Search results for TTR

860 hits were found for TTR

# Family MCID Name MIFTS Score
2
P CRP001 Carpal Tunnel Syndrome 66 37.232
3
P AMY004 Amyloidosis 69 34.520
4
HYP645 Hyperthyroxinemia, Dystransthyretinemic 20 31.338
5
c ATR087 Atrial Standstill 1 74 29.658
6
c HRD039 Hereditary Amyloidosis 45 28.741
7
P PLY019 Polyneuropathy 53 28.066
8
P CHR071 Charcot-Marie-Tooth Disease 64 25.848
9
P HRD207 Hereditary Transthyretin Amyloidosis 25 23.953
10
DFC004 Deficiency Anemia 74 20.480
11
PNC001 Pancytopenia 52 15.025
12
HYP029 Hyperthyroxinemia 32 14.866
13
P HRT032 Heart Disease 84 14.799
14
P NRP001 Neuropathy 59 14.232
15
NTR005 Nutritional Deficiency Disease 60 13.605
16
AMY005 Amyloid Neuropathy 31 13.559
17
P RST002 Restrictive Cardiomyopathy 54 13.169
18
P ALZ034 Alzheimer Disease 87 12.548
19
P KDN018 Kidney Disease 72 12.390
20
ATN004 Autonomic Neuropathy 42 11.883
21
P HYP061 Hypertrophic Cardiomyopathy 69 11.778
22
P DMN002 Dementia 65 11.500
23
c CHR684 Chronic Kidney Disease 74 10.801
24
P HYP086 Hypothyroidism 69 10.794
25
P RHM011 Rheumatoid Arthritis 81 10.680
26
PRT038 Protein-Energy Malnutrition 53 10.654
27
c TYP009 Type 2 Diabetes Mellitus 92 10.550
28
LVR012 Liver Cirrhosis 62 10.517
30
PHN003 Phenylketonuria 76 10.354
31
P CHR573 Choroid Plexus Cancer 48 10.354
32
P RSP003 Respiratory Failure 74 10.251
33
AMY082 Amyloidosis, Familial Visceral 52 10.224
34
P OBS001 Obstructive Jaundice 49 10.224
35
ANR007 Anorexia Nervosa 59 10.046
36
P BRG001 Brugada Syndrome 69 9.731
37
P PRP019 Peripheral Nervous System Disease 57 9.676
38
P DMY001 Demyelinating Polyneuropathy 41 9.631
39
P AMY084 Amyloidosis, Finnish Type 51 9.494
40
INT323 Intraocular Pressure Quantitative Trait Locus 63 9.276
41
P DBT009 Diabetes Mellitus 67 9.272
42
END086 End Stage Renal Disease 54 9.252
43
c BNM010 Bone Marrow Failure Syndrome 1 37 9.225
44
CRB039 Cerebrovascular Disease 65 9.169
45
P HYD006 Hydrocephalus 63 8.900
46
KRT002 Keratomalacia 54 8.811
47
PPL058 Papilloma of Choroid Plexus 54 8.784
48
P NRM002 Normal Pressure Hydrocephalus 49 8.651
49
MTR007 Motor Peripheral Neuropathy 41 8.614
50
P PRK057 Parkinson Disease, Late-Onset 79 8.587
51
c CNT035 Central Nervous System Disease 53 8.587
52
P DRR001 Diarrhea 55 8.543
53
MLY001 Molybdenum Cofactor Deficiency 40 8.528
54
P MYP004 Myopathy 67 8.528
55
P HYP058 Hypervitaminosis a 47 8.454
56
TTH006 Tooth Disease 51 8.454
57
P ART021 Arteriosclerosis 53 8.432
58
BRT005 Barth Syndrome 55 8.408
59
FND001 Fundus Albipunctatus 55 8.408
60
PRT058 Pure Autonomic Failure 58 8.408
61
TST018 Testicular Yolk Sac Tumor 39 8.380
62
P END033 Endocarditis 58 8.305
63
P SHR001 Short Bowel Syndrome 53 8.202
64
DYS015 Dysentery 50 8.202
65
P FCL005 Focal Segmental Glomerulosclerosis 57 8.202
66
HPT019 Hepatic Encephalopathy 59 8.202
67
ATR073 Atrophic Glossitis 28 8.202
68
GLS007 Glossitis 46 8.202
69
CHR096 Chronic Pulmonary Heart Disease 41 8.202
70
DCB001 Decubitus Ulcer 61 8.202
71
c ALM001 Al Amyloidosis 54 7.957
72
HRT008 Heart Conduction Disease 44 7.226
73
MNN017 Mononeuropathy 41 6.824
74
c AMY009 Amyloidosis Aa 47 6.824
75
XRP001 Xerophthalmia 42 6.698
76
ANL018 Analbuminemia 52 6.236
77
P PRC012 Pericardial Effusion 50 6.141
78
PPL013 Papillary Ependymoma 29 6.091
79
MDN002 Median Neuropathy 24 6.006
80
AMY002 Amyloid Tumor 26 5.903
81
MXD001 Mixed Cerebral Palsy 20 5.800
82
ATS009 Autosomal Genetic Disease 24 5.800
83
ATN001 Autonomic Peripheral Neuropathy 17 5.800
84
P ACQ009 Acquired Metabolic Disease 26 5.800
85
c BLC007 Bile Acid Synthesis Defect, Congenital, 1 45 5.800
86
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 5.800
87
GRS011 Gerstmann-Straussler Disease 55 5.800
88
DGR001 Digeorge Syndrome 62 5.800
89
DSS008 Disease of Mental Health 74 5.800
90
P PRC050 Pericardium Disease 31 5.800
91
CHR100 Chronic Ulcer of Skin 57 5.800
92
SPP006 Suppurative Uveitis 14 5.800
93
CRB202 Cerebrovascular Benign Neoplasm 18 5.800
94
ENC002 Eunuchism 22 5.800
95
ESP026 Esophagus Sarcoma 29 5.800
96
INT034 Intracranial Cavernous Angioma 23 5.800
97
INT077 Intracranial Structure Hemangioma 16 5.800
98
KWS001 Kwashiorkor 44 5.800
99
ALC011 Alcoholic Neuropathy 35 5.800
100
MRS001 Marasmus 41 5.800
101
P ATN002 Autonomic Nervous System Disease 51 5.800
102
CNJ011 Conjunctival Deposit 17 5.800
103
CRB040 Cerebrum Cancer 27 5.800
104
BLP001 Blepharochalasis 26 5.800
105
c PRK093 Parkinson Disease 8, Autosomal Dominant 49 5.800
106
CRB038 Cerebral Ventricle Cancer 29 5.800
107
BST003 Bestiality 31 5.800
108
NRV004 Nerve Compression Syndrome 47 5.800
109
ASY004 Asymmetric Motor Neuropathy 18 5.800
110
PDT025 Pediatric Multiple Sclerosis 35 5.800
111
LGN005 Ligneous Conjunctivitis 30 5.800
112
MNN020 Meningococcal Infection 45 5.800
113
CRT011 Carotenemia 23 5.800
114
WLD005 Wild Type Attr Amyloidosis 29 4.525
115
P ATR011 Atrial Fibrillation 66 4.460
116
ATN005 Autonomic Dysfunction 45 3.197
117
CNG034 Congestive Heart Failure 69 2.412
118
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.380
119
P OVR042 Ovarian Cancer 88 2.049
120
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 2.016
121
IMP005 Impotence 52 2.014
122
DBT010 Diabetic Neuropathy 54 1.997
123
P SDR002 Siderosis 42 1.805
124
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.799
125
P NRB001 Neuroblastoma 66 1.798
126
P DYS021 Dysautonomia 38 1.758
127
47X002 47,xyy 48 1.733
128
P AXN001 Axonal Neuropathy 33 1.726
129
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 56 1.681
130
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.669
131
PRT251 Proteinuria, Chronic Benign 58 1.587
132
P THR014 Thrombocytopenia 66 1.551
133
STR067 Stroke, Ischemic 79 1.486
134
c BRG005 Brugada Syndrome 1 56 1.426
135
CRD132 Cardiac Conduction Defect 59 1.426
136
c PRG126 Progressive Familial Heart Block 59 1.426
137
SNS003 Sensory Peripheral Neuropathy 51 1.415
138
P LNG032 Lung Cancer 98 1.374
139
NRL005 Neurilemmoma 60 1.345
140
MCL003 Macular Holes 44 1.315
141
c THR092 Thrombophilia Due to Thrombin Defect 74 1.284
142
P HPT023 Hepatocellular Carcinoma 95 1.280
143
P MYP006 Myopia 55 1.259
144
P TRT010 Teratoma 50 1.241
145
SPR066 Superficial Siderosis 42 1.226
146
P MTR014 Motor Neuron Disease 65 1.210
147
PRS063 Paresthesia 39 1.198
148
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.140
149
P UVT001 Uveitis 57 1.140
150
GST033 Gestational Diabetes 61 1.129
151
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 1.118
152
KRT001 Keratoconjunctivitis Sicca 49 1.062
153
c HYP836 Hypercholesterolemia, Familial, 1 73 1.050
154
HMN044 Human Immunodeficiency Virus Type 1 76 1.030
155
SPR032 Superficial Siderosis of the Central Nervous System 22 1.030
156
P LVR013 Liver Disease 68 1.024
157
P NRV007 Nervous System Disease 66 1.016
158
DYS073 Dysphagia 53 0.982
159
ARG004 Argyria 26 0.982
160
DBT004 Diabetic Polyneuropathy 50 0.951
161
P MSC005 Muscular Dystrophy 66 0.951
162
SXL003 Sexual Disorder 49 0.934
163
P PLY020 Polyradiculoneuropathy 47 0.934
164
P TRM003 Tremor 50 0.916
165
PTH003 Pathologic Nystagmus 52 0.916
166
P VTR007 Vitreoretinopathy 45 0.916
167
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 39 0.913
168
FTL073 Fetal Anticonvulsant Syndrome 24 0.913
169
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 35 0.898
170
c ACT068 Acute Cystitis 61 0.898
171
c MCR115 Microvascular Complications of Diabetes 5 65 0.896
172
P BRS047 Breast Cancer 97 0.889
173
c THR037 Thrombocytopenia 2 37 0.877
175
c PRC016 Pre-Eclampsia 64 0.872
176
P HNT016 Huntington Disease 73 0.856
177
FBR012 Fabry Disease 71 0.856
178
P SZR006 Seizure Disorder 69 0.831
179
P SLP005 Sleep Disorder 62 0.831
180
HLX001 Helix Syndrome 47 0.829
181
DWN001 Down Syndrome 70 0.824
182
P PRS040 Prostate Cancer 95 0.823
183
c SML038 Small Cell Cancer of the Lung 69 0.823
184
PRS012 Pars Planitis 47 0.804
185
P OPN001 Open-Angle Glaucoma 55 0.804
186
c INT064 Intermediate Uveitis 54 0.804
187
P NPH012 Nephrotic Syndrome 62 0.804
188
P TCD001 Tic Disorder 50 0.804
189
SPS019 Spastic Paraparesis 38 0.804
190
P CTR002 Cataract 59 0.804
191
P ADN016 Adenocarcinoma 63 0.796
192
MLD018 Mild Cognitive Impairment 48 0.790
193
P PNC035 Pancreatic Cancer 86 0.763
194
CHR074 Choriocarcinoma 46 0.734
195
TRN015 Transient Cerebral Ischemia 62 0.734
196
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 68 0.728
197
P URN019 Urinary Tract Infection 49 0.728
198
P MYT002 Myotonic Dystrophy 51 0.728
199
P NRF002 Neurofibromatosis 60 0.728
200
ERY029 Erythermalgia, Primary 58 0.727
201
INS024 Insulin-Like Growth Factor I 77 0.727
202
ADL002 Adult Syndrome 69 0.723
203
AND005 Androgen Insensitivity Syndrome, Mild 21 0.723
204
CHL065 Cholangiocarcinoma 58 0.697
205
INT079 Intrahepatic Cholangiocarcinoma 51 0.697
206
c HRD088 Hereditary Neuropathies 34 0.682
207
END057 Endometrial Cancer 71 0.658
208
THR024 Thrombosis 56 0.658
209
SHR107 Short Stature-Obesity Syndrome 25 0.650
210
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 0.646
211
c SPN330 Spondylocostal Dysostosis 5 55 0.646
212
c ORT011 Orthostatic Hypotension 1 43 0.646
213
GST050 Gastrointestinal System Disease 55 0.646
214
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.642
215
P LTR001 Lateral Sclerosis 58 0.642
216
P LKM062 Leukemia, Acute Lymphoblastic 69 0.635
217
P CLR023 Colorectal Cancer 100 0.634
218
P LPR021 Leprosy 3 71 0.626
219
NRG002 Neurogenic Bladder 55 0.626
220
HNS001 Hansen's Disease 32 0.626
221
APM002 Aapoai Amyloidosis 14 0.626
222
ISC004 Ischemia 61 0.625
223
OST012 Osteoarthritis 77 0.625
224
P BCL017 B-Cell Lymphoma 57 0.617
225
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.608
226
CNS004 Constipation 56 0.608
227
DFF005 Diffuse Large B-Cell Lymphoma 55 0.600
228
P LYM118 Lymphoma 69 0.600
229
HYP066 Hyperglycemia 60 0.591
230
HRT012 Heart Valve Disease 53 0.591
231
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.582
232
OVR094 Ovarian Epithelial Cancer 39 0.582
233
PLM033 Pulmonary Embolism 58 0.582
234
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.544
235
GLC003 Glucose Intolerance 53 0.544
236
CLL010 Cellular Ependymoma 58 0.544
237
P GST053 Gastric Cancer 82 0.534
238
P GLM040 Glioma Susceptibility 1 70 0.534
239
CRD223 Cardiac Arrhythmia 63 0.534
240
MLG169 Malignant Astrocytoma 57 0.534
241
P BLD134 Bladder Cancer 79 0.524
242
P PRN023 Prion Disease 60 0.524
243
P VSC007 Vascular Disease 62 0.524
244
P BNG030 Benign Ependymoma 51 0.514
245
PPL022 Papilloma 53 0.504
246
SQM002 Squamous Cell Papilloma 45 0.504
247
EMB004 Embryonal Carcinoma 55 0.504
248
P ART022 Arthritis 70 0.504
249
MYL069 Myeloma, Multiple 77 0.482
250
P NTR004 Neutropenia 62 0.482
251
P EYD002 Eye Disease 57 0.471
252
SPN027 Spinal Stenosis 59 0.460
253
P ENC018 Encephalopathy 62 0.460
254
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.448
255
P SBS003 Substance Abuse 54 0.448
256
GST040 Gastric Adenocarcinoma 66 0.448
257
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.436
258
P MJR001 Major Depressive Disorder 68 0.436
259
ATR057 Atrioventricular Block 54 0.436
260
MNT002 Mental Depression 56 0.436
261
TRM010 Traumatic Brain Injury 50 0.436
262
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.424
263
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.424
264
CRB004 Cerebral Artery Occlusion 46 0.424
265
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.424
266
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.424
267
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.424
268
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.424
269
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.424
270
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.424
271
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.424
272
c MJR024 Major Affective Disorder 9 40 0.424
273
c MJR022 Major Affective Disorder 8 37 0.424
274
HRW001 Hair Whorl 35 0.424
275
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.424
276
P BPL003 Bipolar Disorder 56 0.424
277
P HYP076 Hyperthyroidism 53 0.424
278
GLB002 Glioblastoma 67 0.411
279
P RCT021 Rectum Cancer 54 0.411
280
SQM006 Squamous Cell Carcinoma 59 0.411
281
P VSC011 Vasculitis 61 0.411
282
SYN036 Syncope 44 0.411
283
48X005 48,xyyy 39 0.411
284
c GRV008 Graves Disease 1 54 0.398
286
P ALC033 Alcohol Use Disorder 67 0.398
287
MCN001 Mucinous Adenocarcinoma 49 0.398
288
ANH002 Anhidrosis 45 0.398
289
APP009 Appendix Adenocarcinoma 47 0.398
290
RTN017 Retinal Detachment 60 0.385
291
P CTN015 Cutaneous T Cell Lymphoma 48 0.385
292
PRP080 Peripheral Artery Disease 54 0.385
293
c SVR005 Severe Pre-Eclampsia 50 0.385
294
PLS009 Plasma Cell Neoplasm 64 0.385
295
RTN001 Retinal Vasculitis 46 0.385
296
ART140 Arteries, Anomalies of 52 0.371
297
ESP021 Esophageal Cancer 84 0.371
298
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.371
299
LPP008 Lipoprotein Quantitative Trait Locus 65 0.371
300
P LNG064 Lung Cancer Susceptibility 3 70 0.371
301
c HPT016 Hepatitis B 62 0.371
302
P RTN022 Retinal Vein Occlusion 54 0.371
303
c DLT002 Dilated Cardiomyopathy 79 0.371
304
GST019 Gastrointestinal Stromal Tumor 78 0.371
305
INH007 Inherited Thyroxine-Binding Globulin Deficiency 13 0.371
306
c JVN010 Juvenile Rheumatoid Arthritis 66 0.371
307
FRN006 Frontotemporal Dementia 68 0.356
308
INT395 Intracranial Meningioma 48 0.356
309
MNN043 Meningioma, Familial 79 0.356
310
RDC002 Radiculopathy 51 0.356
311
P MSC003 Muscular Atrophy 52 0.356
312
BRN071 Brain Injury 50 0.356
313
SCR001 Secretory Meningioma 40 0.356
314
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.356
315
THY029 Thyroid Carcinoma 54 0.356
316
P PLM037 Pulmonary Hypertension 69 0.341
317
BCT022 Bacterial Infectious Disease 56 0.341
318
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.341
319
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.341
320
P HYP750 Hypertriglyceridemia, Familial 62 0.341
321
ATM095 Autoimmune Disease 61 0.341
322
HMR039 Hemorrhage, Intracerebral 57 0.341
323
P SCK002 Sick Sinus Syndrome 55 0.341
324
HMS001 Hemosiderosis 48 0.341
325
HMP001 Hemopericardium 47 0.341
326
DMY004 Demyelinating Disease 50 0.341
327
c LKM061 Leukemia, Acute Myeloid 83 0.341
328
KRT006 Keratoconjunctivitis 53 0.341
329
P AVS003 Avascular Necrosis 41 0.341
330
P SPP010 Suppressor of Tumorigenicity 3 51 0.325
331
MYC006 Mycosis Fungoides 65 0.325
332
c BRN108 Branchiootic Syndrome 1 63 0.325
333
ATS010 Autosomal Recessive Disease 42 0.325
334
APH002 Aphasia 55 0.325
335
P MYC007 Myocardial Infarction 69 0.325
336
SRC014 Sarcoma 64 0.325
337
c DPH024 Diaphragmatic Hernia, Congenital 64 0.325
338
P LKM071 Leukemia, Chronic Lymphocytic 74 0.325
339
P MLN008 Melanoma 75 0.325
340
P PLY011 Polycystic Ovary Syndrome 57 0.325
341
INS001 Insulinoma 59 0.325
342
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.325
343
TRC022 Tricuspid Valve Insufficiency 47 0.325
344
SPN035 Spindle Cell Sarcoma 51 0.325
345
c BCT013 Bacterial Pneumonia 47 0.325
346
OLG006 Oligoastrocytoma 35 0.325
347
GLC036 Glucagonoma 45 0.325
348
c ACT075 Acute Myocardial Infarction 55 0.325
349
AGN016 Aging 54 0.308
350
CRV035 Cervical Cancer 72 0.308
351
RLP008 Relapsed/refractory Diffuse Large B-Cell Lymphoma 35 0.308
352
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.308
353
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 0.308
354
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.308
355
P PRG013 Paraganglioma 57 0.308
356
P RTN018 Retinal Disease 53 0.308
357
CRB037 Cerebral Palsy 67 0.308
358
LYM021 Lymphadenitis 56 0.308
359
HLL004 Hellp Syndrome 53 0.308
360
INT010 Intracranial Embolism 48 0.308
361
DPR016 Depression 65 0.308
362
SFT003 Soft Tissue Sarcoma 57 0.308
363
P MYL006 Myeloid Leukemia 60 0.308
364
P INS002 in Situ Carcinoma 53 0.308
365
P HMP007 Hemophilia 52 0.308
366
SPL018 Splenomegaly 47 0.308
367
FTT001 Fatty Liver Disease 61 0.308
368
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.308
369
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.291
370
ADR016 Adrenal Cortical Carcinoma 61 0.291
371
P SNS001 Sensorineural Hearing Loss 59 0.291
372
P VNS003 Venous Insufficiency 54 0.291
373
NNL006 Non-Alcoholic Steatohepatitis 54 0.291
374
P OST002 Osteoporosis 77 0.291
375
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 57 0.291
376
P SLP006 Sleep Apnea 69 0.291
377
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.291
378
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.291
379
c PRG019 Paragangliomas 2 30 0.291
380
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.291
381
KRT019 Keratitis, Hereditary 66 0.291
382
ADN018 Adenoma 58 0.291
383
ANP006 Anaplastic Ependymoma 46 0.291
384
SYN007 Synovitis 54 0.291
385
HYP080 Hypogonadism 49 0.291
386
PLC002 Plica Syndrome 35 0.291
387
P OLG002 Oligodendroglioma 66 0.291
388
ADR004 Adrenal Cortical Adenocarcinoma 38 0.291
389
TRT001 Teratocarcinoma 41 0.291
390
CLR030 Clear Cell Renal Cell Carcinoma 54 0.291
391
GRW007 Growth Hormone Deficiency 47 0.291
392
P SCH015 Schizophrenia 74 0.272
393
c HMP029 Hemophilia a 69 0.272
394
OCL069 Ocular Motor Apraxia 57 0.272
395
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.272
396
c MCR133 Microvascular Complications of Diabetes 4 41 0.272
397
P RST001 Restless Legs Syndrome 52 0.272
398
CMR002 Coumarin Resistance 60 0.272
399
P CLC063 Celiac Disease 1 66 0.272
400
DCT002 Ductal Carcinoma in Situ 58 0.272
401
CLR108 Colorectal Adenoma 63 0.272
402
CLR109 Colorectal Adenocarcinoma 50 0.272
403
c HPT073 Hepatitis C Virus 71 0.272
404
FCT001 Factor Viii Deficiency 62 0.272
405
c MCR113 Microvascular Complications of Diabetes 3 52 0.272
406
c MCR130 Microvascular Complications of Diabetes 6 41 0.272
407
c MCR120 Microvascular Complications of Diabetes 7 47 0.272
408
DRY001 Dry Eye Syndrome 49 0.272
409
RHM028 Rheumatic Heart Disease 56 0.272
410
P ENT005 Entropion 34 0.272
411
c HPT001 Hepatitis C 61 0.272
412
PNM008 Pneumothorax 54 0.272
413
TRN018 Transitional Cell Carcinoma 56 0.272
414
CNT016 Central Retinal Vein Occlusion 54 0.272
415
AMN001 Amenorrhea 53 0.272
416
CHL123 Chlamydia 58 0.272
417
GTR002 Goiter 52 0.272
418
TRC008 Trachoma 53 0.272
419
P GLM007 Glomerulonephritis 59 0.272
420
c ACT071 Acute Kidney Failure 60 0.272
421
CRN036 Craniopharyngioma 63 0.272
422
BLD131 Bladder Urothelial Carcinoma 59 0.272
423
SPN020 Spondylosis 46 0.272
424
SRS001 Serous Cystadenocarcinoma 51 0.272
425
P ORT004 Orthostatic Intolerance 62 0.272
426
P CRN300 Coronary Heart Disease 1 73 0.272
427
P GST044 Gastritis 55 0.272
428
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.272
429
HYP266 Hypoxia 56 0.272
430
P LPS004 Lupus Erythematosus 61 0.272
431
MSL001 Measles 61 0.272
432
HYP056 Hypoglycemia 65 0.272
433
HPR003 Heparin-Induced Thrombocytopenia 47 0.272
434
P ATR005 Atrophic Gastritis 50 0.272
435
PYG006 Pyogenic Granuloma 36 0.272
436
NRT011 Neurotrophic Keratopathy 36 0.272
437
BLP046 Blepharophimosis, Ptosis, and Epicanthus Inversus 56 0.252
438
CYS001 Cystic Fibrosis 77 0.252
439
LYM133 Lymphoma, Hodgkin, Classic 74 0.252
440
DYS182 Dysphasia, Familial Developmental 34 0.252
441
P INF037 Inflammatory Bowel Disease 53 0.252
442
GST105 Gastroesophageal Adenocarcinoma 42 0.252
443
P MLN069 Melanoma, Uveal 59 0.252
444
P SPC019 Specific Language Impairment 31 0.252
445
P LYM033 Lymphoproliferative Syndrome 59 0.252
446
c SYS001 Systemic Lupus Erythematosus 86 0.252
447
c NRB014 Neuroblastoma 3 27 0.252
448
P MTR004 Maturity-Onset Diabetes of the Young 66 0.252
449
URT049 Urate Oxidase, Pseudogene 24 0.252
450
LKS001 Leukostasis 40 0.252
451
CHL068 Cholestasis 61 0.252
452
P HPT021 Hepatitis 68 0.252
453
RTN020 Retinal Vascular Disease 45 0.252
454
P ESP024 Esophagitis 60 0.252
455
LYM009 Lymphocytic Choriomeningitis 46 0.252
456
P GRV001 Graves' Disease 54 0.252
457
P LKM002 Leukemia 66 0.252
458
LNG039 Lung Squamous Cell Carcinoma 57 0.252
459
CLN015 Colon Adenocarcinoma 64 0.252
460
DGN002 Degenerative Myopia 31 0.252
461
IRD001 Iridocyclitis 54 0.252
462
P HDC001 Headache 56 0.252
463
P MNC007 Monocytic Leukemia 48 0.252
464
VSC002 Vascular Dementia 59 0.252
465
PRT036 Peritonitis 65 0.252
466
SKN019 Skin Melanoma 70 0.252
467
SBC016 Subacute Delirium 42 0.252
468
RFR003 Refractive Error 41 0.252
469
HYP141 Hyperphenylalaninemia 42 0.252
470
c GLL024 Gallbladder Disease 1 53 0.230
471
c ORF040 Orofaciodigital Syndrome Viii 49 0.230
472
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.230
473
HMC014 Homocysteinemia 52 0.230
474
P PRK039 Parkinsonism 55 0.230
475
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.230
476
CYC001 Cycloplegia 35 0.230
477
c VRL005 Viral Pneumonia 52 0.230
478
P CHR625 Charcot-Marie-Tooth Disease, Demyelinating, Type 1b 57 0.230
479
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 0.230
480
P FML018 Familial Mediterranean Fever 73 0.230
481
P MYC084 Mycobacterium Tuberculosis 1 68 0.230
482
c SPN294 Spinocerebellar Ataxia 1 53 0.230
483
LPT014 Leptin Deficiency or Dysfunction 77 0.230
484
BRC012 Brucellosis 66 0.230
485
P ANT006 Antiphospholipid Syndrome 55 0.230
486
P MVM001 Movement Disease 61 0.230
487
c INF023 Inflammatory Breast Carcinoma 48 0.230
488
P DYS154 Dystonia 64 0.230
489
P GLL022 Guillain-Barre Syndrome 59 0.230
490
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.230
491
CHL004 Cholelithiasis 48 0.230
492
RTN003 Retinal Ischemia 48 0.230
493
P ART023 Arthropathy 60 0.230
494
P BLD036 Bile Duct Disease 43 0.230
495
P THL005 Thalassemia 56 0.230
496
ACT058 Active Peptic Ulcer Disease 55 0.230
497
P TRC031 Trichorhinophalangeal Syndrome 37 0.230
498
CHR178 Chromosomal Triplication 34 0.230
499
P CHL066 Cholangitis 51 0.230
500
ELS001 Eales Disease 45 0.230
501
P RRT020 Rare Tumor 39 0.230
502
ANX010 Anxiety 70 0.206
503
LYM143 Lymphoma, Non-Hodgkin, Familial 79 0.206
504
c HNT004 Huntington Disease-Like 2 51 0.206
505
P GRF003 Graft-Versus-Host Disease 71 0.206
506
CVD001 Covid-19 58 0.206
507
PLY150 Polykaryocytosis Inducer 29 0.206
508
OBS002 Obsessive-Compulsive Disorder 68 0.206
509
P MLT020 Multiple Sclerosis 79 0.206
510
ORL015 Oral Squamous Cell Carcinoma 43 0.206
511
P EXN002 Exanthem 58 0.206
512
LRG014 Large Cell Neuroendocrine Carcinoma 44 0.206
513
c HNT011 Huntington Disease-Like 3 33 0.206
514
c NMN014 Niemann-Pick Disease, Type C2 49 0.206
515
HYP186 Hypertrophic Neuropathy of Dejerine-Sottas 52 0.206
516
c PLM164 Pulmonary Hypertension, Primary, 1 80 0.206
517
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 54 0.206
518
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 0.206
519
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 16 0.206
520
P EPL164 Epilepsy 70 0.206
521
HYP060 Hyperinsulinism 53 0.206
522
P BND020 Bone Disease 60 0.206
523
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.206
524
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.206
525
TRC005 Tracheal Stenosis 43 0.206
526
BRN004 Brain Edema 54 0.206
527
OVR063 Overnutrition 42 0.206
528
P MTR003 Mitral Valve Stenosis 53 0.206
529
PPL007 Papillary Serous Adenocarcinoma 42 0.206
530
P KDN017 Kidney Cancer 60 0.206
531
P ECL001 Eclampsia 52 0.206
532
PMS001 Poems Syndrome 59 0.206
533
OBS004 Obstructive Hydrocephalus 45 0.206
534
NRN001 Neuroendocrine Carcinoma 47 0.206
535
P HYP024 Hypoparathyroidism 55 0.206
536
CHL039 Choledocholithiasis 37 0.206
537
P FBR017 Fibrosarcoma 55 0.206
538
P BLD062 Bile Duct Cancer 68 0.206
539
PNC034 Pancreas Disease 49 0.206
540
c CHR647 Charcot-Marie-Tooth Disease, Demyelinating, Type 1c 46 0.206
541
TRC110 Tracheobronchial Stenosis, Congenital 28 0.206
542
c PNC106 Pancreatic Agenesis 1 51 0.206
543
P NSP012 Nasopharyngeal Carcinoma 60 0.206
544
DRM006 Dermatitis 62 0.206
545
CHR466 Chronic Thromboembolic Pulmonary Hypertension 47 0.206
546
GLM045 Glioma 62 0.206
547
GLL048 Glial Tumor 52 0.206
548
GST012 Gastroesophageal Junction Adenocarcinoma 45 0.206
549
c RNG015 Ring Chromosome 2 22 0.206
550
HPT022 Hepatoblastoma 54 0.206
551
c ACT135 Acute Graft Versus Host Disease 51 0.206
552
P PRM227 Primary Orthostatic Hypotension 23 0.206
553
ADG002 Audiogenic Seizures 25 0.206
554
RRS004 Rare Systemic Disease 12 0.206
555
P OVR082 Overgrowth Syndrome 42 0.206
556
P MCH002 Machado-Joseph Disease 63 0.178
557
c NPH049 Nephrotic Syndrome, Type 2 52 0.178
558
MYL009 Myelodysplastic Syndrome 67 0.178
559
P STR022 Stargardt Disease 61 0.178
560
PRT013 Portal Hypertension 59 0.178
561
P CRB045 Cerebellar Hypoplasia 40 0.178
562
MRF001 Marfan Syndrome 76 0.178
563
P MYS005 Myositis 56 0.178
564
BRK010 Burkitt Lymphoma 66 0.178
565
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.178
566
c TYP008 Type 1 Diabetes Mellitus 77 0.178
567
END075 Endocervical Adenocarcinoma 37 0.178
568
P PRG002 Progesterone-Receptor Positive Breast Cancer 32 0.178
569
BCT021 Bacterial Sepsis 43 0.178
570
P SLM003 Salmonellosis 54 0.178
571
P FLL037 Follicular Lymphoma 73 0.178
572
ASP030 Aspirin Resistance 40 0.178
573
INC002 Inclusion Body Myositis 57 0.178
574
PPL052 Papillomatosis, Confluent and Reticulated 34 0.178
575
P CRB048 Cerebral Cavernous Malformations 63 0.178
576
c CHL119 Cholangitis, Primary Sclerosing 57 0.178
577
c FML021 Familial Hypercholesterolemia 71 0.178
578
HMG005 Hemoglobinopathy 55 0.178
579
THY020 Thyroid Hyalinizing Trabecular Adenoma 19 0.178
580
BRW004 Brown-Sequard Syndrome 31 0.178
581
FBR047 Fibromyalgia 58 0.178
582
THY030 Thyroid Gland Disease 50 0.178
583
P HMN010 Hemangioma 61 0.178
584
P END039 Endodermal Sinus Tumor 42 0.178
585
NVS001 Neovascular Glaucoma 52 0.178
586
c BPL002 Bipolar I Disorder 47 0.178
587
P NMN002 Niemann-Pick Disease 60 0.178
588
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.178
589
P SCL009 Sclerosing Cholangitis 46 0.178
590
TXC005 Toxic Shock Syndrome 62 0.178
591
PLR008 Pleurisy 49 0.178
592
DDN003 Duodenum Adenocarcinoma 37 0.178
593
PRD004 Prediabetes Syndrome 52 0.178
594
PNC129 Pancreatic Adenocarcinoma 65 0.178
595
P CNT005 Central Nervous System Lymphoma 51 0.178
596
P CRV031 Cervical Adenocarcinoma 48 0.178
597
BLR008 Bilirubin Metabolic Disorder 57 0.178
598
DYS101 Dysgerminoma 44 0.178
599
MDD011 Mood Disorder 62 0.178
600
CYS014 Cystadenocarcinoma 51 0.178
601
PPL002 Papillary Carcinoma 46 0.178
602
P THY023 Thymoma 64 0.178
603
ANP005 Anaplastic Astrocytoma 59 0.178
604
c NPH055 Nephrotic Syndrome, Type 1 52 0.178
605
c THY107 Thymoma, Familial 42 0.178
606
P MYC008 Myocarditis 59 0.178
607
NRM005 Neuromuscular Disease 63 0.178
608
P CMM008 Communicating Hydrocephalus 44 0.178
609
CHL149 Childhood Acute Myeloid Leukemia 42 0.178
610
END029 Endocervical Carcinoma 34 0.178
611
CVR010 Cavernous Malformation 29 0.178
612
STM007 Stomatitis 52 0.178
613
CHR177 Chromophobe Renal Cell Carcinoma 54 0.178
614
OVR012 Ovarian Serous Cystadenocarcinoma 55 0.178
615
PRM226 Primary Central Nervous System Lymphoma 47 0.178
616
AMY010 Amyloidosis Beta2m 16 0.178
617
ANP008 Anaplastic Oligoastrocytoma 31 0.178
618
BLR013 Biliary Tract Cancer 43 0.178
619
ANP009 Anaplastic Oligodendroglioma 41 0.178
620
c SPR009 Sporadic Breast Cancer 42 0.178
621
HVY002 Heavy Metal Poisoning 22 0.178
622
GRM010 Germ Cells Tumors 33 0.178
623
MCR004 Macroglobulinemia 48 0.178
624
MXD032 Mixed Germ Cell Tumor 24 0.178
625
P BCL004 B-Cell Non-Hodgkin Lymphoma 42 0.178
627
AGG011 Aggressive B-Cell Non-Hodgkin Lymphoma 22 0.178
628
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.145
629
c HMC039 Hemochromatosis, Type 1 73 0.145
630
P TYS001 Tay-Sachs Disease 69 0.145
631
P ATX030 Ataxia-Telangiectasia 80 0.145
632
VRC005 Varicose Veins 59 0.145
633
PRP001 Propionic Acidemia 65 0.145
634
KWS002 Kawasaki Disease 65 0.145
635
INV001 Invasive Aspergillosis 48 0.145
636
c BRS111 Breast-Ovarian Cancer, Familial 2 54 0.145
637
c THR102 Thrombocytopenia 5 29 0.145
639
c PCH010 Pachyonychia Congenita 3 43 0.145
640
MRG003 Marginal Zone B-Cell Lymphoma 52 0.145
641
DSS032 Disease by Infectious Agent 55 0.145
642
MLT177 Multisystem Proteinopathy 30 0.145
643
NSP002 Nasopharyngitis 45 0.145
644
MCS002 Mucositis 55 0.145
645
MCR037 Macroglossia 44 0.145
646
THY111 Thyroid Carcinoma, Familial Medullary 67 0.145
647
c MGR028 Migraine with or Without Aura 1 64 0.145
648
c ART115 Aortic Valve Disease 1 72 0.145
649
c SPN225 Spondyloarthropathy 1 70 0.145
650
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.145
651
c HYD064 Hydrocephalus, Congenital, 1 51 0.145
652
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.145
653
TRG002 Trigeminal Neuralgia 61 0.145
654
VNH007 Von Hippel-Lindau Syndrome 73 0.145
655
P SCL018 Scoliosis 57 0.145
656
c ATM089 Autoimmune Neuropathy 28 0.145
657
P APL001 Aplastic Anemia 73 0.145
658
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.145
659
LNG108 Langerhans Cell Histiocytosis 57 0.145
660
c PRG042 Progressive Familial Heart Block, Type Ia 65 0.145
661
MXL016 Maxillonasal Dysplasia, Binder Type 31 0.145
662
CLF027 Cleft Palate, Isolated 64 0.145
663
CRT072 Creutzfeldt-Jakob Disease 67 0.145
664
P ASP006 Aspergillosis 71 0.145
665
c CHR516 Charcot-Marie-Tooth Disease, Type 4c 48 0.145
666
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 34 0.145
667
HYD002 Hydronephrosis 58 0.145
668
c ACT067 Acute Conjunctivitis 37 0.145
669
VTM033 Vitamin K Deficiency Bleeding 50 0.145
670
NRT004 Neuritis 53 0.145
671
P HRD021 Hereditary Sensory Neuropathy 48 0.145
672
CMP034 Complete Androgen Insensitivity Syndrome 55 0.145
673
CRY004 Cryoglobulinemia 47 0.145
674
SPN051 Spondylitis 51 0.145
675
CLC001 Calciphylaxis 50 0.145
676
ACT084 Acute Stress Disorder 53 0.145
677
P CNJ013 Conjunctivitis 66 0.145
678
P PLC011 Pilocytic Astrocytoma 55 0.145
679
c ACT042 Acute Pyelonephritis 45 0.145
680
PST028 Post-Traumatic Stress Disorder 59 0.145
681
c BSL007 Basal Cell Carcinoma 68 0.145
682
TRN003 Transverse Colon Cancer 38 0.145
683
P THR015 Thrombophilia 51 0.145
684
P CRN025 Corneal Dystrophy 49 0.145
685
RGH001 Right Bundle Branch Block 47 0.145
686
TLN003 Telangiectasis 51 0.145
687
BLD009 Bladder Neck Obstruction 33 0.145
688
INF009 Inflammatory Spondylopathy 30 0.145
689
CHG001 Chagas Disease 65 0.145
690
P PYL005 Pyelonephritis 56 0.145
691
P LYN001 Lynch Syndrome 76 0.145
692
INT066 Interstitial Lung Disease 60 0.145
693
P RHB003 Rhabdomyosarcoma 66 0.145
694
ART016 Aortic Aneurysm 69 0.145
695
HST010 Histiocytosis 49 0.145
696
PSY004 Psychotic Disorder 66 0.145
697
THY125 Thyroid Gland Medullary Carcinoma 48 0.145
698
P GLL018 Gallbladder Cancer 53 0.145
699
c RTN041 Retinitis Pigmentosa 11 43 0.145
700
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 54 0.145
701
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.145
702
STN013 Stenotrophomonas Maltophilia Infection 26 0.145
703
CRB086 Cerebral Aneurysms 40 0.145
704
PRP030 Purpura 54 0.145
705
CYT002 Cytokine Deficiency 43 0.145
706
c INF055 Infectious Myocarditis 17 0.145
707
ANX004 Anoxia 40 0.145
708
BCK006 Back Pain 43 0.145
709
HRP004 Herpes Zoster 60 0.145
710
MNN024 Meningitis and Encephalitis 27 0.145
711
PRN039 Paraneoplastic Syndromes 37 0.145
712
P LTT001 Lattice Corneal Dystrophy 30 0.145
713
c INF019 Infectious Anterior Uveitis 31 0.145
714
LNG099 Lung Disease 62 0.145
715
CRH001 Crohn's Disease 80 0.145
716
SKL002 Skeletal Muscle Neoplasm 24 0.145
717
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 68 0.145
718
CLL002 Collecting Duct Carcinoma 53 0.145
719
SCR011 Scrapie 39 0.145
720
MTC005 Mitochondrial Metabolism Disease 45 0.145
721
PRM128 Primary Cutaneous Follicle Center Lymphoma 22 0.145
722
P HRD084 Hereditary Cerebral Amyloid Angiopathy 29 0.145
723
CND006 Candida Glabrata 29 0.145
724
ATM074 Autoimmune Autonomic Ganglionopathy 18 0.145
725
JVN009 Juvenile Pilocytic Astrocytoma 34 0.145
726
P ALP008 Alopecia 53 0.145
727
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.145
728
P ORL007 Oral Cavity Cancer 52 0.145
729
P HYP098 Hypereosinophilic Syndrome 66 0.145
730
ETV001 Etv6 Thrombocytopenia and Predisposition to Leukemia 31 0.145
731
P HMC002 Homocystinuria 52 0.145
732
c PRM299 Primary Cutaneous B-Cell Lymphoma 37 0.145
733
PRM129 Primary Cutaneous Marginal Zone B-Cell Lymphoma 26 0.145
734
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 0.145
735
JVN033 Juvenile Nasopharyngeal Angiofibroma 45 0.145
736
SPC030 Specific Language Disorder 25 0.145
737
P NNN030 Non-Infectious Anterior Uveitis 14 0.145
738
c ACT134 Acute Liver Failure 57 0.145
739
BNG077 Benign Idiopathic Neonatal Seizures 22 0.145
740
CRD137 Cardiogenic Shock 56 0.145
741
P SRC025 Sarcoidosis 1 70 0.103
742
P CRY007 Cryoglobulinemia, Familial Mixed 49 0.103
743
PRS129 Prostatic Hyperplasia, Benign 48 0.103
744
c CRD233 Cardiomyopathy, Dilated, 1b 46 0.103
745
P AST005 Asthma 76 0.103
746
RFS006 Refsum Disease, Classic 63 0.103
747
CRN106 Corneal Dystrophy, Gelatinous Drop-Like 40 0.103
748
c HMP004 Hemophilia B 68 0.103
749
P NRP063 Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive 58 0.103
750
SZR028 Seizures, Scoliosis, and Macrocephaly/microcephaly Syndrome 36 0.103
751
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.103
752
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 0.103
753
P MLT008 Multinodular Goiter 42 0.103
754
GLC105 Glucocorticoid Deficiency 4 with or Without Mineralocorticoid Deficiency 33 0.103
755
P BRW001 Brown-Vialetto-Van Laere Syndrome 50 0.103
756
LWG006 Low Grade Glioma 41 0.103
757
BNR002 Bone Resorption Disease 47 0.103
758
P STC001 Stickler Syndrome 60 0.103
759
END062 Endometrial Hyperplasia 48 0.103
760
MDD018 Middle East Respiratory Syndrome 44 0.103
761
P RNL015 Renal Hypertension 45 0.103
762
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.103
763
ALC007 Alcohol Dependence 65 0.103
764
ATH013 Atherosclerosis Susceptibility 63 0.103
765
BRN032 Brain Glioma 45 0.103
766
P FML011 Familial Adenomatous Polyposis 71 0.103
767
P CRD119 Cardiac Arrest 68 0.103
768
P LFT003 Left Ventricular Noncompaction 57 0.103
769
CRS005 Crest Syndrome 36 0.103
770
CHL147 Chlamydia Pneumonia 47 0.103
771
P HYP097 Hyperekplexia 62 0.103
772
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 63 0.103
773
P SPN408 Spinal Muscular Atrophy, Distal, Autosomal Recessive, 1 52 0.103
774
RDD003 Riddle Syndrome 58 0.103
775
P NNN008 Noonan Syndrome 1 76 0.103
776
NRL016 Neural Tube Defects 81 0.103
777
PRT129 Prothrombin Deficiency, Congenital 48 0.103
778
P HML001 Hemolytic-Uremic Syndrome 52 0.103
779
PRP083 Porphyria, Acute Intermittent 64 0.103
780
MLT157 Multiple System Atrophy 1 69 0.103
781
INT030 Intracranial Aneurysm 55 0.103
782
c VRL010 Viral Hepatitis 52 0.103
783
P BNC003 Bone Cancer 58 0.103
784
EXS001 Exostosis 49 0.103
785
CLT003 Colitis 63 0.103
786
SPN369 Spinal Disease 43 0.103
787
c PRM032 Primary Congenital Glaucoma 40 0.103
788
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.103
789
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.103
790
HYP007 Hypermobility Syndrome 35 0.103
791
TRS001 Tarsal Tunnel Syndrome 26 0.103
792
GT001 Gout 63 0.103
793
CMP010 Complex Regional Pain Syndrome 59 0.103
794
P END044 Endometriosis 62 0.103
795
SVR001 Severe Acute Respiratory Syndrome 68 0.103
796
P LNG028 Long Qt Syndrome 63 0.103
797
PRS021 Prostatic Adenoma 43 0.103
798
PLM001 Pulmonary Tuberculosis 69 0.103
799
LYM027 Lymphopenia 56 0.103
800
P INF032 Infertility 60 0.103
801
P OVR046 Ovarian Cyst 44 0.103
802
EXT007 Extracutaneous Mastocytoma 38 0.103
803
URM002 Uremia 47 0.103
804
PRS045 Prostatic Hypertrophy 52 0.103
805
LPT001 Leptospirosis 66 0.103
806
P PNB001 Pineoblastoma 49 0.103
807
IRN002 Iron Metabolism Disease 56 0.103
808
HYP014 Hyperuricemia 51 0.103
809
P PRP029 Porphyria 60 0.103
810
CRD003 Cardiac Sarcoidosis 44 0.103
811
PPT001 Peptic Esophagitis 51 0.103
812
P INT143 Interstitial Cystitis 59 0.103
813
P CYS018 Cystitis 59 0.103
814
ASP004 Asphyxia Neonatorum 50 0.103
815
DSS009 Disseminated Intravascular Coagulation 56 0.103
816
P OPT009 Optic Neuritis 57 0.103
817
HYP006 Hypertensive Heart Disease 48 0.103
818
VGN017 Vaginal Cancer 58 0.103
819
CDQ001 Cauda Equina Syndrome 37 0.103
820
HYP043 Hyperandrogenism 47 0.103
821
TTN003 Tetanus 64 0.103
822
MTH009 Mouth Disease 57 0.103
823
P PTT006 Pituitary Adenoma 55 0.103
824
MST004 Mast Cell Neoplasm 41 0.103
825
PRT012 Prothrombin Deficiency 48 0.103
826
BRS051 Breast Disease 58 0.103
827
CHR033 Chordoid Glioma 31 0.103
828
MRK001 Merkel Cell Carcinoma 65 0.103
829
MYL001 Myelitis 49 0.103
830
DBT090 Diabetes and Deafness, Maternally Inherited 44 0.103
831
ANR040 Aneurysm 60 0.103
832
P CHR345 Chronic Pain 50 0.103
833
P THY032 Thyroiditis 56 0.103
835
EVN001 Evans' Syndrome 46 0.103
836
P NGH001 Night Blindness 52 0.103
837
END031 Endometrial Stromal Sarcoma 45 0.103
838
CRD016 Cardiac Rupture 34 0.103
839
ULC004 Ulcerative Colitis 74 0.103
840
ILS001 Ileus 49 0.103
841
PRL008 Paralytic Ileus 44 0.103
842
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.103
844
DST006 Diastolic Heart Failure 45 0.103
845
INT040 Intrinsic Asthma 36 0.103
846
ALL006 Allergic Asthma 56 0.103
847
MLT075 Multifocal Motor Neuropathy 45 0.103
848
ORL011 Oral Cancer 60 0.103
849
PNC056 Pineocytoma 44 0.103
850
HYP706 Hypermobile Ehlers-Danlos Syndrome 55 0.103
852
NRM001 Neuromyelitis Optica 60 0.103
853
P TYR004 Tyrosinemia 49 0.103
854
c PSD047 Pseudo-Turner Syndrome 52 0.103
855
LWG005 Low-Grade Astrocytoma 38 0.103
856
PPL050 Papillary Tumor of the Pineal Region 31 0.103
857
MTC111 Mitochondrial Neurogastrointestinal Encephalomyopathy 47 0.103
858
CNG506 Congenital Amyoplasia 27 0.103
859
LRG008 Large Granular Lymphocyte Leukemia 34 0.103
860
PRM163 Primary Mediastinal Large B-Cell Lymphoma 40 0.103
Content
Loading form....