Search results for "fibrosis"

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

2476 hits were found for 'fibrosis'

# Family MCID Name MIFTS Score
1
CYS001 Cystic Fibrosis 87 7.465
2
PLM134 Pulmonary Fibrosis, Idiopathic 61 6.158
3
P CNG047 Congenital Fibrosis of the Extraocular Muscles 37 5.057
4
P PLM036 Pulmonary Fibrosis 69 5.013
5
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 4.977
6
ORL004 Oral Submucous Fibrosis 52 4.892
7
END021 Endomyocardial Fibrosis 47 4.001
8
CNG048 Congenital Hepatic Fibrosis 47 3.828
9
CCH002 Coach Syndrome 53 3.756
10
RTR011 Retroperitoneal Fibrosis 40 3.558
11
c FBR050 Fibrosis of Extraocular Muscles, Congenital, 2 22 3.515
12
c FBR049 Fibrosis of Extraocular Muscles, Congenital, 3a 33 3.504
13
RNL077 Renal Fibrosis 48 3.069
14
PKL002 Poikiloderma, Hereditary Fibrosing, with Tendon Contractures, Myopathy, and Pulmonary Fibrosis 20 2.967
15
c FBR081 Fibrosis of Extraocular Muscles, Congenital, 3c 16 2.967
16
IDP011 Idiopathic Interstitial Pneumonia 57 2.938
17
FBR028 Fibrosing Mediastinitis 24 2.933
18
NPH018 Nephrogenic Systemic Fibrosis 51 2.812
19
DFF002 Diffuse Pulmonary Fibrosis 32 2.792
20
EF001 Eaf 23 2.630
21
PLM139 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 1 30 2.335
22
CYS040 Cystic Fibrosis with Helicobacter Pylori Gastritis, Megaloblastic Anemia, and Mental Retardation 20 2.316
23
PLM141 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 4 19 2.316
24
TKL001 Tukel Syndrome 18 2.302
25
LBN005 Lubani-Al Saleh-Teebi Syndrome 6 2.286
26
PST015 Postinflammatory Pulmonary Fibrosis 11 2.286
27
c PLM044 Pulmonary Fibrosis, Familial 28 1.994
28
ACT029 Acute Interstitial Pneumonia 43 1.980
29
P APL001 Aplastic Anemia 74 1.916
30
IGG007 Igg4-Related Disease 39 1.912
31
c LCL003 Localized Pulmonary Fibrosis 12 1.908
32
PLM143 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 3 15 1.904
33
HRM018 Hermansky-Pudlak Syndrome with Pulmonary Fibrosis 21 1.904
34
PRR004 Preretinal Fibrosis 27 1.899
35
c FBR078 Fibrosis of Extraocular Muscles, Congenital, 5 17 1.889
36
HRM016 Hermansky-Pudlak Syndrome Without Pulmonary Fibrosis 20 1.889
37
BRN075 Bronchiectasis with or Without Elevated Sweat Chloride 2 19 1.884
38
FBR089 Fibrosclerosis, Multifocal 16 1.878
39
IMM129 Immunodeficiency, Ovarian Dysgenesis, and Pulmonary Fibrosis 14 1.878
40
MSC030 Muscular Fibrosis Multifocal Obstructed Vessels 10 1.878
41
FBR086 Fibrolamellar Carcinoma 41 1.855
42
ASB001 Asbestosis 42 1.431
43
TRP020 Tropical Endomyocardial Fibrosis 31 1.423
44
SLC006 Silicosis 53 1.412
45
P MYL005 Myelofibrosis 67 1.388
46
ARW003 Airway-Centered Interstitial Fibrosis 7 1.372
47
FML074 Familial Interstitial Fibrosis 6 1.372
48
IDP016 Idiopathic Diffuse Interstitial Fibrosis 6 1.367
49
c CNG189 Congenital Disorder of Glycosylation, Type Ib 34 1.352
50
BRN077 Bronchiectasis with or Without Elevated Sweat Chloride 3 18 1.346
51
BRN076 Bronchiectasis with or Without Elevated Sweat Chloride 1 27 1.346
52
CRB163 Cerebellar Vermis Aplasia with Associated Features Suggesting Smith-Lemli-Opitz Syndrome and Meckel Syndrome 16 1.340
53
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 5 1.340
54
HPT029 Hepatic Fibrosis Renal Cysts Mental Retardation 3 1.340
55
c NTR031 Neutropenia, Severe Congenital, 5, Autosomal Recessive 28 1.332
56
CMP074 Camptodactyly, Myopia, and Fibrosis of the Medial Rectus Muscle of Eye 15 1.332
57
RZN001 Rozin Hertz Goodman Syndrome 6 1.332
58
FLL047 Follicular Hamartoma-Alopecia-Cystic Fibrosis Syndrome 3 1.332
59
c CNG140 Congenital Fibrosis of the Extraocular Muscles 1a 7 1.332
60
c CNG141 Congenital Fibrosis of the Extraocular Muscles 1b 7 1.332
61
PLM145 Pulmonary Fibrosis-Hepatic Hyperplasia-Bone Marrow Hypoplasia Syndrome 6 1.332
62
c KF2001 Kif21a-Related Congenital Fibrosis of the Extraocular Muscles 7 1.332
63
c PHX001 Phox2a-Related Congenital Fibrosis of the Extraocular Muscles 7 1.332
64
c SFT006 Sftpc-Related Familial Pulmonary Fibrosis 4 1.332
65
c TBB003 Tubb3-Related Congenital Fibrosis of the Extraocular Muscles 7 1.332
66
c TRC066 Terc-Related Familial Pulmonary Fibrosis 4 1.332
67
c TRT009 Tert-Related Familial Pulmonary Fibrosis 4 1.332
68
DBT022 Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism 20 1.323
69
FBR016 Fibrosclerosis of Breast 23 1.323
70
SNR014 Senior-Boichis Syndrome 10 1.323
71
TYL001 Taylor's Syndrome 28 1.312
72
PLM113 Palmoplantar Keratoderma-Sclerodactyly Syndrome 8 1.312
73
SCR009 Scirrhous Adenocarcinoma 14 1.312
74
GRP001 Graphite Pneumoconiosis 10 1.312
75
P HPT021 Hepatitis 74 0.441
76
c PNC106 Pancreatic Agenesis 1 31 0.342
77
PNC034 Pancreas Disease 56 0.341
78
LNG099 Lung Disease 63 0.286
79
c HPT001 Hepatitis C 68 0.251
80
P PNM007 Pneumonia 67 0.243
81
P LVR013 Liver Disease 76 0.240
82
P PNC044 Pancreatitis 62 0.207
83
INT066 Interstitial Lung Disease 60 0.203
84
BRN022 Bronchiectasis 55 0.199
85
RSP006 Respiratory System Disease 61 0.186
86
URT010 Ureteral Obstruction 45 0.167
87
c HPT016 Hepatitis B 61 0.161
88
P ASP006 Aspergillosis 61 0.159
89
LVR012 Liver Cirrhosis 71 0.158
90
c HPT073 Hepatitis C Virus 72 0.156
91
P ALL008 Allergic Bronchopulmonary Aspergillosis 50 0.154
92
c VRL010 Viral Hepatitis 60 0.149
93
FTT001 Fatty Liver Disease 60 0.143
94
P CRD011 Cardiomyopathy 66 0.141
95
P KDN018 Kidney Disease 64 0.138
96
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.132
97
NNL002 Nonalcoholic Steatohepatitis 49 0.131
98
c HPT003 Hepatitis a 55 0.130
99
P PLM037 Pulmonary Hypertension 78 0.124
100
P RSP003 Respiratory Failure 68 0.123
101
MCN017 Meconium Ileus 53 0.123
102
PRM025 Primary Bacterial Infectious Disease 42 0.121
103
NSD001 Nose Disease 51 0.117
104
NTR005 Nutritional Deficiency Disease 51 0.112
105
BRN038 Bronchial Disease 54 0.112
106
P HRT032 Heart Disease 64 0.112
107
P AST005 Asthma 80 0.109
108
EXC002 Exocrine Pancreatic Insufficiency 41 0.109
109
P PRT013 Portal Hypertension 61 0.105
110
END072 Endotheliitis 41 0.104
111
HPT023 Hepatocellular Carcinoma 90 0.101
112
P NNT009 Neonatal Diabetes Mellitus 50 0.101
113
P SPS003 Spastic Diplegia 49 0.099
114
CNN005 Connective Tissue Disease 60 0.096
115
c CNG401 Congenital Heart Disease 67 0.094
116
P CHL066 Cholangitis 48 0.094
117
SCH014 Schistosomiasis 59 0.092
118
P HYP061 Hypertrophic Cardiomyopathy 64 0.091
119
P THY032 Thyroiditis 57 0.089
120
VSC018 Visceral Steatosis 37 0.088
121
P HRM001 Hermansky-Pudlak Syndrome 56 0.087
122
P LNG032 Lung Cancer 92 0.086
123
BLR001 Biliary Atresia 52 0.086
124
P PLY014 Polycystic Kidney Disease 60 0.086
125
MYC013 Mycobacterium Abscessus 41 0.086
126
UPP004 Upper Respiratory Tract Disease 48 0.086
127
NNS002 Nonspecific Interstitial Pneumonia 43 0.085
128
CNG034 Congestive Heart Failure 72 0.084
129
ALR002 Al-Raqad Syndrome 36 0.084
130
VRL011 Viral Infectious Disease 56 0.082
131
PRT036 Peritonitis 65 0.082
132
SKN016 Skin Disease 69 0.080
133
CHL068 Cholestasis 57 0.080
134
P ADN016 Adenocarcinoma 69 0.080
135
ADM013 Adamantinoma of Long Bones 57 0.080
136
P OBS005 Obesity 91 0.079
137
P INF032 Infertility 61 0.079
138
ACR041 Acromelic Frontonasal Dysostosis 45 0.078
139
P LKM002 Leukemia 70 0.078
140
BRT030 Birth Defects 44 0.078
141
P MSC005 Muscular Dystrophy 64 0.076
142
P SCL009 Sclerosing Cholangitis 47 0.076
143
P ART022 Arthritis 73 0.075
144
P MYP004 Myopathy 67 0.075
145
P LYM118 Lymphoma 68 0.075
146
CYS039 Cystic Kidney Disease 49 0.075
147
P PRM006 Primary Biliary Cirrhosis 55 0.075
148
BRN002 Bronchiolitis 56 0.075
149
HYP266 Hypoxia 55 0.075
150
c DLT002 Dilated Cardiomyopathy 75 0.074
151
P ATR011 Atrial Fibrillation 63 0.074
152
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 45 0.074
153
P ESN007 Eosinophilia 61 0.074
154
P SNS014 Sinusitis 66 0.074
155
GLC003 Glucose Intolerance 56 0.074
156
LPD004 Lipoid Nephrosis 49 0.072
157
SKN027 Skin Conditions 44 0.072
158
MDS022 Mediastinitis 37 0.072
159
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 34 0.072
160
P SYS005 Systemic Scleroderma 60 0.071
161
P INT070 Intestinal Obstruction 55 0.071
162
EXT034 Extrinsic Allergic Alveolitis 58 0.071
163
BRN012 Bronchiolitis Obliterans 58 0.071
164
c CRN214 Coronary Heart Disease 5 22 0.071
165
P GLM007 Glomerulonephritis 56 0.071
166
VND001 Vein Disease 51 0.068
167
PLM034 Pulmonary Emphysema 55 0.068
168
ANR040 Aneurysm 56 0.068
169
BLD053 Blood Platelet Disease 44 0.068
170
LKP003 Leukoplakia 44 0.068
171
P PNM006 Pneumoconiosis 51 0.068
172
P RHM011 Rheumatoid Arthritis 87 0.067
173
P HMC003 Hemochromatosis 71 0.067
174
GST050 Gastrointestinal System Disease 58 0.067
175
CHL071 Child Syndrome 58 0.067
176
ATP002 Atopy 62 0.067
177
KDS001 Kid Syndrome 53 0.067
178
CTS003 Coats Disease 57 0.067
179
HYP006 Hypertensive Heart Disease 49 0.067
180
GLC008 Glucose Metabolism Disease 44 0.067
181
WLS001 Wilson Disease 72 0.065
182
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 57 0.065
183
PCK002 Pick Disease 66 0.065
184
PHR003 Pharyngitis 58 0.065
185
CLT003 Colitis 56 0.065
186
PRN021 Paranasal Sinus Disease 50 0.065
187
MSC004 Muscle Tissue Disease 35 0.065
188
c HYP595 Hypertension, Essential 69 0.064
189
BRN024 Bronchitis 67 0.064
190
MTH009 Mouth Disease 63 0.064
191
ATR060 Atrial Standstill, Digenic 51 0.064
192
P ESP024 Esophagitis 62 0.064
193
P CRN178 Coronary Heart Disease 6 22 0.064
194
HPD002 Hepadnavirus Infection 20 0.064
195
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.062
196
PLM129 Pulmonary Disease, Chronic Obstructive 61 0.062
197
P FTT008 Fatty Liver Disease, Nonalcoholic 1 31 0.062
198
SKN023 Skin Tag 48 0.062
199
NNT004 Neonatal Respiratory Failure 38 0.062
200
c FTT007 Fatty Liver Disease, Nonalcoholic 2 17 0.062
201
BLD054 Blood Protein Disease 38 0.062
202
c SYS001 Systemic Lupus Erythematosus 87 0.061
203
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.061
204
P NPH005 Nephronophthisis 55 0.061
205
P LPS004 Lupus Erythematosus 63 0.061
206
P INF038 Influenza 71 0.061
207
ATH003 Atherosclerosis 63 0.061
208
ACQ007 Acquired Immunodeficiency Syndrome 60 0.061
209
P MYC008 Myocarditis 56 0.061
210
MCR088 Microscopic Polyangiitis 47 0.061
211
PRC012 Pericardial Effusion 50 0.061
212
VNT001 Ventilation Pneumonitis 35 0.061
213
SPC003 Specific Developmental Disorder 39 0.061
214
c RNL016 Renal Infectious Disease 22 0.061
215
P PNC035 Pancreatic Cancer 86 0.059
216
P MYC007 Myocardial Infarction 80 0.059
217
P TRC086 Trichohepatoenteric Syndrome 1 46 0.059
218
P PRM011 Primary Ciliary Dyskinesia 56 0.059
219
c HPT015 Hepatitis D 51 0.059
220
VSC007 Vascular Disease 51 0.059
221
MVM001 Movement Disease 45 0.059
222
STM006 Stomach Disease 48 0.059
223
P MSC033 Muscle Disorders 52 0.059
224
c AST039 Asthma 2 28 0.059
225
SPL018 Splenomegaly 45 0.059
226
PLM012 Pulmonary Sarcoidosis 54 0.059
227
ALC006 Alcoholic Hepatitis 60 0.059
228
STT004 Steatorrhea 41 0.059
229
ISC004 Ischemia 56 0.059
230
ORL011 Oral Cancer 53 0.059
231
NSL022 Nasal Cavity Disease 41 0.059
232
ORL015 Oral Squamous Cell Carcinoma 55 0.059
233
GLM011 Glomerulosclerosis 41 0.059
234
GST092 Gastroesophageal Reflux 62 0.057
235
CRH001 Crohn's Disease 76 0.057
236
CNG035 Congenital Bilateral Absence of Vas Deferens 40 0.057
237
c ART101 Aortic Valve Disease 2 56 0.057
238
HYP066 Hyperglycemia 61 0.057
239
ADJ001 Adjustment Disorder 38 0.057
240
P ATX004 Ataxia 53 0.057
241
LKC003 Leukocyte Disease 45 0.057
242
RTN023 Retinitis 49 0.057
243
DCH001 Duchenne Muscular Dystrophy 81 0.056
244
c ACT210 Acute Respiratory Distress Syndrome 55 0.056
245
c TRC078 Trichohepatoenteric Syndrome 2 30 0.056
246
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.056
247
PNM008 Pneumothorax 51 0.056
248
c AST037 Asthma 1 35 0.056
249
SXL003 Sexual Disorder 45 0.056
250
HMN014 Human Immunodeficiency Virus Infectious Disease 46 0.056
251
ALC009 Alcoholic Liver Cirrhosis 53 0.056
252
ORL012 Oral Leukoplakia 41 0.056
253
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.054
254
KRT002 Keratomalacia 50 0.054
255
INS024 Insulin-Like Growth Factor I 75 0.054
256
P DRM010 Dermatomyositis 59 0.054
257
SLP005 Sleep Disorder 52 0.054
258
VSC011 Vasculitis 62 0.054
259
c PLM128 Pulmonary Hypertension, Primary, 2 36 0.054
260
c ATM011 Autoimmune Hepatitis 62 0.054
261
P HYP098 Hypereosinophilic Syndrome 48 0.054
262
ACD009 Acid-Labile Subunit, Deficiency of 37 0.054
263
NWC001 Newcastle Disease 51 0.054
264
c ATM024 Autoimmune Pancreatitis 46 0.054
265
P END033 Endocarditis 52 0.054
266
MCC011 Mucociliary Clearance Disorder 15 0.054
267
P STR020 Strabismus 55 0.052
268
CSY001 C Syndrome 49 0.052
269
ALL026 Allergic Hypersensitivity Disease 53 0.052
270
P THL005 Thalassemia 61 0.052
271
ART017 Aortic Disease 57 0.052
272
PRC013 Pericarditis 52 0.052
273
DDN006 Duodenitis 44 0.052
274
PHY002 Physical Disorder 43 0.052
275
HRT012 Heart Valve Disease 39 0.052
276
c CRN175 Coronary Heart Disease 4 19 0.052
277
RDT005 Radiation Induced Cancer 26 0.052
278
END038 Endocrine Pancreas Disease 42 0.052
279
BRN106 Burns 52 0.052
280
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.050
281
ART016 Aortic Aneurysm 67 0.050
282
MYL009 Myelodysplastic Syndrome 73 0.050
283
TBR010 Tuberculosis 70 0.050
284
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 59 0.050
285
PRP027 Peripheral Vascular Disease 69 0.050
286
AYM001 Ayme-Gripp Syndrome 40 0.050
287
DFF003 Diffuse Scleroderma 39 0.050
288
END030 End Stage Renal Failure 53 0.050
289
P THR014 Thrombocytopenia 63 0.050
290
c ACT027 Acute Pancreatitis 59 0.050
291
BNS002 Bone Structure Disease 37 0.050
292
P BRS047 Breast Cancer 100 0.048
293
DFC004 Deficiency Anemia 64 0.048
294
DRM006 Dermatitis 58 0.048
295
c CHR089 Chronic Kidney Failure 67 0.048
296
P HYP086 Hypothyroidism 63 0.048
297
EYD002 Eye Disease 62 0.048
298
HPT074 Hepatic Adenoma, Somatic 35 0.048
299
ALN001 Aland Island Eye Disease 45 0.048
300
NRM005 Neuromuscular Disease 56 0.048
301
P INT068 Intestinal Disease 60 0.048
302
P PLM006 Pulmonary Alveolar Proteinosis 46 0.048
303
P SDR002 Siderosis 44 0.048
304
ALB002 Albinism 43 0.048
305
P HRT017 Heart Tumor 34 0.048
306
PRT019 Protein-Losing Enteropathy 42 0.048
307
CHL079 Children's Interstitial Lung Disease 18 0.048
308
HPT009 Hepatopulmonary Syndrome 48 0.048
309
ACR005 Acrodermatitis 33 0.048
310
DST006 Diastolic Heart Failure 45 0.048
311
IMP003 Impaired Renal Function Disease 36 0.048
312
WTH001 Withdrawal Disorder 36 0.048
313
CNG039 Congenital Absence of the Vas Deferens 23 0.048
314
P OST002 Osteoporosis 63 0.046
315
P CRN211 Coronary Artery Disease 74 0.046
316
ANX002 Anxiety Disorder 67 0.046
317
P URF003 Urofacial Syndrome 1 51 0.046
318
P PTS002 Ptosis 56 0.046
319
BRC012 Brucellosis 66 0.046
320
ACR003 Acrodermatitis Enteropathica 49 0.046
321
HRT007 Heart Cancer 51 0.046
322
c MCR129 Microvascular Complications of Diabetes 1 55 0.046
323
IMM102 Immunodeficiency 14 33 0.046
324
INC022 Inclusion-Cell Disease 46 0.046
325
LPD008 Lipid Metabolism Disorder 42 0.046
326
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.046
327
ALL006 Allergic Asthma 59 0.046
328
c HPT007 Hepatitis E 51 0.046
329
BLR006 Biliary Tract Disease 50 0.046
330
HMS001 Hemosiderosis 42 0.046
331
c INH020 Inherited Metabolic Disorder 49 0.046
332
P PLY041 Polymyositis 49 0.046
333
CHR008 Choroiditis 43 0.046
334
c CRN172 Coronary Heart Disease 3 19 0.046
335
c CHR096 Chronic Pulmonary Heart Disease 40 0.046
336
ENT007 Enteropathica 26 0.046
337
P DYS007 Dyskeratosis Congenita 64 0.044
338
ADL002 Adult Syndrome 53 0.044
339
c ATM003 Autoimmune Thyroiditis 59 0.044
340
P MTR012 Mitral Valve Disease 59 0.044
341
P MMB011 Membranous Nephropathy 53 0.044
342
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.044
343
P MSC007 Muscle Hypertrophy 55 0.044
344
P DRR001 Diarrhea 60 0.044
345
MXD005 Mixed Connective Tissue Disease 63 0.044
346
STS002 Situs Inversus 43 0.044
347
URT001 Urethritis 39 0.044
348
SCK005 Sickle Cell Disease 51 0.044
349
c CRN177 Coronary Heart Disease 7 21 0.044
350
PRT011 Protein C Deficiency 52 0.044
351
DFF035 Diffuse Cutaneous Systemic Sclerosis 45 0.044
352
PRS047 Prostatitis 56 0.044
353
c ACT075 Acute Myocardial Infarction 61 0.044
354
GLB003 Globe Disease 34 0.044
355
CRN030 Coronary Stenosis 50 0.044
356
PLM015 Pulmonary Systemic Sclerosis 23 0.044
357
P ACT080 Acute Pulmonary Heart Disease 31 0.044
358
c ADL079 Adult Heart Tumor 17 0.044
359
ATS010 Autosomal Recessive Disease 40 0.044
360
c THR092 Thrombophilia Due to Thrombin Defect 56 0.042
361
PLM033 Pulmonary Embolism 59 0.042
362
TTR001 Tetralogy of Fallot 69 0.042
363
PLY022 Polycystic Kidney and Hepatic Disease 47 0.042
364
P RCK004 Rickets 59 0.042
365
CHY002 Chylomicron Retention Disease 54 0.042
366
c JVN010 Juvenile Rheumatoid Arthritis 65 0.042
367
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.042
368
c ACT068 Acute Cystitis 50 0.042
369
SPL012 Splenic Disease 48 0.042
370
P HMN010 Hemangioma 62 0.042
371
P GLL020 Gallbladder Disease 59 0.042
372
c PLM127 Pulmonary Hypertension, Primary, 3 31 0.042
373
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.042
374
P RST002 Restrictive Cardiomyopathy 48 0.042
375
RPR002 Reproductive System Disease 45 0.042
376
OBS061 Obstructive Sleep Apnea 61 0.042
377
P ABD003 Abdominal Aortic Aneurysm 43 0.042
378
P HYP065 Hyperaldosteronism 52 0.042
379
P SLP006 Sleep Apnea 60 0.042
380
P MSC003 Muscular Atrophy 51 0.042
381
DSQ001 Desquamative Interstitial Pneumonia 33 0.042
382
AZS001 Azoospermia 43 0.042
383
P CLL015 Collagen Disease 49 0.042
384
P UVT001 Uveitis 60 0.042
385
P AMY004 Amyloidosis 63 0.042
386
SPR035 Superior Vena Cava Syndrome 31 0.042
387
CHR001 Churg-Strauss Syndrome 48 0.042
388
MTR031 Motor Neuro-Ophthalmic Disorders 22 0.042
389
HYD002 Hydronephrosis 48 0.042
390
GST053 Gastric Cancer 52 0.042
391
RHM009 Rheumatoid Lung Disease 41 0.042
392
BNN003 Bone Inflammation Disease 46 0.042
393
ART012 Aortitis 32 0.042
394
CHL052 Choledochal Cyst 40 0.042
395
HPT020 Hepatic Vascular Disease 43 0.042
396
P BLD051 Blood Coagulation Disease 44 0.042
397
c CRN174 Coronary Heart Disease 2 19 0.042
398
LBR003 Labrador Lung 16 0.042
399
CRB009 Cerebritis 36 0.042
400
SNG003 Single Ventricular Heart 23 0.042
401
MLT035 Multifocal Choroiditis 29 0.042
402
HRP008 Herpes Simiae 13 0.042
403
HRP012 Herpesvirus Simiae B Virus 10 0.042
404
MLR004 Malaria 80 0.039
405
P TYS001 Tay-Sachs Disease 72 0.039
406
EMP007 Emphysema Due to Aat Deficiency 57 0.039
407
ETH011 Ethylmalonic Encephalopathy 57 0.039
408
ART002 Arts Syndrome 53 0.039
409
MSM001 Meesmann Corneal Dystrophy 42 0.039
410
VHW001 Vohwinkel Syndrome 47 0.039
411
P NPH012 Nephrotic Syndrome 55 0.039
412
P MYL006 Myeloid Leukemia 67 0.039
413
GNG013 Gingivitis 61 0.039
414
C3D001 C3 Deficiency 50 0.039
415
SRC014 Sarcoma 66 0.039
416
P ADL010 Adult Respiratory Distress Syndrome 60 0.039
417
DYS073 Dysphagia 51 0.039
418
LYM024 Lymphatic System Disease 49 0.039
419
CHG001 Chagas Disease 62 0.039
420
P HMP007 Hemophilia 55 0.039
421
P LYM025 Lymphedema 60 0.039
422
PMP001 Pemphigus 49 0.039
423
ANG049 Angioedema Induced by Ace Inhibitors 35 0.039
424
TTH006 Tooth Disease 52 0.039
425
c MTR002 Mitral Valve Insufficiency 42 0.039
426
P BRN009 Burning Mouth Syndrome 54 0.039
427
P PLM085 Pulmonary Hemosiderosis 45 0.039
428
CRY004 Cryoglobulinemia 47 0.039
429
ERD001 Erdheim-Chester Disease 51 0.039
430
INT051 Intussusception 50 0.039
431
c PNC111 Pancreatic Cancer 2 33 0.039
432
SLD003 Sialadenitis 45 0.039
433
PLM001 Pulmonary Tuberculosis 69 0.039
434
MGC001 Megacolon 50 0.039
435
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.039
436
DVL001 Developmental Coordination Disorder 36 0.039
437
HMG005 Hemoglobinopathy 49 0.039
438
BRN056 Bronchopulmonary Dysplasia 56 0.039
439
BRW002 Brown's Tendon Sheath Syndrome 14 0.039
440
ISC006 Ischemic Heart Disease 54 0.039
441
STN013 Stenotrophomonas Maltophilia Infection 19 0.039
442
PNC028 Pancreatic Steatorrhea 34 0.039
443
HMP009 Haemophilus Influenzae 44 0.039
444
P PYL005 Pyelonephritis 52 0.039
445
c RCR022 Recurrent Acute Pancreatitis 36 0.039
446
P CRV039 Cervicitis 45 0.039
447
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.039
448
c HYP058 Hypervitaminosis a 35 0.039
449
c HMG004 Hemoglobin D Disease 32 0.039
450
CRD137 Cardiogenic Shock 44 0.039
451
OTP003 Oto-Palatal-Digital Syndrome 14 0.039
452
NNT002 Neonatal Urinary Tract Infectious Disease 12 0.039
453
IMM001 Immune-Complex Glomerulonephritis 41 0.039
454
LYM023 Lymphatic System Cancer 35 0.039
455
c ATM022 Autoimmune Myocarditis 39 0.039
456
PRQ002 Paraquat Poisoning 23 0.039
457
ORL014 Oral Pharyngeal Disorders 13 0.039
458
WRN005 Wrinkles 35 0.039
459
CFT001 Cftr-Related Disorders 14 0.039
460
P PRS040 Prostate Cancer 89 0.037
461
P RNL014 Renal Cell Carcinoma 80 0.037
462
P GCH001 Gaucher's Disease 63 0.037
463
P CMR001 Camurati-Engelmann Disease 63 0.037
464
c INF071 Inflammatory Bowel Disease 1 51 0.037
465
DWN001 Down Syndrome 65 0.037
466
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.037
467
ULC004 Ulcerative Colitis 74 0.037
468
MLD001 Melioidosis 67 0.037
469
MLN007 Male Infertility 56 0.037
470
THR016 Thrombophlebitis 55 0.037
471
P HML002 Hemolytic Anemia 60 0.037
472
P PLY017 Polyarteritis Nodosa 54 0.037
473
ATN002 Autonomic Nervous System Disease 46 0.037
474
P LNG064 Lung Cancer Susceptibility 3 62 0.037
475
TYP007 Typhoid Fever 61 0.037
476
PRP030 Purpura 60 0.037
477
P MNN013 Meningitis 66 0.037
478
AMN002 Amino Acid Metabolic Disorder 48 0.037
479
P ENC018 Encephalopathy 59 0.037
480
P NPH009 Nephrolithiasis 59 0.037
481
IMM090 Immunodeficiency 27a, Mycobacteriosis, Ar 26 0.037
482
ECH003 Echinococcosis 53 0.037
483
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.037
484
P HYP004 Hypercalcemia 54 0.037
485
CNS004 Constipation 57 0.037
486
P GLY013 Glycogen Storage Disease 58 0.037
487
P OCL002 Oculocutaneous Albinism 51 0.037
488
DSS009 Disseminated Intravascular Coagulation 52 0.037
489
c PNC094 Pancreatic Cancer 1 27 0.037
490
ART021 Arteriosclerosis 59 0.037
491
CRB025 Carbohydrate Metabolic Disorder 46 0.037
492
THR004 Thrombocytosis 55 0.037
493
FXF002 Fox-Fordyce Disease 37 0.037
494
NPH003 Nephrocalcinosis 47 0.037
495
FLR002 Filariasis 55 0.037
496
FML039 Female Reproductive System Disease 49 0.037
497
KWS001 Kwashiorkor 45 0.037
498
TNP003 Tn Polyagglutination Syndrome, Somatic 30 0.037
499
RNL078 Renal Dysplasia 48 0.037
500
FSC002 Fascioliasis 39 0.037
501
NDL013 Nodular Regenerative Hyperplasia 46 0.037
502
PRT038 Protein-Energy Malnutrition 48 0.037
503
P LRY019 Laryngitis 55 0.037
504
c CHR417 Chronic Graft Versus Host Disease 50 0.037
505
P NRP001 Neuropathy 57 0.037
506
GRW007 Growth Hormone Deficiency 49 0.037
507
HYP037 Hyperhomocysteinemia 49 0.037
508
CYT008 Cytomegalovirus Infection 51 0.037
509
P RPD001 Rapidly Progressive Glomerulonephritis 43 0.037
510
P SKN013 Skin Benign Neoplasm 38 0.037
511
HYD005 Hydrocele 47 0.037
512
KLD001 Keloids 50 0.037
513
P TRN034 Transverse Myelitis 43 0.037
514
SPN051 Spondylitis 50 0.037
515
ALC005 Alcoholic Pancreatitis 35 0.037
516
P CHR345 Chronic Pain 45 0.037
517
P PSD003 Pseudohypoaldosteronism 42 0.037
518
BCK006 Back Pain 40 0.037
519
NRN002 Neuronitis 40 0.037
520
ATS009 Autosomal Genetic Disease 38 0.037
521
INB001 Inborn Amino Acid Metabolism Disorder 14 0.037
522
P PRL003 Proliferative Glomerulonephritis 40 0.037
523
OST008 Osteosclerotic Myeloma 37 0.037
524
VTM003 Vitamin Metabolic Disorder 31 0.037
525
HDG012 Hodgkin Lymphoma 75 0.034
526
HV1006 Hiv-1 80 0.034
527
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 77 0.034
528
BCK001 Becker Muscular Dystrophy 68 0.034
529
P MCK022 Meckel Syndrome 1 54 0.034
530
GLB001 Gilbert Syndrome 59 0.034
531
c ART115 Aortic Valve Disease 1 53 0.034
532
CMM005 Common Cold 58 0.034
533
GST023 Gastric Ulcer 56 0.034
534
PRP019 Peripheral Nervous System Disease 52 0.034
535
c DYS143 Dyskeratosis Congenita, Autosomal Dominant 2 32 0.034
536
HRY003 Hairy Cell Leukemia 56 0.034
537
P GRV001 Graves' Disease 62 0.034
538
CNT047 Contact Dermatitis 62 0.034
539
INT007 Intermediate Coronary Syndrome 52 0.034
540
ESP023 Esophageal Disease 52 0.034
541
c LCL006 Localized Scleroderma 60 0.034
542
IRN001 Iron Deficiency Anemia 51 0.034
543
P DDN001 Duodenal Ulcer 51 0.034
544
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 30 0.034
545
P ARC016 Auriculocondylar Syndrome 1 44 0.034
546
P LYM026 Lymphoblastic Leukemia 60 0.034
547
P NGH001 Night Blindness 49 0.034
548
P HST010 Histiocytosis 56 0.034
549
P ANT006 Antiphospholipid Syndrome 60 0.034
550
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 42 0.034
551
P THR015 Thrombophilia 59 0.034
552
CRC006 Carcinoid Syndrome 51 0.034
553
P BCL006 B-Cell Lymphomas 64 0.034
554
MDL009 Medullary Sponge Kidney 41 0.034
555
MYX004 Myxedema 36 0.034
556
P PRD008 Periodontitis 46 0.034
557
PRR002 Pure Red-Cell Aplasia 47 0.034
558
MRC001 Marchiafava Bignami Disease 33 0.034
559
VSC006 Vascular Cancer 51 0.034
560
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 21 0.034
561
c SCL052 Scleroderma, Familial Progressive 27 0.034
562
MRB003 Morbid Obesity 59 0.034
563
SYN007 Synovitis 56 0.034
564
DNG002 Dengue Hemorrhagic Fever 60 0.034
565
c ACT071 Acute Kidney Failure 48 0.034
566
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.034
567
P RNL017 Renal Oncocytoma 48 0.034
568
c CNG027 Congenital Hemolytic Anemia 46 0.034
569
BRN014 Bronchopneumonia 45 0.034
570
P RNV001 Renovascular Hypertension 46 0.034
571
OBS001 Obstructive Jaundice 47 0.034
572
HYP063 Hypersplenism 49 0.034
573
DFF005 Diffuse Large B-Cell Lymphoma 57 0.034
574
TRY001 Trypanosomiasis 51 0.034
575
SWT003 Sweat Gland Disease 33 0.034
576
MCN008 Mucinous Cystadenocarcinoma 39 0.034
577
CLL021 Collagenous Colitis 36 0.034
578
c CNG004 Congenital Epulis 34 0.034
579
NNT049 Nontuberculous Mycobacterial Lung Disease 41 0.034
580
CNS002 Constrictive Pericarditis 31 0.034
581
KSH001 Keshan Disease 30 0.034
582
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.034
583
RNL097 Renal Artery Disease 44 0.034
584
c CRN173 Coronary Heart Disease 8 19 0.034
585
P PMP005 Pemphigus Vulgaris 47 0.034
586
P RNL015 Renal Hypertension 47 0.034
587
PRP080 Peripheral Artery Disease 35 0.034
588
MDD010 Middle Ear Disease 47 0.034
589
SYS003 Systolic Heart Failure 42 0.034
590
c ACT042 Acute Pyelonephritis 47 0.034
591
HYP457 Hypertrophic Scars 45 0.034
592
SCR003 Secretory Diarrhea 31 0.034
593
DDN009 Duodenal Obstruction 35 0.034
594
c BNG076 Benign Exophthalmos Syndrome 15 0.034
595
IDP075 Idiopathic and/or Familial Pulmonary Arterial Hypertension 11 0.034
596
IGG011 Igg4-Related Kidney Disease 14 0.034
597
STR067 Stroke, Ischemic 74 0.031
598
SCK003 Sickle Cell Anemia 72 0.031
599
P ATX030 Ataxia-Telangiectasia 78 0.031
600
KPS004 Kaposi Sarcoma 69 0.031
601
P RTN024 Retinoblastoma 75 0.031
602
P KDN017 Kidney Cancer 67 0.031
603
P CLC005 Celiac Disease 67 0.031
604
ACN011 Acne 63 0.031
605
FRB001 Farber Lipogranulomatosis 54 0.031
606
SHW002 Shwachman-Diamond Syndrome 59 0.031
607
P MYS003 Myasthenia Gravis 64 0.031
608
KWS002 Kawasaki Disease 70 0.031
609
c HRM017 Hermansky-Pudlak Syndrome 2 40 0.031
610
ADT003 Auditory System Disease 49 0.031
611
P NRV007 Nervous System Disease 71 0.031
612
CYS010 Cystinosis 51 0.031
613
P LYM007 Lymphangioleiomyomatosis 65 0.031
614
PRD011 Proud Syndrome 42 0.031
615
PPL049 Papillon-Lefevre Syndrome 45 0.031
616
c HMP004 Hemophilia B 61 0.031
617
P BDD001 Budd-Chiari Syndrome 52 0.031
618
KRT010 Kartagener Syndrome 48 0.031
619
PRT037 Pertussis 63 0.031
620
CHR066 Chronic Fatigue Syndrome 63 0.031
621
ACT055 Actinomycosis 42 0.031
622
MSS002 Mass Syndrome 49 0.031
623
P MYS005 Myositis 57 0.031
624
HYP056 Hypoglycemia 60 0.031
625
APP008 Appendicitis 61 0.031
626
NNT012 Neonatal Jaundice 49 0.031
627
HMC038 Hemochromatosis, Neonatal 27 0.031
628
ETN001 Eating Disorder 59 0.031
629
c HYP555 Hypertriglyceridemia, Transient Infantile 26 0.031
630
c BLD124 Bleeding Disorder, Platelet-Type, 11 37 0.031
631
RTN018 Retinal Disease 55 0.031
632
RHM027 Rheumatic Disease 55 0.031
633
c DYS149 Dyskeratosis Congenita, Autosomal Recessive 1 34 0.031
634
GST037 Gastroparesis 54 0.031
635
c NPH046 Nephrolithiasis, Type I 31 0.031
636
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 35 0.031
637
OCL009 Ocular Cancer 61 0.031
638
CHL014 Cholera 56 0.031
639
PLM124 Pulmonary Hypertension, Neonatal 25 0.031
640
c PND001 Pain Disorder 53 0.031
641
CYS008 Cystic Echinococcosis 48 0.031
642
CRY001 Cryptogenic Organizing Pneumonia 44 0.031
643
XRP001 Xerophthalmia 36 0.031
644
PYR010 Peyronie's Disease 52 0.031
645
PRT030 Parathyroid Gland Disease 49 0.031
646
PNB004 Panbronchiolitis, Diffuse 22 0.031
647
P PRX010 Paroxysmal Ventricular Fibrillation 33 0.031
648
HPY002 H. Pylori Infection 58 0.031
649
PLM010 Pulmonary Edema 56 0.031
650
P LCH002 Lichen Planus 61 0.031
651
CVR006 Cavernous Hemangioma 46 0.031
652
GST045 Gastroenteritis 59 0.031
653
NRN004 Neuroendocrine Tumor 54 0.031
654
NSY001 N Syndrome 42 0.031
655
GRD001 Giardiasis 40 0.031
656
MCL006 Macular Retinal Edema 42 0.031
657
ATM052 Autoimmune Disease 1 26 0.031
658
BCT002 Bacterial Vaginosis 53 0.031
659
INT067 Interstitial Nephritis 48 0.031
660
PNN001 Panniculitis 47 0.031
661
HTS001 Hiatus Hernia 40 0.031
662
MNT002 Mental Depression 52 0.031
663
BLD036 Bile Duct Disease 47 0.031
664
ADN018 Adenoma 59 0.031
665
HLL004 Hellp Syndrome 48 0.031
666
SWL001 Swallowing Disorders 33 0.031
667
ATN005 Autonomic Dysfunction 44 0.031
668
c INF067 Inflammatory Bowel Disease 10 31 0.031
669
HYP540 Hypertension, Diastolic 40 0.031
670
ACT084 Acute Stress Disorder 38 0.031
671
CPL005 Capillary Disease 39 0.031
672
c ACT134 Acute Liver Failure 46 0.031
673
URM002 Uremia 36 0.031
674
P RTN016 Retinal Degeneration 50 0.031
675
END040 Endogenous Depression 51 0.031
676
CVT001 Cavitary Optic Disc Anomalies 25 0.031
677
LPM005 Lipomatosis 46 0.031
678
VRR004 Verrucous Carcinoma 54 0.031
679
ORL013 Oral Lichen Planus 53 0.031
680
P EXN002 Exanthem 57 0.031
681
DRM009 Dermatomycosis 33 0.031
682
ESN005 Eosinophilic Gastroenteritis 46 0.031
683
CYS009 Cystadenoma 40 0.031
684
c ANT034 Anterior Uveitis 49 0.031
685
c VRL005 Viral Pneumonia 44 0.031
686
CHR078 Chorioretinitis 41 0.031
687
ANC002 Anca-Associated Vasculitis 43 0.031
688
HRS011 Horseshoe Kidney 34 0.031
689
PST046 Post-Transplant Lymphoproliferative Disease 53 0.031
690
PNC041 Pancreatic Ductal Adenocarcinoma 64 0.031
691
MLT006 Multidrug-Resistant Tuberculosis 46 0.031
692
PRD004 Prediabetes Syndrome 40 0.031
693
SMN007 Seminoma 45 0.031
694
FLL008 Folliculitis 47 0.031
695
PNC002 Pancreatic Mucinous Cystadenoma 35 0.031
696
SPN186 Spinal Cord Injury 62 0.031
697
ART004 Aortic Atherosclerosis 46 0.031
698
VLV010 Vulvovaginitis 41 0.031
699
c CRN176 Coronary Heart Disease 9 19 0.031
700
c INH004 Inherited Blood Coagulation Disease 38 0.031
701
VSC008 Vascular Hemostatic Disease 30 0.031
702
ANG054 Angina Pectoris 48 0.031
703
NRN029 Neuronal Intestinal Dysplasia 31 0.031
704
FNC006 Functional Gastric Disease 33 0.031
705
GRN003 Granulomatous Dermatitis 32 0.031
706
IDP074 Idiopathic Bronchiectasis 34 0.031
707
CRN073 Coronary Arteries Congenital Malformation 11 0.031
708
P FML187 Familial Hypertension 35 0.031
709
BNF002 Bone Fracture 46 0.031
710
c MCL042 Macular Degeneration, Age-Related, 1 71 0.028
711
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 61 0.028
712
c JBR020 Joubert Syndrome 1 57 0.028
713
ALL003 Allergic Rhinitis 67 0.028
714
c PNC108 Pancreatitis, Hereditary 59 0.028
715
P BCK002 Beckwith-Wiedemann Syndrome 56 0.028
716
WRN001 Werner Syndrome 69 0.028
717
KRT004 Keratitis 70 0.028
718
P ESS003 Essential Thrombocythemia 66 0.028
719
MLN008 Melanoma 61 0.028
720
P SPN046 Spinal Muscular Atrophy 62 0.028
721
P NMN002 Niemann-Pick Disease 63 0.028
722
MRF001 Marfan Syndrome 73 0.028
723
P NRF002 Neurofibromatosis 66 0.028
724
ANR002 Aniridia 62 0.028
725
VND002 Van Der Woude Syndrome 50 0.028
726
P ALP004 Alport Syndrome 68 0.028
727
c SRC025 Sarcoidosis 1 58 0.028
728
c FML001 Familial Atrial Fibrillation 59 0.028
729
P PRC031 Preeclampsia/eclampsia 1 53 0.028
730
LNG024 Langerhans-Cell Histiocytosis 64 0.028
731
LPT001 Leptospirosis 65 0.028
732
SPN060 Spondylocarpotarsal Synostosis Syndrome 38 0.028
733
P PSR002 Psoriasis 63 0.028
734
c THR082 Thrombophilia Due to Activated Protein C Resistance 57 0.028
735
TYP011 Typhus 57 0.028
736
HST011 Histoplasmosis 54 0.028
737
MST006 Mast Syndrome 44 0.028
738
P HYP117 Hypertriglyceridemia 65 0.028
739
P GST044 Gastritis 64 0.028
740
URN009 Urinary System Disease 52 0.028
741
c MTB001 Metabolic Syndrome X 61 0.028
742
c HRM005 Hermansky-Pudlak Syndrome 1 47 0.028
743
P RHN004 Rhinitis 59 0.028
744
NCR004 Nocardiosis 44 0.028
745
HNT002 Hantavirus Pulmonary Syndrome 51 0.028
746
TKY002 Takayasu Arteritis 60 0.028
747
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 37 0.028
748
CRN246 Cranioosteoarthropathy 32 0.028
749
DNG003 Dengue Disease 60 0.028
750
c CNG006 Congenital Hypothyroidism 59 0.028
751
CHL127 Cholangiocarcinoma, Susceptibility to 55 0.028
752
c DYS152 Dyskeratosis Congenita, Autosomal Recessive 5 27 0.028
753
ATN011 Autoinflammation with Infantile Enterocolitis 36 0.028
754
IMN002 Iminoglycinuria, Digenic 35 0.028
755
SPT004 Septic Arthritis 60 0.028
756
SML020 Small Patella Syndrome 36 0.028
757
P END044 Endometriosis 53 0.028
758
SPN041 Spinal Cord Disease 50 0.028
759
CMP010 Complex Regional Pain Syndrome 59 0.028
760
P EXP004 Exophthalmos 56 0.028
761
ING001 Inguinal Hernia 57 0.028
762
PLS007 Plasmodium Falciparum Malaria 56 0.028
763
c HRM007 Hermansky-Pudlak Syndrome 4 29 0.028
764
c DYS147 Dyskeratosis Congenita, Autosomal Dominant 3 24 0.028
765
RCT015 Reactive Arthritis 65 0.028
766
P LFT003 Left Ventricular Noncompaction 48 0.028
767
EBS001 Ebstein Anomaly 44 0.028
768
P ECL001 Eclampsia 55 0.028
769
DYS011 Dyskinesia of Esophagus 31 0.028
770
SPT005 Spotted Fever 56 0.028
771
c MCL043 Macular Degeneration, Age-Related, 2 32 0.028
772
EPT021 Epithelial Recurrent Erosion Dystrophy 32 0.028
773
CNV002 Conversion Disorder 45 0.028
774
c RHM021 Rheumatoid Arthritis, Systemic Juvenile 43 0.028
775
c SVR001 Severe Acute Respiratory Syndrome 56 0.028
776
PRL009 Prolactinoma 63 0.028
777
PLM017 Pulmonary Alveolar Microlithiasis 46 0.028
778
c PLY059 Polycystic Kidney Disease, Adult Type I 36 0.028
779
TXC005 Toxic Shock Syndrome 61 0.028
780
HPT019 Hepatic Encephalopathy 58 0.028
781
P FLL037 Follicular Lymphoma 68 0.028
782
BLD034 Bile Duct Carcinoma 56 0.028
783
PRP007 Priapism 48 0.028
784
HMR004 Hemorrhagic Fever with Renal Syndrome 52 0.028
785
CYN002 Cyanosis, Transient Neonatal 29 0.028
786
c PNC103 Pancreatic Cancer 4 30 0.028
787
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 35 0.028
788
WLL006 Wells Syndrome 57 0.028
789
ADL030 Adult-Onset Still's Disease 57 0.028
790
P VNS003 Venous Insufficiency 53 0.028
791
P PLY019 Polyneuropathy 53 0.028
792
CRP010 Corpus Callosum Agenesis 38 0.028
793
ESN015 Eosinophilic Fasciitis 46 0.028
794
P CYS018 Cystitis 54 0.028
795
MYC002 Mycobacterium Avium Complex Disease 52 0.028
796
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.028
797
DNT012 Dental Caries 45 0.028
798
c HMG001 Hemoglobin C Disease 46 0.028
799
PMS001 Poems Syndrome 56 0.028
800
P CTR002 Cataract 57 0.028
801
P GND004 Gonadal Dysgenesis 51 0.028
802
ACT216 Acute Leukemia of Ambiguous Lineage 30 0.028
803
HYP068 Hyperostosis 39 0.028
804
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 36 0.028
805
HYP005 Hypokalemia 52 0.028
806
HPT022 Hepatoblastoma 57 0.028
807
LRN003 Learning Disability 49 0.028
808
RDN001 Reading Disorder 39 0.028
809
CYT004 Cytomegalic Inclusion Disease 29 0.028
810
P HMR012 Hemorrhagic Fever 55 0.028
811
c AST050 Asthma, Phf11-Related 23 0.028
812
SBS003 Substance Abuse 54 0.028
813
ALV002 Alveolar Echinococcosis 50 0.028
814
IRN002 Iron Metabolism Disease 38 0.028
815
ARC002 Arachnoiditis 38 0.028
816
GBL002 Goblet Cell Carcinoid 29 0.028
817
CLN019 Colonic Disease 50 0.028
818
P MCL035 Macular Dystrophy, Retinal, 2 25 0.028
819
HPT046 Hepatic Veno-Occlusive Disease 46 0.028
820
INT079 Intrahepatic Cholangiocarcinoma 55 0.028
821
P HYP060 Hyperinsulinism 58 0.028
822
c INF023 Inflammatory Breast Carcinoma 44 0.028
823
P SHR001 Short Bowel Syndrome 51 0.028
824
DSS008 Disease of Mental Health 48 0.028
825
ELS001 Eales Disease 47 0.028
826
RTC001 Reticulohistiocytic Granuloma 32 0.028
827
MSC072 Muscle Cancer 47 0.028
828
AMB002 Amblyopia 42 0.028
829
P PNC001 Pancytopenia 53 0.028
830
FDL002 Food Allergy 56 0.028
831
PPL022 Papilloma 54 0.028
832
GDS001 Good Syndrome 46 0.028
833
RFR003 Refractive Error 39 0.028
834
ANK001 Ankylosis 52 0.028
835
LYM043 Lymphocytic Hypophysitis 33 0.028
836
NPH004 Nephropathia Epidemica 39 0.028
837
c PST041 Posterior Urethral Valves 46 0.028
838
c CNN010 Connective Tissue Benign Neoplasm 31 0.028
839
FBR003 Fibrous Histiocytoma 46 0.028
840
PRC003 Proctitis 42 0.028
841
SYM002 Sympathetic Ophthalmia 41 0.028
842
INT304 Interstitial Pneumonitis, Desquamative, Familial 14 0.028
843
AQG003 Aquagenic Syringeal Acrokeratoderm 8 0.028
844
P LPD010 Lipodystrophy 51 0.028
845
c ACQ005 Acquired Thrombocytopenia 35 0.028
846
FSC004 Fasciitis 47 0.028
847
ART111 Artery Disease 56 0.028
848
ANG020 Angiosarcoma 53 0.028
849
ISC015 Ischemic Colitis 38 0.028
850
c SBC035 Subacute Cutaneous Lupus Erythematosus 47 0.028
851
LVR014 Liver Sarcoma 37 0.028
852
INS022 in Situ Pulmonary Adenocarcinoma 34 0.028
853
KHN001 Kuhnt-Junius Degeneration 36 0.028
854
PGM003 Pigmentation Disease 34 0.028
855
PLM035 Pulmonary Eosinophilia 46 0.028
856
MYC003 Myocardium Cancer 16 0.028
857
NDL002 Nodular Tenosynovitis 23 0.028
858
SDD007 Sudden Cardiac Death 46 0.028
859
CYS014 Cystadenocarcinoma 47 0.028
860
EPT020 Epithelioid Hemangioendothelioma 46 0.028
861
EXT006 Extrahepatic Cholestasis 35 0.028
862
XNT002 Xanthogranulomatous Cholecystitis 30 0.028
863
DFF013 Diffuse Meningeal Melanocytosis 19 0.028
864
PLS031 Plastic Bronchitis 22 0.028
865
SXD001 Sex Differentiation Disease 39 0.028
866
HNM002 Hinman Syndrome 22 0.028
867
GST039 Gastroduodenitis 32 0.028
868
BNM008 Bone Mineral Density, Low 28 0.028
869
c MYC058 Myocardial Infarction 2 28 0.028
870
XNT001 Xanthogranulomatous Pyelonephritis 32 0.028
871
FXP001 Foxp2-Related Speech and Language Disorders 15 0.028
872
ADS004 Aids Dementia Complex 47 0.028
873
CHL040 Cholangiolocellular Carcinoma 35 0.028
874
c SVR056 Severe Hemophilia a 44 0.028
875
ECT006 Ectodermal Dysplasia 46 0.028
876
EYD001 Eye Degenerative Disease 31 0.028
877
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 19 0.028
878
PNC059 Punctate Inner Choroidopathy 27 0.028
879
EXT035 Extrinsic Cardiomyopathy 38 0.028
880
c CHR098 Chronic Pyelonephritis 38 0.028
881
STR077 Streptococcal Toxic-Shock Syndrome 38 0.028
882
c TRN014 Transient Arthritis 36 0.028
883
ASB003 Asbestos Intoxication 9 0.028
884
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 40 0.028
885
ART031 Aortic Coarctation 42 0.028
886
c INV001 Invasive Aspergillosis 44 0.028
887
SCD003 Scedosporiosis 14 0.028
888
CRT004 Carotid Artery Thrombosis 38 0.028
889
DBT006 Diabetic Macular Edema 46 0.028
890
CNV003 Conventional Fibrosarcoma 31 0.028
891
P ADL037 Adult Xanthogranuloma 22 0.028
892
c CHR036 Chronic Cholangitis 25 0.028
893
BLR002 Bile Reflux 31 0.028
894
PNM022 Pneumonia Caused by Pseudomonas Aeruginosa Infection 8 0.028
895
CRT049 Critical Limb Ischemia 51 0.028
896
DSS024 Disease of Anatomical Entity 40 0.028
897
ISC002 Ischemic Optic Neuropathy 45 0.028
898
PLM007 Pulmonary Aspergilloma 25 0.028
899
PLM062 Pulmonary Hyalinizing Granuloma 12 0.028
900
SKL007 Skeletal Muscle Regeneration 31 0.028
901
THL018 Thalassemia Major 31 0.028
902
P ART084 Arteriovenous Fistula 40 0.028
903
CHR413 Chronic Myocardial Ischemia 39 0.028
904
FBR012 Fabry Disease 68 0.024
905
P HNT016 Huntington Disease 80 0.024
906
PHN003 Phenylketonuria 71 0.024
907
ADN021 Adenomatous Polyposis Coli 71 0.024
908
P PSD087 Pseudoxanthoma Elasticum 65 0.024
909
GLC006 Galactosemia 64 0.024
910
EWN003 Ewing Sarcoma 63 0.024
911
c SPN225 Spondyloarthropathy 1 62 0.024
912
WLM001 Wolman Disease 55 0.024
913
IMG001 Image Syndrome 54 0.024
914
FCT007 Factor Vii Deficiency 60 0.024
915
ANM029 Anemia, Sideroblastic, X-Linked 53 0.024
916
CNT098 Central Core Disease 68 0.024
917
P CSH001 Cushing's Syndrome 65 0.024
918
MCR264 Mcardle Disease 57 0.024
919
c EHL057 Ehlers-Danlos Syndrome, Type Iv 59 0.024
920
c PSD095 Pseudohypoaldosteronism, Type I 50 0.024
921
WLL001 Williams-Beuren Syndrome 61 0.024
922
P WVR001 Weaver Syndrome 54 0.024
923
P OST012 Osteoarthritis 81 0.024
924
P LPR003 Leprosy 70 0.024
925
RBR001 Roberts Syndrome 61 0.024
926
P PLR004 Pleuropulmonary Blastoma 63 0.024
927
CNG368 Congenital Adrenal Hyperplasia 60 0.024
928
P PRD006 Prader-Willi Syndrome 64 0.024
929
ALS001 Alstrom Syndrome 52 0.024
930
URT039 Urticaria 58 0.024
931
LKC001 Leukocyte Adhesion Deficiency 65 0.024
932
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 42 0.024
933
P TRN020 Turner Syndrome 64 0.024
934
c CHL082 Cholestasis, Progressive Familial Intrahepatic 3 33 0.024
935
CRD119 Cardiac Arrest 63 0.024
936
P RTN008 Retinitis Pigmentosa 78 0.024
937
BLL003 Bell's Palsy 47 0.024
938
P SLV001 Silver-Russell Syndrome 54 0.024
939
FCT003 Factor X Deficiency 62 0.024
940
P SHR029 Short Syndrome 60 0.024
941
P EHL001 Ehlers-Danlos Syndrome 61 0.024
942
APP015 Apparent Mineralocorticoid Excess 50 0.024
943
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 32 0.024
944
c NRF018 Neurofibromatosis, Type 1 69 0.024
945
c CHL080 Cholestasis, Progressive Familial Intrahepatic 1 45 0.024
946
PRL019 Prolidase Deficiency 39 0.024
947
CMM004 Common Variable Immunodeficiency 68 0.024
948
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.024
949
P CNG015 Congenital Diaphragmatic Hernia 58 0.024
950
c SRF003 Surfactant Metabolism Dysfunction, Pulmonary, 2 30 0.024
951
CHL067 Cholecystitis 57 0.024
952
P ART023 Arthropathy 63 0.024
953
OVR029 Ovarian Hyperstimulation Syndrome 59 0.024
954
HYP251 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis 34 0.024
955
PRC002 Paracoccidioidomycosis 57 0.024
956
APH001 Aphthous Stomatitis 62 0.024
957
PPT005 Peptic Ulcer Disease 58 0.024
958
CRR007 Cirrhosis, Cryptogenic 38 0.024
959
OCL001 Ocular Albinism 46 0.024
960
MDY005 Mody, Type I 31 0.024
961
c MCK024 Meckel Syndrome 3 25 0.024
962
JJN004 Jejunal Atresia 31 0.024
963
ACT209 Acatalasemia 34 0.024
964
GRF001 Graft-Versus-Host Disease, Protection Against 54 0.024
965
CHR012 Chronic Granulomatous Disease 66 0.024
966
P HLP001 Holoprosencephaly 62 0.024
967
MDD011 Mood Disorder 60 0.024
968
QBC001 Quebec Platelet Disorder 51 0.024
969
ADR038 Adermatoglyphia 39 0.024
970
RBF001 Riboflavin Deficiency 45 0.024
971
IMM066 Immunodeficiency 9 30 0.024
972
FCL012 Facial Paralysis 50 0.024
973
c MCR115 Microvascular Complications of Diabetes 5 60 0.024
974
HPT077 Hepatic Venoocclusive Disease with Immunodeficiency 27 0.024
975
PLY023 Polycystic Liver Disease 57 0.024
976
CNG064 Congenital Chloride Diarrhea 34 0.024
977
OMN001 Omenn Syndrome 61 0.024
978
BRL010 Buruli Ulcer 47 0.024
979
OCL011 Ocular Motility Disease 41 0.024
980
PRS034 Parasitic Helminthiasis Infectious Disease 47 0.024
981
c CRD190 Cardiomyopathy, Hypertrophic, 2 29 0.024
982
OLV001 Olivopontocerebellar Atrophy 53 0.024
983
ALP008 Alopecia 56 0.024
984
MDY006 Mody, Type Iv 31 0.024
985
P CRB042 Cerebellar Ataxia 64 0.024
986
CYS019 Cystathioninuria 30 0.024
987
P EXD001 Exudative Vitreoretinopathy 48 0.024
988
c HRM006 Hermansky-Pudlak Syndrome 3 44 0.024
989
SPC010 Speech and Communication Disorders 42 0.024
990
TRP008 Tropical Calcific Pancreatitis 42 0.024
991
P ANP001 Anaplastic Large Cell Lymphoma 58 0.024
992
LYM017 Lyme Disease 64 0.024
993
P ENC008 Encephalocele 48 0.024
994
P HYP024 Hypoparathyroidism 52 0.024
995
c MCL040 Macular Degeneration, Age-Related, 3 31 0.024
996
c PRM005 Primary Hyperparathyroidism 56 0.024
997
PRR016 Pierre Robin Syndrome 50 0.024
998
P HRT035 Heart Block, Congenital 40 0.024
999
CYS002 Cystic Lymphangioma 45 0.024
1000
ACR002 Acrocapitofemoral Dysplasia 35 0.024
1001
PLR007 Pleural Empyema 45 0.024
1002
TRC097 Tracheomalacia 33 0.024
1003
c NPH053 Nephronophthisis 11 23 0.024
1004
c DYS150 Dyskeratosis Congenita, Autosomal Recessive 3 23 0.024
1005
P PRK001 Porokeratosis 45 0.024
1006
RDD003 Riddle Syndrome 42 0.024
1007
OST015 Osteochondrodysplasia 54 0.024
1008
DBT001 Diabetic Ketoacidosis 45 0.024
1009
MCL027 Macular Dystrophy, Dominant Cystoid 41 0.024
1010
PRX075 Proximal Myopathy and Ophthalmoplegia 33 0.024
1011
P HYP069 Hyperparathyroidism 57 0.024
1012
LYM008 Lymphangiosarcoma 48 0.024
1013
ENT006 Enterokinase Deficiency 23 0.024
1014
P CND004 Candidiasis 58 0.024
1015
PRT014 Protein S Deficiency 54 0.024
1016
c GLL024 Gallbladder Disease 1 34 0.024
1017
ASP001 Asperger Syndrome 49 0.024
1018
ACT058 Active Peptic Ulcer Disease 44 0.024
1019
CND002 Conduct Disorder 54 0.024
1020
c PNC095 Pancreatic Cancer 3 31 0.024
1021
P DBT005 Diabetes Insipidus 53 0.024
1022
c CNT035 Central Nervous System Disease 60 0.024
1023
VLV011 Vulvovaginal Candidiasis 47 0.024
1024
MMB001 Membranoproliferative Glomerulonephritis 44 0.024
1025
CLR096 Ciliary Dyskinesia, Primary, 1, with or Without Situs Inversus 35 0.024
1026
MDN008 Median Arcuate Ligament Syndrome 27 0.024
1027
OST017 Osteomyelitis 60 0.024
1028
RTN017 Retinal Detachment 58 0.024
1029
P SCL018 Scoliosis 56 0.024
1030
IMM071 Immunodeficiency 12 27 0.024
1031
LMT001 Limited Scleroderma 46 0.024
1032
P CRD132 Cardiac Conduction Defect 35 0.024
1033
CRP002 Croup 39 0.024
1034
CRR013 Cirrhosis, North American Indian Childhood Type 19 0.024
1035
CLL003 Cellulitis 49 0.024
1036
TRC003 Trichomoniasis 41 0.024
1037
GNG012 Gingival Overgrowth 52 0.024
1038
RLP001 Relapsing Polychondritis 52 0.024
1039
ANT018 Anthracosis 41 0.024
1040
RCT011 Rectal Prolapse 41 0.024
1041
P HYP083 Hypopituitarism 50 0.024
1042
LYM022 Lymphangioma 55 0.024
1043
TRC040 Tracheoesophageal Fistula 41 0.024
1044
MLT016 Multicentric Reticulohistiocytosis 46 0.024
1045
CRL004 Caroli Disease 40 0.024
1046
HND001 Hand Dermatosis 25 0.024
1047
P THR003 Thoracic Aortic Aneurysm 57 0.024
1048
LNS003 Lens Disease 37 0.024
1049
c HMG003 Hemoglobin E Disease 44 0.024
1050
P FML035 Familial Hyperlipidemia 49 0.024
1051
P SPN052 Spondyloarthropathy 58 0.024
1052
PYM001 Pyomyositis 39 0.024
1053
INT052 Intestinal Volvulus 32 0.024
1054
TRN044 Transposition of the Great Arteries 48 0.024
1055
ACR025 Acrocephalopolydactylous Dysplasia 20 0.024
1056