinoma in Situ 55 0.024
992
SPN051 Spondylitis 55 0.024
993
DGR001 Digeorge Syndrome 55 0.024
994
STR020 Strabismus 55 0.024
995
BRS099 Breast Ductal Carcinoma 55 0.024
996
ALB001 Albright's Hereditary Osteodystrophy 55 0.024
997
P PNM006 Pneumoconiosis 55 0.024
998
P HYP014 Hyperuricemia 54 0.024
999
SPR004 Supravalvular Aortic Stenosis 54 0.024
1000
TMP001 Temporal Lobe Epilepsy 54 0.024
1001
OST015 Osteochondrodysplasia 54 0.024
1002
RST001 Restless Legs Syndrome 54 0.024
1003
QDR001 Quadriplegia 54 0.024
1004
OPT009 Optic Neuritis 53 0.024
1005
GNR004 Generalized Anxiety Disorder 53 0.024
1006
MLN007 Male Infertility 53 0.024
1007
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 53 0.024
1008
MSC072 Muscle Cancer 53 0.024
1009
P TRT010 Teratoma 53 0.024
1010
P BRT004 Bartter Disease 52 0.024
1011
IGG001 Iga Glomerulonephritis 52 0.024
1012
c SCN036 Secondary Progressive Multiple Sclerosis 52 0.024
1013
TLN003 Telangiectasis 52 0.024
1014
BRT005 Barth Syndrome 52 0.024
1015
CHR005 Chorioamnionitis 52 0.024
1016
PLR008 Pleurisy 52 0.024
1017
FML037 Female Breast Cancer 52 0.024
1018
VPM001 Vipoma 52 0.024
1019
ECT026 Ectopic Pregnancy 52 0.024
1020
SPN020 Spondylosis 52 0.024
1021
P PRC012 Pericardial Effusion 52 0.024
1022
DBT004 Diabetic Polyneuropathy 51 0.024
1023
PRN021 Paranasal Sinus Disease 51 0.024
1024
OCL006 Ocular Hypertension 51 0.024
1025
SML036 Small Intestinal Adenocarcinoma 51 0.024
1026
RFL001 Reflex Sympathetic Dystrophy 51 0.024
1027
NTR046 Neutrophil Migration 51 0.024
1028
SRT004 Serotonin Syndrome 51 0.024
1029
SCH012 Schizoaffective Disorder 51 0.024
1030
c HYP739 Hyperlipoproteinemia, Type Iv 51 0.024
1031
HYP006 Hypertensive Heart Disease 51 0.024
1032
RHB001 Rhabdoid Cancer 51 0.024
1033
ATY042 Atypical Chronic Myeloid Leukemia 51 0.024
1034
INT054 Intraocular Lymphoma 50 0.024
1035
ACT017 Acute Chest Syndrome 50 0.024
1036
PLC007 Placental Abruption 50 0.024
1037
HPT014 Hepatorenal Syndrome 49 0.024
1038
CLS016 Clostridium Difficile Colitis 49 0.024
1039
PNC119 Pancreatic Neuroendocrine Tumor 49 0.024
1040
MNC006 Monoclonal Gammopathy of Uncertain Significance 49 0.024
1041
SMN007 Seminoma 49 0.024
1042
P MYP087 Myopathy, Tubular Aggregate, 1 48 0.024
1043
PLM041 Pulmonary Valve Stenosis 48 0.024
1044
c HYP740 Hyperlipoproteinemia, Type V 48 0.024
1045
SPH010 Sphingolipidosis 48 0.024
1046
CNJ012 Conjunctival Disease 48 0.024
1047
SKL017 Skeletal Dysplasias 48 0.024
1048
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.024
1049
c LBR014 Leber Congenital Amaurosis 4 48 0.024
1050
P SDR002 Siderosis 48 0.024
1051
SCT005 Scott Syndrome 48 0.024
1052
RFR010 Refractory Anemia 48 0.024
1053
CRN017 Coronary Thrombosis 48 0.024
1054
P CMP008 Compartment Syndrome 48 0.024
1055
SLV003 Salivary Gland Disease 47 0.024
1056
c ADL096 Adult Hepatocellular Carcinoma 47 0.024
1057
P CRN074 Coronary Artery Aneurysm 47 0.024
1058
c PCH012 Pachyonychia Congenita 2 47 0.024
1059
SGN002 Signet Ring Cell Adenocarcinoma 47 0.024
1060
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 47 0.024
1061
P DYS021 Dysautonomia 47 0.024
1062
PRS129 Prostatic Hyperplasia, Benign 47 0.024
1063
ANP009 Anaplastic Oligodendroglioma 46 0.024
1064
SYN036 Syncope 46 0.024
1065
c PRG126 Progressive Familial Heart Block 46 0.024
1066
NPH010 Nephrosclerosis 46 0.024
1067
CRB004 Cerebral Artery Occlusion 46 0.024
1068
EXS001 Exostosis 46 0.024
1069
MDL009 Medullary Sponge Kidney 46 0.024
1070
FML091 Familial Tumoral Calcinosis 46 0.024
1071
PMP004 Pemphigus Foliaceus 46 0.024
1072
ANS011 Anus Cancer 46 0.024
1073
DDN010 Duodenum Cancer 46 0.024
1074
SQM022 Squamous Cell Carcinoma of the Larynx 45 0.024
1075
GNG003 Gingival Recession 45 0.024
1076
PRM013 Premature Menopause 45 0.024
1077
P HRD001 Hereditary Multiple Exostoses 45 0.024
1078
RFR003 Refractive Error 45 0.024
1079
IRN002 Iron Metabolism Disease 45 0.024
1080
DCB001 Decubitus Ulcer 44 0.024
1081
URT001 Urethritis 44 0.024
1082
BSL008 Basal Ganglia Disease 44 0.024
1083
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 44 0.024
1084
c HYP734 Hypercholesterolemia, Autosomal Dominant, Type B 44 0.024
1085
ASP030 Aspirin Resistance 44 0.024
1086
GST029 Gastric Cardia Adenocarcinoma 44 0.024
1087
MMM006 Mammographic Density 43 0.024
1088
HYD003 Hydrarthrosis 43 0.024
1089
ADS004 Aids Dementia Complex 42 0.024
1090
CNV002 Conversion Disorder 42 0.024
1091
CND005 Cone Dystrophy 42 0.024
1092
MYF001 Myofibroma 42 0.024
1093
SQM021 Squamous Cell Carcinoma of the Hypopharynx 42 0.024
1094
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 42 0.024
1095
LCH004 Lichen Disease 42 0.024
1096
SKN023 Skin Tag 41 0.024
1097
SPN050 Spinocerebellar Degeneration 41 0.024
1098
PNC016 Pancreatic Cholera 41 0.024
1099
SCR001 Secretory Meningioma 41 0.024
1100
c ACT004 Acute Diarrhea 41 0.024
1101
PTT059 Pettigrew Syndrome 40 0.024
1102
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.024
1103
c HYP243 Hyperparathyroidism 1 40 0.024
1104
c ALC033 Alcohol Use Disorder 40 0.024
1105
P FML043 Familial Idiopathic Basal Ganglia Calcification 40 0.024
1106
LTH001 Lethal Midline Granuloma 40 0.024
1107
STR015 Stereotypic Movement Disorder 40 0.024
1108
MVM001 Movement Disease 40 0.024
1109
PRM237 Primary Hypomagnesemia 40 0.024
1110
C1N001 C1 Inhibitor Deficiency 40 0.024
1111
PNC008 Pancreatic Endocrine Carcinoma 40 0.024
1112
ANT018 Anthracosis 39 0.024
1113
BSL009 Basal Ganglia Calcification 39 0.024
1114
MTR007 Motor Peripheral Neuropathy 39 0.024
1115
c HYP601 Hyperinsulinemic Hypoglycemia, Familial, 3 39 0.024
1116
ALG001 Algoneurodystrophy 39 0.024
1117
P CNT036 Central Nervous System Germ Cell Tumor 39 0.024
1118
AMP003 Ampulla of Vater Neoplasm 39 0.024
1119
LTT002 Letterer-Siwe Disease 39 0.024
1120
PNC006 Pancreatic Somatostatinoma 39 0.024
1121
SML014 Small Intestine Leiomyosarcoma 38 0.024