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

2136 hits were found for 'fibrosis'

# ++ Fam MCID Name MIFTS Score
1
CYS001 Cystic Fibrosis 91 7.076
2
IDP003 Idiopathic Pulmonary Fibrosis 62 5.811
3
P PLM036 Pulmonary Fibrosis 59 5.370
4
ORL004 Oral Submucous Fibrosis 51 4.974
5
c CNG047 Congenital Fibrosis of the Extraocular Muscles 20 4.325
6
RTR011 Retroperitoneal Fibrosis 42 4.195
7
END021 Endomyocardial Fibrosis 40 4.113
8
CNG048 Congenital Hepatic Fibrosis 52 3.953
9
P CNG142 Congenital Fibrosis of the Extraocular Muscles 2 24 3.335
10
FBR028 Fibrosing Mediastinitis 25 3.058
11
c CNG144 Congenital Fibrosis of the Extraocular Muscles 3b 5 3.004
12
c CNG145 Congenital Fibrosis of the Extraocular Muscles 3c 4 3.004
13
NPH018 Nephrogenic Systemic Fibrosis 50 2.903
14
CCH002 Coach Syndrome 42 2.728
15
c CNG143 Congenital Fibrosis of the Extraocular Muscles 3a 6 2.694
16
LBN002 Lubani Al Saleh Teebi Syndrome 10 2.687
17
PST015 Postinflammatory Pulmonary Fibrosis 5 2.687
18
DFF002 Diffuse Pulmonary Fibrosis 18 2.510
19
c PLM044 Pulmonary Fibrosis, Familial 22 2.442
20
MCN015 Meconium Ileus in Cystic Fibrosis 15 2.431
21
PRR004 Preretinal Fibrosis 14 2.355
22
HPT065 Hepatic Fibrosis - Renal Cysts - Intellectual Deficit 11 2.335
23
MSC030 Muscular Fibrosis Multifocal Obstructed Vessels 6 2.335
24
LNG082 Lung Fibrosis - Immunodeficiency - 46,xx Gonadal Dysgenesis 5 2.327
25
c LCL003 Localized Pulmonary Fibrosis 3 2.327
26
c CNG146 Congenital Fibrosis of the Extraocular Muscles 4 1 2.327
27
TRP020 Tropical Endomyocardial Fibrosis 14 2.010
28
P HRM005 Hermansky-Pudlak Syndrome 1 44 1.998
29
MLT036 Multifocal Fibrosclerosis 19 1.994
30
P MYL005 Myelofibrosis 67 1.976
31
ACT029 Acute Interstitial Pneumonia 31 1.972
32
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 10 1.954
33
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 8 1.938
34
FML074 Familial Interstitial Fibrosis 3 1.938
35
c HRM009 Hermansky-Pudlak Syndrome 6 28 1.932
36
IDP016 Idiopathic Diffuse Interstitial Fibrosis 3 1.925
37
PSD089 Pseudomonas Aeruginosa Chronic Infection by, in Cystic Fibrosis 5 1.918
38
PLM106 Pulmonary Fibrosis - Hepatic Hyperplasia - Bone Marrow Hypoplasia 2 1.910
39
HPT029 Hepatic Fibrosis Renal Cysts Mental Retardation 0 1.910
40
EF001 Eaf 25 1.900
41
KF2001 Kif21a-Related Congenital Fibrosis of the Extraocular Muscles 10 1.900
42
CYS027 Cystic Fibrosis Lung Disease, Modifier of 5 1.900
43
RCR025 Recurrent Infections-Myelofibrosis-Nephromegaly Syndrome 4 1.900
44
HPT035 Hepatic Fibrosis Susceptibility Due to Schistosoma Mansoni Infection 3 1.900
45
PLM126 Pulmonary Fibrosis, Telomere-Related, 1 3 1.900
46
FLL043 Follicular Hamartoma - Alopecia - Cystic Fibrosis 2 1.900
47
NNC004 Non-Classic Cystic Fibrosis-Like Syndrome 2 1.900
48
PHX001 Phox2a-Related Congenital Fibrosis of the Extraocular Muscles 2 1.900
49
SFT006 Sftpc-Related Familial Pulmonary Fibrosis 2 1.900
50
TBB003 Tubb3-Related Congenital Fibrosis of the Extraocular Muscles 2 1.900
51
TRT009 Tert-Related Familial Pulmonary Fibrosis 2 1.900
52
TRC066 Terc-Related Familial Pulmonary Fibrosis 1 1.900
53
c CNG140 Congenital Fibrosis of the Extraocular Muscles 1a 0 1.900
54
c CNG141 Congenital Fibrosis of the Extraocular Muscles 1b 0 1.900
55
MCN017 Meconium Ileus 41 1.605
56
IDP011 Idiopathic Interstitial Pneumonia 47 1.547
57
ASB001 Asbestosis 49 1.460
58
P MBS002 Moebius Syndrome 45 1.447
59
SLC006 Silicosis 55 1.436
60
HPT012 Hepatocellular Fibrolamellar Carcinoma 23 1.356
61
SCR009 Scirrhous Adenocarcinoma 16 1.343
62
SCL027 Sclerotylosis 12 1.343
63
RZN001 Rozin Hertz Goodman Syndrome 12 1.343
64
TYL001 Taylor's Syndrome 11 1.343
65
c DBT022 Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism 11 1.343
66
FBR016 Fibrosclerosis of Breast 10 1.343
67
c NPH053 Nephronophthisis 11 10 1.343
68
GRP001 Graphite Pneumoconiosis 9 1.343
69
TKL001 Tukel Syndrome 6 1.343
70
c HPT021 Hepatitis 65 0.292
71
P HPT001 Hepatitis C 66 0.266
72
c HPT003 Hepatitis a 57 0.205
73
P LVR013 Liver Disease 62 0.182
74
P BRN022 Bronchiectasis 62 0.178
75
END072 Endotheliitis 51 0.178
76
c HPT007 Hepatitis E 52 0.160
77
ASP006 Aspergillosis 68 0.158
78
ALL008 Allergic Bronchopulmonary Aspergillosis 58 0.158
79
URT010 Ureteral Obstruction 48 0.152
80
P PNM007 Pneumonia 67 0.151
81
P HYP075 Hypertension 76 0.147
82
c HPT015 Hepatitis D 59 0.146
83
c PNC044 Pancreatitis 58 0.144
84
ANK002 Ankylosing Spondylitis 75 0.138
85
ILS001 Ileus 47 0.133
86
c HPT016 Hepatitis B 62 0.130
87
IDP042 Idiopathic Recurrent Stupor 15 0.129
88
PLM074 Pulmonary Function 38 0.123
89
c KDN018 Kidney Disease 52 0.122
90
BRN056 Bronchopulmonary Dysplasia 55 0.118
91
IDP044 Idiopathic Pulmonary Alveolar Proteinosis 47 0.118
92
P IDP049 Idiopathic Anterior Uveitis 30 0.117
93
c XP2001 Xp22.3 Microdeletion Syndrome 17 0.117
94
STN007 Stenotrophomonas Maltophilia 46 0.115
95
c HPT073 Hepatitis C Virus 43 0.114
96
NNL002 Nonalcoholic Steatohepatitis 50 0.113
97
c SCL016 Scleroderma 53 0.111
98
P CRT049 Critical Limb Ischemia 58 0.110
99
CRV045 Cervical Intraepithelial Neoplasia 47 0.110
100
P PNC102 Pancreatitis, Chronic 41 0.110
101
CRK001 Cork-Handlers' Disease 28 0.109
102
THR013 Thoracic Outlet Syndrome 53 0.107
103
c LCL006 Localized Scleroderma 64 0.105
104
c SRC013 Sarcoidosis 60 0.105
105
FTT001 Fatty Liver Disease 58 0.105
106
PNS012 Paine Syndrome 35 0.103
107
LNG032 Lung Cancer 61 0.100
108
CLL021 Collagenous Colitis 48 0.100
109
P PLY014 Polycystic Kidney Disease 62 0.099
110
PLM034 Pulmonary Emphysema 53 0.099
111
P PRT013 Portal Hypertension 65 0.097
112
LVR012 Liver Cirrhosis 69 0.096
113
P CRN074 Coronary Artery Aneurysm 45 0.096
114
BLT018 Bilateral Renal Dysplasia 16 0.096
115
P AST005 Asthma 86 0.095
116
P BLR001 Biliary Atresia 60 0.095
117
SCH014 Schistosomiasis 59 0.095
118
EHL036 Ehlers-Danlos/osteogenesis Imperfecta Syndrome 31 0.095
119
PLM015 Pulmonary Systemic Sclerosis 17 0.095
120
c VRL010 Viral Hepatitis 57 0.094
121
PLM012 Pulmonary Sarcoidosis 52 0.094
122
OCL020 Ocular Cicatricial Pemphigoid 44 0.094
123
SPS077 Sepsis 67 0.092
124
TBR011 Tuberculous Meningitis 51 0.092
125
ENT015 Enthesitis-Related Arthritis 50 0.092
126
EVN001 Evans' Syndrome 50 0.092
127
NNS002 Nonspecific Interstitial Pneumonia 50 0.092
128
P CHL066 Cholangitis 50 0.092
129
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 46 0.092
130
HPT023 Hepatocellular Carcinoma 69 0.091
131
NDL013 Nodular Regenerative Hyperplasia 49 0.091
132
PRL042 Proliferating Trichilemmal Cyst 40 0.091
133
TFT003 Tufting Enteropathy 26 0.091
134
14Q004 14q22q23 Microdeletion Syndrome 25 0.091
135
3Q2005 3q26q27 Microdeletion Syndrome 14 0.091
136
ATX002 Ataxia Telangiectasia 81 0.090
137
OST081 Osteoporosis, Postmenopausal 47 0.090
138
USL001 Usual Interstitial Pneumonia 45 0.089
139
IDP033 Idiopathic Edema 28 0.086
140
c THY032 Thyroiditis 61 0.084
141
PRM126 Primary Peritoneal Carcinoma 51 0.084
142
PCH007 Pouchitis 50 0.084
143
MYC013 Mycobacterium Abscessus 44 0.084
144
SRS007 Sorsby Fundus Dystrophy 33 0.084
145
P INS005 Insulin Resistance 62 0.083
146
ATP002 Atopy 52 0.083
147
SDR002 Siderosis 50 0.083
148
FML089 Familial Thoracic Aortic Aneurysm and Dissection 39 0.083
149
c HYP061 Hypertrophic Cardiomyopathy 59 0.082
150
LNG017 Lung Giant Cell Carcinoma 43 0.082
151
BRN024 Bronchitis 71 0.080
152
DSM004 Desmoid Tumor 63 0.080
153
SQM006 Squamous Cell Carcinoma 58 0.080
154
VSC007 Vascular Disease 69 0.079
155
ACT105 Acute Mountain Sickness 50 0.079
156
c SCL009 Sclerosing Cholangitis 49 0.079
157
EXC002 Exocrine Pancreatic Insufficiency 45 0.079
158
STR077 Streptococcal Toxic-Shock Syndrome 42 0.079
159
P ART022 Arthritis 75 0.077
160
P UVT001 Uveitis 66 0.077
161
P RSP003 Respiratory Failure 60 0.077
162
CHL068 Cholestasis 55 0.077
163
c HRM001 Hermansky-Pudlak Syndrome 55 0.077
164
P ESN007 Eosinophilia 54 0.077
165
INT066 Interstitial Lung Disease 46 0.077
166
P SPR035 Superior Vena Cava Syndrome 34 0.077
167
P SRC025 Sarcoidosis 1 30 0.077
168
HNM001 Hinman's Syndrome 28 0.077
169
TYP018 Type 3 Von Willebrand Disease 17 0.077
170
P DLT002 Dilated Cardiomyopathy 74 0.076
171
P SYS005 Systemic Scleroderma 63 0.076
172
NSY001 N Syndrome 57 0.076
173
SCN006 Secondary Syphilis 53 0.076
174
HYP006 Hypertensive Heart Disease 51 0.076
175
ALB002 Albinism 50 0.076
176
c DBT009 Diabetes Mellitus 68 0.074
177
BRN002 Bronchiolitis 60 0.074
178
EXT034 Extrinsic Allergic Alveolitis 55 0.074
179
SPS019 Spastic Paraparesis 49 0.074
180
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 31 0.074
181
ACN002 Acanthosis Nigricans 70 0.072
182
LKM002 Leukemia 70 0.072
183
P PNM006 Pneumoconiosis 50 0.072
184
LKP003 Leukoplakia 45 0.072
185
ICH002 Ichthyosis Bullosa of Siemens 41 0.072
186
MYC006 Mycosis Fungoides 68 0.071
187
GLL008 Gilles De La Tourette Syndrome 60 0.071
188
P BRN012 Bronchiolitis Obliterans 58 0.071
189
ART031 Aortic Coarctation 56 0.071
190
P INF032 Infertility 55 0.071
191
CNN005 Connective Tissue Disease 51 0.071
192
RSD004 Rosai-Dorfman Disease 44 0.071
193
DFF024 Diffuse Panbronchiolitis 44 0.071
194
c SPN183 Spontaneous Pneumothorax 44 0.071
195
CNG034 Congestive Heart Failure 74 0.069
196
P GLM007 Glomerulonephritis 60 0.069
197
P ADN016 Adenocarcinoma 60 0.069
198
c MSC005 Muscular Dystrophy 54 0.069
199
c ENC008 Encephalocele 47 0.069
200
c INT070 Intestinal Obstruction 46 0.069
201
CRB009 Cerebritis 46 0.069
202
P TRN034 Transverse Myelitis 40 0.069
203
SRF004 Surfactant Metabolism Dysfunction, Pulmonary, 1 24 0.069
204
P STR035 Streptococcal Group a Invasive Disease 15 0.069
205
CRN131 Coronary Artery Disease, Modifier of 12 0.069
206
P RHM011 Rheumatoid Arthritis 83 0.067
207
ART019 Aortic Valve Stenosis 64 0.067
208
SPL018 Splenomegaly 50 0.067
209
P DYS142 Dyskeratosis Congenita, Autosomal Recessive 4 40 0.067
210
RDT013 Radiation Proctitis 36 0.067
211
21Q001 21q22.11q22.12 Microdeletion Syndrome 13 0.067
212
LCH002 Lichen Planus 61 0.065
213
MYC002 Mycobacterium Avium Complex Disease 56 0.065
214
APH001 Aphthous Stomatitis 56 0.065
215
NPH051 Nephritis 55 0.065
216
P PLM129 Pulmonary Disease, Chronic Obstructive 51 0.065
217
GNR017 Generalized Pustular Psoriasis 51 0.065
218
RNL028 Renal Tubular Dysgenesis 49 0.065
219
INT103 Intrauterine Infections 41 0.065
220
P THR045 Thrombotic Thrombocytopenic Purpura, Congenital 35 0.065
221
c ERL004 Early Yaws 29 0.065
222
P DDN001 Duodenal Ulcer 63 0.064
223
DST006 Diastolic Heart Failure 50 0.064
224
ORL011 Oral Cancer 50 0.064
225
PRC013 Pericarditis 48 0.064
226
c NPH005 Nephronophthisis 48 0.064
227
ORL012 Oral Leukoplakia 42 0.064
228
CRY001 Cryptogenic Organizing Pneumonia 41 0.064
229
CLC008 Colchicine Resistance 28 0.064
230
P HMC003 Hemochromatosis 73 0.062
231
P PRM006 Primary Biliary Cirrhosis 69 0.062
232
P INF038 Influenza 63 0.062
233
THR079 Thromboembolism 63 0.062
234
c ATX004 Ataxia 56 0.062
235
DRM004 Dermatofibrosarcoma 51 0.062
236
CYS016 Cystic Kidney 50 0.062
237
CRS001 Crescentic Glomerulonephritis 50 0.062
238
DDF001 Dedifferentiated Liposarcoma 48 0.062
239
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 47 0.062
240
DDN011 Duodenal Atresia 41 0.062
241
ORL015 Oral Squamous Cell Carcinoma 40 0.062
242
PRS115 Prosthetic Joint Infection 36 0.062
243
FCT013 Factor V Leiden Thrombophilia 31 0.062
244
CLR005 Clear Cell Chondrosarcoma 31 0.062
245
ULC004 Ulcerative Colitis 71 0.060
246
ATH003 Atherosclerosis 69 0.060
247
GST023 Gastric Ulcer 67 0.060
248
P ANG001 Angelman Syndrome 67 0.060
249
P HMP004 Hemophilia B 66 0.060
250
P HYP117 Hypertriglyceridemia 63 0.060
251
P HYP098 Hypereosinophilic Syndrome 61 0.060
252
P CNG030 Congenital Muscular Dystrophy 59 0.060
253
c SBC007 Subacute Thyroiditis 55 0.060
254
FBR032 Fibromuscular Dysplasia 54 0.060
255
P END033 Endocarditis 42 0.060
256
P AVS004 Avascular Necrosis of the Femoral Head 40 0.060
257
14Q001 14q12 Microdeletion Syndrome 23 0.060
258
FTL044 Fetal Cytomegalovirus Syndrome 22 0.060
259
PNC077 Pancreatitis, Idiopathic 21 0.060
260
RHM009 Rheumatoid Lung Disease 18 0.060
261
c RNG028 Ring Chromosome Y 17 0.060
262
c 2P1003 2p13.2 Microdeletion Syndrome 11 0.060
263
c ATM064 Autoimmune Pancreatitis Type 1 7 0.060
264
P PNC035 Pancreatic Cancer 82 0.058
265
P ATM003 Autoimmune Thyroiditis 66 0.058
266
LNG024 Langerhans-Cell Histiocytosis 63 0.058
267
ART016 Aortic Aneurysm 62 0.058
268
c ACT027 Acute Pancreatitis 60 0.058
269
DRM014 Dermatofibrosarcoma Protuberans 59 0.058
270
MCR088 Microscopic Polyangiitis 58 0.058
271
CCT002 Cicatricial Pemphigoid 58 0.058
272
c OCL002 Oculocutaneous Albinism 56 0.058
273
P SNS014 Sinusitis 54 0.058
274
INV001 Invasive Aspergillosis 47 0.058
275
PNM013 Pneumococcal Meningitis 47 0.058
276
JVN033 Juvenile Nasopharyngeal Angiofibroma 46 0.058
277
c RSM001 Rasmussen Encephalitis 46 0.058
278
c ACR001 Aicardi-Goutieres Syndrome 46 0.058
279
LKS001 Leukostasis 45 0.058
280
P ATS008 Autosomal Dominant Disease 45 0.058
281
c PLY026 Polycystic Kidney Disease, Autosomal Dominant 45 0.058
282
SPN119 Spondylarthropathy 44 0.058
283
EGG001 Egg Allergy 43 0.058
284
c INT099 Intrahepatic Cholestasis of Pregnancy 37 0.058
285
ALB014 Alobar Holoprosencephaly 36 0.058
286
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 35 0.058
287
LWR010 Low Renin Hypertension 34 0.058
288
HYP114 Hypertensive Nephropathy 34 0.058
289
BNZ002 Benzene Toxicity 28 0.058
290
NNS006 Non-Suppurative Otitis Media 24 0.058
291
P DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 23 0.058
292
MLR006 Male Reproductive Organ Cancer 21 0.058
293
SBL004 Sea-Blue Histiocytosis 17 0.058
294
c DST058 Distal Monosomy 12p 16 0.058
295
RDL021 Riedel Thyroiditis 14 0.058
296
MNS013 Monosomy 13q34 14 0.058
297
c BRN101 Bronchiolitis Obliterans with Obstructive Pulmonary Disease 11 0.058
298
VRS002 Virus-Associated Trichodysplasia Spinulosa 10 0.058
299
P OBS005 Obesity 79 0.056
300
PRT036 Peritonitis 67 0.056
301
RLP001 Relapsing Polychondritis 66 0.056
302
SKN016 Skin Disease 64 0.056
303
URT039 Urticaria 61 0.056
304
HYP266 Hypoxia 60 0.056
305
P PRM054 Primary Sclerosing Cholangitis 57 0.056
306
P PMP005 Pemphigus Vulgaris 57 0.056
307
c MLR021 Malaria, Severe 56 0.056
308
MLN007 Male Infertility 56 0.056
309
CRC006 Carcinoid Syndrome 55 0.056
310
c PRM011 Primary Ciliary Dyskinesia 54 0.056
311
CRT033 Corticobasal Degeneration 53 0.056
312
P CLL015 Collagen Disease 52 0.056
313
EPT020 Epithelioid Hemangioendothelioma 51 0.056
314
c TWN006 Twin Twin Transfusion Syndrome 51 0.056
315
c ATM024 Autoimmune Pancreatitis 51 0.056
316
P INT068 Intestinal Disease 51 0.056
317
OBS006 Obstructive Lung Disease 49 0.056
318
ESN005 Eosinophilic Gastroenteritis 42 0.056
319
c CHR048 Chronic Rhinitis 39 0.056
320
ENT007 Enteropathica 38 0.056
321
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 33 0.056
322
17Q001 17q21.31 Microdeletion Syndrome 29 0.056
323
c CHR226 Chromosome 1q41-Q42 Deletion Syndrome 23 0.056
324
MCR071 Microdeletion 15q11.2 21 0.056
325
ACR022 Acardia 15 0.056
326
GST034 Gastroesophageal Reflux Disease 65 0.053
327
WST001 West Syndrome 64 0.053
328
ERD001 Erdheim-Chester Disease 58 0.053
329
P RNV001 Renovascular Hypertension 56 0.053
330
PRT002 Paratyphoid Fever 55 0.053
331
PRX003 Paroxysmal Nocturnal Hemoglobinuria 55 0.053
332
LPS007 Lupus Nephritis 55 0.053
333
P CRP001 Carpal Tunnel Syndrome 53 0.053
334
ALC006 Alcoholic Hepatitis 52 0.053
335
P MYC008 Myocarditis 51 0.053
336
c EHL021 Ehlers-Danlos Syndrome Type Viib 50 0.053
337
c PRL003 Proliferative Glomerulonephritis 49 0.053
338
CHL056 Cheilitis 49 0.053
339
P THR090 Thrombocythemia 1 48 0.053
340
PRC012 Pericardial Effusion 47 0.053
341
P ECT006 Ectodermal Dysplasia 46 0.053
342
LMB052 Lumbar Disc Herniation 46 0.053
343
VLV044 Vulvar Intraepithelial Neoplasia 45 0.053
344
FCL041 Focal Myositis 44 0.053
345
P HYP090 Hyperalphalipoproteinemia 43 0.053
346
TLY002 T-Lymphocytopenia 42 0.053
347
PST041 Posterior Urethral Valves 42 0.053
348
c RST002 Restrictive Cardiomyopathy 41 0.053
349
CHL079 Children's Interstitial Lung Disease 39 0.053
350
BWN003 Bowenoid Papulosis 39 0.053
351
c ATS010 Autosomal Recessive Disease 39 0.053
352
MCR014 Microcystic Adenoma 38 0.053
353
P PLY027 Polycystic Kidney Disease, Autosomal Recessive 37 0.053
354
P LFT013 Left Ventricular Noncompaction 1, with or Without Congenital Heart Defects 36 0.053
355
PRT082 Preterm Premature Rupture of the Membranes 33 0.053
356
SPR034 Superior Limbic Keratoconjunctivitis 32 0.053
357
c HRM011 Hermansky-Pudlak Syndrome 8 25 0.053
358
ESN020 Eosinophilic Granulomatosis with Polyangiitis 21 0.053
359
GRF006 Grfoma 20 0.053
360
CPD002 Copd, Rate of Decline of Lung Function in 12 0.053
361
CYT018 Cytochrome P450 2d6 Variant 12 0.053
362
c LPS004 Lupus Erythematosus 65 0.051
363
SPT013 Septic Shock 62 0.051
364
ADL030 Adult-Onset Still's Disease 61 0.051
365
DSS009 Disseminated Intravascular Coagulation 59 0.051
366
PRT011 Protein C Deficiency 59 0.051
367
P RHN004 Rhinitis 59 0.051
368
P SYN007 Synovitis 58 0.051
369
CHR001 Churg-Strauss Syndrome 56 0.051
370
c THR003 Thoracic Aortic Aneurysm 54 0.051
371
ACR003 Acrodermatitis Enteropathica 53 0.051
372
P RPD001 Rapidly Progressive Glomerulonephritis 51 0.051
373
PNM008 Pneumothorax 48 0.051
374
ACR005 Acrodermatitis 45 0.051
375
HYP026 Hypoglycemic Coma 43 0.051
376
RHM014 Rheumatoid Vasculitis 41 0.051
377
WRD002 Werdnig-Hoffmann Disease 39 0.051
378
c JBR026 Joubert Syndrome 15 35 0.051
379
c ATX010 Ataxia Neuropathy Spectrum 33 0.051
380
CLL005 Cellular Leiomyoma 30 0.051
381
PRR008 Periarteritis Nodosa 27 0.051
382
HYP319 Hypereosinophilic Syndrome, Idiopathic, Resistant to Imatinib 27 0.051
383
c CNG071 Congenital Disorder of Glycosylation Type 1b 24 0.051
384
c 2Q3005 2q31.1 Microdeletion Syndrome 22 0.051
385
17Q007 17q11 Microdeletion Syndrome 21 0.051
386
SLR005 Solar Urticaria 18 0.051
387
c FRS006 Fraser Like Syndrome 4 0.051
388
P SYS001 Systemic Lupus Erythematosus 83 0.049
389
TBR010 Tuberculosis 82 0.049
390
AND002 Androgen Insensitivity Syndrome 75 0.049
391
THL005 Thalassemia 69 0.049
392
PCK001 Pick's Disease 68 0.049
393
c THR014 Thrombocytopenia 66 0.049
394
P ADL010 Adult Respiratory Distress Syndrome 66 0.049
395
VSC011 Vasculitis 65 0.049
396
CNG368 Congenital Adrenal Hyperplasia 64 0.049
397
GLC003 Glucose Intolerance 62 0.049
398
CRY004 Cryoglobulinemia 59 0.049
399
c AXN002 Axenfeld-Rieger Syndrome 57 0.049
400
VNS009 Venous Thrombosis 56 0.049
401
STR008 Strongyloidiasis 55 0.049
402
P PLM006 Pulmonary Alveolar Proteinosis 55 0.049
403
ESN015 Eosinophilic Fasciitis 54 0.049
404
c MYL014 Myeloproliferative Disorder 54 0.049
405
BCT002 Bacterial Vaginosis 53 0.049
406
c MLG069 Malignant Hypertension 53 0.049
407
LYM019 Lymphosarcoma 53 0.049
408
GRW007 Growth Hormone Deficiency 52 0.049
409
KLD001 Keloids 52 0.049
410
MLT006 Multidrug-Resistant Tuberculosis 51 0.049
411
STT004 Steatorrhea 49 0.049
412
c JBR001 Joubert Syndrome 49 0.049
413
THR035 Thrombasthenia 49 0.049
414
MST002 Mast-Cell Leukemia 47 0.049
415
PRP034 Purpura Fulminans 46 0.049
416
PRT019 Protein-Losing Enteropathy 46 0.049
417
CYC004 Cyclic Hematopoiesis 45 0.049
418
P AZS001 Azoospermia 44 0.049
419
PST055 Postural Hypotension 42 0.049
420
PLM019 Pleomorphic Liposarcoma 42 0.049
421
BRN105 Burn Scar 41 0.049
422
BRN013 Bronchiolitis Obliterans Organizing Pneumonia 41 0.049
423
ZYG002 Zygomycosis 38 0.049
424
GRN037 Granulomatosis with Polyangiitis 36 0.049
425
CNG069 Congenital Cytomegalovirus 33 0.049
426
MYC065 Myocardial Infarction, Decreased 33 0.049
427
CRD132 Cardiac Conduction Defect 32 0.049
428
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 32 0.049
429
BRG002 Berger Disease 30 0.049
430
DSQ001 Desquamative Interstitial Pneumonia 30 0.049
431
PRN029 Parainfluenza Virus Type 3 30 0.049
432
PLM048 Pleomorphic Malignant Fibrous Histiocytoma 23 0.049
433
CHL109 Childhood Apraxia of Speech 19 0.049
434
SCN044 Secondary Ciliary Dyskinesia 17 0.049
435
AML009 Amelogenesis Imperfecta Nephrocalcinosis 15 0.049
436
c MCK009 Meckel Syndrome Type 3 14 0.049
437
IMM048 Immunoglobulin G4-Related Sclerosing Disease 8 0.049
438
ISL072 Isolated Growth Hormone Deficiency, Type Ib, Ghrhr-Related 7 0.049
439
P BRS047 Breast Cancer 85 0.046
440
DCH001 Duchenne Muscular Dystrophy 70 0.046
441
P MLR004 Malaria 66 0.046
442
LRN002 Laron Syndrome 65 0.046
443
P ABD003 Abdominal Aortic Aneurysm 65 0.046
444
ACQ007 Acquired Immunodeficiency Syndrome 62 0.046
445
IRN001 Iron Deficiency Anemia 58 0.046
446
ALL006 Allergic Asthma 58 0.046
447
WLL006 Wells Syndrome 55 0.046
448
c ACT134 Acute Liver Failure 55 0.046
449
c BLN003 Blindness 54 0.046
450
INT075 Intracranial Hypertension 53 0.046
451
P STR020 Strabismus 53 0.046
452
P ESN001 Eosinophilic Esophagitis 52 0.046
453
RHM027 Rheumatic Disease 52 0.046
454
MYL020 Myelomeningocele 51 0.046
455
PGM001 Pigmented Villonodular Synovitis 51 0.046
456
P ESP024 Esophagitis 51 0.046
457
SNG010 Single Median Maxillary Central Incisor 50 0.046
458
P CLC001 Calciphylaxis 49 0.046
459
CNT047 Contact Dermatitis 49 0.046
460
JCB001 Jacobsen Syndrome 49 0.046
461
c CHR417 Chronic Graft Versus Host Disease 49 0.046
462
PNC045 Pancreatic Agenesis 49 0.046
463
BCK006 Back Pain 46 0.046
464
SCL017 Sclerosing Hemangioma 46 0.046
465
P AXN003 Axenfeld-Rieger Syndrome Type 1 39 0.046
466
ENT001 Enterocele 39 0.046
467
GBL002 Goblet Cell Carcinoid 38 0.046
468
FTL021 Fetal Macrosomia 37 0.046
469
HYP226 Hyporeninemic Hypoaldosteronism 33 0.046
470
WRN005 Wrinkles 33 0.046
471
RDT005 Radiation Induced Cancer 27 0.046
472
c HRM006 Hermansky-Pudlak Syndrome 3 24 0.046
473
19Q001 19q13.11 Microdeletion Syndrome 21 0.046
474
c TTL001 Total Internal Ophthalmoplegia 17 0.046
475
c BNG076 Benign Exophthalmos Syndrome 17 0.046
476
P MCL055 Mcleod Syndrome with or Without Chronic Granulomatous Disease 14 0.046
477
RSP001 Respiratory Bronchiolitis-Associated Interstitial Lung Disease 10 0.046
478
P PRM021 Primary Pulmonary Hypertension 74 0.044
479
WLS001 Wilson Disease 74 0.044
480
TRC032 Turcot Syndrome 66 0.044
481
P GRF002 Graft Versus Host Disease 64 0.044
482
PLY017 Polyarteritis Nodosa 62 0.044
483
CHL065 Cholangiocarcinoma 61 0.044
484
PMS001 Poems Syndrome 61 0.044
485
c HYP086 Hypothyroidism 59 0.044
486
c NPH012 Nephrotic Syndrome 57 0.044
487
ANR008 Aneurysm Disease 57 0.044
488
P NPH009 Nephrolithiasis 57 0.044
489
ISC004 Ischemia 57 0.044
490
STF001 Stiff-Person Syndrome 55 0.044
491
APP008 Appendicitis 54 0.044
492
P BRN009 Burning Mouth Syndrome 54 0.044
493
PST046 Post-Transplant Lymphoproliferative Disease 54 0.044
494
HRD057 Hereditary Pancreatitis 53 0.044
495
CHL069 Cholesteatoma 52 0.044
496
ART001 Arterial Tortuosity Syndrome 52 0.044
497
NTR003 Natural Killer Cell Leukemia 52 0.044
498
P EXP004 Exophthalmos 51 0.044
499
HMS001 Hemosiderosis 51 0.044
500
PLY013 Polymyalgia Rheumatica 51 0.044
501
INT146 Intervertebral Disc Disease 50 0.044
502
SLD003 Sialadenitis 50 0.044
503
CYT008 Cytomegalovirus Infection 50 0.044
504
PLY012 Polyhydramnios 49 0.044
505
INT067 Interstitial Nephritis 49 0.044
506
P ORT004 Orthostatic Intolerance 48 0.044
507
c HYD002 Hydronephrosis 48 0.044
508
P NGH001 Night Blindness 47 0.044
509
RNL078 Renal Dysplasia 47 0.044
510
P GND004 Gonadal Dysgenesis 47 0.044
511
CRD003 Cardiac Sarcoidosis 46 0.044
512
P JBR004 Joubert Syndrome 2 45 0.044
513
c CPL003 Capillary Leak Syndrome 44 0.044
514
ALC005 Alcoholic Pancreatitis 44 0.044
515
MLK003 Melkersson-Rosenthal Syndrome 43 0.044
516
CHL052 Choledochal Cyst 43 0.044
517
CNS002 Constrictive Pericarditis 43 0.044
518
P MCK022 Meckel Syndrome 1 41 0.044
519
CLS008 Clostridium Difficile 40 0.044
520
ETH009 Ethmoid Sinusitis 40 0.044
521
AND003 Andersen-Tawil Syndrome 39 0.044
522
STP004 Staphylococcal Toxic Shock Syndrome 39 0.044
523
BGS001 Bagassosis 39 0.044
524
DXR001 Doxorubicin Induced Cardiomyopathy 38 0.044
525
MNN034 Mannose-Binding Lectin Deficiency 37 0.044
526
HPT063 Hepatitis B Virus Infection 36 0.044
527
ART012 Aortitis 36 0.044
528
OST006 Osteoblastoma 35 0.044
529
c RCR022 Recurrent Acute Pancreatitis 35 0.044
530
c CMP058 Complex Regional Pain Syndrome Type 1 35 0.044
531
VND002 Van Der Woude Syndrome 34 0.044
532
c PSD080 Pseudohypoaldosteronism Type 1 33 0.044
533
BST001 Bestrophinopathy 31 0.044
534
XLN005 X-Linked Hyper Igm Syndrome 31 0.044
535
P DNS004 Duane Syndrome Type 2 31 0.044
536
P SLP004 Salpingo-Oophoritis 30 0.044
537
c WRD010 Waardenburg Syndrome Type 4 27 0.044
538
c ICH041 Ichthyosis, Autosomal Recessive 4b 23 0.044
539
c CHR266 Chromosome 8p23.1 Deletion 21 0.044
540
AND005 Androgen Insensitivity Syndrome, Mild 19 0.044
541
c DYS055 Dystonia 10 17 0.044
542
MTH028 Mthfr Thermolabile Variant 17 0.044
543
MDL007 Medial Medullary Syndrome 14 0.044
544
c CTR105 Cataract 12, Multiple Types 13 0.044
545
TNF006 Tnfrsf13b-Related Common Variable Immune Deficiency 12 0.044
546
PLM062 Pulmonary Hyalinizing Granuloma 11 0.044
547
HSL001 House Allergic Alveolitis 7 0.044
548
P MYC007 Myocardial Infarction 82 0.041
549
P OST002 Osteoporosis 73 0.041
550
LYM007 Lymphangioleiomyomatosis 67 0.041
551
P PLY011 Polycystic Ovary Syndrome 66 0.041
552
P AMY004 Amyloidosis 65 0.041
553
P ATP001 Atopic Dermatitis 64 0.041
554
c JVN010 Juvenile Rheumatoid Arthritis 62 0.041
555
PMP001 Pemphigus 60 0.041
556
P DRM010 Dermatomyositis 59 0.041
557
SPN051 Spondylitis 59 0.041
558
STS002 Situs Inversus 56 0.041
559
CMM005 Common Cold 55 0.041
560
SRC014 Sarcoma 54 0.041
561
MLR002 Miliary Tuberculosis 53 0.041
562
c AFB001 Afibrinogenemia 52 0.041
563
CHR008 Choroiditis 51 0.041
564
P PRT039 Proteinuria 51 0.041
565
P MSC003 Muscular Atrophy 51 0.041
566
ANK001 Ankylosis 51 0.041
567
c HYP065 Hyperaldosteronism 50 0.041
568
FLR002 Filariasis 50 0.041
569
c DRR001 Diarrhea 49 0.041
570
MDS022 Mediastinitis 49 0.041
571
c MTR012 Mitral Valve Disease 48 0.041
572
IMM001 Immune-Complex Glomerulonephritis 47 0.041
573
LDP002 Lead Poisoning 47 0.041
574
ADS004 Aids Dementia Complex 47 0.041
575
DFF003 Diffuse Scleroderma 47 0.041
576
CHR031 Chromoblastomycosis 46 0.041
577
LRG008 Large Granular Lymphocyte Leukemia 46 0.041
578
KRT012 Keratoderma 44 0.041
579
P PST022 Posterior Uveal Melanoma 44 0.041
580
PLM035 Pulmonary Eosinophilia 43 0.041
581
KRT002 Keratomalacia 42 0.041
582
RPP001 Rapp-Hodgkin Syndrome 37 0.041
583
17Q004 17q12 Microdeletion Syndrome 32 0.041
584
TRP008 Tropical Calcific Pancreatitis 30 0.041
585
MLT035 Multifocal Choroiditis 29 0.041
586
c MLG033 Malignant Ovarian Cyst 29 0.041
587
EHL006 Ehlers–danlos Syndrome 27 0.041
588
PLM111 Pleomorphic Undifferentiated Sarcoma 21 0.041
589
PTS008 Ptosis, Congenital 21 0.041
590
RTR009 Retroperitoneal Cancer 21 0.041
591
RTR005 Retroperitoneal Lymphoma 14 0.041
592
CLF021 Cleft Palate X-Linked 12 0.041
593
MTR030 Mitral Valve Prolapse, Familial, X-Linked 10 0.041
594
P AMY001 Amyotrophic Lateral Sclerosis 87 0.038
595
MRF001 Marfan Syndrome 78 0.038
596
CRH001 Crohn's Disease 78 0.038
597
KWS002 Kawasaki Disease 69 0.038
598
ACT074 Acute Lymphocytic Leukemia 69 0.038
599
P OST005 Osteogenesis Imperfecta 69 0.038
600
THR006 Thromboangiitis Obliterans 67 0.038
601
ADN018 Adenoma 67 0.038
602
FNC001 Fanconi's Anemia 66 0.038
603
P LSH001 Leishmaniasis 65 0.038
604
ART021 Arteriosclerosis 63 0.038
605
PLM001 Pulmonary Tuberculosis 62 0.038
606
HYP066 Hyperglycemia 59 0.038
607
CRB021 Cerebral Malaria 58 0.038
608
c MLG054 Malignant Histiocytosis 58 0.038
609
DYS007 Dyskeratosis Congenita 58 0.038
610
INT051 Intussusception 57 0.038
611
CLB001 Coloboma 56 0.038
612
c EMR001 Emery-Dreifuss Muscular Dystrophy 56 0.038
613
EPD006 Epidermolysis Bullosa Acquisita 55 0.038
614
HYP458 Hyper Ige Syndrome 54 0.038
615
P MTR005 Mitral Valve Prolapse 54 0.038
616
THY089 Thymic Epithelial Neoplasm 53 0.038
617
P FML052 Familial Cold Autoinflammatory Syndrome 53 0.038
618
RNL015 Renal Hypertension 52 0.038
619
c MYP004 Myopathy 52 0.038
620
NPH003 Nephrocalcinosis 52 0.038
621
HPY002 H. Pylori Infection 52 0.038
622
URN010 Urinary Tract Obstruction 52 0.038
623
DND001 Dandy-Walker Syndrome 52 0.038
624
P GLL020 Gallbladder Disease 52 0.038
625
CRY005 Cryptococcosis 51 0.038
626
MYL001 Myelitis 51 0.038
627
RNL014 Renal Cell Carcinoma 51 0.038
628
c MNT147 Mental Retardation 51 0.038
629
SMT019 Somatostatin Analog 51 0.038
630
ART008 Arteriosclerosis Obliterans 50 0.038
631
MGC001 Megacolon 50 0.038
632
DBT061 Diabetic Nephropathy 50 0.038
633
P PND001 Pain Disorder 49 0.038
634
DNG001 Dengue Shock Syndrome 49 0.038
635
c PST005 Posterior Uveitis 49 0.038
636
TXC012 Toxic Epidermal Necrolysis 49 0.038
637
SYN036 Syncope 49 0.038
638
BRN018 Borna Disease 49 0.038
639
P NRM005 Neuromuscular Disease 48 0.038
640
c PRG060 Pregnancy Loss 48 0.038
641
ISL003 Isolated Growth Hormone Deficiency 47 0.038
642
FBR019 Fibromatosis 47 0.038
643
CVR006 Cavernous Hemangioma 47 0.038
644
PNN001 Panniculitis 47 0.038
645
PST010 Pasteurellosis 47 0.038
646
P CRB126 Cerebral Cavernous Malformation 47 0.038
647
CRN030 Coronary Stenosis 47 0.038
648
SKL017 Skeletal Dysplasias 47 0.038
649
EBS001 Ebstein Anomaly 47 0.038
650
CMB021 Combined Pituitary Hormone Deficiency 46 0.038
651
VRN004 Vernal Keratoconjunctivitis 46 0.038
652
c OPH004 Ophthalmoplegia 46 0.038
653
PLR008 Pleurisy 46 0.038
654
BLR006 Biliary Tract Disease 46 0.038
655
MYX013 Myxofibrosarcoma 45 0.038
656
LKM006 Leukomalacia 45 0.038
657
BLL004 Bullous Keratopathy 45 0.038
658
HYP121 Hypoalphalipoproteinemia 44 0.038
659
PYM001 Pyomyositis 44 0.038
660
FSC004 Fasciitis 44 0.038
661
1P3001 1p36 Deletion Syndrome 44 0.038
662
RCR001 Recurrent Corneal Erosion 43 0.038
663
c FBR045 Fibromatosis, Gingival 43 0.038
664
LMB051 Lumbar Disc Disease 43 0.038
665
ACT093 Actinic Cheilitis 43 0.038
666
MNN021 Meningococcemia 42 0.038
667
NNT016 Neonatal Hemochromatosis 41 0.038
668
CHR078 Chorioretinitis 41 0.038
669
c ATM022 Autoimmune Myocarditis 40 0.038
670
PRM024 Primary Angle-Closure Glaucoma 40 0.038
671
FST010 Fasting Hypoglycemia 40 0.038
672
SCH016 Schimke Immunoosseous Dysplasia 40 0.038
673
CNG116 Congenital Nephrotic Syndrome Finnish Type 39 0.038
674
PRN021 Paranasal Sinus Disease 38 0.038
675
ATP013 Atopic Keratoconjunctivitis 38 0.038
676
RYN001 Raynaud Disease 37 0.038
677
SPR017 Spermatocele 36 0.038
678
TTR016 Tetra-Amelia Syndrome 36 0.038
679
ENC017 Encephaloceles 36 0.038
680
c TRN032 Transient Neonatal Diabetes Mellitus 36 0.038
681
KSH001 Keshan Disease 36 0.038
682
IPX001 Ipex Syndrome 35 0.038
683
CRY008 Cryopyrin-Associated Periodic Syndrome 35 0.038
684
RNL022 Renal Vascular Disease 35 0.038
685
CRB077 Cerebro-Costo-Mandibular Syndrome 32 0.038
686
URT031 Ureteral Disease 32 0.038
687
PPT001 Peptic Esophagitis 32 0.038
688
ACT164 Actinic Prurigo 32 0.038
689
HGH023 High Bone Mass Osteogenesis Imperfecta 27 0.038
690
GST063 Gastric Cancer Risk After H. Pylori Infection 26 0.038
691
INH011 Inherited Bone Marrow Failure Syndromes 25 0.038
692
PLM071 Pulmonary Surfactant Metabolism Dysfunction 25 0.038
693
EMP007 Emphysema Due to Aat Deficiency 23 0.038
694
AML006 Amelogenesis Imperfecta Hypoplastic Type, Ig 23 0.038
695
DDN009 Duodenal Obstruction 22 0.038
696
c DYS040 Dyskeratosis Congenita Autosomal Recessive 20 0.038
697
RPD005 Rapidly Involuting Congenital Hemangioma 19 0.038
698
c PRM041 Primary Cortisol Resistance 19 0.038
699
BLR009 Biliary Atresia Extrahepatic 19 0.038
700
ADM001 Adamantinous Craniopharyngioma 18 0.038
701
P ISC010 Isochromosome Yp 14 0.038
702
12Q001 12q15q21.1 Microdeletion Syndrome 14 0.038
703
c DND010 Dandy-Walker Malformation with Mental Retardation Basal Ganglia Disease and Seizures 12 0.038
704
PRT049 Partial Deletion of Y 9 0.038
705
c FML109 Familial Cerebral Cavernous Malformation 1 7 0.038
706
THM003 Thompson Baraitser Syndrome 1 0.038
707
P NRF002 Neurofibromatosis 86 0.034
708
P PRS040 Prostate Cancer 76 0.034
709
GLC006 Galactosemia 74 0.034
710
P FML018 Familial Mediterranean Fever 73 0.034
711
P TRN020 Turner Syndrome 71 0.034
712
BTT002 Beta Thalassemia 69 0.034
713
CLN016 Colon Cancer 66 0.034
714
DBT011 Diabetic Retinopathy 66 0.034
715
P CNG026 Congenital Heart Defect 65 0.034
716
ANT006 Antiphospholipid Syndrome 64 0.034
717
P ANR007 Anorexia Nervosa 64 0.034
718
PRC002 Paracoccidioidomycosis 64 0.034
719
ALL003 Allergic Rhinitis 62 0.034
720
21H001 21-Hydroxylase Deficiency 62 0.034
721
c MNN013 Meningitis 62 0.034
722
HMN010 Hemangioma 62 0.034
723
OVR029 Ovarian Hyperstimulation Syndrome 61 0.034
724
MLD001 Melioidosis 60 0.034
725
TXC005 Toxic Shock Syndrome 60 0.034
726
MXD005 Mixed Connective Tissue Disease 60 0.034
727
DRM006 Dermatitis 60 0.034
728
PPL022 Papilloma 60 0.034
729
CHG001 Chagas Disease 58 0.034
730
FCL008 Focal Glomerulosclerosis 57 0.034
731
OCC006 Occipital Horn Syndrome 57 0.034
732
P MLN008 Melanoma 56 0.034
733
P DFF005 Diffuse Large B-Cell Lymphoma 56 0.034
734
VRR004 Verrucous Carcinoma 56 0.034
735
KDS001 Kid Syndrome 55 0.034
736
P CND004 Candidiasis 55 0.034
737
FLT001 Felty's Syndrome 54 0.034
738
PRL007 Proliferative Diabetic Retinopathy 54 0.034
739
P OVR049 Ovarian Disease 53 0.034
740
PLY023 Polycystic Liver Disease 53 0.034
741
P DNT039 Dent's Disease 52 0.034
742
DBT004 Diabetic Polyneuropathy 52 0.034
743
HYP063 Hypersplenism 52 0.034
744
LMT001 Limited Scleroderma 52 0.034
745
URN003 Urinary Schistosomiasis 52 0.034
746
DSM007 Desmoplastic Small Round Cell Tumor 51 0.034
747
ART004 Aortic Atherosclerosis 51 0.034
748
ART017 Aortic Disease 51 0.034
749
P PYL005 Pyelonephritis 51 0.034
750
PYR010 Peyronie's Disease 51 0.034
751
GNG012 Gingival Overgrowth 50 0.034
752
ADL002 Adult Syndrome 50 0.034
753
CNS004 Constipation 50 0.034
754
HYP068 Hyperostosis 50 0.034
755
PRC003 Proctitis 49 0.034
756
ACT095 Acute Biphenotypic Leukemia 49 0.034
757
NCR004 Nocardiosis 49 0.034
758
c ACT042 Acute Pyelonephritis 49 0.034
759
LYM022 Lymphangioma 49 0.034
760
MLT113 Multicentric Castleman Disease 48 0.034
761
CYS006 Cystoid Macular Edema 48 0.034
762
HPT009 Hepatopulmonary Syndrome 47 0.034
763
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 47 0.034
764
GST045 Gastroenteritis 46 0.034
765
HYP457 Hypertrophic Scars 46 0.034
766
HMC014 Homocysteinemia 46 0.034
767
c OST025 Osteogenesis Imperfecta Type Iii 45 0.034
768
MDL009 Medullary Sponge Kidney 45 0.034
769
PRL019 Prolidase Deficiency 44 0.034
770
P INF037 Inflammatory Bowel Disease 44 0.034
771
c HMP006 Hemiplegic Migraine 44 0.034
772
KWS001 Kwashiorkor 43 0.034
773
PRR002 Pure Red-Cell Aplasia 42 0.034
774
CHR276 Chronic Active Epstein-Barr Virus Infection 42 0.034
775
LNG029 Lung Adenocarcinoma 42 0.034
776
ENC011 Encephalomyopathy 41 0.034
777
SCT002 Scotoma 41 0.034
778
PGT004 Paget Disease, Juvenile 41 0.034
779
c CHR037 Chronic Eosinophilic Pneumonia 41 0.034
780
HYP030 Hypoactive Sexual Desire Disorder 39 0.034
781
HYD005 Hydrocele 39 0.034
782
CNG064 Congenital Chloride Diarrhea 38 0.034
783
c 3Q2003 3q29 Microdeletion Syndrome 37 0.034
784
DBT007 Diabetic Cataract 36 0.034
785
VRL011 Viral Infectious Disease 35 0.034
786
c BRT034 Bartter Syndrome, Type 2 34 0.034
787
PNC041 Pancreatic Ductal Adenocarcinoma 32 0.034
788
ADS002 Adie Syndrome 32 0.034
789
PRQ002 Paraquat Poisoning 29 0.034
790
12Q002 12q14 Microdeletion Syndrome 28 0.034
791
c HMP017 Hemophilia a, Congenital 26 0.034
792
2Q3003 2q32q33 Microdeletion Syndrome 25 0.034
793
c 2Q2001 2q23.1 Microdeletion Syndrome 25 0.034
794
EHL039 Ehlers-Danlos Syndrome, Periodontitis Type 23 0.034
795
CLD014 Cole Disease 23 0.034
796
P JJN004 Jejunal Atresia 22 0.034
797
CLF029 Cleft Palate and Mental Retardation 21 0.034
798
HYP159 Hyperinsulinism, Focal 20 0.034
799
SNS010 Sine Scleroderma 19 0.034
800
BFD003 Bifid Uvula 18 0.034
801
ATR015 Atresia of Small Intestine 17 0.034
802
CRN197 Coronary Arterial Fistulas 13 0.034
803
SPS044 Spastic Paraplegia Epilepsy Mental Retardation 11 0.034
804
c EHL016 Ehlers-Danlos Syndrome Type 5 11 0.034
805
BNM007 Bone Marrow Failure, Telomere-Related, 1 7 0.034
806
P ALZ001 Alzheimer's Disease 93 0.031
807
P LFR001 Li-Fraumeni Syndrome 75 0.031
808
c NNN003 Noonan Syndrome 73 0.031
809
P GCH001 Gaucher's Disease 73 0.031
810
MYL040 Myelodysplastic Syndromes 72 0.031
811
BRK003 Burkitt's Lymphoma 71 0.031
812
P WGN002 Wegener's Granulomatosis 67 0.031
813
PRT014 Protein S Deficiency 67 0.031
814
P BRD002 Bardet-Biedl Syndrome 67 0.031
815
P TMP003 Temporal Arteritis 64 0.031
816
c ESS002 Essential Hypertension 64 0.031
817
c HMP007 Hemophilia 64 0.031
818
PRC016 Pre-Eclampsia 64 0.031
819
ABT001 Abetalipoproteinemia 64 0.031
820
c PRM002 Primary Hyperoxaluria 63 0.031
821
P GRV001 Graves' Disease 63 0.031
822
ACT073 Acute Leukemia 62 0.031
823
ATM004 Autoimmune Thrombocytopenic Purpura 62 0.031
824
c SPN046 Spinal Muscular Atrophy 60 0.031
825
c ESS003 Essential Thrombocythemia 60 0.031
826
P CLF002 Cleft Palate 60 0.031
827
SPT014 Septo-Optic Dysplasia 59 0.031
828
GNT003 Genital Herpes 59 0.031
829
SCK005 Sickle Cell Disease 58 0.031
830
HYP014 Hyperuricemia 58 0.031
831
SHW002 Shwachman-Diamond Syndrome 58 0.031
832
ZLL002 Zollinger-Ellison Syndrome 58 0.031
833
P PRD008 Periodontitis 58 0.031
834
MLT001 Multiple Chemical Sensitivity 58 0.031
835
TNS005 Tonsillitis 57 0.031
836
P DRM007 Dermatitis Herpetiformis 57 0.031
837
SLP006 Sleep Apnea 57 0.031
838
P MMB002 Membranous Glomerulonephritis 56 0.031
839
GNG013 Gingivitis 56 0.031
840
c ATM011 Autoimmune Hepatitis 56 0.031
841
CLS007 Classic Kaposi Sarcoma 56 0.031
842
P ANP001 Anaplastic Large Cell Lymphoma 56 0.031
843
PPT003 Peptic Ulcer 55 0.031
844
SCR008 Scrub Typhus 55 0.031
845
ANT011 Antisocial Personality Disorder 55 0.031
846
HYP037 Hyperhomocysteinemia 55 0.031
847
P PNC001 Pancytopenia 55 0.031
848
URM002 Uremia 54 0.031
849
FBR003 Fibrous Histiocytoma 54 0.031
850
CRY003 Cryptosporidiosis 54 0.031
851
AVN001 Avian Influenza 54 0.031
852
NRP001 Neuropathy 54 0.031
853
ACT017 Acute Chest Syndrome 53 0.031
854
RNL003 Renal Clear Cell Carcinoma 53 0.031
855
CLL003 Cellulitis 53 0.031
856
LPD010 Lipodystrophy 53 0.031
857
ANR004 Anuria 53 0.031
858
RTN023 Retinitis 53 0.031
859
HRY003 Hairy Cell Leukemia 53 0.031
860
CTS003 Coats Disease 53 0.031
861
SHR001 Short Bowel Syndrome 53 0.031
862
NPH010 Nephrosclerosis 53 0.031
863
SPN020 Spondylosis 53 0.031
864
ARM001 Aromatase Deficiency 53 0.031
865
RTN003 Retinal Ischemia 52 0.031
866
ALV002 Alveolar Echinococcosis 52 0.031
867
STT002 Status Asthmaticus 52 0.031
868
PRP007 Priapism 52 0.031
869
LFT009 Left Ventricular Outflow Tract Obstruction 52 0.031
870
P CYS010 Cystinosis 51 0.031
871
CRD001 Cardiac Tamponade 51 0.031
872
KLB001 Klebsiella 51 0.031
873
P CHR466 Chronic Thromboembolic Pulmonary Hypertension 51 0.031
874
P SCL015 Scleritis 50 0.031
875
OBS001 Obstructive Jaundice 50 0.031
876
RNL011 Renal Osteodystrophy 50 0.031
877
BCL002 B Cell Deficiency 50 0.031
878
FSC002 Fascioliasis 50 0.031
879
c MCK006 Meckel Syndrome 50 0.031
880
PLM010 Pulmonary Edema 50 0.031
881
MLT016 Multicentric Reticulohistiocytosis 50 0.031
882
c CNG018 Congenital Heart Block 50 0.031
883
LYM052 Lymphomatoid Papulosis 50 0.031
884
LYM026 Lymphoblastic Leukemia 49 0.031
885
BLD034 Bile Duct Carcinoma 49 0.031
886
MYX004 Myxedema 49 0.031
887
SYS003 Systolic Heart Failure 48 0.031
888
c OST019 Osteosclerosis 48 0.031
889
CNV002 Conversion Disorder 48 0.031
890
c LFT003 Left Ventricular Noncompaction 48 0.031
891
c RTN014 Retinal Artery Occlusion 47 0.031
892
P ESN008 Eosinophilic Pneumonia 47 0.031
893
EXF001 Exfoliation Syndrome 47 0.031
894
PST087 Posterior Urethral Valve 47 0.031
895
PNC053 Pancreatic Islet Cell Tumors 47 0.031
896
PRT070 Peritoneal Carcinoma 47 0.031
897
ANG011 Angiodysplasia 47 0.031
898
INF023 Inflammatory Breast Carcinoma 47 0.031
899
c PSD003 Pseudohypoaldosteronism 46 0.031
900
MMM001 Mammary Paget's Disease 46 0.031
901
NDL007 Nodular Goiter 46 0.031
902
SRC002 Sarcomatoid Renal Cell Carcinoma 46 0.031
903
MYC012 Mycetoma 46 0.031
904
NPH004 Nephropathia Epidemica 45 0.031
905
FRZ001 Frozen Shoulder 45 0.031
906
SYM002 Sympathetic Ophthalmia 45 0.031
907
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 45 0.031
908
EHL034 Ehlers-Danlos Syndrome, Hypermobility Type 44 0.031
909
P PRK001 Porokeratosis 44 0.031
910
PLM018 Pulmonary Sclerosing Hemangioma 44 0.031
911
GST029 Gastric Cardia Adenocarcinoma 44 0.031
912
IRN002 Iron Metabolism Disease 44 0.031
913
INT191 Intestinal Lymphangiectasia 43 0.031
914
HPT032 Hepatocellular Carcinoma, Somatic 43 0.031
915
c INT064 Intermediate Uveitis 43 0.031
916
PRN049 Paraneoplastic Pemphigus 43 0.031
917
ACT040 Acute Poststreptococcal Glomerulonephritis 43 0.031
918
ANG002 Angiostrongyliasis 42 0.031
919
CRB138 Core Binding Factor Acute Myeloid Leukemia 42 0.031
920
LYM014 Lymphangitis 42 0.031
921
PRL011 Proliferative Vitreoretinopathy 42 0.031
922
P HYP231 Hypothalamic Hamartomas 42 0.031
923
WRT003 Warthin Tumor 42 0.031
924
P LSS005 Lissencephaly 1 42 0.031
925
PLP001 Pulpitis 41 0.031
926
P CRV039 Cervicitis 41 0.031
927
DNR001 Duane Retraction Syndrome 41 0.031
928
PPL006 Papillon-Lefevre Disease 41 0.031
929
c WRD015 Waardenburg Syndrome Type Iva 41 0.031
930
LYM043 Lymphocytic Hypophysitis 41 0.031
931
BNG016 Benign Migratory Glossitis 40 0.031
932
ACT055 Actinomycosis 40 0.031
933
CHL039 Choledocholithiasis 40 0.031
934
HRS011 Horseshoe Kidney 39 0.031
935
OST032 Osteofibrous Dysplasia 39 0.031
936
STC004 Stachybotrys Chartarum 39 0.031
937
PNC033 Pancreas Adenocarcinoma 39 0.031
938
CHR370 Chronic Granulomatous Disease, Autosomal, Due to Deficiency of Cyba 38 0.031
939
BRN038 Bronchial Disease 38 0.031
940
P HYP058 Hypervitaminosis a 38 0.031
941
BLD101 Bladder Cancer Susceptibility 38 0.031
942
HLM001 Helminthiasis 37 0.031
943
CRD016 Cardiac Rupture 37 0.031
944
P SCL025 Scleromyxedema 37 0.031
945
EXT006 Extrahepatic Cholestasis 37 0.031
946
HYD028 Hydrops, Ectopic Calcification, Moth-Eaten Skeletal Dysplasia 37 0.031
947
CNJ007 Conjunctivochalasis 36 0.031
948
HTL002 Htlv-1 Associated Myelopathy 36 0.031
949
c NMN004 Niemann-Pick Disease Type C1 36 0.031
950
SCR003 Secretory Diarrhea 36 0.031
951
c SVR056 Severe Hemophilia a 35 0.031
952
BLD054 Blood Protein Disease 35 0.031
953
EMN001 Emanuel Syndrome 34 0.031
954
PTY004 Pityriasis Lichenoides 34 0.031
955
XRP001 Xerophthalmia 34 0.031
956
EHL010 Ehlers-Danlos Syndrome Arthrochalasia Type 33 0.031
957
CHR415 Chronic Venous Leg Ulcers 33 0.031
958
CRR001 Carrion's Disease 32 0.031
959
OVR054 Ovarian Mucinous Neoplasm 32 0.031
960
URT036 Urethral Obstruction 31 0.031
961
GRN003 Granulomatous Dermatitis 31 0.031
962
NRT005 North Carolina Macular Dystrophy 31 0.031
963
SLL001 Sialolithiasis 30 0.031
964
HYP034 Hypertensive Encephalopathy 30 0.031
965
PNC028 Pancreatic Steatorrhea 29 0.031
966
EHL012 Ehlers-Danlos Syndrome Dermatosparaxis Type 29 0.031
967
MNT053 Mental Retardation, Stereotypic Movements, Epilepsy, and/or Cerebral Malformations 29 0.031
968
TXC001 Toxic Megacolon 28 0.031
969
ACT022 Acute Retinal Necrosis Syndrome 28 0.031
970
PTL001 Patulous Eustachian Tube 28 0.031
971
END048 Endotoxin Hyporesponsiveness 28 0.031
972
PLM007 Pulmonary Aspergilloma 28 0.031
973
c PDT025 Pediatric Multiple Sclerosis 27 0.031
974
c CHR036 Chronic Cholangitis 27 0.031
975
NNT039 Neonatal Marfan Syndrome 27 0.031
976
SML020 Small Patella Syndrome 26 0.031
977
PNC002 Pancreatic Mucinous Cystadenoma 26 0.031
978
YCH001 Y Chromosome Infertility 25 0.031
979
CL1004 Col1a1/2-Related Osteogenesis Imperfecta 25 0.031
980
CSC001 Cascade Stomach 24 0.031
981
INT011 Interstitial Emphysema 24 0.031
982
c CNG372 Congenital Generalized Lipodystrophy Type 3 24 0.031
983
GNT018 Gianotti Crosti Syndrome 23 0.031
984
c BRN078 Bronchiectasis with or Without Elevated Sweat Chloride 1, Modifier of 23 0.031
985
STR015 Stereotypic Movement Disorder 22 0.031
986
P HYP078 Hypertrophy of Breast 20 0.031
987
BLD063 Bile Duct Cysts 20 0.031
988
ISL074 Isolated Pierre Robin Sequence 20 0.031
989
BDN001 Bednar's Tumor 20 0.031
990
HRL001 Harlequin Type Ichthyosis 20 0.031
991
PRT015 Partial Third-Nerve Palsy 19 0.031
992
TMP006 Temporomandibular Ankylosis 19 0.031
993
NNT025 Neonatal Systemic Lupus Erythematosus 19 0.031
994
ANG022 Angel Shaped Phalangoepiphyseal Dysplasia 18 0.031
995
PLM108 Pulmonary Interstitial Glycogenosis 18 0.031
996
EPT021 Epithelial Recurrent Erosion Dystrophy 17 0.031
997
CFT001 Cftr-Related Disorders 17 0.031
998
THY020 Thyroid Hyalinizing Trabecular Adenoma 16 0.031
999
EHL008 Ehlers–danlos Syndrome, Vascular Type 15 0.031
1000
ABD007 Abdominal Cystic Lymphangioma 13 0.031
1001
c 9P1001 9p13 Microdeletion Syndrome 13 0.031
1002
c 5Q3002 5q31.3 Microdeletion Syndrome 13 0.031
1003
PTT043 Pituitary Hormone Deficiency, Combined, 6 13 0.031
1004
c EHL019 Ehlers-Danlos Syndrome Type Via 12 0.031
1005
SPS082 Spastic Paraplegia - Epilepsy - Intellectual Deficit 12 0.031
1006
c FML136 Familial Mediterranean Fever Type 1 11 0.031
1007
PLM051 Pulmonary Arterio-Veinous Fistula 8 0.031
1008
LBR003 Labrador Lung 7 0.031
1009
APL001 Aplastic Anemia 77 0.027
1010
P RTT002 Rett Syndrome 75 0.027
1011
P MLT020 Multiple Sclerosis 75 0.027
1012
FBR012 Fabry Disease 74 0.027
1013
KPS001 Kaposi's Sarcoma 73 0.027
1014
P NMN002 Niemann-Pick Disease 72 0.027
1015
PRP027 Peripheral Vascular Disease 71 0.027
1016
P CLC005 Celiac Disease 71 0.027
1017
P MCP002 Mucopolysaccharidosis I 70 0.027
1018
P CHR089 Chronic Kidney Failure 68 0.027
1019
BHC002 Behcet's Disease 68 0.027
1020
P PRP003 Porphyria Cutanea Tarda 68 0.027
1021
GLN003 Glanzmann's Thrombasthenia 68 0.027
1022
DBT001 Diabetic Ketoacidosis 67 0.027
1023
SCK003 Sickle Cell Anemia 67 0.027
1024
P PRM005 Primary Hyperparathyroidism 66 0.027
1025
HYP056 Hypoglycemia 66 0.027
1026
P FRD001 Friedreich Ataxia 64 0.027
1027
PRL009 Prolactinoma 64 0.027
1028
P FCL005 Focal Segmental Glomerulosclerosis 64 0.027
1029
SPN186 Spinal Cord Injury 63 0.027
1030
ISC006 Ischemic Heart Disease 62 0.027
1031
PSY004 Psychotic Disorder 62 0.027
1032
P HLP001 Holoprosencephaly 61 0.027
1033
MYS005 Myositis 61 0.027
1034
VLV011 Vulvovaginal Candidiasis 61 0.027
1035
P HMC002 Homocystinuria 61 0.027
1036
LMY002 Leiomyoma 61 0.027
1037
PLY041 Polymyositis 61 0.027
1038
THR016 Thrombophlebitis 61 0.027
1039
P HST010 Histiocytosis 61 0.027
1040
P END044 Endometriosis 61 0.027
1041
BRN106 Burns 61 0.027
1042
MRB003 Morbid Obesity 60 0.027
1043
PPL002 Papillary Carcinoma 60 0.027
1044
P HYD006 Hydrocephalus 60 0.027
1045
ACT010 Acth-Secreting Pituitary Adenoma 60 0.027
1046
PLM033 Pulmonary Embolism 60 0.027
1047
TYP007 Typhoid Fever 60 0.027
1048
c ACT075 Acute Myocardial Infarction 59 0.027
1049
ANR002 Aniridia 59 0.027
1050
VTL002 Vitiligo 59 0.027
1051
SPT004 Septic Arthritis 59 0.027
1052
HPT002 Hepatic Vein Thrombosis 59 0.027
1053
P AGM001 Agammaglobulinemia 58 0.027
1054
PSD007 Pseudomyxoma Peritonei 58 0.027
1055
P CMP010 Complex Regional Pain Syndrome 57 0.027
1056
CRB042 Cerebellar Ataxia 57 0.027
1057
c HYP069 Hyperparathyroidism 57 0.027
1058
P DBT005 Diabetes Insipidus 56 0.027
1059
CMP002 Campylobacteriosis 56 0.027
1060
OST011 Osteomalacia 56 0.027
1061
ASP003 Aseptic Meningitis 56 0.027
1062
HPT022 Hepatoblastoma 56 0.027
1063
PLS006 Plasmodium Vivax Malaria 56 0.027
1064
ERY003 Erythema Multiforme 56 0.027
1065
CHL014 Cholera 56 0.027
1066
P MTB001 Metabolic Syndrome X 56 0.027
1067
P QFV001 Q Fever 56 0.027
1068
P SHR029 Short Syndrome 55 0.027
1069
HPR003 Heparin-Induced Thrombocytopenia 55 0.027
1070
ALL009 Allergic Conjunctivitis 55 0.027
1071
MCK007 Muckle-Wells Syndrome 55 0.027
1072
ALP007 Alpha 1-Antitrypsin Deficiency 54 0.027
1073
ACN011 Acne 54 0.027
1074
P LPS002 Liposarcoma 54 0.027
1075
PRV004 Periventricular Leukomalacia 54 0.027
1076
P LNG044 Long Qt Syndrome 1 53 0.027
1077
CHR282 Chronic Infantile Neurological Cutaneous Articular Syndrome 53 0.027
1078
ACR008 Acrocallosal Syndrome 53 0.027
1079
PRD007 Periodontal Disease 53 0.027
1080
P RTN022 Retinal Vein Occlusion 53 0.027
1081
P ISC002 Ischemic Optic Neuropathy 52 0.027
1082
CHR005 Chorioamnionitis 52 0.027
1083
P MMB001 Membranoproliferative Glomerulonephritis 52 0.027
1084
ALL010 Allergic Contact Dermatitis 52 0.027
1085
P ATN005 Autonomic Dysfunction 52 0.027
1086
CHR074 Choriocarcinoma 52 0.027
1087
KRT006 Keratoconjunctivitis 52 0.027
1088
CYT005 Cytomegalovirus Retinitis 52 0.027
1089
P CNG015 Congenital Diaphragmatic Hernia 52 0.027
1090
ALC009 Alcoholic Liver Cirrhosis 52 0.027
1091
BCT015 Bacteremia 52 0.027
1092
PSR002 Psoriasis 51 0.027
1093
ARC002 Arachnoiditis 51 0.027
1094
LPM004 Lipoma 51 0.027
1095
IDP064 Idiopathic Neutropenia 51 0.027
1096
c ATM019 Autoimmune Polyendocrine Syndrome 51 0.027
1097
PRS047 Prostatitis 50 0.027
1098
LPC002 Lip Cancer 50 0.027
1099
INT054 Intraocular Lymphoma 50 0.027
1100
c WLM002 Wilms Tumor 50 0.027
1101
c CNT016 Central Retinal Vein Occlusion 50 0.027
1102
RFR010 Refractory Anemia 50 0.027
1103
AMY053 Amyloidosis, Secondary 50 0.027
1104
SPN035 Spindle Cell Sarcoma 50 0.027
1105
CRT016 Carotid Artery Disease 49 0.027
1106
HST009 Histiocytoma 49 0.027
1107
P PRM100 Primary Spontaneous Pneumothorax 49 0.027
1108
P LYM025 Lymphedema 49 0.027
1109
CYS002 Cystic Lymphangioma 49 0.027
1110
P GLC007 Glaucoma 49 0.027
1111
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 48 0.027
1112
c CTR002 Cataract 48 0.027
1113
CRB086 Cerebral Aneurysms 48 0.027
1114
TCL002 T-Cell Large Granular Lymphocyte Leukemia 48 0.027
1115
CRN024 Corneal Disease 48 0.027
1116
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 48 0.027
1117
NRR001 Neuroretinitis 48 0.027
1118
HRD004 Hereditary Breast Ovarian Cancer 48 0.027
1119
P END047 Endophthalmitis 48 0.027
1120
HMG005 Hemoglobinopathy 47 0.027
1121
MCN007 Meconium Aspiration Syndrome 47 0.027
1122
INF058 Inflammatory Myofibroblastic Tumor 47 0.027
1123
KRT008 Keratopathy 47 0.027
1124
LCH009 Lichen Sclerosus 47 0.027
1125
c KBK001 Kabuki Syndrome 47 0.027
1126
VLL003 Villonodular Synovitis 47 0.027
1127
TRN007 Transsexualism 47 0.027
1128
VSM001 Vasomotor Rhinitis 46 0.027
1129
DNT012 Dental Caries 46 0.027
1130
PRP023 Peripheral Neuropathy 46 0.027
1131
SCN036 Secondary Progressive Multiple Sclerosis 46 0.027
1132
LGN001 Legionnaires' Disease 46 0.027
1133
DBT006 Diabetic Macular Edema 46 0.027
1134
TLN003 Telangiectasis 46 0.027
1135
NPH017 Nephrosis 45 0.027
1136
PLY020 Polyradiculoneuropathy 45 0.027
1137
TND004 Tendinopathy 45 0.027
1138
LPM005 Lipomatosis 45 0.027
1139
c ACQ014 Acquired Hemophilia 45 0.027
1140
ART006 Arthus Reaction 45 0.027
1141
PRT038 Protein-Energy Malnutrition 45 0.027
1142
INF034 Infective Endocarditis 44 0.027
1143
CLN019 Colonic Disease 44 0.027
1144
EXT033 Extrapulmonary Tuberculosis 44 0.027
1145
PYL006 Pyloric Stenosis 44 0.027
1146
MCN008 Mucinous Cystadenocarcinoma 44 0.027
1147
ALC010 Alcoholic Cardiomyopathy 44 0.027
1148
HST016 Histiocytic Sarcoma 43 0.027
1149
NNS005 Non-Small Cell Lung Carcinoma 43 0.027
1150
DYS073 Dysphagia 42 0.027
1151
HRT012 Heart Valve Disease 42 0.027
1152
NNT012 Neonatal Jaundice 42 0.027
1153
c LNG063 Lung Cancer Susceptibility 42 0.027
1154
BRN014 Bronchopneumonia 42 0.027
1155
PRP002 Periapical Granuloma 42 0.027
1156
c MYT011 Myotonia 41 0.027
1157
NNT019 Neonatal Hypothyroidism 41 0.027
1158
CMP009 Complement Deficiency 41 0.027
1159
c MLG086 Malignant Hyperthermia Susceptibility 41 0.027
1160
DFF016 Diffuse Astrocytoma 41 0.027
1161
c HYP057 Hypervitaminosis D 41 0.027
1162
MNN014 Mononeuritis 40 0.027
1163
INT052 Intestinal Volvulus 40 0.027
1164
CRP018 Cor Pulmonale 40 0.027
1165
ATX019 Ataxia with Vitamin E Deficiency 40 0.027
1166
PRX015 Paroxysmal Extreme Pain Disorder 39 0.027
1167
GST039 Gastroduodenitis 39 0.027
1168
SKL007 Skeletal Muscle Regeneration 39 0.027
1169
MCR020 Microsporidiosis 39 0.027
1170
MRS001 Marasmus 39 0.027
1171
HTS001 Hiatus Hernia 39 0.027
1172
SGN002 Signet Ring Cell Adenocarcinoma 38 0.027
1173
ODN005 Odontogenic Myxoma 38 0.027
1174
PLR007 Pleural Empyema 37 0.027
1175
c CHR098 Chronic Pyelonephritis 37 0.027
1176
VLV042 Vulvar Vestibulitis Syndrome 37 0.027
1177
ACL001 Acalculous Cholecystitis 37 0.027
1178
FNS001 Funisitis 37 0.027
1179
c ACQ022 Acquired Generalized Lipodystrophy 36 0.027
1180
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 36 0.027
1181
PST062 Pustulosis Palmaris Et Plantaris 36 0.027
1182
SML032 Small Bowel Adenocarcinoma 36 0.027
1183
RTC003 Root Caries 35 0.027
1184
SRF006 Surfactant Dysfunction 34 0.027
1185
TND006 Tendinosis 34 0.027
1186
INT079 Intrahepatic Cholangiocarcinoma 34 0.027
1187
LPG001 Lipogranulomatosis 34 0.027
1188
P INF131 Infant Acute Respiratory Distress Syndrome 33 0.027
1189
MTR001 Mature Cataract 32 0.027
1190
c PLY084 Polycystic Kidney Disease, Type 2 31 0.027
1191
GRD005 Geroderma Osteodysplasticum 31 0.027
1192
MTC028 Mitochondrial Cardiomyopathy 31 0.027
1193
CLT002 Cluttering 31 0.027
1194
DDN007 Duodenal Disease 31 0.027
1195
DFF031 Diffuse Alveolar Hemorrhage 30 0.027
1196
ELS002 Elastosis Perforans Serpiginosa 29 0.027
1197
15Q001 15q13.3 Microdeletion 29 0.027
1198
CRY006 Cryofibrinogenemia 29 0.027
1199
NMN003 Niemann–pick Disease 29 0.027
1200
ANT018 Anthracosis 28 0.027
1201
JVN024 Juvenile Hereditary Hemochromatosis 28 0.027
1202
TYP024 Type Ii Mixed Cryoglobulinemia 28 0.027
1203
c DYS039 Dyskeratosis Congenita Autosomal Dominant 28 0.027
1204
PTT021 Pituitary Hormone Deficiency, Combined 2 28 0.027
1205
c DPH016 Diaphragmatic Hernia 3 27 0.027
1206
NNH002 Non-a-E Hepatitis 27