Search results for "nephropathy"

The MalaCard for "nephropathy" has been retired.
Searching MalaCards for entries containing "nephropathy"

1362 hits were found for 'nephropathy'

# Family MCID Name MIFTS Score
1
BLK001 Balkan Nephropathy 35 4.726
2
FML076 Familial Juvenile Hyperuricaemic Nephropathy 24 4.595
3
ANG060 Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle Cramps 33 4.099
4
P MMB011 Membranous Nephropathy 43 3.927
5
P HYP623 Hyperuricemic Nephropathy, Familial Juvenile 1 37 3.854
6
UMD001 Umod-Associated Kidney Disease 19 3.810
7
c HYP616 Hyperuricemic Nephropathy, Familial Juvenile 2 22 3.578
8
IGG001 Iga Glomerulonephritis 40 3.543
9
c MCR113 Microvascular Complications of Diabetes 3 46 3.103
10
ACT043 Acute Urate Nephropathy 30 3.057
11
c BKV001 Bk-Virus Nephropathy 20 3.037
12
NPH037 Nephronophthisis-Like Nephropathy 1 21 3.025
13
HYP114 Hypertensive Nephropathy 28 2.901
14
HMT008 Hematuria, Benign Familial 32 2.755
15
NPH014 Nephropathy with Pretibial Epidermolysis Bullosa and Deafness 17 2.718
16
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 30 2.703
17
NPH023 Nephropathy, Deafness, and Hyperparathyroidism 14 2.703
18
P IGN003 Iga Nephropathy 1 24 2.612
19
P ALP004 Alport Syndrome 66 2.469
20
DNY001 Denys-Drash Syndrome 57 2.400
21
LMY009 Leiomyomatosis, Esophageal and Vulval, with Nephropathy 8 2.383
22
NPH066 Nephropathy Due to Cfhr5 Deficiency 14 2.345
23
P AMY082 Amyloidosis, Familial Visceral 43 2.336
24
EPL108 Epilepsy, Progressive Myoclonic 4, with or Without Renal Failure 24 2.336
25
P KDN018 Kidney Disease 57 2.135
26
MMB002 Membranous Glomerulonephritis 40 2.118
27
c IGN002 Iga Nephropathy 2 11 2.090
28
ALP047 Alport Syndrome and Thin Basement Membrane Nephropathy 22 1.998
29
PLY043 Polyomavirus Allograft Nephropathy 9 1.987
30
HRD044 Hereditary Endotheliopathy, Retinopathy, Nephropathy, and Stroke 18 1.955
31
NPH003 Nephrocalcinosis 39 1.948
32
MCK007 Muckle-Wells Syndrome 58 1.940
33
RNL051 Renal Cysts and Diabetes Syndrome 46 1.940
34
MLT033 Multicentric Osteolysis Nephropathy 5 1.940
35
MLT102 Multicentric Carpo-Tarsal Osteolysis with or Without Nephropathy 12 1.931
36
FGN001 Feigenbaum Bergeron Richardson Syndrome 12 1.931
37
c HYP529 Hyperuricemic Nephropathy, Familial Juvenile, 3 10 1.931
38
c ALP073 Alport Syndrome, Autosomal Recessive 40 1.922
39
DNT019 Daentl Towsend Siegel Syndrome 18 1.922
40
NPH050 Nephropathy, Progressive, with Deafness 6 1.922
41
c RNR002 Ren-Related Kidney Disease 11 1.911
42
HYP632 Hyperuricemia - Anemia - Renal Failure 10 1.911
43
FNC009 Fanconi-Bickel Syndrome 50 1.898
44
c ALM001 Al Amyloidosis 45 1.898
45
HRD176 Hereditary Amyloidosis with Primary Renal Involement 21 1.898
46
APM001 Aapoaii Amyloidosis 14 1.898
47
APM002 Aapoai Amyloidosis 12 1.898
48
c ATS141 Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease Type E 12 1.898
49
AFB003 Afib Amyloidosis 11 1.898
50
P C1Q005 C1q Nephropathy 20 1.534
51
P MCR115 Microvascular Complications of Diabetes 5 47 1.447
52
c MCR112 Microvascular Complications of Diabetes 2 22 1.423
53
c MCR129 Microvascular Complications of Diabetes 1 41 1.416
54
c MCR120 Microvascular Complications of Diabetes 7 25 1.409
55
c MCR130 Microvascular Complications of Diabetes 6 23 1.409
56
c MCR133 Microvascular Complications of Diabetes 4 21 1.409
57
HMR004 Hemorrhagic Fever with Renal Syndrome 53 1.401
58
NPH004 Nephropathia Epidemica 40 1.392
59
VSC016 Vasculopathy, Retinal, with Cerebral Leukodystrophy 30 1.383
60
ATH009 Atherosclerosis - Deafness - Diabetes - Epilepsy - Nephropathy 13 1.383
61
c CL4008 Col4a4-Related Nephropathy 6 1.383
62
ADN024 Adenine Phosphoribosyltransferase Deficiency 43 1.372
63
CTR091 Cataract - Nephropathy - Encephalopathy 12 1.372
64
c CNG407 Congenital Membranous Nephropathy Due to Maternal Anti-Neutral Endopeptidase Alloimmunization 9 1.372
65
ATS138 Autosomal Dominant Progressive Nephropathy with Hypertension 6 1.372
66
c CL4006 Col4a5-Related Nephropathy 5 1.372
67
c CL4007 Col4a3-Related Nephropathy 5 1.372
68
NPH022 Nephropathy Familial with Hyperuricemia 2 1.372
69
c ALP074 Alport Syndrome, Autosomal Dominant 36 1.359
70
FTZ004 Fitzsimmons Walson Mellor Syndrome 12 1.359
71
ALL011 Allain-Babin-Demarquez Syndrome 4 1.342
72
HRR004 Herrmann Syndrome 3 1.342
73
P PRM002 Primary Hyperoxaluria 64 0.395
74
URN009 Urinary System Disease 33 0.371
75
P GLM007 Glomerulonephritis 49 0.268
76
c CHR089 Chronic Kidney Failure 61 0.229
77
END030 End Stage Renal Failure 51 0.207
78
P HYP071 Hypersensitivity Reaction Type Ii Disease 38 0.194
79
P GLM044 Glomerular Disease 32 0.193
80
IMP003 Impaired Renal Function Disease 23 0.192
81
END072 Endotheliitis 39 0.168
82
MDY003 Mody, Type Ii 32 0.156
83
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 84 0.155
84
P DBT085 Diabetes Mellitus, Insulin-Dependent 82 0.154
85
ATM052 Autoimmune Disease 1 15 0.154
86
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 11 0.153
87
ATM053 Autoimmune Disease 2 5 0.151
88
P NPH012 Nephrotic Syndrome 52 0.147
89
GLM011 Glomerulosclerosis 38 0.143
90
GLC008 Glucose Metabolism Disease 30 0.138
91
P CNG401 Congenital Heart Disease 68 0.134
92
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 15 0.134
93
ATM054 Autoimmune Disease 3 5 0.134
94
c ACT071 Acute Kidney Failure 45 0.126
95
c MTB001 Metabolic Syndrome X 52 0.123
96
GMM002 Gamma Chain Deficiency 44 0.120
97
RNL015 Renal Hypertension 38 0.118
98
BLD054 Blood Protein Disease 24 0.118
99
PRP030 Purpura 47 0.116
100
ATM055 Autoimmune Disease 4 5 0.116
101
P FCL005 Focal Segmental Glomerulosclerosis 65 0.112
102
ATM059 Autoimmune Disease 6 16 0.112
103
ATM012 Autoimmune Disease of Blood 24 0.111
104
c HYP595 Hypertension, Essential 68 0.109
105
IDP077 Idiopathic Membranous Glomerulonephritis 29 0.109
106
P NRP001 Neuropathy 48 0.105
107
c CRN175 Coronary Heart Disease 4 9 0.105
108
P MYC007 Myocardial Infarction 76 0.103
109
P HPT021 Hepatitis 58 0.103
110
RNL097 Renal Artery Disease 32 0.101
111
MDY005 Mody, Type I 27 0.101
112
RNL077 Renal Fibrosis 37 0.099
113
CNG034 Congestive Heart Failure 65 0.095
114
TNS005 Tonsillitis 47 0.095
115
P TRC086 Trichohepatoenteric Syndrome 1 42 0.095
116
INT067 Interstitial Nephritis 41 0.095
117
c CRN172 Coronary Heart Disease 3 9 0.095
118
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 13 0.093
119
P CRN214 Coronary Heart Disease 5 10 0.093
120
c CRN178 Coronary Heart Disease 6 10 0.093
121
ISC004 Ischemia 47 0.090
122
CRS001 Crescentic Glomerulonephritis 38 0.090
123
P HYP014 Hyperuricemia 45 0.088
124
NTR005 Nutritional Deficiency Disease 41 0.086
125
NNS006 Non-Suppurative Otitis Media 36 0.086
126
ATN002 Autonomic Nervous System Disease 27 0.086
127
PRP027 Peripheral Vascular Disease 62 0.083
128
THR013 Thoracic Outlet Syndrome 47 0.083
129
MMB001 Membranoproliferative Glomerulonephritis 44 0.083
130
c MYC058 Myocardial Infarction 2 19 0.083
131
c ACT075 Acute Myocardial Infarction 50 0.081
132
FBR012 Fabry Disease 75 0.078
133
P CRN211 Coronary Artery Disease 68 0.078
134
STR067 Stroke, Ischemic 68 0.078
135
HYP066 Hyperglycemia 50 0.078
136
ART111 Artery Disease 48 0.078
137
CRB009 Cerebritis 37 0.078
138
ATM013 Autoimmune Disease of Cardiovascular System 4 0.078
139
c SYS001 Systemic Lupus Erythematosus 90 0.076
140
P ART022 Arthritis 61 0.076
141
NLP001 Nail-Patella Syndrome 59 0.076
142
P MYL007 Myeloma 54 0.076
143
DFC004 Deficiency Anemia 52 0.076
144
c MLG069 Malignant Hypertension 46 0.076
145
LPD008 Lipid Metabolism Disorder 45 0.076
146
P PRL003 Proliferative Glomerulonephritis 36 0.076
147
ANR002 Aniridia 72 0.073
148
ISC006 Ischemic Heart Disease 56 0.073
149
ACN002 Acanthosis Nigricans 53 0.073
150
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 34 0.073
151
BLD053 Blood Platelet Disease 32 0.073
152
P ATX010 Ataxia Neuropathy Spectrum 31 0.073
153
c SPN225 Spondyloarthropathy 1 66 0.070
154
P HRM001 Hermansky-Pudlak Syndrome 62 0.070
155
P KDN017 Kidney Cancer 60 0.070
156
c PNC108 Pancreatitis, Hereditary 59 0.070
157
P RSP003 Respiratory Failure 58 0.070
158
VSC007 Vascular Disease 55 0.070
159
c ART101 Aortic Valve Disease 2 46 0.070
160
DBT084 Diabetes Mellitus, Ketosis-Prone 30 0.070
161
c SCN053 Secondary Glomerular Disease 4 0.070
162
P RHM011 Rheumatoid Arthritis 88 0.067
163
P ANG001 Angelman Syndrome 66 0.067
164
P LPS004 Lupus Erythematosus 61 0.067
165
P PLY014 Polycystic Kidney Disease 60 0.067
166
c HPT016 Hepatitis B 59 0.067
167
P HMP002 Hemophagocytic Lymphohistiocytosis 59 0.067
168
HNT002 Hantavirus Pulmonary Syndrome 52 0.067
169
P GT001 Gout 51 0.067
170
ATH003 Atherosclerosis 50 0.067
171
MTH009 Mouth Disease 44 0.067
172
P SPS003 Spastic Diplegia 37 0.067
173
c HMG001 Hemoglobin C Disease 36 0.067
174
c ATM017 Autoimmune Disease of the Nervous System 26 0.067
175
c ATM007 Autoimmune Disease of Central Nervous System 22 0.067
176
P FNC004 Fanconi Syndrome 46 0.064
177
P VSC005 Vesicoureteral Reflux 44 0.064
178
CYS016 Cystic Kidney 43 0.064
179
RTN023 Retinitis 43 0.064
180
ADJ001 Adjustment Disorder 30 0.064
181
c RNL016 Renal Infectious Disease 7 0.064
182
TBR010 Tuberculosis 64 0.061
183
ART021 Arteriosclerosis 51 0.061
184
VSC011 Vasculitis 50 0.061
185
MYC002 Mycobacterium Avium Complex Disease 46 0.061
186
LPD004 Lipoid Nephrosis 38 0.061
187
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 19 0.061
188
c MLT019 Multiple Myeloma 77 0.057
189
PCK002 Pick Disease 61 0.057
190
P LKM002 Leukemia 61 0.057
191
RTN018 Retinal Disease 46 0.057
192
HYP266 Hypoxia 42 0.057
193
P PYL005 Pyelonephritis 42 0.057
194
P EXN002 Exanthem 41 0.057
195
ANG054 Angina Pectoris 41 0.057
196
P RPD001 Rapidly Progressive Glomerulonephritis 39 0.057
197
ATN004 Autonomic Neuropathy 39 0.057
198
WTH001 Withdrawal Disorder 27 0.057
199
P OBS005 Obesity 89 0.053
200
P AST005 Asthma 77 0.053
201
HV1006 Hiv-1 77 0.053
202
P ATX030 Ataxia-Telangiectasia 76 0.053
203
c HPT001 Hepatitis C 64 0.053
204
P AMY004 Amyloidosis 60 0.053
205
ART001 Arterial Tortuosity Syndrome 59 0.053
206
PRT036 Peritonitis 58 0.053
207
P AND016 Andersen Syndrome 58 0.053
208
P CMP010 Complex Regional Pain Syndrome 51 0.053
209
c SCN006 Secondary Syphilis 48 0.053
210
LRN003 Learning Disability 47 0.053
211
P HML001 Hemolytic-Uremic Syndrome 44 0.053
212
ANR040 Aneurysm 43 0.053
213
MCR004 Macroglobulinemia 43 0.053
214
NPH018 Nephrogenic Systemic Fibrosis 43 0.053
215
HNC001 Henoch-Schoenlein Purpura 41 0.053
216
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 30 0.053
217
BSM001 Basement Membrane Disease 26 0.053
218
HPT023 Hepatocellular Carcinoma 90 0.049
219
P WSK001 Wiskott-Aldrich Syndrome 68 0.049
220
AND015 Androgen Insensitivity 65 0.049
221
P PSR002 Psoriasis 64 0.049
222
P AXN010 Axenfeld-Rieger Syndrome, Type 3 60 0.049
223
ACQ007 Acquired Immunodeficiency Syndrome 55 0.049
224
CHR001 Churg-Strauss Syndrome 53 0.049
225
P NPH005 Nephronophthisis 53 0.049
226
P PNC044 Pancreatitis 51 0.049
227
P HYP069 Hyperparathyroidism 50 0.049
228
VRL011 Viral Infectious Disease 50 0.049
229
CNN005 Connective Tissue Disease 49 0.049
230
P SPN052 Spondyloarthropathy 49 0.049
231
P UVT001 Uveitis 49 0.049
232
P THY032 Thyroiditis 48 0.049
233
P SZR006 Seizure Disorder 48 0.049
234
CSY001 C Syndrome 44 0.049
235
FCT013 Factor V Leiden Thrombophilia 43 0.049
236
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 43 0.049
237
P RNV001 Renovascular Hypertension 43 0.049
238
PRP080 Peripheral Artery Disease 39 0.049
239
LGH004 Light Chain Deposition Disease 38 0.049
240
NRR001 Neuroretinitis 38 0.049
241
TFT003 Tufting Enteropathy 27 0.049
242
ALR002 Al-Raqad Syndrome 23 0.049
243
AND005 Androgen Insensitivity Syndrome, Mild 19 0.049
244
c CRN177 Coronary Heart Disease 7 10 0.049
245
c CRN174 Coronary Heart Disease 2 9 0.049
246
GTL001 Gitelman Syndrome 63 0.045
247
KWS002 Kawasaki Disease 62 0.045
248
c HPT073 Hepatitis C Virus 60 0.045
249
ACR008 Acrocallosal Syndrome 58 0.045
250
CRB039 Cerebrovascular Disease 58 0.045
251
P ADN016 Adenocarcinoma 56 0.045
252
P THL005 Thalassemia 56 0.045
253
P RCK004 Rickets 55 0.045
254
SCH016 Schimke Immunoosseous Dysplasia 51 0.045
255
SNS001 Sensorineural Hearing Loss 49 0.045
256
P SCK005 Sickle Cell Disease 49 0.045
257
P NPH009 Nephrolithiasis 48 0.045
258
WLL006 Wells Syndrome 48 0.045
259
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 46 0.045
260
P DRR001 Diarrhea 45 0.045
261
CRY004 Cryoglobulinemia 45 0.045
262
INT007 Intermediate Coronary Syndrome 45 0.045
263
TRN018 Transitional Cell Carcinoma 44 0.045
264
HYP037 Hyperhomocysteinemia 40 0.045
265
VSC006 Vascular Cancer 40 0.045
266
P PRP023 Peripheral Neuropathy 40 0.045
267
PRT019 Protein-Losing Enteropathy 40 0.045
268
MNN014 Mononeuritis 39 0.045
269
MSN001 Mesangial Proliferative Glomerulonephritis 39 0.045
270
TTR016 Tetra-Amelia Syndrome 38 0.045
271
RTN020 Retinal Vascular Disease 38 0.045
272
RTR011 Retroperitoneal Fibrosis 38 0.045
273
NPH010 Nephrosclerosis 38 0.045
274
IMM001 Immune-Complex Glomerulonephritis 35 0.045
275
VND001 Vein Disease 34 0.045
276
ADS002 Adie Syndrome 34 0.045
277
c CHR098 Chronic Pyelonephritis 33 0.045
278
STR044 Steroid-Resistant Nephrotic Syndrome 31 0.045
279
VSL002 Visual Epilepsy 31 0.045
280
HPT074 Hepatic Adenoma, Somatic 30 0.045
281
c ARC016 Auriculocondylar Syndrome 1 30 0.045
282
CHR413 Chronic Myocardial Ischemia 29 0.045
283
HYP540 Hypertension, Diastolic 29 0.045
284
P MDL021 Medullary Cystic Kidney Disease 2 27 0.045
285
HNM002 Hinman Syndrome 27 0.045
286
BNS002 Bone Structure Disease 24 0.045
287
PLS010 Plasma Protein Metabolism Disease 23 0.045
288
ACD004 Acdc 23 0.045
289
ATM014 Autoimmune Disease of Endocrine System 21 0.045
290
c BNG076 Benign Exophthalmos Syndrome 21 0.045
291
c AST037 Asthma 1 20 0.045
292
c TRC078 Trichohepatoenteric Syndrome 2 20 0.045
293
VTM003 Vitamin Metabolic Disorder 18 0.045
294
c CRN173 Coronary Heart Disease 8 9 0.045
295
DWS002 Dawson Disease 3 0.045
296
c AMY091 Amyotrophic Lateral Sclerosis 1 83 0.040
297
MLR004 Malaria 72 0.040
298
SCK003 Sickle Cell Anemia 71 0.040
299
CDS001 Cadasil 70 0.040
300
P APL001 Aplastic Anemia 70 0.040
301
P PND002 Pendred Syndrome 63 0.040
302
MYC006 Mycosis Fungoides 60 0.040
303
PLM001 Pulmonary Tuberculosis 60 0.040
304
P LVR013 Liver Disease 59 0.040
305
BRN024 Bronchitis 56 0.040
306
P ANT006 Antiphospholipid Syndrome 55 0.040
307
P CMR001 Camurati-Engelmann Disease 54 0.040
308
c ATM011 Autoimmune Hepatitis 53 0.040
309
MXD005 Mixed Connective Tissue Disease 53 0.040
310
DBT010 Diabetic Neuropathy 53 0.040
311
P HML002 Hemolytic Anemia 52 0.040
312
PMS001 Poems Syndrome 51 0.040
313
P GRV001 Graves' Disease 51 0.040
314
FRS002 Frasier Syndrome 50 0.040
315
EPD016 Epidermolysis Bullosa 49 0.040
316
P ACT074 Acute Lymphocytic Leukemia 48 0.040
317
CLT003 Colitis 47 0.040
318
PLS011 Plasmacytoma 46 0.040
319
P FML035 Familial Hyperlipidemia 46 0.040
320
HMT018 Hematopoietic Stem Cell Transplantation 45 0.040
321
P SCL015 Scleritis 45 0.040
322
P HYP060 Hyperinsulinism 44 0.040
323
URM002 Uremia 44 0.040
324
P HMR012 Hemorrhagic Fever 44 0.040
325
P CLL015 Collagen Disease 43 0.040
326
c PND001 Pain Disorder 43 0.040
327
IPX001 Ipex Syndrome 43 0.040
328
ADL002 Adult Syndrome 43 0.040
329
OST011 Osteomalacia 42 0.040
330
ADT003 Auditory System Disease 42 0.040
331
c CMP058 Complex Regional Pain Syndrome Type 1 40 0.040
332
NRN002 Neuronitis 40 0.040
333
SPN051 Spondylitis 39 0.040
334
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 39 0.040
335
DBT008 Diabetic Angiopathy 38 0.040
336
LMB062 Limb Ischemia 38 0.040
337
CRB025 Carbohydrate Metabolic Disorder 32 0.040
338
CHL070 Cholesterol Embolism 31 0.040
339
PRP019 Peripheral Nervous System Disease 31 0.040
340
UND005 Undifferentiated Pleomorphic Sarcoma 31 0.040
341
P HYP120 Hypoaldosteronism 31 0.040
342
c JVN024 Juvenile Hereditary Hemochromatosis 30 0.040
343
CLC007 Calcium Metabolism Disease 28 0.040
344
PRM025 Primary Bacterial Infectious Disease 27 0.040
345
RDN001 Reading Disorder 25 0.040
346
MDY006 Mody, Type Iv 24 0.040
347
c CMR004 Camurati Engelmann Disease, Type 2 11 0.040
348
c DBT055 Diabetes Mellitus, Insulin-Dependent, 3 9 0.040
349
c DBT056 Diabetes Mellitus, Insulin-Dependent, 4 9 0.040
350
P PRS040 Prostate Cancer 90 0.035
351
CRH001 Crohn's Disease 80 0.035
352
P HYP607 Hypercholesterolemia, Familial 79 0.035
353
P HNT016 Huntington Disease 78 0.035
354
GLC006 Galactosemia 76 0.035
355
c CHR090 Chronic Lymphocytic Leukemia 70 0.035
356
BRK010 Burkitt Lymphoma 68 0.035
357
BHC002 Behcet's Disease 63 0.035
358
c ATM003 Autoimmune Thyroiditis 57 0.035
359
P PSR001 Psoriatic Arthritis 57 0.035
360
P HYP117 Hypertriglyceridemia 56 0.035
361
c PRM005 Primary Hyperparathyroidism 56 0.035
362
c ATM010 Autoimmune Hemolytic Anemia 56 0.035
363
RCT015 Reactive Arthritis 55 0.035
364
TTN003 Tetanus 55 0.035
365
P EPL002 Epilepsy Syndrome 54 0.035
366
EYD002 Eye Disease 54 0.035
367
P ACR001 Aicardi-Goutieres Syndrome 53 0.035
368
CHG001 Chagas Disease 53 0.035
369
YLL002 Yellow Fever 52 0.035
370
RLP001 Relapsing Polychondritis 52 0.035
371
STT001 Status Epilepticus 51 0.035
372
CHL071 Child Syndrome 51 0.035
373
P CHL002 Childhood Absence Epilepsy 51 0.035
374
P MNN013 Meningitis 51 0.035
375
VHW001 Vohwinkel Syndrome 50 0.035
376
PRS047 Prostatitis 50 0.035
377
P MTR004 Maturity-Onset Diabetes of the Young 49 0.035
378
P SHR029 Short Syndrome 49 0.035
379
c THR092 Thrombophilia Due to Thrombin Defect 49 0.035
380
P PLY017 Polyarteritis Nodosa 49 0.035
381
LYM021 Lymphadenitis 48 0.035
382
CYT008 Cytomegalovirus Infection 47 0.035
383
c CNG124 Congenital Rubella 47 0.035
384
P SLP006 Sleep Apnea 46 0.035
385
P SPR013 Spiradenoma 46 0.035
386
RNL007 Renal Tubular Acidosis 46 0.035
387
EVN001 Evans' Syndrome 46 0.035
388
P PLY019 Polyneuropathy 46 0.035
389
SPN020 Spondylosis 46 0.035
390
PRT011 Protein C Deficiency 46 0.035
391
NWC001 Newcastle Disease 45 0.035
392
P RTN022 Retinal Vein Occlusion 45 0.035
393
PLS009 Plasma Cell Neoplasm 45 0.035
394
P LPD010 Lipodystrophy 45 0.035
395
PLM010 Pulmonary Edema 45 0.035
396
GRF001 Graft-Versus-Host Disease, Protection Against 44 0.035
397
ESN015 Eosinophilic Fasciitis 44 0.035
398
GLL032 Galloway-Mowat Syndrome 44 0.035
399
P SYP003 Syphilis 44 0.035
400
c ANT034 Anterior Uveitis 44 0.035
401
KDS001 Kid Syndrome 44 0.035
402
TRN015 Transient Cerebral Ischemia 43 0.035
403
c PLY026 Polycystic Kidney Disease, Autosomal Dominant 43 0.035
404
P HYD002 Hydronephrosis 42 0.035
405
ART017 Aortic Disease 42 0.035
406
P GND004 Gonadal Dysgenesis 41 0.035
407
c CHR417 Chronic Graft Versus Host Disease 41 0.035
408
URT001 Urethritis 40 0.035
409
CRN030 Coronary Stenosis 40 0.035
410
HYP006 Hypertensive Heart Disease 40 0.035
411
HPT014 Hepatorenal Syndrome 39 0.035
412
GDS001 Good Syndrome 37 0.035
413
LMY003 Leiomyomatosis 36 0.035
414
c PLY059 Polycystic Kidney Disease, Adult Type I 36 0.035
415
IRN002 Iron Metabolism Disease 36 0.035
416
IDP033 Idiopathic Edema 36 0.035
417
c HMG003 Hemoglobin E Disease 35 0.035
418
c SYS043 Systemic Lupus Erythematosus 1 34 0.035
419
THL010 Thalassemia Minor 34 0.035
420
NSY001 N Syndrome 34 0.035
421
ACT084 Acute Stress Disorder 34 0.035
422
UPP004 Upper Respiratory Tract Disease 34 0.035
423
CRN019 Coronary Artery Vasospasm 32 0.035
424
CRB086 Cerebral Aneurysms 32 0.035
425
SCN001 Secondary Hyperparathyroidism of Renal Origin 32 0.035
426
ART012 Aortitis 32 0.035
427
CRT004 Carotid Artery Thrombosis 32 0.035
428
c CRN159 Craniosynostosis, Type 1 32 0.035
429
c ACT004 Acute Diarrhea 31 0.035
430
MDY004 Mody, Type Iii 30 0.035
431
SXL003 Sexual Disorder 30 0.035
432
HRS011 Horseshoe Kidney 29 0.035
433
PST011 Pustulosis of Palm and Sole 28 0.035
434
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 28 0.035
435
MCR039 Macrophagic Myofasciitis 28 0.035
436
c NPH049 Nephrotic Syndrome, Type 2 27 0.035
437
SPC003 Specific Developmental Disorder 25 0.035
438
MNG003 Mungan Syndrome 24 0.035
439
c AST039 Asthma 2 23 0.035
440
c HMG004 Hemoglobin D Disease 22 0.035
441
RNL001 Renal Artery Obstruction 22 0.035
442
c SYS038 Systemic Lupus Erythematosus 2 20 0.035
443
CRB031 Cerebral Arterial Disease 19 0.035
444
DHL001 Dahlberg Borer Newcomer Syndrome 17 0.035
445
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 16 0.035
446
CLL035 Collagen Type Iii Glomerulopathy 9 0.035
447
c DBT038 Diabetes Mellitus, Insulin-Dependent, 5 8 0.035
448
P SYS050 Systemic Lupus Erythematosus with Nephritis 2 5 0.035
449
P ALZ034 Alzheimer Disease 98 0.029
450
P CLR023 Colorectal Cancer 95 0.029
451
P RNL014 Renal Cell Carcinoma 81 0.029
452
P OST012 Osteoarthritis 79 0.029
453
P PNC035 Pancreatic Cancer 78 0.029
454
P PLM037 Pulmonary Hypertension 78 0.029
455
ULC004 Ulcerative Colitis 75 0.029
456
P HMC003 Hemochromatosis 75 0.029
457
c PRK057 Parkinson Disease, Late-Onset 73 0.029
458
P SCL016 Scleroderma 69 0.029
459
P CLC005 Celiac Disease 69 0.029
460
P BRD002 Bardet-Biedl Syndrome 68 0.029
461
P FML161 Familial Mediterranean Fever, Ar 67 0.029
462
P STH001 Saethre-Chotzen Syndrome 65 0.029
463
CMM004 Common Variable Immunodeficiency 64 0.029
464
c LKM062 Leukemia, Acute Lymphoblastic 63 0.029
465
APR006 Apert Syndrome 63 0.029
466
P WLF004 Wolfram Syndrome 62 0.029
467
WRN001 Werner Syndrome 61 0.029
468
P LYM007 Lymphangioleiomyomatosis 61 0.029
469
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 0.029
470
LDD001 Ladd Syndrome 60 0.029
471
c BRD010 Bardet-Biedl Syndrome 1 59 0.029
472
P AGM001 Agammaglobulinemia 59 0.029
473
LVR012 Liver Cirrhosis 59 0.029
474
CYS010 Cystinosis 59 0.029
475
P MYL006 Myeloid Leukemia 59 0.029
476
ALC007 Alcohol Dependence 59 0.029
477
GST092 Gastroesophageal Reflux 58 0.029
478
P BCK002 Beckwith-Wiedemann Syndrome 58 0.029
479
BLD087 Bladder Cancer, Somatic 58 0.029
480
P DRM010 Dermatomyositis 57 0.029
481
P ATP001 Atopic Dermatitis 57 0.029
482
P PNM007 Pneumonia 56 0.029
483
c SYS004 Systemic Mastocytosis 56 0.029
484
P PRM006 Primary Biliary Cirrhosis 56 0.029
485
BLL006 Bullous Pemphigoid 55 0.029
486
BRC012 Brucellosis 55 0.029
487
SCH014 Schistosomiasis 55 0.029
488
SMT008 Smith-Magenis Syndrome 54 0.029
489
FCT006 Factor V Deficiency 54 0.029
490
P HYD006 Hydrocephalus 54 0.029
491
c HRD002 Hereditary Angioedema 54 0.029
492
P LDD002 Liddle Syndrome 54 0.029
493
DRM006 Dermatitis 54 0.029
494
P CRD011 Cardiomyopathy 53 0.029
495
DMN002 Dementia 53 0.029
496
PLM033 Pulmonary Embolism 53 0.029
497
CHR020 Chronic Interstitial Cystitis 53 0.029
498
P HYP086 Hypothyroidism 52 0.029
499
c ACT210 Acute Respiratory Distress Syndrome 52 0.029
500
ASP005 Asphyxiating Thoracic Dystrophy 52 0.029
501
APH001 Aphthous Stomatitis 52 0.029
502
P HYP004 Hypercalcemia 52 0.029
503
FCS012 Facioscapulohumeral Muscular Dystrophy 1 51 0.029
504
HST011 Histoplasmosis 51 0.029
505
MLL005 Miller-Dieker Syndrome 50 0.029
506
PLS006 Plasmodium Vivax Malaria 50 0.029
507
P THR014 Thrombocytopenia 50 0.029
508
PTY003 Pityriasis Rubra Pilaris 50 0.029
509
c VRL010 Viral Hepatitis 49 0.029
510
P SNS014 Sinusitis 49 0.029
511
MCR088 Microscopic Polyangiitis 49 0.029
512
P GST044 Gastritis 49 0.029
513
ATX019 Ataxia with Vitamin E Deficiency 49 0.029
514
GLC003 Glucose Intolerance 49 0.029
515
FTT001 Fatty Liver Disease 49 0.029
516
KRT002 Keratomalacia 49 0.029
517
P GLY013 Glycogen Storage Disease 49 0.029
518
c HPT015 Hepatitis D 48 0.029
519
INT002 Intermittent Claudication 48 0.029
520
P CTR002 Cataract 48 0.029
521
P MST009 Mastocytosis 48 0.029
522
GNG013 Gingivitis 47 0.029
523
MGL001 Megaloblastic Anemia 47 0.029
524
THR100 Thrombocytopenic Purpura, Autoimmune 47 0.029
525
ALP008 Alopecia 47 0.029
526
P ANP001 Anaplastic Large Cell Lymphoma 47 0.029
527
P TYR004 Tyrosinemia 47 0.029
528
P RNL028 Renal Tubular Dysgenesis 47 0.029
529
SND002 Sneddon Syndrome 47 0.029
530
P SLD010 Sialidosis, Type I 46 0.029
531
OBS061 Obstructive Sleep Apnea 46 0.029
532
P DBT005 Diabetes Insipidus 46 0.029
533
P ANG015 Angioedema 46 0.029
534
CND002 Conduct Disorder 45 0.029
535
P PLY041 Polymyositis 45 0.029
536
GST045 Gastroenteritis 45 0.029
537
PRG009 Progressive Multifocal Leukoencephalopathy 45 0.029
538
P LKD001 Leukodystrophy 45 0.029
539
P VNS003 Venous Insufficiency 44 0.029
540
PRL019 Prolidase Deficiency 44 0.029
541
PRN011 Pernicious Anemia 44 0.029
542
PLY013 Polymyalgia Rheumatica 44 0.029
543
P ACT135 Acute Graft Versus Host Disease 44 0.029
544
c CCK005 Cockayne Syndrome, Type a 43 0.029
545
BRN106 Burns 43 0.029
546
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 43 0.029
547
SCH002 Schnitzler Syndrome 43 0.029
548
P CST005 Castleman Disease 43 0.029
549
P TRM003 Tremor 43 0.029
550
ANK001 Ankylosis 43 0.029
551
RTC005 Reticulosarcoma 42 0.029
552
FBR032 Fibromuscular Dysplasia 42 0.029
553
PST062 Pustulosis Palmaris Et Plantaris 42 0.029
554
c HPT007 Hepatitis E 42 0.029
555
WLC001 Wolcott-Rallison Syndrome 42 0.029
556
DWR001 Dwarfism 42 0.029
557
C3D001 C3 Deficiency 42 0.029
558
P PLM006 Pulmonary Alveolar Proteinosis 41 0.029
559
c NPH048 Nephronophthisis 1, Juvenile 41 0.029
560
FRN012 Frontometaphyseal Dysplasia 41 0.029
561
HMG005 Hemoglobinopathy 40 0.029
562
HMS001 Hemosiderosis 40 0.029
563
FSC004 Fasciitis 40 0.029
564
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 40 0.029
565
P PSD003 Pseudohypoaldosteronism 40 0.029
566
FLL008 Folliculitis 40 0.029
567
c CNT016 Central Retinal Vein Occlusion 40 0.029
568
LYM012 Lymphoplasmacytic Lymphoma 40 0.029
569
MNN009 Meningoencephalitis 40 0.029
570
JBR006 Joubert Syndrome with Oculorenal Anomalies 40 0.029
571
DDN006 Duodenitis 40 0.029
572
BCT015 Bacteremia 40 0.029
573
BNF002 Bone Fracture 39 0.029
574
ART004 Aortic Atherosclerosis 39 0.029
575
c ATM024 Autoimmune Pancreatitis 39 0.029
576
P EHL015 Ehlers-Danlos Syndrome Progeroid Type 39 0.029
577
MCL027 Macular Dystrophy, Dominant Cystoid 39 0.029
578
c CNG027 Congenital Hemolytic Anemia 39 0.029
579
RNL011 Renal Osteodystrophy 39 0.029
580
CRY021 Cryoglobulinemic Vasculitis 38 0.029
581
P HYP599 Hypoparathyroidism, Familial Isolated 38 0.029
582
URT010 Ureteral Obstruction 38 0.029
583
IMN002 Iminoglycinuria, Digenic 38 0.029
584
CLL002 Collecting Duct Carcinoma 38 0.029
585
c ACT042 Acute Pyelonephritis 38 0.029
586
PLY020 Polyradiculoneuropathy 38 0.029
587
PLS025 Plasmablastic Lymphoma 38 0.029
588
CNV002 Conversion Disorder 37 0.029
589
DBT006 Diabetic Macular Edema 37 0.029
590
P DMY001 Demyelinating Polyneuropathy 36 0.029
591
EPS006 Epstein Syndrome 36 0.029
592
RNL012 Renal Tuberculosis 36 0.029
593
c CNG033 Congenital Syphilis 35 0.029
594
PRT030 Parathyroid Gland Disease 35 0.029
595
PTT009 Pituitary Gland Disease 34 0.029
596
MCL006 Macular Retinal Edema 34 0.029
597
HRT007 Heart Cancer 34 0.029
598
CRT008 Carotid Artery Dissection 34 0.029
599
HMN032 Human Herpesvirus 8 34 0.029
600
SPL018 Splenomegaly 34 0.029
601
SKN023 Skin Tag 33 0.029
602
TBL013 Tubulointerstitial Nephritis and Uveitis 33 0.029
603
ANG046 Angioimmunoblastic T-Cell Lymphoma 33 0.029
604
CHY006 Chylous Ascites 33 0.029
605
P CRB059 Cerebellar Degeneration 32 0.029
606
CLS016 Clostridium Difficile Colitis 32 0.029
607
c HYP248 Hyperprolinemia, Type I 32 0.029
608
c AML044 Amelogenesis Imperfecta, Type Ig 31 0.029
609
c NPH055 Nephrotic Syndrome, Type 1 31 0.029
610
C4B001 C4b Deficiency 30 0.029
611
P ATM020 Autoimmune Enteropathy 30 0.029
612
ADR009 Adrenal Cortex Disease 30 0.029
613
IGG007 Igg4-Related Disease 30 0.029
614
P HYP111 Hyperprolinemia 30 0.029
615
BLD039 Bladder Adenocarcinoma 29 0.029
616
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 29 0.029
617
CRB001 Cerebral Lymphoma 29 0.029
618
c PSR017 Psoriasis 2 28 0.029
619
P PSR004 Psoriasis Susceptibility 1 28 0.029
620
c HYP073 Hypersensitivity Reaction Type Iv Disease 28 0.029
621
P SCK034 Sickle Beta Thalassemia 28 0.029
622
ORT001 Orthostatic Proteinuria 28 0.029
623
C4D002 C4a Deficiency 27 0.029
624
ACT003 Acute Kidney Tubular Necrosis 27 0.029
625
JBR007 Joubert Syndrome with Renal Anomalies 27 0.029
626
KDN013 Kidney Hypertrophy 26 0.029
627
ART010 Arteriolosclerosis 26 0.029
628
c AML006 Amelogenesis Imperfecta Hypoplastic Type, Ig 26 0.029
629
RNL021 Renal Tubular Transport Disease 25 0.029
630
c HYD047 Hydrocephalus, Nonsyndromic, Autosomal Recessive 25 0.029
631
c HYD043 Hydrocephalus, Nonsyndromic, Autosomal Recessive 2 25 0.029
632
c MDL008 Medullary Cystic Kidney Disease 1 25 0.029
633
HNS001 Hansen's Disease 25 0.029
634
c PSR019 Psoriasis Susceptibility 13 23 0.029
635
P GLM015 Glomerulopathy with Fibronectin Deposits 2 23 0.029
636
c NPH047 Nephrotic Syndrome, Type 4 22 0.029
637
c GLM029 Glomerulosclerosis, Focal Segmental, 1 22 0.029
638
ANT030 Antecubital Pterygium 22 0.029
639
VSC008 Vascular Hemostatic Disease 22 0.029
640
GLB003 Globe Disease 22 0.029
641
P HRT017 Heart Tumor 21 0.029
642
CHR476 Chronic Angina 21 0.029
643
c NPH070 Nephrotic Syndrome, Type 6 21 0.029
644
PSR005 Psoriasis, Protection Against 21 0.029
645
CRB157 Cerebroretinal Vasculopathy 19 0.029
646
ATM018 Autoimmune Disease of Urogenital Tract 19 0.029
647
PLL005 Pallister-Killian Mosaic Syndrome 18 0.029
648
FBR085 Fibrillary Glomerulonephritis 18 0.029
649
c ERC007 Ercc8-Related Cockayne Syndrome 18 0.029
650
TRT006 Torticollis Keloids Cryptorchidism Renal Dysplasia 18 0.029
651
c SYS046 Systemic Lupus Erythematosus 3 17 0.029
652
EXD002 Exudative Glomerulonephritis 17 0.029
653
HRD064 Hereditary Vascular Retinopathy 15 0.029
654
SNG003 Single Ventricular Heart 14 0.029
655
DFN014 Deafness Nephritis Anorectal Malformation 13 0.029
656
IND008 Indomethacin Embryofetopathy 13 0.029
657
c DBT054 Diabetes Mellitus, Insulin-Dependent, 24 9 0.029
658
c DBT059 Diabetes Mellitus, Insulin-Dependent, 8 9 0.029
659
c CRN176 Coronary Heart Disease 9 9 0.029
660
c ADL079 Adult Heart Tumor 7 0.029
661
CMP052 Complication in Hemodialysis 6 0.029
662
GLC077 Glucocorticoid Therapy, Response to 6 0.029
663
c SYS054 Systemic Lupus Erythematosus with Nephritis 3 5 0.029
664
c SYS056 Systemic Lupus Erythematosus with Nephritis 1 5 0.029
665
CMP062 Complication After Organ Transplantation 4 0.029
666
PRT056 Protein R Deficiency 4 0.029
667
P BRS047 Breast Cancer 100 0.020
668
P LNG032 Lung Cancer 91 0.020
669
CYS001 Cystic Fibrosis 90 0.020
670
P SCH015 Schizophrenia 79 0.020
671
P RTN008 Retinitis Pigmentosa 75 0.020
672
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 75 0.020
673
HDG012 Hodgkin Lymphoma 75 0.020
674
P OST002 Osteoporosis 75 0.020
675
c MCL042 Macular Degeneration, Age-Related, 1 74 0.020
676
c LKM061 Leukemia, Acute Myeloid 74 0.020
677
c DLT002 Dilated Cardiomyopathy 73 0.020
678
PHN003 Phenylketonuria 73 0.020
679
P PFF001 Pfeiffer Syndrome 71 0.020
680
c FNC027 Fanconi Anemia, Complementation Group a 71 0.020
681
MYL009 Myelodysplastic Syndrome 69 0.020
682
P LGH007 Leigh Syndrome 67 0.020
683
END057 Endometrial Cancer 67 0.020
684
GLL008 Gilles De La Tourette Syndrome 67 0.020
685
P FRG001 Fragile X Syndrome 66 0.020
686
ATT013 Attention Deficit-Hyperactivity Disorder 66 0.020
687
c HMP004 Hemophilia B 65 0.020
688
P ATM006 Autoimmune Lymphoproliferative Syndrome 65 0.020
689
P RNL101 Renal Cell Carcinoma, Papillary 65 0.020
690
P CRD013 Cardiofaciocutaneous Syndrome 65 0.020
691
GLN010 Glanzmann Thrombasthenia 65 0.020
692
c HMP029 Hemophilia a 64 0.020
693
P GCH001 Gaucher's Disease 64 0.020
694
CST001 Costello Syndrome 64 0.020
695
P MYL005 Myelofibrosis 64 0.020
696
c JVN010 Juvenile Rheumatoid Arthritis 64 0.020
697
P STM004 Stomach Cancer 63 0.020
698
VNW001 Von Willebrand's Disease 63 0.020
699
c MLT136 Multiple Endocrine Neoplasia 1 62 0.020
700
ATS001 Autistic Disorder 62 0.020
701
DWN001 Down Syndrome 62 0.020
702
c SYS005 Systemic Scleroderma 62 0.020
703
P PRD006 Prader-Willi Syndrome 62 0.020
704
MLD001 Melioidosis 61 0.020
705
P FRD001 Friedreich Ataxia 61 0.020
706
P ALX003 Alexander Disease 61 0.020
707
CHD001 Chediak-Higashi Syndrome 61 0.020
708
CRV047 Cervical Cancer, Somatic 61 0.020
709
ACR007 Acromegaly 61 0.020
710
SKN016 Skin Disease 61 0.020
711
PLL001 Pallister-Hall Syndrome 60 0.020
712
c SRC025 Sarcoidosis 1 60 0.020
713
TNG009 Tongue Squamous Cell Carcinoma 60 0.020
714
WGN006 Wegener Granulomatosis 59 0.020
715
BRN028 Brain Cancer 59 0.020
716
TYP007 Typhoid Fever 59 0.020
717
WLL001 Williams-Beuren Syndrome 59 0.020
718
OMN001 Omenn Syndrome 59 0.020
719
PYR013 Pyruvate Kinase Deficiency 59 0.020
720
LKN001 Leukoencephalopathy with Vanishing White Matter 59 0.020
721
FCL009 Focal Dermal Hypoplasia 58 0.020
722
CNG368 Congenital Adrenal Hyperplasia 58 0.020
723
LSH001 Leishmaniasis 58 0.020
724
MSM014 Mismatch Repair Cancer Syndrome 58 0.020
725
PRC002 Paracoccidioidomycosis 57 0.020
726
P LYM026 Lymphoblastic Leukemia 57 0.020
727
TWN003 Townes-Brocks Syndrome 57 0.020
728
OTT002 Otitis Media 57 0.020
729
BLS001 Blau Syndrome 57 0.020
730
P RTH001 Rothmund-Thomson Syndrome 57 0.020
731
c CNG006 Congenital Hypothyroidism 57 0.020
732
OVR029 Ovarian Hyperstimulation Syndrome 57 0.020
733
TKY001 Takayasu's Arteritis 57 0.020
734
c ESS001 Essential Tremor 57 0.020
735
P BCL006 B-Cell Lymphomas 57 0.020
736
MBS002 Moebius Syndrome 57 0.020
737
P ASP006 Aspergillosis 56 0.020
738
KND001 Kindler Syndrome 56 0.020
739
LWS003 Lowe Syndrome 56 0.020
740
LYS003 Lysinuric Protein Intolerance 56 0.020
741
OVR078 Ovarian Cancer, Somatic 56 0.020
742
c GCH015 Gaucher Disease, Type I 56 0.020
743
IMG001 Image Syndrome 56 0.020
744
DBT088 Diabetes Insipidus, Nephrogenic 56 0.020
745
CTN007 Cutaneous Leishmaniasis 55 0.020
746
ART016 Aortic Aneurysm 55 0.020
747
DNG002 Dengue Hemorrhagic Fever 55 0.020
748
LPT001 Leptospirosis 55 0.020
749
P ATR011 Atrial Fibrillation 55 0.020
750
c MCL062 Mucolipidosis Ii Alpha/beta 55 0.020
751
PSY004 Psychotic Disorder 55 0.020
752
P PTT014 Pitt-Hopkins Syndrome 55 0.020
753
P ORT004 Orthostatic Intolerance 55 0.020
754
ALP007 Alpha 1-Antitrypsin Deficiency 55 0.020
755
WST001 West Syndrome 54 0.020
756
CRB037 Cerebral Palsy 54 0.020
757
P TXP001 Toxoplasmosis 54 0.020
758
HRP004 Herpes Zoster 54 0.020
759
GLL022 Guillain-Barre Syndrome 54 0.020
760
P FND001 Fundus Albipunctatus 54 0.020
761
MLN008 Melanoma 54 0.020
762
PNC041 Pancreatic Ductal Adenocarcinoma 53 0.020
763
CNT047 Contact Dermatitis 53 0.020
764
HMT002 Hematologic Cancer 53 0.020
765
GRY002 Gray Platelet Syndrome 53 0.020
766
DHY002 Dihydropyrimidine Dehydrogenase Deficiency 53 0.020
767
ADL030 Adult-Onset Still's Disease 53 0.020
768
QFV001 Q Fever 53 0.020
769
KLP010 Klippel-Trenaunay-Weber Syndrome 53 0.020
770
P LPR002 Leopard Syndrome 53 0.020
771
MLK003 Melkersson-Rosenthal Syndrome 53 0.020
772
ALC006 Alcoholic Hepatitis 53 0.020
773
RBS003 Rabson-Mendenhall Syndrome 53 0.020
774
CCH002 Coach Syndrome 53 0.020
775
LKM066 Leukemia, Acute Myelomonocytic, Somatic, Somatic 53 0.020
776
P TMP003 Temporal Arteritis 53 0.020
777
P MLS001 Melas Syndrome 53 0.020
778
IRR002 Irritable Bowel Syndrome 53 0.020
779
PLS007 Plasmodium Falciparum Malaria 52 0.020
780
P HRD011 Hereditary Spherocytosis 52 0.020
781
PLM031 Poliomyelitis 52 0.020
782
CHR029 Choroid Plexus Papilloma 52 0.020
783
P INF032 Infertility 52 0.020
784
ETN001 Eating Disorder 52 0.020
785
CHR063 Chronic Mucocutaneous Candidiasis 52 0.020
786
CLF027 Cleft Palate, Isolated 52 0.020
787
c SVR001 Severe Acute Respiratory Syndrome 52 0.020
788
P ANR007 Anorexia Nervosa 52 0.020
789
APP008 Appendicitis 52 0.020
790
HSH003 Hashimoto Thyroiditis 51 0.020
791
SCH063 Schimmelpenning-Feuerstein-Mims Syndrome, Somatic Mosaic 51 0.020
792
SCR002 Scurvy 51 0.020
793
P HMP007 Hemophilia 51 0.020
794
ECH003 Echinococcosis 51 0.020
795
c PRC016 Pre-Eclampsia 51 0.020
796
LST001 Listeriosis 51 0.020
797
ICH002 Ichthyosis Bullosa of Siemens 51 0.020
798
P ESP024 Esophagitis 51 0.020
799
TRP002 Tropical Spastic Paraparesis 51 0.020
800
PLM129 Pulmonary Disease, Chronic Obstructive 51 0.020
801
P HST010 Histiocytosis 51 0.020
802
P FTL001 Fetal Alcohol Syndrome 50 0.020
803
THL016 Thalassemias, Alpha- 50 0.020
804
ALL010 Allergic Contact Dermatitis 50 0.020
805
STR008 Strongyloidiasis 50 0.020
806
P RBL001 Rubella 50 0.020
807
P CNJ013 Conjunctivitis 50 0.020
808
HPY002 H. Pylori Infection 50 0.020
809
HYD012 Hydrops Fetalis 50 0.020
810
P ABD003 Abdominal Aortic Aneurysm 50 0.020
811
URT039 Urticaria 50 0.020
812
SPT005 Spotted Fever 49 0.020
813
KRT001 Keratoconjunctivitis Sicca 49 0.020
814
BRN012 Bronchiolitis Obliterans 49 0.020
815
c ACT073 Acute Leukemia 49 0.020
816
ACT049 Acute Disseminated Encephalomyelitis 49 0.020
817
P MTC069 Mitochondrial Disorders 49 0.020
818
P MMP001 Mumps 49 0.020
819
NTR040 Neutropenia, Cyclic 49 0.020
820
TXC005 Toxic Shock Syndrome 49 0.020
821
MGR028 Migraine with or Without Aura 1 49 0.020
822
THR004 Thrombocytosis 48 0.020
823
VGT001 Vogt-Koyanagi-Harada Disease 48 0.020
824
GLC012 Galactosialidosis 48 0.020
825
P ENC004 Encephalitis 48 0.020
826
ERD001 Erdheim-Chester Disease 48 0.020
827
P LNG064 Lung Cancer Susceptibility 3 48 0.020
828
P BRT004 Bartter Disease 48 0.020
829
CHL028 Childhood Type Dermatomyositis 48 0.020
830
P FNG005 Feingold Syndrome 48 0.020
831
CRM001 Crimean-Congo Hemorrhagic Fever 48 0.020
832
PHR003 Pharyngitis 48 0.020
833
CRV038 Cervical Squamous Cell Carcinoma 48 0.020
834
BRN002 Bronchiolitis 48 0.020
835
SZR001 Sezary's Disease 48 0.020
836
BLS002 Blastomycosis 48 0.020
837
c GLY019 Glycogen Storage Disease Iiia 48 0.020
838
P LYM025 Lymphedema 48 0.020
839
P HML033 Hemolytic Uremic Syndrome, Atypical 1 48 0.020
840
KRT006 Keratoconjunctivitis 48 0.020
841
GST060 Gastric Cancer, Somatic 48 0.020
842
SLC006 Silicosis 47 0.020
843
BRN004 Brain Edema 47 0.020
844
c VRL007 Viral Encephalitis 47 0.020
845
LYM019 Lymphosarcoma 47 0.020
846
PRM042 Primary Effusion Lymphoma 47 0.020
847
GDP001 Goodpasture Syndrome 47 0.020
848
SPT004 Septic Arthritis 47 0.020
849
P PRC031 Preeclampsia/eclampsia 1 47 0.020
850
c ACT027 Acute Pancreatitis 47 0.020
851
FCT022 Factor Xi Deficiency, Autosomal Recessive 47 0.020
852
PRN038 Prune Belly Syndrome 47 0.020
853
FDL002 Food Allergy 47 0.020
854
BLD044 Bladder Disease 47 0.020
855
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.020
856
LPR001 Lepromatous Leprosy 47 0.020
857
RNL024 Renal Glucosuria 47 0.020
858
TTH006 Tooth Disease 47 0.020
859
PLV003 Pelvic Inflammatory Disease 47 0.020
860
VSC002 Vascular Dementia 47 0.020
861
ALL006 Allergic Asthma 46 0.020
862
ALL009 Allergic Conjunctivitis 46 0.020
863
SCR008 Scrub Typhus 46 0.020
864
P LTR001 Lateral Sclerosis 46 0.020
865
PSD007 Pseudomyxoma Peritonei 46 0.020
866
RST001 Restless Legs Syndrome 46 0.020
867
ADR005 Adrenal Carcinoma 46 0.020
868
IDP011 Idiopathic Interstitial Pneumonia 46 0.020
869
PRD019 Periodic Fever, Familial 46 0.020
870
ALP014 Alpha-Thalassemia/mental Retardation Syndrome 46 0.020
871
c INF069 Infantile Neuroaxonal Dystrophy 1 46 0.020
872
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 46 0.020
873
FLR002 Filariasis 46 0.020
874
P AGN002 Agnosia 46 0.020
875
PRT014 Protein S Deficiency 46 0.020
876
P HYP065 Hyperaldosteronism 45 0.020
877
TYP011 Typhus 45 0.020
878
OBS006 Obstructive Lung Disease 45 0.020
879
P PRT013 Portal Hypertension 45 0.020
880
P MNC007 Monocytic Leukemia 45 0.020
881
OCL005 Oculocerebrorenal Syndrome 45 0.020
882
PMP001 Pemphigus 45 0.020
883
LRW001 Leri-Weill Dyschondrosteosis 45 0.020
884
P CTN015 Cutaneous T Cell Lymphoma 45 0.020
885
CRD119 Cardiac Arrest 45 0.020
886
STT007 Steatocystoma Multiplex 45 0.020
887
TRY001 Trypanosomiasis 45 0.020
888
P PLM085 Pulmonary Hemosiderosis 44 0.020
889
P FNC044 Fanconi Anemia, Complementation Group C 44 0.020
890
P CNT005 Central Nervous System Lymphoma 44 0.020
891
ING001 Inguinal Hernia 44 0.020
892
P INT068 Intestinal Disease 44 0.020
893
c GMM003 Gamma Heavy Chain Disease 44 0.020
894
CTS003 Coats Disease 44 0.020
895
BLM002 Bulimia Nervosa 44 0.020
896
RTN017 Retinal Detachment 44 0.020
897
SLP001 Sleeping Sickness 44 0.020
898
MLN014 Melnick-Needles Syndrome 44 0.020
899
CLN003 Clonorchiasis 44 0.020
900
CRT049 Critical Limb Ischemia 44 0.020
901
CNS004 Constipation 44 0.020
902
HMR039 Hemorrhage, Intracerebral 44 0.020
903
c CNG411 Congenital Disorder of Glycosylation, Type in 44 0.020
904
ASP003 Aseptic Meningitis 44 0.020
905
VGN023 Vaginitis 44 0.020
906
GST040 Gastric Adenocarcinoma 44 0.020
907
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 44 0.020
908
c HYP163 Hyperlipidemia Type 3 44 0.020
909
P EXP004 Exophthalmos 44 0.020
910
MTR046 Maternally Inherited Diabetes and Deafness 43 0.020
911
NNL002 Nonalcoholic Steatohepatitis 43 0.020
912
BLC001 Blue Cone Monochromacy 43 0.020
913
LPD009 Lipid Storage Disease 43 0.020
914
c PST041 Posterior Urethral Valves 43 0.020
915
SML033 Small Cell Cancer of the Lung, Somatic 43 0.020
916
P GST049 Gastrointestinal System Cancer 43 0.020
917
GST027 Gastric Lymphoma 43 0.020
918
TBR006 Tuberculoid Leprosy 43 0.020
919
LMR001 Lemierre's Syndrome 43 0.020
920
P BRS044 Breast Adenocarcinoma 43 0.020
921
INC001 Incontinentia Pigmenti Achromians 43 0.020
922
ARC002 Arachnoiditis 43 0.020
923
GRN039 Greenberg Skeletal Dysplasia 43 0.020
924
URN003 Urinary Schistosomiasis 43 0.020
925
ANR004 Anuria 43 0.020
926
c CNT075 Central Precocious Puberty 43 0.020
927
CLD007 Cold Agglutinin Disease 43 0.020
928
BRL010 Buruli Ulcer 43 0.020
929
MYH001 May-Hegglin Anomaly 43 0.020
930
P MLT074 Multiple Endocrine Neoplasia 43 0.020
931
c SVR005 Severe Pre-Eclampsia 43 0.020
932
PPL002 Papillary Carcinoma 43 0.020
933
P ATX004 Ataxia 43 0.020
934
PRR002 Pure Red-Cell Aplasia 43 0.020
935
PRN014 Paronychia 43 0.020
936
HMP005 Hemiplegia 43 0.020
937
MCN007 Meconium Aspiration Syndrome 43 0.020
938
ELS001 Eales Disease 43 0.020
939
GNG012 Gingival Overgrowth 43 0.020
940
MLT113 Multicentric Castleman Disease 42 0.020
941
PSD002 Pseudotumor Cerebri 42 0.020
942
FSC002 Fascioliasis 42 0.020
943
PLM070 Pulmonic Stenosis 42 0.020
944
P RTN016 Retinal Degeneration 42 0.020
945
P PSD015 Pseudohypoparathyroidism 42 0.020
946
BRN071 Brain Injury 42 0.020
947
P CRV039 Cervicitis 42 0.020
948
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 42 0.020
949
MRC001 Marchiafava Bignami Disease 42 0.020
950
HDC001 Headache 42 0.020
951
GNT031 Genitopatellar Syndrome 42 0.020
952
RNL078 Renal Dysplasia 42 0.020
953
P SCL009 Sclerosing Cholangitis 42 0.020
954
c VRL012 Viral Meningitis 42 0.020
955
P ENC018 Encephalopathy 42 0.020
956
TLN003 Telangiectasis 41 0.020
957
PRS045 Prostatic Hypertrophy 41 0.020
958
PYM001 Pyomyositis 41 0.020
959
P AFB001 Afibrinogenemia 41 0.020
960
VNW005 Von Willebrand Disease, Type 1 41 0.020
961
RSD004 Rosai-Dorfman Disease 41 0.020
962
INT051 Intussusception 41 0.020
963
ALC009 Alcoholic Liver Cirrhosis 41 0.020
964
CLL003 Cellulitis 41 0.020
965
CNN003 Conn's Syndrome 41 0.020
966
c INF023 Inflammatory Breast Carcinoma 41 0.020
967
PST021 Postpartum Depression 41 0.020
968
EWN002 Ewing's Family of Tumors 41 0.020
969
LYM029 Lymphedema-Distichiasis Syndrome 41 0.020
970
RDC002 Radiculopathy 41 0.020
971
P HYL004 Hyaline Fibromatosis Syndrome 41 0.020
972
ACN001 Acinar Cell Carcinoma 41 0.020
973
HRT012 Heart Valve Disease 40 0.020
974
FRM003 Farmer's Lung 40 0.020
975
APR001 Apraxia 40 0.020
976
OBS001 Obstructive Jaundice 40 0.020
977
P SDR002 Siderosis 40 0.020
978
CHL018 Childhood Medulloblastoma 40 0.020
979
MDL009 Medullary Sponge Kidney 40 0.020
980
DFF036 Differentiated Thyroid Carcinoma 40 0.020
981
CHR005 Chorioamnionitis 40 0.020
982
SHR075 Short-Rib Thoracic Dysplasia 9 with or Without Polydactyly 40 0.020
983
STM007 Stomatitis 40 0.020
984
DBT062 Diabetic Foot Ulcers 40 0.020
985
CRD137 Cardiogenic Shock 39 0.020
986
HPT009 Hepatopulmonary Syndrome 39 0.020
987
MNT002 Mental Depression 39 0.020
988
TBR008 Tuberculous Peritonitis 39 0.020
989
ARC007 Arachnoid Cysts 39 0.020
990
ACT017 Acute Chest Syndrome 39 0.020
991
CRD001 Cardiac Tamponade 39 0.020
992
c SML016 Small Intestine Cancer 39 0.020
993
MLT006 Multidrug-Resistant Tuberculosis 39 0.020
994
PRT082 Preterm Premature Rupture of the Membranes 39 0.020
995
P CHL066 Cholangitis 39 0.020
996
FCT005 Factor Xiii Deficiency 39 0.020
997
PLY012 Polyhydramnios 39 0.020
998
HYP017 Hypophosphatemia 39 0.020
999
EPD053 Epidermal Nevus, Somatic 39 0.020
1000
CRP017 Carpal Tunnel Syndrome, Familial 39 0.020
1001
NCR007 Necrotizing Fasciitis 39 0.020
1002
HYP005 Hypokalemia 39 0.020
1003
PSD009 Pseudohermaphroditism 39 0.020
1004
c EPD044 Epidermolysis Bullosa Dystrophica, Ar 39 0.020
1005
P HRD018 Hair Disease 39 0.020
1006
GGR001 Geographic Tongue 38 0.020
1007
ESN002 Eosinophilia-Myalgia Syndrome 38 0.020
1008
ESN011 Eisenmenger Syndrome 38 0.020
1009
PTY001 Pityriasis Rosea 38 0.020
1010
KMR001 Kimura Disease 38 0.020
1011
c INT064 Intermediate Uveitis 38 0.020
1012
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 38 0.020
1013
ONC003 Oncogenic Osteomalacia 38 0.020
1014
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 38 0.020
1015
EXT033 Extrapulmonary Tuberculosis 38 0.020
1016
DST006 Diastolic Heart Failure 38 0.020
1017
HND002 Hand, Foot and Mouth Disease 38 0.020
1018
PRN021 Paranasal Sinus Disease 38 0.020
1019
NSP002 Nasopharyngitis 38 0.020
1020
P RTN014 Retinal Artery Occlusion 38 0.020
1021
c EYC002 Eye Carcinoma 38 0.020
1022
c SBC007 Subacute Thyroiditis 38 0.020
1023
PNC034 Pancreas Disease 38 0.020
1024
RTN021 Retinal Vascular Occlusion 38 0.020
1025
BRD025 Birdshot Chorioretinopathy 38 0.020
1026
NCR001 Necrotizing Ulcerative Gingivitis 38 0.020
1027
HRM002 Hermaphroditism 37 0.020
1028
LCN001 Lice Infestation 37 0.020
1029
RTN015 Retinal Cancer 37 0.020
1030
CLC001 Calciphylaxis 37 0.020
1031
c ACQ014 Acquired Hemophilia 37 0.020
1032
P MRC003 Mercury Poisoning 37 0.020
1033
GLC011 Galactose Epimerase Deficiency 37 0.020
1034
PMP004 Pemphigus Foliaceus 37 0.020
1035
P EST001 Estrogen-Receptor Positive Breast Cancer 37 0.020
1036
c PRG011 Progressive Myoclonus Epilepsy 37 0.020
1037
INT054 Intraocular Lymphoma 37 0.020
1038
FML038 Female Reproductive Organ Cancer 37 0.020
1039
BRN080 Brain Ischemia 37 0.020
1040
c CHR037 Chronic Eosinophilic Pneumonia 37 0.020
1041
SPL012 Splenic Disease 37 0.020
1042
BRB001 Beriberi 37 0.020
1043
P LRG017 Large Intestine Cancer 37 0.020
1044
MLN054 Melanocytic Nevus Syndrome, Congenital, Somatic 37 0.020
1045
CNG116 Congenital Nephrotic Syndrome Finnish Type 37 0.020
1046
SYS003 Systolic Heart Failure 37 0.020
1047
c SVR056 Severe Hemophilia a