Search results for Calcium Phosphate

2117 hits were found for Calcium Phosphate

# Family MCID Name MIFTS Score
1
P HYP069 Hyperparathyroidism 63 0.507
2
RCK004 Rickets 68 0.431
3
P KDN018 Kidney Disease 72 0.411
4
HYP025 Hyperphosphatemia 48 0.383
5
BNR002 Bone Resorption Disease 48 0.372
6
c CHR684 Chronic Kidney Disease 70 0.362
7
NPH009 Nephrolithiasis 55 0.360
8
P OST002 Osteoporosis 74 0.350
9
PRT037 Pertussis 65 0.349
10
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.336
11
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.336
12
c SCN007 Secondary Hyperparathyroidism 51 0.334
13
URL001 Urolithiasis 45 0.304
14
HYP017 Hypophosphatemia 50 0.285
15
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.278
16
P BND020 Bone Disease 59 0.277
17
c HYP595 Hypertension, Essential 84 0.270
18
c PRM005 Primary Hyperparathyroidism 58 0.261
19
END086 End Stage Renal Disease 51 0.258
20
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.243
21
P NRB001 Neuroblastoma 72 0.240
22
P LKM002 Leukemia 68 0.238
23
OST011 Osteomalacia 52 0.232
24
P CLR023 Colorectal Cancer 99 0.226
25
P LYM118 Lymphoma 68 0.220
26
LYM019 Lymphosarcoma 46 0.215
27
DNT012 Dental Caries 53 0.213
28
HLX001 Helix Syndrome 47 0.210
29
P HYP024 Hypoparathyroidism 56 0.209
30
48X005 48,xyyy 39 0.205
31
CNG034 Congestive Heart Failure 69 0.200
32
LPP008 Lipoprotein Quantitative Trait Locus 62 0.199
33
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.196
34
ISC004 Ischemia 58 0.195
35
OST159 Osteogenic Sarcoma 66 0.191
36
P ADN016 Adenocarcinoma 64 0.190
37
ANG054 Angina Pectoris 66 0.189
38
ART140 Arteries, Anomalies of 52 0.188
39
P LKM062 Leukemia, Acute Lymphoblastic 69 0.185
40
NPH003 Nephrocalcinosis 51 0.184
41
ATH013 Atherosclerosis Susceptibility 65 0.183
42
ADN018 Adenoma 59 0.180
43
HYP266 Hypoxia 57 0.179
44
ANX004 Anoxia 40 0.179
45
MTB004 Metabolic Acidosis 50 0.177
46
P MYL006 Myeloid Leukemia 60 0.176
47
ALL026 Allergic Hypersensitivity Disease 62 0.175
48
P HRT032 Heart Disease 75 0.175
49
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.174
50
P CRN300 Coronary Heart Disease 1 63 0.174
51
CHL014 Cholera 59 0.174
52
P GLM045 Glioma 63 0.172
53
GLL048 Glial Tumor 45 0.171
54
OST017 Osteomyelitis 64 0.170
55
c LKM061 Leukemia, Acute Myeloid 84 0.169
56
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.169
57
P PRS040 Prostate Cancer 97 0.169
58
LYM040 Lymphoblastic Lymphoma 54 0.168
59
P PRD008 Periodontitis 64 0.167
60
P VSC007 Vascular Disease 63 0.167
61
P GRF003 Graft-Versus-Host Disease 72 0.166
62
URM002 Uremia 49 0.165
63
c RHB024 Rhabdomyosarcoma 2 67 0.165
64
P LKM071 Leukemia, Chronic Lymphocytic 79 0.164
65
CLC006 Calcinosis 48 0.163
66
P MSC005 Muscular Dystrophy 66 0.163
67
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.162
68
TTN003 Tetanus 65 0.159
69
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.158
70
HRW001 Hair Whorl 36 0.158
71
c PRC016 Pre-Eclampsia 63 0.158
72
IDP073 Idiopathic Hypercalciuria 43 0.155
73
MYL069 Myeloma, Multiple 85 0.155
74
P DBT009 Diabetes Mellitus 64 0.155
75
ADL002 Adult Syndrome 70 0.153
76
RNL011 Renal Osteodystrophy 50 0.153
77
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.153
78
P NRP001 Neuropathy 56 0.153
79
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.152
80
c ACT071 Acute Kidney Failure 60 0.151
81
LYM133 Lymphoma, Hodgkin, Classic 69 0.150
82
HYP005 Hypokalemia 55 0.150
83
P BCL017 B-Cell Lymphoma 58 0.149
84
47X002 47,xyy 49 0.149
85
HYP056 Hypoglycemia 66 0.148
86
P CHN059 Chondrocalcinosis 52 0.147
87
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.147
88
P CRD119 Cardiac Arrest 67 0.146
89
DWN001 Down Syndrome 70 0.146
90
DFC004 Deficiency Anemia 70 0.145
91
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.145
92
P SRC025 Sarcoidosis 1 70 0.143
93
c LKM063 Leukemia, Chronic Myeloid 72 0.143
94
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.142
95
OST012 Osteoarthritis 78 0.141
96
CNS004 Constipation 58 0.140
97
INS001 Insulinoma 60 0.140
98
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.140
99
MYL009 Myelodysplastic Syndrome 70 0.140
100
P DRR001 Diarrhea 55 0.139
101
c NRF023 Neurofibromatosis, Type Ii 80 0.139
102
GT001 Gout 64 0.137
103
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.137
104
P TRN020 Turner Syndrome 67 0.137
105
P LTR001 Lateral Sclerosis 54 0.137
106
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.136
107
P MYC007 Myocardial Infarction 70 0.136
108
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.135
109
P SZR006 Seizure Disorder 56 0.135
110
AGN016 Aging 56 0.134
111
P HYP076 Hyperthyroidism 55 0.133
112
P MYP004 Myopathy 70 0.133
113
LPD008 Lipid Metabolism Disorder 62 0.133
114
VSL002 Visual Epilepsy 59 0.133
115
P BRS047 Breast Cancer 97 0.133
116
P ALZ034 Alzheimer Disease 88 0.132
117
P ART023 Arthropathy 62 0.132
118
c ATR087 Atrial Standstill 1 75 0.132
119
P PHC003 Pheochromocytoma 71 0.131
120
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.131
121
ADR040 Adrenal Gland Pheochromocytoma 46 0.131
122
c MGR028 Migraine with or Without Aura 1 67 0.130
123
HYP066 Hyperglycemia 61 0.130
124
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.128
125
CYS001 Cystic Fibrosis 81 0.128
126
P HYP086 Hypothyroidism 69 0.128
127
HMN044 Human Immunodeficiency Virus Type 1 71 0.126
128
IRN002 Iron Metabolism Disease 57 0.126
129
P RCT021 Rectum Cancer 52 0.126
130
P MLG056 Malignant Hyperthermia 67 0.125
131
P OVR042 Ovarian Cancer 88 0.124
132
P CTR002 Cataract 60 0.124
133
c HYP836 Hypercholesterolemia, Familial, 1 73 0.124
134
P HYP726 Hypercalcemia, Infantile, 1 58 0.123
135
P CRD246 Cardiovascular System Disease 57 0.122
136
LMB002 Lambert-Eaton Myasthenic Syndrome 53 0.122
137
P ENC018 Encephalopathy 61 0.120
138
c ACT027 Acute Pancreatitis 60 0.120
139
P FLL037 Follicular Lymphoma 67 0.120
140
P LVR013 Liver Disease 68 0.119
141
MNT001 Mantle Cell Lymphoma 69 0.119
142
c DLT002 Dilated Cardiomyopathy 79 0.119
143
PPL052 Papillomatosis, Confluent and Reticulated 33 0.119
144
P ART021 Arteriosclerosis 54 0.118
145
c GLL024 Gallbladder Disease 1 53 0.118
146
PLS009 Plasma Cell Neoplasm 51 0.118
147
c MCR113 Microvascular Complications of Diabetes 3 52 0.117
148
c FLL041 Follicular Lymphoma 1 49 0.117
149
BRK010 Burkitt Lymphoma 67 0.117
150
c MCR120 Microvascular Complications of Diabetes 7 47 0.117
151
CYT002 Cytokine Deficiency 42 0.117
152
P NTR004 Neutropenia 63 0.116
153
c MCR130 Microvascular Complications of Diabetes 6 41 0.116
154
c MCR133 Microvascular Complications of Diabetes 4 41 0.116
155
c PRM038 Primary Agammaglobulinemia 44 0.116
156
THY029 Thyroid Carcinoma 59 0.115
157
PNG002 Pain Agnosia 51 0.115
158
INS024 Insulin-Like Growth Factor I 79 0.115
159
IMM167 Immune Deficiency Disease 78 0.115
160
c CHR064 Chronic Monocytic Leukemia 33 0.115
161
P PLM037 Pulmonary Hypertension 67 0.114
162
LVR012 Liver Cirrhosis 62 0.114
163
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.114
164
MSC157 Muscular Dystrophy, Duchenne Type 72 0.114
165
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.114
166
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.114
167
P PRP019 Peripheral Nervous System Disease 58 0.113
168
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.112
169
P FML068 Familial Hypocalciuric Hypercalcemia 54 0.112
170
c LKM005 Leukemia, T-Cell, Chronic 34 0.111
171
INT007 Intermediate Coronary Syndrome 55 0.111
172
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.111
173
PLS025 Plasmablastic Lymphoma 47 0.110
174
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.110
175
P CNR004 Cone-Rod Dystrophy 2 73 0.110
176
ATM095 Autoimmune Disease 62 0.110
177
P BPL003 Bipolar Disorder 56 0.110
178
CLN015 Colon Adenocarcinoma 65 0.110
179
P ATR011 Atrial Fibrillation 66 0.109
180
c MJR024 Major Affective Disorder 9 41 0.109
181
c MJR022 Major Affective Disorder 8 38 0.109
182
HMT002 Hematologic Cancer 62 0.109
183
P PSR002 Psoriasis 62 0.109
184
CRB039 Cerebrovascular Disease 67 0.109
185
P CHR345 Chronic Pain 44 0.108
186
c ACT075 Acute Myocardial Infarction 57 0.107
187
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.106
188
P ECL001 Eclampsia 50 0.106
189
ACQ007 Acquired Immunodeficiency Syndrome 60 0.106
190
P HYP061 Hypertrophic Cardiomyopathy 70 0.106
191
GLB015 Glioblastoma Multiforme 75 0.106
192
P PNC035 Pancreatic Cancer 84 0.105
193
c ACT073 Acute Leukemia 58 0.105
194
STR067 Stroke, Ischemic 81 0.105
195
ATX019 Ataxia with Vitamin E Deficiency 42 0.105
196
NTR005 Nutritional Deficiency Disease 62 0.105
197
HYP060 Hyperinsulinism 54 0.105
198
OST003 Osteonecrosis 61 0.105
199
TRM010 Traumatic Brain Injury 51 0.105
200
BRN071 Brain Injury 49 0.105
201
HML018 Homologous Wasting Disease 22 0.105
202
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.105
203
CRN030 Coronary Stenosis 50 0.105
204
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.105
205
MYL031 Myeloproliferative Neoplasm 66 0.104
206
P AST007 Astrocytoma 51 0.104
207
FML307 Familial Calcium Pyrophosphate Deposition 40 0.104
208
SKN016 Skin Disease 63 0.104
209
PST011 Pustulosis of Palm and Sole 52 0.104
210
P OVR082 Overgrowth Syndrome 50 0.104
211
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.103
212
BNM001 Bone Marrow Cancer 43 0.103
213
DPR016 Depression 63 0.103
214
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.102
215
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.102
216
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.102
217
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.102
218
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.102
219
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.102
220
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.102
221
RTR008 Root Resorption 45 0.102
222
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.102
223
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.102
224
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.102
225
SPN186 Spinal Cord Injury 60 0.102
226
P PNC044 Pancreatitis 61 0.102
227
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.102
228
P MCR115 Microvascular Complications of Diabetes 5 66 0.102
229
P MLN008 Melanoma 69 0.101
230
PLY150 Polykaryocytosis Inducer 31 0.101
231
P LNG032 Lung Cancer 98 0.101
232
MLR004 Malaria 81 0.101
233
P HML002 Hemolytic Anemia 63 0.100
234
P ADL017 Adult T-Cell Leukemia 56 0.100
235
c CHR417 Chronic Graft Versus Host Disease 57 0.099
236
LNG099 Lung Disease 60 0.099
237
P PSD015 Pseudohypoparathyroidism 56 0.099
238
OCL069 Ocular Motor Apraxia 51 0.099
239
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 60 0.099
240
P PLY014 Polycystic Kidney Disease 62 0.099
241
P RNL007 Renal Tubular Acidosis 51 0.098
242
MRG003 Marginal Zone B-Cell Lymphoma 52 0.098
243
ALC007 Alcohol Dependence 66 0.098
244
c ACT135 Acute Graft Versus Host Disease 52 0.098
245
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.098
246
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.098
247
P CHR285 Chronic Myelomonocytic Leukemia 60 0.097
248
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.097
249
DRM006 Dermatitis 61 0.097
250
TXC005 Toxic Shock Syndrome 62 0.097
251
FTT001 Fatty Liver Disease 61 0.097
252
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.096
253
PRT029 Parathyroid Adenoma 50 0.096
254
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.096
255
P HYP733 Hypercalciuria, Absorptive, 2 45 0.095
256
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.095
257
CRB004 Cerebral Artery Occlusion 45 0.095
258
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.094
259
c PRS136 Prostate Cancer, Hereditary, 6 33 0.094
260
c PRS130 Prostate Cancer, Hereditary, 8 32 0.094
261
c SML038 Small Cell Cancer of the Lung 65 0.094
262
P NPH012 Nephrotic Syndrome 60 0.094
263
P HPT023 Hepatocellular Carcinoma 100 0.093
264
P GST053 Gastric Cancer 83 0.093
265
c ACT068 Acute Cystitis 63 0.093
266
MCS002 Mucositis 56 0.093
267
MYL005 Myelofibrosis 70 0.093
268
STT001 Status Epilepticus 60 0.092
269
P ART022 Arthritis 69 0.092
270
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.092
271
MMM001 Mammary Paget's Disease 53 0.091
272
P EPL164 Epilepsy 71 0.091
273
CLR108 Colorectal Adenoma 64 0.091
274
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.091
275
ATR057 Atrioventricular Block 55 0.091
276
PRP027 Peripheral Vascular Disease 71 0.091
277
MCR004 Macroglobulinemia 49 0.091
278
STM007 Stomatitis 50 0.091
279
PRS021 Prostatic Adenoma 51 0.090
280
PRS045 Prostatic Hypertrophy 53 0.089
281
P PNM007 Pneumonia 68 0.089
282
P THR014 Thrombocytopenia 67 0.089
283
PRS129 Prostatic Hyperplasia, Benign 49 0.089
284
MNT002 Mental Depression 58 0.089
285
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.089
286
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.088
287
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.088
288
RFR010 Refractory Anemia 48 0.088
289
SVR004 Severe Combined Immunodeficiency 73 0.087
290
DPH001 Diphtheria 60 0.087
291
CRD132 Cardiac Conduction Defect 58 0.087
292
P RHM011 Rheumatoid Arthritis 80 0.087
293
P TRM003 Tremor 54 0.087
294
BCT022 Bacterial Infectious Disease 56 0.086
295
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.086
296
ERY051 Erythroleukemia, Familial 56 0.086
297
ONC003 Oncogenic Osteomalacia 42 0.086
298
SPL004 Splenic Marginal Zone Lymphoma 51 0.085
299
c SYS001 Systemic Lupus Erythematosus 86 0.085
300
GNG003 Gingival Recession 44 0.085
301
P HNT016 Huntington Disease 72 0.085
302
HYP014 Hyperuricemia 52 0.085
303
SQM006 Squamous Cell Carcinoma 60 0.085
304
P INF037 Inflammatory Bowel Disease 54 0.085
305
PPT005 Peptic Ulcer Disease 59 0.084
306
CRD223 Cardiac Arrhythmia 60 0.084
307
WLD007 Waldenstroem's Macroglobulinemia 61 0.084
308
SCK003 Sickle Cell Anemia 74 0.084
309
HMS001 Hemosiderosis 54 0.084
310
FCT007 Factor Vii Deficiency 67 0.083
311
ESP021 Esophageal Cancer 90 0.083
312
PTT037 Pituitary Tumors 44 0.083
313
P HRP006 Herpes Simplex 65 0.083
314
P RSP003 Respiratory Failure 74 0.083
315
GLS018 Glass Syndrome 57 0.082
316
P HDC001 Headache 57 0.082
317
SYN007 Synovitis 54 0.082
318
PLC002 Plica Syndrome 36 0.082
319
CHL149 Childhood Acute Myeloid Leukemia 44 0.082
320
PRT036 Peritonitis 64 0.082
321
P THL005 Thalassemia 60 0.081
322
LYM012 Lymphoplasmacytic Lymphoma 47 0.081
323
P INF032 Infertility 57 0.081
324
AST005 Asthma 76 0.081
325
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.081
326
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.081
327
P ANP001 Anaplastic Large Cell Lymphoma 58 0.081
328
c PRD040 Periodontitis, Chronic 53 0.080
329
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.080
330
ANK001 Ankylosis 51 0.080
331
P RRH023 Rare Hereditary Hemochromatosis 41 0.080
332
P FNC004 Fanconi Syndrome 50 0.080
333
GLC003 Glucose Intolerance 54 0.080
334
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.080
335
P TXP001 Toxoplasmosis 60 0.079
336
P DMN002 Dementia 66 0.079
337
MYC006 Mycosis Fungoides 66 0.078
338
P GLM007 Glomerulonephritis 57 0.078
339
P BLD134 Bladder Cancer 79 0.078
340
P FNC034 Fanconi Renotubular Syndrome 2 40 0.078
341
P MSC003 Muscular Atrophy 52 0.078
342
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.078
343
GTR002 Goiter 53 0.077
344
P DDN001 Duodenal Ulcer 52 0.077
345
P LPS004 Lupus Erythematosus 61 0.077
346
ENM002 Enamel Erosion 26 0.077
347
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.077
348
c THR092 Thrombophilia Due to Thrombin Defect 73 0.076
349
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.076
350
BNN003 Bone Inflammation Disease 48 0.076
351
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.076
352
P SCK005 Sickle Cell Disease 50 0.076
353
WTH001 Withdrawal Disorder 48 0.075
354
P PRM002 Primary Hyperoxaluria 62 0.075
355
FNG017 Fungal Infectious Disease 53 0.075
356
ACR007 Acromegaly 71 0.075
357
P KDN017 Kidney Cancer 60 0.075
358
RTC005 Reticulosarcoma 47 0.075
359
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.075
360
PLM033 Pulmonary Embolism 59 0.075
361
P SCL018 Scoliosis 60 0.075
362
P LCT001 Lactic Acidosis 51 0.075
363
c FNC043 Fanconi Anemia, Complementation Group E 62 0.075
364
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.074
365
CLN045 Colonic Benign Neoplasm 46 0.074
366
P MLN007 Male Infertility 55 0.074
367
P SKN015 Skin Carcinoma 66 0.074
368
P ALP008 Alopecia 54 0.074
369
P HYP776 Hyperparathyroidism, Neonatal Severe 47 0.074
370
P PLY018 Polycythemia 56 0.074
371
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.074
372
SCN001 Secondary Hyperparathyroidism of Renal Origin 27 0.074
373
SKN019 Skin Melanoma 68 0.074
374
SYN036 Syncope 45 0.074
375
DFF005 Diffuse Large B-Cell Lymphoma 55 0.073
376
c BRN108 Branchiootic Syndrome 1 62 0.073
377
TND005 Tendinitis 54 0.073
378
SZR001 Sezary's Disease 60 0.073
379
SRC014 Sarcoma 65 0.073
380
P INF038 Influenza 68 0.073
381
HYP789 Hypophosphatemic Rickets with Hypercalciuria, Hereditary 51 0.073
382
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.073
383
P PLY019 Polyneuropathy 56 0.073
384
P TMR018 Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 61 0.072
385
ALL014 Allergic Encephalomyelitis 38 0.072
386
c DRR009 Diarrhea 6 46 0.072
387
PST092 Posttransplant Acute Limbic Encephalitis 29 0.072
388
IRR002 Irritable Bowel Syndrome 65 0.072
389
P LCT002 Lactose Intolerance 53 0.072
390
SPN035 Spindle Cell Sarcoma 53 0.072
391
P MYS003 Myasthenia Gravis 68 0.072
392
P DRM053 Dermatitis, Atopic 66 0.072
393
P RHN004 Rhinitis 57 0.072
394
CHL079 Children's Interstitial Lung Disease 26 0.072
395
P EXN002 Exanthem 57 0.071
396
c SVR001 Severe Acute Respiratory Syndrome 62 0.071
397
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.071
398
P PLY011 Polycystic Ovary Syndrome 56 0.071
399
c GRV008 Graves Disease 1 56 0.071
400
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.071
401
PLP001 Pulpitis 49 0.071
402
PRM020 Premenstrual Tension 40 0.071
403
c HPT016 Hepatitis B 59 0.071
404
PRL017 Prolymphocytic Leukemia 47 0.071
405
HMP009 Haemophilus Influenzae 43 0.071
406
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.071
407
CLC001 Calciphylaxis 51 0.071
408
NRM005 Neuromuscular Disease 64 0.071
409
IMP005 Impotence 52 0.071
410
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.071
411
P PLM036 Pulmonary Fibrosis 65 0.071
412
TLN003 Telangiectasis 52 0.071
413
ATY042 Atypical Chronic Myeloid Leukemia 49 0.071
414
CHL068 Cholestasis 61 0.071
415
P HYP035 Hypophosphatasia 61 0.070
416
c SCL052 Scleroderma, Familial Progressive 61 0.070
417
DNT006 Dental Pulp Necrosis 41 0.070
418
P HYP265 Hypotonia 43 0.070
419
MYC005 Myocardial Stunning 46 0.070
420
ANX010 Anxiety 73 0.070
421
BRN004 Brain Edema 56 0.070
422
PLM001 Pulmonary Tuberculosis 69 0.070
423
ATS010 Autosomal Recessive Disease 48 0.070
424
P SYS005 Systemic Scleroderma 68 0.069
425
P UVT001 Uveitis 57 0.069
426
MRF001 Marfan Syndrome 77 0.069
427
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.069
428
HDG004 Hodgkin's Granuloma 23 0.069
429
HDG006 Hodgkin's Paragranuloma 22 0.069
430
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.069
431
P FBR017 Fibrosarcoma 56 0.069
432
BRN024 Bronchitis 68 0.069
433
P SCH015 Schizophrenia 74 0.069
434
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 19 0.069
435
RYN005 Raynaud Phenomenon 47 0.069
436
c MLG068 Malignant Glioma 46 0.068
437
END057 Endometrial Cancer 74 0.068
438
CLT003 Colitis 62 0.068
439
P ALC033 Alcohol Use Disorder 58 0.068
440
c ATS007 Autism Spectrum Disorder 67 0.068
441
P HYP750 Hypertriglyceridemia, Familial 62 0.068
442
CHG001 Chagas Disease 66 0.068
443
HRY003 Hairy Cell Leukemia 55 0.067
444
ENM001 Enamel Caries 28 0.067
445
ART016 Aortic Aneurysm 69 0.067
446
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.067
447
P MLT020 Multiple Sclerosis 72 0.067
448
CRH001 Crohn's Disease 74 0.067
449
49X006 49, Xxxxy Syndrome 41 0.066
450
GST050 Gastrointestinal System Disease 56 0.066
451
PLY001 Polycythemia Vera 69 0.066
452
P PRK057 Parkinson Disease, Late-Onset 78 0.066
453
P ENC004 Encephalitis 61 0.066
454
P DST107 Distal Renal Tubular Acidosis 42 0.066
455
P PGT001 Paget's Disease of Bone 58 0.065
456
c PCH010 Pachyonychia Congenita 3 44 0.065
457
c CHR682 Chronic Bilirubin Encephalopathy 39 0.065
458
VCC001 Vaccinia 49 0.065
459
P MJR001 Major Depressive Disorder 68 0.065
460
MSC007 Muscle Hypertrophy 64 0.065
461
ANR040 Aneurysm 59 0.065
462
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.065
463
PYR009 Pyridoxine Deficiency Anemia 34 0.065
464
P LNG064 Lung Cancer Susceptibility 3 78 0.065
465
MDD011 Mood Disorder 62 0.065
466
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.064
467
P MYC008 Myocarditis 59 0.064
468
P ATS364 Autism 70 0.064
469
P MNC007 Monocytic Leukemia 53 0.064
470
P FML187 Familial Hypertension 37 0.064
471
P ESS003 Essential Thrombocythemia 68 0.064
472
P AMY004 Amyloidosis 70 0.064
473
LSH001 Leishmaniasis 63 0.064
474
P KLZ004 Kala-Azar 1 41 0.064
475
P CHR012 Chronic Granulomatous Disease 67 0.064
476
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.064
477
OST004 Osteitis Fibrosa 41 0.064
478
SFT003 Soft Tissue Sarcoma 56 0.064
479
TRN015 Transient Cerebral Ischemia 63 0.064
480
P TMP001 Temporal Lobe Epilepsy 50 0.064
481
P BRB001 Beriberi 46 0.064
482
THY111 Thyroid Carcinoma, Familial Medullary 67 0.064
483
c PNS012 Paine Syndrome 61 0.064
484
PNC129 Pancreatic Adenocarcinoma 68 0.064
485
BRT054 Brittle Bone Disorder 72 0.063
486
CRY024 Crystal Arthropathies 20 0.063
487
ENT004 Enthesopathy 49 0.063
488
VRL011 Viral Infectious Disease 61 0.063
489
P PYL005 Pyelonephritis 56 0.063
490
P BSL038 Basal Ganglia Calcification, Idiopathic, 1 52 0.063
491
P LNG028 Long Qt Syndrome 66 0.063
492
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.063
493
FBR047 Fibromyalgia 58 0.063
494
CNT047 Contact Dermatitis 58 0.063
496
KRT002 Keratomalacia 47 0.063
497
ALL003 Allergic Rhinitis 67 0.063
498
PLM031 Poliomyelitis 64 0.063
499
CHR074 Choriocarcinoma 47 0.063
500
BCK006 Back Pain 42 0.063
501
LPT014 Leptin Deficiency or Dysfunction 74 0.063
502
c PRM012 Primary Polycythemia 50 0.062
503
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.062
504
SCH014 Schistosomiasis 57 0.062
505
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.062
506
PLM017 Pulmonary Alveolar Microlithiasis 50 0.062
507
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.062
508
THY125 Thyroid Gland Medullary Carcinoma 50 0.062
509
P PRD021 Periodic Paralysis 45 0.062
510
P GLM040 Glioma Susceptibility 1 81 0.062
511
P GRV001 Graves' Disease 55 0.062
512
LYM051 Lymphomatoid Granulomatosis 45 0.062
513
LNG031 Lung Benign Neoplasm 51 0.062
514
OVR094 Ovarian Epithelial Cancer 38 0.062
515
THY030 Thyroid Gland Disease 52 0.062
516
P MTR014 Motor Neuron Disease 65 0.061
517
BRR014 Barrett Esophagus 65 0.061
518
PRM329 Premature Aging 35 0.061
519
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.061
520
CVD001 Covid-19 44 0.061
521
WLL004 Wallerian Degeneration 39 0.061
522
ZLL002 Zollinger-Ellison Syndrome 55 0.061
523
BLR008 Bilirubin Metabolic Disorder 57 0.061
524
MGK001 Megakaryocytic Leukemia 64 0.061
526
ULC004 Ulcerative Colitis 73 0.060
527
P END044 Endometriosis 63 0.060
528
GST023 Gastric Ulcer 53 0.060
529
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.060
530
P CYS018 Cystitis 59 0.060
531
P MLG074 Malignant Mesenchymoma 40 0.060
532
THR024 Thrombosis 57 0.060
533
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.060
534
DBT010 Diabetic Neuropathy 54 0.060
535
P GST044 Gastritis 56 0.060
536
PRP080 Peripheral Artery Disease 53 0.060
537
ANR007 Anorexia Nervosa 63 0.060
538
IDP070 Idiopathic Scoliosis 42 0.060
539
c THR090 Thrombocythemia 1 49 0.060
540
FBR009 Fibrous Dysplasia 48 0.059
541
c EPS035 Episodic Ataxia, Type 2 63 0.059
542
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.059
543
KRT008 Keratopathy 47 0.059
544
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.059
545
P RTN024 Retinoblastoma 73 0.059
546
P SLP006 Sleep Apnea 69 0.059
547
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.059
548
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.059
549
CLR109 Colorectal Adenocarcinoma 51 0.059
550
CNN005 Connective Tissue Disease 68 0.059
551
PRT013 Portal Hypertension 59 0.059
552
P MYT002 Myotonic Dystrophy 49 0.059
553
P DNT020 Dent Disease 1 62 0.058
554
MTH071 Methane Production 26 0.058
555
c HPT073 Hepatitis C Virus 72 0.058
556
CMM004 Common Variable Immunodeficiency 68 0.058
557
PRP016 Paraplegia 52 0.058
558
c INH020 Inherited Metabolic Disorder 47 0.058
559
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.058
560
ENT011 Enterocolitis 51 0.058
561
c FML001 Familial Atrial Fibrillation 65 0.058
562
TXC002 Toxic Encephalopathy 53 0.058
563
c FML008 Familial Retinoblastoma 53 0.058
564
PRR001 Periarthritis 32 0.058
565
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.058
566
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.058
567
HPT004 Hepatic Coma 45 0.058
568
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.058
569
P LYM033 Lymphoproliferative Syndrome 59 0.058
570
HYD002 Hydronephrosis 60 0.057
571
GST092 Gastroesophageal Reflux 67 0.057
572
P DYS154 Dystonia 65 0.057
573
VSC002 Vascular Dementia 57 0.057
574
P MYS005 Myositis 56 0.057
575
EWN003 Ewing Sarcoma 69 0.057
576
P HPT021 Hepatitis 67 0.057
577
P GLY013 Glycogen Storage Disease 60 0.057
578
LYM027 Lymphopenia 58 0.057
579
c DBT099 Diabetes Mellitus, Type I 65 0.057
580
FRZ001 Frozen Shoulder 53 0.057
581
c CHR418 Chronic Leukemia 49 0.057
582
P BRS044 Breast Adenocarcinoma 59 0.057
583
GST045 Gastroenteritis 59 0.057
584
c PSR017 Psoriasis 2 53 0.057
585
c PSR023 Psoriasis 1 52 0.057
586
c PSR032 Psoriasis 11 47 0.057
587
c PSR028 Psoriasis 7 42 0.057
588
c PSR018 Psoriasis 13 41 0.057
589
CHL065 Cholangiocarcinoma 68 0.057
590
c HYP794 Hyperoxaluria, Primary, Type I 63 0.057
591
PLM010 Pulmonary Edema 54 0.057
592
P NRV007 Nervous System Disease 66 0.056
593
P BNC003 Bone Cancer 58 0.056
594
GRN017 Granulocytopenia 44 0.056
595
P CYS039 Cystic Kidney Disease 54 0.056
596
c HYP272 Hypercholesterolemia, Familial, 3 44 0.056
597
SPN027 Spinal Stenosis 59 0.056
598
EYD002 Eye Disease 58 0.056
599
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.056
600
TRP009 Triple X Syndrome 42 0.056
601
c HMC039 Hemochromatosis, Type 1 74 0.056
602
P RTN016 Retinal Degeneration 53 0.056
603
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.056
604
PPL022 Papilloma 54 0.056
605
c ART101 Aortic Valve Disease 2 65 0.056
606
PTH003 Pathologic Nystagmus 52 0.056
607
CRD137 Cardiogenic Shock 47 0.056
608
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.056
609
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.056
610
c FML035 Familial Hyperlipidemia 55 0.055
611
SBC016 Subacute Delirium 44 0.055
612
BRN028 Brain Cancer 74 0.055
613
CRP001 Carpal Tunnel Syndrome 67 0.055
614
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.055
615
DGN001 Degenerative Disc Disease 48 0.055
616
c MCR129 Microvascular Complications of Diabetes 1 66 0.055
617
P PMP001 Pemphigus 54 0.055
618
c SPN225 Spondyloarthropathy 1 73 0.055
619
P THY023 Thymoma 65 0.055
620
SPT004 Septic Arthritis 58 0.055
621
c THY107 Thymoma, Familial 52 0.055
622
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 37 0.055
623
P DRM010 Dermatomyositis 61 0.055
624
GST020 Gastric Antral Vascular Ectasia 41 0.055
625
P RHB003 Rhabdomyosarcoma 63 0.055
626
P ATX030 Ataxia-Telangiectasia 82 0.055
627
CNT033 Central Nervous System Cancer 47 0.054
628
P SCK002 Sick Sinus Syndrome 55 0.054
629
HYP081 Hypolipoproteinemia 51 0.054
630
HYP080 Hypogonadism 50 0.054
631
SYS003 Systolic Heart Failure 49 0.054
632
PRT010 Parathyroid Carcinoma 67 0.054
633
P SNS001 Sensorineural Hearing Loss 60 0.054
634
HRT012 Heart Valve Disease 53 0.054
635
P PNC025 Panic Disorder 53 0.054
636
BRS064 Bursitis 48 0.054
637
HPT019 Hepatic Encephalopathy 60 0.054
638
PRP030 Purpura 54 0.054
639
RTN023 Retinitis 46 0.054
640
PPL001 Papillary Adenoma 44 0.054
641
NRR001 Neuroretinitis 42 0.054
642
P OPT006 Optic Nerve Disease 60 0.054
643
P RNL015 Renal Hypertension 47 0.054
644
AMN003 Amnestic Disorder 54 0.054
645
P SCL057 Scoliosis, Isolated 1 41 0.054
646
c VRL010 Viral Hepatitis 52 0.053
647
CHL004 Cholelithiasis 49 0.053
648
LMB062 Limb Ischemia 55 0.053
649
URT010 Ureteral Obstruction 45 0.053
650
GNG013 Gingivitis 59 0.053
651
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.053
652
P HYP098 Hypereosinophilic Syndrome 67 0.053
653
P TRT010 Teratoma 52 0.053
654
P MLT074 Multiple Endocrine Neoplasia 56 0.053
655
GRM010 Germ Cells Tumors 34 0.053
656
c LKM070 Leukemia, Acute Monocytic 57 0.053
657
DYS073 Dysphagia 50 0.053
658
c HYP057 Hypervitaminosis D 42 0.053
659
INT079 Intrahepatic Cholangiocarcinoma 51 0.053
660
P CHN012 Chondrosarcoma 56 0.053
661
END040 Endogenous Depression 55 0.053
662
HMC014 Homocysteinemia 53 0.053
663
MDL009 Medullary Sponge Kidney 40 0.053
664
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.052
665
P CLC063 Celiac Disease 1 66 0.052
666
PNM001 Pneumocystosis 59 0.052
667
TRD006 Tardive Dyskinesia 54 0.052
668
CHR286 Chronic Neutrophilic Leukemia 42 0.052
669
P BRT004 Bartter Disease 52 0.052
670
RST023 Resting Heart Rate, Variation in 41 0.052
671
KHL003 Kohlschutter-Tonz Syndrome 65 0.052
672
P GCH001 Gaucher's Disease 63 0.052
673
c HYP864 Hypoparathyroidism, Familial Isolated, 1 48 0.052
674
P NSP012 Nasopharyngeal Carcinoma 66 0.052
675
c DWL002 Dowling-Degos Disease 1 58 0.052
676
SLP001 Sleeping Sickness 54 0.052
677
P AVS003 Avascular Necrosis 42 0.052
678
KRT019 Keratitis, Hereditary 65 0.052
679
P MDL005 Medulloblastoma 77 0.052
680
c HPT001 Hepatitis C 62 0.052
681
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.052
682
c XNT010 Xanthinuria, Type I 53 0.052
683
AYM001 Ayme-Gripp Syndrome 57 0.052
684
NNT012 Neonatal Jaundice 53 0.052
685
PRS063 Paresthesia 41 0.052
686
ANT024 Anthrax Disease 58 0.051
687
P RNV001 Renovascular Hypertension 48 0.051
688
P NGH001 Night Blindness 48 0.051
689
INT054 Intraocular Lymphoma 48 0.051
690
PLS011 Plasmacytoma 56 0.051
691
P SLP005 Sleep Disorder 59 0.051
692
P CND004 Candidiasis 58 0.051
693
RDC002 Radiculopathy 50 0.051
694
ARG004 Argyria 27 0.051
695
NRL016 Neural Tube Defects 82 0.051
696
HYP020 Hyperprolactinemia 64 0.051
697
P RTN018 Retinal Disease 53 0.051
698
OTT002 Otitis Media 72 0.051
699
INT002 Intermittent Claudication 61 0.051
700
P SPP010 Suppressor of Tumorigenicity 3 51 0.051
701
P APL001 Aplastic Anemia 74 0.051
702
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.051
703
c MNN043 Meningioma, Familial 74 0.051
704
MNN042 Meningioma, Radiation-Induced 62 0.051
705
SPN021 Spinal Meningioma 50 0.051
706
SCR001 Secretory Meningioma 41 0.051
707
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.051
708
CHL123 Chlamydia 59 0.051
709
ALL006 Allergic Asthma 56 0.051
710
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.050
711
VLK001 Volkmann Contracture 25 0.050
712
P SYP003 Syphilis 58 0.050
713
ILS001 Ileus 51 0.050
714
INT067 Interstitial Nephritis 48 0.050
715
HMG002 Hemoglobinuria 50 0.050
716
RTC003 Root Caries 33 0.050
717
P OST001 Osteopetrosis 70 0.050
718
SNS003 Sensory Peripheral Neuropathy 54 0.050
719
MST005 Mastitis 53 0.050
720
CRB090 Cerebral Hypoxia 44 0.050
721
IRN001 Iron Deficiency Anemia 59 0.050
722
P ANG015 Angioedema 57 0.050
723
c PRM226 Primary Central Nervous System Lymphoma 48 0.050
724
SQM002 Squamous Cell Papilloma 46 0.050
725
P BRG001 Brugada Syndrome 71 0.050
726
P ASP006 Aspergillosis 69 0.050
727
P PSD087 Pseudoxanthoma Elasticum 65 0.050
728
P SML001 Small Cell Carcinoma 52 0.050
729
GST040 Gastric Adenocarcinoma 70 0.049
730
P LPR021 Leprosy 3 69 0.049
731
VTM033 Vitamin K Deficiency Bleeding 48 0.049
732
HNS001 Hansen's Disease 34 0.049
733
CLC004 Calcific Tendinitis 30 0.049
734
CRV035 Cervical Cancer 76 0.049
735
NNL006 Non-Alcoholic Steatohepatitis 54 0.049
736
P CNJ013 Conjunctivitis 65 0.049
737
P INT070 Intestinal Obstruction 58 0.049
738
KRT013 Keratolytic Winter Erythema 46 0.049
739
c SVR005 Severe Pre-Eclampsia 50 0.049
740
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.049
741
THR004 Thrombocytosis 51 0.049
742
PLS007 Plasmodium Falciparum Malaria 52 0.049
743
ACT119 Acute Promyelocytic Leukemia 63 0.049
744
P SJG008 Sjogren Syndrome 61 0.049
745
CMR002 Coumarin Resistance 56 0.049
746
CLL003 Cellulitis 54 0.049
747
CHN010 Chondroma 43 0.049
748
GST033 Gestational Diabetes 61 0.049
749
c HYP243 Hyperparathyroidism 1 51 0.049
750
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 30 0.049
751
c PSD108 Pseudohypoparathyroidism, Type Ia 66 0.049
752
PRS047 Prostatitis 56 0.049
753
RDN001 Reading Disorder 40 0.049
754
PRN019 Perinatal Necrotizing Enterocolitis 59 0.048
755
P MYP006 Myopia 55 0.048
756
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.048
757
OST115 Osteonecrosis of the Jaw 40 0.048
758
OST016 Osteochondrosis 53 0.048
759
CHR178 Chromosomal Triplication 35 0.048
760
MYT011 Myotonia 34 0.048
761
P CNT005 Central Nervous System Lymphoma 53 0.048
762
NWC001 Newcastle Disease 45 0.048
763
LTH001 Lethal Midline Granuloma 44 0.048
764
MXD050 Mixed Phenotype Acute Leukemia 43 0.048
765
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.048
766
APP009 Appendix Adenocarcinoma 44 0.048
767
PRP036 Peripheral T-Cell Lymphoma 53 0.048
768
HST010 Histiocytosis 48 0.048
769
SPL018 Splenomegaly 48 0.048
770
MXD026 Mixed Glioma 45 0.048
771
KPS004 Kaposi Sarcoma 75 0.048
772
P HMN010 Hemangioma 61 0.048
773
c ACT134 Acute Liver Failure 56 0.048
774
MTH009 Mouth Disease 56 0.048
775
RYS001 Reye Syndrome 51 0.048
776
EMB004 Embryonal Carcinoma 56 0.047
777
P SHR001 Short Bowel Syndrome 53 0.047
778
P HMP007 Hemophilia 51 0.047
779
CYS014 Cystadenocarcinoma 51 0.047
780
IDP085 Idiopathic Infantile Hypercalcemia 28 0.047
781
P ADL010 Adult Respiratory Distress Syndrome 65 0.047
782
RNL077 Renal Fibrosis 47 0.047
783
IRD001 Iridocyclitis 53 0.047
784
c PNC108 Pancreatitis, Hereditary 70 0.047
785
ACH005 Achalasia 51 0.047
786
SPS057 Spasticity 45 0.047
787
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.047
788
OVR029 Ovarian Hyperstimulation Syndrome 64 0.047
789
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.047
790
LRG008 Large Granular Lymphocyte Leukemia 41 0.047
791
INT066 Interstitial Lung Disease 60 0.047
792
TRY001 Trypanosomiasis 50 0.047
793
P BNG032 Benign Mesothelioma 46 0.047
794
P TST021 Testicular Germ Cell Tumor 60 0.047
795
GST030 Gastrinoma 45 0.047
796
CRT015 Carotid Artery Occlusion 45 0.047
797
c BTT014 Beta-Thalassemia 74 0.046
798
P ESP024 Esophagitis 62 0.046
799
P URT039 Urticaria 58 0.046
800
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.046
801
ENC014 Enchondroma 29 0.046
802
VTM027 Vitamin D-Dependent Rickets, Type 2a 56 0.046
803
P INS002 in Situ Carcinoma 53 0.046
804
ADR007 Adrenoleukodystrophy 75 0.046
805
PYR016 Pyridoxine Deficiency 30 0.046
806
TBC004 Tobacco Addiction 64 0.046
807
P VSC011 Vasculitis 62 0.046
808
c MCR112 Microvascular Complications of Diabetes 2 41 0.046
809
P RTN008 Retinitis Pigmentosa 79 0.046
810
CRB037 Cerebral Palsy 69 0.046
811
PLG002 Plague 63 0.046
812
BRN056 Bronchopulmonary Dysplasia 57 0.046
813
GRM005 Germ Cell Cancer 47 0.046
814
P HYD006 Hydrocephalus 66 0.046
815
c ALP101 Alpha-Thalassemia 62 0.046
816
THY122 Thyroid Gland Cancer 57 0.046
817
P SBS003 Substance Abuse 55 0.046
818
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.046
819
MCC012 Mccune-Albright Syndrome 70 0.045
820
P MYC084 Mycobacterium Tuberculosis 1 68 0.045
821
c PLY105 Polycystic Ovary Syndrome 1 38 0.045
822
HYP006 Hypertensive Heart Disease 49 0.045
823
HDN002 Head Injury 46 0.045
824
P VNS003 Venous Insufficiency 55 0.045
825
P OPN001 Open-Angle Glaucoma 49 0.045
826
c MCL013 Mucolipidosis Iv 66 0.045
827
CYT018 Cytochrome P450 2d6 Variant 27 0.045
828
WST001 West Syndrome 61 0.045
829
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.045
830
c HPT003 Hepatitis a 62 0.045
831
CRC021 Carcinosarcoma 62 0.045
832
P PRP029 Porphyria 62 0.045
833
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.045
834
P LCH002 Lichen Planus 53 0.045
835
CLF001 Cleft Lip 53 0.045
836
P OCL013 Oculodentodigital Dysplasia 69 0.044
837
VSC003 Visceral Leishmaniasis 55 0.044
838
P MYC033 Myoclonus 46 0.044
839
ACT003 Acute Kidney Tubular Necrosis 45 0.044
840
c JVN010 Juvenile Rheumatoid Arthritis 64 0.044
841
CHL067 Cholecystitis 57 0.044
842
SKN013 Skin Benign Neoplasm 51 0.044
843
MSL001 Measles 62 0.044
844
OCL006 Ocular Hypertension 53 0.044
845
TST015 Testicular Disease 43 0.044
846
GLM044 Glomerular Disease 37 0.044
847
c INF071 Inflammatory Bowel Disease 1 67 0.044
848
P MVM001 Movement Disease 63 0.044
849
P PRM006 Primary Biliary Cirrhosis 62 0.044
850
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.044
851
P INT068 Intestinal Disease 53 0.044
852
GRW007 Growth Hormone Deficiency 46 0.044
853
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.044
854
CHR563 Chronic Eosinophilic Leukemia 48 0.044
855
CNN003 Conn's Syndrome 79 0.044
856
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.044
857
P NMN002 Niemann-Pick Disease 59 0.044
858
INC002 Inclusion Body Myositis 58 0.044
859
SPN019 Spondylolisthesis 51 0.044
860
PRD004 Prediabetes Syndrome 47 0.044
861
BCT002 Bacterial Vaginosis 53 0.043
862
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.043
863
VRC005 Varicose Veins 60 0.043
864
DSS009 Disseminated Intravascular Coagulation 57 0.043
865
NRN004 Neuroendocrine Tumor 55 0.043
866
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.043
867
GSG001 Gas Gangrene 53 0.043
868
P MGR003 Migraine with Aura 52 0.043
869
c MTR002 Mitral Valve Insufficiency 48 0.043
870
ATN005 Autonomic Dysfunction 46 0.043
871
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.043
872
P TRC086 Trichohepatoenteric Syndrome 1 62 0.043
873
CLR030 Clear Cell Renal Cell Carcinoma 53 0.043
874
KRT009 Keratosis 51 0.043
875
P MTC069 Mitochondrial Disorders 56 0.043
876
P PTT006 Pituitary Adenoma 55 0.043
877
ACR041 Acromelic Frontonasal Dysostosis 52 0.043
878
HVY002 Heavy Metal Poisoning 22 0.043
879
c GCH015 Gaucher Disease, Type I 70 0.043
880
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.043
881
PSR001 Psoriatic Arthritis 61 0.043
882
PMP006 Pemphigus Vulgaris, Familial 57 0.043
883
P ANG001 Angelman Syndrome 69 0.043
884
PSY004 Psychotic Disorder 67 0.043
885
P PNM006 Pneumoconiosis 56 0.043
886
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.043
887
BNG036 Bone Giant Cell Tumor 49 0.043
888
ANT018 Anthracosis 48 0.043
889
P EPN001 Ependymoblastoma 44 0.043
890
P ALP009 Alopecia Areata 60 0.043
891
AMN001 Amenorrhea 54 0.042
892
LWC001 Low Compliance Bladder 43 0.042
893
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.042
894
P DNG005 Dengue Virus 59 0.042
895
PLC008 Placenta Disease 50 0.042
896
SPN020 Spondylosis 46 0.042
897
URN010 Urinary Tract Obstruction 55 0.042
898
SPN051 Spondylitis 51 0.042
899
CCN002 Cocaine Abuse 49 0.042
900
c CHL157 Childhood B-Cell Acute Lymphoblastic Leukemia 33 0.042
901
HPT046 Hepatic Veno-Occlusive Disease 56 0.042
902
ACT200 Acute Monoblastic Leukemia 52 0.042
903
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.042
904
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 45 0.042
905
FML091 Familial Tumoral Calcinosis 44 0.042
906
PRT058 Pure Autonomic Failure 59 0.042
907
CRN288 Corneal Dystrophy, Band-Shaped 38 0.042
908
P MCR010 Microcephaly 59 0.042
909
PRT038 Protein-Energy Malnutrition 54 0.042
910
CRH005 Crohn's Colitis 53 0.042
911
LYS002 Lysosomal Storage Disease 52 0.042
912
DYS015 Dysentery 52 0.042
913
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.042
914
URC002 Urea Cycle Disorder 51 0.041
915
CLF004 Cleft Lip/palate 54 0.041
916
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.041
917
c BCT013 Bacterial Pneumonia 48 0.041
918
P BCT020 Bacteremia 2 44 0.041
919
ATM052 Autoimmune Disease 1 37 0.041
920
WLF001 Wolff-Parkinson-White Syndrome 66 0.041
921
MCL006 Macular Retinal Edema 55 0.041
922
RSC001 Rosacea 54 0.041
923
c INF145 Infantile Liver Failure Syndrome 1 50 0.041
924
DRY001 Dry Eye Syndrome 47 0.041
925
SPR008 Supratentorial Primitive Neuroectodermal Tumor 43 0.041
926
BSL009 Basal Ganglia Calcification 41 0.041
927
c OVR114 Ovarian Cancer 1 38 0.041
928
BLL006 Bullous Pemphigoid 62 0.041
929
INF009 Inflammatory Spondylopathy 31 0.041
930
P OLG002 Oligodendroglioma 67 0.041
931
ALL010 Allergic Contact Dermatitis 56 0.041
932
MDD018 Middle East Respiratory Syndrome 43 0.041
933
ANG049 Angioedema Induced by Ace Inhibitors 40 0.041
934
RFR009 Refractory Cytopenia with Multilineage Dysplasia 31 0.041
935
P MNN013 Meningitis 66 0.041
936
INT146 Intervertebral Disc Disease 63 0.041
937
ERY003 Erythema Multiforme 58 0.041
938
NRT004 Neuritis 52 0.041
939
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.041
940
INT253 Intestinal Benign Neoplasm 45 0.041
941
TND004 Tendinopathy 43 0.041
942
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.041
943
P ZLL001 Zellweger Syndrome 57 0.041
944
CLS052 Classic Hairy Cell Leukemia 27 0.041
945
c CNG027 Congenital Hemolytic Anemia 50 0.041
946
NPH010 Nephrosclerosis 50 0.041
947
c MLG069 Malignant Hypertension 47 0.041
948
PRT030 Parathyroid Gland Disease 45 0.041
949
PHS001 Phosphorus Metabolism Disease 40 0.041
950
INT075 Intracranial Hypertension 53 0.040
951
SCH012 Schizoaffective Disorder 50 0.040
952
NRT001 Neurotic Disorder 53 0.040
953
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.040
954
P BCL013 B-Cell Adult Acute Lymphocytic Leukemia 32 0.040
955
CHC001 Chickenpox 60 0.040
956
RBS001 Rabies 58 0.040
957
NWB001 Newborn Respiratory Distress Syndrome 58 0.040
958
DFF003 Diffuse Scleroderma 41 0.040
959
c SYS043 Systemic Lupus Erythematosus 1 38 0.040
960
RYN001 Raynaud Disease 48 0.040
961
DST006 Diastolic Heart Failure 45 0.040
963
c ALM001 Al Amyloidosis 50 0.039
964
RFR002 Refractory Hairy Cell Leukemia 33 0.039
965
CRN036 Craniopharyngioma 65 0.039
966
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.039
967
LNG108 Langerhans Cell Histiocytosis 58 0.039
968
THR013 Thoracic Outlet Syndrome 54 0.039
969
P MST002 Mast-Cell Leukemia 49 0.039
970
CND006 Candida Glabrata 32 0.039
971
HRP008 Herpes Simiae 25 0.039
972
FLL027 Fallopian Tube Carcinoma 67 0.039
973
AVN001 Avian Influenza 59 0.039
974
CMM005 Common Cold 57 0.039
975
c HYP292 Hypophosphatasia, Infantile 57 0.039
976
P PRC012 Pericardial Effusion 51 0.039
977
NPH018 Nephrogenic Systemic Fibrosis 50 0.039
978
HMP001 Hemopericardium 48 0.039
979
TST014 Testicular Cancer 46 0.039
980
ERY066 Erythema Multiforme Major 30 0.039
981
TRN018 Transitional Cell Carcinoma 56 0.039
982
CRT017 Cartilage Disease 54 0.039
983
P MJR007 Major Affective Disorder 1 43 0.039
984
AMN006 Aminoaciduria 38 0.039
985
DNT010 Dentin Caries 32 0.039
986
CLF027 Cleft Palate, Isolated 64 0.039
987
ALL009 Allergic Conjunctivitis 50 0.039
988
GYN001 Gynecomastia 49 0.039
989
P END039 Endodermal Sinus Tumor 44 0.039
990
TST018 Testicular Yolk Sac Tumor 39 0.039
991
INF021 Infant Gynecomastia 31 0.039
992
P BLD062 Bile Duct Cancer 67 0.039
993
RHM001 Rheumatic Fever 60 0.039
994
P PRN023 Prion Disease 57 0.039
995
P THY032 Thyroiditis 52 0.039
996
c BPL002 Bipolar I Disorder 49 0.039
997
BCK003 Background Diabetic Retinopathy 46 0.039
998
P HMR005 Hemorrhoid 46 0.039
999
MST004 Mast Cell Neoplasm 42 0.039
1000
P CLS010 Cluster Headache 42 0.039
1001
EXT007 Extracutaneous Mastocytoma 38 0.039
1002
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.039
1003
P DNT007 Dentin Sensitivity 36 0.039
1004
P INT143 Interstitial Cystitis 61 0.039
1005
ALC006 Alcoholic Hepatitis 61 0.039
1006
ACT058 Active Peptic Ulcer Disease 55 0.039
1007
c CNT035 Central Nervous System Disease 52 0.039
1008
HYP781 Hypoascorbemia 51 0.039
1009
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.039
1010
SML008 Small Intestine Lymphoma 33 0.039
1011
TTH007 Tooth Erosion 31 0.039
1012
BRS051 Breast Disease 58 0.038
1013
BRD001 Brody Myopathy 57 0.038
1014
P LMB006 Limb-Girdle Muscular Dystrophy 53 0.038
1015
FDL002 Food Allergy 51 0.038
1016
P ART018 Aortic Valve Insufficiency 49 0.038
1017
THR035 Thrombasthenia 40 0.038
1018
MCN008 Mucinous Cystadenocarcinoma 40 0.038
1019
CYS010 Cystinosis 59 0.038
1020
PHN003 Phenylketonuria 75 0.038
1021
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.038
1022
P END033 Endocarditis 57 0.038
1023
CHR073 Choreatic Disease 52 0.038
1024
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.038
1025
CNT017 Central Nervous System Origin Vertigo 45 0.038
1026
URM005 Uremic Pruritus 42 0.038
1027
SCR011 Scrapie 39 0.038
1028
ADG002 Audiogenic Seizures 25 0.038
1029
P SPN046 Spinal Muscular Atrophy 62 0.038
1030
P BNG030 Benign Ependymoma 60 0.038
1031
CLL010 Cellular Ependymoma 54 0.038
1032
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.038
1033
DWR001 Dwarfism 44 0.038
1034
GRM004 Germinoma 40 0.038
1035
ACT011 Acute Contagious Conjunctivitis 40 0.038
1036
c PRG106 Progressive Muscular Dystrophy 33 0.038
1037
ACN002 Acanthosis Nigricans 60 0.038
1038
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.038
1039
CLS016 Clostridium Difficile Colitis 48 0.038
1040
C1N001 C1 Inhibitor Deficiency 39 0.038
1041
PPL049 Papillon-Lefevre Syndrome 65 0.038
1042
END081 Endosteal Hyperostosis, Autosomal Dominant 60 0.038
1043
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.038
1044
ISL001 Islet Cell Tumor 56 0.038
1045
ART074 Aortic Dissection 52 0.038
1046
BHR001 Behr Syndrome 51 0.038
1047
OPT003 Opiate Dependence 50 0.038
1048
SNT005 Sinoatrial Node Disease 49 0.038
1049
P CHL156 Childhood T-Cell Acute Lymphoblastic Leukemia 38 0.038
1050
c HNT011 Huntington Disease-Like 3 38 0.038
1051
HRN029 Hearing Loss, Noise-Induced 37 0.038
1052
ENP001 Enophthalmos 35 0.038
1053
P GLL018 Gallbladder Cancer 57 0.037
1054
c VSC019 Vesicoureteral Reflux 1 57 0.037
1055
RTN020 Retinal Vascular Disease 46 0.037
1056
KLD004 Keloid Disorder 40 0.037
1057
P WSK001 Wiskott-Aldrich Syndrome 72 0.037
1058
KRT006 Keratoconjunctivitis 53 0.037
1059
CHL018 Childhood Medulloblastoma 49 0.037
1060
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.037
1061
SVR097 Severe Cutaneous Adverse Reaction 69 0.037
1062
c PRM196 Premature Ovarian Failure 1 67 0.037
1063
P HRD011 Hereditary Spherocytosis 60 0.037
1064
CRY005 Cryptococcosis 58 0.037
1065
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.037
1066
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 43 0.037
1067
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.037
1068
CHN016 Cohen Syndrome 63 0.036
1069
P HMC002 Homocystinuria 53 0.036
1070