Search results for Cyclosporin A

1376 hits were found for Cyclosporin A

# Family MCID Name MIFTS Score
1
P GRF003 Graft-Versus-Host Disease 71 16.699
2
PST011 Pustulosis of Palm and Sole 52 14.326
3
P PSR002 Psoriasis 63 14.281
4
P APL001 Aplastic Anemia 72 14.031
5
P NPH012 Nephrotic Syndrome 61 12.752
6
DFC004 Deficiency Anemia 74 11.837
7
PRT251 Proteinuria, Chronic Benign 58 11.435
8
KRT006 Keratoconjunctivitis 53 11.374
10
c ACT135 Acute Graft Versus Host Disease 51 10.681
11
c HYP836 Hypercholesterolemia, Familial, 1 73 9.862
12
P DRM053 Dermatitis, Atopic 65 9.742
13
CRH001 Crohn's Disease 80 9.700
14
GNG012 Gingival Overgrowth 49 9.679
15
P OVR082 Overgrowth Syndrome 41 9.668
16
P BRS047 Breast Cancer 97 9.275
17
MYL009 Myelodysplastic Syndrome 67 9.189
18
DRM006 Dermatitis 61 9.161
19
P EYD002 Eye Disease 57 9.140
20
ULC004 Ulcerative Colitis 74 8.789
21
CLT003 Colitis 63 8.779
22
KRT001 Keratoconjunctivitis Sicca 49 8.658
23
P UVT001 Uveitis 57 8.625
24
c LKM061 Leukemia, Acute Myeloid 83 8.606
25
P LKM002 Leukemia 65 8.480
26
P GLM007 Glomerulonephritis 59 8.374
27
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 8.346
28
c ATR087 Atrial Standstill 1 74 8.343
29
P KDN018 Kidney Disease 71 8.287
30
DRY001 Dry Eye Syndrome 49 8.233
31
P CNR004 Cone-Rod Dystrophy 2 74 7.634
32
P ANR048 Aniridia 1 66 7.375
33
HML018 Homologous Wasting Disease 21 7.252
34
P FCL005 Focal Segmental Glomerulosclerosis 57 7.248
35
P THR014 Thrombocytopenia 66 7.169
36
P MYL006 Myeloid Leukemia 60 7.163
37
c ACT071 Acute Kidney Failure 60 7.056
38
ANT039 Antisynthetase Syndrome 55 6.943
39
PRP030 Purpura 54 6.844
40
P RTN008 Retinitis Pigmentosa 79 6.708
41
P HML002 Hemolytic Anemia 62 6.688
42
P MMB011 Membranous Nephropathy 50 6.657
43
P SJG008 Sjogren Syndrome 60 6.635
44
ATM095 Autoimmune Disease 61 6.503
45
c FNC027 Fanconi Anemia, Complementation Group a 80 6.502
46
P CNJ013 Conjunctivitis 66 6.451
47
c SYS001 Systemic Lupus Erythematosus 85 6.413
48
CYS001 Cystic Fibrosis 77 6.400
49
P LPS004 Lupus Erythematosus 61 6.373
50
P LYM118 Lymphoma 66 6.360
51
PNC001 Pancytopenia 52 6.358
52
48X005 48,xyyy 39 6.329
53
P HPT021 Hepatitis 68 6.261
54
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 6.235
55
c HPT001 Hepatitis C 61 6.206
56
P SZR006 Seizure Disorder 69 6.122
57
P HYP061 Hypertrophic Cardiomyopathy 68 6.049
58
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 6.003
59
IMM167 Immune Deficiency Disease 76 5.999
60
END086 End Stage Renal Disease 54 5.972
61
ADL002 Adult Syndrome 69 5.906
62
P LKM062 Leukemia, Acute Lymphoblastic 69 5.881
63
IDP091 Idiopathic Nephrotic Syndrome 49 5.694
64
c TYP008 Type 1 Diabetes Mellitus 77 5.693
65
c FML021 Familial Hypercholesterolemia 71 5.690
66
MYL069 Myeloma, Multiple 76 5.674
67
P ALP008 Alopecia 53 5.666
68
KRT019 Keratitis, Hereditary 66 5.618
69
RHB024 Rhabdomyosarcoma 2 65 5.588
70
BRN012 Bronchiolitis Obliterans 56 5.574
71
P NRB001 Neuroblastoma 66 5.563
72
c LKM063 Leukemia, Chronic Myeloid 70 5.559
73
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 5.540
74
P VSC011 Vasculitis 61 5.529
75
BRN002 Bronchiolitis 57 5.516
76
P LKM071 Leukemia, Chronic Lymphocytic 74 5.497
77
P CLR023 Colorectal Cancer 100 5.457
78
P INF037 Inflammatory Bowel Disease 53 5.429
79
c PSR017 Psoriasis 2 53 5.411
80
P TRM003 Tremor 50 5.382
81
P LYM033 Lymphoproliferative Syndrome 59 5.372
82
P PRR002 Pure Red-Cell Aplasia 46 5.359
83
CYT002 Cytokine Deficiency 43 5.324
84
c TBR025 Tuberous Sclerosis 1 84 5.309
85
c AMY091 Amyotrophic Lateral Sclerosis 1 87 5.300
86
RNL114 Renal Cell Carcinoma, Nonpapillary 79 5.295
87
P NTR004 Neutropenia 62 5.273
88
P MYC007 Myocardial Infarction 69 5.255
89
VRN004 Vernal Keratoconjunctivitis 47 5.245
90
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 5.245
91
P ART022 Arthritis 70 5.242
92
SKN016 Skin Disease 63 5.234
93
LNG099 Lung Disease 62 5.226
94
HMN044 Human Immunodeficiency Virus Type 1 76 5.150
95
PLM134 Pulmonary Fibrosis, Idiopathic 76 5.132
96
P DBT009 Diabetes Mellitus 67 5.124
97
P PNM007 Pneumonia 64 5.091
98
P TRN020 Turner Syndrome 67 5.033
99
c HYP595 Hypertension, Essential 84 4.987
100
c HPT073 Hepatitis C Virus 70 4.925
101
LVR012 Liver Cirrhosis 62 4.884
102
P BTH005 Bethlem Myopathy 1 62 4.870
103
c TYP009 Type 2 Diabetes Mellitus 91 4.863
104
c HPT003 Hepatitis a 63 4.856
105
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 65 4.805
106
ISC004 Ischemia 61 4.782
107
P RHM011 Rheumatoid Arthritis 81 4.775
108
CNN005 Connective Tissue Disease 66 4.774
109
P PRS040 Prostate Cancer 95 4.738
110
SVR097 Severe Cutaneous Adverse Reaction 68 4.724
111
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 4.710
112
P ALP004 Alport Syndrome 69 4.688
113
P MYP004 Myopathy 67 4.676
114
P ATX030 Ataxia-Telangiectasia 80 4.658
115
c ACT073 Acute Leukemia 59 4.647
116
P LNG032 Lung Cancer 98 4.636
117
LYM019 Lymphosarcoma 46 4.624
118
P HYP098 Hypereosinophilic Syndrome 66 4.589
119
ALL029 Allergic Disease 61 4.582
120
P LNG028 Long Qt Syndrome 63 4.556
121
P SRC025 Sarcoidosis 1 70 4.531
122
c DLT002 Dilated Cardiomyopathy 79 4.530
123
c FML346 Familial Adenomatous Polyposis 1 65 4.530
124
PRM236 Primary Biliary Cholangitis 62 4.524
125
P ALP009 Alopecia Areata 59 4.521
126
P NRP001 Neuropathy 59 4.444
127
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 41 4.410
128
BRN071 Brain Injury 50 4.390
129
c CHR417 Chronic Graft Versus Host Disease 55 4.383
130
MSC157 Muscular Dystrophy, Duchenne Type 78 4.378
131
c BLD140 Blood Group, I System 47 4.375
132
P ENC018 Encephalopathy 62 4.334
133
c CHR684 Chronic Kidney Disease 73 4.333
134
P BCL017 B-Cell Lymphoma 57 4.333
135
TRM010 Traumatic Brain Injury 50 4.327
136
INT066 Interstitial Lung Disease 60 4.318
137
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 4.303
138
P RTN024 Retinoblastoma 72 4.282
139
P SKN015 Skin Carcinoma 71 4.252
140
c NRF024 Neurofibromatosis, Type I 76 4.235
141
INT323 Intraocular Pressure Quantitative Trait Locus 63 4.232
142
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 4.229
143
LBR036 Leber Plus Disease 67 4.184
144
PSR001 Psoriatic Arthritis 61 4.178
145
P EXN002 Exanthem 58 4.170
146
AGN016 Aging 53 4.155
147
P THR005 Thrombotic Thrombocytopenic Purpura 64 4.128
148
HMG002 Hemoglobinuria 50 4.111
149
c ACT075 Acute Myocardial Infarction 55 4.104
150
c ATM011 Autoimmune Hepatitis 62 4.099
151
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 4.090
152
LYM133 Lymphoma, Hodgkin, Classic 69 4.044
153
GLC003 Glucose Intolerance 53 4.028
154
ALL009 Allergic Conjunctivitis 51 4.022
155
c PST005 Posterior Uveitis 54 4.011
156
GNG013 Gingivitis 59 4.003
157
LYM143 Lymphoma, Non-Hodgkin, Familial 74 3.984
158
P HYP750 Hypertriglyceridemia, Familial 61 3.979
159
BRT054 Brittle Bone Disorder 74 3.951
160
GST019 Gastrointestinal Stromal Tumor 78 3.946
161
BNR002 Bone Resorption Disease 47 3.922
162
HMT002 Hematologic Cancer 61 3.920
163
P LCH002 Lichen Planus 54 3.902
164
c ACT027 Acute Pancreatitis 60 3.876
165
P ACN011 Acne 55 3.868
166
ERY003 Erythema Multiforme 56 3.864
167
P VSC007 Vascular Disease 62 3.836
168
THR024 Thrombosis 56 3.827
169
LPD008 Lipid Metabolism Disorder 61 3.815
170
LPP008 Lipoprotein Quantitative Trait Locus 65 3.814
171
THR100 Thrombocytopenic Purpura, Autoimmune 60 3.802
172
P DRR001 Diarrhea 55 3.788
173
PLS009 Plasma Cell Neoplasm 64 3.774
174
P MLN008 Melanoma 75 3.766
175
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 3.758
176
RNL065 Renal Cell Carcinoma, Papillary, 1 79 3.735
177
P CYS018 Cystitis 58 3.730
178
INS024 Insulin-Like Growth Factor I 77 3.724
179
P HRT032 Heart Disease 84 3.719
180
CVD001 Covid-19 59 3.712
181
LGH007 Leigh Syndrome 70 3.712
182
SCH036 Scheie Syndrome 73 3.712
183
ERY066 Erythema Multiforme Major 29 3.711
184
P INT143 Interstitial Cystitis 59 3.642
185
P HMP002 Hemophagocytic Lymphohistiocytosis 60 3.641
186
c PSR023 Psoriasis 1 52 3.621
187
P NJM001 Nijmegen Breakage Syndrome 75 3.612
188
P PTY003 Pityriasis Rubra Pilaris 57 3.606
189
P NPH005 Nephronophthisis 59 3.601
190
SVR004 Severe Combined Immunodeficiency 70 3.600
191
c PSR018 Psoriasis 13 40 3.592
192
MCS002 Mucositis 55 3.577
193
AND005 Androgen Insensitivity Syndrome, Mild 21 3.554
194
P LVR013 Liver Disease 68 3.551
195
P BRD002 Bardet-Biedl Syndrome 66 3.547
196
c CHR064 Chronic Monocytic Leukemia 35 3.547
197
PMP006 Pemphigus Vulgaris, Familial 57 3.546
198
P PRD008 Periodontitis 63 3.534
199
CRD223 Cardiac Arrhythmia 63 3.533
200
BCT022 Bacterial Infectious Disease 55 3.528
201
HMN014 Human Immunodeficiency Virus Infectious Disease 54 3.526
202
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 3.515
203
DWN001 Down Syndrome 70 3.511
204
c MCR113 Microvascular Complications of Diabetes 3 52 3.507
205
P PNC044 Pancreatitis 61 3.493
206
STR067 Stroke, Ischemic 79 3.491
207
P SYS005 Systemic Scleroderma 73 3.486
208
SPN186 Spinal Cord Injury 60 3.484
209
c PSR028 Psoriasis 7 42 3.472
210
c PSR032 Psoriasis 11 47 3.472
211
c FML191 Familial Long Qt Syndrome 54 3.468
212
c NRB014 Neuroblastoma 3 28 3.465
213
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 3.455
214
P PMP001 Pemphigus 54 3.446
215
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 3.437
216
P PLY014 Polycystic Kidney Disease 71 3.430
217
c INF071 Inflammatory Bowel Disease 1 65 3.426
218
P OVR042 Ovarian Cancer 88 3.426
219
P CTR002 Cataract 59 3.415
220
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 3.406
221
HMZ003 Homozygous Familial Hypercholesterolemia 60 3.405
222
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 3.396
223
c HPT016 Hepatitis B 62 3.392
224
RFR010 Refractory Anemia 49 3.390
225
P PRK039 Parkinsonism 55 3.387
226
VSL013 Visual Impairment and Progressive Phthisis Bulbi 36 3.369
227
c MCR120 Microvascular Complications of Diabetes 7 47 3.344
228
ACQ007 Acquired Immunodeficiency Syndrome 58 3.336
229
GLL048 Glial Tumor 51 3.335
230
P RSP003 Respiratory Failure 73 3.320
231
P CHL066 Cholangitis 51 3.318
232
LYM040 Lymphoblastic Lymphoma 53 3.312
234
FCT001 Factor Viii Deficiency 61 3.278
235
c HMP029 Hemophilia a 69 3.272
236
P HDC001 Headache 56 3.235
237
c SML038 Small Cell Cancer of the Lung 68 3.221
238
c SCL052 Scleroderma, Familial Progressive 60 3.217
239
P CRD119 Cardiac Arrest 68 3.214
240
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 3.210
241
P ULL002 Ullrich Congenital Muscular Dystrophy 1 56 3.202
242
KRT009 Keratosis 52 3.202
243
SKN019 Skin Melanoma 70 3.201
244
MYL005 Myelofibrosis 70 3.197
245
P EPL164 Epilepsy 70 3.190
246
c PSR021 Psoriasis 14, Pustular 57 3.190
247
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 3.181
248
ART140 Arteries, Anomalies of 52 3.178
249
HYP066 Hyperglycemia 60 3.161
250
IGG001 Iga Glomerulonephritis 50 3.154
251
GNT179 Genetic Steroid-Resistant Nephrotic Syndrome 40 3.135
252
P ART021 Arteriosclerosis 53 3.130
253
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 3.111
254
CHD001 Chediak-Higashi Syndrome 66 3.085
255
c MCR133 Microvascular Complications of Diabetes 4 41 3.075
256
c MCR130 Microvascular Complications of Diabetes 6 41 3.075
257
SVR001 Severe Acute Respiratory Syndrome 68 3.071
258
c JVN010 Juvenile Rheumatoid Arthritis 52 3.065
259
SRC014 Sarcoma 64 3.056
260
c WLM013 Wilms Tumor 1 65 3.045
261
P OPN001 Open-Angle Glaucoma 55 3.018
262
P THY032 Thyroiditis 56 3.011
263
HYP266 Hypoxia 56 3.010
264
KPS004 Kaposi Sarcoma 76 3.007
265
P DYS154 Dystonia 64 2.996
266
PLM129 Pulmonary Disease, Chronic Obstructive 74 2.982
267
P EPD016 Epidermolysis Bullosa 53 2.977
268
SPS057 Spasticity 43 2.967
269
ALP097 Alopecia Universalis Congenita 57 2.964
270
P ASP006 Aspergillosis 71 2.959
271
XLN231 X-Linked Alport Syndrome 41 2.958
272
c BTT014 Beta-Thalassemia 72 2.954
273
ACT113 Acute Myeloblastic Leukemia with Maturation 46 2.945
274
ALC007 Alcohol Dependence 65 2.928
275
c PLM164 Pulmonary Hypertension, Primary, 1 75 2.920
276
MMB001 Membranoproliferative Glomerulonephritis 56 2.919
277
ACT011 Acute Contagious Conjunctivitis 41 2.918
278
ATX019 Ataxia with Vitamin E Deficiency 44 2.913
279
P PNC035 Pancreatic Cancer 87 2.909
280
CRT012 Cortical Blindness 42 2.901
281
MYL031 Myeloproliferative Neoplasm 66 2.895
282
P DMN001 Diamond-Blackfan Anemia 73 2.884
283
P PNV001 Panuveitis 48 2.884
284
P THY023 Thymoma 64 2.884
285
P PHC003 Pheochromocytoma 70 2.878
286
GLB002 Glioblastoma 67 2.876
287
P PLM036 Pulmonary Fibrosis 65 2.874
288
STM007 Stomatitis 52 2.869
289
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 2.867
290
P CHR012 Chronic Granulomatous Disease 69 2.865
291
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 2.864
292
MSC007 Muscle Hypertrophy 64 2.827
293
P ALC033 Alcohol Use Disorder 67 2.826
294
c THR092 Thrombophilia Due to Thrombin Defect 74 2.825
295
P MSC005 Muscular Dystrophy 66 2.818
296
BLR008 Bilirubin Metabolic Disorder 57 2.815
297
PMP014 Pemphigoid 48 2.806
298
WST001 West Syndrome 64 2.794
299
P LTR001 Lateral Sclerosis 57 2.788
300
P DYS007 Dyskeratosis Congenita 66 2.784
301
P PLY019 Polyneuropathy 52 2.779
302
P OPT006 Optic Nerve Disease 57 2.767
303
NRT004 Neuritis 53 2.766
304
P HRP006 Herpes Simplex 65 2.758
305
P URN019 Urinary Tract Infection 48 2.756
306
HYP005 Hypokalemia 55 2.754
307
RSC001 Rosacea 55 2.750
308
P PRP019 Peripheral Nervous System Disease 57 2.746
309
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 2.746
310
P CRN300 Coronary Heart Disease 1 73 2.739
311
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 2.728
312
P AMY004 Amyloidosis 69 2.727
313
CRY008 Cryopyrin-Associated Periodic Syndrome 48 2.725
314
P TBR001 Tuberous Sclerosis 69 2.716
315
GLM045 Glioma 62 2.709
316
SPN035 Spindle Cell Sarcoma 51 2.704
317
RTN001 Retinal Vasculitis 46 2.701
318
P FML018 Familial Mediterranean Fever 73 2.697
319
P ADN016 Adenocarcinoma 63 2.693
320
c PRM038 Primary Agammaglobulinemia 47 2.680
321
P BND020 Bone Disease 60 2.679
322
LPT014 Leptin Deficiency or Dysfunction 77 2.674
323
CMM004 Common Variable Immunodeficiency 71 2.661
324
P RHN004 Rhinitis 56 2.657
325
CRB039 Cerebrovascular Disease 65 2.652
326
P LNG064 Lung Cancer Susceptibility 3 69 2.647
327
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 2.647
328
OST012 Osteoarthritis 77 2.647
329
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.645
330
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 2.645
331
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 37 2.628
332
CNG034 Congestive Heart Failure 69 2.628
333
GLS018 Glass Syndrome 60 2.622
334
SQM006 Squamous Cell Carcinoma 59 2.620
335
P OST135 Osteogenesis Imperfecta, Type I 60 2.607
336
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.596
337
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.596
338
RSP023 Rasopathy 54 2.589
339
P MLT020 Multiple Sclerosis 79 2.587
340
PRS047 Prostatitis 57 2.587
341
ORL013 Oral Lichen Planus 45 2.586
342
P MTR004 Maturity-Onset Diabetes of the Young 66 2.581
343
P OST001 Osteopetrosis 70 2.576
344
P PRK057 Parkinson Disease, Late-Onset 79 2.571
345
P THL005 Thalassemia 56 2.565
346
NRR001 Neuroretinitis 42 2.551
347
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 2.549
348
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 2.545
349
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 57 2.532
350
c ANM038 Anemia, Autoimmune Hemolytic 63 2.518
351
PRP036 Peripheral T-Cell Lymphoma 52 2.518
352
CRH005 Crohn's Colitis 53 2.517
353
P HPT023 Hepatocellular Carcinoma 95 2.508
354
P FNG006 Feingold Syndrome 1 61 2.498
355
OCL069 Ocular Motor Apraxia 57 2.488
356
IRD001 Iridocyclitis 54 2.480
357
c MGR028 Migraine with or Without Aura 1 63 2.478
358
PNC129 Pancreatic Adenocarcinoma 64 2.477
359
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 2.475
360
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 2.475
361
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 2.475
362
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.475
363
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.475
364
CRV035 Cervical Cancer 72 2.473
365
c ATS013 Autosomal Recessive Congenital Ichthyosis 66 2.463
366
P OST002 Osteoporosis 76 2.462
367
P MLG056 Malignant Hyperthermia 65 2.462
368
RTN023 Retinitis 45 2.453
369
P ALZ034 Alzheimer Disease 87 2.449
370
WLS001 Wilson Disease 70 2.448
371
47X002 47,xyy 47 2.445
372
c DRM054 Dermatitis, Atopic, 2 47 2.444
373
P LFR001 Li-Fraumeni Syndrome 73 2.444
374
TXC005 Toxic Shock Syndrome 61 2.436
375
HST010 Histiocytosis 49 2.431
376
PRT036 Peritonitis 65 2.430
377
LYM027 Lymphopenia 56 2.430
378
ENH001 Enhanced S-Cone Syndrome 58 2.427
379
P ART023 Arthropathy 59 2.421
380
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 43 2.408
381
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 2.405
382
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 2.402
383
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 2.394
384
XRD010 Xeroderma Pigmentosum, Variant Type 72 2.389
385
HYP056 Hypoglycemia 65 2.380
386
P SCK005 Sickle Cell Disease 56 2.356
387
VRL011 Viral Infectious Disease 60 2.355
388
BRK010 Burkitt Lymphoma 65 2.350
389
ADR007 Adrenoleukodystrophy 73 2.342
390
BHC003 Behcet Syndrome 70 2.338
391
CMB007 Combined Immunodeficiency 56 2.337
392
GLM044 Glomerular Disease 34 2.337
393
c ACT068 Acute Cystitis 60 2.336
394
P MDL005 Medulloblastoma 75 2.331
395
CLN015 Colon Adenocarcinoma 64 2.324
396
BRN028 Brain Cancer 73 2.324
397
P HMP007 Hemophilia 52 2.320
398
c LKM056 Leukemia, Chronic Lymphocytic 2 47 2.320
399
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 59 2.320
400
FRS002 Frasier Syndrome 54 2.312
401
P KDN017 Kidney Cancer 60 2.311
402
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 66 2.293
403
FSC004 Fasciitis 49 2.293
404
P BRL012 Bare Lymphocyte Syndrome, Type Ii 65 2.289
405
FML035 Familial Hyperlipidemia 54 2.289
406
ALL003 Allergic Rhinitis 66 2.281
407
RPD005 Rapidly Involuting Congenital Hemangioma 48 2.279
408
c PRC016 Pre-Eclampsia 64 2.279
409
P ESP024 Esophagitis 60 2.276
410
c NPH049 Nephrotic Syndrome, Type 2 49 2.275
411
P GLM040 Glioma Susceptibility 1 70 2.264
412
P ADL010 Adult Respiratory Distress Syndrome 70 2.262
413
RYN005 Raynaud Phenomenon 45 2.253
414
PRT037 Pertussis 49 2.249
415
BNM001 Bone Marrow Cancer 45 2.249
416
c GLY008 Glycogen Storage Disease Ii 72 2.249
417
P INF032 Infertility 60 2.244
418
CNS004 Constipation 56 2.241
419
c MCR115 Microvascular Complications of Diabetes 5 65 2.239
420
CRD137 Cardiogenic Shock 56 2.231
421
ESP021 Esophageal Cancer 84 2.225
422
BP1002 Bap1 Tumor Predisposition Syndrome 42 2.222
423
SQM013 Squamous Cell Carcinoma, Head and Neck 75 2.214
424
P PLM037 Pulmonary Hypertension 69 2.207
425
LNG108 Langerhans Cell Histiocytosis 57 2.203
426
P RNL100 Renal Hypodysplasia/aplasia 1 63 2.196
427
P INF038 Influenza 68 2.193
428
c SPN225 Spondyloarthropathy 1 70 2.191
429
c HMC039 Hemochromatosis, Type 1 73 2.184
430
P EPD009 Epidermolysis Bullosa Dystrophica 66 2.182
431
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 2.182
432
P AST005 Asthma 75 2.179
433
BLL006 Bullous Pemphigoid 61 2.178
434
P GST053 Gastric Cancer 82 2.175
435
P FML068 Familial Hypocalciuric Hypercalcemia 55 2.174
436
c MCP001 Mucopolysaccharidosis Iii 69 2.167
437
c NPH055 Nephrotic Syndrome, Type 1 52 2.162
438
PNG002 Pain Agnosia 51 2.162
439
P ALG028 Alagille Syndrome 1 73 2.159
440
c ACT134 Acute Liver Failure 57 2.159
441
BTT017 Beta-Thalassemia Major 54 2.157
442
c FML094 Familial Wilms Tumor 2 28 2.157
443
P BLP003 Blepharospasm 45 2.152
444
END057 Endometrial Cancer 76 2.147
445
MSN001 Mesangial Proliferative Glomerulonephritis 44 2.140
446
P HYP069 Hyperparathyroidism 62 2.131
447
DNY001 Denys-Drash Syndrome 57 2.119
448
P HYP086 Hypothyroidism 68 2.118
449
CNT105 Central Core Disease of Muscle 59 2.115
450
CRT084 Creatinine Clearance Quantitative Trait Locus 25 2.111
451
c FML015 Familial Nephrotic Syndrome 48 2.102
452
P MTC003 Metachromatic Leukodystrophy 71 2.099
453
ENT011 Enterocolitis 55 2.091
454
P HYP838 Hyperlipidemia, Familial Combined, 3 61 2.091
455
IGR001 Ige Responsiveness, Atopic 58 2.088
456
c GLC092 Glaucoma, Primary Open Angle 60 2.083
457
CRB009 Cerebritis 43 2.083
458
JVN004 Juvenile Myelomonocytic Leukemia 66 2.080
459
c ACQ016 Acquired Pure Red Cell Aplasia 29 2.079
460
BRN024 Bronchitis 67 2.077
461
P CHR285 Chronic Myelomonocytic Leukemia 59 2.074
462
HRL003 Hurler Syndrome 66 2.072
463
PHN003 Phenylketonuria 76 2.069
464
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 2.064
466
OST159 Osteogenic Sarcoma 66 2.052
467
P HRM001 Hermansky-Pudlak Syndrome 65 2.050
468
P HML033 Hemolytic Uremic Syndrome, Atypical 1 67 2.040
469
P CRV039 Cervicitis 52 2.037
470
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 56 2.035
471
INV001 Invasive Aspergillosis 48 2.030
472
LKC009 Leukocyte Adhesion Deficiency, Type I 69 2.028
473
ANR040 Aneurysm 60 2.022
474
OMN001 Omenn Syndrome 63 2.021
475
NTR005 Nutritional Deficiency Disease 60 2.020
476
P ICH004 Ichthyosis 56 2.013
477
FBR012 Fabry Disease 71 2.011
478
P KRT007 Keratoconus 49 2.010
479
SPL018 Splenomegaly 47 2.010
480
ATH013 Atherosclerosis Susceptibility 63 2.001
481
PRL017 Prolymphocytic Leukemia 47 2.000
482
P FLL037 Follicular Lymphoma 66 1.995
483
END072 Endotheliitis 36 1.994
484
P TXP001 Toxoplasmosis 59 1.993
485
PPL022 Papilloma 53 1.986
486
MLR004 Malaria 77 1.984
487
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 1.984
488
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.966
489
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.966
490
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.964
491
HYP020 Hyperprolactinemia 63 1.959
492
MCR004 Macroglobulinemia 48 1.955
493
c LKM060 Leukemia, Acute Lymphoblastic 3 49 1.951
494
MCR013 Microphthalmia 59 1.950
495
c PRS130 Prostate Cancer, Hereditary, 8 32 1.942
496
c PRS136 Prostate Cancer, Hereditary, 6 33 1.942
497
SCK003 Sickle Cell Anemia 74 1.940
498
BRN101 Bronchiolitis Obliterans with Obstructive Pulmonary Disease 27 1.938
499
P MCR129 Microvascular Complications of Diabetes 1 67 1.936
500
c HYP724 Hyperlipoproteinemia, Type Iii 66 1.935
501
PRS063 Paresthesia 39 1.934
502
DSS032 Disease by Infectious Agent 55 1.923
503
P PRM002 Primary Hyperoxaluria 65 1.919
505
VNH007 Von Hippel-Lindau Syndrome 72 1.917
506
CHR103 Charge Syndrome 65 1.909
507
P HYP055 Hypoplastic Left Heart Syndrome 65 1.903
508
c BRN108 Branchiootic Syndrome 1 63 1.902
509
CTS005 Catastrophic Antiphospholipid Syndrome 43 1.899
510
MNT001 Mantle Cell Lymphoma 65 1.894
511
WLD007 Waldenstroem's Macroglobulinemia 59 1.894
512
LYM012 Lymphoplasmacytic Lymphoma 50 1.894
513
GST037 Gastroparesis 52 1.893
514
c BSL007 Basal Cell Carcinoma 67 1.882
515
P HMN038 Human Coronavirus Sensitivity 30 1.880
516
P KLZ004 Kala-Azar 1 41 1.879
517
LSH001 Leishmaniasis 63 1.879
518
IRN002 Iron Metabolism Disease 56 1.876
519
HGH043 High Grade Glioma 46 1.874
520
HDG004 Hodgkin's Granuloma 22 1.873
521
HDG006 Hodgkin's Paragranuloma 22 1.873
522
TTN003 Tetanus 64 1.871
523
CHR063 Chronic Mucocutaneous Candidiasis 68 1.869
524
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.863
525
P ANP001 Anaplastic Large Cell Lymphoma 59 1.863
526
EHL079 Ehlers-Danlos Syndrome, Dermatosparaxis Type 52 1.859
527
c MTC056 Mitochondrial Dna Depletion Syndrome 4a 62 1.857
528
P ECL001 Eclampsia 52 1.856
529
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.852
530
OCL006 Ocular Hypertension 53 1.846
531
HRY003 Hairy Cell Leukemia 53 1.844
532
P GRV001 Graves' Disease 54 1.843
533
c DWL002 Dowling-Degos Disease 1 58 1.838
534
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 63 1.830
535
CYT018 Cytochrome P450 2d6 Variant 26 1.830
536
c SYS043 Systemic Lupus Erythematosus 1 38 1.824
537
HYP080 Hypogonadism 49 1.823
538
P ANG015 Angioedema 56 1.822
539
CNG116 Congenital Nephrotic Syndrome Finnish Type 33 1.821
540
P PTS002 Ptosis 52 1.820
541
PRT013 Portal Hypertension 59 1.812
542
HMC014 Homocysteinemia 52 1.810
543
P HYD006 Hydrocephalus 62 1.809
544
c LCL006 Localized Scleroderma 64 1.807
545
P ACT008 Actinic Keratosis 53 1.806
546
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.801
547
P GLC113 Galactosemia I 65 1.795
548
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 35 1.794
549
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 1.794
550
MYL075 Myelodysplastic/myeloproliferative Neoplasm 51 1.794
551
P MYC084 Mycobacterium Tuberculosis 1 68 1.793
552
DYS073 Dysphagia 53 1.792
553
CRB011 Cerebrotendinous Xanthomatosis 64 1.788
554
P NRV007 Nervous System Disease 65 1.787
555
SPL004 Splenic Marginal Zone Lymphoma 50 1.777
556
P SCH015 Schizophrenia 74 1.773
557
c VRL010 Viral Hepatitis 52 1.771
558
WLM014 Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome 53 1.769
559
c GLL024 Gallbladder Disease 1 53 1.768
560
BNG091 Benign Chronic Pemphigus 56 1.763
561
CYS010 Cystinosis 61 1.759
562
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 1.759
563
CYS036 Cystinosis, Nephropathic 51 1.752
564
c PRD040 Periodontitis, Chronic 52 1.750
565
THR004 Thrombocytosis 52 1.750
566
c MCP052 Mucopolysaccharidosis, Type Vi 67 1.749
567
SQM002 Squamous Cell Papilloma 45 1.744
568
P HRS035 Hirschsprung Disease 1 66 1.743
569
MCL006 Macular Retinal Edema 56 1.743
570
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.742
571
c INH020 Inherited Metabolic Disorder 47 1.739
572
PRR013 Prurigo Nodularis 38 1.734
573
MLT134 Multiple Pterygium Syndrome, Lethal Type 56 1.734
574
RCK004 Rickets 64 1.732
575
c NMN015 Niemann-Pick Disease, Type C1 68 1.730
576
P SNS001 Sensorineural Hearing Loss 60 1.724
577
P BLD134 Bladder Cancer 79 1.722
578
THR035 Thrombasthenia 48 1.721
579
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.719
580
SCH014 Schistosomiasis 56 1.719
581
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 44 1.718
582
AYM001 Ayme-Gripp Syndrome 57 1.716
583
AGG012 Aggressive Nk-Cell Leukemia 47 1.715
584
ALP103 Alpha-1-Antitrypsin Deficiency 67 1.713
586
P RTN016 Retinal Degeneration 52 1.697
587
c MCL046 Mucolipidosis Iii Alpha/beta 61 1.696
588
CHL004 Cholelithiasis 48 1.693
589
HMP005 Hemiplegia 53 1.686
590
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 1.681
591
P HYP730 Hypogonadotropic Hypogonadism 57 1.668
592
SHP001 Shipyard Eye 30 1.666
593
ERL001 Early Myoclonic Encephalopathy 62 1.663
594
GTL001 Gitelman Syndrome 65 1.662
595
PST092 Posttransplant Acute Limbic Encephalitis 29 1.659
596
PRN019 Perinatal Necrotizing Enterocolitis 60 1.659
597
HRW001 Hair Whorl 35 1.657
598
P MLN007 Male Infertility 56 1.656
599
LWC001 Low Compliance Bladder 44 1.655
600
HSH003 Hashimoto Thyroiditis 60 1.654
601
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 57 1.654
602
c ATS007 Autism Spectrum Disorder 71 1.648
603
AMN001 Amenorrhea 53 1.646
604
APH001 Aphthous Stomatitis 57 1.639
605
NRL016 Neural Tube Defects 80 1.637
606
P ATR011 Atrial Fibrillation 66 1.633
607
HMG005 Hemoglobinopathy 55 1.631
608
BLS001 Blau Syndrome 68 1.631
609
CHL152 Childhood Acute Lymphocytic Leukemia 50 1.620
610
INS001 Insulinoma 59 1.619
611
INF021 Infant Gynecomastia 30 1.617
612
GYN001 Gynecomastia 48 1.617
613
c HYP543 Hypoplastic Left Heart Syndrome 1 46 1.611
614
PRM013 Premature Menopause 57 1.611
615
CHR008 Choroiditis 48 1.610
616
ALL006 Allergic Asthma 55 1.610
617
KNB006 Knobloch Syndrome 1 44 1.606
618
P KNB001 Knobloch Syndrome 37 1.606
619
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 1.600
620
IMP005 Impotence 52 1.600
621
P VTR007 Vitreoretinopathy 45 1.599
622
P MTR014 Motor Neuron Disease 65 1.593
623
PRS045 Prostatic Hypertrophy 53 1.591
624
PCH007 Pouchitis 42 1.591
625
BRS051 Breast Disease 58 1.586
626
ALP048 Alopecia Totalis 31 1.579
627
BLP005 Blepharitis 50 1.579
628
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 1.574
629
PRS021 Prostatic Adenoma 43 1.571
630
PYG003 Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, and Acne 57 1.570
631
c MCR112 Microvascular Complications of Diabetes 2 42 1.563
632
SPP011 Suppression of Tumorigenicity 12 61 1.558
633
TLN003 Telangiectasis 51 1.555
634
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 62 1.554
635
INT075 Intracranial Hypertension 52 1.553
636
c JVN061 Juvenile Arthritis 56 1.553
637
LNG039 Lung Squamous Cell Carcinoma 57 1.550
638
CMM005 Common Cold 55 1.550
639
DFF003 Diffuse Scleroderma 41 1.549
640
STT001 Status Epilepticus 58 1.549
641
ILS001 Ileus 49 1.546
642
P STR020 Strabismus 56 1.542
643
IMM055 Immunodeficiency, Common Variable, 8, with Autoimmunity 42 1.540
644
P FML011 Familial Adenomatous Polyposis 70 1.537
645
P NSP012 Nasopharyngeal Carcinoma 60 1.533
646
c DMN023 Diamond-Blackfan Anemia 1 68 1.529
647
RNL078 Renal Dysplasia 46 1.528
648
GST040 Gastric Adenocarcinoma 66 1.526
649
BDD001 Budd-Chiari Syndrome 62 1.524
650
P SPP010 Suppressor of Tumorigenicity 3 50 1.517
651
VSC003 Visceral Leishmaniasis 54 1.516
652
LYM051 Lymphomatoid Granulomatosis 44 1.515
653
P EPD083 Epidermodysplasia Verruciformis 1 57 1.513
654
P ATS364 Autism 72 1.512
655
PLC008 Placenta Disease 48 1.512
656
c FCL025 Focal Segmental Glomerulosclerosis 1 49 1.511
657
P MST009 Mastocytosis 64 1.507
658
LYM094 Lymphedema, Primary, with Myelodysplasia 40 1.505
659
P RHB003 Rhabdomyosarcoma 66 1.499
661
LPD004 Lipoid Nephrosis 44 1.496
662
SZR001 Sezary's Disease 60 1.495
663
P MYP006 Myopia 55 1.494
664
ANG054 Angina Pectoris 65 1.490
665
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 1.489
666
NNN026 Noonan Syndrome with Multiple Lentigines 64 1.488
667
ADN001 Adenosine Deaminase Deficiency 59 1.487
668
LNG073 Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 58 1.479
669
MVL001 Mevalonic Aciduria 65 1.465
670
PPT005 Peptic Ulcer Disease 58 1.465
671
THY029 Thyroid Carcinoma 55 1.461
672
ENT004 Enthesopathy 51 1.459
673
c HMP004 Hemophilia B 68 1.459
674
HMF011 Hemifacial Spasm, Familial 33 1.453
675
P HMF004 Hemifacial Spasm 38 1.453
676
VCC001 Vaccinia 49 1.449
677
P KRT028 Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant 54 1.440
678
GST045 Gastroenteritis 58 1.438
679
RNL024 Renal Glucosuria 60 1.433
680
c EXD008 Exudative Vitreoretinopathy 1 71 1.429
681
CYC010 Cyclic Neutropenia 63 1.428
682
OPT003 Opiate Dependence 49 1.422
683
P SBS003 Substance Abuse 54 1.419
684
HYP457 Hypertrophic Scars 42 1.417
685
PLM033 Pulmonary Embolism 58 1.413
686
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 47 1.410
687
P TRC086 Trichohepatoenteric Syndrome 1 59 1.407
688
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 69 1.406
689
ART016 Aortic Aneurysm 68 1.406
690
P ESN008 Eosinophilic Pneumonia 50 1.402
691
TNG002 Tangier Disease 63 1.402
692
P PRC012 Pericardial Effusion 50 1.401
693
CHR682 Chronic Bilirubin Encephalopathy 37 1.397
694
FBR047 Fibromyalgia 57 1.396
695
P PLY018 Polycythemia 56 1.396
696
BCK006 Back Pain 43 1.395
697
P HRD012 Hereditary Elliptocytosis 55 1.394
698
PRG009 Progressive Multifocal Leukoencephalopathy 58 1.391
699
ANX010 Anxiety 70 1.390
700
BRT059 Bartsocas-Papas Syndrome 55 1.389
701
c HPT015 Hepatitis D 49 1.386
702
SBC016 Subacute Delirium 42 1.384
703
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 1.383
704
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 1.381
705
P MVM001 Movement Disease 61 1.376
706
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 1.375
707
THY111 Thyroid Carcinoma, Familial Medullary 67 1.372
708
P MCR010 Microcephaly 59 1.372
709
PFF001 Pfeiffer Syndrome 77 1.372
710
c ATS282 Autosomal Recessive Malignant Osteopetrosis 45 1.369
711
PTR032 Peters-Plus Syndrome 63 1.369
712
c BRT028 Brittle Cornea Syndrome 1 39 1.366
713
PRS129 Prostatic Hyperplasia, Benign 48 1.366
714
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.366
715
OTT002 Otitis Media 70 1.364
716
P SLP006 Sleep Apnea 69 1.363
717
FLL041 Follicular Lymphoma 1 44 1.362
718
RTC005 Reticulosarcoma 47 1.362
719
c HYP794 Hyperoxaluria, Primary, Type I 63 1.360
720
EXP004 Exophthalmos 50 1.358
721
PLM010 Pulmonary Edema 54 1.356
722
FCL012 Facial Paralysis 49 1.353
723
P RTN018 Retinal Disease 53 1.353
724
c ATS383 Autosomal Dominant Non-Syndromic Intellectual Disability 1 36 1.352
725
GRG001 Greig Cephalopolysyndactyly Syndrome 64 1.351
726
HMR023 Hemorrhagic Cystitis 43 1.351
727
PRP001 Propionic Acidemia 65 1.349
728
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 44 1.349
729
CYS013 Cystinuria 66 1.348
730
P JNC001 Junctional Epidermolysis Bullosa 54 1.343
731
GST071 Gastrointestinal Carcinoma 46 1.342
732
OPD006 Opioid Addiction 48 1.340
733
P HNT016 Huntington Disease 73 1.338
734
WTH001 Withdrawal Disorder 47 1.337
735
P BRN022 Bronchiectasis 59 1.335
736
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 51 1.334
737
URN010 Urinary Tract Obstruction 55 1.333
738
LNG015 Lingual-Facial-Buccal Dyskinesia 47 1.329
739
HPT004 Hepatic Coma 43 1.326
740
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 64 1.324
741
P MNN013 Meningitis 65 1.324
742
LMB062 Limb Ischemia 55 1.324
743
FDL002 Food Allergy 47 1.322
744
ART002 Arts Syndrome 66 1.322
745
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 1.322
746
HYP810 Hypereosinophilic Syndrome, Idiopathic 61 1.321
747
P RNL007 Renal Tubular Acidosis 52 1.319
748
RLP002 Relapsing-Remitting Multiple Sclerosis 56 1.318
749
HYP458 Hyper Ige Syndrome 60 1.314
750
LWC002 Lowe Oculocerebrorenal Syndrome 68 1.313
751
c NPH054 Nephrotic Syndrome, Type 3 44 1.312
752
ACH005 Achalasia 54 1.312
753
SMT004 Smith-Lemli-Opitz Syndrome 69 1.310
754
INT002 Intermittent Claudication 61 1.310
755
ACT088 Acute Insulin Response 39 1.308
756
c HRD142 Hereditary Xanthinuria 44 1.297
757
MNC001 Monocular Esotropia 30 1.296
758
EST005 Esotropia 43 1.296
759
RTN017 Retinal Detachment 60 1.289
760
HYP088 Hyper-Igd Syndrome 51 1.284
761
ORB013 Orbital Disease 42 1.281
762
PLM035 Pulmonary Eosinophilia 49 1.281
763
AMB002 Amblyopia 49 1.279
764
CHL067 Cholecystitis 59 1.279
765
CRV002 Cervix Uteri Carcinoma in Situ 48 1.278
766
CRV045 Cervical Intraepithelial Neoplasia 38 1.278
767
GST092 Gastroesophageal Reflux 59 1.277
768
c OPT053 Optic Atrophy 1 62 1.275
769
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 1.273
770
c PRG042 Progressive Familial Heart Block, Type Ia 65 1.273
771
GRY002 Gray Platelet Syndrome 57 1.267
772
PLY001 Polycythemia Vera 69 1.265
773
DFF021 Diffuse Mesangial Sclerosis 41 1.264
774
FTT001 Fatty Liver Disease 61 1.262
775
GLS001 Gliosarcoma 63 1.262
776
BLD131 Bladder Urothelial Carcinoma 59 1.261
777
GLT035 Glutaric Acidemia I 57 1.261
778
GLC106 Glucocorticoid Resistance, Generalized 47 1.260
779
NPH009 Nephrolithiasis 54 1.258
780
P CRN037 Craniosynostosis 67 1.255
781
RSP027 Respiratory Papillomatosis, Juvenile Recurrent, Congenital 47 1.254
782
c PSD093 Pseudohypoaldosteronism, Type Iid 31 1.253
783
FCT007 Factor Vii Deficiency 64 1.251
784
P CRN025 Corneal Dystrophy 49 1.246
785
IDP011 Idiopathic Interstitial Pneumonia 59 1.241
786
FLL027 Fallopian Tube Carcinoma 66 1.239
787
LYM007 Lymphangioleiomyomatosis 68 1.236
788
MNN043 Meningioma, Familial 79 1.235
789
P VNW001 Von Willebrand's Disease 64 1.235
790
c THR090 Thrombocythemia 1 50 1.234
791
c THR124 Thrombotic Thrombocytopenic Purpura, Hereditary 53 1.234
792
P WSK001 Wiskott-Aldrich Syndrome 72 1.232
793
P PRG092 Pregnancy Loss, Recurrent 1 42 1.231
794
MTH076 Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency 50 1.230
795
P DMY001 Demyelinating Polyneuropathy 41 1.229
796
GRN037 Granulomatosis with Polyangiitis 66 1.226
797
TFR002 Tafro Syndrome 34 1.224
798
c ART115 Aortic Valve Disease 1 72 1.221
799
PRT019 Protein-Losing Enteropathy 44 1.219
800
ACT119 Acute Promyelocytic Leukemia 62 1.219
801
KLD004 Keloid Disorder 38 1.218
802
c HRM005 Hermansky-Pudlak Syndrome 1 55 1.217
803
FCS002 Fucosidosis 61 1.217
804
ICH001 Ichthyosis Vulgaris 53 1.216
805
LYS003 Lysinuric Protein Intolerance 57 1.215
806
CRS001 Crescentic Glomerulonephritis 42 1.210
807
ANC002 Anca-Associated Vasculitis 44 1.208
808
APH002 Aphasia 55 1.206
809
CCT002 Cicatricial Pemphigoid 53 1.201
810
c OST126 Osteopetrosis, Autosomal Recessive 1 51 1.200
811
IMM136 Immune System Disease 46 1.197
812
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 47 1.196
813
NRM005 Neuromuscular Disease 62 1.196
814
P AGM001 Agammaglobulinemia 67 1.193
815
MLT163 Multiple Pterygium Syndrome, Escobar Variant 62 1.188
816
AND014 Androgenic Alopecia 46 1.188
817
P ALP061 Alopecia, Androgenetic, 1 48 1.188
818
ERY029 Erythermalgia, Primary 57 1.185
819
c NRB010 Neuroblastoma 1 59 1.183
820
SVR066 Severe Combined Immunodeficiency, X-Linked 65 1.174
821
DFF005 Diffuse Large B-Cell Lymphoma 55 1.173
822
P TRT019 Torticollis 47 1.173
823
c SCK017 Sick Sinus Syndrome 1 34 1.172
824
P DMN002 Dementia 65 1.172
825
P ESS003 Essential Thrombocythemia 68 1.171
826
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 54 1.169
827
P CHR345 Chronic Pain 50 1.165
828
P MLN069 Melanoma, Uveal 59 1.164
829
MSL001 Measles 61 1.164
830
P OCL013 Oculodentodigital Dysplasia 66 1.164
831
P RCT021 Rectum Cancer 54 1.162
832
P TMT001 Timothy Syndrome 55 1.162
833
ADN018 Adenoma 58 1.161
834
MCH006 Mechanical Strabismus 40 1.161
835
P MSC003 Muscular Atrophy 52 1.159
836
c GLY060 Glycogen Storage Disease Ia 62 1.159
837
SPC005 Speech Disorder 46 1.156
838
c SPN330 Spondylocostal Dysostosis 5 55 1.154
839
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 66 1.153
840
c 46X055 46,xy Sex Reversal 3 40 1.153
841
CHR003 Cherubism 57 1.152
842
PYR041 Pyruvate Kinase Deficiency of Red Cells 56 1.151
843
c BSL024 Basal Cell Carcinoma 1 55 1.143
844
EXC003 Excessive Tearing 33 1.143
845
P LCR008 Lacrimal Apparatus Disease 41 1.143
846
HPT019 Hepatic Encephalopathy 59 1.142
847
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 58 1.138
848
EPD022 Epidermolysis Bullosa Pruriginosa 41 1.135
849
DPH001 Diphtheria 59 1.133
850
RFL001 Reflex Sympathetic Dystrophy 51 1.132
851
ALG001 Algoneurodystrophy 37 1.132
852
THY030 Thyroid Gland Disease 50 1.131
853
P GCH001 Gaucher's Disease 69 1.130
854
PLY023 Polycystic Liver Disease 62 1.128
855
MYS016 Myosclerosis, Autosomal Recessive 32 1.127
856
HMN048 Human Papillomavirus Infectious Disease 45 1.127
857
GST050 Gastrointestinal System Disease 55 1.127
858
CNN003 Conn's Syndrome 77 1.114
859
P PRP003 Porphyria Cutanea Tarda 66 1.114
860
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 1.113
861
DBT010 Diabetic Neuropathy 54 1.112
862
P HYP076 Hyperthyroidism 53 1.111
863
NRG002 Neurogenic Bladder 54 1.111
864
NNL006 Non-Alcoholic Steatohepatitis 54 1.109
865
ANG049 Angioedema Induced by Ace Inhibitors 38 1.108
866
PLS025 Plasmablastic Lymphoma 47 1.108
867
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.107
868
PRP027 Peripheral Vascular Disease 71 1.106
869
P CMP005 Campomelic Dysplasia 65 1.104
870
MCR088 Microscopic Polyangiitis 51 1.103
871
ACT098 Acute Erythroid Leukemia 55 1.101
872
CRD132 Cardiac Conduction Defect 59 1.101
873
IMM065 Immunodeficiency 10 47 1.097
874
HYD002 Hydronephrosis 58 1.092
875
c ESS001 Essential Tremor 56 1.088
876
P CLC063 Celiac Disease 1 65 1.086
877
PRP016 Paraplegia 52 1.086
878
MLG169 Malignant Astrocytoma 57 1.085
879
P MJR001 Major Depressive Disorder 68 1.084
880
CLF027 Cleft Palate, Isolated 64 1.081
881
OVR094 Ovarian Epithelial Cancer 39 1.077
882
P HMR003 Hemorrhagic Disease 59 1.077
883
P LPR021 Leprosy 3 71 1.076
884
P NGH001 Night Blindness 52 1.073
885
PRP083 Porphyria, Acute Intermittent 64 1.070
886
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 1.069
887
c HRD002 Hereditary Angioedema 61 1.068
888
c PRT132 Protoporphyria, Erythropoietic, 1 61 1.066
889
CMB081 Combined Immunodeficiency, X-Linked 39 1.066
890
c TYR012 Tyrosinemia, Type I 61 1.061
891
PMP010 Pompholyx 33 1.061
892
MRT001 Muir-Torre Syndrome 59 1.059
893
MST024 Mastocytosis, Cutaneous 66 1.059
894
DSC009 Discoid Lupus Erythematosus 42 1.059
895
END020 Endocardial Fibroelastosis 53 1.058
896
SCT005 Scott Syndrome 51 1.056
897
FCT006 Factor V Deficiency 55 1.053
898
P RNV001 Renovascular Hypertension 48 1.049
899
AMG001 Amegakaryocytic Thrombocytopenia, Congenital 55 1.046
900
P PSD003 Pseudohypoaldosteronism 45 1.040
901
SPP007 Suppression Amblyopia 38 1.038
902
c ART101 Aortic Valve Disease 2 65 1.038
903
P CYS039 Cystic Kidney Disease 52 1.036
904
ADR022 Adrenomyeloneuropathy 38 1.029
905
SRT004 Serotonin Syndrome 54 1.028
906
CCN002 Cocaine Abuse 49 1.026
907
P GNG025 Gingival Fibromatosis 48 1.026
908
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 1.023
909
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 34 1.023
910
BRN009 Burning Mouth Syndrome 51 1.022
911
P END044 Endometriosis 62 1.022
912
c CHL137 Cholestasis, Progressive Familial Intrahepatic, 3 53 1.018
913
DNT012 Dental Caries 53 1.016
914
c LYM106 Lymphoproliferative Syndrome 1 45 1.015
915
ISL099 Isolated Methylmalonic Acidemia 35 1.015
916
P BRN035 Brain Stem Glioma 49 1.013
917
P PLY006 Polydactyly 58 1.007
918
LYS012 Lysosomal Acid Lipase Deficiency 64 1.007
919
PSY004 Psychotic Disorder 66 1.007
920
P CRD246 Cardiovascular System Disease 55 1.006
921
c SVR003 Severe Congenital Neutropenia 59 1.006
922
P LRY044 Larynx Cancer 53 1.005
923
LYM048 Lymphoma, Large-Cell, Immunoblastic 27 1.002
924
VLV010 Vulvovaginitis 42 1.002
925
STT009 Sutton Disease 2 30 1.002
926
SPS019 Spastic Paraparesis 38 0.997
927
MRK001 Merkel Cell Carcinoma 64 0.993
928
IMM003 Immunoglobulin Alpha Deficiency 44 0.993
929
TRN015 Transient Cerebral Ischemia 62 0.993
930
P MTC133 Mitochondrial Myopathy 51 0.992
931
c CRD093 Cardiomyopathy, Dilated, 1a 55 0.992
932
MYP035 Myopathy, Distal, with Anterior Tibial Onset 33 0.990
933
ATM052 Autoimmune Disease 1 36 0.988
934
c ANG068 Angioedema, Hereditary, Type I 58 0.988
935
GLC009 Glucosephosphate Dehydrogen