Search results for Phosphoric acid

937 hits were found for Phosphoric acid

# Family MCID Name MIFTS Score
1
LPD008 Lipid Metabolism Disorder 62 39.465
2
RPD005 Rapidly Involuting Congenital Hemangioma 46 36.260
3
NNL005 Non-Alcoholic Fatty Liver Disease 63 35.573
4
GST092 Gastroesophageal Reflux 61 35.410
5
FTT001 Fatty Liver Disease 62 33.724
6
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 33.444
7
CHL068 Cholestasis 61 32.192
8
HYP014 Hyperuricemia 51 29.994
9
MTB004 Metabolic Acidosis 48 28.318
10
HLX001 Helix Syndrome 48 27.895
11
P LVR013 Liver Disease 69 27.307
12
c CHR684 Chronic Kidney Disease 69 27.307
13
NRL016 Neural Tube Defects 81 25.553
14
P NRB001 Neuroblastoma 66 25.530
15
BNR002 Bone Resorption Disease 47 25.434
16
P KDN018 Kidney Disease 72 25.244
17
GT001 Gout 64 25.108
18
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 24.516
19
c TYP009 Type 2 Diabetes Mellitus 92 24.434
20
LVR012 Liver Cirrhosis 63 24.227
21
P CRN300 Coronary Heart Disease 1 73 23.141
22
CLT003 Colitis 63 23.114
23
HYP781 Hypoascorbemia 52 23.008
24
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 22.931
25
ACT119 Acute Promyelocytic Leukemia 62 22.924
26
48X005 48,xyyy 39 22.894
27
P DDN001 Duodenal Ulcer 53 22.875
28
P SZR006 Seizure Disorder 70 22.797
29
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 22.620
30
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 22.620
31
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 22.617
32
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 22.617
33
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 22.612
34
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 22.612
35
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 22.612
36
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 22.612
37
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 22.612
38
HYP066 Hyperglycemia 61 22.511
39
c HYP836 Hypercholesterolemia, Familial, 1 73 22.489
40
P HYP750 Hypertriglyceridemia, Familial 62 22.311
41
ISV001 Isovaleric Acidemia 54 22.123
42
P OST002 Osteoporosis 76 21.933
43
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 21.928
44
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 21.928
45
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 21.902
46
GLL048 Glial Tumor 52 21.178
47
OST012 Osteoarthritis 77 21.133
48
GLM045 Glioma 63 21.084
49
P DBT009 Diabetes Mellitus 67 20.948
50
ATH013 Atherosclerosis Susceptibility 63 20.873
51
AGN016 Aging 54 20.535
52
HRW001 Hair Whorl 35 20.498
53
PPT005 Peptic Ulcer Disease 58 20.473
54
HMN044 Human Immunodeficiency Virus Type 1 78 20.453
55
P BRS047 Breast Cancer 98 20.371
56
ISC004 Ischemia 61 20.333
57
c GLL024 Gallbladder Disease 1 52 20.210
58
IRN002 Iron Metabolism Disease 57 20.006
59
c DNT047 Dentinogenesis Imperfecta Type 2 35 19.961
60
P GST044 Gastritis 55 19.843
61
P ENC018 Encephalopathy 62 19.828
62
P DRR001 Diarrhea 55 19.708
63
NNL006 Non-Alcoholic Steatohepatitis 54 19.647
64
P CLR023 Colorectal Cancer 100 19.509
65
RCK004 Rickets 68 19.391
66
P LKM002 Leukemia 67 19.248
67
PHS025 Phosphatase, Acid, of Tissues 28 19.215
68
CYS001 Cystic Fibrosis 78 19.214
69
ULC004 Ulcerative Colitis 74 19.096
70
PRT037 Pertussis 65 18.987
71
END086 End Stage Renal Disease 52 18.969
72
GLB002 Glioblastoma 67 18.756
73
HYP056 Hypoglycemia 65 18.536
74
ALL029 Allergic Disease 59 18.531
75
HYP266 Hypoxia 57 18.433
76
P INF038 Influenza 68 18.427
77
DFC004 Deficiency Anemia 74 18.271
78
P INF037 Inflammatory Bowel Disease 53 18.263
79
P HPT023 Hepatocellular Carcinoma 96 18.185
80
P BND020 Bone Disease 59 18.142
81
P MYP004 Myopathy 67 18.131
82
P PRD008 Periodontitis 64 18.086
83
HMC014 Homocysteinemia 52 18.005
84
P BPL003 Bipolar Disorder 56 17.944
85
P EPL164 Epilepsy 68 17.873
86
P HPT021 Hepatitis 69 17.867
87
P ALZ034 Alzheimer Disease 87 17.851
88
c MJR022 Major Affective Disorder 8 38 17.844
89
c MJR024 Major Affective Disorder 9 41 17.844
90
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 17.738
91
ORG002 Organic Acidemia 44 17.734
92
NPH009 Nephrolithiasis 54 17.732
93
CYT002 Cytokine Deficiency 43 17.638
94
OST159 Osteogenic Sarcoma 66 17.579
95
P PRS040 Prostate Cancer 95 17.551
96
c PRC016 Pre-Eclampsia 65 17.443
97
PHN003 Phenylketonuria 76 17.431
98
P PNC035 Pancreatic Cancer 86 17.413
99
HYP060 Hyperinsulinism 54 17.401
100
P PSR002 Psoriasis 63 17.129
101
P HYP069 Hyperparathyroidism 62 17.019
102
IMM167 Immune Deficiency Disease 78 17.012
103
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 17.002
104
GST023 Gastric Ulcer 52 16.973
105
47X002 47,xyy 48 16.902
106
PPL052 Papillomatosis, Confluent and Reticulated 34 16.858
107
c HYP595 Hypertension, Essential 85 16.810
108
KRT002 Keratomalacia 55 16.729
109
c TYP008 Type 1 Diabetes Mellitus 70 16.606
110
c ACT027 Acute Pancreatitis 60 16.595
111
DNT012 Dental Caries 53 16.526
112
P ADN016 Adenocarcinoma 63 16.521
113
c HPT073 Hepatitis C Virus 71 16.502
114
PST011 Pustulosis of Palm and Sole 52 16.400
115
P VSC007 Vascular Disease 63 16.391
116
P HRP006 Herpes Simplex 65 16.379
117
P HRT032 Heart Disease 81 16.354
118
CRH001 Crohn's Disease 80 16.350
119
PRT251 Proteinuria, Chronic Benign 57 16.339
120
c LKM061 Leukemia, Acute Myeloid 83 16.283
121
P MYC084 Mycobacterium Tuberculosis 1 68 16.267
122
c HPT016 Hepatitis B 62 16.153
123
c ACT071 Acute Kidney Failure 60 16.101
124
SKN016 Skin Disease 63 16.031
125
MNT002 Mental Depression 57 15.975
126
CHL014 Cholera 62 15.892
127
DRM006 Dermatitis 62 15.891
128
P ART022 Arthritis 71 15.873
129
P HNT016 Huntington Disease 73 15.846
130
MYL069 Myeloma, Multiple 77 15.788
131
P PNC044 Pancreatitis 61 15.784
132
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 15.750
133
URL001 Urolithiasis 46 15.693
134
P GST053 Gastric Cancer 83 15.483
135
BRR014 Barrett Esophagus 66 15.480
136
HPT019 Hepatic Encephalopathy 59 15.478
137
BCT022 Bacterial Infectious Disease 56 15.456
138
HPT004 Hepatic Coma 43 15.451
139
c HPT001 Hepatitis C 62 15.444
140
P MYL006 Myeloid Leukemia 61 15.254
141
P LNG032 Lung Cancer 98 15.199
142
BRN071 Brain Injury 50 15.081
143
P OVR042 Ovarian Cancer 88 15.030
144
INS024 Insulin-Like Growth Factor I 78 14.995
145
P NRP001 Neuropathy 60 14.933
146
DPR016 Depression 65 14.907
147
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 14.868
148
P URN019 Urinary Tract Infection 49 14.708
149
c MCR120 Microvascular Complications of Diabetes 7 47 14.678
150
ADN018 Adenoma 59 14.637
151
GLC003 Glucose Intolerance 54 14.580
152
TRM010 Traumatic Brain Injury 51 14.564
153
P ATS364 Autism 69 14.545
154
c MCR113 Microvascular Complications of Diabetes 3 52 14.543
155
LNG099 Lung Disease 62 14.539
156
P BLD134 Bladder Cancer 79 14.525
157
c AMY091 Amyotrophic Lateral Sclerosis 1 88 14.442
158
STT001 Status Epilepticus 59 14.408
159
P OVR082 Overgrowth Syndrome 49 14.395
160
c MCR133 Microvascular Complications of Diabetes 4 41 14.366
161
c MCR130 Microvascular Complications of Diabetes 6 41 14.361
162
P LCT001 Lactic Acidosis 51 14.311
163
URM002 Uremia 47 14.301
164
HMP009 Haemophilus Influenzae 41 14.245
165
P GLM040 Glioma Susceptibility 1 71 14.232
166
c ATS007 Autism Spectrum Disorder 72 14.160
167
P LTR001 Lateral Sclerosis 58 14.143
168
P MYC007 Myocardial Infarction 70 14.128
169
CRV035 Cervical Cancer 73 14.127
170
P MLN008 Melanoma 76 14.008
171
P BCL017 B-Cell Lymphoma 59 13.966
172
OCL069 Ocular Motor Apraxia 57 13.948
173
MTH071 Methane Production 25 13.937
174
P RHM011 Rheumatoid Arthritis 82 13.933
175
PRT036 Peritonitis 65 13.838
176
P DRM053 Dermatitis, Atopic 65 13.828
177
c ACT068 Acute Cystitis 61 13.796
178
P HYP086 Hypothyroidism 69 13.793
179
SVR001 Severe Acute Respiratory Syndrome 67 13.712
180
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 13.659
181
P MJR001 Major Depressive Disorder 68 13.653
182
SPN186 Spinal Cord Injury 61 13.596
183
KRT009 Keratosis 53 13.520
184
ATM095 Autoimmune Disease 61 13.509
185
P SCH015 Schizophrenia 74 13.509
186
BRN024 Bronchitis 67 13.447
187
OST003 Osteonecrosis 61 13.374
188
c PCH010 Pachyonychia Congenita 3 43 13.307
189
TXC005 Toxic Shock Syndrome 62 13.301
190
NPH091 Nephrolithiasis, Calcium Oxalate 61 13.141
191
CRB004 Cerebral Artery Occlusion 45 13.132
192
P INF032 Infertility 57 13.119
193
P THR014 Thrombocytopenia 66 13.062
194
VCC001 Vaccinia 47 13.058
195
P ALC033 Alcohol Use Disorder 61 13.021
196
DSS032 Disease by Infectious Agent 55 12.954
197
ANX004 Anoxia 40 12.904
198
c ATR087 Atrial Standstill 1 74 12.797
199
P MSC003 Muscular Atrophy 52 12.786
200
c HPT003 Hepatitis a 63 12.650
201
P MLT020 Multiple Sclerosis 79 12.600
202
MLG169 Malignant Astrocytoma 57 12.568
203
ESP021 Esophageal Cancer 83 12.532
204
P TRM003 Tremor 48 12.497
205
P ENC004 Encephalitis 61 12.479
206
c MGR028 Migraine with or Without Aura 1 64 12.475
207
P PRP019 Peripheral Nervous System Disease 58 12.448
208
SRC014 Sarcoma 65 12.445
209
ZLL002 Zollinger-Ellison Syndrome 55 12.433
210
P ADL010 Adult Respiratory Distress Syndrome 71 12.408
211
SPN035 Spindle Cell Sarcoma 54 12.399
212
P GLM007 Glomerulonephritis 60 12.397
214
PLM129 Pulmonary Disease, Chronic Obstructive 74 12.335
215
HYP005 Hypokalemia 55 12.318
216
P SKN015 Skin Carcinoma 71 12.305
217
P LNG064 Lung Cancer Susceptibility 3 70 12.303
218
GST033 Gestational Diabetes 61 12.280
219
c SML038 Small Cell Cancer of the Lung 69 12.275
220
P AMY004 Amyloidosis 70 12.256
221
P ATT013 Attention Deficit-Hyperactivity Disorder 64 12.213
222
P AST005 Asthma 76 12.199
223
SQM006 Squamous Cell Carcinoma 60 12.170
224
P THL005 Thalassemia 56 12.161
225
CNG034 Congestive Heart Failure 69 12.011
226
P LPS004 Lupus Erythematosus 61 12.008
227
P MSC005 Muscular Dystrophy 67 11.991
228
GST045 Gastroenteritis 58 11.926
229
P TMP001 Temporal Lobe Epilepsy 49 11.910
230
CYS013 Cystinuria 66 11.757
231
c MCR115 Microvascular Complications of Diabetes 5 65 11.721
232
RNL114 Renal Cell Carcinoma, Nonpapillary 80 11.716
233
c SYS001 Systemic Lupus Erythematosus 87 11.696
234
AVN001 Avian Influenza 61 11.678
235
P GLY013 Glycogen Storage Disease 60 11.641
236
P PHC003 Pheochromocytoma 69 11.626
237
HGH043 High Grade Glioma 45 11.619
238
HYP017 Hypophosphatemia 49 11.588
239
PRP027 Peripheral Vascular Disease 71 11.583
240
MDD011 Mood Disorder 62 11.570
241
P RTN024 Retinoblastoma 73 11.547
242
c ACT075 Acute Myocardial Infarction 56 11.539
243
CRB039 Cerebrovascular Disease 66 11.534
244
ADR040 Adrenal Gland Pheochromocytoma 46 11.520
245
P CTR002 Cataract 60 11.502
246
ATS010 Autosomal Recessive Disease 42 11.476
247
THY029 Thyroid Carcinoma 51 11.463
248
c DWL002 Dowling-Degos Disease 1 58 11.463
249
CNS004 Constipation 56 11.446
250
HYP025 Hyperphosphatemia 48 11.425
251
MLR004 Malaria 80 11.423
252
CHL004 Cholelithiasis 49 11.351
253
P FRG001 Fragile X Syndrome 70 11.321
254
IRR002 Irritable Bowel Syndrome 65 11.299
255
CRD132 Cardiac Conduction Defect 60 11.284
256
c ACT134 Acute Liver Failure 59 11.269
257
TTN003 Tetanus 65 11.256
258
P LKM062 Leukemia, Acute Lymphoblastic 69 11.248
259
P RSP003 Respiratory Failure 74 11.245
260
PPL022 Papilloma 53 11.178
261
MYL009 Myelodysplastic Syndrome 67 11.176
262
P PLY019 Polyneuropathy 52 11.159
263
P PRK039 Parkinsonism 55 11.111
264
P PLM036 Pulmonary Fibrosis 66 11.105
265
P NPH012 Nephrotic Syndrome 60 11.082
266
CLN015 Colon Adenocarcinoma 65 11.042
267
P HYP265 Hypotonia 42 11.025
268
NRR001 Neuroretinitis 42 11.007
269
RTN023 Retinitis 46 11.004
270
PLM010 Pulmonary Edema 55 10.997
271
P ART021 Arteriosclerosis 54 10.992
272
PST092 Posttransplant Acute Limbic Encephalitis 28 10.974
273
P ART023 Arthropathy 61 10.956
274
NWC001 Newcastle Disease 47 10.932
275
DBT010 Diabetic Neuropathy 54 10.884
276
PRP001 Propionic Acidemia 65 10.871
277
SVR004 Severe Combined Immunodeficiency 72 10.831
278
P PRP029 Porphyria 60 10.806
279
HMS001 Hemosiderosis 48 10.787
280
SQM002 Squamous Cell Papilloma 46 10.785
281
P RHN004 Rhinitis 57 10.769
282
c SCN007 Secondary Hyperparathyroidism 51 10.722
283
P CHR345 Chronic Pain 50 10.693
284
P FBR017 Fibrosarcoma 56 10.673
285
P LYM118 Lymphoma 67 10.660
286
P PNM007 Pneumonia 67 10.581
287
P PLY011 Polycystic Ovary Syndrome 57 10.558
288
P EYD002 Eye Disease 57 10.498
289
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 10.493
290
NTR005 Nutritional Deficiency Disease 61 10.493
291
PLM033 Pulmonary Embolism 58 10.493
292
P CRD246 Cardiovascular System Disease 56 10.418
293
HNS001 Hansen's Disease 32 10.413
294
P CYS018 Cystitis 59 10.378
295
P LPR021 Leprosy 3 71 10.370
296
ALL014 Allergic Encephalomyelitis 34 10.354
297
P PLM037 Pulmonary Hypertension 72 10.333
298
P EXN002 Exanthem 58 10.303
299
P HYP076 Hyperthyroidism 53 10.272
300
P DMN002 Dementia 66 10.266
301
GNG013 Gingivitis 59 10.246
302
CLF027 Cleft Palate, Isolated 64 10.243
303
P RTN008 Retinitis Pigmentosa 80 10.239
304
P NSP012 Nasopharyngeal Carcinoma 61 10.218
305
P RRH023 Rare Hereditary Hemochromatosis 54 10.194
306
ANG054 Angina Pectoris 66 10.115
307
CHL065 Cholangiocarcinoma 58 10.071
308
BRN004 Brain Edema 54 10.068
309
MCS002 Mucositis 56 10.060
310
PRS045 Prostatic Hypertrophy 53 10.052
311
OST115 Osteonecrosis of the Jaw 41 10.028
312
INT079 Intrahepatic Cholangiocarcinoma 51 10.025
313
ARG004 Argyria 26 10.008
314
PLY150 Polykaryocytosis Inducer 29 9.967
315
LPT014 Leptin Deficiency or Dysfunction 78 9.953
316
P NMN002 Niemann-Pick Disease 60 9.925
317
P BRS044 Breast Adenocarcinoma 58 9.893
318
P ALP008 Alopecia 54 9.862
319
P RCT021 Rectum Cancer 54 9.782
320
SCH014 Schistosomiasis 56 9.780
321
CNT047 Contact Dermatitis 57 9.779
322
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 9.774
323
P SPP010 Suppressor of Tumorigenicity 3 51 9.761
324
P KLZ004 Kala-Azar 1 41 9.742
325
LSH001 Leishmaniasis 64 9.742
326
c VRL010 Viral Hepatitis 53 9.740
327
IRN001 Iron Deficiency Anemia 58 9.740
328
P LKM071 Leukemia, Chronic Lymphocytic 75 9.683
329
DYS073 Dysphagia 53 9.662
330
P SYS005 Systemic Scleroderma 74 9.639
331
MST005 Mastitis 53 9.548
332
MLD018 Mild Cognitive Impairment 48 9.531
333
P PRK057 Parkinson Disease, Late-Onset 80 9.528
334
INS001 Insulinoma 59 9.515
335
c ACT073 Acute Leukemia 58 9.480
336
P SCK005 Sickle Cell Disease 56 9.441
337
MDD018 Middle East Respiratory Syndrome 44 9.423
338
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 9.404
339
ACY011 Acyl-Coa Dehydrogenase Deficiency 30 9.391
340
P HYP098 Hypereosinophilic Syndrome 66 9.328
341
ENT011 Enterocolitis 55 9.320
342
P ATR005 Atrophic Gastritis 50 9.316
343
P RNL007 Renal Tubular Acidosis 50 9.283
344
c PRD040 Periodontitis, Chronic 52 9.277
345
P CND004 Candidiasis 58 9.266
346
ORL011 Oral Cancer 60 9.260
347
P SCL018 Scoliosis 57 9.241
348
P CNJ013 Conjunctivitis 66 9.239
349
c LKM063 Leukemia, Chronic Myeloid 71 9.223
350
ENT004 Enthesopathy 51 9.221
351
PRS021 Prostatic Adenoma 43 9.211
352
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 9.209
353
MNN043 Meningioma, Familial 79 9.188
354
c LKM005 Leukemia, T-Cell, Chronic 34 9.181
355
P MLN007 Male Infertility 56 9.056
356
SCR001 Secretory Meningioma 40 9.005
357
LYM002 Lymphoplasmacyte-Rich Meningioma 35 9.005
358
SPN021 Spinal Meningioma 50 9.005
359
PNG002 Pain Agnosia 51 8.994
360
AMN006 Aminoaciduria 37 8.994
361
ANX010 Anxiety 70 8.938
362
P MNN013 Meningitis 65 8.923
363
PRS129 Prostatic Hyperplasia, Benign 49 8.898
364
ACT098 Acute Erythroid Leukemia 55 8.888
365
c DLT002 Dilated Cardiomyopathy 78 8.875
366
P PLY014 Polycystic Kidney Disease 69 8.873
367
P HDC001 Headache 57 8.871
368
ALL003 Allergic Rhinitis 67 8.849
369
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 8.800
370
P DYS154 Dystonia 64 8.784
371
P INT068 Intestinal Disease 53 8.773
372
P URT039 Urticaria 58 8.766
373
c BSL007 Basal Cell Carcinoma 68 8.764
374
c BTT014 Beta-Thalassemia 72 8.760
375
P CLC063 Celiac Disease 1 66 8.715
376
OST017 Osteomyelitis 63 8.688
377
P ANP001 Anaplastic Large Cell Lymphoma 61 8.686
378
INT323 Intraocular Pressure Quantitative Trait Locus 64 8.673
379
P CRD119 Cardiac Arrest 67 8.671
380
c PRM005 Primary Hyperparathyroidism 59 8.636
381
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 8.605
382
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 8.587
383
ORL015 Oral Squamous Cell Carcinoma 43 8.513
384
SCR011 Scrapie 39 8.508
385
P GRF003 Graft-Versus-Host Disease 71 8.499
386
BRN028 Brain Cancer 74 8.479
387
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 8.446
388
HDN002 Head Injury 44 8.427
389
P KDN017 Kidney Cancer 61 8.427
390
MMM001 Mammary Paget's Disease 53 8.405
391
P PRN023 Prion Disease 60 8.403
392
RNL077 Renal Fibrosis 46 8.332
393
END057 Endometrial Cancer 72 8.320
394
P PYL005 Pyelonephritis 57 8.285
395
CHC001 Chickenpox 57 8.268
396
GST040 Gastric Adenocarcinoma 67 8.256
397
INT066 Interstitial Lung Disease 60 8.223
398
CHR074 Choriocarcinoma 46 8.220
399
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 8.215
400
PRN019 Perinatal Necrotizing Enterocolitis 60 8.204
401
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 8.196
402
TLN003 Telangiectasis 51 8.194
403
P TYR004 Tyrosinemia 50 8.154
404
PRT013 Portal Hypertension 59 8.131
405
c SCL052 Scleroderma, Familial Progressive 61 8.110
406
BRK010 Burkitt Lymphoma 66 8.088
407
P BNG032 Benign Mesothelioma 53 8.050
408
PNC129 Pancreatic Adenocarcinoma 65 8.048
409
P SRC025 Sarcoidosis 1 71 8.037
410
P FML011 Familial Adenomatous Polyposis 71 7.936
411
P HML002 Hemolytic Anemia 62 7.912
412
SPL018 Splenomegaly 49 7.911
413
DBT084 Diabetes Mellitus, Ketosis-Prone 60 7.903
414
PSY004 Psychotic Disorder 66 7.895
415
SBC016 Subacute Delirium 43 7.872
416
DYS015 Dysentery 50 7.851
417
MSC007 Muscle Hypertrophy 64 7.848
418
P FNC004 Fanconi Syndrome 60 7.818
419
MSC157 Muscular Dystrophy, Duchenne Type 79 7.792
420
P MDL005 Medulloblastoma 75 7.763
421
P THY032 Thyroiditis 57 7.757
422
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 7.752
423
ANT024 Anthrax Disease 58 7.740
424
P HYP061 Hypertrophic Cardiomyopathy 69 7.713
425
ANR007 Anorexia Nervosa 60 7.677
426
PLG002 Plague 58 7.673
428
P RTN018 Retinal Disease 53 7.617
429
PNC041 Pancreatic Ductal Adenocarcinoma 51 7.616
430
TRN015 Transient Cerebral Ischemia 63 7.574
431
SQM013 Squamous Cell Carcinoma, Head and Neck 73 7.556
432
P SLP006 Sleep Apnea 69 7.535
433
PRT038 Protein-Energy Malnutrition 53 7.504
434
ALL006 Allergic Asthma 56 7.448
435
P MCR010 Microcephaly 60 7.442
436
CLR109 Colorectal Adenocarcinoma 50 7.418
437
PLC002 Plica Syndrome 35 7.299
438
SYN007 Synovitis 55 7.299
439
P VSC011 Vasculitis 61 7.259
440
ETN001 Eating Disorder 59 7.246
441
TRN018 Transitional Cell Carcinoma 56 7.221
442
c PLM164 Pulmonary Hypertension, Primary, 1 76 7.090
443
CLF001 Cleft Lip 53 7.076
444
P HYD006 Hydrocephalus 61 7.064
445
OST011 Osteomalacia 52 7.029
446
GST030 Gastrinoma 45 7.029
447
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 7.019
448
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 7.019
449
PRP083 Porphyria, Acute Intermittent 65 7.013
450
PTT037 Pituitary Tumors 44 7.005
451
P RHB003 Rhabdomyosarcoma 66 6.994
452
P HYP024 Hypoparathyroidism 55 6.987
453
BRT054 Brittle Bone Disorder 74 6.964
454
P CTN015 Cutaneous T Cell Lymphoma 48 6.958
455
DSS009 Disseminated Intravascular Coagulation 57 6.948
456
SPN051 Spondylitis 51 6.935
457
INF009 Inflammatory Spondylopathy 30 6.935
458
P PLY018 Polycythemia 56 6.932
459
NPH003 Nephrocalcinosis 49 6.875
460
IMP005 Impotence 52 6.864
461
AMN003 Amnestic Disorder 54 6.844
462
c PLM127 Pulmonary Hypertension, Primary, 3 34 6.788
463
CND006 Candida Glabrata 30 6.761
464
PRP080 Peripheral Artery Disease 54 6.717
465
SFT003 Soft Tissue Sarcoma 57 6.684
466
PLM134 Pulmonary Fibrosis, Idiopathic 76 6.684
467
PNC001 Pancytopenia 53 6.666
468
GTR002 Goiter 53 6.646
469
P DST107 Distal Renal Tubular Acidosis 48 6.639
470
LNG031 Lung Benign Neoplasm 51 6.634
471
c HNT004 Huntington Disease-Like 2 52 6.624
472
CRB037 Cerebral Palsy 67 6.624
473
OVR094 Ovarian Epithelial Cancer 39 6.620
474
LWC002 Lowe Oculocerebrorenal Syndrome 68 6.594
475
PST021 Postpartum Depression 50 6.555
476
HND015 Hand Skill, Relative 30 6.524
477
STN013 Stenotrophomonas Maltophilia Infection 26 6.512
478
P SPN046 Spinal Muscular Atrophy 63 6.492
479
P OPN001 Open-Angle Glaucoma 55 6.461
480
CRC006 Carcinoid Syndrome 55 6.459
481
MST004 Mast Cell Neoplasm 42 6.435
482
CYS010 Cystinosis 62 6.431
483
RTN017 Retinal Detachment 60 6.431
484
P MYC008 Myocarditis 59 6.423
485
EXT007 Extracutaneous Mastocytoma 38 6.421
486
c SPN225 Spondyloarthropathy 1 70 6.406
487
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 6.404
488
LKP003 Leukoplakia 39 6.401
489
MLT157 Multiple System Atrophy 1 69 6.389
490
PNM008 Pneumothorax 54 6.381
491
KWS001 Kwashiorkor 45 6.370
492
P SLP005 Sleep Disorder 61 6.343
493
HYP080 Hypogonadism 50 6.334
494
URT010 Ureteral Obstruction 45 6.318
495
ADG002 Audiogenic Seizures 25 6.314
496
INT002 Intermittent Claudication 61 6.309
497
FBR047 Fibromyalgia 58 6.306
498
PLS011 Plasmacytoma 56 6.295
499
VSC003 Visceral Leishmaniasis 55 6.288
500
ILS001 Ileus 50 6.275
501
NRN004 Neuroendocrine Tumor 59 6.274
502
P GRV001 Graves' Disease 55 6.265
503
RTR008 Root Resorption 44 6.226
504
P MTC069 Mitochondrial Disorders 57 6.209
505
ENM002 Enamel Erosion 25 6.207
506
PLM031 Poliomyelitis 63 6.180
507
FCL014 Focal Epilepsy 53 6.151
508
HYD002 Hydronephrosis 58 6.117
509
P PGT001 Paget's Disease of Bone 61 6.067
510
P NRV007 Nervous System Disease 67 6.062
511
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 6.025
512
ASP007 Aspiration Pneumonia 49 5.911
513
TRY001 Trypanosomiasis 50 5.904
514
THY030 Thyroid Gland Disease 50 5.897
515
DNT001 Dental Fluorosis 43 5.890
516
MCR013 Microphthalmia 60 5.887
517
CLC006 Calcinosis 47 5.883
518
HRY003 Hairy Cell Leukemia 61 5.881
519
c BCT007 Bacterial Meningitis 55 5.874
520
DDN006 Duodenitis 50 5.818
521
DMP001 Dumping Syndrome 43 5.805
522
CRD223 Cardiac Arrhythmia 63 5.789
523
P ASP006 Aspergillosis 72 5.780
524
P MYS005 Myositis 56 5.775
525
PLY001 Polycythemia Vera 69 5.761
526
ART002 Arts Syndrome 66 5.755
527
GLS001 Gliosarcoma 64 5.747
528
P PTT006 Pituitary Adenoma 55 5.722
529
CRT015 Carotid Artery Occlusion 45 5.722
530
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 5.715
531
LYM027 Lymphopenia 56 5.686
532
P ADL017 Adult T-Cell Leukemia 56 5.658
533
EXN003 Exencephaly 30 5.645
534
P SPR120 Supranuclear Palsy, Progressive, 1 69 5.636
535
P TRT010 Teratoma 51 5.625
536
RNL011 Renal Osteodystrophy 49 5.625
537
P SBS003 Substance Abuse 54 5.598
538
PSR001 Psoriatic Arthritis 62 5.596
539
BRN056 Bronchopulmonary Dysplasia 56 5.587
540
c HMC039 Hemochromatosis, Type 1 73 5.583
541
ENM001 Enamel Caries 27 5.580
542
P DBT005 Diabetes Insipidus 54 5.515
543
c EXD008 Exudative Vitreoretinopathy 1 71 5.510
544
P BRB001 Beriberi 44 5.496
545
ACR007 Acromegaly 70 5.475
546
P ATX030 Ataxia-Telangiectasia 80 5.463
547
P SYP003 Syphilis 59 5.462
548
NRM005 Neuromuscular Disease 63 5.448
549
P RBL001 Rubella 58 5.447
550
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 5.434
551
P LRY044 Larynx Cancer 54 5.426
552
ACT003 Acute Kidney Tubular Necrosis 46 5.409
553
c GRV008 Graves Disease 1 54 5.400
554
c HPT007 Hepatitis E 51 5.376
555
P THY023 Thymoma 64 5.340
556
c THY107 Thymoma, Familial 42 5.336
557
BRS051 Breast Disease 58 5.315
558
c THY109 Thyroid Cancer, Nonmedullary, 1 55 5.314
559
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 5.300
560
THR004 Thrombocytosis 53 5.273
561
INT067 Interstitial Nephritis 46 5.272
562
c ACT135 Acute Graft Versus Host Disease 51 5.256
563
P RTT002 Rett Syndrome 79 5.253
564
c RTN047 Retinitis Pigmentosa 18 46 5.250
565
FRN006 Frontotemporal Dementia 68 5.211
566
RTN020 Retinal Vascular Disease 46 5.200
567
DFF005 Diffuse Large B-Cell Lymphoma 54 5.194
568
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 5.183
569
P PNC025 Panic Disorder 52 5.181
570
P INT070 Intestinal Obstruction 57 5.158
571
CHL045 Choline Deficiency Disease 39 5.157
572
APP008 Appendicitis 62 5.153
573
ANP008 Anaplastic Oligoastrocytoma 29 5.138
574
MYM001 Myoma 54 5.126
575
TND005 Tendinitis 54 5.120
576
BRC012 Brucellosis 66 5.115
577
URN010 Urinary Tract Obstruction 55 5.108
578
P MYP006 Myopia 56 5.058
579
P MTC133 Mitochondrial Myopathy 50 5.056
580
BNG077 Benign Idiopathic Neonatal Seizures 23 5.053
581
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 5.050
582
P HMN010 Hemangioma 62 5.024
583
P ANT006 Antiphospholipid Syndrome 55 4.995
584
VTM033 Vitamin K Deficiency Bleeding 48 4.990
585
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 4.984
586
LYM017 Lyme Disease 62 4.963
587
VLV047 Volvulus of Midgut 52 4.959
588
BNN003 Bone Inflammation Disease 48 4.948
589
HVY002 Heavy Metal Poisoning 22 4.948
590
P PMP001 Pemphigus 55 4.944
591
IDP070 Idiopathic Scoliosis 42 4.911
592
TTH007 Tooth Erosion 29 4.896
593
P PTS002 Ptosis 52 4.881
594
P GLL022 Guillain-Barre Syndrome 60 4.843
595
BTT017 Beta-Thalassemia Major 51 4.839
596
MNT001 Mantle Cell Lymphoma 67 4.774
597
CCC002 Coccidiosis 50 4.737
598
P FCL005 Focal Segmental Glomerulosclerosis 57 4.692
599
PRM329 Premature Aging 36 4.692
600
P HML001 Hemolytic-Uremic Syndrome 52 4.687
601
XRD010 Xeroderma Pigmentosum, Variant Type 73 4.686
602
ORL012 Oral Leukoplakia 36 4.679
603
APN008 Apnea, Obstructive Sleep 67 4.678
604
CLL003 Cellulitis 53 4.660
605
GSG001 Gas Gangrene 52 4.651
606
MYL005 Myelofibrosis 71 4.645
607
c RNG015 Ring Chromosome 2 22 4.623
608
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 4.615
609
PLR007 Pleural Empyema 51 4.613
610
GST037 Gastroparesis 52 4.608
611
DRM011 Dermatophytosis 52 4.606
612
GLC036 Glucagonoma 46 4.605
613
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 4.580
614
P DRM010 Dermatomyositis 61 4.559
615
MYL031 Myeloproliferative Neoplasm 66 4.538
616
AMN001 Amenorrhea 54 4.522
617
MCL006 Macular Retinal Edema 57 4.508
618
SLC006 Silicosis 56 4.488
619
GLC086 Glucocorticoid-Induced Osteoporosis 43 4.472
620
NNT012 Neonatal Jaundice 53 4.468
621
ANT018 Anthracosis 51 4.453
622
DNT010 Dentin Caries 31 4.447
623
c ACT004 Acute Diarrhea 40 4.384
624
P RNL015 Renal Hypertension 45 4.381
625
CRB090 Cerebral Hypoxia 42 4.362
626
HST010 Histiocytosis 49 4.352
627
ASP004 Asphyxia Neonatorum 50 4.340
628
PLY100 Polyploidy 36 4.328
629
P BRN022 Bronchiectasis 60 4.323
630
BNG036 Bone Giant Cell Tumor 49 4.316
631
P HYP040 Hypospadias 51 4.285
632
P EHL001 Ehlers-Danlos Syndrome 58 4.284
633
P PNM006 Pneumoconiosis 55 4.239
634
P LMY004 Leiomyosarcoma 62 4.238
635
ALV005 Alveolar Soft Part Sarcoma 61 4.218
636
P OST001 Osteopetrosis 71 4.216
637
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 4.212
638
ART004 Aortic Atherosclerosis 47 4.201
639
ANR004 Anuria 44 4.196
640
PRT058 Pure Autonomic Failure 58 4.189
641
P HRD086 Hereditary Hypophosphatemic Rickets 40 4.152
642
SML019 Smallpox 55 4.149
643
GLM044 Glomerular Disease 35 4.139
644
INV001 Invasive Aspergillosis 49 4.137
645
GRW007 Growth Hormone Deficiency 46 4.137
646
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 4.126
647
P PSD015 Pseudohypoparathyroidism 55 4.123
648
PCK003 Pick Disease of Brain 69 4.120
649
SYN036 Syncope 45 4.116
650
FLR002 Filariasis 55 4.116
651
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 4.110
652
P PRC012 Pericardial Effusion 50 4.090
653
KLB003 Klebsiella Pneumonia 50 4.085
654
BRN014 Bronchopneumonia 53 4.085
656
HMP001 Hemopericardium 47 4.079
657
LMB062 Limb Ischemia 55 4.078
658
RTN003 Retinal Ischemia 49 4.073
659
P AML002 Amelogenesis Imperfecta 56 4.059
660
RTC012 Reticuloendotheliosis, X-Linked 35 4.041
661
P ESS003 Essential Thrombocythemia 69 4.031
662
LGN006 Legionnaire Disease 52 4.022
663
HYP020 Hyperprolactinemia 63 4.016
664
ACT055 Actinomycosis 55 4.009
665
END041 Endometrial Adenocarcinoma 64 3.997
666
P NGH001 Night Blindness 52 3.997
667
CLF056 Cleft Lip with or Without Cleft Palate 42 3.991
668
ING001 Inguinal Hernia 59 3.984
669
P SCL057 Scoliosis, Isolated 1 40 3.976
670
WLS001 Wilson Disease 70 3.944
671
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 3.942
672
P GLL018 Gallbladder Cancer 53 3.925
673
CHL152 Childhood Acute Lymphocytic Leukemia 50 3.922
674
ADN011 Adenoid Cystic Carcinoma 68 3.900
675
HMR002 Hemarthrosis 44 3.888
676
CRY035 Cryptorchidism, Unilateral or Bilateral 58 3.881
677
P HRD008 Hereditary Hemorrhagic Telangiectasia 65 3.869
678
CYS005 Cysticercosis 60 3.867
679
PPL002 Papillary Carcinoma 46 3.859
680
PRT029 Parathyroid Adenoma 51 3.853
681
ALL009 Allergic Conjunctivitis 51 3.816
682
P MYG005 Myoglobinuria 40 3.814
683
KRT008 Keratopathy 46 3.772
684
P HYP726 Hypercalcemia, Infantile, 1 58 3.766
685
PRM020 Premenstrual Tension 39 3.759
686
IDP073 Idiopathic Hypercalciuria 40 3.752
687
QFV001 Q Fever 62 3.730
688
c SPR086 Spermatogenic Failure 3 46 3.725
689
P FML018 Familial Mediterranean Fever 73 3.723
690
MTB016 Metabolic Myopathy 30 3.716
691
CRB086 Cerebral Aneurysms 40 3.689
692
P PTN014 Patent Ductus Arteriosus 1 59 3.689
693
P AVS003 Avascular Necrosis 41 3.675
694
THR016 Thrombophlebitis 50 3.665
695
P BNG095 Benign Giant Cell Tumor 43 3.621
696
CRY005 Cryptococcosis 60 3.610
697
TLR001 Tularemia 56 3.578
698
VRL003 Variola Major 43 3.558
699
P HYP083 Hypopituitarism 52 3.532
700
PRM003 Premature Ejaculation 44 3.518
701
ART074 Aortic Dissection 53 3.513
702
CHR072 Chordoma 57 3.501
703
DSS012 Disseminated Infection with Mycobacterium Avium Complex 19 3.487
704
c AMY009 Amyloidosis Aa 47 3.483
705
MST021 Meester-Loeys Syndrome 42 3.471
706
P HYP733 Hypercalciuria, Absorptive, 2 45 3.470
707
CRN036 Craniopharyngioma 64 3.464
708
RTC003 Root Caries 32 3.463
709
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 3.409
710
PLP001 Pulpitis 48 3.397
711
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 3.338
712
P RST001 Restless Legs Syndrome 52 3.333
713
P FNG006 Feingold Syndrome 1 62 3.276
714
DFF036 Differentiated Thyroid Carcinoma 51 3.211
715
c PRG106 Progressive Muscular Dystrophy 32 3.206
716
THY128 Thyroid Tumor 35 3.146
717
P EPL140 Epilepsy, Idiopathic Generalized 62 3.138
718
P SDR003 Sideroblastic Anemia 51 3.133
719
BRX001 Bruxism 51 3.084
720
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 3.076
721
MNC019 Monocarboxylate Transporter 1 Deficiency 47 3.076
722
DRG003 Drug Dependence 46 3.067
723
P CYS039 Cystic Kidney Disease 53 3.067
724
PRX085 Preaxial Hallucal Polydactyly 28 3.062
725
GRM010 Germ Cells Tumors 33 3.047
726
CNG092 Congenital Extrahepatic Portosystemic Shunt 24 3.047
727
HMR023 Hemorrhagic Cystitis 43 3.017
728
RHM028 Rheumatic Heart Disease 56 3.016
729
PNN001 Panniculitis 52 3.013
730
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 65 3.005
731
ATR057 Atrioventricular Block 54 2.986
732
P DYS021 Dysautonomia 38 2.981
733
INT017 Intestinal Schistosomiasis 51 2.975
734
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 2.954
735
ANK001 Ankylosis 51 2.947
736
LNN001 Lennox-Gastaut Syndrome 61 2.945
737
P DNT007 Dentin Sensitivity 34 2.918
738
c GLY004 Glycogen Storage Disease V 62 2.900
739
CRT055 Creatine Deficiency Syndromes 37 2.888
740
FBR009 Fibrous Dysplasia 48 2.883
741
SHR097 Short Tarsus with Absence of Lower Eyelashes 25 2.882
742
HYP114 Hypertensive Nephropathy 36 2.872
743
NPH018 Nephrogenic Systemic Fibrosis 49 2.867
744
P ART005 Arteriovenous Malformation 65 2.856
745
P HYP035 Hypophosphatasia 62 2.836
746
FSR001 Fusariosis 45 2.832
747
PNM010 Pneumothorax, Primary Spontaneous 58 2.823
748
MSN004 Mesenchymal Cell Neoplasm 42 2.820
749
INT078 Intracranial Thrombosis 50 2.813
750
ACR008 Acrocallosal Syndrome 70 2.796
751
RFR007 Refractory Anemia with Excess Blasts in Transformation 26 2.753
752
OST016 Osteochondrosis 52 2.737
753
CLS052 Classic Hairy Cell Leukemia 25 2.736
754
PTT046 Pituitary Hormone Deficiency, Combined, 2 62 2.736
755
DBT006 Diabetic Macular Edema 48 2.717
756
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 61 2.713
757
PLR022 Pleural Disease 45 2.709
758
INF118 Inflammatory Myopathy with Abundant Macrophages 27 2.695
759
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 38 2.682
760
P VNS003 Venous Insufficiency 55 2.678
761
c LRG001 Large Cell Carcinoma 48 2.672
762
OBS082 Obstructive Nephropathy 41 2.662
763
P FML340 Familial Episodic Pain Syndrome 50 2.647
764
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 2.643
765
ANS011 Anus Cancer 57 2.639
766
CLN044 Colon Adenoma 44 2.631
767
PRQ002 Paraquat Poisoning 28 2.612
768
P CHN059 Chondrocalcinosis 52 2.609
769
MCR141 Mucormycosis 59 2.602
770
TNP004 Tn Polyagglutination Syndrome 42 2.592
771
P SPN052 Spondyloarthropathy 55 2.585
772
P LNG035 Lung Large Cell Carcinoma 54 2.553
773
NND010 Nondisjunction 34 2.519
774
TNG009 Tongue Squamous Cell Carcinoma 43 2.516
775
SCR015 Scarlet Fever 38 2.516
776
ART010 Arteriolosclerosis 37 2.502
777
CRT033 Corticobasal Degeneration 47 2.501
778
CLC001 Calciphylaxis 51 2.495
779
HMM004 Hamamy Syndrome 39 2.488
780
RNL024 Renal Glucosuria 60 2.487
781
PTN004 Patent Ductus Venosus 31 2.450
782
P ALP004 Alport Syndrome 69 2.450
783
URM005 Uremic Pruritus 45 2.449
784
c HNT010 Huntington Disease-Like 1 55 2.449
785
P LSS002 Lissencephaly 50 2.423
786
OPD006 Opioid Addiction 48 2.389
787
GLN002 Glanders 38 2.385
788
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 2.379
789
P DNT011 Dentinogenesis Imperfecta 52 2.378
790
PSD007 Pseudomyxoma Peritonei 53 2.355
791
ART008 Arteriosclerosis Obliterans 40 2.324
792
LYS029 Lysosomal Disease 30 2.323
793
ERY069 Erythrokeratoderma ''en Cocardes'' 27 2.299
794
P PRD037 Periodontal Ehlers-Danlos Syndrome 49 2.280
795
DNT002 Dentine Erosion 18 2.275
796
PCT003 Pectus Excavatum 46 2.267
797
P CRB048 Cerebral Cavernous Malformations 63 2.263
798
CRL001 Cerulean Cataract 26 2.250
799
PRR019 Perioral Myoclonia with Absences 27 2.243
800
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 57 2.239
801
c CNG413 Congenital Short Bowel Syndrome 42 2.222
802
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 2.215
803
P PSD087 Pseudoxanthoma Elasticum 67 2.213
804
PRT010 Parathyroid Carcinoma 68 2.211
805
DST006 Diastolic Heart Failure 45 2.190
806
P VTM027 Vitamin D-Dependent Rickets, Type 2a 53 2.189
807
DMN026 Dementia Pugilistica 27 2.180
808
c PLM128 Pulmonary Hypertension, Primary, 2 28 2.178
809
c CNG411 Congenital Disorder of Glycosylation, Type in 67 2.161
810
PRR015 Preauricular Fistulae, Congenital 19 2.159
811
PRS115 Prosthetic Joint Infection 42 2.157
812
BLP046 Blepharophimosis, Ptosis, and Epicanthus Inversus 56 2.145
813
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 19 2.135
814
P SCL048 Sclerosteosis 58 2.129
815
OCL008 Oculopharyngeal Muscular Dystrophy 53 2.098
816
SLD003 Sialadenitis 48 2.094
817
STN011 Sting-Associated Vasculopathy with Onset in Infancy 45 2.087
818
DRR014 Darier-White Disease 59 2.074
819
P STN012 Sting-Associated Vasculopathy, Infantile-Onset 42 2.073
820
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 49 2.066
821
NRL004 Neuroleptic Malignant Syndrome 52 2.055
822
PHS027 Phosphoglycoprotein 1 15 2.045
823
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 47 2.042
824
c PSD108 Pseudohypoparathyroidism, Type Ia 65 2.038
825
SMT003 Somatostatinoma 52 2.035
826
MLL002 Miller Fisher Syndrome 40 2.032
827
HMP018 Hemophilic Arthropathy 34 2.005
828
OST004 Osteitis Fibrosa 38 1.985
829
PLM028 Pulmonary Coin Lesion 30 1.964
830
c ALB021 Albinism, Oculocutaneous, Type Ii 59 1.963
831
HYP057 Hypervitaminosis D 37 1.960
832
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 1.956
833
P MTR012 Mitral Valve Disease 57 1.951
834
MLT134 Multiple Pterygium Syndrome, Lethal Type 56 1.947
835
NPH113 Nephroma 37 1.937
836
DSS010 Dissociative Disorder 39 1.936
837
MLK004 Malakoplakia 33 1.919
838
P CND005 Cone Dystrophy 47 1.889
839
MYS004 Myiasis 39 1.875
840
DBT081 Diabetic Encephalopathy 36 1.860
841
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 55 1.859
842
P CLR019 Color Blindness 48 1.859
843
TQP001 Taqi Polymorphism 29 1.834
844
P BRC006 Brachydactyly 51 1.827
845
c CRN243 Carney Complex, Type 1 53 1.827
846
c NRP064 Neuropathy, Congenital Hypomyelinating, 2 35 1.822
847
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 66 1.794
848
ONC003 Oncogenic Osteomalacia 42 1.733
849
CHR515 Chronic Atrial and Intestinal Dysrhythmia 43 1.702
850
CYT018 Cytochrome P450 2d6 Variant 26 1.700
851
CLR033 Color Vision Deficiency 40 1.698
852
P CRT085 Carotid Intimal Medial Thickness 2 22 1.686
853
PRT030 Parathyroid Gland Disease 45 1.685
854
P TRM004 Trimethylaminuria 45 1.684
855
P DNT020 Dent Disease 1 63 1.682
856
P FML023 Familial Hemiplegic Migraine 53 1.654
857
MYX013 Myxofibrosarcoma 44 1.640
858
c ACT076 Acute Myocarditis 47 1.640
859
CRY024 Crystal Arthropathies 18 1.640
860
RDD003 Riddle Syndrome 58 1.635
861
CTN011 Cutaneous Porphyria 45 1.623
862
STR081 Stormorken Syndrome 55 1.622
863
PSD014 Pseudopseudohypoparathyroidism 54 1.612
864
SCR035 Sacral Agenesis with Vertebral Anomalies 38 1.604
865
SMT007 Smith-Fineman-Myers Syndrome 32 1.596
866
c CRB094 Cerebral Cavernous Malformations 3 41 1.585
867
SLN001 Silent Myocardial Infarction 33 1.579
868
c CRB191 Cerebral Cavernous Malformations 2 45 1.545
869
LGH004 Light Chain Deposition Disease 40 1.543
870
VPM001 Vipoma 49 1.505
871
CHN016 Cohen Syndrome 60 1.495
872
CRD016 Cardiac Rupture 34 1.485
873
DNT006 Dental Pulp Necrosis 43 1.483
874
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 18 1.453
875
SPR004 Supravalvular Aortic Stenosis 57 1.448
876
P NLD001 Nail Disease 51 1.448
877
c HYP292 Hypophosphatasia, Infantile 55 1.443
878
c ADL052 Adult Acute Lymphocytic Leukemia 46 1.420
879
DSR072 Disorder of Energy Metabolism 10 1.419
880
HYD005 Hydrocele 46 1.411
881
NRD102 Neurodevelopmental Disorder with Progressive Microcephaly, Spasticity, and Brain Imaging Abnormalities 33 1.398
882
BTT018 Beta-Thalassemia Intermedia 31 1.398
883
STV003 Stuve-Wiedemann Syndrome 52 1.392
884
BSL009 Basal Ganglia Calcification 45 1.353
885
GNT001 Giant Cell Reparative Granuloma 40 1.353
886
CHL028 Childhood Type Dermatomyositis 59 1.353
887
P QLT041 Qualitative or Quantitative Defects of Alpha-Dystroglycan 18 1.352
888
CVR006 Cavernous Hemangioma 51 1.352
889
c CNG441 Congenital Muscular Dystrophy Due to Dystroglycanopathy 28 1.352
890
GMS001 Gemistocytic Astrocytoma 32 1.341
891
BNS001 Bone Osteosarcoma 40 1.334
892
TXC011 Toxocariasis 46 1.324
893
EPL001 Epilepsy with Generalized Tonic-Clonic Seizures 40 1.315
894
c ALB019 Albinism, Oculocutaneous, Type Iv 48 1.288
895
HYP789 Hypophosphatemic Rickets with Hypercalciuria, Hereditary 49 1.281
896
P SKL032 Skeletal Muscle Disease 25 1.255
897
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 53 1.246
898
MLG061 Malignant Choroid Melanoma 33 1.237
899
P MYP087 Myopathy, Tubular Aggregate, 1 49 1.188
900
FSS001 Fissured Tongue 30 1.165
901
CNR001 Coenurosis 26 1.153
902
P BSL038 Basal Ganglia Calcification, Idiopathic, 1 53 1.143
903
CTN020 Cutaneous Sclerosis 16 1.140
904
FML327 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis 18 1.140
905
P VTM026 Vitamin D Hydroxylation-Deficient Rickets, Type 1a 45 1.114
906
HYP636 Hypocalcemic Vitamin D-Dependent Rickets 38 1.114
907
c ALB017 Albinism, Oculocutaneous, Type Vi 30 1.089
908
TTH032 Tooth Size 35 1.057
909
c MGR030 Migraine, Familial Hemiplegic, 2 49 1.057
910
SLL001 Sialolithiasis 36 1.049
911
c CRD163 Cardiofaciocutaneous Syndrome 2 37 1.016
912
FML091 Familial Tumoral Calcinosis 43 1.009
913
RGH006 Right Aortic Arch 29 0.991
914
TYM001 Tympanosclerosis 36 0.991
915
ALX002 Alexithymia 37 0.956
916
c MSC037 Muscular Dystrophy-Dystroglycanopathy , Type a, 4 60 0.956
917
DSR031 Disorder of Copper Metabolism 25 0.932
918
MXD032 Mixed Germ Cell Tumor 24 0.932
919
FML008 Familial Retinoblastoma 50 0.921
920
PRN038 Prune Belly Syndrome 56 0.858
921
HYD001 Hydranencephaly 43 0.858
922
LRR002 Lrrk2 Parkinson Disease 9 0.853
923
SLR005 Solar Urticaria 29 0.824
924
TRD003 Taurodontism 30 0.824
925
ANG004 Angioid Streaks 40 0.792
926
P TMR018 Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 60 0.792
927
PLM017 Pulmonary Alveolar Microlithiasis 47 0.757
928
c LBR012 Leber Congenital Amaurosis 2 52 0.722
929
DNT046 Dental Abscess 32 0.719
930
PNK001 Pink1 Type of Young-Onset Parkinson Disease 8 0.676
931
DNT021 Dent Disease 2 37 0.625
932
ORM002 Oromandibular Dystonia 40 0.625
933
RGN005 Regional Odontodysplasia 23 0.625
934
GST111 Gastroenteropancreatic Neuroendocrine Neoplasm 18 0.558
935
c SPN314 Spinocerebellar Ataxia 10 47 0.558
936
c RTN050 Retinitis Pigmentosa 20 38 0.558
937
ERB002 Erb's Palsy 13 0.558
Content
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