Search results for "fibrosis"

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

2544 hits were found for 'fibrosis'

# Family MCID Name MIFTS Score
1
CYS001 Cystic Fibrosis 83 7.467
2
PLM134 Pulmonary Fibrosis, Idiopathic 61 6.015
3
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 5.565
4
TKL001 Tukel Syndrome 34 5.456
5
P PLM036 Pulmonary Fibrosis 71 5.019
6
ORL004 Oral Submucous Fibrosis 51 4.895
7
END021 Endomyocardial Fibrosis 49 3.997
8
PKL002 Poikiloderma, Hereditary Fibrosing, with Tendon Contractures, Myopathy, and Pulmonary Fibrosis 24 3.988
9
RTR011 Retroperitoneal Fibrosis 39 3.830
10
CNG048 Congenital Hepatic Fibrosis 44 3.823
11
CCH002 Coach Syndrome 54 3.748
12
c FBR049 Fibrosis of Extraocular Muscles, Congenital, 3a 24 3.496
13
c FBR050 Fibrosis of Extraocular Muscles, Congenital, 2 23 3.496
14
RNL077 Renal Fibrosis 47 3.083
15
P FBR081 Fibrosis of Extraocular Muscles, Congenital, 3c 15 2.955
16
c FBR078 Fibrosis of Extraocular Muscles, Congenital, 5 13 2.951
17
FBR028 Fibrosing Mediastinitis 25 2.929
18
NPH018 Nephrogenic Systemic Fibrosis 51 2.802
19
DFF002 Diffuse Pulmonary Fibrosis 33 2.787
20
PLM139 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 1 27 2.675
21
PLM141 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 4 18 2.656
22
FBR089 Fibrosclerosis, Multifocal 16 2.633
23
EF001 Eaf 26 2.627
24
IDP011 Idiopathic Interstitial Pneumonia 56 2.597
25
CYS040 Cystic Fibrosis with Helicobacter Pylori Gastritis, Megaloblastic Anemia, and Mental Retardation 20 2.313
26
PST015 Postinflammatory Pulmonary Fibrosis 11 2.283
27
LBN005 Lubani-Al Saleh-Teebi Syndrome 6 2.277
28
c PLM044 Pulmonary Fibrosis, Familial 31 1.984
29
ACT029 Acute Interstitial Pneumonia 41 1.982
30
IGG007 Igg4-Related Disease 38 1.909
31
c LCL003 Localized Pulmonary Fibrosis 12 1.905
32
P APL001 Aplastic Anemia 75 1.897
33
PRR004 Preretinal Fibrosis 36 1.897
34
HRM018 Hermansky-Pudlak Syndrome with Pulmonary Fibrosis 23 1.897
35
PLM143 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 3 14 1.897
36
HRM016 Hermansky-Pudlak Syndrome Without Pulmonary Fibrosis 22 1.887
37
BRN075 Bronchiectasis with or Without Elevated Sweat Chloride 2 19 1.875
38
IMM129 Immunodeficiency, Ovarian Dysgenesis, and Pulmonary Fibrosis 15 1.875
39
MSC030 Muscular Fibrosis Multifocal Obstructed Vessels 10 1.875
40
FBR086 Fibrolamellar Carcinoma 45 1.853
41
ASB001 Asbestosis 42 1.423
42
TRP020 Tropical Endomyocardial Fibrosis 30 1.418
43
SLC006 Silicosis 53 1.403
44
P MYL005 Myelofibrosis 67 1.396
45
FML074 Familial Interstitial Fibrosis 7 1.370
46
ARW003 Airway-Centered Interstitial Fibrosis 7 1.370
47
IDP016 Idiopathic Diffuse Interstitial Fibrosis 8 1.365
48
c CNG189 Congenital Disorder of Glycosylation, Type Ib 33 1.350
49
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 7 1.350
50
BRN076 Bronchiectasis with or Without Elevated Sweat Chloride 1 29 1.338
51
BRN077 Bronchiectasis with or Without Elevated Sweat Chloride 3 17 1.338
52
CRB163 Cerebellar Vermis Aplasia with Associated Features Suggesting Smith-Lemli-Opitz Syndrome and Meckel Syndrome 16 1.338
53
PLM155 Pulmonary Fibrosis, Idiopathic Susceptibility 7 1.338
54
HPT029 Hepatic Fibrosis Renal Cysts Mental Retardation 3 1.338
55
c NTR031 Neutropenia, Severe Congenital, 5, Autosomal Recessive 28 1.330
56
CMP074 Camptodactyly, Myopia, and Fibrosis of the Medial Rectus Muscle of Eye 15 1.330
57
c CNG140 Congenital Fibrosis of the Extraocular Muscles 1a 6 1.330
58
c CNG141 Congenital Fibrosis of the Extraocular Muscles 1b 6 1.330
59
PLM145 Pulmonary Fibrosis-Hepatic Hyperplasia-Bone Marrow Hypoplasia Syndrome 6 1.330
60
c PHX001 Phox2a-Related Congenital Fibrosis of the Extraocular Muscles 5 1.330
61
c KF2001 Kif21a-Related Congenital Fibrosis of the Extraocular Muscles 5 1.330
62
c TBB003 Tubb3-Related Congenital Fibrosis of the Extraocular Muscles 5 1.330
63
c SFT006 Sftpc-Related Familial Pulmonary Fibrosis 4 1.330
64
c TRC066 Terc-Related Familial Pulmonary Fibrosis 4 1.330
65
c TRT009 Tert-Related Familial Pulmonary Fibrosis 4 1.330
66
FLL047 Follicular Hamartoma-Alopecia-Cystic Fibrosis Syndrome 3 1.330
67
CYS042 Cystic Fibrosis and Congenital Absence of the Vas Deferens 0 1.330
68
FBR016 Fibrosclerosis of Breast 24 1.322
69
DBT022 Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism 21 1.322
70
SNR014 Senior-Boichis Syndrome 13 1.322
71
RZN001 Rozin Hertz Goodman Syndrome 5 1.322
72
TYL001 Taylor's Syndrome 26 1.310
73
SCR009 Scirrhous Adenocarcinoma 21 1.310
74
GRP001 Graphite Pneumoconiosis 10 1.310
75
PLM113 Palmoplantar Keratoderma-Sclerodactyly Syndrome 9 1.310
76
P HPT021 Hepatitis 69 0.440
77
c PNC106 Pancreatic Agenesis 1 37 0.349
78
PNC034 Pancreas Disease 58 0.349
79
LNG099 Lung Disease 64 0.283
80
c HPT001 Hepatitis C 68 0.253
81
P PNM007 Pneumonia 68 0.243
82
P LVR013 Liver Disease 75 0.240
83
RSP006 Respiratory System Disease 58 0.207
84
P PNC044 Pancreatitis 61 0.204
85
INT066 Interstitial Lung Disease 59 0.203
86
BRN022 Bronchiectasis 50 0.202
87
URT010 Ureteral Obstruction 45 0.169
88
c HPT016 Hepatitis B 65 0.162
89
LVR012 Liver Cirrhosis 67 0.161
90
c HPT073 Hepatitis C Virus 73 0.160
91
P ASP006 Aspergillosis 61 0.159
92
P ALL008 Allergic Bronchopulmonary Aspergillosis 51 0.156
93
c VRL010 Viral Hepatitis 60 0.149
94
FTT001 Fatty Liver Disease 59 0.148
95
P CRD011 Cardiomyopathy 68 0.142
96
NNL002 Nonalcoholic Steatohepatitis 50 0.142
97
P KDN018 Kidney Disease 66 0.137
98
c HPT003 Hepatitis a 59 0.133
99
P HRT032 Heart Disease 75 0.131
100
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.127
101
PRM025 Primary Bacterial Infectious Disease 41 0.124
102
MCN017 Meconium Ileus 54 0.122
103
P RSP003 Respiratory Failure 71 0.120
104
GST050 Gastrointestinal System Disease 56 0.118
105
NSD001 Nose Disease 48 0.118
106
P PLM037 Pulmonary Hypertension 79 0.117
107
BRN038 Bronchial Disease 51 0.111
108
P AST005 Asthma 82 0.110
109
EXC002 Exocrine Pancreatic Insufficiency 43 0.109
110
P HPT023 Hepatocellular Carcinoma 92 0.103
111
P NNT009 Neonatal Diabetes Mellitus 52 0.103
112
NTR005 Nutritional Deficiency Disease 36 0.102
113
P PRT013 Portal Hypertension 60 0.100
114
P SPS003 Spastic Diplegia 52 0.100
115
END072 Endotheliitis 42 0.100
116
VSC018 Visceral Steatosis 37 0.094
117
SCH014 Schistosomiasis 58 0.092
118
CNN005 Connective Tissue Disease 62 0.089
119
UPP004 Upper Respiratory Tract Disease 46 0.086
120
P CHL066 Cholangitis 42 0.086
121
NNS002 Nonspecific Interstitial Pneumonia 45 0.085
122
MYC013 Mycobacterium Abscessus 41 0.085
123
P LNG032 Lung Cancer 95 0.084
124
P HRM001 Hermansky-Pudlak Syndrome 59 0.084
125
P THY032 Thyroiditis 54 0.084
126
P PLY014 Polycystic Kidney Disease 53 0.084
127
BLR001 Biliary Atresia 52 0.084
128
CNG034 Congestive Heart Failure 72 0.080
129
SQM006 Squamous Cell Carcinoma 70 0.080
130
SKN016 Skin Disease 66 0.080
131
ADM013 Adamantinoma of Long Bones 57 0.080
132
P OBS005 Obesity 92 0.079
133
PRT036 Peritonitis 63 0.079
134
P INF032 Infertility 59 0.078
135
CHL068 Cholestasis 59 0.078
136
CYS039 Cystic Kidney Disease 52 0.078
137
ACR041 Acromelic Frontonasal Dysostosis 45 0.078
138
P MSC005 Muscular Dystrophy 65 0.077
139
BRT030 Birth Defects 43 0.077
140
c DLT002 Dilated Cardiomyopathy 76 0.076
141
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.076
142
LPD004 Lipoid Nephrosis 48 0.076
143
P ATR011 Atrial Fibrillation 66 0.073
144
P SNS014 Sinusitis 60 0.073
145
BRN002 Bronchiolitis 56 0.073
146
VRL011 Viral Infectious Disease 55 0.073
147
MSC004 Muscle Tissue Disease 34 0.073
148
P ART022 Arthritis 75 0.072
149
HYP266 Hypoxia 56 0.072
150
P SCL009 Sclerosing Cholangitis 48 0.072
151
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 33 0.072
152
P ADN016 Adenocarcinoma 69 0.070
153
P INT070 Intestinal Obstruction 57 0.070
154
GLC003 Glucose Intolerance 55 0.070
155
P PRM006 Primary Biliary Cirrhosis 51 0.070
156
HYP006 Hypertensive Heart Disease 50 0.070
157
P LKM002 Leukemia 71 0.069
158
MDS022 Mediastinitis 41 0.069
159
c CRN214 Coronary Heart Disease 5 22 0.069
160
P LYM118 Lymphoma 69 0.068
161
P MYP004 Myopathy 67 0.068
162
P SYS005 Systemic Scleroderma 61 0.068
163
P GLM007 Glomerulonephritis 59 0.068
164
THR024 Thrombosis 57 0.068
165
EXT034 Extrinsic Allergic Alveolitis 55 0.068
166
VND001 Vein Disease 47 0.068
167
LKP003 Leukoplakia 38 0.068
168
MCS002 Mucositis 55 0.066
169
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 54 0.066
170
VNT001 Ventilation Pneumonitis 35 0.066
171
ATP002 Atopy 66 0.065
172
CTS003 Coats Disease 57 0.065
173
ANR040 Aneurysm 57 0.065
174
PRN021 Paranasal Sinus Disease 49 0.065
175
NNT004 Neonatal Respiratory Failure 37 0.065
176
P PNC035 Pancreatic Cancer 87 0.063
177
P HMC003 Hemochromatosis 72 0.063
178
MTH009 Mouth Disease 61 0.063
179
BRN012 Bronchiolitis Obliterans 58 0.063
180
PHR003 Pharyngitis 56 0.063
181
PLM034 Pulmonary Emphysema 55 0.063
182
ATR060 Atrial Standstill, Digenic 51 0.063
183
P PNM006 Pneumoconiosis 51 0.063
184
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.063
185
BLD053 Blood Platelet Disease 46 0.063
186
P FTT008 Fatty Liver Disease, Nonalcoholic 1 30 0.063
187
c TRC078 Trichohepatoenteric Syndrome 2 29 0.063
188
HPD002 Hepadnavirus Infection 22 0.063
189
c FTT007 Fatty Liver Disease, Nonalcoholic 2 16 0.063
190
P MYC007 Myocardial Infarction 79 0.062
191
c HYP595 Hypertension, Essential 69 0.062
192
BRN024 Bronchitis 64 0.062
193
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.062
194
ORL011 Oral Cancer 56 0.062
195
STM006 Stomach Disease 50 0.062
196
ALR002 Al-Raqad Syndrome 36 0.062
197
P CRN178 Coronary Heart Disease 6 21 0.062
198
c RNL016 Renal Infectious Disease 20 0.062
199
P RHM011 Rheumatoid Arthritis 89 0.060
200
ISC004 Ischemia 61 0.060
201
ORL015 Oral Squamous Cell Carcinoma 57 0.060
202
P PRM011 Primary Ciliary Dyskinesia 57 0.060
203
P NPH005 Nephronophthisis 55 0.060
204
NWC001 Newcastle Disease 54 0.060
205
c HPT015 Hepatitis D 52 0.060
206
SKN027 Skin Conditions 43 0.060
207
LKC003 Leukocyte Disease 43 0.060
208
NSL022 Nasal Cavity Disease 38 0.060
209
ADJ001 Adjustment Disorder 38 0.060
210
SPC003 Specific Developmental Disorder 38 0.060
211
P INF038 Influenza 72 0.059
212
PCK002 Pick Disease 68 0.059
213
CLT003 Colitis 60 0.059
214
CHL071 Child Syndrome 58 0.059
215
KDS001 Kid Syndrome 53 0.059
216
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.059
217
INC022 Inclusion-Cell Disease 46 0.059
218
STT004 Steatorrhea 40 0.059
219
c AST039 Asthma 2 28 0.059
220
CRH001 Crohn's Disease 75 0.057
221
WLS001 Wilson Disease 72 0.057
222
ACQ007 Acquired Immunodeficiency Syndrome 60 0.057
223
PLM012 Pulmonary Sarcoidosis 54 0.057
224
P MSC033 Muscle Disorders 52 0.057
225
P TRC086 Trichohepatoenteric Syndrome 1 48 0.057
226
SKN023 Skin Tag 44 0.057
227
SPL018 Splenomegaly 44 0.057
228
PHY002 Physical Disorder 43 0.057
229
c AST037 Asthma 1 29 0.057
230
MCC011 Mucociliary Clearance Disorder 16 0.057
231
ATH003 Atherosclerosis 65 0.055
232
P ESP024 Esophagitis 61 0.055
233
HYP066 Hyperglycemia 61 0.055
234
ART017 Aortic Disease 57 0.055
235
P MYC008 Myocarditis 54 0.055
236
MCR088 Microscopic Polyangiitis 49 0.055
237
ORL012 Oral Leukoplakia 46 0.055
238
ACD009 Acid-Labile Subunit, Deficiency of 45 0.055
239
CNG035 Congenital Bilateral Absence of Vas Deferens 36 0.055
240
DCH001 Duchenne Muscular Dystrophy 79 0.053
241
P HYP098 Hypereosinophilic Syndrome 63 0.053
242
GST092 Gastroesophageal Reflux 62 0.053
243
ALC006 Alcoholic Hepatitis 59 0.053
244
ALL026 Allergic Hypersensitivity Disease 52 0.053
245
CSY001 C Syndrome 50 0.053
246
MVM001 Movement Disease 49 0.053
247
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.053
248
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.053
249
P LPS004 Lupus Erythematosus 64 0.052
250
c ATS347 Autosomal Dominant Polycystic Kidney Disease 63 0.052
251
VSC011 Vasculitis 62 0.052
252
c ATM011 Autoimmune Hepatitis 60 0.052
253
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.052
254
PNM008 Pneumothorax 53 0.052
255
KRT002 Keratomalacia 52 0.052
256
SXL003 Sexual Disorder 42 0.052
257
DFF003 Diffuse Scleroderma 41 0.052
258
END038 Endocrine Pancreas Disease 41 0.052
259
HRT012 Heart Valve Disease 40 0.052
260
c CHR096 Chronic Pulmonary Heart Disease 40 0.052
261
BNS002 Bone Structure Disease 37 0.052
262
IMP003 Impaired Renal Function Disease 34 0.052
263
RDT005 Radiation Induced Cancer 28 0.052
264
CHL079 Children's Interstitial Lung Disease 18 0.052
265
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.050
266
INS024 Insulin-Like Growth Factor I 75 0.050
267
TBR010 Tuberculosis 70 0.050
268
c CHR089 Chronic Kidney Failure 66 0.050
269
PRM097 Primary Immunodeficiency Disease 60 0.050
270
c ACT210 Acute Respiratory Distress Syndrome 57 0.050
271
BRN106 Burns 52 0.050
272
PRC012 Pericardial Effusion 51 0.050
273
ALC009 Alcoholic Liver Cirrhosis 49 0.050
274
c ATM024 Autoimmune Pancreatitis 47 0.050
275
DST006 Diastolic Heart Failure 46 0.050
276
GLC008 Glucose Metabolism Disease 42 0.050
277
AYM001 Ayme-Gripp Syndrome 41 0.050
278
WTH001 Withdrawal Disorder 37 0.050
279
c CRN177 Coronary Heart Disease 7 20 0.050
280
c CRN175 Coronary Heart Disease 4 19 0.050
281
c SYS001 Systemic Lupus Erythematosus 86 0.048
282
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.048
283
ART016 Aortic Aneurysm 69 0.048
284
PRP027 Peripheral Vascular Disease 69 0.048
285
P OST002 Osteoporosis 64 0.048
286
P ATX004 Ataxia 53 0.048
287
RTN023 Retinitis 50 0.048
288
URN009 Urinary System Disease 50 0.048
289
P PLM006 Pulmonary Alveolar Proteinosis 48 0.048
290
DFF035 Diffuse Cutaneous Systemic Sclerosis 45 0.048
291
ALN001 Aland Island Eye Disease 45 0.048
292
c MTR002 Mitral Valve Insufficiency 44 0.048
293
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.048
294
DDN006 Duodenitis 42 0.048
295
c CRN172 Coronary Heart Disease 3 19 0.048
296
P BRS047 Breast Cancer 100 0.046
297
ANX002 Anxiety Disorder 67 0.046
298
VSC007 Vascular Disease 67 0.046
299
BRC012 Brucellosis 66 0.046
300
P THL005 Thalassemia 64 0.046
301
P THR014 Thrombocytopenia 64 0.046
302
P DRM010 Dermatomyositis 62 0.046
303
P LYM025 Lymphedema 61 0.046
304
LPD008 Lipid Metabolism Disorder 58 0.046
305
P MSC007 Muscle Hypertrophy 58 0.046
306
c ACT027 Acute Pancreatitis 57 0.046
307
SLP005 Sleep Disorder 53 0.046
308
PRC013 Pericarditis 51 0.046
309
P URF003 Urofacial Syndrome 1 50 0.046
310
HMS001 Hemosiderosis 46 0.046
311
BLD054 Blood Protein Disease 37 0.046
312
ACR005 Acrodermatitis 36 0.046
313
P HRT017 Heart Tumor 32 0.046
314
c ADL096 Adult Hepatocellular Carcinoma 24 0.046
315
PLM015 Pulmonary Systemic Sclerosis 23 0.046
316
GST053 Gastric Cancer 78 0.044
317
DRM006 Dermatitis 66 0.044
318
ALL006 Allergic Asthma 58 0.044
319
P MTR012 Mitral Valve Disease 58 0.044
320
PRS047 Prostatitis 56 0.044
321
c ART101 Aortic Valve Disease 2 53 0.044
322
BLR006 Biliary Tract Disease 52 0.044
323
P STR020 Strabismus 51 0.044
324
CRN030 Coronary Stenosis 51 0.044
325
c ACT068 Acute Cystitis 50 0.044
326
ACR003 Acrodermatitis Enteropathica 49 0.044
327
c INH020 Inherited Metabolic Disorder 49 0.044
328
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.044
329
HRT007 Heart Cancer 46 0.044
330
P SDR002 Siderosis 44 0.044
331
PRT019 Protein-Losing Enteropathy 42 0.044
332
URT001 Urethritis 41 0.044
333
P ACT080 Acute Pulmonary Heart Disease 31 0.044
334
c HMG004 Hemoglobin D Disease 31 0.044
335
ENT007 Enteropathica 31 0.044
336
SNG003 Single Ventricular Heart 22 0.044
337
CNG039 Congenital Absence of the Vas Deferens 22 0.044
338
c CRN174 Coronary Heart Disease 2 20 0.044
339
AND005 Androgen Insensitivity Syndrome, Mild 16 0.044
340
P CRN211 Coronary Artery Disease 74 0.041
341
MYL009 Myelodysplastic Syndrome 73 0.041
342
TTR001 Tetralogy of Fallot 71 0.041
343
P HYP086 Hypothyroidism 64 0.041
344
P INF037 Inflammatory Bowel Disease 63 0.041
345
P RCK004 Rickets 61 0.041
346
EYD002 Eye Disease 61 0.041
347
ETH011 Ethylmalonic Encephalopathy 56 0.041
348
NRM005 Neuromuscular Disease 56 0.041
349
END030 End Stage Renal Failure 55 0.041
350
P MCR129 Microvascular Complications of Diabetes 1 54 0.041
351
c HPT007 Hepatitis E 54 0.041
352
P END033 Endocarditis 54 0.041
353
ADL002 Adult Syndrome 52 0.041
354
P HYP065 Hyperaldosteronism 50 0.041
355
HPT009 Hepatopulmonary Syndrome 48 0.041
356
ALB002 Albinism 46 0.041
357
STS002 Situs Inversus 46 0.041
358
CHR008 Choroiditis 44 0.041
359
ATS010 Autosomal Recessive Disease 41 0.041
360
PNC028 Pancreatic Steatorrhea 34 0.041
361
ANG049 Angioedema Induced by Ace Inhibitors 34 0.041
362
ART012 Aortitis 30 0.041
363
VTM003 Vitamin Metabolic Disorder 30 0.041
364
c PLM127 Pulmonary Hypertension, Primary, 3 28 0.041
365
c ADL079 Adult Heart Tumor 16 0.041
366
HRP008 Herpes Simiae 12 0.041
367
NNT002 Neonatal Urinary Tract Infectious Disease 11 0.041
368
HRP012 Herpesvirus Simiae B Virus 10 0.041
369
BCK001 Becker Muscular Dystrophy 69 0.039
370
P DYS007 Dyskeratosis Congenita 63 0.039
371
P INT068 Intestinal Disease 60 0.039
372
P DRR001 Diarrhea 60 0.039
373
P GLL020 Gallbladder Disease 59 0.039
374
PLY022 Polycystic Kidney and Hepatic Disease 58 0.039
375
P CMR001 Camurati-Engelmann Disease 58 0.039
376
CHY002 Chylomicron Retention Disease 57 0.039
377
P MMB011 Membranous Nephropathy 54 0.039
378
P PLY041 Polymyositis 52 0.039
379
ERD001 Erdheim-Chester Disease 52 0.039
380
LYM024 Lymphatic System Disease 52 0.039
381
ART002 Arts Syndrome 51 0.039
382
RHM028 Rheumatic Heart Disease 50 0.039
383
P RNL015 Renal Hypertension 48 0.039
384
HYD002 Hydronephrosis 47 0.039
385
CRB025 Carbohydrate Metabolic Disorder 46 0.039
386
CRY004 Cryoglobulinemia 46 0.039
387
P ABD003 Abdominal Aortic Aneurysm 45 0.039
388
HRT015 Heritable Pulmonary Arterial Hypertension 45 0.039
389
AZS001 Azoospermia 44 0.039
390
CRR007 Cirrhosis, Cryptogenic 43 0.039
391
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.039
392
c ATM022 Autoimmune Myocarditis 42 0.039
393
c RCR022 Recurrent Acute Pancreatitis 41 0.039
394
PRP080 Peripheral Artery Disease 37 0.039
395
DVL001 Developmental Coordination Disorder 36 0.039
396
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.039
397
SPR035 Superior Vena Cava Syndrome 31 0.039
398
c PNC111 Pancreatic Cancer 2 28 0.039
399
c PNC094 Pancreatic Cancer 1 27 0.039
400
c CRN173 Coronary Heart Disease 8 18 0.039
401
ORL014 Oral Pharyngeal Disorders 11 0.039
402
P RNL014 Renal Cell Carcinoma 82 0.037
403
P TYS001 Tay-Sachs Disease 71 0.037
404
ISC006 Ischemic Heart Disease 68 0.037
405
DWN001 Down Syndrome 66 0.037
406
P AMY004 Amyloidosis 65 0.037
407
DFC004 Deficiency Anemia 64 0.037
408
MXD005 Mixed Connective Tissue Disease 62 0.037
409
P GCH001 Gaucher's Disease 62 0.037
410
c ACT075 Acute Myocardial Infarction 60 0.037
411
OCL009 Ocular Cancer 59 0.037
412
MRB003 Morbid Obesity 59 0.037
413
EMP007 Emphysema Due to Aat Deficiency 58 0.037
414
P MYS005 Myositis 57 0.037
415
ESP023 Esophageal Disease 54 0.037
416
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.037
417
TTH006 Tooth Disease 52 0.037
418
P PYL005 Pyelonephritis 52 0.037
419
HMG005 Hemoglobinopathy 52 0.037
420
PRT011 Protein C Deficiency 52 0.037
421
SCK005 Sickle Cell Disease 51 0.037
422
P RST002 Restrictive Cardiomyopathy 50 0.037
423
P MSC003 Muscular Atrophy 50 0.037
424
P CHR345 Chronic Pain 50 0.037
425
P CLL015 Collagen Disease 50 0.037
426
c ACT071 Acute Kidney Failure 49 0.037
427
SLD003 Sialadenitis 49 0.037
428
CHR001 Churg-Strauss Syndrome 49 0.037
429
DYS073 Dysphagia 48 0.037
430
AMN002 Amino Acid Metabolic Disorder 47 0.037
431
SPL012 Splenic Disease 46 0.037
432
P CRV039 Cervicitis 45 0.037
433
HMP009 Haemophilus Influenzae 45 0.037
434
CRY001 Cryptogenic Organizing Pneumonia 44 0.037
435
BNN003 Bone Inflammation Disease 44 0.037
436
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.037
437
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.037
438
CHL052 Choledochal Cyst 41 0.037
439
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.037
440
c HYP058 Hypervitaminosis a 39 0.037
441
RHM009 Rheumatoid Lung Disease 38 0.037
442
ALC005 Alcoholic Pancreatitis 36 0.037
443
ATS009 Autosomal Genetic Disease 35 0.037
444
LYM023 Lymphatic System Cancer 33 0.037
445
GLB003 Globe Disease 32 0.037
446
MLT035 Multifocal Choroiditis 32 0.037
447
INT304 Interstitial Pneumonitis, Desquamative, Familial 31 0.037
448
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.037
449
IMM090 Immunodeficiency 27a, Mycobacteriosis, Ar 26 0.037
450
PRQ002 Paraquat Poisoning 25 0.037
451
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.037
452
STN013 Stenotrophomonas Maltophilia Infection 20 0.037
453
LBR003 Labrador Lung 13 0.037
454
INB001 Inborn Amino Acid Metabolism Disorder 12 0.037
455
MLR004 Malaria 83 0.034
456
HV1006 Hiv-1 80 0.034
457
HDG012 Hodgkin Lymphoma 77 0.034
458
PLM001 Pulmonary Tuberculosis 67 0.034
459
CHG001 Chagas Disease 67 0.034
460
OBS061 Obstructive Sleep Apnea 66 0.034
461
SRC014 Sarcoma 66 0.034
462
P HML002 Hemolytic Anemia 62 0.034
463
P SLP006 Sleep Apnea 61 0.034
464
c SRC025 Sarcoidosis 1 61 0.034
465
P NRP001 Neuropathy 59 0.034
466
P NPH012 Nephrotic Syndrome 59 0.034
467
WLL006 Wells Syndrome 59 0.034
468
P UVT001 Uveitis 58 0.034
469
CNS004 Constipation 57 0.034
470
ART111 Artery Disease 55 0.034
471
MLN007 Male Infertility 55 0.034
472
P OCL002 Oculocutaneous Albinism 54 0.034
473
P MCK022 Meckel Syndrome 1 54 0.034
474
CRC006 Carcinoid Syndrome 52 0.034
475
KLD001 Keloids 51 0.034
476
SPN051 Spondylitis 51 0.034
477
NDL013 Nodular Regenerative Hyperplasia 50 0.034
478
c ART115 Aortic Valve Disease 1 50 0.034
479
GRW007 Growth Hormone Deficiency 50 0.034
480
PMP001 Pemphigus 50 0.034
481
HPT074 Hepatic Adenoma, Somatic 50 0.034
482
LRN003 Learning Disability 49 0.034
483
NPH003 Nephrocalcinosis 48 0.034
484
PRM236 Primary Biliary Cholangitis 47 0.034
485
MGC001 Megacolon 45 0.034
486
RNL078 Renal Dysplasia 45 0.034
487
P RPD001 Rapidly Progressive Glomerulonephritis 45 0.034
488
GDS001 Good Syndrome 44 0.034
489
P PLM085 Pulmonary Hemosiderosis 44 0.034
490
P SKN013 Skin Benign Neoplasm 43 0.034
491
PRD004 Prediabetes Syndrome 43 0.034
492
BCK006 Back Pain 43 0.034
493
HPT020 Hepatic Vascular Disease 42 0.034
494
IMM001 Immune-Complex Glomerulonephritis 42 0.034
495
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.034
496
NRN002 Neuronitis 41 0.034
497
CHR078 Chorioretinitis 40 0.034
498
CRB009 Cerebritis 39 0.034
499
MCN008 Mucinous Cystadenocarcinoma 39 0.034
500
HYP540 Hypertension, Diastolic 39 0.034
501
NSY001 N Syndrome 36 0.034
502
SWT003 Sweat Gland Disease 34 0.034
503
c SRC023 Sarcoidosis 2 33 0.034
504
c DYS143 Dyskeratosis Congenita, Autosomal Dominant 2 27 0.034
505
PLM124 Pulmonary Hypertension, Neonatal 22 0.034
506
IDP075 Idiopathic and/or Familial Pulmonary Arterial Hypertension 11 0.034
507
CRN073 Coronary Arteries Congenital Malformation 10 0.034
508
P PRS040 Prostate Cancer 90 0.031
509
ULC004 Ulcerative Colitis 76 0.031
510
P RTN024 Retinoblastoma 74 0.031
511
SCK003 Sickle Cell Anemia 71 0.031
512
P ESS003 Essential Thrombocythemia 70 0.031
513
MLD001 Melioidosis 67 0.031
514
P MYL006 Myeloid Leukemia 66 0.031
515
P BCL006 B-Cell Lymphomas 65 0.031
516
PNC041 Pancreatic Ductal Adenocarcinoma 64 0.031
517
P PRD008 Periodontitis 63 0.031
518
GNG013 Gingivitis 61 0.031
519
P NPH009 Nephrolithiasis 60 0.031
520
GLB001 Gilbert Syndrome 60 0.031
521
P GRV001 Graves' Disease 59 0.031
522
P ENC018 Encephalopathy 59 0.031
523
P ALC004 Alcohol Abuse 59 0.031
524
DFF005 Diffuse Large B-Cell Lymphoma 59 0.031
525
CMM005 Common Cold 59 0.031
526
MYL031 Myeloproliferative Neoplasm 58 0.031
527
ART021 Arteriosclerosis 58 0.031
528
ETN001 Eating Disorder 58 0.031
529
ADN018 Adenoma 58 0.031
530
P HST010 Histiocytosis 58 0.031
531
HRY003 Hairy Cell Leukemia 57 0.031
532
P HMR003 Hemorrhagic Disease 57 0.031
533
P RTN016 Retinal Degeneration 54 0.031
534
FLR002 Filariasis 54 0.031
535
VRR004 Verrucous Carcinoma 54 0.031
536
PYR010 Peyronie's Disease 53 0.031
537
RTN018 Retinal Disease 53 0.031
538
CHL014 Cholera 53 0.031
539
MNT002 Mental Depression 53 0.031
540
CYT008 Cytomegalovirus Infection 52 0.031
541
P PTS002 Ptosis 51 0.031
542
c CHR417 Chronic Graft Versus Host Disease 51 0.031
543
P PLY017 Polyarteritis Nodosa 51 0.031
544
INT051 Intussusception 50 0.031
545
BNF002 Bone Fracture 50 0.031
546
c ACT134 Acute Liver Failure 50 0.031
547
HYP063 Hypersplenism 48 0.031
548
URM002 Uremia 48 0.031
549
ATN002 Autonomic Nervous System Disease 48 0.031
550
P NGH001 Night Blindness 48 0.031
551
FML039 Female Reproductive System Disease 48 0.031
552
BLD036 Bile Duct Disease 48 0.031
553
c HMG001 Hemoglobin C Disease 47 0.031
554
PRT030 Parathyroid Gland Disease 47 0.031
555
SDD007 Sudden Cardiac Death 47 0.031
556
CYS014 Cystadenocarcinoma 47 0.031
557
HYD005 Hydrocele 46 0.031
558
BRN014 Bronchopneumonia 45 0.031
559
CRD118 Cardiovascular Cancer 44 0.031
560
SYS003 Systolic Heart Failure 43 0.031
561
P PRL003 Proliferative Glomerulonephritis 43 0.031
562
NNT049 Nontuberculous Mycobacterial Lung Disease 43 0.031
563
P BLD051 Blood Coagulation Disease 42 0.031
564
c VRL005 Viral Pneumonia 42 0.031
565
PRD011 Proud Syndrome 42 0.031
566
MDL009 Medullary Sponge Kidney 41 0.031
567
RPR002 Reproductive System Disease 41 0.031
568
ACT084 Acute Stress Disorder 40 0.031
569
ADT003 Auditory System Disease 40 0.031
570
c HRM017 Hermansky-Pudlak Syndrome 2 39 0.031
571
CLL021 Collagenous Colitis 39 0.031
572
BNR001 Bone Remodeling Disease 37 0.031
573
WRN005 Wrinkles 37 0.031
574
CPL005 Capillary Disease 36 0.031
575
FXF002 Fox-Fordyce Disease 36 0.031
576
DRM009 Dermatomycosis 35 0.031
577
CNS002 Constrictive Pericarditis 34 0.031
578
KSH001 Keshan Disease 33 0.031
579
SWL001 Swallowing Disorders 33 0.031
580
c DYS149 Dyskeratosis Congenita, Autosomal Recessive 1 33 0.031
581
DDN009 Duodenal Obstruction 32 0.031
582
FNC006 Functional Gastric Disease 32 0.031
583
SKL007 Skeletal Muscle Regeneration 32 0.031
584
CVT001 Cavitary Optic Disc Anomalies 31 0.031
585
VSC008 Vascular Hemostatic Disease 30 0.031
586
c PNC103 Pancreatic Cancer 4 29 0.031
587
c MYC058 Myocardial Infarction 2 28 0.031
588
HNM002 Hinman Syndrome 25 0.031
589
ATM052 Autoimmune Disease 1 25 0.031
590
MTR031 Motor Neuro-Ophthalmic Disorders 19 0.031
591
c CRN176 Coronary Heart Disease 9 18 0.031
592
CFT001 Cftr-Related Disorders 14 0.031
593
IGG011 Igg4-Related Kidney Disease 13 0.031
594
P OST012 Osteoarthritis 83 0.028
595
P HNT016 Huntington Disease 80 0.028
596
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.028
597
P ATX030 Ataxia-Telangiectasia 77 0.028
598
c MCL042 Macular Degeneration, Age-Related, 1 73 0.028
599
P CLC005 Celiac Disease 68 0.028
600
P MNN013 Meningitis 67 0.028
601
P END044 Endometriosis 66 0.028
602
P LYM007 Lymphangioleiomyomatosis 66 0.028
603
P TRN020 Turner Syndrome 65 0.028
604
P KDN017 Kidney Cancer 65 0.028
605
P AGM001 Agammaglobulinemia 64 0.028
606
P ANR002 Aniridia 64 0.028
607
MLN008 Melanoma 62 0.028
608
P LNG064 Lung Cancer Susceptibility 3 62 0.028
609
P LYM026 Lymphoblastic Leukemia 62 0.028
610
ACN011 Acne 62 0.028
611
P CRD194 Cardiomyopathy, Familial Hypertrophic 62 0.028
612
HYP056 Hypoglycemia 61 0.028
613
SHW002 Shwachman-Diamond Syndrome 61 0.028
614
c LCL006 Localized Scleroderma 61 0.028
615
HPY002 H. Pylori Infection 61 0.028
616
PLM033 Pulmonary Embolism 60 0.028
617
P NRV006 Nervous System Cancer 60 0.028
618
P GST049 Gastrointestinal System Cancer 60 0.028
619
P GLY013 Glycogen Storage Disease 60 0.028
620
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.028
621
P ORL007 Oral Cavity Cancer 59 0.028
622
P HMN010 Hemangioma 59 0.028
623
c FML001 Familial Atrial Fibrillation 58 0.028
624
P HYP060 Hyperinsulinism 58 0.028
625
P EXN002 Exanthem 57 0.028
626
NRN004 Neuroendocrine Tumor 56 0.028
627
INT079 Intrahepatic Cholangiocarcinoma 56 0.028
628
BLD034 Bile Duct Carcinoma 56 0.028
629
PRP019 Peripheral Nervous System Disease 55 0.028
630
THR004 Thrombocytosis 55 0.028
631
PPL022 Papilloma 55 0.028
632
ECH003 Echinococcosis 54 0.028
633
c THR092 Thrombophilia Due to Thrombin Defect 54 0.028
634
GST037 Gastroparesis 54 0.028
635
SBS003 Substance Abuse 54 0.028
636
FRB001 Farber Lipogranulomatosis 53 0.028
637
END040 Endogenous Depression 53 0.028
638
P DBT005 Diabetes Insipidus 53 0.028
639
CYS010 Cystinosis 53 0.028
640
DSS008 Disease of Mental Health 52 0.028
641
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.028
642
c INF023 Inflammatory Breast Carcinoma 52 0.028
643
PNN001 Panniculitis 51 0.028
644
VSC006 Vascular Cancer 51 0.028
645
GNR004 Generalized Anxiety Disorder 51 0.028
646
INT007 Intermediate Coronary Syndrome 50 0.028
647
HYP037 Hyperhomocysteinemia 50 0.028
648
c HRM005 Hermansky-Pudlak Syndrome 1 49 0.028
649
P SHR001 Short Bowel Syndrome 49 0.028
650
PRT038 Protein-Energy Malnutrition 49 0.028
651
ATN005 Autonomic Dysfunction 49 0.028
652
MSS002 Mass Syndrome 48 0.028
653
MDD010 Middle Ear Disease 48 0.028
654
FSC004 Fasciitis 48 0.028
655
THL018 Thalassemia Major 48 0.028
656
c CNG027 Congenital Hemolytic Anemia 48 0.028
657
P RNV001 Renovascular Hypertension 47 0.028
658
c INV001 Invasive Aspergillosis 47 0.028
659
LPM005 Lipomatosis 47 0.028
660
MLT016 Multicentric Reticulohistiocytosis 46 0.028
661
ART004 Aortic Atherosclerosis 46 0.028
662
c MLG002 Malignant Peritoneal Mesothelioma 46 0.028
663
INT067 Interstitial Nephritis 46 0.028
664
PRP007 Priapism 46 0.028
665
KRT010 Kartagener Syndrome 45 0.028
666
HYP457 Hypertrophic Scars 45 0.028
667
P PSD003 Pseudohypoaldosteronism 44 0.028
668
RNL097 Renal Artery Disease 43 0.028
669
FBR003 Fibrous Histiocytoma 43 0.028
670
P CRD132 Cardiac Conduction Defect 43 0.028
671
SPC010 Speech and Communication Disorders 41 0.028
672
CHR413 Chronic Myocardial Ischemia 41 0.028
673
ARC002 Arachnoiditis 41 0.028
674
CNV002 Conversion Disorder 41 0.028
675
KWS001 Kwashiorkor 40 0.028
676
ACT055 Actinomycosis 40 0.028
677
PGM003 Pigmentation Disease 39 0.028
678
P MXL015 Maxillary Sinusitis 38 0.028
679
SXD001 Sex Differentiation Disease 38 0.028
680
EXT006 Extrahepatic Cholestasis 37 0.028
681
PNC002 Pancreatic Mucinous Cystadenoma 36 0.028
682
SCR003 Secretory Diarrhea 36 0.028
683
MYX004 Myxedema 35 0.028
684
RDN001 Reading Disorder 34 0.028
685
XRP001 Xerophthalmia 33 0.028
686
LNS003 Lens Disease 33 0.028
687
c CNN010 Connective Tissue Benign Neoplasm 32 0.028
688
c MCL043 Macular Degeneration, Age-Related, 2 32 0.028
689
GST039 Gastroduodenitis 31 0.028
690
CYT004 Cytomegalic Inclusion Disease 31 0.028
691
c HRM007 Hermansky-Pudlak Syndrome 4 31 0.028
692
EYD001 Eye Degenerative Disease 30 0.028
693
MRG013 Mirage Syndrome 29 0.028
694
c HYP555 Hypertriglyceridemia, Transient Infantile 29 0.028
695
HMC038 Hemochromatosis, Neonatal 29 0.028
696
c SCL052 Scleroderma, Familial Progressive 27 0.028
697
IMM071 Immunodeficiency 12 26 0.028
698
c DYS152 Dyskeratosis Congenita, Autosomal Recessive 5 26 0.028
699
P MCL035 Macular Dystrophy, Retinal, 2 25 0.028
700
c DYS147 Dyskeratosis Congenita, Autosomal Dominant 3 24 0.028
701
EYC003 Eye Accommodation Disease 24 0.028
702
HND001 Hand Dermatosis 23 0.028
703
c MLT093 Multiple Sclerosis 2 18 0.028
704
BRW002 Brown's Tendon Sheath Syndrome 16 0.028
705
BNM008 Bone Mineral Density, Low 16 0.028
706
PNM022 Pneumonia Caused by Pseudomonas Aeruginosa Infection 10 0.028
707
P OVR042 Ovarian Cancer 76 0.024
708
MRF001 Marfan Syndrome 73 0.024
709
P NRF002 Neurofibromatosis 71 0.024
710
KWS002 Kawasaki Disease 70 0.024
711
P FLL037 Follicular Lymphoma 70 0.024
712
FBR012 Fabry Disease 69 0.024
713
P ALP004 Alport Syndrome 69 0.024
714
SVR004 Severe Combined Immunodeficiency 69 0.024
715
CMM004 Common Variable Immunodeficiency 68 0.024
716
CRV047 Cervical Cancer, Somatic 65 0.024
717
P CSH001 Cushing's Syndrome 65 0.024
718
P NMN002 Niemann-Pick Disease 65 0.024
719
CNT098 Central Core Disease 65 0.024
720
P SPN046 Spinal Muscular Atrophy 65 0.024
721
P ART023 Arthropathy 64 0.024
722
HMT002 Hematologic Cancer 64 0.024
723
ALL003 Allergic Rhinitis 63 0.024
724
CNT047 Contact Dermatitis 61 0.024
725
P PSR002 Psoriasis 61 0.024
726
P ADL010 Adult Respiratory Distress Syndrome 61 0.024
727
P HYP117 Hypertriglyceridemia 61 0.024
728
BRS051 Breast Disease 61 0.024
729
MDD011 Mood Disorder 61 0.024
730
c JBR020 Joubert Syndrome 1 60 0.024
731
c CNG006 Congenital Hypothyroidism 60 0.024
732
P CNG015 Congenital Diaphragmatic Hernia 60 0.024
733
WLL001 Williams-Beuren Syndrome 60 0.024
734
P RHN004 Rhinitis 60 0.024
735
RBR001 Roberts Syndrome 60 0.024
736
SPT004 Septic Arthritis 60 0.024
737
CRV038 Cervical Squamous Cell Carcinoma 60 0.024
738
P THR015 Thrombophilia 59 0.024
739
c RHM021 Rheumatoid Arthritis, Systemic Juvenile 59 0.024
740
ADL030 Adult-Onset Still's Disease 59 0.024
741
LPR018 Leprechaunism 58 0.024
742
P SHR029 Short Syndrome 58 0.024
743
P CTR002 Cataract 58 0.024
744
P HYP069 Hyperparathyroidism 58 0.024
745
c PNC108 Pancreatitis, Hereditary 58 0.024
746
SYN007 Synovitis 58 0.024
747
ING001 Inguinal Hernia 58 0.024
748
P HMP007 Hemophilia 57 0.024
749
WLM001 Wolman Disease 57 0.024
750
CHL067 Cholecystitis 57 0.024
751
ALP008 Alopecia 57 0.024
752
SFT003 Soft Tissue Sarcoma 57 0.024
753
c SVR001 Severe Acute Respiratory Syndrome 57 0.024
754
P ANP001 Anaplastic Large Cell Lymphoma 57 0.024
755
P BCK002 Beckwith-Wiedemann Syndrome 56 0.024
756
P LYM033 Lymphoproliferative Syndrome 56 0.024
757
GST023 Gastric Ulcer 56 0.024
758
P ANT006 Antiphospholipid Syndrome 56 0.024
759
P LPD010 Lipodystrophy 55 0.024
760
HPT022 Hepatoblastoma 55 0.024
761
HDC001 Headache 54 0.024
762
c PND001 Pain Disorder 54 0.024
763
CND002 Conduct Disorder 54 0.024
764
P BRN009 Burning Mouth Syndrome 54 0.024
765
PST046 Post-Transplant Lymphoproliferative Disease 54 0.024
766
C3D001 C3 Deficiency 53 0.024
767
FDL002 Food Allergy 53 0.024
768
P EXP004 Exophthalmos 53 0.024
769
OLV001 Olivopontocerebellar Atrophy 53 0.024
770
ANG020 Angiosarcoma 53 0.024
771
ALS001 Alstrom Syndrome 53 0.024
772
P PNC001 Pancytopenia 52 0.024
773
ECT006 Ectodermal Dysplasia 52 0.024
774
HST011 Histoplasmosis 52 0.024
775
P PRT096 Peritoneal Mesothelioma 52 0.024
776
IRN001 Iron Deficiency Anemia 52 0.024
777
ANK001 Ankylosis 51 0.024
778
PLR022 Pleural Disease 51 0.024
779
P GND004 Gonadal Dysgenesis 51 0.024
780
P PMP005 Pemphigus Vulgaris 51 0.024
781
IMM136 Immune System Disease 51 0.024
782
TRY001 Trypanosomiasis 51 0.024
783
CLN019 Colonic Disease 51 0.024
784
P LFT003 Left Ventricular Noncompaction 50 0.024
785
ESN005 Eosinophilic Gastroenteritis 50 0.024
786
P DDN001 Duodenal Ulcer 50 0.024
787
FML038 Female Reproductive Organ Cancer 50 0.024
788
IMG001 Image Syndrome 50 0.024
789
FML037 Female Breast Cancer 50 0.024
790
PLR008 Pleurisy 50 0.024
791
OVR063 Overnutrition 50 0.024
792
MSC072 Muscle Cancer 49 0.024
793
BCL002 B Cell Deficiency 49 0.024
794
TRN044 Transposition of the Great Arteries 48 0.024
795
P CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 48 0.024
796
P FML035 Familial Hyperlipidemia 48 0.024
797
OBS001 Obstructive Jaundice 48 0.024
798
BCT015 Bacteremia 48 0.024
799
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.024
800
PSD007 Pseudomyxoma Peritonei 48 0.024
801
BRN056 Bronchopulmonary Dysplasia 48 0.024
802
PPL049 Papillon-Lefevre Syndrome 48 0.024
803
P RNL017 Renal Oncocytoma 47 0.024
804
ESN015 Eosinophilic Fasciitis 47 0.024
805
PRR002 Pure Red-Cell Aplasia 47 0.024
806
LMT001 Limited Scleroderma 46 0.024
807
PRP021 Peripheral Nervous System Neoplasm 46 0.024
808
CLC001 Calciphylaxis 46 0.024
809
DNT012 Dental Caries 46 0.024
810
c HRM006 Hermansky-Pudlak Syndrome 3 46 0.024
811
c CLL013 Cell Type Cancer 46 0.024
812
c CHL080 Cholestasis, Progressive Familial Intrahepatic 1 46 0.024
813
CRD137 Cardiogenic Shock 46 0.024
814
FLT011 Felty Syndrome 46 0.024
815
PLM035 Pulmonary Eosinophilia 46 0.024
816
PLM017 Pulmonary Alveolar Microlithiasis 46 0.024
817
INT017 Intestinal Schistosomiasis 45 0.024
818
c CHL082 Cholestasis, Progressive Familial Intrahepatic 3 45 0.024
819
MMM001 Mammary Paget's Disease 45 0.024
820
VSC047 Vascular Malformation 45 0.024
821
EBS001 Ebstein Anomaly 45 0.024
822
c ACT042 Acute Pyelonephritis 45 0.024
823
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.024
824
RGH009 Right Atrial Isomerism 44 0.024
825
P ART084 Arteriovenous Fistula 44 0.024
826
GRN017 Granulocytopenia 44 0.024
827
c CHL119 Cholangitis, Primary Sclerosing 44 0.024
828
c HMG003 Hemoglobin E Disease 44 0.024
829
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.024
830
NCR004 Nocardiosis 43 0.024
831
SNS023 Sensory System Cancer 43 0.024
832
c ACT076 Acute Myocarditis 42 0.024
833
SPS057 Spasticity 42 0.024
834
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.024
835
OCL001 Ocular Albinism 42 0.024
836
FSC002 Fascioliasis 42 0.024
837
DPH021 Diaphragm Disease 41 0.024
838
PRC003 Proctitis 41 0.024
839
c PRM023 Pre-Malignant Neoplasm 41 0.024
840
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.024
841
PRX075 Proximal Myopathy and Ophthalmoplegia 41 0.024
842
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.024
843
c PRG106 Progressive Muscular Dystrophy 40 0.024
844
P CNN004 Connective Tissue Cancer 40 0.024
845
HTS001 Hiatus Hernia 40 0.024
846
MYC017 Mycobacterium Kansasii 40 0.024
847
CRL004 Caroli Disease 40 0.024
848
RCT017 Rectal Disease 40 0.024
849
CYS009 Cystadenoma 40 0.024
850
IMP006 Impulse Control Disorder 40 0.024
851
HYP068 Hyperostosis 40 0.024
852
P ARC016 Auriculocondylar Syndrome 1 40 0.024
853
BND014 Bone Development Disease 40 0.024
854
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.024
855
c HMC009 Hemochromatosis Type 2 39 0.024
856
ANT039 Antisynthetase Syndrome 39 0.024
857
c CRD190 Cardiomyopathy, Hypertrophic, 2 39 0.024
858
MNR003 Mineral Metabolism Disease 38 0.024
859
P FML187 Familial Hypertension 38 0.024
860
LRN001 Laurence-Moon Syndrome 38 0.024
861
GLC086 Glucocorticoid-Induced Osteoporosis 38 0.024
862
P HRT035 Heart Block, Congenital 38 0.024
863
c ALP005 Alpha Chain Disease 37 0.024
864
STR089 Storage Pool Platelet Disease 37 0.024
865
IDP074 Idiopathic Bronchiectasis 36 0.024
866
c INH004 Inherited Blood Coagulation Disease 36 0.024
867
ISC005 Ischemic Bone Disease 36 0.024
868
c CHR098 Chronic Pyelonephritis 36 0.024
869
INT052 Intestinal Volvulus 36 0.024
870
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.024
871
c PLM022 Pulmonary Valve Insufficiency 34 0.024
872
c GLL024 Gallbladder Disease 1 34 0.024
873
P DXT004 Dextro-Looped Transposition of the Great Arteries 34 0.024
874
ACR002 Acrocapitofemoral Dysplasia 33 0.024
875
HRS011 Horseshoe Kidney 33 0.024
876
c MCL040 Macular Degeneration, Age-Related, 3 33 0.024
877
c NPH046 Nephrolithiasis, Type I 32 0.024
878
MYC014 Mycobacterium Chelonae 32 0.024
879
SRN001 Serine Deficiency 32 0.024
880
BLR002 Bile Reflux 31 0.024
881
LYM043 Lymphocytic Hypophysitis 31 0.024
882
SBV001 Subvalvular Aortic Stenosis 31 0.024
883
c INF078 Inflammatory Bowel Disease 2 31 0.024
884
c PNC095 Pancreatic Cancer 3 30 0.024
885
MDY005 Mody, Type I 30 0.024
886
MDY006 Mody, Type Iv 30 0.024
887
HNS001 Hansen's Disease 30 0.024
888
IMM066 Immunodeficiency 9 30 0.024
889
c TRN038 Transposition of the Great Arteries, Dextro-Looped 1 29 0.024
890
DYS011 Dyskinesia of Esophagus 28 0.024
891
CRB031 Cerebral Arterial Disease 27 0.024
892
PLM007 Pulmonary Aspergilloma 27 0.024
893
HPT077 Hepatic Venoocclusive Disease with Immunodeficiency 27 0.024
894
c CHR036 Chronic Cholangitis 26 0.024
895
UNV002 Univentricular Heart 26 0.024
896
c DYS141 Dyskeratosis Congenita, Autosomal Dominant 1 25 0.024
897
c MLT094 Multiple Sclerosis 3 24 0.024
898
PLS031 Plastic Bronchitis 24 0.024
899
c NPH053 Nephronophthisis 11 24 0.024
900
PNB004 Panbronchiolitis, Diffuse 24 0.024
901
NPH064 Nipah Virus Disease 22 0.024
902
c DYS150 Dyskeratosis Congenita, Autosomal Recessive 3 22 0.024
903
LVR004 Liver Inflammatory Pseudotumor 22 0.024
904
HYP213 Hypomelanotic Disorder 21 0.024
905
CRC034 Carcinoma Showing Thymus-Like Differentiation 21 0.024
906
ATX038 Ataxia and Polyneuropathy, Adult-Onset 21 0.024
907
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 21 0.024
908
IMM142 Immunodeficiency 50 20 0.024
909
ACR025 Acrocephalopolydactylous Dysplasia 19 0.024
910
CRR013 Cirrhosis, North American Indian Childhood Type 17 0.024
911
c RNL092 Renal-Hepatic-Pancreatic Dysplasia 1 16 0.024
912
ATM053 Autoimmune Disease 2 16 0.024
913
c MCL026 Macular Dystrophy, Retinal, 3 16 0.024
914
SCD003 Scedosporiosis 15 0.024
915
c BNG076 Benign Exophthalmos Syndrome 15 0.024
916
MYC003 Myocardium Cancer 14 0.024
917
c DLT001 Delta Chain Disease 13 0.024
918
PLM062 Pulmonary Hyalinizing Granuloma 12 0.024
919
AQG003 Aquagenic Syringeal Acrokeratoderm 7 0.024
920
P MLT019 Multiple Myeloma 83 0.020
921
P RTN008 Retinitis Pigmentosa 80 0.020
922
c CHR090 Chronic Lymphocytic Leukemia 76 0.020
923
PHN003 Phenylketonuria 72 0.020
924
ADN021 Adenomatous Polyposis Coli 70 0.020
925
SQM013 Squamous Cell Carcinoma, Head and Neck 70 0.020
926
WRN001 Werner Syndrome 67 0.020
927
KPS004 Kaposi Sarcoma 67 0.020
928
c NRF018 Neurofibromatosis, Type 1 67 0.020
929
P MYS003 Myasthenia Gravis 67 0.020
930
P PSD087 Pseudoxanthoma Elasticum 66 0.020
931
CHR012 Chronic Granulomatous Disease 65 0.020
932
P PLY011 Polycystic Ovary Syndrome 65 0.020
933
PRT037 Pertussis 64 0.020
934
GLC006 Galactosemia 64 0.020
935
CHR066 Chronic Fatigue Syndrome 64 0.020
936
P BRD002 Bardet-Biedl Syndrome 63 0.020
937
P HLP001 Holoprosencephaly 63 0.020
938
ALC007 Alcohol Dependence 63 0.020
939
LYM017 Lyme Disease 63 0.020
940
RCT015 Reactive Arthritis 63 0.020
941
WGN006 Wegener Granulomatosis 63 0.020
942
P OST001 Osteopetrosis 63 0.020
943
SPN186 Spinal Cord Injury 63 0.020
944
P EHL001 Ehlers-Danlos Syndrome 63 0.020
945
c HMP004 Hemophilia B 62 0.020
946
P PRD006 Prader-Willi Syndrome 62 0.020
947
CNG368 Congenital Adrenal Hyperplasia 62 0.020
948
OST017 Osteomyelitis 61 0.020
949
P SLV002 Salivary Gland Cancer 61 0.020
950
CRD119 Cardiac Arrest 61 0.020
951
FCT007 Factor Vii Deficiency 61 0.020
952
P DNT015 Dent Disease 61 0.020
953
TYP007 Typhoid Fever 61 0.020
954
OVR029 Ovarian Hyperstimulation Syndrome 61 0.020
955
CHR072 Chordoma 61 0.020
956
c EHL057 Ehlers-Danlos Syndrome, Type Iv 60 0.020
957
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 0.020
958
APP008 Appendicitis 60 0.020
959
c ADL017 Adult T-Cell Leukemia 60 0.020
960
P SPN052 Spondyloarthropathy 60 0.020
961
TNG009 Tongue Squamous Cell Carcinoma 59 0.020
962
CNT097 Central Hypoventilation Syndrome, Congenital 59 0.020
963
GST045 Gastroenteritis 59 0.020
964
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.020
965
P PRP029 Porphyria 59 0.020
966
PGT001 Paget's Disease of Bone 59 0.020
967
P PLY018 Polycythemia 58 0.020
968
P MTR004 Maturity-Onset Diabetes of the Young 58 0.020
969
RHM027 Rheumatic Disease 58 0.020
970
P BRS044 Breast Adenocarcinoma 58 0.020
971
TNG003 Tongue Cancer 58 0.020
972
BNC003 Bone Cancer 58 0.020
973
P THR003 Thoracic Aortic Aneurysm 57 0.020
974
KND001 Kindler Syndrome 57 0.020
975
P CND004 Candidiasis 57 0.020
976
P LRY044 Larynx Cancer 57 0.020
977
URT039 Urticaria 57 0.020
978
PNC033 Pancreas Adenocarcinoma 57 0.020
979
WST001 West Syndrome 57 0.020
980
ARG002 Argininosuccinic Aciduria 57 0.020
981
c MCR115 Microvascular Complications of Diabetes 5 57 0.020
982
P INT143 Interstitial Cystitis 57 0.020
983
P MST009 Mastocytosis 56 0.020
984
PLY023 Polycystic Liver Disease 56 0.020
985
PTT006 Pituitary Adenoma 56 0.020
986
P SML001 Small Cell Carcinoma 56 0.020
987
P PLY019 Polyneuropathy 56 0.020
988
P BDD001 Budd-Chiari Syndrome 56 0.020
989
P WVR001 Weaver Syndrome 56 0.020
990
c MLG077 Malignant Peripheral Nerve Sheath Tumor 56 0.020
991
HPT019 Hepatic Encephalopathy 56 0.020
992
P SCL018 Scoliosis 55 0.020
993
P LPS002 Liposarcoma 55 0.020
994
P FNC043 Fanconi Anemia, Complementation Group E 55 0.020
995
LKC001 Leukocyte Adhesion Deficiency 55 0.020
996
SPN027 Spinal Stenosis 55 0.020
997
VGT001 Vogt-Koyanagi-Harada Disease 55 0.020
998
P SLV001 Silver-Russell Syndrome 54 0.020
999
P HYP083 Hypopituitarism 54 0.020
1000
P NLD001 Nail Disease 54 0.020
1001
RCT018 Rectal Neoplasm 54 0.020
1002
LNG039 Lung Squamous Cell Carcinoma 54 0.020
1003
LYM022 Lymphangioma 54 0.020
1004
CHL127 Cholangiocarcinoma, Susceptibility to 54 0.020
1005
LMY002 Leiomyoma 54 0.020
1006
P LRY019 Laryngitis 54 0.020
1007
PLV003 Pelvic Inflammatory Disease 54 0.020
1008
P VNS003 Venous Insufficiency 54 0.020
1009
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 53 0.020
1010
P HYP027 Hypobetalipoproteinemia 53 0.020
1011
P LCH002 Lichen Planus 53 0.020
1012
P HYP024 Hypoparathyroidism 53 0.020
1013
c INS002 in Situ Carcinoma 53 0.020
1014
THR016 Thrombophlebitis 53 0.020
1015
P CYS018 Cystitis 52 0.020
1016
GRF001 Graft-Versus-Host Disease, Protection Against 52 0.020
1017
P SML016 Small Intestine Cancer 52 0.020
1018
LYS002 Lysosomal Storage Disease 52 0.020
1019
ISL003 Isolated Growth Hormone Deficiency 52 0.020
1020
OST015 Osteochondrodysplasia 52 0.020
1021
BCT002 Bacterial Vaginosis 52 0.020
1022
CRH005 Crohn's Colitis 52 0.020
1023
MYC002 Mycobacterium Avium Complex Disease 52 0.020
1024
PLM014 Pleomorphic Adenoma 52 0.020
1025
MSS001 Masa Syndrome 52 0.020
1026
APP015 Apparent Mineralocorticoid Excess 51 0.020
1027
SRS001 Serous Cystadenocarcinoma 51 0.020
1028
STR008 Strongyloidiasis 51 0.020
1029
PPL002 Papillary Carcinoma 51 0.020
1030
CLL003 Cellulitis 51 0.020
1031
HYP005 Hypokalemia 51 0.020
1032
MYL001 Myelitis 51 0.020
1033
DSS009 Disseminated Intravascular Coagulation 51 0.020
1034
HMP005 Hemiplegia 51 0.020
1035
c GLY019 Glycogen Storage Disease Iiia 50 0.020
1036
VND002 Van Der Woude Syndrome 50 0.020
1037
ASP001 Asperger Syndrome 50 0.020
1038
SHR072 Short-Rib Thoracic Dysplasia 3 with or Without Polydactyly 50 0.020
1039
CCT002 Cicatricial Pemphigoid 50 0.020
1040
RLP001 Relapsing Polychondritis 50 0.020
1041
MCN001 Mucinous Adenocarcinoma 50 0.020
1042
NNT012 Neonatal Jaundice 50 0.020
1043
P HMC002 Homocystinuria 50 0.020
1044
PRR016 Pierre Robin Syndrome 50 0.020
1045
HLL004 Hellp Syndrome 50 0.020
1046
ANG054 Angina Pectoris 50 0.020
1047
ERY017 Erythema Elevatum Diutinum 49 0.020
1048
P GNT008 Giant Cell Tumor 49 0.020
1049
LPD009 Lipid Storage Disease 49 0.020
1050
P SNR012 Senior-Loken Syndrome-1 49 0.020
1051
P TRN034 Transverse Myelitis 49 0.020
1052
ATR057 Atrioventricular Block