Search results for "fibrosis"

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

2455 hits were found for 'fibrosis'

# Family MCID Name MIFTS Score
1
CYS001 Cystic Fibrosis 86 7.481
2
PLM134 Pulmonary Fibrosis, Idiopathic 61 6.160
3
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 5.562
4
TKL001 Tukel Syndrome 33 5.459
5
P PLM036 Pulmonary Fibrosis 68 5.028
6
ORL004 Oral Submucous Fibrosis 51 4.906
7
RTR011 Retroperitoneal Fibrosis 38 3.839
8
CNG048 Congenital Hepatic Fibrosis 45 3.827
9
CCH002 Coach Syndrome 54 3.751
10
c FBR049 Fibrosis of Extraocular Muscles, Congenital, 3a 24 3.500
11
c FBR050 Fibrosis of Extraocular Muscles, Congenital, 2 23 3.500
12
c MYT012 Myotonia Congenita, Recessive 42 3.488
13
PKL002 Poikiloderma, Hereditary Fibrosing, with Tendon Contractures, Myopathy, and Pulmonary Fibrosis 22 3.248
14
RNL077 Renal Fibrosis 47 3.088
15
P FBR081 Fibrosis of Extraocular Muscles, Congenital, 3c 15 2.958
16
IDP011 Idiopathic Interstitial Pneumonia 57 2.940
17
FBR028 Fibrosing Mediastinitis 24 2.932
18
NPH018 Nephrogenic Systemic Fibrosis 51 2.811
19
DFF002 Diffuse Pulmonary Fibrosis 33 2.790
20
PLM139 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 1 27 2.678
21
PLM141 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 4 17 2.659
22
FBR089 Fibrosclerosis, Multifocal 14 2.635
23
EF001 Eaf 24 2.629
24
CYS040 Cystic Fibrosis with Helicobacter Pylori Gastritis, Megaloblastic Anemia, and Mental Retardation 19 2.315
25
c FBR078 Fibrosis of Extraocular Muscles, Congenital, 5 13 2.297
26
PST015 Postinflammatory Pulmonary Fibrosis 11 2.285
27
LBN005 Lubani-Al Saleh-Teebi Syndrome 6 2.278
28
c PLM044 Pulmonary Fibrosis, Familial 30 1.985
29
ACT029 Acute Interstitial Pneumonia 43 1.978
30
IGG007 Igg4-Related Disease 37 1.912
31
c LCL003 Localized Pulmonary Fibrosis 13 1.908
32
P APL001 Aplastic Anemia 73 1.899
33
PRR004 Preretinal Fibrosis 36 1.899
34
HRM018 Hermansky-Pudlak Syndrome with Pulmonary Fibrosis 22 1.899
35
PLM143 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 3 15 1.899
36
HRM016 Hermansky-Pudlak Syndrome Without Pulmonary Fibrosis 21 1.889
37
BRN075 Bronchiectasis with or Without Elevated Sweat Chloride 2 19 1.877
38
IMM129 Immunodeficiency, Ovarian Dysgenesis, and Pulmonary Fibrosis 15 1.877
39
MSC030 Muscular Fibrosis Multifocal Obstructed Vessels 10 1.877
40
FBR086 Fibrolamellar Carcinoma 39 1.854
41
ASB001 Asbestosis 42 1.426
42
TRP020 Tropical Endomyocardial Fibrosis 30 1.420
43
SLC006 Silicosis 53 1.408
44
P MYL005 Myelofibrosis 67 1.399
45
FML074 Familial Interstitial Fibrosis 8 1.372
46
ARW003 Airway-Centered Interstitial Fibrosis 7 1.372
47
IDP016 Idiopathic Diffuse Interstitial Fibrosis 8 1.367
48
c CNG189 Congenital Disorder of Glycosylation, Type Ib 33 1.352
49
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 7 1.352
50
BRN076 Bronchiectasis with or Without Elevated Sweat Chloride 1 28 1.339
51
BRN077 Bronchiectasis with or Without Elevated Sweat Chloride 3 17 1.339
52
CRB163 Cerebellar Vermis Aplasia with Associated Features Suggesting Smith-Lemli-Opitz Syndrome and Meckel Syndrome 16 1.339
53
PLM155 Pulmonary Fibrosis, Idiopathic Susceptibility 7 1.339
54
HPT029 Hepatic Fibrosis Renal Cysts Mental Retardation 3 1.339
55
c NTR031 Neutropenia, Severe Congenital, 5, Autosomal Recessive 29 1.332
56
CMP074 Camptodactyly, Myopia, and Fibrosis of the Medial Rectus Muscle of Eye 15 1.332
57
c KF2001 Kif21a-Related Congenital Fibrosis of the Extraocular Muscles 6 1.332
58
c PHX001 Phox2a-Related Congenital Fibrosis of the Extraocular Muscles 6 1.332
59
c TBB003 Tubb3-Related Congenital Fibrosis of the Extraocular Muscles 6 1.332
60
c CNG140 Congenital Fibrosis of the Extraocular Muscles 1a 6 1.332
61
c CNG141 Congenital Fibrosis of the Extraocular Muscles 1b 6 1.332
62
PLM145 Pulmonary Fibrosis-Hepatic Hyperplasia-Bone Marrow Hypoplasia Syndrome 6 1.332
63
c SFT006 Sftpc-Related Familial Pulmonary Fibrosis 4 1.332
64
c TRC066 Terc-Related Familial Pulmonary Fibrosis 4 1.332
65
c TRT009 Tert-Related Familial Pulmonary Fibrosis 4 1.332
66
FLL047 Follicular Hamartoma-Alopecia-Cystic Fibrosis Syndrome 3 1.332
67
FBR016 Fibrosclerosis of Breast 25 1.323
68
DBT022 Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism 21 1.323
69
SNR014 Senior-Boichis Syndrome 10 1.323
70
RZN001 Rozin Hertz Goodman Syndrome 5 1.323
71
TYL001 Taylor's Syndrome 29 1.311
72
SCR009 Scirrhous Adenocarcinoma 14 1.311
73
GRP001 Graphite Pneumoconiosis 10 1.311
74
PLM113 Palmoplantar Keratoderma-Sclerodactyly Syndrome 7 1.311
75
P HPT021 Hepatitis 70 0.443
76
c PNC106 Pancreatic Agenesis 1 40 0.348
77
PNC034 Pancreas Disease 57 0.348
78
LNG099 Lung Disease 62 0.285
79
c HPT001 Hepatitis C 68 0.253
80
P PNM007 Pneumonia 66 0.244
81
P LVR013 Liver Disease 72 0.239
82
RSP006 Respiratory System Disease 62 0.231
83
P PNC044 Pancreatitis 60 0.206
84
INT066 Interstitial Lung Disease 58 0.202
85
BRN022 Bronchiectasis 47 0.201
86
URT010 Ureteral Obstruction 45 0.171
87
c HPT016 Hepatitis B 64 0.162
88
P ASP006 Aspergillosis 60 0.160
89
LVR012 Liver Cirrhosis 67 0.159
90
c HPT073 Hepatitis C Virus 72 0.158
91
P ALL008 Allergic Bronchopulmonary Aspergillosis 49 0.156
92
c VRL010 Viral Hepatitis 61 0.150
93
FTT001 Fatty Liver Disease 60 0.146
94
P CRD011 Cardiomyopathy 67 0.142
95
NNL002 Nonalcoholic Steatohepatitis 53 0.141
96
c HPT003 Hepatitis a 59 0.132
97
P HRT032 Heart Disease 76 0.131
98
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.131
99
PRM025 Primary Bacterial Infectious Disease 43 0.127
100
MCN017 Meconium Ileus 54 0.123
101
P RSP003 Respiratory Failure 70 0.120
102
NSD001 Nose Disease 52 0.119
103
P PLM037 Pulmonary Hypertension 79 0.117
104
GST050 Gastrointestinal System Disease 54 0.115
105
P AST005 Asthma 82 0.110
106
BRN038 Bronchial Disease 54 0.110
107
EXC002 Exocrine Pancreatic Insufficiency 43 0.109
108
NTR005 Nutritional Deficiency Disease 39 0.107
109
P PRT013 Portal Hypertension 59 0.103
110
P NNT009 Neonatal Diabetes Mellitus 52 0.103
111
HPT023 Hepatocellular Carcinoma 91 0.102
112
END072 Endotheliitis 42 0.100
113
P SPS003 Spastic Diplegia 53 0.099
114
SCH014 Schistosomiasis 58 0.092
115
VSC018 Visceral Steatosis 37 0.092
116
CNN005 Connective Tissue Disease 61 0.090
117
P CHL066 Cholangitis 49 0.089
118
UPP004 Upper Respiratory Tract Disease 48 0.086
119
MYC013 Mycobacterium Abscessus 40 0.086
120
P THY032 Thyroiditis 54 0.085
121
BLR001 Biliary Atresia 51 0.085
122
NNS002 Nonspecific Interstitial Pneumonia 44 0.084
123
P LNG032 Lung Cancer 94 0.083
124
CNG034 Congestive Heart Failure 71 0.080
125
SKN016 Skin Disease 68 0.080
126
PRT036 Peritonitis 62 0.080
127
P OBS005 Obesity 93 0.079
128
P INF032 Infertility 61 0.079
129
CHL068 Cholestasis 58 0.079
130
ADM013 Adamantinoma of Long Bones 59 0.078
131
BRT030 Birth Defects 43 0.078
132
VRL011 Viral Infectious Disease 59 0.077
133
CYS039 Cystic Kidney Disease 52 0.077
134
ACR041 Acromelic Frontonasal Dysostosis 46 0.077
135
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 47 0.075
136
c DLT002 Dilated Cardiomyopathy 75 0.074
137
LPD004 Lipoid Nephrosis 48 0.074
138
P ATR011 Atrial Fibrillation 64 0.073
139
P MSC005 Muscular Dystrophy 64 0.073
140
BRN002 Bronchiolitis 56 0.073
141
P PRM006 Primary Biliary Cirrhosis 52 0.073
142
P SNS014 Sinusitis 60 0.071
143
P INT070 Intestinal Obstruction 56 0.071
144
HYP266 Hypoxia 55 0.071
145
VND001 Vein Disease 52 0.071
146
P SCL009 Sclerosing Cholangitis 47 0.071
147
MSC004 Muscle Tissue Disease 36 0.071
148
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 34 0.071
149
c CRN214 Coronary Heart Disease 5 23 0.071
150
P MYP004 Myopathy 67 0.070
151
GLC003 Glucose Intolerance 55 0.070
152
HYP006 Hypertensive Heart Disease 50 0.070
153
MDS022 Mediastinitis 41 0.070
154
P ART022 Arthritis 75 0.069
155
P LKM002 Leukemia 70 0.069
156
P ADN016 Adenocarcinoma 69 0.069
157
P ESN007 Eosinophilia 61 0.069
158
LKP003 Leukoplakia 41 0.069
159
P HMC003 Hemochromatosis 72 0.067
160
P LYM118 Lymphoma 70 0.067
161
P GLM007 Glomerulonephritis 56 0.067
162
MTH009 Mouth Disease 63 0.066
163
ATP002 Atopy 63 0.066
164
CTS003 Coats Disease 57 0.066
165
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 55 0.066
166
P PNM006 Pneumoconiosis 51 0.066
167
BLD053 Blood Platelet Disease 46 0.066
168
c HYP595 Hypertension, Essential 69 0.064
169
P SYS005 Systemic Scleroderma 58 0.064
170
BRN012 Bronchiolitis Obliterans 58 0.064
171
PHR003 Pharyngitis 58 0.064
172
ANR040 Aneurysm 57 0.064
173
EXT034 Extrinsic Allergic Alveolitis 56 0.064
174
PLM034 Pulmonary Emphysema 54 0.064
175
PRN021 Paranasal Sinus Disease 50 0.064
176
NNT004 Neonatal Respiratory Failure 41 0.064
177
P FTT008 Fatty Liver Disease, Nonalcoholic 1 33 0.064
178
HPD002 Hepadnavirus Infection 23 0.064
179
c FTT007 Fatty Liver Disease, Nonalcoholic 2 18 0.064
180
PLM129 Pulmonary Disease, Chronic Obstructive 62 0.063
181
VNT001 Ventilation Pneumonitis 37 0.063
182
P MYC007 Myocardial Infarction 79 0.061
183
PCK002 Pick Disease 67 0.061
184
ORL011 Oral Cancer 55 0.061
185
P NPH005 Nephronophthisis 55 0.061
186
ATR060 Atrial Standstill, Digenic 53 0.061
187
SKN023 Skin Tag 46 0.061
188
SKN027 Skin Conditions 45 0.061
189
PHY002 Physical Disorder 44 0.061
190
SPC003 Specific Developmental Disorder 40 0.061
191
ADJ001 Adjustment Disorder 38 0.061
192
ALR002 Al-Raqad Syndrome 36 0.061
193
c RNL016 Renal Infectious Disease 24 0.061
194
P CRN178 Coronary Heart Disease 6 24 0.061
195
P RHM011 Rheumatoid Arthritis 88 0.059
196
HV1006 Hiv-1 82 0.059
197
P INF038 Influenza 74 0.059
198
WLS001 Wilson Disease 72 0.059
199
BRN024 Bronchitis 63 0.059
200
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.059
201
CHL071 Child Syndrome 58 0.059
202
ORL015 Oral Squamous Cell Carcinoma 56 0.059
203
KDS001 Kid Syndrome 53 0.059
204
STM006 Stomach Disease 50 0.059
205
LKC003 Leukocyte Disease 47 0.059
206
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.059
207
NSL022 Nasal Cavity Disease 42 0.059
208
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.059
209
c TRC078 Trichohepatoenteric Syndrome 2 31 0.059
210
P PNC035 Pancreatic Cancer 85 0.058
211
CRH001 Crohn's Disease 76 0.058
212
P ESP024 Esophagitis 62 0.058
213
CLT003 Colitis 59 0.058
214
P PRM011 Primary Ciliary Dyskinesia 58 0.058
215
MVM001 Movement Disease 54 0.058
216
P MYC008 Myocarditis 54 0.058
217
MCR088 Microscopic Polyangiitis 48 0.058
218
STT004 Steatorrhea 40 0.058
219
c AST039 Asthma 2 31 0.058
220
ATH003 Atherosclerosis 62 0.056
221
HYP066 Hyperglycemia 60 0.056
222
ALC006 Alcoholic Hepatitis 59 0.056
223
ISC004 Ischemia 59 0.056
224
PLM012 Pulmonary Sarcoidosis 54 0.056
225
P MSC033 Muscle Disorders 52 0.056
226
HMN014 Human Immunodeficiency Virus Infectious Disease 49 0.056
227
ACD009 Acid-Labile Subunit, Deficiency of 48 0.056
228
CNG035 Congenital Bilateral Absence of Vas Deferens 36 0.056
229
MCC011 Mucociliary Clearance Disorder 17 0.056
230
DCH001 Duchenne Muscular Dystrophy 80 0.054
231
GST092 Gastroesophageal Reflux 61 0.054
232
ART017 Aortic Disease 58 0.054
233
NWC001 Newcastle Disease 54 0.054
234
ALL026 Allergic Hypersensitivity Disease 53 0.054
235
c HPT015 Hepatitis D 52 0.054
236
ORL012 Oral Leukoplakia 46 0.054
237
GLM011 Glomerulosclerosis 44 0.054
238
c AST037 Asthma 1 31 0.054
239
c PLM128 Pulmonary Hypertension, Primary, 2 30 0.054
240
c ATM011 Autoimmune Hepatitis 58 0.052
241
KRT002 Keratomalacia 54 0.052
242
PNM008 Pneumothorax 52 0.052
243
CSY001 C Syndrome 49 0.052
244
SXL003 Sexual Disorder 47 0.052
245
GLC008 Glucose Metabolism Disease 47 0.052
246
SPL018 Splenomegaly 44 0.052
247
END038 Endocrine Pancreas Disease 43 0.052
248
HRT012 Heart Valve Disease 41 0.052
249
WTH001 Withdrawal Disorder 41 0.052
250
RDT005 Radiation Induced Cancer 28 0.052
251
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.050
252
INS024 Insulin-Like Growth Factor I 74 0.050
253
PRP027 Peripheral Vascular Disease 69 0.050
254
P LPS004 Lupus Erythematosus 63 0.050
255
c ACT210 Acute Respiratory Distress Syndrome 57 0.050
256
SLP005 Sleep Disorder 53 0.050
257
P HYP098 Hypereosinophilic Syndrome 51 0.050
258
PRC012 Pericardial Effusion 50 0.050
259
c ATM024 Autoimmune Pancreatitis 46 0.050
260
AYM001 Ayme-Gripp Syndrome 45 0.050
261
DFF003 Diffuse Scleroderma 41 0.050
262
BNS002 Bone Structure Disease 36 0.050
263
c CRN175 Coronary Heart Disease 4 21 0.050
264
c SYS001 Systemic Lupus Erythematosus 87 0.049
265
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.049
266
ART016 Aortic Aneurysm 67 0.049
267
c CHR089 Chronic Kidney Failure 66 0.049
268
BRC012 Brucellosis 65 0.049
269
P OST002 Osteoporosis 64 0.049
270
VSC011 Vasculitis 62 0.049
271
PRM097 Primary Immunodeficiency Disease 61 0.049
272
P THL005 Thalassemia 61 0.049
273
P ATX004 Ataxia 53 0.049
274
BRN106 Burns 52 0.049
275
RTN023 Retinitis 49 0.049
276
ALC009 Alcoholic Liver Cirrhosis 48 0.049
277
P PLM006 Pulmonary Alveolar Proteinosis 48 0.049
278
P TRC086 Trichohepatoenteric Syndrome 1 46 0.049
279
DST006 Diastolic Heart Failure 46 0.049
280
ALN001 Aland Island Eye Disease 45 0.049
281
DDN006 Duodenitis 44 0.049
282
IMP003 Impaired Renal Function Disease 37 0.049
283
P HRT017 Heart Tumor 35 0.049
284
CHL079 Children's Interstitial Lung Disease 19 0.049
285
P BRS047 Breast Cancer 100 0.046
286
ANX002 Anxiety Disorder 69 0.046
287
TBR010 Tuberculosis 69 0.046
288
P THR014 Thrombocytopenia 64 0.046
289
EYD002 Eye Disease 63 0.046
290
P LYM025 Lymphedema 61 0.046
291
LPD008 Lipid Metabolism Disorder 58 0.046
292
URN009 Urinary System Disease 53 0.046
293
END030 End Stage Renal Failure 52 0.046
294
P END033 Endocarditis 52 0.046
295
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.046
296
HRT007 Heart Cancer 50 0.046
297
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.046
298
P SDR002 Siderosis 44 0.046
299
c CHR096 Chronic Pulmonary Heart Disease 40 0.046
300
BLD054 Blood Protein Disease 40 0.046
301
ACR005 Acrodermatitis 34 0.046
302
c CRN172 Coronary Heart Disease 3 21 0.046
303
VSC007 Vascular Disease 67 0.044
304
DRM006 Dermatitis 61 0.044
305
P MSC007 Muscle Hypertrophy 59 0.044
306
P MTR012 Mitral Valve Disease 59 0.044
307
P DRM010 Dermatomyositis 58 0.044
308
ALL006 Allergic Asthma 58 0.044
309
NRM005 Neuromuscular Disease 57 0.044
310
P MCR129 Microvascular Complications of Diabetes 1 57 0.044
311
c ACT027 Acute Pancreatitis 56 0.044
312
c ART101 Aortic Valve Disease 2 55 0.044
313
c HPT007 Hepatitis E 54 0.044
314
P STR020 Strabismus 53 0.044
315
P URF003 Urofacial Syndrome 1 52 0.044
316
PRC013 Pericarditis 52 0.044
317
BLR006 Biliary Tract Disease 51 0.044
318
CRN030 Coronary Stenosis 50 0.044
319
c ACT068 Acute Cystitis 50 0.044
320
c INH020 Inherited Metabolic Disorder 49 0.044
321
HPT009 Hepatopulmonary Syndrome 48 0.044
322
ACR003 Acrodermatitis Enteropathica 48 0.044
323
c MTR002 Mitral Valve Insufficiency 44 0.044
324
CHR008 Choroiditis 43 0.044
325
PRT019 Protein-Losing Enteropathy 41 0.044
326
P ACT080 Acute Pulmonary Heart Disease 32 0.044
327
ENT007 Enteropathica 26 0.044
328
SNG003 Single Ventricular Heart 24 0.044
329
PLM015 Pulmonary Systemic Sclerosis 24 0.044
330
CNG039 Congenital Absence of the Vas Deferens 22 0.044
331
c CRN177 Coronary Heart Disease 7 22 0.044
332
c ADL079 Adult Heart Tumor 19 0.044
333
AND005 Androgen Insensitivity Syndrome, Mild 16 0.044
334
GST053 Gastric Cancer 77 0.042
335
MYL009 Myelodysplastic Syndrome 74 0.042
336
TTR001 Tetralogy of Fallot 71 0.042
337
c PNC108 Pancreatitis, Hereditary 67 0.042
338
P HYP086 Hypothyroidism 65 0.042
339
P INT068 Intestinal Disease 61 0.042
340
P RCK004 Rickets 59 0.042
341
ETH011 Ethylmalonic Encephalopathy 59 0.042
342
ADL002 Adult Syndrome 53 0.042
343
P HYP065 Hyperaldosteronism 51 0.042
344
LYM024 Lymphatic System Disease 50 0.042
345
DFF035 Diffuse Cutaneous Systemic Sclerosis 45 0.042
346
HMS001 Hemosiderosis 45 0.042
347
ALB002 Albinism 43 0.042
348
ATS010 Autosomal Recessive Disease 41 0.042
349
URT001 Urethritis 40 0.042
350
c HMG004 Hemoglobin D Disease 33 0.042
351
c PLM127 Pulmonary Hypertension, Primary, 3 30 0.042
352
c CRN174 Coronary Heart Disease 2 22 0.042
353
HRP008 Herpes Simiae 15 0.042
354
HRP012 Herpesvirus Simiae B Virus 13 0.042
355
NNT002 Neonatal Urinary Tract Infectious Disease 13 0.042
356
P CRN211 Coronary Artery Disease 75 0.040
357
PLY022 Polycystic Kidney and Hepatic Disease 66 0.040
358
DFC004 Deficiency Anemia 65 0.040
359
P DYS007 Dyskeratosis Congenita 63 0.040
360
c ACT075 Acute Myocardial Infarction 60 0.040
361
CHY002 Chylomicron Retention Disease 59 0.040
362
P GLL020 Gallbladder Disease 59 0.040
363
PRS047 Prostatitis 56 0.040
364
P MMB011 Membranous Nephropathy 56 0.040
365
ART002 Arts Syndrome 53 0.040
366
P MSC003 Muscular Atrophy 51 0.040
367
P PLY041 Polymyositis 51 0.040
368
PRT011 Protein C Deficiency 51 0.040
369
P DRR001 Diarrhea 51 0.040
370
RHM028 Rheumatic Heart Disease 51 0.040
371
HMG005 Hemoglobinopathy 50 0.040
372
AZS001 Azoospermia 48 0.040
373
SPL012 Splenic Disease 47 0.040
374
HYD002 Hydronephrosis 47 0.040
375
BNN003 Bone Inflammation Disease 46 0.040
376
HRT015 Heritable Pulmonary Arterial Hypertension 45 0.040
377
CRR007 Cirrhosis, Cryptogenic 44 0.040
378
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 44 0.040
379
P ABD003 Abdominal Aortic Aneurysm 43 0.040
380
c BLD124 Bleeding Disorder, Platelet-Type, 11 42 0.040
381
c ATM022 Autoimmune Myocarditis 41 0.040
382
DVL001 Developmental Coordination Disorder 37 0.040
383
PRP080 Peripheral Artery Disease 36 0.040
384
ANG049 Angioedema Induced by Ace Inhibitors 35 0.040
385
LYM023 Lymphatic System Cancer 35 0.040
386
PNC028 Pancreatic Steatorrhea 35 0.040
387
VTM003 Vitamin Metabolic Disorder 33 0.040
388
SPR035 Superior Vena Cava Syndrome 32 0.040
389
ART012 Aortitis 31 0.040
390
MLT035 Multifocal Choroiditis 30 0.040
391
ORL014 Oral Pharyngeal Disorders 14 0.040
392
P TYS001 Tay-Sachs Disease 71 0.037
393
ISC006 Ischemic Heart Disease 68 0.037
394
PLM001 Pulmonary Tuberculosis 68 0.037
395
OBS061 Obstructive Sleep Apnea 66 0.037
396
DWN001 Down Syndrome 65 0.037
397
P AMY004 Amyloidosis 64 0.037
398
P SLP006 Sleep Apnea 61 0.037
399
GNG013 Gingivitis 60 0.037
400
P CMR001 Camurati-Engelmann Disease 59 0.037
401
MRB003 Morbid Obesity 58 0.037
402
EMP007 Emphysema Due to Aat Deficiency 56 0.037
403
P MYS005 Myositis 56 0.037
404
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.037
405
P PYL005 Pyelonephritis 52 0.037
406
TTH006 Tooth Disease 52 0.037
407
ERD001 Erdheim-Chester Disease 51 0.037
408
MRC001 Marchiafava Bignami Disease 50 0.037
409
P CLL015 Collagen Disease 49 0.037
410
DYS073 Dysphagia 49 0.037
411
P CHR345 Chronic Pain 49 0.037
412
SCK005 Sickle Cell Disease 49 0.037
413
AMN002 Amino Acid Metabolic Disorder 48 0.037
414
SLD003 Sialadenitis 48 0.037
415
P RNL015 Renal Hypertension 47 0.037
416
CRB025 Carbohydrate Metabolic Disorder 47 0.037
417
ATN002 Autonomic Nervous System Disease 47 0.037
418
CRY004 Cryoglobulinemia 47 0.037
419
P BLD051 Blood Coagulation Disease 45 0.037
420
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.037
421
HMP009 Haemophilus Influenzae 45 0.037
422
P CRV039 Cervicitis 44 0.037
423
HPT020 Hepatic Vascular Disease 44 0.037
424
c RCR022 Recurrent Acute Pancreatitis 41 0.037
425
CHL052 Choledochal Cyst 40 0.037
426
RHM009 Rheumatoid Lung Disease 40 0.037
427
ATS009 Autosomal Genetic Disease 39 0.037
428
c HYP058 Hypervitaminosis a 38 0.037
429
GLB003 Globe Disease 35 0.037
430
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 34 0.037
431
INT304 Interstitial Pneumonitis, Desquamative, Familial 32 0.037
432
c PNC111 Pancreatic Cancer 2 30 0.037
433
c PLM121 Pulmonary Hypertension, Primary, 4 29 0.037
434
c PNC094 Pancreatic Cancer 1 29 0.037
435
IMM090 Immunodeficiency 27a, Mycobacteriosis, Ar 28 0.037
436
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 26 0.037
437
PRQ002 Paraquat Poisoning 24 0.037
438
c CRN173 Coronary Heart Disease 8 20 0.037
439
INB001 Inborn Amino Acid Metabolism Disorder 15 0.037
440
LBR003 Labrador Lung 15 0.037
441
P RNL014 Renal Cell Carcinoma 81 0.034
442
SRC014 Sarcoma 66 0.034
443
CHG001 Chagas Disease 62 0.034
444
P HML002 Hemolytic Anemia 60 0.034
445
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 60 0.034
446
P NRP001 Neuropathy 60 0.034
447
P UVT001 Uveitis 59 0.034
448
MSS002 Mass Syndrome 59 0.034
449
P HMR003 Hemorrhagic Disease 57 0.034
450
ART111 Artery Disease 57 0.034
451
CNS004 Constipation 57 0.034
452
MLN007 Male Infertility 56 0.034
453
THR004 Thrombocytosis 55 0.034
454
MNT002 Mental Depression 54 0.034
455
ESP023 Esophageal Disease 53 0.034
456
c ART115 Aortic Valve Disease 1 53 0.034
457
P MCK022 Meckel Syndrome 1 53 0.034
458
CRC006 Carcinoid Syndrome 51 0.034
459
CYT008 Cytomegalovirus Infection 51 0.034
460
LRN003 Learning Disability 51 0.034
461
HPT074 Hepatic Adenoma, Somatic 51 0.034
462
KLD001 Keloids 51 0.034
463
P OCL002 Oculocutaneous Albinism 51 0.034
464
c CHR417 Chronic Graft Versus Host Disease 50 0.034
465
SPN051 Spondylitis 50 0.034
466
INT051 Intussusception 50 0.034
467
c ACT071 Acute Kidney Failure 50 0.034
468
P RST002 Restrictive Cardiomyopathy 50 0.034
469
MGC001 Megacolon 50 0.034
470
NDL013 Nodular Regenerative Hyperplasia 49 0.034
471
PMP001 Pemphigus 49 0.034
472
CHR001 Churg-Strauss Syndrome 49 0.034
473
GRW007 Growth Hormone Deficiency 48 0.034
474
c HRM005 Hermansky-Pudlak Syndrome 1 48 0.034
475
NPH003 Nephrocalcinosis 46 0.034
476
RNL078 Renal Dysplasia 45 0.034
477
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.034
478
P PLM085 Pulmonary Hemosiderosis 44 0.034
479
BCK006 Back Pain 42 0.034
480
NRN002 Neuronitis 42 0.034
481
IMM001 Immune-Complex Glomerulonephritis 42 0.034
482
HYP540 Hypertension, Diastolic 41 0.034
483
P HRM017 Hermansky-Pudlak Syndrome 2 40 0.034
484
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 38 0.034
485
CRB009 Cerebritis 38 0.034
486
SWT003 Sweat Gland Disease 37 0.034
487
WRN005 Wrinkles 37 0.034
488
ALC005 Alcoholic Pancreatitis 36 0.034
489
c SCL052 Scleroderma, Familial Progressive 27 0.034
490
c DYS143 Dyskeratosis Congenita, Autosomal Dominant 2 27 0.034
491
PLM124 Pulmonary Hypertension, Neonatal 27 0.034
492
STN013 Stenotrophomonas Maltophilia Infection 19 0.034
493
CFT001 Cftr-Related Disorders 14 0.034
494
IDP075 Idiopathic and/or Familial Pulmonary Arterial Hypertension 13 0.034
495
CRN073 Coronary Arteries Congenital Malformation 13 0.034
496
P PRS040 Prostate Cancer 89 0.031
497
MLR004 Malaria 79 0.031
498
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 76 0.031
499
P RTN024 Retinoblastoma 75 0.031
500
HDG012 Hodgkin Lymphoma 73 0.031
501
BCK001 Becker Muscular Dystrophy 68 0.031
502
P MYL006 Myeloid Leukemia 67 0.031
503
MLD001 Melioidosis 67 0.031
504
P MNN013 Meningitis 65 0.031
505
OCL009 Ocular Cancer 62 0.031
506
GLB001 Gilbert Syndrome 61 0.031
507
P GRV001 Graves' Disease 61 0.031
508
P NPH009 Nephrolithiasis 60 0.031
509
P HMN010 Hemangioma 60 0.031
510
P ADL010 Adult Respiratory Distress Syndrome 60 0.031
511
ETN001 Eating Disorder 60 0.031
512
c LCL006 Localized Scleroderma 59 0.031
513
P ENC018 Encephalopathy 59 0.031
514
ART021 Arteriosclerosis 59 0.031
515
CMM005 Common Cold 58 0.031
516
WLL006 Wells Syndrome 56 0.031
517
RTN018 Retinal Disease 56 0.031
518
P PTS002 Ptosis 56 0.031
519
CHL014 Cholera 55 0.031
520
P PLY017 Polyarteritis Nodosa 55 0.031
521
DSS008 Disease of Mental Health 55 0.031
522
NRN004 Neuroendocrine Tumor 54 0.031
523
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.031
524
VSC006 Vascular Cancer 54 0.031
525
P RTN016 Retinal Degeneration 54 0.031
526
PYR010 Peyronie's Disease 53 0.031
527
ECH003 Echinococcosis 53 0.031
528
INT007 Intermediate Coronary Syndrome 52 0.031
529
FRB001 Farber Lipogranulomatosis 51 0.031
530
c INF067 Inflammatory Bowel Disease 10 51 0.031
531
ADT003 Auditory System Disease 51 0.031
532
URM002 Uremia 50 0.031
533
c ACT134 Acute Liver Failure 50 0.031
534
HYP037 Hyperhomocysteinemia 50 0.031
535
P NGH001 Night Blindness 49 0.031
536
PRT038 Protein-Energy Malnutrition 49 0.031
537
PRT030 Parathyroid Gland Disease 49 0.031
538
c CNG027 Congenital Hemolytic Anemia 48 0.031
539
HYP063 Hypersplenism 48 0.031
540
BLD036 Bile Duct Disease 48 0.031
541
BNF002 Bone Fracture 47 0.031
542
CRD118 Cardiovascular Cancer 47 0.031
543
c HMG001 Hemoglobin C Disease 47 0.031
544
P RNV001 Renovascular Hypertension 47 0.031
545
HYD005 Hydrocele 47 0.031
546
SDD007 Sudden Cardiac Death 46 0.031
547
P SKN013 Skin Benign Neoplasm 46 0.031
548
GDS001 Good Syndrome 45 0.031
549
RNL097 Renal Artery Disease 45 0.031
550
KWS001 Kwashiorkor 44 0.031
551
CRY001 Cryptogenic Organizing Pneumonia 44 0.031
552
P RPD001 Rapidly Progressive Glomerulonephritis 44 0.031
553
PRD004 Prediabetes Syndrome 43 0.031
554
P PRL003 Proliferative Glomerulonephritis 43 0.031
555
P PSD003 Pseudohypoaldosteronism 43 0.031
556
SYS003 Systolic Heart Failure 43 0.031
557
PRD011 Proud Syndrome 42 0.031
558
THL018 Thalassemia Major 42 0.031
559
c VRL005 Viral Pneumonia 42 0.031
560
CHR078 Chorioretinitis 41 0.031
561
MDL009 Medullary Sponge Kidney 40 0.031
562
CPL005 Capillary Disease 40 0.031
563
ACT084 Acute Stress Disorder 40 0.031
564
NSY001 N Syndrome 39 0.031
565
FSC002 Fascioliasis 38 0.031
566
DRM009 Dermatomycosis 36 0.031
567
FNC006 Functional Gastric Disease 34 0.031
568
SWL001 Swallowing Disorders 34 0.031
569
VSC008 Vascular Hemostatic Disease 33 0.031
570
c DYS149 Dyskeratosis Congenita, Autosomal Recessive 1 33 0.031
571
DDN009 Duodenal Obstruction 32 0.031
572
CVT001 Cavitary Optic Disc Anomalies 32 0.031
573
KSH001 Keshan Disease 31 0.031
574
ATM052 Autoimmune Disease 1 28 0.031
575
MLN012 Melanoma and Neural System Tumor Syndrome 27 0.031
576
HNM002 Hinman Syndrome 25 0.031
577
MTR031 Motor Neuro-Ophthalmic Disorders 23 0.031
578
c CRN176 Coronary Heart Disease 9 20 0.031
579
IGG011 Igg4-Related Kidney Disease 13 0.031
580
P ATX030 Ataxia-Telangiectasia 76 0.028
581
ULC004 Ulcerative Colitis 75 0.028
582
c MCL042 Macular Degeneration, Age-Related, 1 71 0.028
583
KWS002 Kawasaki Disease 70 0.028
584
SCK003 Sickle Cell Anemia 68 0.028
585
P ESS003 Essential Thrombocythemia 68 0.028
586
P KDN017 Kidney Cancer 67 0.028
587
WRN001 Werner Syndrome 67 0.028
588
P CLC005 Celiac Disease 67 0.028
589
c GCH015 Gaucher Disease, Type I 66 0.028
590
P LYM007 Lymphangioleiomyomatosis 65 0.028
591
P BCL006 B-Cell Lymphomas 64 0.028
592
P CRD194 Cardiomyopathy, Familial Hypertrophic 64 0.028
593
PNC041 Pancreatic Ductal Adenocarcinoma 63 0.028
594
ACN011 Acne 63 0.028
595
P LNG064 Lung Cancer Susceptibility 3 62 0.028
596
CNT047 Contact Dermatitis 62 0.028
597
HYP056 Hypoglycemia 61 0.028
598
SHW002 Shwachman-Diamond Syndrome 60 0.028
599
ANR002 Aniridia 60 0.028
600
P GST049 Gastrointestinal System Cancer 60 0.028
601
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.028
602
HRY003 Hairy Cell Leukemia 60 0.028
603
PLM033 Pulmonary Embolism 59 0.028
604
P THR015 Thrombophilia 59 0.028
605
P HYP060 Hyperinsulinism 59 0.028
606
c FML001 Familial Atrial Fibrillation 59 0.028
607
PRP030 Purpura 59 0.028
608
ADN018 Adenoma 59 0.028
609
P GLY013 Glycogen Storage Disease 59 0.028
610
HPY002 H. Pylori Infection 58 0.028
611
P ORL007 Oral Cavity Cancer 58 0.028
612
c SVR001 Severe Acute Respiratory Syndrome 57 0.028
613
P BRN009 Burning Mouth Syndrome 57 0.028
614
DFF005 Diffuse Large B-Cell Lymphoma 56 0.028
615
SBS003 Substance Abuse 56 0.028
616
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 56 0.028
617
c THR092 Thrombophilia Due to Thrombin Defect 56 0.028
618
P HMP007 Hemophilia 56 0.028
619
FLR002 Filariasis 55 0.028
620
P HST010 Histiocytosis 55 0.028
621
P LRY019 Laryngitis 55 0.028
622
P PRP019 Peripheral Nervous System Disease 54 0.028
623
GST037 Gastroparesis 53 0.028
624
VRR004 Verrucous Carcinoma 53 0.028
625
P DBT005 Diabetes Insipidus 53 0.028
626
THR016 Thrombophlebitis 52 0.028
627
CYS010 Cystinosis 51 0.028
628
IRN001 Iron Deficiency Anemia 51 0.028
629
HYP005 Hypokalemia 51 0.028
630
ANG054 Angina Pectoris 51 0.028
631
MSC072 Muscle Cancer 51 0.028
632
P DDN001 Duodenal Ulcer 51 0.028
633
PNN001 Panniculitis 50 0.028
634
HLL004 Hellp Syndrome 49 0.028
635
c HTR008 Heterotaxy, Visceral, 5 48 0.028
636
P SHR001 Short Bowel Syndrome 48 0.028
637
FML039 Female Reproductive System Disease 48 0.028
638
OBS001 Obstructive Jaundice 48 0.028
639
KRT010 Kartagener Syndrome 48 0.028
640
PRP007 Priapism 47 0.028
641
INT067 Interstitial Nephritis 47 0.028
642
LPM005 Lipomatosis 47 0.028
643
MDD010 Middle Ear Disease 46 0.028
644
RPR002 Reproductive System Disease 46 0.028
645
P PRD008 Periodontitis 46 0.028
646
P RNL017 Renal Oncocytoma 46 0.028
647
ART004 Aortic Atherosclerosis 46 0.028
648
PRR002 Pure Red-Cell Aplasia 46 0.028
649
CRD137 Cardiogenic Shock 46 0.028
650
ATN005 Autonomic Dysfunction 45 0.028
651
c HRM006 Hermansky-Pudlak Syndrome 3 45 0.028
652
HYP457 Hypertrophic Scars 45 0.028
653
BRN014 Bronchopneumonia 45 0.028
654
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.028
655
PRM236 Primary Biliary Cholangitis 43 0.028
656
CNV002 Conversion Disorder 42 0.028
657
PGM003 Pigmentation Disease 42 0.028
658
ACT055 Actinomycosis 41 0.028
659
NNT049 Nontuberculous Mycobacterial Lung Disease 41 0.028
660
P FML187 Familial Hypertension 41 0.028
661
CHR413 Chronic Myocardial Ischemia 40 0.028
662
SXD001 Sex Differentiation Disease 40 0.028
663
P CRD132 Cardiac Conduction Defect 40 0.028
664
RDN001 Reading Disorder 39 0.028
665
c INH004 Inherited Blood Coagulation Disease 39 0.028
666
FXF002 Fox-Fordyce Disease 39 0.028
667
CLL021 Collagenous Colitis 38 0.028
668
MYX004 Myxedema 38 0.028
669
ARC002 Arachnoiditis 38 0.028
670
EXT006 Extrahepatic Cholestasis 36 0.028
671
OST008 Osteosclerotic Myeloma 36 0.028
672
c CNN010 Connective Tissue Benign Neoplasm 35 0.028
673
XRP001 Xerophthalmia 35 0.028
674
CNS002 Constrictive Pericarditis 34 0.028
675
c MCL043 Macular Degeneration, Age-Related, 2 34 0.028
676
c SRC023 Sarcoidosis 2 33 0.028
677
SKL007 Skeletal Muscle Regeneration 32 0.028
678
SCR003 Secretory Diarrhea 32 0.028
679
EYD001 Eye Degenerative Disease 31 0.028
680
c PNC103 Pancreatic Cancer 4 31 0.028
681
c HRM007 Hermansky-Pudlak Syndrome 4 30 0.028
682
CYT004 Cytomegalic Inclusion Disease 30 0.028
683
c HYP555 Hypertriglyceridemia, Transient Infantile 29 0.028
684
c MYC058 Myocardial Infarction 2 29 0.028
685
P MCL035 Macular Dystrophy, Retinal, 2 27 0.028
686
HMC038 Hemochromatosis, Neonatal 27 0.028
687
MRG013 Mirage Syndrome 26 0.028
688
EYC003 Eye Accommodation Disease 26 0.028
689
c DYS152 Dyskeratosis Congenita, Autosomal Recessive 5 26 0.028
690
c DYS147 Dyskeratosis Congenita, Autosomal Dominant 3 24 0.028
691
BNM008 Bone Mineral Density, Low 19 0.028
692
MYC003 Myocardium Cancer 17 0.028
693
BRW002 Brown's Tendon Sheath Syndrome 16 0.028
694
PNM022 Pneumonia Caused by Pseudomonas Aeruginosa Infection 10 0.028
695
P OST012 Osteoarthritis 82 0.024
696
P HNT016 Huntington Disease 80 0.024
697
MRF001 Marfan Syndrome 73 0.024
698
FBR012 Fabry Disease 69 0.024
699
P ALP004 Alport Syndrome 68 0.024
700
CNT098 Central Core Disease 66 0.024
701
KPS004 Kaposi Sarcoma 66 0.024
702
P HYP117 Hypertriglyceridemia 65 0.024
703
P PLR004 Pleuropulmonary Blastoma 64 0.024
704
PRT037 Pertussis 64 0.024
705
P TRN020 Turner Syndrome 64 0.024
706
ALL003 Allergic Rhinitis 64 0.024
707
CHR066 Chronic Fatigue Syndrome 64 0.024
708
P CSH001 Cushing's Syndrome 64 0.024
709
P SPN046 Spinal Muscular Atrophy 63 0.024
710
P PSR002 Psoriasis 63 0.024
711
P NMN002 Niemann-Pick Disease 63 0.024
712
P SPN301 Spinocerebellar Ataxia 2 63 0.024
713
c HMP004 Hemophilia B 62 0.024
714
RCT015 Reactive Arthritis 62 0.024
715
SPN186 Spinal Cord Injury 62 0.024
716
DNG002 Dengue Hemorrhagic Fever 62 0.024
717
BRS051 Breast Disease 62 0.024
718
MDD011 Mood Disorder 61 0.024
719
WLL001 Williams-Beuren Syndrome 61 0.024
720
TYP007 Typhoid Fever 61 0.024
721
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 61 0.024
722
P RHN004 Rhinitis 61 0.024
723
P LYM026 Lymphoblastic Leukemia 60 0.024
724
OVR029 Ovarian Hyperstimulation Syndrome 60 0.024
725
APP008 Appendicitis 60 0.024
726
P SHR029 Short Syndrome 60 0.024
727
GST045 Gastroenteritis 60 0.024
728
SPT004 Septic Arthritis 59 0.024
729
c JBR020 Joubert Syndrome 1 59 0.024
730
c CNG006 Congenital Hypothyroidism 59 0.024
731
P ANT006 Antiphospholipid Syndrome 58 0.024
732
c SRC025 Sarcoidosis 1 58 0.024
733
P CTR002 Cataract 57 0.024
734
RHM027 Rheumatic Disease 57 0.024
735
ING001 Inguinal Hernia 57 0.024
736
PLY023 Polycystic Liver Disease 57 0.024
737
P EXN002 Exanthem 57 0.024
738
ADL030 Adult-Onset Still's Disease 57 0.024
739
P PLY018 Polycythemia 57 0.024
740
P BCK002 Beckwith-Wiedemann Syndrome 56 0.024
741
HPT019 Hepatic Encephalopathy 56 0.024
742
CND002 Conduct Disorder 56 0.024
743
WLM001 Wolman Disease 56 0.024
744
PLM010 Pulmonary Edema 56 0.024
745
INT079 Intrahepatic Cholangiocarcinoma 55 0.024
746
c PND001 Pain Disorder 55 0.024
747
BLD034 Bile Duct Carcinoma 55 0.024
748
GST023 Gastric Ulcer 55 0.024
749
PPL022 Papilloma 55 0.024
750
IMG001 Image Syndrome 55 0.024
751
P HMR012 Hemorrhagic Fever 55 0.024
752
HDC001 Headache 54 0.024
753
P EXP004 Exophthalmos 54 0.024
754
HST011 Histoplasmosis 54 0.024
755
FDL002 Food Allergy 54 0.024
756
P VNS003 Venous Insufficiency 53 0.024
757
P END044 Endometriosis 53 0.024
758
PST046 Post-Transplant Lymphoproliferative Disease 53 0.024
759
C3D001 C3 Deficiency 53 0.024
760
P LYM033 Lymphoproliferative Syndrome 53 0.024
761
HPT022 Hepatoblastoma 53 0.024
762
P CYS018 Cystitis 53 0.024
763
P GND004 Gonadal Dysgenesis 53 0.024
764
P LPD010 Lipodystrophy 52 0.024
765
ANK001 Ankylosis 52 0.024
766
ALS001 Alstrom Syndrome 52 0.024
767
ANG020 Angiosarcoma 52 0.024
768
P PNC001 Pancytopenia 52 0.024
769
TRY001 Trypanosomiasis 52 0.024
770
ALV002 Alveolar Echinococcosis 51 0.024
771
GNR004 Generalized Anxiety Disorder 51 0.024
772
BCT002 Bacterial Vaginosis 51 0.024
773
P HYP237 Hypercalcemia, Infantile 51 0.024
774
DSS009 Disseminated Intravascular Coagulation 51 0.024
775
HNT002 Hantavirus Pulmonary Syndrome 51 0.024
776
MYC002 Mycobacterium Avium Complex Disease 51 0.024
777
FML037 Female Breast Cancer 51 0.024
778
P FML035 Familial Hyperlipidemia 50 0.024
779
CLN019 Colonic Disease 50 0.024
780
c INF023 Inflammatory Breast Carcinoma 50 0.024
781
IMM136 Immune System Disease 50 0.024
782
PLR008 Pleurisy 50 0.024
783
PRP021 Peripheral Nervous System Neoplasm 50 0.024
784
CYS008 Cystic Echinococcosis 50 0.024
785
OVR063 Overnutrition 49 0.024
786
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 49 0.024
787
ESN005 Eosinophilic Gastroenteritis 49 0.024
788
BRN056 Bronchopulmonary Dysplasia 49 0.024
789
P TRN034 Transverse Myelitis 48 0.024
790
c INV001 Invasive Aspergillosis 47 0.024
791
DBT006 Diabetic Macular Edema 47 0.024
792
ORL013 Oral Lichen Planus 47 0.024
793
ECT006 Ectodermal Dysplasia 47 0.024
794
TRN044 Transposition of the Great Arteries 47 0.024
795
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.024
796
HST009 Histiocytoma 47 0.024
797
ESN015 Eosinophilic Fasciitis 46 0.024
798
SPC010 Speech and Communication Disorders 46 0.024
799
MLT006 Multidrug-Resistant Tuberculosis 46 0.024
800
INT017 Intestinal Schistosomiasis 46 0.024
801
DNT012 Dental Caries 46 0.024
802
c CHL080 Cholestasis, Progressive Familial Intrahepatic 1 46 0.024
803
PLM035 Pulmonary Eosinophilia 46 0.024
804
CYS014 Cystadenocarcinoma 46 0.024
805
FSC004 Fasciitis 46 0.024
806
PLM017 Pulmonary Alveolar Microlithiasis 46 0.024
807
c CHL082 Cholestasis, Progressive Familial Intrahepatic 3 46 0.024
808
c ACT042 Acute Pyelonephritis 46 0.024
809
DPH021 Diaphragm Disease 45 0.024
810
VSC047 Vascular Malformation 45 0.024
811
LMT001 Limited Scleroderma 45 0.024
812
P ARC016 Auriculocondylar Syndrome 1 44 0.024
813
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 44 0.024
814
P ART084 Arteriovenous Fistula 44 0.024
815
c HMG003 Hemoglobin E Disease 44 0.024
816
PRC003 Proctitis 43 0.024
817
CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 43 0.024
818
OCL001 Ocular Albinism 43 0.024
819
P PMP005 Pemphigus Vulgaris 43 0.024
820
IRN002 Iron Metabolism Disease 43 0.024
821
CRD003 Cardiac Sarcoidosis 43 0.024
822
PRX075 Proximal Myopathy and Ophthalmoplegia 43 0.024
823
ART031 Aortic Coarctation 42 0.024
824
SMN007 Seminoma 42 0.024
825
c ACT076 Acute Myocarditis 42 0.024
826
FBR003 Fibrous Histiocytoma 42 0.024
827
VLV010 Vulvovaginitis 42 0.024
828
BND014 Bone Development Disease 42 0.024
829
NCR004 Nocardiosis 42 0.024
830
CPL007 Capillary Malformation-Arteriovenous Malformation 41 0.024
831
SPN119 Spondylarthropathy 41 0.024
832
SMT002 Smooth Muscle Tumor 41 0.024
833
c PRG106 Progressive Muscular Dystrophy 41 0.024
834
ANC002 Anca-Associated Vasculitis 41 0.024
835
MNR003 Mineral Metabolism Disease 41 0.024
836
PLT002 Platelet Storage Pool Deficiency 41 0.024
837
IMP006 Impulse Control Disorder 40 0.024
838
SYM002 Sympathetic Ophthalmia 40 0.024
839
GRD001 Giardiasis 40 0.024
840
MCN008 Mucinous Cystadenocarcinoma 40 0.024
841
CYS009 Cystadenoma 40 0.024
842
HYP068 Hyperostosis 40 0.024
843
THL017 Thalassemia Intermedia 40 0.024
844
RCT017 Rectal Disease 39 0.024
845
P HRT035 Heart Block, Congenital 39 0.024
846
MDY003 Mody, Type Ii 38 0.024
847
c PLM022 Pulmonary Valve Insufficiency 38 0.024
848
P MXL015 Maxillary Sinusitis 38 0.024
849
c GLL024 Gallbladder Disease 1 38 0.024
850
LNS003 Lens Disease 38 0.024
851
HTS001 Hiatus Hernia 38 0.024
852
LRN001 Laurence-Moon Syndrome 38 0.024
853
c CHR098 Chronic Pyelonephritis 38 0.024
854
ANT039 Antisynthetase Syndrome 37 0.024
855
IDP074 Idiopathic Bronchiectasis 37 0.024
856
INT052 Intestinal Volvulus 36 0.024
857
ACR002 Acrocapitofemoral Dysplasia 36 0.024
858
PNC002 Pancreatic Mucinous Cystadenoma 35 0.024
859
HRS011 Horseshoe Kidney 35 0.024
860
ADP007 Adie Pupil 34 0.024
861
c MCL040 Macular Degeneration, Age-Related, 3 34 0.024
862
c CNG004 Congenital Epulis 33 0.024
863
MDY005 Mody, Type I 33 0.024
864
DYS011 Dyskinesia of Esophagus 33 0.024
865
MDY006 Mody, Type Iv 33 0.024
866
c NPH046 Nephrolithiasis, Type I 33 0.024
867
SRN001 Serine Deficiency 32 0.024
868
IMM066 Immunodeficiency 9 32 0.024
869
c PNC095 Pancreatic Cancer 3 32 0.024
870
c CRD190 Cardiomyopathy, Hypertrophic, 2 32 0.024
871
BLR002 Bile Reflux 32 0.024
872
CRB031 Cerebral Arterial Disease 31 0.024
873
c TRN038 Transposition of the Great Arteries, Dextro-Looped 1 31 0.024
874
GRN003 Granulomatous Dermatitis 31 0.024
875
IMM102 Immunodeficiency 14 31 0.024
876
SBV001 Subvalvular Aortic Stenosis 31 0.024
877
GST039 Gastroduodenitis 31 0.024
878
LYM043 Lymphocytic Hypophysitis 31 0.024
879
HNS001 Hansen's Disease 29 0.024
880
IMM071 Immunodeficiency 12 28 0.024
881
c CHR036 Chronic Cholangitis 27 0.024
882
PLM007 Pulmonary Aspergilloma 27 0.024
883
HPT077 Hepatic Venoocclusive Disease with Immunodeficiency 27 0.024
884
c MLT094 Multiple Sclerosis 3 26 0.024
885
PNC059 Punctate Inner Choroidopathy 26 0.024
886
KHL001 Kohler's Disease 26 0.024
887
UNV002 Univentricular Heart 26 0.024
888
HND001 Hand Dermatosis 25 0.024
889
c DYS141 Dyskeratosis Congenita, Autosomal Dominant 1 25 0.024
890
NPH064 Nipah Virus Disease 25 0.024
891
PLS031 Plastic Bronchitis 24 0.024
892
c NPH053 Nephronophthisis 11 23 0.024
893
PNB004 Panbronchiolitis, Diffuse 23 0.024
894
c DYS150 Dyskeratosis Congenita, Autosomal Recessive 3 22 0.024
895
HYP213 Hypomelanotic Disorder 21 0.024
896
c MLT093 Multiple Sclerosis 2 20 0.024
897
ATM053 Autoimmune Disease 2 19 0.024
898
ACR025 Acrocephalopolydactylous Dysplasia 18 0.024
899
c MCL026 Macular Dystrophy, Retinal, 3 18 0.024
900
CRR013 Cirrhosis, North American Indian Childhood Type 17 0.024
901
c RNL092 Renal-Hepatic-Pancreatic Dysplasia 1 17 0.024
902
c DLT001 Delta Chain Disease 16 0.024
903
SCD003 Scedosporiosis 15 0.024
904
c BNG076 Benign Exophthalmos Syndrome 14 0.024
905
PLM062 Pulmonary Hyalinizing Granuloma 12 0.024
906
P RTN008 Retinitis Pigmentosa 79 0.020
907
STR067 Stroke, Ischemic 77 0.020
908
ADN021 Adenomatous Polyposis Coli 76 0.020
909
P OVR042 Ovarian Cancer 75 0.020
910
PHN003 Phenylketonuria 73 0.020
911
P NRV007 Nervous System Disease 71 0.020
912
KRT004 Keratitis 70 0.020
913
c NRF018 Neurofibromatosis, Type 1 68 0.020
914
P LPR003 Leprosy 68 0.020
915
SVR004 Severe Combined Immunodeficiency 68 0.020
916
CMM004 Common Variable Immunodeficiency 67 0.020
917
GLC006 Galactosemia 67 0.020
918
P PSD087 Pseudoxanthoma Elasticum 67 0.020
919
P PLY011 Polycystic Ovary Syndrome 66 0.020
920
P FLL037 Follicular Lymphoma 66 0.020
921
P MYS003 Myasthenia Gravis 65 0.020
922
ALC007 Alcohol Dependence 65 0.020
923
LKC001 Leukocyte Adhesion Deficiency 65 0.020
924
CHR012 Chronic Granulomatous Disease 65 0.020
925
c HMP029 Hemophilia a 64 0.020
926
HMT002 Hematologic Cancer 64 0.020
927
P AGM001 Agammaglobulinemia 64 0.020
928
EWN003 Ewing Sarcoma 64 0.020
929
P HMP002 Hemophagocytic Lymphohistiocytosis 63 0.020
930
P ART023 Arthropathy 63 0.020
931
LPT001 Leptospirosis 63 0.020
932
P PRD006 Prader-Willi Syndrome 63 0.020
933
CRD119 Cardiac Arrest 63 0.020
934
c SPN225 Spondyloarthropathy 1 63 0.020
935
LYM017 Lyme Disease 63 0.020
936
P HLP001 Holoprosencephaly 62 0.020
937
P NRV006 Nervous System Cancer 62 0.020
938
APH001 Aphthous Stomatitis 62 0.020
939
FCT003 Factor X Deficiency 62 0.020
940
WGN006 Wegener Granulomatosis 62 0.020
941
FCT007 Factor Vii Deficiency 62 0.020
942
P EHL001 Ehlers-Danlos Syndrome 61 0.020
943
OMN001 Omenn Syndrome 61 0.020
944
GTL001 Gitelman Syndrome 60 0.020
945
CNT097 Central Hypoventilation Syndrome, Congenital 60 0.020
946
P SPN052 Spondyloarthropathy 60 0.020
947
TKY002 Takayasu Arteritis 60 0.020
948
c EHL057 Ehlers-Danlos Syndrome, Type Iv 60 0.020
949
c MCR115 Microvascular Complications of Diabetes 5 60 0.020
950
c ATM010 Autoimmune Hemolytic Anemia 60 0.020
951
P ALC004 Alcohol Abuse 60 0.020
952
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.020
953
RBR001 Roberts Syndrome 59 0.020
954
LPR018 Leprechaunism 59 0.020
955
OST017 Osteomyelitis 59 0.020
956
c NPH055 Nephrotic Syndrome, Type 1 59 0.020
957
URT039 Urticaria 59 0.020
958
P CNG015 Congenital Diaphragmatic Hernia 58 0.020
959
P ANP001 Anaplastic Large Cell Lymphoma 58 0.020
960
P PRP029 Porphyria 58 0.020
961
RTN017 Retinal Detachment 57 0.020
962
P PRC031 Preeclampsia/eclampsia 1 57 0.020
963
ARG002 Argininosuccinic Aciduria 57 0.020
964
P HYP069 Hyperparathyroidism 57 0.020
965
P MTR004 Maturity-Onset Diabetes of the Young 57 0.020
966
c THR082 Thrombophilia Due to Activated Protein C Resistance 57 0.020
967
P CND004 Candidiasis 57 0.020
968
P THR003 Thoracic Aortic Aneurysm 57 0.020
969
P INT143 Interstitial Cystitis 57 0.020
970
PPT005 Peptic Ulcer Disease 56 0.020
971
SPT005 Spotted Fever 56 0.020
972
CHL067 Cholecystitis 56 0.020
973
P SCL018 Scoliosis 56 0.020
974
NRP015 Neuropathy, Congenital Hypomyelinating 56 0.020
975
P BDD001 Budd-Chiari Syndrome 56 0.020
976
FCT022 Factor Xi Deficiency, Autosomal Recessive 56 0.020
977
SPN027 Spinal Stenosis 56 0.020
978
PMS001 Poems Syndrome 55 0.020
979
ALP008 Alopecia 55 0.020
980
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.020
981
PRC002 Paracoccidioidomycosis 55 0.020
982
CHL127 Cholangiocarcinoma, Susceptibility to 55 0.020
983
PTT006 Pituitary Adenoma 55 0.020
984
SCR008 Scrub Typhus 54 0.020
985
P SLV001 Silver-Russell Syndrome 54 0.020
986
c VRL007 Viral Encephalitis 54 0.020
987
CRM001 Crimean-Congo Hemorrhagic Fever 54 0.020
988
P PLY019 Polyneuropathy 54 0.020
989
GRF001 Graft-Versus-Host Disease, Protection Against 54 0.020
990
LYM022 Lymphangioma 54 0.020
991
c AFB002 Afibrinogenemia, Congenital 54 0.020
992
P MST009 Mastocytosis 54 0.020
993
CHR177 Chromophobe Renal Cell Carcinoma 53 0.020
994
P LCH002 Lichen Planus 53 0.020
995
OST015 Osteochondrodysplasia 53 0.020
996
LYM019 Lymphosarcoma 53 0.020
997
P SJG001 Sjogren's Syndrome 53 0.020
998
P HYP027 Hypobetalipoproteinemia 52 0.020
999
LYS002 Lysosomal Storage Disease 52 0.020
1000
PRT014 Protein S Deficiency 52 0.020
1001
CRH005 Crohn's Colitis 52 0.020
1002
P HYP083 Hypopituitarism 52 0.020
1003
VGT001 Vogt-Koyanagi-Harada Disease 52 0.020
1004
PLR022 Pleural Disease 52 0.020
1005
P HYP024 Hypoparathyroidism 52 0.020
1006
APP015 Apparent Mineralocorticoid Excess 52 0.020
1007
GNG012 Gingival Overgrowth 52 0.020
1008
P PRT096 Peritoneal Mesothelioma 51 0.020
1009
NNT012 Neonatal Jaundice 51 0.020
1010
P WVR001 Weaver Syndrome 51 0.020
1011
ACR008 Acrocallosal Syndrome 51 0.020
1012
VND002 Van Der Woude Syndrome 51 0.020
1013
CRT049 Critical Limb Ischemia 51 0.020
1014
CCT002 Cicatricial Pemphigoid 51 0.020
1015
c INF071 Inflammatory Bowel Disease 1 51 0.020
1016
P LPS002 Liposarcoma 50 0.020
1017
MCN001 Mucinous Adenocarcinoma 50 0.020
1018
QBC001 Quebec Platelet Disorder 50 0.020
1019
FCL012 Facial Paralysis 50 0.020
1020
c GLY019 Glycogen Storage Disease Iiia 50 0.020
1021
DBT084 Diabetes Mellitus, Ketosis-Prone 50 0.020
1022
STR008 Strongyloidiasis 50 0.020
1023
PST095 Post-Thrombotic Syndrome 50 0.020
1024
BCL002 B Cell Deficiency 50 0.020
1025
c PSD095 Pseudohypoaldosteronism, Type I 49 0.020
1026
LPD009 Lipid Storage Disease 49 0.020
1027
ASP001 Asperger Syndrome 49 0.020
1028
PRR016 Pierre Robin Syndrome 49 0.020
1029
RLP001 Relapsing Polychondritis 49 0.020
1030
MSS001 Masa Syndrome 49 0.020
1031
P SNR012 Senior-Loken Syndrome-1 49 0.020
1032
ATR057 Atrioventricular Block 49 0.020
1033
P PNV001 Panuveitis 49 0.020
1034
c ANT034 Anterior Uveitis 49 0.020
1035
P LFT003 Left Ventricular Noncompaction 49 0.020
1036
ILT001 Ileitis 49 0.020
1037
CLL003 Cellulitis 49 0.020
1038
PRT018 Portal Vein Thrombosis 49 0.020
1039
PTT009 Pituitary Gland Disease 48 0.020
1040
SHR074 Short-Rib Thoracic Dysplasia 1 with or Without Polydactyly 48 0.020
1041
CRN027 Corneal Neovascularization 48 0.020
1042
ACT017 Acute Chest Syndrome 48 0.020
1043
ADR038 Adermatoglyphia 48 0.020
1044
RSP002 Respiratory Syncytial Virus Infectious Disease 48 0.020
1045
GLT021 Glutaricaciduria, Type I 48 0.020
1046
LYM008 Lymphangiosarcoma 48 0.020
1047
BCT015 Bacteremia 48 0.020
1048
CHL004 Cholelithiasis 48 0.020
1049
CRN017 Coronary Thrombosis 48 0.020
1050
P ADM011 Adams-Oliver Syndrome 48 0.020
1051
MYL001 Myelitis 48 0.020
1052
BRL010 Buruli Ulcer 47 0.020
1053
P MYT002 Myotonic Dystrophy 47 0.020
1054