Search results for fibrosis

2104 hits were found for fibrosis

# Family MCID Name MIFTS Score
1
CYS001 Cystic Fibrosis 85 8.362
2
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 7.936
3
PLM134 Pulmonary Fibrosis, Idiopathic 73 7.322
4
TKL001 Tukel Syndrome 46 5.883
5
ORL004 Oral Submucous Fibrosis 56 5.336
6
P PLM036 Pulmonary Fibrosis 68 5.135
7
PKL002 Poikiloderma, Hereditary Fibrosing, with Tendon Contractures, Myopathy, and Pulmonary Fibrosis 29 4.571
8
END021 Endomyocardial Fibrosis 51 4.433
9
CCH002 Coach Syndrome 51 4.116
10
RTR011 Retroperitoneal Fibrosis 43 4.037
11
P CNG048 Congenital Hepatic Fibrosis 41 3.732
12
FBR089 Fibrosclerosis, Multifocal 28 3.677
13
c FBR050 Fibrosis of Extraocular Muscles, Congenital, 2 25 3.630
14
FBR094 Fibrosis of Extraocular Muscles, Congenital, 3a, with or Without Extraocular Involvement 25 3.622
15
RNL077 Renal Fibrosis 49 3.222
16
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 48 3.088
17
CYS047 Cystic Fibrosis, Modifier of, 1 15 3.080
18
FBR028 Fibrosing Mediastinitis 28 3.029
19
NPH018 Nephrogenic Systemic Fibrosis 56 2.960
20
DFF002 Diffuse Pulmonary Fibrosis 29 2.869
21
PLM139 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 1 22 2.771
22
c HPT084 Hepatic Fibrosis, Severe Due to Schistosoma Mansoni Infection 14 2.745
23
IDP011 Idiopathic Interstitial Pneumonia 60 2.742
24
P FBR081 Fibrosis of Extraocular Muscles, Congenital, 3c 16 2.735
25
c FBR078 Fibrosis of Extraocular Muscles, Congenital, 5 14 2.735
26
EF001 Eaf 27 2.723
27
CYS040 Cystic Fibrosis with Helicobacter Pylori Gastritis, Megaloblastic Anemia, and Mental Retardation 21 2.395
28
PLM141 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 4 17 2.391
29
PLM143 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 3 16 2.391
30
FBR096 Fibrosis of Extraocular Muscles, Congenital, with Synergistic Divergence 11 2.369
31
PST015 Postinflammatory Pulmonary Fibrosis 12 2.362
32
LBN005 Lubani-Al Saleh-Teebi Syndrome 7 2.355
33
IGG007 Igg4-Related Disease 43 1.988
34
ACT029 Acute Interstitial Pneumonia 41 1.984
35
PRR004 Preretinal Fibrosis 37 1.970
36
c CNG189 Congenital Disorder of Glycosylation, Type Ib 36 1.965
37
HRM018 Hermansky-Pudlak Syndrome with Pulmonary Fibrosis 19 1.954
38
BRN075 Bronchiectasis with or Without Elevated Sweat Chloride 2 19 1.954
39
IMM129 Immunodeficiency, Ovarian Dysgenesis, and Pulmonary Fibrosis 17 1.954
40
BRN077 Bronchiectasis with or Without Elevated Sweat Chloride 3 17 1.954
41
BRN076 Bronchiectasis with or Without Elevated Sweat Chloride 1 26 1.948
42
HRM016 Hermansky-Pudlak Syndrome Without Pulmonary Fibrosis 17 1.941
43
MSC030 Muscular Fibrosis Multifocal Obstructed Vessels 14 1.941
44
c LCL003 Localized Pulmonary Fibrosis 5 1.934
45
FBR086 Fibrolamellar Carcinoma 50 1.916
46
ASB001 Asbestosis 45 1.488
47
SLC006 Silicosis 57 1.485
48
TRP020 Tropical Endomyocardial Fibrosis 32 1.482
49
P MYL005 Myelofibrosis 75 1.473
50
c PLM044 Pulmonary Fibrosis, Familial 12 1.431
51
ARW003 Airway-Centered Interstitial Fibrosis 9 1.427
52
PLM145 Pulmonary Fibrosis-Hepatic Hyperplasia-Bone Marrow Hypoplasia Syndrome 15 1.406
53
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 9 1.400
54
ISL112 Isolated Congenital Hepatic Fibrosis 7 1.400
55
DBT022 Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism 28 1.393
56
CRB163 Cerebellar Vermis Aplasia with Associated Features Suggesting Smith-Lemli-Opitz Syndrome and Meckel Syndrome 21 1.393
57
c NTR031 Neutropenia, Severe Congenital, 5, Autosomal Recessive 29 1.386
58
FML074 Familial Interstitial Fibrosis 2 1.386
59
FBR016 Fibrosclerosis of Breast 21 1.377
60
CMP074 Camptodactyly, Myopia, and Fibrosis of the Medial Rectus Muscle of Eye 18 1.377
61
SNR014 Senior-Boichis Syndrome 13 1.377
62
RZN001 Rozin Hertz Goodman Syndrome 7 1.377
63
CYS042 Cystic Fibrosis and Congenital Absence of the Vas Deferens 0 1.377
64
TYL001 Taylor's Syndrome 33 1.355
65
SCR009 Scirrhous Adenocarcinoma 22 1.355
66
PLM113 Palmoplantar Keratoderma-Sclerodactyly Syndrome 16 1.355
67
GRP001 Graphite Pneumoconiosis 11 1.355
68
P HPT021 Hepatitis 75 0.509
69
PNC034 Pancreas Disease 59 0.405
70
LNG099 Lung Disease 67 0.346
71
c HPT001 Hepatitis C 73 0.291
72
P LVR013 Liver Disease 76 0.289
73
P PNM007 Pneumonia 70 0.285
74
RSP006 Respiratory System Disease 63 0.265
75
BRN022 Bronchiectasis 55 0.235
76
P PNC044 Pancreatitis 64 0.234
77
URT010 Ureteral Obstruction 49 0.200
78
c HPT073 Hepatitis C Virus 73 0.190
79
LVR012 Liver Cirrhosis 73 0.189
80
P ASP006 Aspergillosis 65 0.187
81
P ALL008 Allergic Bronchopulmonary Aspergillosis 56 0.180
82
FTT001 Fatty Liver Disease 62 0.179
83
c HPT016 Hepatitis B 68 0.177
84
c SCL052 Scleroderma, Familial Progressive 60 0.175
85
P KDN018 Kidney Disease 69 0.168
86
NNL002 Nonalcoholic Steatohepatitis 56 0.161
87
c HPT003 Hepatitis a 63 0.157
88
c BLD140 Blood Group, I System 37 0.153
89
GST050 Gastrointestinal System Disease 66 0.148
90
P HRT032 Heart Disease 80 0.142
91
MCN017 Meconium Ileus 52 0.142
92
INT066 Interstitial Lung Disease 63 0.140
93
AST005 Asthma 83 0.133
94
P PLM037 Pulmonary Hypertension 79 0.129
95
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.129
96
VRL011 Viral Infectious Disease 64 0.128
97
AGN016 Aging 65 0.127
98
c VRL010 Viral Hepatitis 59 0.125
99
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.124
100
EXC002 Exocrine Pancreatic Insufficiency 45 0.123
101
P PRT013 Portal Hypertension 59 0.121
102
END072 Endotheliitis 46 0.119
103
P DBT009 Diabetes Mellitus 72 0.117
104
SCH014 Schistosomiasis 62 0.117
105
SPS003 Spastic Diplegia 55 0.116
106
P VSC018 Visceral Steatosis 38 0.115
107
BRN038 Bronchial Disease 58 0.110
108
P HPT023 Hepatocellular Carcinoma 94 0.109
109
CNN005 Connective Tissue Disease 65 0.106
110
BLR001 Biliary Atresia 56 0.104
111
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 27 0.103
112
P LNG032 Lung Cancer 99 0.102
113
P HYP061 Hypertrophic Cardiomyopathy 65 0.102
114
P CHL066 Cholangitis 52 0.102
115
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.101
116
P PLY014 Polycystic Kidney Disease 60 0.100
117
PRT036 Peritonitis 67 0.098
118
P THY032 Thyroiditis 56 0.097
119
NNS002 Nonspecific Interstitial Pneumonia 46 0.097
120
MYC013 Mycobacterium Abscessus 45 0.097
121
SQM006 Squamous Cell Carcinoma 74 0.096
122
CNG034 Congestive Heart Failure 74 0.096
123
P HRM001 Hermansky-Pudlak Syndrome 62 0.096
124
CHL068 Cholestasis 60 0.092
125
P DLT002 Dilated Cardiomyopathy 76 0.089
126
P ADN016 Adenocarcinoma 71 0.089
127
P MSC005 Muscular Dystrophy 66 0.089
128
HYP266 Hypoxia 61 0.089
129
BRN002 Bronchiolitis 59 0.089
130
P INF032 Infertility 59 0.089
131
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.088
132
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.088
133
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.088
134
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.088
135
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.088
136
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.088
137
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.088
138
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.088
139
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.088
140
P LKM002 Leukemia 75 0.087
141
P ART022 Arthritis 77 0.085
142
P ATR011 Atrial Fibrillation 68 0.085
143
P SCL009 Sclerosing Cholangitis 53 0.085
144
ACQ007 Acquired Immunodeficiency Syndrome 65 0.084
145
P SNS014 Sinusitis 62 0.084
146
ANR040 Aneurysm 61 0.084
147
HYP006 Hypertensive Heart Disease 51 0.084
148
ISC004 Ischemia 66 0.082
149
c CHR089 Chronic Kidney Failure 72 0.081
150
P LYM118 Lymphoma 71 0.081
151
P GLM007 Glomerulonephritis 61 0.081
152
GLC003 Glucose Intolerance 58 0.081
153
P INT070 Intestinal Obstruction 55 0.081
154
MDS022 Mediastinitis 44 0.081
155
VSC007 Vascular Disease 71 0.079
156
SKN016 Skin Disease 68 0.079
157
P SYS005 Systemic Scleroderma 67 0.079
158
THR024 Thrombosis 61 0.079
159
BRN012 Bronchiolitis Obliterans 60 0.079
160
P PLM034 Pulmonary Emphysema 59 0.079
161
P PNM006 Pneumoconiosis 55 0.079
162
LKP003 Leukoplakia 42 0.079
163
ASB003 Asbestos Intoxication 19 0.079
164
P RHM011 Rheumatoid Arthritis 91 0.078
165
MCS002 Mucositis 61 0.078
166
P PRM011 Primary Ciliary Dyskinesia 57 0.078
167
BRN024 Bronchitis 67 0.076
168
SKN027 Skin Conditions 48 0.076
169
ANX010 Anxiety 72 0.075
170
CLT003 Colitis 63 0.075
171
ORL015 Oral Squamous Cell Carcinoma 59 0.075
172
MCR088 Microscopic Polyangiitis 58 0.075
173
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.075
174
P MYC007 Myocardial Infarction 81 0.073
175
P ANR048 Aniridia 1 68 0.073
176
BRR014 Barrett Esophagus 64 0.073
177
P NPH005 Nephronophthisis 57 0.073
178
PLY156 Polycystic Kidney Disease 4 with or Without Hepatic Disease 56 0.073
179
P PRM006 Primary Biliary Cirrhosis 55 0.073
180
HPD002 Hepadnavirus Infection 14 0.073
181
P INF038 Influenza 77 0.071
182
P RSP003 Respiratory Failure 71 0.071
183
P ESP024 Esophagitis 64 0.070
184
PRN021 Paranasal Sinus Disease 51 0.070
185
P BRS047 Breast Cancer 100 0.068
186
ALL026 Allergic Hypersensitivity Disease 59 0.068
187
SPL018 Splenomegaly 45 0.068
188
c TRC078 Trichohepatoenteric Syndrome 2 34 0.068
189
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.068
190
CRH001 Crohn's Disease 80 0.066
191
DFF003 Diffuse Scleroderma 44 0.066
192
STT004 Steatorrhea 41 0.066
193
P FTT008 Fatty Liver Disease, Nonalcoholic 1 25 0.066
194
ANR038 Anorexia Nervosa 1 21 0.066
195
BLD137 Blood Group--Ahonen 17 0.066
196
BRC012 Brucellosis 71 0.064
197
VSC011 Vasculitis 66 0.064
198
HYP066 Hyperglycemia 64 0.064
199
GST092 Gastroesophageal Reflux 64 0.064
200
c ATM011 Autoimmune Hepatitis 63 0.064
201
MNT002 Mental Depression 60 0.064
202
ORL011 Oral Cancer 60 0.064
203
PRS047 Prostatitis 59 0.064
204
P MYC008 Myocarditis 58 0.064
205
ORL012 Oral Leukoplakia 45 0.064
206
c BLR024 Biliary Cirrhosis, Primary, 1 35 0.064
207
VSD002 Vas Deferens, Congenital Bilateral Aplasia of 34 0.064
208
ALR002 Al-Raqad Syndrome 30 0.064
209
P LPS004 Lupus Erythematosus 69 0.062
210
c ART101 Aortic Valve Disease 2 65 0.062
211
c CHL119 Cholangitis, Primary Sclerosing 60 0.062
212
PLM012 Pulmonary Sarcoidosis 58 0.062
213
PNM008 Pneumothorax 57 0.062
214
P PLM006 Pulmonary Alveolar Proteinosis 49 0.062
215
c PLY141 Polycystic Kidney Disease 5 42 0.062
216
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.062
217
ALP046 Alport Syndrome, X-Linked 74 0.060
218
P HYP098 Hypereosinophilic Syndrome 65 0.060
219
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.060
220
URN009 Urinary System Disease 58 0.060
221
BRN106 Burns 57 0.060
222
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.060
223
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.060
224
c SYS001 Systemic Lupus Erythematosus 86 0.058
225
INS024 Insulin-Like Growth Factor I 83 0.058
226
P OST002 Osteoporosis 75 0.058
227
MSC157 Muscular Dystrophy, Duchenne Type 74 0.058
228
P MYP004 Myopathy 69 0.058
229
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.058
230
P THR014 Thrombocytopenia 65 0.058
231
EXT034 Extrinsic Allergic Alveolitis 57 0.058
232
c MCR113 Microvascular Complications of Diabetes 3 55 0.058
233
RTN023 Retinitis 52 0.058
234
P PRC012 Pericardial Effusion 52 0.058
235
NSD001 Nose Disease 51 0.058
236
HMS001 Hemosiderosis 50 0.058
237
c ATM024 Autoimmune Pancreatitis 49 0.058
238
HRT012 Heart Valve Disease 45 0.058
239
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.058
240
ISC006 Ischemic Heart Disease 73 0.056
241
P GRF003 Graft-Versus-Host Disease 72 0.056
242
P INT068 Intestinal Disease 65 0.056
243
P END033 Endocarditis 58 0.056
244
P CRN300 Coronary Heart Disease 1 57 0.056
245
STR020 Strabismus 55 0.056
246
CHR008 Choroiditis 47 0.056
247
DDN006 Duodenitis 46 0.056
248
P RNG031 Ring Chromosome Y Syndrome 29 0.056
249
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.054
250
ART016 Aortic Aneurysm 70 0.054
251
P MYC084 Mycobacterium Tuberculosis 1 69 0.054
252
P CRN018 Coronary Artery Anomaly 69 0.054
253
P DYS007 Dyskeratosis Congenita 68 0.054
254
c SML038 Small Cell Cancer of the Lung 67 0.054
255
P DRM010 Dermatomyositis 65 0.054
256
P THL005 Thalassemia 65 0.054
257
P LYM025 Lymphedema 63 0.054
258
ALC006 Alcoholic Hepatitis 62 0.054
259
c ACT027 Acute Pancreatitis 61 0.054
260
P MTR012 Mitral Valve Disease 59 0.054
261
IGR001 Ige Responsiveness, Atopic 56 0.054
262
PRC013 Pericarditis 55 0.054
263
DFF035 Diffuse Cutaneous Systemic Sclerosis 53 0.054
264
HYD002 Hydronephrosis 49 0.054
265
c MCR130 Microvascular Complications of Diabetes 6 42 0.054
266
ACR005 Acrodermatitis 35 0.054
267
c MCR120 Microvascular Complications of Diabetes 7 34 0.054
268
c MCR133 Microvascular Complications of Diabetes 4 32 0.054
269
MYL009 Myelodysplastic Syndrome 75 0.052
270
P TTR001 Tetralogy of Fallot 70 0.052
271
DRM006 Dermatitis 67 0.052
272
ATM095 Autoimmune Disease 66 0.052
273
NRM005 Neuromuscular Disease 60 0.052
274
P PYL005 Pyelonephritis 56 0.052
275
P ESP035 Esophagitis, Eosinophilic, 1 55 0.052
276
P TRC086 Trichohepatoenteric Syndrome 1 54 0.052
277
STS002 Situs Inversus 48 0.052
278
P SDR002 Siderosis 48 0.052
279
c MTR002 Mitral Valve Insufficiency 46 0.052
280
PRT019 Protein-Losing Enteropathy 40 0.052
281
MLT035 Multifocal Choroiditis 35 0.052
282
ENT007 Enteropathica 29 0.052
283
P STR035 Streptococcal Group a Invasive Disease 28 0.052
284
PLM001 Pulmonary Tuberculosis 72 0.049
285
MXD005 Mixed Connective Tissue Disease 66 0.049
286
c LCL006 Localized Scleroderma 66 0.049
287
GNG013 Gingivitis 64 0.049
288
c ACT210 Acute Respiratory Distress Syndrome 63 0.049
289
P MYS005 Myositis 63 0.049
290
P HYP086 Hypothyroidism 62 0.049
291
P UVT001 Uveitis 61 0.049
292
ALP103 Alpha-1-Antitrypsin Deficiency 60 0.049
293
RHM028 Rheumatic Heart Disease 54 0.049
294
HPT009 Hepatopulmonary Syndrome 53 0.049
295
HPT082 Hepatic Adenomas, Familial 52 0.049
296
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.049
297
KLD001 Keloids 50 0.049
298
ALB002 Albinism 45 0.049
299
URT001 Urethritis 44 0.049
300
c ATM022 Autoimmune Myocarditis 40 0.049
301
ART012 Aortitis 33 0.049
302
HRP008 Herpes Simiae 16 0.049
303
GST053 Gastric Cancer 84 0.047
304
WLS001 Wilson Disease 72 0.047
305
DWN001 Down Syndrome 70 0.047
306
c CHR417 Chronic Graft Versus Host Disease 65 0.047
307
P RHN004 Rhinitis 62 0.047
308
ALL006 Allergic Asthma 60 0.047
309
P DRR001 Diarrhea 60 0.047
310
HYP810 Hypereosinophilic Syndrome, Idiopathic 57 0.047
311
P PLY041 Polymyositis 57 0.047
312
ERD001 Erdheim-Chester Disease 57 0.047
313
P MSC003 Muscular Atrophy 55 0.047
314
c PYR010 Peyronie's Disease 54 0.047
315
NDL013 Nodular Regenerative Hyperplasia 53 0.047
316
ACR056 Acrodermatitis Enteropathica, Zinc-Deficiency Type 51 0.047
317
HMP009 Haemophilus Influenzae 49 0.047
318
HYP457 Hypertrophic Scars 48 0.047
319
AZS001 Azoospermia 47 0.047
320
c RCR022 Recurrent Acute Pancreatitis 43 0.047
321
CRB009 Cerebritis 41 0.047
322
ANT018 Anthracosis 39 0.047
323
PLY112 Polyarteritis Nodosa, Childhood-Onset 39 0.047
324
DSQ001 Desquamative Interstitial Pneumonia 37 0.047
325
HMP001 Hemopericardium 34 0.047
326
INT304 Interstitial Pneumonitis, Desquamative, Familial 31 0.047
327
c DYS143 Dyskeratosis Congenita, Autosomal Dominant 2 28 0.047
328
BLD163 Blood Group, Dombrock System 23 0.047
329
STN013 Stenotrophomonas Maltophilia Infection 22 0.047
330
MLR004 Malaria 86 0.044
331
CHG001 Chagas Disease 72 0.044
332
WGN006 Wegener Granulomatosis 71 0.044
333
P TYS001 Tay-Sachs Disease 71 0.044
334
c JVN010 Juvenile Rheumatoid Arthritis 71 0.044
335
P TRN020 Turner Syndrome 69 0.044
336
P AMY004 Amyloidosis 69 0.044
337
P PRD008 Periodontitis 67 0.044
338
HSH003 Hashimoto Thyroiditis 67 0.044
339
P SLP006 Sleep Apnea 65 0.044
340
P SRC025 Sarcoidosis 1 63 0.044
341
P ART021 Arteriosclerosis 62 0.044
342
P MCK013 Meckel Syndrome, Type 1 62 0.044
343
P CMR001 Camurati-Engelmann Disease 62 0.044
344
MRB003 Morbid Obesity 61 0.044
345
BRN056 Bronchopulmonary Dysplasia 61 0.044
346
P NPH012 Nephrotic Syndrome 60 0.044
347
SLP005 Sleep Disorder 59 0.044
348
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.044
349
P OCL002 Oculocutaneous Albinism 57 0.044
350
IMM158 Immune Suppression 57 0.044
351
IMM136 Immune System Disease 57 0.044
352
CYT008 Cytomegalovirus Infection 57 0.044
353
P MMB011 Membranous Nephropathy 55 0.044
354
P PMP001 Pemphigus 55 0.044
355
BLR006 Biliary Tract Disease 55 0.044
356
SCK005 Sickle Cell Disease 54 0.044
357
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.044
358
HMG005 Hemoglobinopathy 53 0.044
359
P OBS001 Obstructive Jaundice 53 0.044
360
CHR001 Churg-Strauss Syndrome 51 0.044
361
P RST002 Restrictive Cardiomyopathy 51 0.044
362
CRY004 Cryoglobulinemia 49 0.044
363
P CRV039 Cervicitis 49 0.044
364
SLD003 Sialadenitis 49 0.044
365
P PLM085 Pulmonary Hemosiderosis 48 0.044
366
P HYP058 Hypervitaminosis a 48 0.044
367
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.044
368
P RPD001 Rapidly Progressive Glomerulonephritis 48 0.044
369
DST006 Diastolic Heart Failure 47 0.044
370
BCK006 Back Pain 46 0.044
371
IMM001 Immune-Complex Glomerulonephritis 39 0.044
372
GLC008 Glucose Metabolism Disease 38 0.044
373
c DYS149 Dyskeratosis Congenita, Autosomal Recessive 1 35 0.044
374
PNB004 Panbronchiolitis, Diffuse 34 0.044
375
c SRC023 Sarcoidosis 2 30 0.044
376
PRQ002 Paraquat Poisoning 27 0.044
377
P PNC035 Pancreatic Cancer 89 0.041
378
P PRS040 Prostate Cancer 88 0.041
379
ULC004 Ulcerative Colitis 80 0.041
380
c MCL042 Macular Degeneration, Age-Related, 1 79 0.041
381
P MYS003 Myasthenia Gravis 73 0.041
382
MLD001 Melioidosis 73 0.041
383
c SPN225 Spondyloarthropathy 1 71 0.041
384
P MNN013 Meningitis 71 0.041
385
P ESS003 Essential Thrombocythemia 71 0.041
386
c BTT014 Beta-Thalassemia 70 0.041
387
CHL065 Cholangiocarcinoma 70 0.041
388
P JBR020 Joubert Syndrome 1 68 0.041
389
SRC014 Sarcoma 68 0.041
390
P ADL010 Adult Respiratory Distress Syndrome 67 0.041
391
P LYM026 Lymphoblastic Leukemia 66 0.041
392
GST045 Gastroenteritis 65 0.041
393
APP008 Appendicitis 64 0.041
394
P GLL020 Gallbladder Disease 64 0.041
395
MYL031 Myeloproliferative Neoplasm 64 0.041
396
MSC152 Muscular Dystrophy, Becker Type 64 0.041
397
ADN018 Adenoma 63 0.041
398
P NRP001 Neuropathy 63 0.041
399
P SPN046 Spinal Muscular Atrophy 63 0.041
400
PLM033 Pulmonary Embolism 62 0.041
401
P GCH001 Gaucher's Disease 62 0.041
402
VTR013 Vitreoretinopathy, Neovascular Inflammatory 61 0.041
403
PRC002 Paracoccidioidomycosis 59 0.041
404
CRC006 Carcinoid Syndrome 59 0.041
405
FLR002 Filariasis 58 0.041
406
P ENC018 Encephalopathy 58 0.041
407
URN010 Urinary Tract Obstruction 57 0.041
408
CNS004 Constipation 57 0.041
409
ECH003 Echinococcosis 57 0.041
410
SPN051 Spondylitis 55 0.041
411
KRT002 Keratomalacia 55 0.041
412
P CLL015 Collagen Disease 53 0.041
413
MLN007 Male Infertility 53 0.041
414
c PNS012 Paine Syndrome 52 0.041
415
BLD036 Bile Duct Disease 52 0.041
416
PLR008 Pleurisy 52 0.041
417
P PLY017 Polyarteritis Nodosa 51 0.041
418
ART140 Arteries, Anomalies of 51 0.041
419
CHN070 Cohen-Gibson Syndrome 51 0.041
420
MGC001 Megacolon 50 0.041
421
RNL078 Renal Dysplasia 49 0.041
422
NPH003 Nephrocalcinosis 49 0.041
423
PRD004 Prediabetes Syndrome 46 0.041
424
P HRT035 Heart Block, Congenital 45 0.041
425
P PRL003 Proliferative Glomerulonephritis 45 0.041
426
NRN002 Neuronitis 43 0.041
427
CTS003 Coats Disease 42 0.041
428
HRN026 Hernia, Hiatus 42 0.041
429
WRN005 Wrinkles 41 0.041
430
CHP002 Chops Syndrome 40 0.041
431
ALC005 Alcoholic Pancreatitis 39 0.041
432
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.041
433
P BLD124 Bleeding Disorder, Platelet-Type, 11 38 0.041
434
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.041
435
CHL045 Choline Deficiency Disease 27 0.041
436
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.041
437
P ATX030 Ataxia-Telangiectasia 80 0.038
438
c HYP595 Hypertension, Essential 78 0.038
439
APL001 Aplastic Anemia 74 0.038
440
SCK003 Sickle Cell Anemia 73 0.038
441
MLN008 Melanoma 72 0.038
442
P END044 Endometriosis 71 0.038
443
c HMC039 Hemochromatosis, Type 1 71 0.038
444
HMN044 Human Immunodeficiency Virus Type 1 71 0.038
445
CNN003 Conn's Syndrome 70 0.038
446
P MYL006 Myeloid Leukemia 69 0.038
447
LYM007 Lymphangioleiomyomatosis 68 0.038
448
PNC041 Pancreatic Ductal Adenocarcinoma 67 0.038
449
CNT047 Contact Dermatitis 64 0.038
450
SHW002 Shwachman-Diamond Syndrome 63 0.038
451
HYP056 Hypoglycemia 62 0.038
452
c MCR129 Microvascular Complications of Diabetes 1 62 0.038
453
c THR092 Thrombophilia Due to Thrombin Defect 61 0.038
454
P HST010 Histiocytosis 60 0.038
455
HRY003 Hairy Cell Leukemia 60 0.038
456
c ATR087 Atrial Standstill 1 59 0.038
457
PHR003 Pharyngitis 59 0.038
458
P LCH002 Lichen Planus 58 0.038
459
NRN004 Neuroendocrine Tumor 58 0.038
460
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.038
461
PLM010 Pulmonary Edema 57 0.038
462
NPH009 Nephrolithiasis 57 0.038
463
CHL014 Cholera 56 0.038
464
BCT002 Bacterial Vaginosis 56 0.038
465
P RTN016 Retinal Degeneration 56 0.038
466
PST046 Post-Transplant Lymphoproliferative Disease 56 0.038
467
PRM236 Primary Biliary Cholangitis 56 0.038
468
THR004 Thrombocytosis 55 0.038
469
TRY001 Trypanosomiasis 55 0.038
470
P TRN034 Transverse Myelitis 53 0.038
471
ESN015 Eosinophilic Fasciitis 52 0.038
472
P INF037 Inflammatory Bowel Disease 52 0.038
473
URM002 Uremia 52 0.038
474
GNG012 Gingival Overgrowth 52 0.038
475
INT051 Intussusception 51 0.038
476
c INV001 Invasive Aspergillosis 51 0.038
477
HYD005 Hydrocele 51 0.038
478
P NGH001 Night Blindness 51 0.038
479
P LPM005 Lipomatosis 50 0.038
480
HYP063 Hypersplenism 49 0.038
481
PRP007 Priapism 49 0.038
482
FSC004 Fasciitis 48 0.038
483
P RNV001 Renovascular Hypertension 48 0.038
484
PNN001 Panniculitis 48 0.038
485
KRT010 Kartagener Syndrome 46 0.038
486
NPH010 Nephrosclerosis 46 0.038
487
MDL009 Medullary Sponge Kidney 46 0.038
488
LYM024 Lymphatic System Disease 45 0.038
489
CRY001 Cryptogenic Organizing Pneumonia 45 0.038
490
IRN002 Iron Metabolism Disease 45 0.038
491
c HRM017 Hermansky-Pudlak Syndrome 2 45 0.038
492
CHR078 Chorioretinitis 41 0.038
493
DRM009 Dermatomycosis 39 0.038
494
HMC038 Hemochromatosis, Neonatal 38 0.038
495
SRF006 Surfactant Dysfunction 37 0.038
496
CNS002 Constrictive Pericarditis 37 0.038
497
c PNC106 Pancreatic Agenesis 1 36 0.038
498
XRP001 Xerophthalmia 35 0.038
499
MSC012 Muscular Dystrophy, Duchenne and Becker Type 35 0.038
500
c DYS141 Dyskeratosis Congenita, Autosomal Dominant 1 34 0.038
501
c HYP555 Hypertriglyceridemia, Transient Infantile 34 0.038
502
SPN331 Spondyloocular Syndrome 34 0.038
503
DDN009 Duodenal Obstruction 34 0.038
504
RHM009 Rheumatoid Lung Disease 34 0.038
505
BLC007 Bile Acid Synthesis Defect, Congenital, 1 34 0.038
506
KSH001 Keshan Disease 33 0.038
507
ACR025 Acrocephalopolydactylous Dysplasia 33 0.038
508
c NPH031 Nephronophthisis 3 32 0.038
509
IGG011 Igg4-Related Kidney Disease 15 0.038
510
OST012 Osteoarthritis 88 0.035
511
P RTN024 Retinoblastoma 76 0.035
512
MRF001 Marfan Syndrome 75 0.035
513
P CRV035 Cervical Cancer 72 0.035
514
FBR012 Fabry Disease 72 0.035
515
P BCL006 B-Cell Lymphomas 70 0.035
516
P FRG001 Fragile X Syndrome 69 0.035
517
P ORT004 Orthostatic Intolerance 68 0.035
518
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.035
519
P ART023 Arthropathy 68 0.035
520
APN008 Apnea, Obstructive Sleep 67 0.035
521
ADL030 Adult-Onset Still's Disease 65 0.035
522
DFF005 Diffuse Large B-Cell Lymphoma 64 0.035
523
VRC005 Varicose Veins 64 0.035
524
OST017 Osteomyelitis 64 0.035
525
CRP001 Carpal Tunnel Syndrome 64 0.035
526
c ACT075 Acute Myocardial Infarction 64 0.035
527
MTH009 Mouth Disease 64 0.035
528
LNG108 Langerhans Cell Histiocytosis 63 0.035
529
P CHR285 Chronic Myelomonocytic Leukemia 63 0.035
530
RHM027 Rheumatic Disease 62 0.035
531
CMM005 Common Cold 62 0.035
532
P HML002 Hemolytic Anemia 62 0.035
533
P GRV001 Graves' Disease 62 0.035
534
P CND004 Candidiasis 61 0.035
535
P GLY013 Glycogen Storage Disease 61 0.035
536
P HMN010 Hemangioma 61 0.035
537
P SPN052 Spondyloarthropathy 61 0.035
538
P CTR002 Cataract 60 0.035
539
P ANT006 Antiphospholipid Syndrome 59 0.035
540
END030 End Stage Renal Failure 59 0.035
541
PPL022 Papilloma 58 0.035
542
c SVR001 Severe Acute Respiratory Syndrome 58 0.035
543
HMT018 Hematopoietic Stem Cell Transplantation 58 0.035
544
RTN018 Retinal Disease 56 0.035
545
BNF002 Bone Fracture 56 0.035
546
ESN005 Eosinophilic Gastroenteritis 56 0.035
547
GST037 Gastroparesis 56 0.035
548
CYS010 Cystinosis 55 0.035
549
c INT064 Intermediate Uveitis 54 0.035
550
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 54 0.035
551
P DBT005 Diabetes Insipidus 54 0.035
552
SHR074 Short-Rib Thoracic Dysplasia 1 with or Without Polydactyly 54 0.035
553
RSP002 Respiratory Syncytial Virus Infectious Disease 53 0.035
554
MSC033 Muscle Disorders 53 0.035
555
P DDN001 Duodenal Ulcer 53 0.035
556
ALC009 Alcoholic Liver Cirrhosis 53 0.035
557
FBR032 Fibromuscular Dysplasia 53 0.035
558
PRT038 Protein-Energy Malnutrition 52 0.035
559
c CHL132 Cholestasis, Progressive Familial Intrahepatic, 1 52 0.035
560
ENT011 Enterocolitis 52 0.035
561
P SHR001 Short Bowel Syndrome 52 0.035
562
c ACT134 Acute Liver Failure 52 0.035
563
PRR002 Pure Red-Cell Aplasia 52 0.035
564
NTR046 Neutrophil Migration 51 0.035
565
BRL010 Buruli Ulcer 51 0.035
566
ATN005 Autonomic Dysfunction 51 0.035
567
INT067 Interstitial Nephritis 51 0.035
568
CYS014 Cystadenocarcinoma 51 0.035
569
MDD010 Middle Ear Disease 50 0.035
570
PNC001 Pancytopenia 50 0.035
571
P PTS002 Ptosis 50 0.035
572
P GNG025 Gingival Fibromatosis 50 0.035
573
TRN044 Transposition of the Great Arteries 49 0.035
574
ANX004 Anoxia 49 0.035
575
ANR004 Anuria 49 0.035
576
PLM017 Pulmonary Alveolar Microlithiasis 48 0.035
577
c ACT042 Acute Pyelonephritis 48 0.035
578
MLT006 Multidrug-Resistant Tuberculosis 48 0.035
579
ART004 Aortic Atherosclerosis 48 0.035
580
DYS073 Dysphagia 47 0.035
581
c HRM005 Hermansky-Pudlak Syndrome 1 47 0.035
582
P PSD003 Pseudohypoaldosteronism 47 0.035
583
CLP005 Ciliopathy 46 0.035
584
CLN003 Clonorchiasis 46 0.035
585
ARC002 Arachnoiditis 45 0.035
586
PRS127 Pearson Marrow-Pancreas Syndrome 45 0.035
587
FSC002 Fascioliasis 45 0.035
588
BRN014 Bronchopneumonia 45 0.035
589
MYX004 Myxedema 44 0.035
590
c WLM011 Wilms Tumor 6 44 0.035
591
BLD063 Bile Duct Cysts 44 0.035
592
TTH032 Tooth Size 44 0.035
593
STR089 Storage Pool Platelet Disease 43 0.035
594
CLL021 Collagenous Colitis 43 0.035
595
ACT055 Actinomycosis 43 0.035
596
KWS001 Kwashiorkor 43 0.035
597
RDD003 Riddle Syndrome 41 0.035
598
MCN008 Mucinous Cystadenocarcinoma 41 0.035
599
SLL001 Sialolithiasis 41 0.035
600
MVM001 Movement Disease 40 0.035
601
MSC004 Muscle Tissue Disease 39 0.035
602
EXT006 Extrahepatic Cholestasis 39 0.035
603
DYS011 Dyskinesia of Esophagus 39 0.035
604
ATN011 Autoinflammation with Infantile Enterocolitis 39 0.035
605
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.035
606
BTL002 Beta-Lactam Allergy 37 0.035
607
SCR003 Secretory Diarrhea 36 0.035
608
c SRF005 Surfactant Metabolism Dysfunction, Pulmonary, 3 35 0.035
609
CYT004 Cytomegalic Inclusion Disease 35 0.035
610
LNG095 Lung Abscess 34 0.035
611
GRW036 Growth Control, Y-Chromosome Influenced 33 0.035
612
CYN002 Cyanosis, Transient Neonatal 32 0.035
613
c SRF008 Surfactant Metabolism Dysfunction, Pulmonary, 4 32 0.035
614
INF009 Inflammatory Spondylopathy 32 0.035
615
PNC059 Punctate Inner Choroidopathy 30 0.035
616
P SRF003 Surfactant Metabolism Dysfunction, Pulmonary, 2 29 0.035
617
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 29 0.035
618
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 29 0.035
619
c HRM007 Hermansky-Pudlak Syndrome 4 28 0.035
620
c DYS147 Dyskeratosis Congenita, Autosomal Dominant 3 24 0.035
621
c NPH053 Nephronophthisis 11 23 0.035
622
c RNL092 Renal-Hepatic-Pancreatic Dysplasia 1 23 0.035
623
BLD159 Blood Group, Junior System 20 0.035
624
BRN101 Bronchiolitis Obliterans with Obstructive Pulmonary Disease 17 0.035
625
LYM133 Lymphoma, Hodgkin, Classic 78 0.031
626
P NRV007 Nervous System Disease 75 0.031
627
P FML018 Familial Mediterranean Fever 73 0.031
628
NRF026 Neurofibromatosis, Type Iv, of Riccardi 72 0.031
629
SVR004 Severe Combined Immunodeficiency 71 0.031
630
PRT037 Pertussis 70 0.031
631
c WLM013 Wilms Tumor 1 69 0.031
632
OMN001 Omenn Syndrome 68 0.031
633
ALL003 Allergic Rhinitis 68 0.031
634
P NMN002 Niemann-Pick Disease 68 0.031
635
CHR066 Chronic Fatigue Syndrome 67 0.031
636
BRS051 Breast Disease 67 0.031
637
P TXP001 Toxoplasmosis 65 0.031
638
P PSR002 Psoriasis 65 0.031
639
SYS004 Systemic Mastocytosis 65 0.031
640
RCT015 Reactive Arthritis 65 0.031
641
c CNG006 Congenital Hypothyroidism 62 0.031
642
SYN007 Synovitis 61 0.031
643
P HMP007 Hemophilia 61 0.031
644
c PNC108 Pancreatitis, Hereditary 60 0.031
645
VGT001 Vogt-Koyanagi-Harada Disease 60 0.031
646
SPT004 Septic Arthritis 60 0.031
647
PPT005 Peptic Ulcer Disease 60 0.031
648
BLD034 Bile Duct Carcinoma 60 0.031
649
INT079 Intrahepatic Cholangiocarcinoma 60 0.031
650
LYS012 Lysosomal Acid Lipase Deficiency 60 0.031
651
DNH001 Donohue Syndrome 60 0.031
652
SPN027 Spinal Stenosis 60 0.031
653
ING001 Inguinal Hernia 59 0.031
654
P BCK002 Beckwith-Wiedemann Syndrome 58 0.031
655
CMP010 Complex Regional Pain Syndrome 58 0.031
656
OCL020 Ocular Cicatricial Pemphigoid 58 0.031
657
P THR015 Thrombophilia 58 0.031
658
ARG002 Argininosuccinic Aciduria 57 0.031
659
P LPD010 Lipodystrophy 57 0.031
660
P CYS018 Cystitis 57 0.031
661
GST023 Gastric Ulcer 57 0.031
662
P SLV001 Silver-Russell Syndrome 57 0.031
663
ECT006 Ectodermal Dysplasia 57 0.031
664
P LRY019 Laryngitis 57 0.031
665
ISL003 Isolated Growth Hormone Deficiency 57 0.031
666
NWB001 Newborn Respiratory Distress Syndrome 56 0.031
667
P BRN009 Burning Mouth Syndrome 56 0.031
668
P ALP008 Alopecia 56 0.031
669
c GLY003 Glycogen Storage Disease Iii 56 0.031
670
P PMP005 Pemphigus Vulgaris 56 0.031
671
HYP060 Hyperinsulinism 56 0.031
672
P MYP006 Myopia 56 0.031
673
DSS009 Disseminated Intravascular Coagulation 56 0.031
674
ANK001 Ankylosis 56 0.031
675
IRN001 Iron Deficiency Anemia 55 0.031
676
HPT022 Hepatoblastoma 55 0.031
677
GLB001 Gilbert Syndrome 55 0.031
678
NRT004 Neuritis 55 0.031
679
P AGG001 Aggressive Periodontitis 55 0.031
680
MGR028 Migraine with or Without Aura 1 55 0.031
681
STR008 Strongyloidiasis 54 0.031
682
c CLR131 Ciliary Dyskinesia, Primary, 1 54 0.031
683
c INF023 Inflammatory Breast Carcinoma 54 0.031
684
P SNR003 Senior-Loken Syndrome 1 54 0.031
685
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 54 0.031
686
STF002 Stiff Skin Syndrome 53 0.031
687
P PNV001 Panuveitis 52 0.031
688
EBS001 Ebstein Anomaly 52 0.031
689
HYP068 Hyperostosis 52 0.031
690
P LFT003 Left Ventricular Noncompaction 52 0.031
691
GRW007 Growth Hormone Deficiency 52 0.031
692
MYL001 Myelitis 52 0.031
693
ORL013 Oral Lichen Planus 51 0.031
694
HST009 Histiocytoma 51 0.031
695
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 51 0.031
696
P GND004 Gonadal Dysgenesis 50 0.031
697
PPL049 Papillon-Lefevre Syndrome 50 0.031
698
DNT012 Dental Caries 50 0.031
699
EXP004 Exophthalmos 50 0.031
700
URT031 Ureteral Disease 50 0.031
701
ESN011 Eisenmenger Syndrome 49 0.031
702
P RNL017 Renal Oncocytoma 49 0.031
703
GRN017 Granulocytopenia 49 0.031
704
PRT011 Protein C Deficiency 48 0.031
705
PLM035 Pulmonary Eosinophilia 48 0.031
706
c ACT076 Acute Myocarditis 48 0.031
707
ART031 Aortic Coarctation 48 0.031
708
LMT001 Limited Scleroderma 47 0.031
709
MLT016 Multicentric Reticulohistiocytosis 47 0.031
710
MYC012 Mycetoma 46 0.031
711
P ART084 Arteriovenous Fistula 46 0.031
712
c LSS005 Lissencephaly 1 46 0.031
713
CHR100 Chronic Ulcer of Skin 46 0.031
714
ANT039 Antisynthetase Syndrome 46 0.031
715
FBR003 Fibrous Histiocytoma 46 0.031
716
LRN001 Laurence-Moon Syndrome 46 0.031
717
P HRD009 Hereditary Wilms' Tumor 46 0.031
718
CRD137 Cardiogenic Shock 45 0.031
719
NNT049 Nontuberculous Mycobacterial Lung Disease 45 0.031
720
PRN049 Paraneoplastic Pemphigus 45 0.031
721
PRC003 Proctitis 44 0.031
722
MCL003 Macular Holes 44 0.031
723
MNN034 Mannose-Binding Lectin Deficiency 44 0.031
724
OST062 Osteoarthritis with Mild Chondrodysplasia 43 0.031
725
NCR004 Nocardiosis 43 0.031
726
PYM001 Pyomyositis 42 0.031
727
ANC002 Anca-Associated Vasculitis 42 0.031
728
BCL014 B-Cell Growth Factor 42 0.031
729
PNM010 Pneumothorax, Primary Spontaneous 41 0.031
730
c HRM008 Hermansky-Pudlak Syndrome 5 41 0.031
731
SPN060 Spondylocarpotarsal Synostosis Syndrome 41 0.031
732
c HMC035 Hemochromatosis, Type 4 40 0.031
733
c RTN177 Retinitis Pigmentosa 73 39 0.031
734
P MXL015 Maxillary Sinusitis 39 0.031
735
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 38 0.031
736
INT052 Intestinal Volvulus 38 0.031
737
ALC010 Alcoholic Cardiomyopathy 38 0.031
738
IMM078 Immunodeficiency 21 38 0.031
739
c CHR098 Chronic Pyelonephritis 38 0.031
740
DLT018 Dilution, Pigmentary 37 0.031
741
PNL013 Penile Disease 37 0.031
742
MCR001 Microcystic Meningioma 36 0.031
743
PLS002 Peliosis Hepatis 36 0.031
744
P ART106 Arterial Calcification, Generalized, of Infancy, 1 36 0.031
745
CRL004 Caroli Disease 35 0.031
746
EPT021 Epithelial Recurrent Erosion Dystrophy 35 0.031
747
LYM043 Lymphocytic Hypophysitis 34 0.031
748
SCL025 Scleromyxedema 34 0.031
749
c HRM009 Hermansky-Pudlak Syndrome 6 33 0.031
750
c INF145 Infantile Liver Failure Syndrome 1 33 0.031
751
GST039 Gastroduodenitis 33 0.031
752
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 33 0.031
753
c SRF004 Surfactant Metabolism Dysfunction, Pulmonary, 1 33 0.031
754
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 33 0.031
755
SCL056 Sclerosing Cholangitis, Neonatal 32 0.031
756
OCL011 Ocular Motility Disease 31 0.031
757
c GLY044 Glycogen Storage Disease Ixc 30 0.031
758
ACT216 Acute Leukemia of Ambiguous Lineage 30 0.031
759
PLM007 Pulmonary Aspergilloma 28 0.031
760
c HTR021 Heterotaxy, Visceral, 5, Autosomal 28 0.031
761
PLS031 Plastic Bronchitis 28 0.031
762
UND007 Undifferentiated Connective Tissue Disease 28 0.031
763
SCL022 Scleredema 27 0.031
764
c SPN381 Spinocerebellar Ataxia, Autosomal Recessive 21 26 0.031
765
ARM010 Arima Syndrome 26 0.031
766
HPT077 Hepatic Venoocclusive Disease with Immunodeficiency 26 0.031
767
c DYS152 Dyskeratosis Congenita, Autosomal Recessive 5 25 0.031
768
HYP213 Hypomelanotic Disorder 25 0.031
769
HLX001 Helix Syndrome 25 0.031
770
CRC034 Carcinoma Showing Thymus-Like Differentiation 24 0.031
771
NRL023 Neurologic, Endocrine, and Pancreatic Disease, Multisystem, Infantile-Onset 23 0.031
772
c CHR036 Chronic Cholangitis 22 0.031
773
IDP086 Idiopathic Pleuroparenchymal Fibroelastosis 19 0.031
774
BRW002 Brown's Tendon Sheath Syndrome 19 0.031
775
BLC016 Bile Acid Synthesis Defect, Congenital, 5 18 0.031
776
SCD003 Scedosporiosis 16 0.031
777
AND005 Androgen Insensitivity Syndrome, Mild 16 0.031
778
IGG008 Igg4-Related Mesenteritis 15 0.031
779
PLM062 Pulmonary Hyalinizing Granuloma 14 0.031
780
AQG003 Aquagenic Syringeal Acrokeratoderm 12 0.031
781
P OVR042 Ovarian Cancer 82 0.027
782
P RTN008 Retinitis Pigmentosa 81 0.027
783
P FLL037 Follicular Lymphoma 76 0.027
784
PLY001 Polycythemia Vera 75 0.027
785
KPS004 Kaposi Sarcoma 73 0.027
786
PHN003 Phenylketonuria 73 0.027
787
KWS002 Kawasaki Disease 72 0.027
788
LSH001 Leishmaniasis 71 0.027
789
CMM004 Common Variable Immunodeficiency 71 0.027
790
WRN001 Werner Syndrome 70 0.027
791
P AGM001 Agammaglobulinemia 70 0.027
792
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 70 0.027
793
P CHR012 Chronic Granulomatous Disease 69 0.027
794
P PSD087 Pseudoxanthoma Elasticum 67 0.027
795
P HLP001 Holoprosencephaly 67 0.027
796
OTT002 Otitis Media 67 0.027
797
SPN186 Spinal Cord Injury 67 0.027
798
TYP007 Typhoid Fever 67 0.027
799
P MCR115 Microvascular Complications of Diabetes 5 66 0.027
800
P PRD006 Prader-Willi Syndrome 66 0.027
801
P ENC004 Encephalitis 66 0.027
802
CTN007 Cutaneous Leishmaniasis 66 0.027
803
P PLY011 Polycystic Ovary Syndrome 65 0.027
804
P CLC063 Celiac Disease 1 65 0.027
805
OVR029 Ovarian Hyperstimulation Syndrome 64 0.027
806
LPT001 Leptospirosis 64 0.027
807
GLC006 Galactosemia 64 0.027
808
HYP020 Hyperprolactinemia 64 0.027
809
P LNG028 Long Qt Syndrome 63 0.027
810
KRT001 Keratoconjunctivitis Sicca 63 0.027
811
DSM004 Desmoid Tumor 63 0.027
812
CRD119 Cardiac Arrest 63 0.027
813
IRR002 Irritable Bowel Syndrome 63 0.027
814
P PRP029 Porphyria 62 0.027
815
FCT007 Factor Vii Deficiency 62 0.027
816
LYM021 Lymphadenitis 62 0.027
817
DFC004 Deficiency Anemia 62 0.027
818
P EXN002 Exanthem 62 0.027
819
PRP030 Purpura 61 0.027
820
P EHL001 Ehlers-Danlos Syndrome 61 0.027
821
TXC005 Toxic Shock Syndrome 61 0.027
822
P HMR003 Hemorrhagic Disease 61 0.027
823
TNS005 Tonsillitis 61 0.027
824
P ANP001 Anaplastic Large Cell Lymphoma 60 0.027
825
ALL010 Allergic Contact Dermatitis 60 0.027
826
P FCL005 Focal Segmental Glomerulosclerosis 60 0.027
827
P PLY018 Polycythemia 60 0.027
828
c PRM005 Primary Hyperparathyroidism 59 0.027
829
MSC165 Muscular Dystrophy, Congenital, Lmna-Related 59 0.027
830
URT039 Urticaria 59 0.027
831
c BCT007 Bacterial Meningitis 59 0.027
832
VSC003 Visceral Leishmaniasis 59 0.027
833
RLP002 Relapsing-Remitting Multiple Sclerosis 59 0.027
834
PLS007 Plasmodium Falciparum Malaria 59 0.027
835
P HYP083 Hypopituitarism 59 0.027
836
CHL067 Cholecystitis 58 0.027
837
P HYP069 Hyperparathyroidism 58 0.027
838
LMY002 Leiomyoma 58 0.027
839
P FRD012 Friedreich Ataxia 1 58 0.027
840
BDD001 Budd-Chiari Syndrome 58 0.027
841
GNT003 Genital Herpes 58 0.027
842
ESP023 Esophageal Disease 58 0.027
843
PTT046 Pituitary Hormone Deficiency, Combined, 2 57 0.027
844
ART017 Aortic Disease 57 0.027
845
c ACT135 Acute Graft Versus Host Disease 57 0.027
846
ANG020 Angiosarcoma 57 0.027
847
VND007 Van Der Woude Syndrome 1 57 0.027
848
ADN027 Adenomyosis 57 0.027
849
P PTT006 Pituitary Adenoma 57 0.027
850
PRR016 Pierre Robin Syndrome 57 0.027
851
P RTH001 Rothmund-Thomson Syndrome 57 0.027
852
MSC007 Muscle Hypertrophy 57 0.027
853
c HPT007 Hepatitis E 57 0.027
854
SPT005 Spotted Fever 57 0.027
855
P SCL018 Scoliosis 56 0.027
856
HST011 Histoplasmosis 56 0.027
857
KRT006 Keratoconjunctivitis 56 0.027
858
c HYP731 Hyperaldosteronism, Familial, Type I 56 0.027
859
ACR008 Acrocallosal Syndrome 56 0.027
860
ALS001 Alstrom Syndrome 55 0.027
861
FDL002 Food Allergy 55 0.027
862
RLP001 Relapsing Polychondritis 55 0.027
863
CLN019 Colonic Disease 55 0.027
864
P ESN008 Eosinophilic Pneumonia 55 0.027
865
HDC001 Headache 55 0.027
866
DXT001 Dextrocardia 55 0.027
867
END081 Endosteal Hyperostosis, Autosomal Dominant 55 0.027
868
P HYP024 Hypoparathyroidism 55 0.027
869
ASP003 Aseptic Meningitis 54 0.027
870
SMT003 Somatostatinoma 54 0.027
871
APP015 Apparent Mineralocorticoid Excess 54 0.027
872
CCT002 Cicatricial Pemphigoid 54 0.027
873
PRP080 Peripheral Artery Disease 54 0.027
874
OST015 Osteochondrodysplasia 54 0.027
875
ALL009 Allergic Conjunctivitis 53 0.027
876
CLC001 Calciphylaxis 53 0.027
877
OVR063 Overnutrition 53 0.027
878
LYM022 Lymphangioma 53 0.027
879
HYP005 Hypokalemia 53 0.027
880
ANG054 Angina Pectoris 53 0.027
881
CRH005 Crohn's Colitis 53 0.027
882
MBS002 Moebius Syndrome 53 0.027
883
P RTN022 Retinal Vein Occlusion 53 0.027
884
c VRL007 Viral Encephalitis 53 0.027
885
CLL003 Cellulitis 53 0.027
886
P CRD132 Cardiac Conduction Defect 53 0.027
887
P CRN108 Cranioectodermal Dysplasia 1 53 0.027
888
HLL004 Hellp Syndrome 53 0.027
889
VLV011 Vulvovaginal Candidiasis 53 0.027
890
THR016 Thrombophlebitis 53 0.027
891
CRD223 Cardiac Arrhythmia 52 0.027
892
c HPT015 Hepatitis D 52 0.027
893
P FNC043 Fanconi Anemia, Complementation Group E 52 0.027
894
c ORF037 Orofaciodigital Syndrome I 51 0.027
895
P ASP001 Asperger Syndrome 51 0.027
896
MMB001 Membranoproliferative Glomerulonephritis 51 0.027
897
MCL006 Macular Retinal Edema 51 0.027
898
CRT033 Corticobasal Degeneration 51 0.027
899
NNT012 Neonatal Jaundice 51 0.027
900
LYM051 Lymphomatoid Granulomatosis 51 0.027
901
P EXD001 Exudative Vitreoretinopathy 51 0.027
902
RPP001 Rapp-Hodgkin Syndrome 51 0.027
903
CHR563 Chronic Eosinophilic Leukemia 51 0.027
904
c ART115 Aortic Valve Disease 1 51 0.027
905
P MYT002 Myotonic Dystrophy 50 0.027
906
VCC001 Vaccinia 50 0.027
907
PLR001 Pleural Tuberculosis 50 0.027
908
FLL008 Folliculitis 50 0.027
909
GNG011 Gingival Disease 50 0.027
910
P HMC002 Homocystinuria 50 0.027
911
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 50 0.027
912
P SCL015 Scleritis 50 0.027
913
c CNT016 Central Retinal Vein Occlusion 50 0.027
914
TRC012 Trichuriasis 50 0.027
915
c SPS215 Spastic Paraplegia 3, Autosomal Dominant 50 0.027
916
ALV002 Alveolar Echinococcosis 49 0.027
917
SHR069 Short-Rib Thoracic Dysplasia 6 with or Without Polydactyly 49 0.027
918
c FBR084 Fibromatosis, Gingival, 1 49 0.027
919
P HMP006 Hemiplegic Migraine 49 0.027
920
INF058 Inflammatory Myofibroblastic Tumor 49 0.027
921
CLS016 Clostridium Difficile Colitis 49 0.027
922
c INH020 Inherited Metabolic Disorder 49 0.027
923
SMN007 Seminoma 49 0.027
924
ONC007 Oncocytoma 48 0.027
925
P ENC008 Encephalocele 48 0.027
926
CYS008 Cystic Echinococcosis 47 0.027
927
DNN001 Danon Disease 47 0.027
928
INT017 Intestinal Schistosomiasis 47 0.027
929
c CHL137 Cholestasis, Progressive Familial Intrahepatic, 3 47 0.027
930
c PSD114 Pseudohypoaldosteronism, Type I, Autosomal Recessive 47 0.027
931
CYS002 Cystic Lymphangioma 47 0.027
932
PYL006 Pyloric Stenosis 47 0.027
933
c HRM006 Hermansky-Pudlak Syndrome 3 47 0.027
934
P RSM001 Rasmussen Encephalitis 46 0.027
935
SYN036 Syncope 46 0.027
936
SPN119 Spondylarthropathy 46 0.027
937
NSP002 Nasopharyngitis 46 0.027
938
EPD070 Epidermoid Cysts 46 0.027
939
P HYP009 Hypertrophic Pyloric Stenosis 45 0.027
940
P TRT019 Torticollis 45 0.027
941
NTR003 Natural Killer Cell Leukemia 45 0.027
942
BLD053 Blood Platelet Disease 45 0.027
943
PRS034 Parasitic Helminthiasis Infectious Disease 45 0.027
944
RSP019 Respiratory Distress Syndrome in Premature Infants 45 0.027
945
GRD001 Giardiasis 45 0.027
946
VLV010 Vulvovaginitis 45 0.027
947
IDP064 Idiopathic Neutropenia 45 0.027
948
TRP008 Tropical Calcific Pancreatitis 45 0.027
949
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 44 0.027
950
CRS001 Crescentic Glomerulonephritis 44 0.027
951
MYF002 Myofascial Pain Syndrome 44 0.027
952
CYS009 Cystadenoma 44 0.027
953
TRC003 Trichomoniasis 44 0.027
954
CRB108 Cerebral Palsy, Ataxic, Autosomal Recessive 43 0.027
955
SYM002 Sympathetic Ophthalmia 43 0.027
956
CHR466 Chronic Thromboembolic Pulmonary Hypertension 43 0.027
957
UTR011 Uterine Corpus Serous Adenocarcinoma 43 0.027
958
c HMC009 Hemochromatosis Type 2 43 0.027
959
CRV045 Cervical Intraepithelial Neoplasia 43 0.027
960
c NPH019 Nephronophthisis 1 42 0.027
961
UPP004 Upper Respiratory Tract Disease 42 0.027
962
MYC017 Mycobacterium Kansasii 42 0.027
963
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 42 0.027
964
SHR075 Short-Rib Thoracic Dysplasia 9 with or Without Polydactyly 42 0.027
965
SRC002 Sarcomatoid Renal Cell Carcinoma 42 0.027
966
c NPH068 Nephronophthisis 16 42 0.027
967
CRB086 Cerebral Aneurysms 42 0.027
968
c CNG208 Congenital Disorder of Glycosylation, Type Iic 42 0.027
969
LCH004 Lichen Disease 42 0.027
970
c NNN010 Noonan Syndrome 3 42 0.027
971
PRL019 Prolidase Deficiency 41 0.027
972
c ALZ056 Alzheimer Disease 3 41 0.027
973
ADP007 Adie Pupil 41 0.027
974
SPS057 Spasticity 41 0.027
975
CRP002 Croup 41 0.027
976
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 41 0.027
977
MYH012 Myhre Syndrome 41 0.027
978
ORF044 Orofacial Granulomatosis 41 0.027
979
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 41 0.027
980
c MSC117 Muscular Dystrophy, Limb-Girdle, Type 1e 41 0.027
981
c HYP057 Hypervitaminosis D 40 0.027
982
DYS164 Dyskeratosis Congenita, X-Linked 40 0.027
983
CRD003 Cardiac Sarcoidosis 40 0.027
984
ATS010 Autosomal Recessive Disease 40 0.027
985
TTR025 Tetraamelia Syndrome, Autosomal Recessive 40 0.027
986
VTR003 Vitreous Detachment 40 0.027
987
CNG069 Congenital Cytomegalovirus 40 0.027
988
CHL013 Cholecystolithiasis 39 0.027
989
ACL001 Acalculous Cholecystitis 39 0.027
990
c GLL024 Gallbladder Disease 1 39 0.027
991
AMN002 Amino Acid Metabolic Disorder 38 0.027
992
OST008 Osteosclerotic Myeloma 38 0.027
993
c BRD035 Bardet-Biedl Syndrome 15 38 0.027
994
P BLD051 Blood Coagulation Disease 38 0.027
995
PNC002 Pancreatic Mucinous Cystadenoma 38 0.027
996
P DXT004 Dextro-Looped Transposition of the Great Arteries 38 0.027
997
c PLM022 Pulmonary Valve Insufficiency 38 0.027
998
GRN003 Granulomatous Dermatitis 38 0.027
999
CHL039 Choledocholithiasis 38 0.027
1000
GBL002 Goblet Cell Carcinoid 37 0.027
1001
IMM064 Immunodeficiency, Common Variable, 10 37 0.027
1002
IDP074 Idiopathic Bronchiectasis 37 0.027
1003
ALB014 Alobar Holoprosencephaly 37 0.027
1004
P ANX007 Anauxetic Dysplasia 1 36 0.027
1005
GPS001 Gapo Syndrome 36 0.027
1006
TST043 Testicular Seminoma 36 0.027
1007
PGM003 Pigmentation Disease 36 0.027
1008
URT037 Urethral Stricture 35 0.027
1009
PST030 Postcholecystectomy Syndrome 35 0.027
1010
P LYM124 Lymphangiectasia, Intestinal 35 0.027
1011
HRS011 Horseshoe Kidney 35 0.027
1012
GNR003 Generalized Atherosclerosis 35 0.027
1013
MNN028 Mononeuropathy of the Median Nerve, Mild 35 0.027
1014
BLR002 Bile Reflux 34 0.027
1015
MYC014 Mycobacterium Chelonae 34 0.027
1016
HYP034 Hypertensive Encephalopathy 34 0.027
1017
PRN007 Perinephritis 34 0.027
1018
TXC001 Toxic Megacolon 34 0.027
1019
46X053 46,xy Gonadal Dysgenesis, Partial, with Minifascicular Neuropathy 34 0.027
1020
CRD016 Cardiac Rupture 34 0.027
1021
ACT209 Acatalasemia 33 0.027
1022
SPS019 Spastic Paraparesis 33 0.027
1023
APP016 Apple Allergy 33 0.027
1024
EXT035 Extrinsic Cardiomyopathy 33 0.027
1025
c NPH032 Nephronophthisis 4 33 0.027
1026
PLM151 Pulmonary Arteriovenous Fistulas 33 0.027
1027
ANG066 Angel-Shaped Phalangoepiphyseal Dysplasia 33 0.027
1028
TRC097 Tracheomalacia 32 0.027
1029
HYP540 Hypertension, Diastolic 32 0.027
1030
SPL005 Splenic Artery Aneurysm 32 0.027
1031
SPP004 Suppurative Cholangitis 32 0.027
1032
BLR028 Biliary Atresia, Extrahepatic 32 0.027
1033
SLR005 Solar Urticaria 32 0.027
1034
c MYT029 Myotonia Congenita, Autosomal Recessive 32 0.027
1035
SBD001 Subdural Empyema 31 0.027
1036
HYP048 Hypotropia 31 0.027
1037
CYS019 Cystathioninuria 30 0.027
1038
c DYS039 Dyskeratosis Congenita Autosomal Dominant 30 0.027
1039
OVL001 Ovalocytosis, Southeast Asian 30 0.027
1040
PCM002 Pauci-Immune Glomerulonephritis 30 0.027
1041
MYC015 Mycobacterium Fortuitum 30 0.027
1042
DDN005 Duodenal Somatostatinoma 30 0.027
1043
MCP039 Mucoepithelial Dysplasia, Hereditary 30 0.027
1044
ENP001 Enophthalmos 29 0.027
1045
c INH004 Inherited Blood Coagulation Disease 29 0.027
1046
UNV002 Univentricular Heart 29 0.027
1047
CNG064 Congenital Chloride Diarrhea 29 0.027
1048
INH011 Inherited Bone Marrow Failure Syndromes 28 0.027
1049
TRC038 Tracheobronchomegaly 28 0.027
1050
INT258 Interstitial Nephritis, Karyomegalic 28 0.027
1051
c MDL008 Medullary Cystic Kidney Disease 1 28 0.027
1052
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 27 0.027
1053
CLN022 Colonic Atresia 27 0.027
1054
LFF001 Loeffler Endocarditis 27 0.027
1055
AST054 Australia Antigen 26 0.027
1056
HMX003 Heme Oxygenase 1 Deficiency 26 0.027
1057
c LPD034 Lipodystrophy, Familial Partial, Type 4 26 0.027
1058
RDT005 Radiation Induced Cancer 26 0.027
1059
LVR004 Liver Inflammatory Pseudotumor 25 0.027
1060
MYC016 Mycobacterium Gordonae 24 0.027
1061
c JBR031 Joubert Syndrome 21 24 0.027
1062
BLC011 Bile Acid Synthesis Defect, Congenital, 3 23 0.027
1063
SNG003 Single Ventricular Heart 23 0.027
1064
NRT006 North American Indian Childhood Cirrhosis 23 0.027
1065
MCN022 Mucinous Cystadenocarcinoma of the Pancreas 22 0.027
1066
CRD237 Cardiomyopathy, Dilated, 1aa, with or Without Left Ventricular Noncompaction 22 0.027
1067
c CRD083 Cardiomyopathy, Familial Hypertrophic, 15 21 0.027
1068
c SNR016 Senior-Loken Syndrome 9 21 0.027
1069
MNR004 Mounier-Kuhn Syndrome 21 0.027
1070
c DYS150 Dyskeratosis Congenita, Autosomal Recessive 3 21 0.027
1071
c RNL095 Renal-Hepatic-Pancreatic Dysplasia 2 21 0.027
1072
NNN007 Non-Involuting Congenital Hemangioma 20 0.027
1073
c NPH077 Nephronophthisis 19 20 0.027
1074
NPH037 Nephronophthisis-Like Nephropathy 1 20 0.027
1075
c CRB168 Cerebroretinal Microangiopathy with Calcifications and Cysts 2 20 0.027
1076
c NPH086 Nephronophthisis 20 19 0.027
1077
CRN197 Coronary Arterial Fistulas 19 0.027
1078
P NRN029 Neuronal Intestinal Dysplasia 19 0.027
1079
TFR002 Tafro Syndrome 18 0.027
1080
BLD138 Blood Group--Diego System 18 0.027
1081
EXT039 Extrapontine Myelinolysis 18 0.027
1082
PLM051 Pulmonary Arterio-Veinous Fistula 17 0.027
1083
c NRN038 Neuronal Intestinal Dysplasia, Type B 17 0.027
1084
INB001 Inborn Amino Acid Metabolism Disorder 16 0.027
1085
MST022 Masticatory Muscles, Hypertrophy of 16 0.027
1086
IMM162 Immunoglobulin E Concentration, Serum 16 0.027
1087
RTN191 Retinal Dystrophy with or Without Extraocular Anomalies 16 0.027
1088
AMN012 Aminoacidopathies 15 0.027
1089
ACR022 Acardia 13 0.027
1090
SPL069 Splenoportal Vascular Anomalies 11 0.027
1091
MYL069 Myeloma, Multiple 86 0.022
1092
P MLT020 Multiple Sclerosis 85 0.022
1093
P PHC003 Pheochromocytoma 72 0.022
1094
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.022
1095
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.022
1096
P NRF023 Neurofibromatosis, Type Ii 69 0.022
1097
P DRM053 Dermatitis, Atopic 68 0.022
1098
c MYT021 Myotonic Dystrophy 1 68 0.022
1099
BHC003 Behcet Syndrome 68 0.022
1100
P HYD006 Hydrocephalus 68 0.022
1101
c HMP004 Hemophilia B 67 0.022
1102
P CNJ013 Conjunctivitis 67 0.022
1103
P PRP003 Porphyria Cutanea Tarda 67 0.022
1104
DNG002 Dengue Hemorrhagic Fever 66 0.022
1105
PCK003 Pick Disease of Brain 66 0.022
1106
TTN003 Tetanus 65 0.022
1107
SCR008 Scrub Typhus 65 0.022
1108
P ART067 Aortic Aneurysm, Familial Thoracic 1 65 0.022
1109
CHL123 Chlamydia 64 0.022
1110
PMS001 Poems Syndrome 64 0.022
1111
P ALP009 Alopecia Areata 64 0.022
1112
APH001 Aphthous Stomatitis 64 0.022
1113
HLC007 Helicobacter Pylori Infection 64 0.022
1114
PLM031 Poliomyelitis 64 0.022
1115
c DPH024 Diaphragmatic Hernia, Congenital 63 0.022
1116
PNC033 Pancreas Adenocarcinoma 63 0.022
1117
P INT143 Interstitial Cystitis 63 0.022
1118
PTT048 Pituitary Adenoma, Prolactin-Secreting 63 0.022
1119
c ADL017 Adult T-Cell Leukemia 63 0.022
1120
HMR004 Hemorrhagic Fever with Renal Syndrome 63 0.022
1121
P ALC004 Alcohol Abuse