Search results for "fibrosis"

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

2472 hits were found for 'fibrosis'

# Family MCID Name MIFTS Score
1
CYS001 Cystic Fibrosis 90 7.509
2
PLM134 Pulmonary Fibrosis, Idiopathic 54 5.911
3
P PLM036 Pulmonary Fibrosis 59 4.783
4
ORL004 Oral Submucous Fibrosis 46 4.713
5
P CNG047 Congenital Fibrosis of the Extraocular Muscles 33 4.334
6
END021 Endomyocardial Fibrosis 44 4.032
7
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 29 3.789
8
CNG048 Congenital Hepatic Fibrosis 49 3.609
9
RTR011 Retroperitoneal Fibrosis 38 3.589
10
c FBR050 Fibrosis of Extraocular Muscles, Congenital, 2 26 3.291
11
c FBR049 Fibrosis of Extraocular Muscles, Congenital, 3a 32 3.279
12
RNL077 Renal Fibrosis 37 3.057
13
CCH002 Coach Syndrome 53 3.017
14
FBR028 Fibrosing Mediastinitis 25 2.970
15
c FBR081 Fibrosis of Extraocular Muscles, Congenital, 3c 17 2.679
16
DFF002 Diffuse Pulmonary Fibrosis 28 2.470
17
NPH018 Nephrogenic Systemic Fibrosis 43 2.425
18
PLM139 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 1 33 2.360
19
TKL001 Tukel Syndrome 19 2.310
20
PST015 Postinflammatory Pulmonary Fibrosis 5 2.310
21
LBN002 Lubani Al Saleh Teebi Syndrome 13 2.296
22
IDP011 Idiopathic Interstitial Pneumonia 46 2.209
23
ACT029 Acute Interstitial Pneumonia 35 2.000
24
c PLM044 Pulmonary Fibrosis, Familial 19 1.990
25
P APL001 Aplastic Anemia 70 1.933
26
IGG007 Igg4-Related Disease 30 1.928
27
PLM141 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 4 19 1.924
28
PRR004 Preretinal Fibrosis 22 1.919
29
PKL002 Poikiloderma, Hereditary Fibrosing, with Tendon Contractures, Myopathy, and Pulmonary Fibrosis 20 1.919
30
HRM018 Hermansky-Pudlak Syndrome with Pulmonary Fibrosis 19 1.919
31
c LCL003 Localized Pulmonary Fibrosis 18 1.919
32
PLM143 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 3 18 1.919
33
HRM016 Hermansky-Pudlak Syndrome Without Pulmonary Fibrosis 19 1.915
34
c FBR078 Fibrosis of Extraocular Muscles, Congenital, 5 16 1.904
35
BRN075 Bronchiectasis with or Without Elevated Sweat Chloride 2 22 1.898
36
MSC030 Muscular Fibrosis Multifocal Obstructed Vessels 12 1.898
37
JBR033 Joubert Syndrome with Hepatic Defect 32 1.891
38
EF001 Eaf 17 1.883
39
FBR086 Fibrolamellar Carcinoma 30 1.874
40
RCR027 Recurrent Infections-Myelofibrosis-Nephromegaly Syndrome 9 1.874
41
MCN017 Meconium Ileus 45 1.556
42
ASB001 Asbestosis 39 1.430
43
TRP020 Tropical Endomyocardial Fibrosis 30 1.427
44
SLC006 Silicosis 47 1.417
45
P MYL005 Myelofibrosis 64 1.403
46
ARW003 Airway-Centered Interstitial Fibrosis 6 1.387
47
IDP016 Idiopathic Diffuse Interstitial Fibrosis 3 1.382
48
FML074 Familial Interstitial Fibrosis 3 1.377
49
c CNG189 Congenital Disorder of Glycosylation, Type Ib 40 1.360
50
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 9 1.360
51
BRN076 Bronchiectasis with or Without Elevated Sweat Chloride 1 28 1.354
52
BRN077 Bronchiectasis with or Without Elevated Sweat Chloride 3 20 1.354
53
HPT076 Hepatic Fibrosis - Renal Cysts - Intellectual Disability 15 1.354
54
HPT029 Hepatic Fibrosis Renal Cysts Mental Retardation 3 1.354
55
c CNG140 Congenital Fibrosis of the Extraocular Muscles 1a 8 1.346
56
c CNG141 Congenital Fibrosis of the Extraocular Muscles 1b 8 1.346
57
c KF2001 Kif21a-Related Congenital Fibrosis of the Extraocular Muscles 7 1.346
58
c PHX001 Phox2a-Related Congenital Fibrosis of the Extraocular Muscles 7 1.346
59
c TBB003 Tubb3-Related Congenital Fibrosis of the Extraocular Muscles 7 1.346
60
LNG082 Lung Fibrosis - Immunodeficiency - 46,xx Gonadal Dysgenesis 6 1.346
61
PLM106 Pulmonary Fibrosis - Hepatic Hyperplasia - Bone Marrow Hypoplasia 6 1.346
62
c SFT006 Sftpc-Related Familial Pulmonary Fibrosis 5 1.346
63
c TRC066 Terc-Related Familial Pulmonary Fibrosis 5 1.346
64
c TRT009 Tert-Related Familial Pulmonary Fibrosis 5 1.346
65
NNT051 Neonatal Diabetes - Congenital Hypothyroidism - Congenital Glaucoma - Hepatic Fibrosis - Polycystic Kidneys 5 1.346
66
FLL043 Follicular Hamartoma - Alopecia - Cystic Fibrosis 4 1.346
67
FBR016 Fibrosclerosis of Breast 23 1.337
68
SNR014 Senior-Boichis Syndrome 10 1.337
69
HRZ001 Huriez Syndrome 28 1.325
70
TYL001 Taylor's Syndrome 16 1.325
71
RZN001 Rozin Hertz Goodman Syndrome 16 1.325
72
SCR009 Scirrhous Adenocarcinoma 15 1.325
73
GRP001 Graphite Pneumoconiosis 10 1.325
74
P HPT021 Hepatitis 58 0.435
75
PNC034 Pancreas Disease 38 0.336
76
c HPT001 Hepatitis C 64 0.249
77
P PNM007 Pneumonia 56 0.235
78
P LVR013 Liver Disease 59 0.232
79
CRK001 Cork-Handlers' Disease 40 0.228
80
P PNC044 Pancreatitis 51 0.207
81
BRN022 Bronchiectasis 49 0.196
82
P INT066 Interstitial Lung Disease 46 0.196
83
RSP006 Respiratory System Disease 36 0.193
84
USL001 Usual Interstitial Pneumonia 28 0.192
85
GLC006 Galactosemia 76 0.164
86
c HPT016 Hepatitis B 59 0.160
87
URT010 Ureteral Obstruction 38 0.158
88
P ASP006 Aspergillosis 56 0.156
89
c HPT073 Hepatitis C Virus 60 0.154
90
ALL008 Allergic Bronchopulmonary Aspergillosis 47 0.152
91
c VRL010 Viral Hepatitis 49 0.145
92
LVR012 Liver Cirrhosis 59 0.143
93
FTT001 Fatty Liver Disease 49 0.139
94
P CRD011 Cardiomyopathy 53 0.138
95
NNL002 Nonalcoholic Steatohepatitis 43 0.132
96
P KDN018 Kidney Disease 57 0.131
97
c HPT003 Hepatitis a 47 0.129
98
P RSP003 Respiratory Failure 58 0.129
99
P SCL016 Scleroderma 69 0.119
100
NSD001 Nose Disease 28 0.117
101
NTR005 Nutritional Deficiency Disease 41 0.114
102
P PLM037 Pulmonary Hypertension 78 0.114
103
PRM025 Primary Bacterial Infectious Disease 27 0.113
104
P AST005 Asthma 77 0.111
105
BRN038 Bronchial Disease 41 0.107
106
EXC002 Exocrine Pancreatic Insufficiency 36 0.107
107
HPT023 Hepatocellular Carcinoma 90 0.104
108
SPN020 Spondylosis 46 0.102
109
P PRT013 Portal Hypertension 45 0.098
110
P NNT009 Neonatal Diabetes Mellitus 41 0.097
111
P HRM001 Hermansky-Pudlak Syndrome 62 0.096
112
CNN005 Connective Tissue Disease 49 0.093
113
END072 Endotheliitis 39 0.093
114
P SPS003 Spastic Diplegia 37 0.093
115
P CNG401 Congenital Heart Disease 68 0.092
116
SCH014 Schistosomiasis 55 0.089
117
P CHL066 Cholangitis 39 0.089
118
SKN016 Skin Disease 61 0.088
119
P HYP061 Hypertrophic Cardiomyopathy 56 0.088
120
VRL011 Viral Infectious Disease 50 0.088
121
P THY032 Thyroiditis 48 0.088
122
VSC018 Visceral Steatosis 26 0.088
123
P PLY014 Polycystic Kidney Disease 60 0.086
124
P TRC086 Trichohepatoenteric Syndrome 1 42 0.085
125
UPP004 Upper Respiratory Tract Disease 34 0.085
126
P LNG032 Lung Cancer 91 0.084
127
BLR001 Biliary Atresia 44 0.084
128
NNS002 Nonspecific Interstitial Pneumonia 40 0.084
129
PRT036 Peritonitis 58 0.083
130
MYC013 Mycobacterium Abscessus 35 0.083
131
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 30 0.083
132
NNS006 Non-Suppurative Otitis Media 36 0.082
133
c SYS005 Systemic Scleroderma 62 0.080
134
CHL068 Cholestasis 45 0.080
135
CNG034 Congestive Heart Failure 65 0.079
136
P INF032 Infertility 52 0.079
137
P OBS005 Obesity 89 0.078
138
P PRM002 Primary Hyperoxaluria 64 0.078
139
OBS006 Obstructive Lung Disease 45 0.078
140
GLC003 Glucose Intolerance 49 0.076
141
P MSC005 Muscular Dystrophy 52 0.075
142
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 28 0.075
143
c HYP595 Hypertension, Essential 68 0.074
144
P SCL009 Sclerosing Cholangitis 42 0.074
145
MSC004 Muscle Tissue Disease 23 0.074
146
c DLT002 Dilated Cardiomyopathy 73 0.072
147
P LKM002 Leukemia 61 0.072
148
P ART022 Arthritis 61 0.072
149
BRN002 Bronchiolitis 48 0.072
150
CYS016 Cystic Kidney 43 0.072
151
LPD004 Lipoid Nephrosis 38 0.072
152
SKN027 Skin Conditions 34 0.072
153
P PRM006 Primary Biliary Cirrhosis 56 0.071
154
HYP006 Hypertensive Heart Disease 40 0.071
155
P ADN016 Adenocarcinoma 56 0.070
156
P ATR011 Atrial Fibrillation 55 0.070
157
P MYP004 Myopathy 50 0.070
158
c ART101 Aortic Valve Disease 2 46 0.070
159
VND001 Vein Disease 34 0.070
160
MDS022 Mediastinitis 33 0.070
161
c CRN178 Coronary Heart Disease 6 10 0.070
162
P SNS014 Sinusitis 49 0.068
163
P ESN007 Eosinophilia 48 0.068
164
P PNM006 Pneumoconiosis 45 0.068
165
P INT070 Intestinal Obstruction 45 0.068
166
HYP266 Hypoxia 42 0.068
167
P CRN214 Coronary Heart Disease 5 10 0.068
168
ACQ007 Acquired Immunodeficiency Syndrome 55 0.067
169
EYD002 Eye Disease 54 0.067
170
CHL071 Child Syndrome 51 0.067
171
PLM129 Pulmonary Disease, Chronic Obstructive 51 0.067
172
THR013 Thoracic Outlet Syndrome 47 0.067
173
P SPR013 Spiradenoma 46 0.067
174
KDS001 Kid Syndrome 44 0.067
175
ANR002 Aniridia 72 0.065
176
BRN012 Bronchiolitis Obliterans 49 0.065
177
P GLM007 Glomerulonephritis 49 0.065
178
PHR003 Pharyngitis 48 0.065
179
P RHM011 Rheumatoid Arthritis 88 0.063
180
P DBT085 Diabetes Mellitus, Insulin-Dependent 82 0.063
181
P HMC003 Hemochromatosis 75 0.063
182
PCK002 Pick Disease 61 0.063
183
CLT003 Colitis 47 0.063
184
P CLL015 Collagen Disease 43 0.063
185
ANR040 Aneurysm 43 0.063
186
BLD053 Blood Platelet Disease 32 0.063
187
LKP003 Leukoplakia 32 0.063
188
NNT004 Neonatal Respiratory Failure 28 0.063
189
P FTT008 Fatty Liver Disease, Nonalcoholic 1 23 0.063
190
c FTT007 Fatty Liver Disease, Nonalcoholic 2 9 0.063
191
P PNC035 Pancreatic Cancer 78 0.062
192
c SPN225 Spondyloarthropathy 1 66 0.062
193
PLM034 Pulmonary Emphysema 49 0.062
194
CTS003 Coats Disease 44 0.062
195
EXT034 Extrinsic Allergic Alveolitis 44 0.062
196
MTH009 Mouth Disease 44 0.062
197
SPC003 Specific Developmental Disorder 25 0.062
198
BLD054 Blood Protein Disease 24 0.062
199
CRH001 Crohn's Disease 80 0.060
200
VSC007 Vascular Disease 55 0.060
201
P PRM011 Primary Ciliary Dyskinesia 54 0.060
202
P NPH005 Nephronophthisis 53 0.060
203
c MTB001 Metabolic Syndrome X 52 0.060
204
KRT002 Keratomalacia 49 0.060
205
c HPT015 Hepatitis D 48 0.060
206
GST050 Gastrointestinal System Disease 43 0.060
207
NRN002 Neuronitis 40 0.060
208
STT004 Steatorrhea 33 0.060
209
SKN023 Skin Tag 33 0.060
210
MVM001 Movement Disease 31 0.060
211
P ANG001 Angelman Syndrome 66 0.059
212
P INF038 Influenza 64 0.059
213
ACN002 Acanthosis Nigricans 53 0.059
214
PLM012 Pulmonary Sarcoidosis 46 0.059
215
P MSC033 Muscle Disorders 38 0.059
216
PRN021 Paranasal Sinus Disease 38 0.059
217
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 34 0.059
218
P ATX010 Ataxia Neuropathy Spectrum 31 0.059
219
LKC003 Leukocyte Disease 28 0.059
220
HPD002 Hepadnavirus Infection 13 0.059
221
c RNL016 Renal Infectious Disease 7 0.059
222
P MYC007 Myocardial Infarction 76 0.057
223
AND015 Androgen Insensitivity 65 0.057
224
c CHR089 Chronic Kidney Failure 61 0.057
225
P AXN010 Axenfeld-Rieger Syndrome, Type 3 60 0.057
226
c PNC108 Pancreatitis, Hereditary 59 0.057
227
IMG001 Image Syndrome 56 0.057
228
HNT002 Hantavirus Pulmonary Syndrome 52 0.057
229
P ESP024 Esophagitis 51 0.057
230
P CMP010 Complex Regional Pain Syndrome 51 0.057
231
ATH003 Atherosclerosis 50 0.057
232
HYP066 Hyperglycemia 50 0.057
233
MCR088 Microscopic Polyangiitis 49 0.057
234
ADJ001 Adjustment Disorder 30 0.057
235
GLC008 Glucose Metabolism Disease 30 0.057
236
ALR002 Al-Raqad Syndrome 23 0.057
237
DCH001 Duchenne Muscular Dystrophy 78 0.055
238
WLS001 Wilson Disease 74 0.055
239
P HMP002 Hemophagocytic Lymphohistiocytosis 59 0.055
240
GST092 Gastroesophageal Reflux 58 0.055
241
BRN024 Bronchitis 56 0.055
242
ALC006 Alcoholic Hepatitis 53 0.055
243
c SCN006 Secondary Syphilis 48 0.055
244
EVN001 Evans' Syndrome 46 0.055
245
ORL015 Oral Squamous Cell Carcinoma 45 0.055
246
CNG035 Congenital Bilateral Absence of Vas Deferens 44 0.055
247
PNM008 Pneumothorax 41 0.055
248
DFF003 Diffuse Scleroderma 39 0.055
249
STM006 Stomach Disease 36 0.055
250
c PLM128 Pulmonary Hypertension, Primary, 2 25 0.055
251
c AST039 Asthma 2 23 0.055
252
VNT001 Ventilation Pneumonitis 22 0.055
253
c AST037 Asthma 1 20 0.055
254
P ATX030 Ataxia-Telangiectasia 76 0.053
255
ISC004 Ischemia 47 0.053
256
MYC002 Mycobacterium Avium Complex Disease 46 0.053
257
GLM011 Glomerulosclerosis 38 0.053
258
HMN014 Human Immunodeficiency Virus Infectious Disease 33 0.053
259
WTH001 Withdrawal Disorder 27 0.053
260
c TRC078 Trichohepatoenteric Syndrome 2 20 0.053
261
MCC011 Mucociliary Clearance Disorder 12 0.053
262
c CRN175 Coronary Heart Disease 4 9 0.053
263
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 84 0.051
264
HV1006 Hiv-1 77 0.051
265
INS024 Insulin-Like Growth Factor I 64 0.051
266
P LPS004 Lupus Erythematosus 61 0.051
267
VSC011 Vasculitis 50 0.051
268
P MYC008 Myocarditis 47 0.051
269
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 46 0.051
270
NWC001 Newcastle Disease 45 0.051
271
RTN023 Retinitis 43 0.051
272
c ATM024 Autoimmune Pancreatitis 39 0.051
273
SPL018 Splenomegaly 34 0.051
274
PHY002 Physical Disorder 33 0.051
275
NSL022 Nasal Cavity Disease 28 0.051
276
c BNG076 Benign Exophthalmos Syndrome 21 0.051
277
c SYS001 Systemic Lupus Erythematosus 90 0.049
278
TTR001 Tetralogy of Fallot 68 0.049
279
TBR010 Tuberculosis 64 0.049
280
ART001 Arterial Tortuosity Syndrome 59 0.049
281
P AND016 Andersen Syndrome 58 0.049
282
ANX002 Anxiety Disorder 57 0.049
283
P THL005 Thalassemia 56 0.049
284
P RCK004 Rickets 55 0.049
285
ART016 Aortic Aneurysm 55 0.049
286
P ACR001 Aicardi-Goutieres Syndrome 53 0.049
287
c ACT210 Acute Respiratory Distress Syndrome 52 0.049
288
ACR003 Acrodermatitis Enteropathica 51 0.049
289
P HYP098 Hypereosinophilic Syndrome 49 0.049
290
SLP005 Sleep Disorder 47 0.049
291
P STR020 Strabismus 47 0.049
292
BRN106 Burns 43 0.049
293
ORL011 Oral Cancer 43 0.049
294
ART017 Aortic Disease 42 0.049
295
DDN006 Duodenitis 40 0.049
296
ORL012 Oral Leukoplakia 35 0.049
297
URN009 Urinary System Disease 33 0.049
298
BNS002 Bone Structure Disease 24 0.049
299
CHL079 Children's Interstitial Lung Disease 8 0.049
300
P OST002 Osteoporosis 75 0.047
301
PRP027 Peripheral Vascular Disease 62 0.047
302
P DRM010 Dermatomyositis 57 0.047
303
BRC012 Brucellosis 55 0.047
304
ALP007 Alpha 1-Antitrypsin Deficiency 55 0.047
305
END030 End Stage Renal Failure 51 0.047
306
P THR014 Thrombocytopenia 50 0.047
307
ERD001 Erdheim-Chester Disease 48 0.047
308
LPD008 Lipid Metabolism Disorder 45 0.047
309
PRC013 Pericarditis 44 0.047
310
IPX001 Ipex Syndrome 43 0.047
311
ADL002 Adult Syndrome 43 0.047
312
P ATX004 Ataxia 43 0.047
313
PRC012 Pericardial Effusion 41 0.047
314
HRT012 Heart Valve Disease 40 0.047
315
BLR006 Biliary Tract Disease 38 0.047
316
c CHR096 Chronic Pulmonary Heart Disease 30 0.047
317
IMP003 Impaired Renal Function Disease 23 0.047
318
P HRT017 Heart Tumor 21 0.047
319
RDT005 Radiation Induced Cancer 20 0.047
320
AND005 Androgen Insensitivity Syndrome, Mild 19 0.047
321
P BRS047 Breast Cancer 100 0.045
322
c AMY091 Amyotrophic Lateral Sclerosis 1 83 0.045
323
P CRN211 Coronary Artery Disease 68 0.045
324
P NNN008 Noonan Syndrome 1 62 0.045
325
P HYP086 Hypothyroidism 52 0.045
326
P ABD003 Abdominal Aortic Aneurysm 50 0.045
327
c ACT027 Acute Pancreatitis 47 0.045
328
PRT011 Protein C Deficiency 46 0.045
329
NRM005 Neuromuscular Disease 45 0.045
330
P OPH004 Ophthalmoplegia 43 0.045
331
c PND001 Pain Disorder 43 0.045
332
GST053 Gastric Cancer 41 0.045
333
PRT019 Protein-Losing Enteropathy 40 0.045
334
CRB009 Cerebritis 37 0.045
335
CHR008 Choroiditis 37 0.045
336
CRR007 Cirrhosis, Cryptogenic 36 0.045
337
HRT007 Heart Cancer 34 0.045
338
DSQ001 Desquamative Interstitial Pneumonia 34 0.045
339
ACR005 Acrodermatitis 34 0.045
340
BRN013 Bronchiolitis Obliterans Organizing Pneumonia 33 0.045
341
SXL003 Sexual Disorder 30 0.045
342
ENT007 Enteropathica 28 0.045
343
PLM015 Pulmonary Systemic Sclerosis 17 0.045
344
MYL009 Myelodysplastic Syndrome 69 0.043
345
P GCH001 Gaucher's Disease 64 0.043
346
P DYS007 Dyskeratosis Congenita 60 0.043
347
c ATM003 Autoimmune Thyroiditis 57 0.043
348
c MCL062 Mucolipidosis Ii Alpha/beta 55 0.043
349
DRM006 Dermatitis 54 0.043
350
c ATM011 Autoimmune Hepatitis 53 0.043
351
DFC004 Deficiency Anemia 52 0.043
352
ATP002 Atopy 50 0.043
353
P SCK005 Sickle Cell Disease 49 0.043
354
P MTR012 Mitral Valve Disease 46 0.043
355
P MSC003 Muscular Atrophy 45 0.043
356
P FNC044 Fanconi Anemia, Complementation Group C 44 0.043
357
GMM002 Gamma Chain Deficiency 44 0.043
358
CSY001 C Syndrome 44 0.043
359
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 43 0.043
360
P PTS002 Ptosis 42 0.043
361
c HPT007 Hepatitis E 42 0.043
362
P PLM006 Pulmonary Alveolar Proteinosis 41 0.043
363
P SDR002 Siderosis 40 0.043
364
ALB002 Albinism 40 0.043
365
CRP017 Carpal Tunnel Syndrome, Familial 39 0.043
366
DST006 Diastolic Heart Failure 38 0.043
367
ATS010 Autosomal Recessive Disease 33 0.043
368
UND005 Undifferentiated Pleomorphic Sarcoma 31 0.043
369
TFT003 Tufting Enteropathy 27 0.043
370
ATN002 Autonomic Nervous System Disease 27 0.043
371
CNG039 Congenital Absence of the Vas Deferens 24 0.043
372
c PLM127 Pulmonary Hypertension, Primary, 3 21 0.043
373
c ADL079 Adult Heart Tumor 7 0.043
374
HRP008 Herpes Simiae 4 0.043
375
HRP012 Herpesvirus Simiae B Virus 1 0.043
376
BRK010 Burkitt Lymphoma 68 0.040
377
c JVN010 Juvenile Rheumatoid Arthritis 64 0.040
378
c SRC025 Sarcoidosis 1 60 0.040
379
PLY022 Polycystic Kidney and Hepatic Disease 57 0.040
380
ISC006 Ischemic Heart Disease 56 0.040
381
P SHR029 Short Syndrome 49 0.040
382
P UVT001 Uveitis 49 0.040
383
P GLL020 Gallbladder Disease 48 0.040
384
P LYM025 Lymphedema 48 0.040
385
TTH006 Tooth Disease 47 0.040
386
ALL006 Allergic Asthma 46 0.040
387
STS002 Situs Inversus 46 0.040
388
P HYP065 Hyperaldosteronism 45 0.040
389
P DRR001 Diarrhea 45 0.040
390
P PLY041 Polymyositis 45 0.040
391
P INT068 Intestinal Disease 44 0.040
392
P MMB011 Membranous Nephropathy 43 0.040
393
AZS001 Azoospermia 43 0.040
394
P END033 Endocarditis 43 0.040
395
P HYD002 Hydronephrosis 42 0.040
396
ALC009 Alcoholic Liver Cirrhosis 41 0.040
397
HMS001 Hemosiderosis 40 0.040
398
URT001 Urethritis 40 0.040
399
CRN030 Coronary Stenosis 40 0.040
400
DFF035 Diffuse Cutaneous Systemic Sclerosis 40 0.040
401
MNT002 Mental Depression 39 0.040
402
P CHR345 Chronic Pain 39 0.040
403
P RST002 Restrictive Cardiomyopathy 38 0.040
404
IRN002 Iron Metabolism Disease 36 0.040
405
NNT049 Nontuberculous Mycobacterial Lung Disease 30 0.040
406
PNC028 Pancreatic Steatorrhea 29 0.040
407
DVL001 Developmental Coordination Disorder 28 0.040
408
SPR035 Superior Vena Cava Syndrome 27 0.040
409
AMY016 Amyopathic Dermatomyositis 25 0.040
410
c PNC111 Pancreatic Cancer 2 24 0.040
411
GLB003 Globe Disease 22 0.040
412
IDP075 Idiopathic and/or Familial Pulmonary Arterial Hypertension 16 0.040
413
c CRN172 Coronary Heart Disease 3 9 0.040
414
LBR003 Labrador Lung 7 0.040
415
P TYS001 Tay-Sachs Disease 70 0.038
416
DWN001 Down Syndrome 62 0.038
417
P AMY004 Amyloidosis 60 0.038
418
SRC014 Sarcoma 57 0.038
419
CHG001 Chagas Disease 53 0.038
420
MLK003 Melkersson-Rosenthal Syndrome 53 0.038
421
CHR001 Churg-Strauss Syndrome 53 0.038
422
MXD005 Mixed Connective Tissue Disease 53 0.038
423
P NPH012 Nephrotic Syndrome 52 0.038
424
VHW001 Vohwinkel Syndrome 50 0.038
425
PRS047 Prostatitis 50 0.038
426
c THR092 Thrombophilia Due to Thrombin Defect 49 0.038
427
GNG013 Gingivitis 47 0.038
428
THR100 Thrombocytopenic Purpura, Autoimmune 47 0.038
429
LRN003 Learning Disability 47 0.038
430
CRY004 Cryoglobulinemia 45 0.038
431
CRC006 Carcinoid Syndrome 44 0.038
432
FCT013 Factor V Leiden Thrombophilia 43 0.038
433
P CRV039 Cervicitis 42 0.038
434
SLD003 Sialadenitis 42 0.038
435
RNL078 Renal Dysplasia 42 0.038
436
P CNG018 Congenital Heart Block 41 0.038
437
c CHR417 Chronic Graft Versus Host Disease 41 0.038
438
HPT009 Hepatopulmonary Syndrome 39 0.038
439
P RPD001 Rapidly Progressive Glomerulonephritis 39 0.038
440
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 39 0.038
441
c RCR022 Recurrent Acute Pancreatitis 38 0.038
442
c DYS143 Dyskeratosis Congenita, Autosomal Dominant 2 36 0.038
443
HRT015 Heritable Pulmonary Arterial Hypertension 36 0.038
444
c ACT068 Acute Cystitis 36 0.038
445
LYM024 Lymphatic System Disease 36 0.038
446
AMN002 Amino Acid Metabolic Disorder 35 0.038
447
ADS002 Adie Syndrome 34 0.038
448
CHL052 Choledochal Cyst 34 0.038
449
c ATM022 Autoimmune Myocarditis 34 0.038
450
DYS073 Dysphagia 33 0.038
451
ART012 Aortitis 32 0.038
452
c HYP058 Hypervitaminosis a 31 0.038
453
HPT074 Hepatic Adenoma, Somatic 30 0.038
454
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 29 0.038
455
ATS009 Autosomal Genetic Disease 28 0.038
456
HNM002 Hinman Syndrome 27 0.038
457
RPR002 Reproductive System Disease 26 0.038
458
MLT035 Multifocal Choroiditis 25 0.038
459
PRQ002 Paraquat Poisoning 24 0.038
460
P ACT080 Acute Pulmonary Heart Disease 20 0.038
461
c PLM121 Pulmonary Hypertension, Primary, 4 20 0.038
462
STN013 Stenotrophomonas Maltophilia Infection 18 0.038
463
VTM003 Vitamin Metabolic Disorder 18 0.038
464
c PNC094 Pancreatic Cancer 1 17 0.038
465
PLM133 Pulmonary Non-Tuberculous Mycobacterial Infection 11 0.038
466
c CRN177 Coronary Heart Disease 7 10 0.038
467
c CRN174 Coronary Heart Disease 2 9 0.038
468
INB001 Inborn Amino Acid Metabolism Disorder 4 0.038
469
ORL014 Oral Pharyngeal Disorders 2 0.038
470
ULC004 Ulcerative Colitis 75 0.035
471
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 75 0.035
472
MLR004 Malaria 72 0.035
473
SCK003 Sickle Cell Anemia 71 0.035
474
PLM001 Pulmonary Tuberculosis 60 0.035
475
SHW002 Shwachman-Diamond Syndrome 58 0.035
476
P MCK022 Meckel Syndrome 1 58 0.035
477
CHL065 Cholangiocarcinoma 56 0.035
478
P CMR001 Camurati-Engelmann Disease 54 0.035
479
P PRD008 Periodontitis 52 0.035
480
SCH016 Schimke Immunoosseous Dysplasia 51 0.035
481
P MNN013 Meningitis 51 0.035
482
MLN007 Male Infertility 50 0.035
483
HPY002 H. Pylori Infection 50 0.035
484
P OCL002 Oculocutaneous Albinism 48 0.035
485
P NRP001 Neuropathy 48 0.035
486
MRB003 Morbid Obesity 47 0.035
487
P SLP006 Sleep Apnea 46 0.035
488
RTN018 Retinal Disease 46 0.035
489
c ACT071 Acute Kidney Failure 45 0.035
490
MGC001 Megacolon 45 0.035
491
ART002 Arts Syndrome 44 0.035
492
CNS004 Constipation 44 0.035
493
c HRM005 Hermansky-Pudlak Syndrome 1 42 0.035
494
P PYL005 Pyelonephritis 42 0.035
495
NDL013 Nodular Regenerative Hyperplasia 42 0.035
496
MRC001 Marchiafava Bignami Disease 42 0.035
497
KLD001 Keloids 42 0.035
498
CHR078 Chorioretinitis 41 0.035
499
HMG005 Hemoglobinopathy 40 0.035
500
SPN051 Spondylitis 39 0.035
501
NPH003 Nephrocalcinosis 39 0.035
502
GRW007 Growth Hormone Deficiency 38 0.035
503
TTR016 Tetra-Amelia Syndrome 38 0.035
504
RNL015 Renal Hypertension 38 0.035
505
SPL012 Splenic Disease 37 0.035
506
P PRL003 Proliferative Glomerulonephritis 36 0.035
507
HMP009 Haemophilus Influenzae 36 0.035
508
IMM001 Immune-Complex Glomerulonephritis 35 0.035
509
c HRM017 Hermansky-Pudlak Syndrome 2 33 0.035
510
c MTR002 Mitral Valve Insufficiency 32 0.035
511
ALC005 Alcoholic Pancreatitis 32 0.035
512
RHM009 Rheumatoid Lung Disease 32 0.035
513
CRB025 Carbohydrate Metabolic Disorder 32 0.035
514
P GLM044 Glomerular Disease 32 0.035
515
BCK006 Back Pain 32 0.035
516
HYP047 Hypertropia 31 0.035
517
PRP019 Peripheral Nervous System Disease 31 0.035
518
c JVN024 Juvenile Hereditary Hemochromatosis 30 0.035
519
END038 Endocrine Pancreas Disease 28 0.035
520
P PLM071 Pulmonary Surfactant Metabolism Dysfunction 28 0.035
521
c SRC023 Sarcoidosis 2 27 0.035
522
SWT003 Sweat Gland Disease 25 0.035
523
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 15 0.035
524
RSP017 Response to Antiviral Treatment in Hepatitis C 11 0.035
525
NNT002 Neonatal Urinary Tract Infectious Disease 7 0.035
526
P PRS040 Prostate Cancer 90 0.032
527
P RNL014 Renal Cell Carcinoma 81 0.032
528
P LFR001 Li-Fraumeni Syndrome 79 0.032
529
P HNT016 Huntington Disease 78 0.032
530
HDG012 Hodgkin Lymphoma 75 0.032
531
c MCL042 Macular Degeneration, Age-Related, 1 74 0.032
532
PHN003 Phenylketonuria 73 0.032
533
BCK001 Becker Muscular Dystrophy 66 0.032
534
KWS002 Kawasaki Disease 62 0.032
535
P LYM007 Lymphangioleiomyomatosis 61 0.032
536
c JBR020 Joubert Syndrome 1 60 0.032
537
c BRD010 Bardet-Biedl Syndrome 1 59 0.032
538
WGN006 Wegener Granulomatosis 59 0.032
539
P MYL006 Myeloid Leukemia 59 0.032
540
P NMN002 Niemann-Pick Disease 59 0.032
541
ALC007 Alcohol Dependence 59 0.032
542
CHR066 Chronic Fatigue Syndrome 55 0.032
543
P HMN010 Hemangioma 54 0.032
544
CNT047 Contact Dermatitis 53 0.032
545
PLM033 Pulmonary Embolism 53 0.032
546
P HML002 Hemolytic Anemia 52 0.032
547
CMM005 Common Cold 52 0.032
548
ETN001 Eating Disorder 52 0.032
549
P HYP004 Hypercalcemia 52 0.032
550
ART021 Arteriosclerosis 51 0.032
551
c ACT075 Acute Myocardial Infarction 50 0.032
552
ATX019 Ataxia with Vitamin E Deficiency 49 0.032
553
P PLY017 Polyarteritis Nodosa 49 0.032
554
P NPH009 Nephrolithiasis 48 0.032
555
NRT001 Neurotic Disorder 48 0.032
556
WLL006 Wells Syndrome 48 0.032
557
P CTR002 Cataract 48 0.032
558
P PTT050 Pituitary Adenoma, Growth Hormone-Secreting 47 0.032
559
CYT008 Cytomegalovirus Infection 47 0.032
560
OBS061 Obstructive Sleep Apnea 46 0.032
561
PRD019 Periodic Fever, Familial 46 0.032
562
FLR002 Filariasis 46 0.032
563
PMP001 Pemphigus 45 0.032
564
TRY001 Trypanosomiasis 45 0.032
565
PLM010 Pulmonary Edema 45 0.032
566
P PLM085 Pulmonary Hemosiderosis 44 0.032
567
PYR010 Peyronie's Disease 44 0.032
568
URM002 Uremia 44 0.032
569
P THR012 Thoracic Cancer 44 0.032
570
P NGH001 Night Blindness 43 0.032
571
c ART115 Aortic Valve Disease 1 43 0.032
572
MSM001 Meesmann Corneal Dystrophy 42 0.032
573
P RTN016 Retinal Degeneration 42 0.032
574
ADT003 Auditory System Disease 42 0.032
575
INT051 Intussusception 41 0.032
576
PLR008 Pleurisy 41 0.032
577
BRN014 Bronchopneumonia 40 0.032
578
HYP063 Hypersplenism 40 0.032
579
HYD005 Hydrocele 40 0.032
580
CHL073 Cholestasis-Lymphedema Syndrome 40 0.032
581
MDL009 Medullary Sponge Kidney 40 0.032
582
BNF002 Bone Fracture 39 0.032
583
PRP080 Peripheral Artery Disease 39 0.032
584
P HYP071 Hypersensitivity Reaction Type Ii Disease 38 0.032
585
NRR001 Neuroretinitis 38 0.032
586
CLL021 Collagenous Colitis 37 0.032
587
c HRM006 Hermansky-Pudlak Syndrome 3 36 0.032
588
PRT030 Parathyroid Gland Disease 35 0.032
589
AMB002 Amblyopia 35 0.032
590
c SYS043 Systemic Lupus Erythematosus 1 34 0.032
591
CRY001 Cryptogenic Organizing Pneumonia 34 0.032
592
ACT084 Acute Stress Disorder 34 0.032
593
BLD036 Bile Duct Disease 33 0.032
594
CNS002 Constrictive Pericarditis 33 0.032
595
MLN012 Melanoma and Neural System Tumor Syndrome 33 0.032
596
WRN005 Wrinkles 31 0.032
597
SPN331 Spondyloocular Syndrome 30 0.032
598
P BLD051 Blood Coagulation Disease 30 0.032
599
c CHL119 Cholangitis, Primary Sclerosing 30 0.032
600
DDN009 Duodenal Obstruction 30 0.032
601
c DYS149 Dyskeratosis Congenita, Autosomal Recessive 1 29 0.032
602
HYP540 Hypertension, Diastolic 29 0.032
603
c HRM007 Hermansky-Pudlak Syndrome 4 28 0.032
604
KSH001 Keshan Disease 26 0.032
605
URT036 Urethral Obstruction 26 0.032
606
FNC006 Functional Gastric Disease 22 0.032
607
c HMG004 Hemoglobin D Disease 22 0.032
608
VSC008 Vascular Hemostatic Disease 22 0.032
609
LYM023 Lymphatic System Cancer 20 0.032
610
SWL001 Swallowing Disorders 20 0.032
611
ATM052 Autoimmune Disease 1 15 0.032
612
PLM124 Pulmonary Hypertension, Neonatal 15 0.032
613
SNG003 Single Ventricular Heart 14 0.032
614
c CRN176 Coronary Heart Disease 9 9 0.032
615
FCT015 Factor 2 Deficiency 7 0.032
616
MTR031 Motor Neuro-Ophthalmic Disorders 6 0.032
617
LYM036 Lymphatic Neoplasm 3 0.032
618
CRN073 Coronary Arteries Congenital Malformation 1 0.032
619
P CLC005 Celiac Disease 69 0.028
620
STR067 Stroke, Ischemic 68 0.028
621
P BRD002 Bardet-Biedl Syndrome 68 0.028
622
P FML161 Familial Mediterranean Fever, Ar 67 0.028
623
P FCL005 Focal Segmental Glomerulosclerosis 65 0.028
624
MLD001 Melioidosis 61 0.028
625
CHR012 Chronic Granulomatous Disease 60 0.028
626
PLL001 Pallister-Hall Syndrome 60 0.028
627
CNT098 Central Core Disease 60 0.028
628
TYP007 Typhoid Fever 59 0.028
629
CYS010 Cystinosis 59 0.028
630
P LYM026 Lymphoblastic Leukemia 57 0.028
631
P ATP001 Atopic Dermatitis 57 0.028
632
c CNG006 Congenital Hypothyroidism 57 0.028
633
P BCL006 B-Cell Lymphomas 57 0.028
634
P ADL010 Adult Respiratory Distress Syndrome 55 0.028
635
P ANT006 Antiphospholipid Syndrome 55 0.028
636
P PTT014 Pitt-Hopkins Syndrome 55 0.028
637
SMT008 Smith-Magenis Syndrome 54 0.028
638
ADN018 Adenoma 54 0.028
639
MLN008 Melanoma 54 0.028
640
PNC041 Pancreatic Ductal Adenocarcinoma 53 0.028
641
FRB001 Farber Lipogranulomatosis 53 0.028
642
GST023 Gastric Ulcer 53 0.028
643
ADL030 Adult-Onset Still's Disease 53 0.028
644
P THR015 Thrombophilia 52 0.028
645
c SVR001 Severe Acute Respiratory Syndrome 52 0.028
646
P HMP007 Hemophilia 51 0.028
647
P GRV001 Graves' Disease 51 0.028
648
CHL014 Cholera 50 0.028
649
HYP056 Hypoglycemia 49 0.028
650
P GLY013 Glycogen Storage Disease 49 0.028
651
THR004 Thrombocytosis 48 0.028
652
CHL028 Childhood Type Dermatomyositis 48 0.028
653
P FNG005 Feingold Syndrome 48 0.028
654
DFF005 Diffuse Large B-Cell Lymphoma 48 0.028
655
SPT004 Septic Arthritis 47 0.028
656
P LRY019 Laryngitis 46 0.028
657
P DDN001 Duodenal Ulcer 46 0.028
658
CND002 Conduct Disorder 45 0.028
659
VRR004 Verrucous Carcinoma 45 0.028
660
ING001 Inguinal Hernia 44 0.028
661
P HYP060 Hyperinsulinism 44 0.028
662
ESN015 Eosinophilic Fasciitis 44 0.028
663
c ACT134 Acute Liver Failure 44 0.028
664
ARC002 Arachnoiditis 43 0.028
665
BRN056 Bronchopulmonary Dysplasia 43 0.028
666
GRN039 Greenberg Skeletal Dysplasia 43 0.028
667
CVR006 Cavernous Hemangioma 43 0.028
668
LMT001 Limited Scleroderma 42 0.028
669
P SHR001 Short Bowel Syndrome 42 0.028
670
P BRN009 Burning Mouth Syndrome 42 0.028
671
ACT055 Actinomycosis 41 0.028
672
PRP007 Priapism 41 0.028
673
INT067 Interstitial Nephritis 41 0.028
674
SPN035 Spindle Cell Sarcoma 41 0.028
675
LFT009 Left Ventricular Outflow Tract Obstruction 41 0.028
676
c INF023 Inflammatory Breast Carcinoma 41 0.028
677
c INV001 Invasive Aspergillosis 40 0.028
678
HYP037 Hyperhomocysteinemia 40 0.028
679
FSC004 Fasciitis 40 0.028
680
OBS001 Obstructive Jaundice 40 0.028
681
P PSD003 Pseudohypoaldosteronism 40 0.028
682
VSC006 Vascular Cancer 40 0.028
683
PRT038 Protein-Energy Malnutrition 40 0.028
684
TRN044 Transposition of the Great Arteries 39 0.028
685
KRT010 Kartagener Syndrome 39 0.028
686
P INT191 Intestinal Lymphangiectasia 39 0.028
687
ART004 Aortic Atherosclerosis 39 0.028
688
MNN014 Mononeuritis 39 0.028
689
LPM005 Lipomatosis 39 0.028
690
EXT022 Exotropia 38 0.028
691
PLT002 Platelet Storage Pool Deficiency 38 0.028
692
HTS001 Hiatus Hernia 38 0.028
693
c ACT042 Acute Pyelonephritis 38 0.028
694
HRM002 Hermaphroditism 37 0.028
695
GDS001 Good Syndrome 37 0.028
696
NNT016 Neonatal Hemochromatosis 37 0.028
697
CNV002 Conversion Disorder 37 0.028
698
HYP457 Hypertrophic Scars 37 0.028
699
PNN001 Panniculitis 37 0.028
700
KWS001 Kwashiorkor 37 0.028
701
CLP005 Ciliopathy 37 0.028
702
FBR003 Fibrous Histiocytoma 37 0.028
703
SDD007 Sudden Cardiac Death 36 0.028
704
PRC003 Proctitis 36 0.028
705
XRP001 Xerophthalmia 36 0.028
706
MYX004 Myxedema 36 0.028
707
c PLY059 Polycystic Kidney Disease, Adult Type I 36 0.028
708
ATN005 Autonomic Dysfunction 36 0.028
709
MCN008 Mucinous Cystadenocarcinoma 35 0.028
710
NSY001 N Syndrome 34 0.028
711
c HRM009 Hermansky-Pudlak Syndrome 6 34 0.028
712
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 34 0.028
713
c VRL005 Viral Pneumonia 33 0.028
714
c GLL024 Gallbladder Disease 1 33 0.028
715
EXT006 Extrahepatic Cholestasis 32 0.028
716
RNL097 Renal Artery Disease 32 0.028
717
PRD004 Prediabetes Syndrome 31 0.028
718
DRM009 Dermatomycosis 31 0.028
719
c DYS141 Dyskeratosis Congenita, Autosomal Dominant 1 30 0.028
720
SCR003 Secretory Diarrhea 30 0.028
721
SPP007 Suppression Amblyopia 28 0.028
722
MDY005 Mody, Type I 27 0.028
723
PGM003 Pigmentation Disease 26 0.028
724
c DYS152 Dyskeratosis Congenita, Autosomal Recessive 5 26 0.028
725
RDN001 Reading Disorder 25 0.028
726
c DYS147 Dyskeratosis Congenita, Autosomal Dominant 3 25 0.028
727
c MCL043 Macular Degeneration, Age-Related, 2 24 0.028
728
c PNC103 Pancreatic Cancer 4 21 0.028
729
PLL005 Pallister-Killian Mosaic Syndrome 18 0.028
730
P MCL035 Macular Dystrophy, Retinal, 2 18 0.028
731
EYD001 Eye Degenerative Disease 17 0.028
732
CFT001 Cftr-Related Disorders 14 0.028
733
BRW002 Brown's Tendon Sheath Syndrome 12 0.028
734
BNM008 Bone Mineral Density, Low 10 0.028
735
MYC003 Myocardium Cancer 9 0.028
736
c CRN173 Coronary Heart Disease 8 9 0.028
737
FML066 Familial Hypersensitivity Pneumonitis 8 0.028
738
SKN025 Skin Pigmentation Disorders 5 0.028
739
DWS002 Dawson Disease 3 0.028
740
P OST012 Osteoarthritis 79 0.025
741
FBR012 Fabry Disease 75 0.025
742
c LKM061 Leukemia, Acute Myeloid 74 0.025
743
MRF001 Marfan Syndrome 72 0.025
744
SQM013 Squamous Cell Carcinoma, Head and Neck 71 0.025
745
GLL008 Gilles De La Tourette Syndrome 67 0.025
746
P ALP004 Alport Syndrome 66 0.025
747
P NRF002 Neurofibromatosis 66 0.025
748
c HMP004 Hemophilia B 65 0.025
749
GLN010 Glanzmann Thrombasthenia 65 0.025
750
P PSR002 Psoriasis 64 0.025
751
P ESS003 Essential Thrombocythemia 63 0.025
752
LNG024 Langerhans-Cell Histiocytosis 63 0.025
753
P FRD001 Friedreich Ataxia 61 0.025
754
ALL003 Allergic Rhinitis 61 0.025
755
P END044 Endometriosis 61 0.025
756
P KDN017 Kidney Cancer 60 0.025
757
TNG009 Tongue Squamous Cell Carcinoma 60 0.025
758
P AGM001 Agammaglobulinemia 59 0.025
759
P TRN020 Turner Syndrome 59 0.025
760
WLL001 Williams-Beuren Syndrome 59 0.025
761
PYR013 Pyruvate Kinase Deficiency 59 0.025
762
ACR008 Acrocallosal Syndrome 58 0.025
763
P BCK002 Beckwith-Wiedemann Syndrome 58 0.025
764
P SPN046 Spinal Muscular Atrophy 58 0.025
765
CRB039 Cerebrovascular Disease 58 0.025
766
ABT001 Abetalipoproteinemia 57 0.025
767
P RTH001 Rothmund-Thomson Syndrome 57 0.025
768
P HYP117 Hypertriglyceridemia 56 0.025
769
SND007 Sandhoff Disease, Infantile, Juvenile, and Adult Forms 56 0.025
770
c GCH015 Gaucher Disease, Type I 56 0.025
771
P BDD001 Budd-Chiari Syndrome 56 0.025
772
RCT015 Reactive Arthritis 55 0.025
773
c CRD194 Cardiomyopathy, Familial Hypertrophic 55 0.025
774
P MYS005 Myositis 54 0.025
775
RBR001 Roberts Syndrome 54 0.025
776
WLM001 Wolman Disease 54 0.025
777
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 53 0.025
778
c LCL006 Localized Scleroderma 52 0.025
779
APP008 Appendicitis 52 0.025
780
MDD011 Mood Disorder 52 0.025
781
SCR002 Scurvy 51 0.025
782
ALS001 Alstrom Syndrome 51 0.025
783
P ICH001 Ichthyosis Vulgaris 51 0.025
784
VLV011 Vulvovaginal Candidiasis 51 0.025
785
P HST010 Histiocytosis 51 0.025
786
HST011 Histoplasmosis 51 0.025
787
P HYP069 Hyperparathyroidism 50 0.025
788
STR008 Strongyloidiasis 50 0.025
789
PPL049 Papillon-Lefevre Syndrome 50 0.025
790
URT039 Urticaria 50 0.025
791
PPL022 Papilloma 49 0.025
792
PRL009 Prolactinoma 49 0.025
793
CMP002 Campylobacteriosis 49 0.025
794
P LPS002 Liposarcoma 49 0.025
795
PRD007 Periodontal Disease 49 0.025
796
PNM001 Pneumocystosis 49 0.025
797
LMY002 Leiomyoma 49 0.025
798
HPT022 Hepatoblastoma 49 0.025
799
P RNL017 Renal Oncocytoma 48 0.025
800
c INF071 Inflammatory Bowel Disease 1 48 0.025
801
46X003 46,xx Testicular Disorder of Sex Development 48 0.025
802
OST017 Osteomyelitis 48 0.025
803
ART111 Artery Disease 48 0.025
804
INT146 Intervertebral Disc Disease 48 0.025
805
THR016 Thrombophlebitis 48 0.025
806
GST060 Gastric Cancer, Somatic 48 0.025
807
P RHN004 Rhinitis 47 0.025
808
OCL001 Ocular Albinism 47 0.025
809
LYM019 Lymphosarcoma 47 0.025
810
ALP008 Alopecia 47 0.025
811
P MCR115 Microvascular Complications of Diabetes 5 47 0.025
812
BCT002 Bacterial Vaginosis 47 0.025
813
FLT001 Felty's Syndrome 47 0.025
814
P SLL003 Salla Disease 46 0.025
815
P FML035 Familial Hyperlipidemia 46 0.025
816
EXF001 Exfoliation Syndrome 45 0.025
817
c CNT033 Central Nervous System Cancer 45 0.025
818
GST045 Gastroenteritis 45 0.025
819
BLD034 Bile Duct Carcinoma 45 0.025
820
INT007 Intermediate Coronary Syndrome 45 0.025
821
HYP068 Hyperostosis 45 0.025
822
P RTN022 Retinal Vein Occlusion 45 0.025
823
P LPD010 Lipodystrophy 45 0.025
824
NCR004 Nocardiosis 44 0.025
825
PRL019 Prolidase Deficiency 44 0.025
826
c CHL080 Cholestasis, Progressive Familial Intrahepatic 1 44 0.025
827
INT079 Intrahepatic Cholangiocarcinoma 44 0.025
828
ESP023 Esophageal Disease 44 0.025
829
SYN007 Synovitis 44 0.025
830
P SCL018 Scoliosis 44 0.025
831
VGN023 Vaginitis 44 0.025
832
BRS051 Breast Disease 44 0.025
833
P LFT003 Left Ventricular Noncompaction 44 0.025
834
NRN004 Neuroendocrine Tumor 44 0.025
835
P EXP004 Exophthalmos 44 0.025
836
ECT006 Ectodermal Dysplasia 44 0.025
837
SML033 Small Cell Cancer of the Lung, Somatic 43 0.025
838
P PMP005 Pemphigus Vulgaris 43 0.025
839
PLR001 Pleural Tuberculosis 43 0.025
840
PRR002 Pure Red-Cell Aplasia 43 0.025
841
ANK001 Ankylosis 43 0.025
842
P RNV001 Renovascular Hypertension 43 0.025
843
FSC002 Fascioliasis 42 0.025
844
c CHL082 Cholestasis, Progressive Familial Intrahepatic 3 42 0.025
845
CRT016 Carotid Artery Disease 42 0.025
846
HLL004 Hellp Syndrome 42 0.025
847
URN010 Urinary Tract Obstruction 42 0.025
848
PLM019 Pleomorphic Liposarcoma 42 0.025
849
EBS001 Ebstein Anomaly 42 0.025
850
P ENC018 Encephalopathy 42 0.025
851
P PNC001 Pancytopenia 41 0.025
852
P GND004 Gonadal Dysgenesis 41 0.025
853
c NPH032 Nephronophthisis 4 41 0.025
854
CLN019 Colonic Disease 41 0.025
855
P MSC007 Muscle Hypertrophy 41 0.025
856
LRN001 Laurence-Moon Syndrome 40 0.025
857
MYC012 Mycetoma 40 0.025
858
CYS014 Cystadenocarcinoma 40 0.025
859
P PRP023 Peripheral Neuropathy 40 0.025
860
c CNT016 Central Retinal Vein Occlusion 40 0.025
861
CYS009 Cystadenoma 40 0.025
862
CHR005 Chorioamnionitis 40 0.025
863
CRD137 Cardiogenic Shock 39 0.025
864
MDD010 Middle Ear Disease 39 0.025
865
ACT017 Acute Chest Syndrome 39 0.025
866
DNT012 Dental Caries 39 0.025
867
BCL002 B Cell Deficiency 39 0.025
868
P SKN013 Skin Benign Neoplasm 39 0.025
869
c CNG027 Congenital Hemolytic Anemia 39 0.025
870
CRL004 Caroli Disease 39 0.025
871
CRS001 Crescentic Glomerulonephritis 38 0.025
872
ORL013 Oral Lichen Planus 38 0.025
873
NPH010 Nephrosclerosis 38 0.025
874
SMT002 Smooth Muscle Tumor 37 0.025
875
CLR096 Ciliary Dyskinesia, Primary, 1, with or Without Situs Inversus 37 0.025
876
PLM035 Pulmonary Eosinophilia 37 0.025
877
DBT006 Diabetic Macular Edema 37 0.025
878
MCL003 Macular Holes 37 0.025
879
ANT039 Antisynthetase Syndrome 36 0.025
880
MSS002 Mass Syndrome 36 0.025
881
c HMG001 Hemoglobin C Disease 36 0.025
882
PLR007 Pleural Empyema 36 0.025
883
PLS002 Peliosis Hepatis 36 0.025
884
RGH009 Right Atrial Isomerism 36 0.025
885
c HRM008 Hermansky-Pudlak Syndrome 5 35 0.025
886
VSC047 Vascular Malformation 35 0.025
887
ESN005 Eosinophilic Gastroenteritis 35 0.025
888
CRH005 Crohn's Colitis 35 0.025
889
ERY004 Erysipelas 35 0.025
890
c HMG003 Hemoglobin E Disease 35 0.025
891
LPD001 Lipid Pneumonia 34 0.025
892
ENT001 Enterocele 34 0.025
893
PRP021 Peripheral Nervous System Neoplasm 34 0.025
894
ELP001 Elephantiasis 34 0.025
895
P EPS030 Episodic Kinesigenic Dyskinesia 1 34 0.025
896
BNN003 Bone Inflammation Disease 33 0.025
897
HPT020 Hepatic Vascular Disease 33 0.025
898
HMP001 Hemopericardium 33 0.025
899
PLC008 Placenta Disease 33 0.025
900
HPT002 Hepatic Vein Thrombosis 32 0.025
901
CRB086 Cerebral Aneurysms 32 0.025
902
LYM043 Lymphocytic Hypophysitis 31 0.025
903
MCR019 Microglandular Adenosis 31 0.025
904
CHR100 Chronic Ulcer of Skin 31 0.025
905
GNG011 Gingival Disease 31 0.025
906
SPC010 Speech and Communication Disorders 31 0.025
907
SKL007 Skeletal Muscle Regeneration 31 0.025
908
SPS057 Spasticity 30 0.025
909
GST039 Gastroduodenitis 30 0.025
910
BLR002 Bile Reflux 30 0.025
911
c ARC016 Auriculocondylar Syndrome 1 30 0.025
912
DXT002 Dextrocardia with Situs Inversus 30 0.025
913
HYP048 Hypotropia 30 0.025
914
MNR003 Mineral Metabolism Disease 29 0.025
915
c RNL092 Renal-Hepatic-Pancreatic Dysplasia 1 29 0.025
916
c PRG106 Progressive Muscular Dystrophy 28 0.025
917
FXF001 Fox Fordyce Disease 28 0.025
918
PLM007 Pulmonary Aspergilloma 28 0.025
919
SPS016 Spasmodic Dysphonia 28 0.025
920
FML039 Female Reproductive System Disease 28 0.025
921
CYT004 Cytomegalic Inclusion Disease 27 0.025
922
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 27 0.025
923
LNS003 Lens Disease 26 0.025
924
c NPH053 Nephronophthisis 11 26 0.025
925
OCL011 Ocular Motility Disease 26 0.025
926
CPL005 Capillary Disease 26 0.025
927
c PTS008 Ptosis, Congenital 26 0.025
928
c PLM022 Pulmonary Valve Insufficiency 26 0.025
929
PRL014 Paralytic Squint 25 0.025
930
c INH004 Inherited Blood Coagulation Disease 25 0.025
931
SRN001 Serine Deficiency 25 0.025
932
c DYS150 Dyskeratosis Congenita, Autosomal Recessive 3 24 0.025
933
MDY006 Mody, Type Iv 24 0.025
934
c ACT219 Acute Myeloid Leukemia, Flt3-Related 23 0.025
935
c DYS173 Dyskeratosis Congenita, Autosomal Recessive 6 23 0.025
936
DYS011 Dyskinesia of Esophagus 23 0.025
937
GRN008 Granular Cell Carcinoma 23 0.025
938
HPT077 Hepatic Venoocclusive Disease with Immunodeficiency 22 0.025
939
c CHR036 Chronic Cholangitis 22 0.025
940
UNV002 Univentricular Heart 22 0.025
941
PNB004 Panbronchiolitis, Diffuse 21 0.025
942
PLS031 Plastic Bronchitis 21 0.025
943
c MCL040 Macular Degeneration, Age-Related, 3 21 0.025
944
TMR013 Tumor Necrosis Factor Receptor 1 Associated Periodic Syndrome 20 0.025
945
c MYC058 Myocardial Infarction 2 19 0.025
946
HND001 Hand Dermatosis 19 0.025
947
c HYP555 Hypertriglyceridemia, Transient Infantile 19 0.025
948
KHL001 Kohler's Disease 18 0.025
949
c PNC095 Pancreatic Cancer 3 18 0.025
950
BLD063 Bile Duct Cysts 18 0.025
951
c MLT094 Multiple Sclerosis 3 18 0.025
952
NPH064 Nipah Virus Disease 17 0.025
953
ALT003 Alternating Exotropia 17 0.025
954
HYP213 Hypomelanotic Disorder 15 0.025
955
IMM071 Immunodeficiency 12 15 0.025
956
EYC003 Eye Accommodation Disease 14 0.025
957
PLM062 Pulmonary Hyalinizing Granuloma 12 0.025
958
c MLT093 Multiple Sclerosis 2 9 0.025
959
c MCL026 Macular Dystrophy, Retinal, 3 8 0.025
960
HRT029 Heart Tumor of the Child 7 0.025
961
ATM053 Autoimmune Disease 2 5 0.025
962
c DLT001 Delta Chain Disease 5 0.025
963
P ALZ034 Alzheimer Disease 98 0.020
964
P CLR023 Colorectal Cancer 95 0.020
965
P RTT002 Rett Syndrome 79 0.020
966
c PRK057 Parkinson Disease, Late-Onset 73 0.020
967
ADN021 Adenomatous Polyposis Coli 71 0.020
968
c FNC027 Fanconi Anemia, Complementation Group a 71 0.020
969
CDS001 Cadasil 70 0.020
970
P CSH001 Cushing's Syndrome 67 0.020
971
P RBN001 Rubinstein-Taybi Syndrome 66 0.020
972
FCT007 Factor Vii Deficiency 66 0.020
973
P PSD087 Pseudoxanthoma Elasticum 65 0.020
974
KPS004 Kaposi Sarcoma 65 0.020
975
SVR004 Severe Combined Immunodeficiency 65 0.020
976
CMM004 Common Variable Immunodeficiency 64 0.020
977
P KRT004 Keratitis 63 0.020
978
c LKM062 Leukemia, Acute Lymphoblastic 63 0.020
979
BLM001 Bloom Syndrome 63 0.020
980
GTL001 Gitelman Syndrome 63 0.020
981
c NRF018 Neurofibromatosis, Type 1 63 0.020
982
P HLP001 Holoprosencephaly 62 0.020
983
P PRD006 Prader-Willi Syndrome 62 0.020
984
P FLL037 Follicular Lymphoma 62 0.020
985
LKC001 Leukocyte Adhesion Deficiency 61 0.020
986
WRN001 Werner Syndrome 61 0.020
987
c GLY008 Glycogen Storage Disease Ii 61 0.020
988
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 0.020
989
ARG002 Argininosuccinic Aciduria 59 0.020
990
c EHL057 Ehlers-Danlos Syndrome, Type Iv 58 0.020
991
P MRT001 Muir-Torre Syndrome 58 0.020
992
P PLY011 Polycystic Ovary Syndrome 58 0.020
993
P CNG015 Congenital Diaphragmatic Hernia 58 0.020
994
P SLV001 Silver-Russell Syndrome 58 0.020
995
CNG368 Congenital Adrenal Hyperplasia 58 0.020
996
INC021 Incontinentia Pigmenti 58 0.020
997
P AGM005 Agammaglobulinemia, X-Linked 1 58 0.020
998
TWN003 Townes-Brocks Syndrome 57 0.020
999
OVR029 Ovarian Hyperstimulation Syndrome 57 0.020
1000
MLG068 Malignant Glioma 57 0.020
1001
KND001 Kindler Syndrome 56 0.020
1002
LYM017 Lyme Disease 56 0.020
1003
c PRM005 Primary Hyperparathyroidism 56 0.020
1004
P CRB042 Cerebellar Ataxia 56 0.020
1005
P EMR001 Emery-Dreifuss Muscular Dystrophy 56 0.020
1006
CLB001 Coloboma 55 0.020
1007
PRT037 Pertussis 55 0.020
1008
ACN011 Acne 55 0.020
1009
LPT001 Leptospirosis 55 0.020
1010
HJD001 Hajdu-Cheney Syndrome 55 0.020
1011
SPN186 Spinal Cord Injury 55 0.020
1012
P MYM002 Moyamoya Disease 55 0.020
1013
DRM014 Dermatofibrosarcoma Protuberans 54 0.020
1014
P HYD006 Hydrocephalus 54 0.020
1015
P FND001 Fundus Albipunctatus 54 0.020
1016
P SJG001 Sjogren's Syndrome 54 0.020
1017
P MYL007 Myeloma 54 0.020
1018
VND002 Van Der Woude Syndrome 54 0.020
1019
P PRP029 Porphyria 54 0.020
1020
c FML001 Familial Atrial Fibrillation 53 0.020
1021
P PLY018 Polycythemia 53 0.020
1022
CHR020 Chronic Interstitial Cystitis 53 0.020
1023
APP015 Apparent Mineralocorticoid Excess 52 0.020
1024
APH001 Aphthous Stomatitis 52 0.020
1025
GLB001 Gilbert Syndrome 52 0.020
1026
P ALP009 Alopecia Areata 52 0.020
1027
RLP001 Relapsing Polychondritis 52 0.020
1028
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 52 0.020
1029
c CNT035 Central Nervous System Disease 52 0.020
1030
P EHL001 Ehlers-Danlos Syndrome 51 0.020
1031
PMS001 Poems Syndrome 51 0.020
1032
P ADM011 Adams-Oliver Syndrome 51 0.020
1033
ECH003 Echinococcosis 51 0.020
1034
CHL067 Cholecystitis 51 0.020
1035
MSS001 Masa Syndrome 51 0.020
1036
P FTL001 Fetal Alcohol Syndrome 50 0.020
1037
ALV002 Alveolar Echinococcosis 50 0.020
1038
P CND004 Candidiasis 50 0.020
1039
P FBR017 Fibrosarcoma 50 0.020
1040
DBT001 Diabetic Ketoacidosis 50 0.020
1041
c THR082 Thrombophilia Due to Activated Protein C Resistance 50 0.020
1042
P CNJ013 Conjunctivitis 50 0.020
1043
PRN023 Prion Disease 50 0.020
1044
HYD012 Hydrops Fetalis 50 0.020
1045
P ART023 Arthropathy 50 0.020
1046
P LCH002 Lichen Planus 50 0.020
1047
c LSS005 Lissencephaly 1 49 0.020
1048
SNS001 Sensorineural Hearing Loss 49 0.020
1049
P NRV007 Nervous System Disease 49 0.020
1050
ACT049 Acute Disseminated Encephalomyelitis 49 0.020
1051
P SPN052 Spondyloarthropathy 49 0.020
1052
P SNR012 Senior-Loken Syndrome-1 49 0.020
1053
P INT001 Intrahepatic Cholestasis 49 0.020