Search results for Calcium Phosphate

3638 hits were found for Calcium Phosphate

# Family MCID Name MIFTS Score
1
P HYP069 Hyperparathyroidism 62 75.576
2
NPH091 Nephrolithiasis, Calcium Oxalate 61 66.312
3
RCK004 Rickets 68 64.348
4
HYP025 Hyperphosphatemia 48 56.539
5
c CHR684 Chronic Kidney Disease 69 54.232
6
c SCN007 Secondary Hyperparathyroidism 51 51.671
7
BNR002 Bone Resorption Disease 47 50.576
8
GLC009 Glucosephosphate Dehydrogenase Deficiency 53 49.637
9
P OST002 Osteoporosis 76 48.895
10
P KDN018 Kidney Disease 72 48.083
11
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 47.341
12
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 47.341
13
NPH009 Nephrolithiasis 54 47.054
14
PRT037 Pertussis 65 43.426
15
P BND020 Bone Disease 59 43.085
16
c CHN022 Chondrocalcinosis 2 39 41.921
17
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 41.377
18
c PRM005 Primary Hyperparathyroidism 59 41.251
19
P GLC113 Galactosemia I 66 40.696
20
HYP017 Hypophosphatemia 49 40.513
21
URL001 Urolithiasis 46 37.381
22
END086 End Stage Renal Disease 52 36.961
23
OST011 Osteomalacia 52 35.761
24
P HYP024 Hypoparathyroidism 55 35.073
25
FML307 Familial Calcium Pyrophosphate Deposition 38 33.949
26
c HYP595 Hypertension, Essential 85 32.220
27
P CHN059 Chondrocalcinosis 52 28.265
28
RPD005 Rapidly Involuting Congenital Hemangioma 46 27.470
29
NPH003 Nephrocalcinosis 49 26.973
30
ATH013 Atherosclerosis Susceptibility 63 26.936
31
P NRB001 Neuroblastoma 66 26.604
32
HLX001 Helix Syndrome 48 25.653
33
DNT012 Dental Caries 53 24.978
34
MTB004 Metabolic Acidosis 48 24.946
35
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 24.429
36
LPP008 Lipoprotein Quantitative Trait Locus 65 24.399
37
ADN018 Adenoma 59 24.176
38
CLC006 Calcinosis 47 24.089
39
ART140 Arteries, Anomalies of 53 23.369
40
RNL011 Renal Osteodystrophy 49 23.226
41
48X005 48,xyyy 39 22.955
42
AGN016 Aging 54 22.921
43
ISC004 Ischemia 61 22.734
44
c GLY016 Glycogen Storage Disease Ib 40 22.596
45
OST159 Osteogenic Sarcoma 66 22.322
46
URM002 Uremia 47 22.018
47
PRT251 Proteinuria, Chronic Benign 57 22.010
48
c PRC016 Pre-Eclampsia 65 21.703
49
P CRN300 Coronary Heart Disease 1 73 21.615
50
IDP073 Idiopathic Hypercalciuria 40 21.455
51
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 21.248
52
P PRD008 Periodontitis 64 20.745
53
P VSC007 Vascular Disease 63 20.700
54
ANG054 Angina Pectoris 66 20.659
55
HYP266 Hypoxia 57 20.539
56
CHL014 Cholera 62 20.506
57
c TYP009 Type 2 Diabetes Mellitus 92 20.309
58
ANX004 Anoxia 40 20.304
59
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 20.148
60
c ACT071 Acute Kidney Failure 60 20.084
61
HRW001 Hair Whorl 35 20.042
62
FRC011 Fructose Intolerance, Hereditary 55 20.041
63
HYP005 Hypokalemia 55 19.983
64
c GLY060 Glycogen Storage Disease Ia 63 19.976
65
P MSC005 Muscular Dystrophy 67 19.872
66
ALL029 Allergic Disease 59 19.707
67
P DBT009 Diabetes Mellitus 67 19.535
68
LPD008 Lipid Metabolism Disorder 62 19.521
69
P MYP004 Myopathy 67 19.492
70
GLM045 Glioma 63 19.471
71
DFC004 Deficiency Anemia 74 19.444
72
GLL048 Glial Tumor 52 19.309
73
MYL069 Myeloma, Multiple 77 19.196
74
IRN002 Iron Metabolism Disease 57 19.125
75
TTN003 Tetanus 65 19.107
76
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 65 18.920
77
P LKM002 Leukemia 67 18.778
78
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 18.774
79
P CLR023 Colorectal Cancer 100 18.666
80
c ACT027 Acute Pancreatitis 60 18.605
81
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 18.382
82
c HYP836 Hypercholesterolemia, Familial, 1 73 18.306
83
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 18.206
84
HYP056 Hypoglycemia 65 18.033
85
P HML002 Hemolytic Anemia 62 17.991
86
HYP066 Hyperglycemia 61 17.820
87
P HRD086 Hereditary Hypophosphatemic Rickets 40 17.809
88
P PNC044 Pancreatitis 61 17.799
89
47X002 47,xyy 48 17.655
90
PRT029 Parathyroid Adenoma 51 17.646
91
P HRT032 Heart Disease 81 17.645
92
GT001 Gout 64 17.619
93
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 17.562
94
c MCR120 Microvascular Complications of Diabetes 7 47 17.556
95
c GLL024 Gallbladder Disease 1 52 17.445
96
c MCR113 Microvascular Complications of Diabetes 3 52 17.434
97
CNS004 Constipation 56 17.363
98
c ATR087 Atrial Standstill 1 74 17.305
99
P FML068 Familial Hypocalciuric Hypercalcemia 55 17.147
100
P LYM118 Lymphoma 67 17.043
101
c MCR130 Microvascular Complications of Diabetes 6 41 17.017
102
c MCR133 Microvascular Complications of Diabetes 4 41 17.017
103
P ALZ034 Alzheimer Disease 87 17.003
104
P SRC025 Sarcoidosis 1 71 16.953
105
P PRS040 Prostate Cancer 95 16.928
106
P SZR006 Seizure Disorder 70 16.885
107
OST017 Osteomyelitis 63 16.639
108
OST012 Osteoarthritis 77 16.572
109
P HYP076 Hyperthyroidism 53 16.570
110
CNG034 Congestive Heart Failure 69 16.548
111
P LTR001 Lateral Sclerosis 58 16.375
112
c AMY091 Amyotrophic Lateral Sclerosis 1 88 16.344
113
P HYP086 Hypothyroidism 69 16.293
114
THY029 Thyroid Carcinoma 51 16.095
115
P CRD119 Cardiac Arrest 67 16.020
116
P PHC003 Pheochromocytoma 69 15.848
117
ADR040 Adrenal Gland Pheochromocytoma 46 15.833
118
P ACN011 Acne 57 15.810
119
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 15.775
120
P HYP726 Hypercalcemia, Infantile, 1 58 15.707
121
P ART022 Arthritis 71 15.703
122
P BRS047 Breast Cancer 98 15.698
123
CYS001 Cystic Fibrosis 78 15.586
124
P ART021 Arteriosclerosis 54 15.574
125
P PSD015 Pseudohypoparathyroidism 55 15.569
126
INS001 Insulinoma 59 15.511
127
KRT002 Keratomalacia 55 15.468
128
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 15.442
129
CYT002 Cytokine Deficiency 43 15.432
130
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 15.415
131
INS024 Insulin-Like Growth Factor I 78 15.413
132
P CTR002 Cataract 60 15.388
133
P PLM037 Pulmonary Hypertension 72 15.341
134
MLR004 Malaria 80 15.326
135
P ECL001 Eclampsia 52 15.220
136
P URN019 Urinary Tract Infection 49 15.106
137
P NRP001 Neuropathy 60 15.066
138
HMN044 Human Immunodeficiency Virus Type 1 78 14.935
139
NTR005 Nutritional Deficiency Disease 61 14.902
140
FTT001 Fatty Liver Disease 62 14.891
141
BLR008 Bilirubin Metabolic Disorder 57 14.855
142
P LKM062 Leukemia, Acute Lymphoblastic 69 14.805
143
P ADN016 Adenocarcinoma 63 14.694
144
P ENC018 Encephalopathy 62 14.688
145
NNL005 Non-Alcoholic Fatty Liver Disease 63 14.682
146
c DLT002 Dilated Cardiomyopathy 78 14.645
147
P EPL164 Epilepsy 68 14.547
148
P MLT020 Multiple Sclerosis 79 14.543
149
P THL005 Thalassemia 56 14.478
150
P RNL007 Renal Tubular Acidosis 50 14.469
151
CLC001 Calciphylaxis 51 14.446
152
GLB002 Glioblastoma 67 14.425
153
MSC157 Muscular Dystrophy, Duchenne Type 79 14.412
154
P MYC007 Myocardial Infarction 70 14.388
155
P ART023 Arthropathy 61 14.378
156
P RHM011 Rheumatoid Arthritis 82 14.375
157
SPN186 Spinal Cord Injury 61 14.281
158
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 14.264
159
P OVR042 Ovarian Cancer 88 14.219
160
P PSR002 Psoriasis 63 14.194
161
P MLG056 Malignant Hyperthermia 66 14.097
162
P GLM040 Glioma Susceptibility 1 71 14.057
163
P PRP019 Peripheral Nervous System Disease 58 14.001
164
P DRR001 Diarrhea 55 13.970
165
HYP060 Hyperinsulinism 54 13.968
166
P BPL003 Bipolar Disorder 56 13.914
167
P BCL017 B-Cell Lymphoma 59 13.876
168
c MJR022 Major Affective Disorder 8 38 13.861
169
c MJR024 Major Affective Disorder 9 41 13.861
170
PRT036 Peritonitis 65 13.805
171
LYM019 Lymphosarcoma 46 13.789
172
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 13.769
173
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 13.769
174
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 13.769
175
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 13.769
176
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 13.769
177
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 13.769
178
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 13.769
179
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 13.769
180
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 13.769
181
PST011 Pustulosis of Palm and Sole 52 13.761
182
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 13.742
183
CRB004 Cerebral Artery Occlusion 45 13.716
184
CRB039 Cerebrovascular Disease 66 13.647
185
PLY150 Polykaryocytosis Inducer 29 13.594
186
STR067 Stroke, Ischemic 80 13.578
187
CLS031 Classic Galactosemia and Clinical Variant Galactosemia 18 13.567
188
LMB002 Lambert-Eaton Myasthenic Syndrome 52 13.498
189
PPL052 Papillomatosis, Confluent and Reticulated 34 13.464
190
c MGR028 Migraine with or Without Aura 1 64 13.400
191
c MCR115 Microvascular Complications of Diabetes 5 65 13.337
192
BRN071 Brain Injury 50 13.309
193
TRM010 Traumatic Brain Injury 51 13.297
194
P INF037 Inflammatory Bowel Disease 53 13.286
195
P LKM071 Leukemia, Chronic Lymphocytic 75 13.276
196
P PLY014 Polycystic Kidney Disease 69 13.239
197
MMM001 Mammary Paget's Disease 53 13.233
198
ONC003 Oncogenic Osteomalacia 42 13.173
199
BNN003 Bone Inflammation Disease 48 13.153
200
P HYP733 Hypercalciuria, Absorptive, 2 45 13.152
201
SKN016 Skin Disease 63 13.147
202
LVR012 Liver Cirrhosis 63 13.134
203
CRN030 Coronary Stenosis 50 13.024
204
ATM095 Autoimmune Disease 61 13.004
205
IMM167 Immune Deficiency Disease 78 12.996
206
P PRM002 Primary Hyperoxaluria 65 12.973
207
RNL114 Renal Cell Carcinoma, Nonpapillary 80 12.970
208
c ACT075 Acute Myocardial Infarction 56 12.950
209
P HYP061 Hypertrophic Cardiomyopathy 69 12.946
210
c LKM061 Leukemia, Acute Myeloid 83 12.939
211
BCT022 Bacterial Infectious Disease 56 12.822
212
P PNC035 Pancreatic Cancer 86 12.797
213
TXC005 Toxic Shock Syndrome 62 12.794
214
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 12.781
215
OST003 Osteonecrosis 61 12.765
216
P ATR011 Atrial Fibrillation 66 12.719
217
P GLM007 Glomerulonephritis 60 12.652
218
PRP027 Peripheral Vascular Disease 71 12.612
219
P CHR345 Chronic Pain 50 12.552
220
MLG169 Malignant Astrocytoma 57 12.539
221
DWN001 Down Syndrome 70 12.521
222
P FNC004 Fanconi Syndrome 60 12.493
223
CRH001 Crohn's Disease 80 12.429
224
P NPH012 Nephrotic Syndrome 60 12.347
225
P LNG032 Lung Cancer 98 12.301
226
INT007 Intermediate Coronary Syndrome 54 12.282
227
P MYL006 Myeloid Leukemia 61 12.223
228
P HNT016 Huntington Disease 73 12.211
229
P LVR013 Liver Disease 69 12.194
230
P MYC084 Mycobacterium Tuberculosis 1 68 12.164
231
P OVR082 Overgrowth Syndrome 49 12.136
232
ALC007 Alcohol Dependence 66 12.113
233
P HPT023 Hepatocellular Carcinoma 96 12.106
234
P HPT021 Hepatitis 69 12.053
235
P SCK005 Sickle Cell Disease 56 11.967
236
P INF032 Infertility 57 11.908
237
P RSP003 Respiratory Failure 74 11.905
238
ATS010 Autosomal Recessive Disease 42 11.892
239
STM007 Stomatitis 54 11.860
240
P GLY013 Glycogen Storage Disease 60 11.860
241
PNG002 Pain Agnosia 51 11.840
242
HYP014 Hyperuricemia 51 11.823
243
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 53 11.810
244
CLT003 Colitis 63 11.792
245
CLR108 Colorectal Adenoma 64 11.753
246
HYP789 Hypophosphatemic Rickets with Hypercalciuria, Hereditary 49 11.744
247
OST004 Osteitis Fibrosa 38 11.742
248
GLC003 Glucose Intolerance 54 11.660
249
CRD132 Cardiac Conduction Defect 60 11.634
250
CLN015 Colon Adenocarcinoma 65 11.612
251
P MLN008 Melanoma 76 11.553
252
P TMR018 Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 60 11.509
253
c TYP008 Type 1 Diabetes Mellitus 70 11.447
254
c SYS001 Systemic Lupus Erythematosus 87 11.436
255
P MSC003 Muscular Atrophy 52 11.339
256
ULC004 Ulcerative Colitis 74 11.310
257
P HRP006 Herpes Simplex 65 11.279
258
P LPS004 Lupus Erythematosus 61 11.268
259
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 11.201
260
GTR002 Goiter 53 11.200
261
P PRK039 Parkinsonism 55 11.156
262
P DRM053 Dermatitis, Atopic 65 11.140
263
PRT010 Parathyroid Carcinoma 68 11.140
264
c PLM164 Pulmonary Hypertension, Primary, 1 76 11.083
265
c SCL052 Scleroderma, Familial Progressive 61 11.066
266
OCL069 Ocular Motor Apraxia 57 11.054
267
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 11.022
268
MNT002 Mental Depression 57 11.001
269
P TRM003 Tremor 48 10.968
270
SVR004 Severe Combined Immunodeficiency 72 10.936
271
STT001 Status Epilepticus 59 10.935
272
HMP009 Haemophilus Influenzae 41 10.892
273
SCK003 Sickle Cell Anemia 74 10.875
274
HMS001 Hemosiderosis 48 10.875
275
NNT012 Neonatal Jaundice 53 10.780
276
SCN001 Secondary Hyperparathyroidism of Renal Origin 24 10.743
277
P GST053 Gastric Cancer 83 10.688
278
LNG099 Lung Disease 62 10.654
279
IMP005 Impotence 52 10.651
280
P RRH023 Rare Hereditary Hemochromatosis 54 10.635
281
P SYS005 Systemic Scleroderma 74 10.586
282
ACQ007 Acquired Immunodeficiency Syndrome 59 10.567
283
P THR014 Thrombocytopenia 66 10.557
284
PRS021 Prostatic Adenoma 43 10.534
285
ALL014 Allergic Encephalomyelitis 34 10.532
286
DPH001 Diphtheria 59 10.518
287
P NTR004 Neutropenia 63 10.496
288
RTR008 Root Resorption 44 10.453
289
ATR057 Atrioventricular Block 54 10.443
290
P PNM007 Pneumonia 67 10.430
291
DPR016 Depression 65 10.430
292
PRS045 Prostatic Hypertrophy 53 10.400
293
CRD223 Cardiac Arrhythmia 63 10.384
294
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 10.369
295
SQM006 Squamous Cell Carcinoma 60 10.363
296
P LCT001 Lactic Acidosis 51 10.359
297
HYP080 Hypogonadism 50 10.353
298
CHL068 Cholestasis 61 10.350
299
P INF038 Influenza 68 10.337
300
P HYP035 Hypophosphatasia 62 10.330
301
PLM129 Pulmonary Disease, Chronic Obstructive 74 10.307
302
MCS002 Mucositis 56 10.301
303
PRS129 Prostatic Hyperplasia, Benign 49 10.292
304
c ACT068 Acute Cystitis 61 10.288
305
c LKM063 Leukemia, Chronic Myeloid 71 10.250
306
P ALC033 Alcohol Use Disorder 61 10.246
307
P TRN020 Turner Syndrome 67 10.182
308
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 10.176
309
P DST107 Distal Renal Tubular Acidosis 48 10.140
310
LYM133 Lymphoma, Hodgkin, Classic 74 10.131
311
PST092 Posttransplant Acute Limbic Encephalitis 28 10.120
312
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 10.078
313
P HYP265 Hypotonia 42 10.071
314
c DNT047 Dentinogenesis Imperfecta Type 2 35 10.070
315
P RHN004 Rhinitis 57 10.069
316
c HYP794 Hyperoxaluria, Primary, Type I 63 10.065
317
PTT037 Pituitary Tumors 44 10.031
318
DSS032 Disease by Infectious Agent 55 10.005
319
ESP021 Esophageal Cancer 83 10.002
320
AML006 Amelogenesis Imperfecta Hypoplastic Type, Ig 21 9.934
321
P AST005 Asthma 76 9.913
322
P BLD134 Bladder Cancer 79 9.876
323
P PGT001 Paget's Disease of Bone 61 9.876
325
P MLT074 Multiple Endocrine Neoplasia 59 9.802
326
c BRN108 Branchiootic Syndrome 1 62 9.773
327
P MLN007 Male Infertility 56 9.772
328
c ATS007 Autism Spectrum Disorder 72 9.760
329
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 9.697
330
P GRV001 Graves' Disease 55 9.643
331
LYM027 Lymphopenia 56 9.618
332
P PLY011 Polycystic Ovary Syndrome 57 9.605
333
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 9.602
334
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 9.587
335
ACR007 Acromegaly 70 9.586
336
P SCL018 Scoliosis 57 9.576
337
PRS047 Prostatitis 58 9.559
338
LYM143 Lymphoma, Non-Hodgkin, Familial 75 9.543
339
MYC005 Myocardial Stunning 46 9.528
340
IRR002 Irritable Bowel Syndrome 65 9.527
341
c LKM005 Leukemia, T-Cell, Chronic 34 9.519
342
c HPT016 Hepatitis B 62 9.492
343
P GRF003 Graft-Versus-Host Disease 71 9.469
344
P HYP750 Hypertriglyceridemia, Familial 62 9.448
345
P PRK057 Parkinson Disease, Late-Onset 80 9.445
346
TND005 Tendinitis 54 9.430
347
P ALP008 Alopecia 54 9.410
348
PPT005 Peptic Ulcer Disease 58 9.397
349
PLM017 Pulmonary Alveolar Microlithiasis 47 9.388
350
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 9.372
351
MYL009 Myelodysplastic Syndrome 67 9.367
352
P AMY004 Amyloidosis 70 9.364
353
LPT014 Leptin Deficiency or Dysfunction 78 9.331
354
c HPT003 Hepatitis a 63 9.322
355
PLM010 Pulmonary Edema 55 9.259
356
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 9.252
357
P TXP001 Toxoplasmosis 60 9.241
358
P KLZ004 Kala-Azar 1 41 9.220
359
LSH001 Leishmaniasis 64 9.220
360
c ART115 Aortic Valve Disease 1 74 9.190
361
P CHR012 Chronic Granulomatous Disease 69 9.190
362
GLC086 Glucocorticoid-Induced Osteoporosis 43 9.176
363
P CRD246 Cardiovascular System Disease 56 9.167
364
DRM006 Dermatitis 62 9.145
365
RLP002 Relapsing-Remitting Multiple Sclerosis 56 9.143
366
P SCH015 Schizophrenia 74 9.140
367
P PLM036 Pulmonary Fibrosis 66 9.069
368
P KDN017 Kidney Cancer 61 9.069
369
P CLC063 Celiac Disease 1 66 9.061
370
SRC014 Sarcoma 65 9.049
371
P THY032 Thyroiditis 57 9.032
372
c ACT073 Acute Leukemia 58 9.026
373
c INH020 Inherited Metabolic Disorder 48 9.020
374
P LCT002 Lactose Intolerance 52 9.004
375
P END044 Endometriosis 62 8.999
376
PLC002 Plica Syndrome 35 8.992
377
SYN007 Synovitis 55 8.992
378
BRT054 Brittle Bone Disorder 74 8.984
379
ANK001 Ankylosis 51 8.957
380
CNN003 Conn's Syndrome 79 8.948
381
P PSD087 Pseudoxanthoma Elasticum 67 8.921
382
P RCT021 Rectum Cancer 54 8.907
383
P LNG064 Lung Cancer Susceptibility 3 70 8.903
384
c PRD040 Periodontitis, Chronic 52 8.887
385
SPN035 Spindle Cell Sarcoma 54 8.881
386
P ANR048 Aniridia 1 64 8.880
387
INT323 Intraocular Pressure Quantitative Trait Locus 64 8.872
388
P MYS003 Myasthenia Gravis 68 8.867
389
CHG001 Chagas Disease 66 8.863
390
P MYC008 Myocarditis 59 8.863
391
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 8.827
392
P HYP776 Hyperparathyroidism, Neonatal Severe 46 8.818
393
P ADL010 Adult Respiratory Distress Syndrome 71 8.776
394
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 8.761
395
P ATS364 Autism 69 8.748
396
P UVT001 Uveitis 57 8.735
397
PYR009 Pyridoxine Deficiency Anemia 35 8.725
398
c SML038 Small Cell Cancer of the Lung 69 8.714
399
c ART101 Aortic Valve Disease 2 66 8.670
400
ART016 Aortic Aneurysm 68 8.668
401
ALL003 Allergic Rhinitis 67 8.667
402
c GRV008 Graves Disease 1 54 8.644
403
RYN005 Raynaud Phenomenon 45 8.627
404
P FBR017 Fibrosarcoma 56 8.591
405
END057 Endometrial Cancer 72 8.582
406
c HPT001 Hepatitis C 62 8.577
407
c PCH010 Pachyonychia Congenita 3 43 8.533
408
P DDN001 Duodenal Ulcer 53 8.531
409
P ENC004 Encephalitis 61 8.474
410
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 8.473
411
DBT084 Diabetes Mellitus, Ketosis-Prone 60 8.453
412
P CNJ013 Conjunctivitis 66 8.452
413
DNT006 Dental Pulp Necrosis 43 8.440
414
ANR007 Anorexia Nervosa 60 8.419
415
THY111 Thyroid Carcinoma, Familial Medullary 67 8.418
416
BRN004 Brain Edema 54 8.386
417
BRK010 Burkitt Lymphoma 66 8.383
418
SYN036 Syncope 45 8.374
419
HMC014 Homocysteinemia 52 8.340
420
P DNT020 Dent Disease 1 63 8.337
421
CVD001 Covid-19 57 8.309
422
P SKN015 Skin Carcinoma 71 8.270
423
PRM020 Premenstrual Tension 39 8.244
424
SVR001 Severe Acute Respiratory Syndrome 67 8.227
425
P ANP001 Anaplastic Large Cell Lymphoma 61 8.212
426
VCC001 Vaccinia 47 8.185
427
MDD011 Mood Disorder 62 8.178
428
P BSL038 Basal Ganglia Calcification, Idiopathic, 1 53 8.137
429
ADL002 Adult Syndrome 70 8.128
430
RHB024 Rhabdomyosarcoma 2 67 8.120
431
c BTT014 Beta-Thalassemia 72 8.103
432
c PSD108 Pseudohypoparathyroidism, Type Ia 65 8.090
433
P EYD002 Eye Disease 57 8.078
434
PRP080 Peripheral Artery Disease 54 8.064
435
P ESP024 Esophagitis 60 8.058
436
ACT098 Acute Erythroid Leukemia 55 8.040
437
MSC007 Muscle Hypertrophy 64 8.037
438
P HDC001 Headache 57 8.036
439
P FML187 Familial Hypertension 34 8.035
440
P PLY019 Polyneuropathy 52 8.034
441
ANR040 Aneurysm 61 8.013
442
THY125 Thyroid Gland Medullary Carcinoma 48 7.999
443
P EXN002 Exanthem 58 7.997
444
P DMN002 Dementia 66 7.982
445
P LNG028 Long Qt Syndrome 64 7.968
446
c MCL062 Mucolipidosis Ii Alpha/beta 68 7.945
447
ENM002 Enamel Erosion 25 7.932
448
P GST044 Gastritis 55 7.924
449
P OST001 Osteopetrosis 71 7.901
450
ENM001 Enamel Caries 27 7.898
451
P ADL017 Adult T-Cell Leukemia 56 7.892
452
GST092 Gastroesophageal Reflux 61 7.874
453
P DRM010 Dermatomyositis 61 7.858
454
P BRT004 Bartter Disease 58 7.825
455
NRL016 Neural Tube Defects 81 7.818
456
ZLL002 Zollinger-Ellison Syndrome 55 7.815
457
DYS073 Dysphagia 53 7.801
458
TRN015 Transient Cerebral Ischemia 63 7.793
459
LWC002 Lowe Oculocerebrorenal Syndrome 68 7.791
460
NRR001 Neuroretinitis 42 7.781
461
RTN023 Retinitis 46 7.773
462
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 7.767
463
P MJR001 Major Depressive Disorder 68 7.761
464
P RTN016 Retinal Degeneration 52 7.757
465
THR024 Thrombosis 56 7.741
466
P RTN024 Retinoblastoma 73 7.722
467
IRN001 Iron Deficiency Anemia 58 7.716
468
P HYP098 Hypereosinophilic Syndrome 66 7.693
469
CHL004 Cholelithiasis 49 7.670
470
KRT019 Keratitis, Hereditary 66 7.667
471
P PRD021 Periodic Paralysis 41 7.655
472
HGH043 High Grade Glioma 45 7.652
473
CHL123 Chlamydia 58 7.651
474
PLM001 Pulmonary Tuberculosis 69 7.644
475
c MLT156 Multiple Endocrine Neoplasia, Type I 72 7.640
476
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 7.622
477
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 7.620
478
SCH014 Schistosomiasis 56 7.620
479
IDP085 Idiopathic Infantile Hypercalcemia 32 7.620
480
AMN001 Amenorrhea 54 7.594
481
c HYP752 Hypocalciuric Hypercalcemia, Familial, Type I 46 7.575
482
TLN003 Telangiectasis 51 7.566
483
c HPT073 Hepatitis C Virus 71 7.562
484
MST005 Mastitis 53 7.560
485
P PLY018 Polycythemia 56 7.552
486
CRY024 Crystal Arthropathies 18 7.548
487
NRM005 Neuromuscular Disease 63 7.544
488
BCK006 Back Pain 47 7.541
489
HRT012 Heart Valve Disease 53 7.527
491
PRP016 Paraplegia 52 7.503
492
PLP001 Pulpitis 48 7.485
493
SPL018 Splenomegaly 49 7.484
494
P CYS018 Cystitis 59 7.481
495
LYM040 Lymphoblastic Lymphoma 53 7.470
496
c HYP243 Hyperparathyroidism 1 47 7.430
497
P TMP001 Temporal Lobe Epilepsy 49 7.421
498
DBT010 Diabetic Neuropathy 54 7.409
499
CNN005 Connective Tissue Disease 67 7.402
500
LYS002 Lysosomal Storage Disease 51 7.394
501
P VSC011 Vasculitis 61 7.389
502
AMN006 Aminoaciduria 37 7.384
503
WTH001 Withdrawal Disorder 48 7.380
504
SLP001 Sleeping Sickness 56 7.372
505
CYS013 Cystinuria 66 7.363
506
HYP057 Hypervitaminosis D 37 7.362
507
P PYL005 Pyelonephritis 57 7.342
508
OTT002 Otitis Media 71 7.331
509
BSL009 Basal Ganglia Calcification 45 7.311
510
FBR009 Fibrous Dysplasia 48 7.305
511
MRF001 Marfan Syndrome 76 7.301
512
CHL065 Cholangiocarcinoma 58 7.288
513
INT079 Intrahepatic Cholangiocarcinoma 51 7.288
514
HPT004 Hepatic Coma 43 7.265
515
P MYT002 Myotonic Dystrophy 51 7.263
516
SPN051 Spondylitis 51 7.253
517
ALL006 Allergic Asthma 56 7.251
518
THY030 Thyroid Gland Disease 50 7.235
519
CRD137 Cardiogenic Shock 56 7.233
520
P MTR014 Motor Neuron Disease 65 7.227
521
GNG012 Gingival Overgrowth 49 7.225
522
ENT004 Enthesopathy 51 7.223
523
MYL005 Myelofibrosis 71 7.212
524
P DYS154 Dystonia 64 7.199
525
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 7.191
526
P SLP006 Sleep Apnea 69 7.188
527
BRN024 Bronchitis 67 7.184
528
PPL022 Papilloma 53 7.152
529
GST045 Gastroenteritis 58 7.149
530
HMN014 Human Immunodeficiency Virus Infectious Disease 54 7.143
531
LMB062 Limb Ischemia 55 7.140
532
PNC129 Pancreatic Adenocarcinoma 65 7.127
533
PRP030 Purpura 54 7.123
534
c THR092 Thrombophilia Due to Thrombin Defect 74 7.120
535
ARG004 Argyria 26 7.115
536
P SJG008 Sjogren Syndrome 61 7.107
537
DGN001 Degenerative Disc Disease 49 7.095
538
c VRL010 Viral Hepatitis 53 7.089
539
CRB037 Cerebral Palsy 67 7.082
540
PRM329 Premature Aging 36 7.070
541
VSC002 Vascular Dementia 60 7.060
542
HPT019 Hepatic Encephalopathy 59 7.016
543
URT010 Ureteral Obstruction 45 7.009
544
c SPN225 Spondyloarthropathy 1 70 7.003
545
c THY107 Thymoma, Familial 42 6.966
546
P THY023 Thymoma 64 6.966
547
PLS009 Plasma Cell Neoplasm 64 6.958
548
P CND004 Candidiasis 58 6.945
549
INT067 Interstitial Nephritis 46 6.930
550
P BRS044 Breast Adenocarcinoma 58 6.896
551
P SNS001 Sensorineural Hearing Loss 59 6.895
552
P BRG001 Brugada Syndrome 69 6.873
553
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 6.872
554
HYD002 Hydronephrosis 58 6.845
555
RNL077 Renal Fibrosis 46 6.804
556
FBR047 Fibromyalgia 58 6.801
557
INF009 Inflammatory Spondylopathy 30 6.792
558
c SVR005 Severe Pre-Eclampsia 50 6.788
559
FML091 Familial Tumoral Calcinosis 43 6.787
560
CRV035 Cervical Cancer 73 6.779
561
P BNC003 Bone Cancer 58 6.777
562
P KRN004 Kernicterus 46 6.774
563
P RHB003 Rhabdomyosarcoma 66 6.771
564
OVR094 Ovarian Epithelial Cancer 39 6.747
565
c JVN010 Juvenile Rheumatoid Arthritis 66 6.746
566
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 6.740
567
CLC004 Calcific Tendinitis 33 6.702
568
DFF005 Diffuse Large B-Cell Lymphoma 54 6.701
569
URN010 Urinary Tract Obstruction 55 6.682
570
CHR074 Choriocarcinoma 46 6.649
571
HDN002 Head Injury 44 6.636
572
GNG013 Gingivitis 59 6.621
573
P RNV001 Renovascular Hypertension 49 6.619
574
ANT024 Anthrax Disease 58 6.605
575
P MYS005 Myositis 56 6.591
576
CRT015 Carotid Artery Occlusion 45 6.584
577
KRT008 Keratopathy 46 6.581
578
ACT003 Acute Kidney Tubular Necrosis 46 6.574
579
HYP020 Hyperprolactinemia 63 6.569
580
P CNR004 Cone-Rod Dystrophy 2 74 6.560
581
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 6.556
582
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 6.556
583
RTC003 Root Caries 32 6.551
584
MYL031 Myeloproliferative Neoplasm 66 6.548
585
GST033 Gestational Diabetes 61 6.543
586
CNT047 Contact Dermatitis 57 6.531
587
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 6.527
588
CMB007 Combined Immunodeficiency 57 6.524
589
SBC016 Subacute Delirium 43 6.504
590
GNG003 Gingival Recession 49 6.504
591
P HMP007 Hemophilia 52 6.486
592
IDP070 Idiopathic Scoliosis 42 6.482
593
P VTM027 Vitamin D-Dependent Rickets, Type 2a 53 6.471
594
P RTN018 Retinal Disease 53 6.465
595
P GCH001 Gaucher's Disease 70 6.465
596
c DWL002 Dowling-Degos Disease 1 58 6.446
597
P ASP006 Aspergillosis 72 6.422
598
ANX010 Anxiety 70 6.420
599
SQM002 Squamous Cell Papilloma 46 6.409
600
MTH071 Methane Production 25 6.407
601
CRB090 Cerebral Hypoxia 42 6.404
602
P TRC031 Trichorhinophalangeal Syndrome 38 6.397
603
c BLD140 Blood Group, I System 46 6.397
604
P MCL001 Mucolipidosis 49 6.397
605
OST115 Osteonecrosis of the Jaw 41 6.396
606
HMG002 Hemoglobinuria 50 6.384
607
P CYS039 Cystic Kidney Disease 53 6.377
608
SYS003 Systolic Heart Failure 49 6.372
609
MNT001 Mantle Cell Lymphoma 67 6.355
610
MDL009 Medullary Sponge Kidney 39 6.338
611
P BRB001 Beriberi 44 6.337
612
P OPN001 Open-Angle Glaucoma 55 6.337
613
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 6.306
614
NNL006 Non-Alcoholic Steatohepatitis 54 6.284
615
HNS001 Hansen's Disease 32 6.284
616
ANT039 Antisynthetase Syndrome 55 6.276
617
GST050 Gastrointestinal System Disease 55 6.276
618
ENT011 Enterocolitis 55 6.265
619
c CRN243 Carney Complex, Type 1 53 6.257
620
PRM236 Primary Biliary Cholangitis 60 6.255
621
PRT013 Portal Hypertension 59 6.243
622
P LPR021 Leprosy 3 71 6.233
623
PLM033 Pulmonary Embolism 58 6.210
624
PLM031 Poliomyelitis 63 6.207
625
WLL004 Wallerian Degeneration 38 6.200
626
PRS063 Paresthesia 39 6.194
627
c HMC039 Hemochromatosis, Type 1 73 6.187
628
CHL067 Cholecystitis 60 6.185
629
P NSP012 Nasopharyngeal Carcinoma 61 6.178
630
PRR001 Periarthritis 34 6.164
631
GST030 Gastrinoma 45 6.153
632
P DBT005 Diabetes Insipidus 54 6.129
633
P CHN012 Chondrosarcoma 57 6.127
634
P ATX030 Ataxia-Telangiectasia 80 6.125
635
VLK001 Volkmann Contracture 23 6.109
636
c FML021 Familial Hypercholesterolemia 72 6.098
637
MCC012 Mccune-Albright Syndrome 70 6.081
638
SPT004 Septic Arthritis 58 6.056
639
PHN003 Phenylketonuria 76 6.052
640
P EPS003 Episodic Ataxia 59 6.047
641
P SHR001 Short Bowel Syndrome 53 6.045
642
P HMC002 Homocystinuria 53 6.043
643
PLS007 Plasmodium Falciparum Malaria 52 6.043
644
ILS001 Ileus 50 6.040
645
P TRT010 Teratoma 51 6.035
646
c ACT134 Acute Liver Failure 59 6.031
647
CRN019 Coronary Artery Vasospasm 47 6.030
648
P HRD011 Hereditary Spherocytosis 64 6.020
649
CMM004 Common Variable Immunodeficiency 72 6.015
650
GRW007 Growth Hormone Deficiency 46 6.012
651
TRD006 Tardive Dyskinesia 53 6.002
652
c PRG042 Progressive Familial Heart Block, Type Ia 66 5.989
653
P MYC033 Myoclonus 47 5.974
654
P MYP006 Myopia 56 5.960
655
c PNS012 Paine Syndrome 60 5.949
656
GTL001 Gitelman Syndrome 65 5.944
657
PLG002 Plague 58 5.938
658
CRT013 Carotid Stenosis 51 5.919
659
MYT011 Myotonia 39 5.917
660
ETN001 Eating Disorder 59 5.916
661
GST023 Gastric Ulcer 52 5.913
662
P MDL005 Medulloblastoma 75 5.911
663
P SML001 Small Cell Carcinoma 52 5.904
664
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 5.901
665
MCR004 Macroglobulinemia 49 5.898
666
P HYD006 Hydrocephalus 61 5.891
667
P MCR129 Microvascular Complications of Diabetes 1 68 5.886
668
EMB004 Embryonal Carcinoma 56 5.886
669
PTH003 Pathologic Nystagmus 52 5.885
670
SPS057 Spasticity 42 5.879
671
P RTN008 Retinitis Pigmentosa 80 5.872
672
TRY001 Trypanosomiasis 50 5.844
673
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 5.843
674
VSC003 Visceral Leishmaniasis 55 5.839
675
BRN056 Bronchopulmonary Dysplasia 56 5.828
676
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 5.819
677
P NRF002 Neurofibromatosis 57 5.818
678
HMG005 Hemoglobinopathy 56 5.807
679
P INT143 Interstitial Cystitis 60 5.798
680
P MVM001 Movement Disease 61 5.790
681
VTM033 Vitamin K Deficiency Bleeding 48 5.789
682
KLD004 Keloid Disorder 39 5.788
683
P END033 Endocarditis 58 5.778
684
PLY001 Polycythemia Vera 69 5.772
685
P PMP001 Pemphigus 55 5.769
686
P OPT006 Optic Nerve Disease 58 5.765
687
HYP068 Hyperostosis 47 5.761
688
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 5.759
689
P AVS003 Avascular Necrosis 41 5.756
690
P SPP010 Suppressor of Tumorigenicity 3 51 5.749
691
WLL001 Williams-Beuren Syndrome 61 5.749
692
P INS002 in Situ Carcinoma 53 5.748
693
P NMN002 Niemann-Pick Disease 60 5.742
694
P PTT006 Pituitary Adenoma 55 5.716
695
P SCL048 Sclerosteosis 58 5.706
696
END040 Endogenous Depression 55 5.699
697
P ATT013 Attention Deficit-Hyperactivity Disorder 64 5.682
698
P CRP001 Carpal Tunnel Syndrome 66 5.678
699
P ESS003 Essential Thrombocythemia 69 5.666
700
c EPS035 Episodic Ataxia, Type 2 63 5.654
701
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 5.638
702
FDL002 Food Allergy 47 5.637
703
P NRV007 Nervous System Disease 67 5.635
704
LWC001 Low Compliance Bladder 45 5.632
705
PNC041 Pancreatic Ductal Adenocarcinoma 51 5.632
706
P RNL015 Renal Hypertension 45 5.627
707
ORL015 Oral Squamous Cell Carcinoma 43 5.627
708
P INT068 Intestinal Disease 53 5.625
709
RST023 Resting Heart Rate, Variation in 40 5.611
710
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 5.606
711
TRN018 Transitional Cell Carcinoma 56 5.604
712
DYS015 Dysentery 50 5.597
713
DMY004 Demyelinating Disease 50 5.590
714
PRT030 Parathyroid Gland Disease 45 5.575
715
DSS009 Disseminated Intravascular Coagulation 57 5.574
716
IRD001 Iridocyclitis 53 5.567
717
CNT105 Central Core Disease of Muscle 59 5.543
718
P SCL057 Scoliosis, Isolated 1 40 5.541
719
P FLL037 Follicular Lymphoma 74 5.532
720
BRN028 Brain Cancer 74 5.532
721
c THY109 Thyroid Cancer, Nonmedullary, 1 55 5.527
722
SQM013 Squamous Cell Carcinoma, Head and Neck 73 5.527
723
GST040 Gastric Adenocarcinoma 67 5.515
724
c PRS136 Prostate Cancer, Hereditary, 6 33 5.508
725
c PRS130 Prostate Cancer, Hereditary, 8 32 5.508
726
KRT009 Keratosis 53 5.507
727
PRM013 Premature Menopause 58 5.493
728
RTN020 Retinal Vascular Disease 46 5.485
729
MTR002 Mitral Valve Insufficiency 52 5.484
730
P DNG005 Dengue Virus 56 5.480
731
P URT039 Urticaria 58 5.477
732
P HMN010 Hemangioma 62 5.474
733
P FCL005 Focal Segmental Glomerulosclerosis 57 5.466
734
P PRN023 Prion Disease 60 5.465
735
c CHR064 Chronic Monocytic Leukemia 36 5.463
736
P MTH007 Methemoglobinemia 46 5.462
737
HMT002 Hematologic Cancer 61 5.462
738
c MCR112 Microvascular Complications of Diabetes 2 42 5.458
739
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 5.450
740
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 5.427
741
DWR001 Dwarfism 44 5.426
742
NWC001 Newcastle Disease 47 5.419
743
SKN019 Skin Melanoma 71 5.414
744
IGG001 Iga Glomerulonephritis 50 5.414
745
PYR016 Pyridoxine Deficiency 29 5.412
746
NPH010 Nephrosclerosis 50 5.399
747
EWN003 Ewing Sarcoma 70 5.397
748
ART002 Arts Syndrome 66 5.396
749
SNS003 Sensory Peripheral Neuropathy 52 5.388
750
CHR178 Chromosomal Triplication 34 5.388
751
PLS011 Plasmacytoma 56 5.385
752
SFT003 Soft Tissue Sarcoma 57 5.379
753
CYS010 Cystinosis 62 5.371
754
GLM044 Glomerular Disease 35 5.363
755
AMN003 Amnestic Disorder 54 5.361
756
P CNT004 Centronuclear Myopathy 57 5.340
757
FRZ001 Frozen Shoulder 55 5.339
758
MTH009 Mouth Disease 57 5.307
759
PSR001 Psoriatic Arthritis 62 5.301
760
MNN043 Meningioma, Familial 79 5.297
761
SPN027 Spinal Stenosis 59 5.291
762
CLR030 Clear Cell Renal Cell Carcinoma 54 5.290
763
INT066 Interstitial Lung Disease 60 5.284
764
MLG086 Malignant Hyperthermia Susceptibility 39 5.271
765
P SLP005 Sleep Disorder 61 5.265
766
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 5.257
767
BNM001 Bone Marrow Cancer 46 5.249
768
SCR001 Secretory Meningioma 40 5.248
769
LYM002 Lymphoplasmacyte-Rich Meningioma 35 5.248
770
SPN021 Spinal Meningioma 50 5.248
771
PRT058 Pure Autonomic Failure 58 5.247
772
P FRG001 Fragile X Syndrome 70 5.246
773
MDD018 Middle East Respiratory Syndrome 44 5.241
774
CLR109 Colorectal Adenocarcinoma 50 5.233
775
BRS064 Bursitis 51 5.229
776
ORL011 Oral Cancer 60 5.225
777
KPS004 Kaposi Sarcoma 77 5.224
778
OVR029 Ovarian Hyperstimulation Syndrome 63 5.220
779
INT002 Intermittent Claudication 61 5.219
780
OCL006 Ocular Hypertension 53 5.217
781
P BNG032 Benign Mesothelioma 53 5.214
782
THR004 Thrombocytosis 53 5.207
783
DNT001 Dental Fluorosis 43 5.200
784
MLD018 Mild Cognitive Impairment 48 5.196
785
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 5.191
786
MST004 Mast Cell Neoplasm 42 5.186
787
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 5.180
788
P NRN021 Neuronal Ceroid Lipofuscinosis 65 5.173
789
MSL001 Measles 61 5.164
790
RYS001 Reye Syndrome 49 5.163
791
P ICH004 Ichthyosis 56 5.161
792
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 5.161
793
CND006 Candida Glabrata 30 5.159
794
HRY003 Hairy Cell Leukemia 61 5.158
795
ATN005 Autonomic Dysfunction 46 5.147
796
DST006 Diastolic Heart Failure 45 5.132
797
P PTT014 Pitt-Hopkins Syndrome 64 5.126
798
EXT007 Extracutaneous Mastocytoma 38 5.108
799
P MNN013 Meningitis 65 5.092
800
CHR682 Chronic Bilirubin Encephalopathy 37 5.076
801
c HNT011 Huntington Disease-Like 3 34 5.074
802
OST016 Osteochondrosis 52 5.067
803
BRS051 Breast Disease 58 5.057
804
PRT038 Protein-Energy Malnutrition 53 5.030
805
GLY081 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency 47 5.025
806
P SCK002 Sick Sinus Syndrome 55 5.019
807
CRC021 Carcinosarcoma 64 5.017
808
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 5.010
809
P LCH002 Lichen Planus 54 5.004
810
CLL003 Cellulitis 53 4.999
811
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 4.997
812
P PRP029 Porphyria 60 4.994
813
INT075 Intracranial Hypertension 53 4.992
814
HVY002 Heavy Metal Poisoning 22 4.991
815
DGR001 Digeorge Syndrome 62 4.975
816
GRN017 Granulocytopenia 42 4.967
817
MCL006 Macular Retinal Edema 57 4.966
818
CHC001 Chickenpox 57 4.957
819
PLM134 Pulmonary Fibrosis, Idiopathic 76 4.953
820
PRN019 Perinatal Necrotizing Enterocolitis 60 4.950
821
P SPN046 Spinal Muscular Atrophy 63 4.942
822
c ACT135 Acute Graft Versus Host Disease 51 4.931
823
P WSK001 Wiskott-Aldrich Syndrome 72 4.924
824
P PNC025 Panic Disorder 52 4.920
825
P ANG015 Angioedema 56 4.916
826
TND004 Tendinopathy 45 4.915
827
LMY002 Leiomyoma 51 4.907
828
BRR014 Barrett Esophagus 66 4.901
829
DRY001 Dry Eye Syndrome 50 4.896
830
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 4.894
831
CHL152 Childhood Acute Lymphocytic Leukemia 50 4.894
832
P MGR003 Migraine with Aura 52 4.894
833
P MCR010 Microcephaly 60 4.886
834
GSG001 Gas Gangrene 52 4.883
835
HLC007 Helicobacter Pylori Infection 67 4.871
836
PST028 Post-Traumatic Stress Disorder 59 4.864
837
VRC005 Varicose Veins 60 4.860
838
P ART018 Aortic Valve Insufficiency 52 4.858
839
FNG017 Fungal Infectious Disease 54 4.843
840
P CHL066 Cholangitis 52 4.842
841
URM005 Uremic Pruritus 45 4.840
842
ATX019 Ataxia with Vitamin E Deficiency 44 4.839
843
ART035 Arterial Calcification of Infancy 58 4.838
844
P INT070 Intestinal Obstruction 57 4.837
845
MSN004 Mesenchymal Cell Neoplasm 42 4.834
846
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 4.821
847
P LMB006 Limb-Girdle Muscular Dystrophy 52 4.815
848
c ATS239 Autosomal Recessive Hypophosphatemic Rickets 50 4.813
849
P FML011 Familial Adenomatous Polyposis 71 4.810
850
WST001 West Syndrome 59 4.805
851
AND005 Androgen Insensitivity Syndrome, Mild 21 4.799
852
CRN288 Corneal Dystrophy, Band-Shaped 36 4.786
853
RBS001 Rabies 58 4.785
854
c HYP608 Hypocalciuric Hypercalcemia, Familial, Type Iii 42 4.785
855
P MNC007 Monocytic Leukemia 47 4.780
856
PRL017 Prolymphocytic Leukemia 47 4.774
857
c GLY008 Glycogen Storage Disease Ii 72 4.771
858
BCT002 Bacterial Vaginosis 53 4.770
859
NRN005 Neuronal Ceroid-Lipofuscinoses 61 4.768
860
ACT119 Acute Promyelocytic Leukemia 62 4.763
861
PRN039 Paraneoplastic Syndromes 37 4.759
862
c BCT013 Bacterial Pneumonia 48 4.756
863
BNG018 Benign Paroxysmal Positional Nystagmus 41 4.751
864
PSY004 Psychotic Disorder 66 4.742
865
TRT001 Teratocarcinoma 42 4.739
866
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 4.720
867
c PNC108 Pancreatitis, Hereditary 69 4.717
868
c GLC092 Glaucoma, Primary Open Angle 62 4.710
869
CRH005 Crohn's Colitis 53 4.701
870
HML018 Homologous Wasting Disease 21 4.700
871
P PRC019 Precocious Puberty 47 4.697
872
P PLY041 Polymyositis 59 4.691
873
c HNT004 Huntington Disease-Like 2 52 4.686
874
RFR010 Refractory Anemia 49 4.678
875
P MTR003 Mitral Valve Stenosis 53 4.672
876
NRT004 Neuritis 53 4.668
877
c PRG020 Paragangliomas 3 39 4.668
878
c SCN036 Secondary Progressive Multiple Sclerosis 55 4.666
879
SCR011 Scrapie 39 4.664
880
SCH012 Schizoaffective Disorder 50 4.653
881
HYP006 Hypertensive Heart Disease 49 4.650
882
CHR100 Chronic Ulcer of Skin 57 4.646
883
TYP007 Typhoid Fever 64 4.643
884
RTN017 Retinal Detachment 60 4.642
885
THR035 Thrombasthenia 48 4.634
886
SXL003 Sexual Disorder 49 4.634
887
P CRB059 Cerebellar Degeneration 36 4.630
888
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 49 4.626
889
VRL011 Viral Infectious Disease 61 4.625
890
RSC001 Rosacea 55 4.591
891
c BCT007 Bacterial Meningitis 55 4.586
892
MLK006 Milk Allergy 47 4.584
893
NPH018 Nephrogenic Systemic Fibrosis 49 4.575
894
CHP002 Chops Syndrome 47 4.567
895
KRT006 Keratoconjunctivitis 53 4.558
896
RDC002 Radiculopathy 52 4.554
897
P NGH001 Night Blindness 52 4.552
898
c ALP101 Alpha-Thalassemia 62 4.543
899
CRY005 Cryptococcosis 60 4.531
900
P MJR007 Major Affective Disorder 1 42 4.526
901
c HYP602 Hyperoxaluria, Primary, Type Ii 49 4.525
902
ACH005 Achalasia 55 4.524
903
CTN007 Cutaneous Leishmaniasis 62 4.521
904
P PTS002 Ptosis 52 4.510
905
MYC006 Mycosis Fungoides 65 4.502
906
c HYP724 Hyperlipoproteinemia, Type Iii 67 4.500
907
CYN002 Cyanosis, Transient Neonatal 43 4.496
908
CLF027 Cleft Palate, Isolated 64 4.480
909
HLL004 Hellp Syndrome 53 4.480
910
P FML362 Familial Isolated Hypoparathyroidism 48 4.473
911
P RTT002 Rett Syndrome 79 4.471
912
RNL065 Renal Cell Carcinoma, Papillary, 1 79 4.464
913
LNG031 Lung Benign Neoplasm 51 4.449
914
c HYP292 Hypophosphatasia, Infantile 55 4.445
915
CHN010 Chondroma 43 4.443
916
CRT084 Creatinine Clearance Quantitative Trait Locus 25 4.434
917
INF034 Infective Endocarditis 54 4.430
918
PLS006 Plasmodium Vivax Malaria 51 4.425
919
HST010 Histiocytosis 49 4.420
920
ART074 Aortic Dissection 53 4.417
921
c EPS039 Episodic Pain Syndrome, Familial, 1 42 4.417
922
NRN004 Neuroendocrine Tumor 59 4.416
923
PMP014 Pemphigoid 51 4.415
924
AVN001 Avian Influenza 61 4.413
925
c CNG411 Congenital Disorder of Glycosylation, Type in 67 4.412
926
SPN020 Spondylosis 46 4.409
927
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 4.405
928
P MLT008 Multinodular Goiter 42 4.398
929
BNG036 Bone Giant Cell Tumor 49 4.389
930
AZS001 Azoospermia 45 4.386
931
P LYM033 Lymphoproliferative Syndrome 59 4.382
932
ART004 Aortic Atherosclerosis 47 4.382
933
ATN004 Autonomic Neuropathy 42 4.368
934
DMP001 Dumping Syndrome 43 4.365
935
PMP006 Pemphigus Vulgaris, Familial 58 4.361
936
TTH006 Tooth Disease 51 4.356
937
c VSC019 Vesicoureteral Reflux 1 57 4.354
938
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 4.344
939
CHR073 Choreatic Disease 54 4.344
940
P TBR001 Tuberous Sclerosis 69 4.342
941
CHD004 Chudley-Mccullough Syndrome 48 4.340
942
ALL010 Allergic Contact Dermatitis