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

2005 hits were found for 'fibrosis'

# Family MCID Name MIFTS Score
1
CYS001 Cystic Fibrosis 103 7.119
2
IDP003 Idiopathic Pulmonary Fibrosis 69 5.822
3
P PLM036 Pulmonary Fibrosis 66 5.395
4
ORL004 Oral Submucous Fibrosis 57 4.978
5
c CNG047 Congenital Fibrosis of the Extraocular Muscles 27 4.361
6
END021 Endomyocardial Fibrosis 42 4.123
7
CNG048 Congenital Hepatic Fibrosis 53 3.944
8
RTR011 Retroperitoneal Fibrosis 31 3.609
9
P CNG142 Congenital Fibrosis of the Extraocular Muscles 2 32 3.323
10
FBR028 Fibrosing Mediastinitis 18 2.992
11
c CNG144 Congenital Fibrosis of the Extraocular Muscles 3b 11 2.992
12
c CNG145 Congenital Fibrosis of the Extraocular Muscles 3c 5 2.992
13
CCH002 Coach Syndrome 48 2.719
14
PST015 Postinflammatory Pulmonary Fibrosis 6 2.691
15
c CNG143 Congenital Fibrosis of the Extraocular Muscles 3a 14 2.684
16
LBN002 Lubani Al Saleh Teebi Syndrome 15 2.676
17
DFF002 Diffuse Pulmonary Fibrosis 19 2.495
18
c PLM044 Pulmonary Fibrosis, Familial 27 2.449
19
NPH018 Nephrogenic Systemic Fibrosis 44 2.435
20
MCN015 Meconium Ileus in Cystic Fibrosis 11 2.419
21
c LCL003 Localized Pulmonary Fibrosis 8 2.364
22
PRR004 Preretinal Fibrosis 14 2.347
23
HPT065 Hepatic Fibrosis - Renal Cysts - Intellectual Deficit 16 2.326
24
MSC030 Muscular Fibrosis Multifocal Obstructed Vessels 10 2.326
25
LNG082 Lung Fibrosis - Immunodeficiency - 46,xx Gonadal Dysgenesis 11 2.318
26
c CNG146 Congenital Fibrosis of the Extraocular Muscles 4 2 2.318
27
P HRM005 Hermansky-Pudlak Syndrome 1 51 1.994
28
P MYL005 Myelofibrosis 75 1.971
29
ACT029 Acute Interstitial Pneumonia 32 1.967
30
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 15 1.932
31
c HRM009 Hermansky-Pudlak Syndrome 6 34 1.926
32
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 7 1.919
33
PSD089 Pseudomonas Aeruginosa Chronic Infection by, in Cystic Fibrosis 15 1.911
34
MLT036 Multifocal Fibrosclerosis 13 1.911
35
TRP020 Tropical Endomyocardial Fibrosis 8 1.911
36
ARW003 Airway-Centered Interstitial Fibrosis 1 1.911
37
c NTR031 Neutropenia, Severe Congenital, 5, Autosomal Recessive 18 1.903
38
HPT029 Hepatic Fibrosis Renal Cysts Mental Retardation 2 1.903
39
FML074 Familial Interstitial Fibrosis 1 1.903
40
IDP016 Idiopathic Diffuse Interstitial Fibrosis 0 1.903
41
EF001 Eaf 18 1.893
42
c KF2001 Kif21a-Related Congenital Fibrosis of the Extraocular Muscles 16 1.893
43
CYS027 Cystic Fibrosis Lung Disease, Modifier of 14 1.893
44
PLM126 Pulmonary Fibrosis, Telomere-Related, 1 9 1.893
45
PLM106 Pulmonary Fibrosis - Hepatic Hyperplasia - Bone Marrow Hypoplasia 7 1.893
46
c PHX001 Phox2a-Related Congenital Fibrosis of the Extraocular Muscles 4 1.893
47
c SFT006 Sftpc-Related Familial Pulmonary Fibrosis 4 1.893
48
c TBB003 Tubb3-Related Congenital Fibrosis of the Extraocular Muscles 4 1.893
49
c TRT009 Tert-Related Familial Pulmonary Fibrosis 4 1.893
50
FLL043 Follicular Hamartoma - Alopecia - Cystic Fibrosis 3 1.893
51
HPT035 Hepatic Fibrosis Susceptibility Due to Schistosoma Mansoni Infection 3 1.893
52
NNC004 Non-Classic Cystic Fibrosis-Like Syndrome 3 1.893
53
c TRC066 Terc-Related Familial Pulmonary Fibrosis 3 1.893
54
c CNG140 Congenital Fibrosis of the Extraocular Muscles 1a 1 1.893
55
c CNG141 Congenital Fibrosis of the Extraocular Muscles 1b 1 1.893
56
IDP011 Idiopathic Interstitial Pneumonia 53 1.560
57
MCN017 Meconium Ileus 37 1.556
58
ASB001 Asbestosis 52 1.460
59
P MBS002 Moebius Syndrome 42 1.446
60
SLC006 Silicosis 58 1.434
61
HPT012 Hepatocellular Fibrolamellar Carcinoma 24 1.351
62
c NPH053 Nephronophthisis 11 18 1.338
63
SCR009 Scirrhous Adenocarcinoma 17 1.338
64
RZN001 Rozin Hertz Goodman Syndrome 16 1.338
65
DBT022 Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism 15 1.338
66
SCL027 Sclerotylosis 12 1.338
67
FBR016 Fibrosclerosis of Breast 11 1.338
68
TYL001 Taylor's Syndrome 10 1.338
69
TKL001 Tukel Syndrome 7 1.338
70
GRP001 Graphite Pneumoconiosis 6 1.338
71
c HPT021 Hepatitis 75 0.445
72
P HPT001 Hepatitis C 66 0.252
73
c PNC044 Pancreatitis 67 0.227
74
c HPT003 Hepatitis a 60 0.212
75
P LVR013 Liver Disease 70 0.188
76
BRN022 Bronchiectasis 64 0.184
77
END072 Endotheliitis 47 0.184
78
P HYP075 Hypertension 86 0.182
79
ASP006 Aspergillosis 73 0.164
80
ALL008 Allergic Bronchopulmonary Aspergillosis 64 0.164
81
URT010 Ureteral Obstruction 49 0.162
82
P PNM007 Pneumonia 79 0.156
83
IDP042 Idiopathic Recurrent Stupor 15 0.147
84
c HPT016 Hepatitis B 65 0.144
85
ANK002 Ankylosing Spondylitis 75 0.139
86
c KDN018 Kidney Disease 58 0.126
87
P SRC025 Sarcoidosis 1 32 0.124
88
P IDP049 Idiopathic Anterior Uveitis 30 0.122
89
c XP2001 Xp22.3 Microdeletion Syndrome 21 0.122
90
BRN056 Bronchopulmonary Dysplasia 47 0.121
91
IDP044 Idiopathic Pulmonary Alveolar Proteinosis 44 0.121
92
c SCL016 Scleroderma 59 0.114
93
THR013 Thoracic Outlet Syndrome 54 0.114
94
CRV045 Cervical Intraepithelial Neoplasia 36 0.114
95
ICH002 Ichthyosis Bullosa of Siemens 50 0.111
96
P LNG032 Lung Cancer 74 0.108
97
FTT001 Fatty Liver Disease 61 0.108
98
TFT003 Tufting Enteropathy 21 0.107
99
c RNG028 Ring Chromosome Y 14 0.107
100
c SRC013 Sarcoidosis 69 0.106
101
BRN101 Bronchiolitis Obliterans with Obstructive Pulmonary Disease 13 0.104
102
P PLY014 Polycystic Kidney Disease 67 0.102
103
PLM034 Pulmonary Emphysema 60 0.102
104
CRK001 Cork-Handlers' Disease 32 0.101
105
P PRT013 Portal Hypertension 67 0.100
106
P CRN074 Coronary Artery Aneurysm 34 0.100
107
LVR012 Liver Cirrhosis 75 0.099
108
BLR001 Biliary Atresia 67 0.099
109
c VRL010 Viral Hepatitis 61 0.099
110
EHL036 Ehlers-Danlos/osteogenesis Imperfecta Syndrome 32 0.099
111
PLM015 Pulmonary Systemic Sclerosis 18 0.099
112
PLM012 Pulmonary Sarcoidosis 55 0.097
113
P AST005 Asthma 88 0.096
114
SCH014 Schistosomiasis 72 0.096
115
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 43 0.096
116
TBR011 Tuberculous Meningitis 40 0.096
117
OCL020 Ocular Cicatricial Pemphigoid 37 0.096
118
c PRT070 Peritoneal Carcinoma 37 0.096
119
HPT023 Hepatocellular Carcinoma 89 0.095
120
P CHL066 Cholangitis 57 0.095
121
NNS002 Nonspecific Interstitial Pneumonia 55 0.095
122
BLT018 Bilateral Renal Dysplasia 13 0.093
123
c THY032 Thyroiditis 67 0.092
124
SPS077 Sepsis 58 0.092
125
EVN001 Evans' Syndrome 54 0.092
126
CLL021 Collagenous Colitis 41 0.090
127
TYP018 Type 3 Von Willebrand Disease 23 0.089
128
P ATX002 Ataxia Telangiectasia 93 0.088
129
P PRM126 Primary Peritoneal Carcinoma 47 0.088
130
NDL013 Nodular Regenerative Hyperplasia 42 0.088
131
PCH007 Pouchitis 40 0.088
132
SRS007 Sorsby Fundus Dystrophy 38 0.088
133
PRL042 Proliferating Trichilemmal Cyst 38 0.088
134
PNS012 Paine Syndrome 35 0.088
135
FTL044 Fetal Cytomegalovirus Syndrome 28 0.088
136
IDP033 Idiopathic Edema 20 0.088
137
P STR035 Streptococcal Group a Invasive Disease 14 0.088
138
PRT036 Peritonitis 78 0.086
139
c LCL006 Localized Scleroderma 68 0.086
140
c HYP061 Hypertrophic Cardiomyopathy 61 0.086
141
SQM006 Squamous Cell Carcinoma 61 0.086
142
SDR002 Siderosis 53 0.086
143
SYN053 Syndromic Diarrhea 42 0.086
144
NNN017 Noonan/ Costello/ Leopard/ Cardiofaciocutaneous Syndrome Multi-Gene Panels 13 0.086
145
GLL008 Gilles De La Tourette Syndrome 73 0.085
146
LNG017 Lung Giant Cell Carcinoma 47 0.085
147
HNM002 Hinman Syndrome 24 0.085
148
PLM051 Pulmonary Arterio-Veinous Fistula 10 0.085
149
BRN024 Bronchitis 76 0.083
150
DSM004 Desmoid Tumor 58 0.082
151
P INF032 Infertility 56 0.082
152
EXC002 Exocrine Pancreatic Insufficiency 47 0.082
153
STR077 Streptococcal Toxic-Shock Syndrome 34 0.082
154
P RSP003 Respiratory Failure 70 0.080
155
P UVT001 Uveitis 67 0.080
156
c HRM001 Hermansky-Pudlak Syndrome 57 0.080
157
c SCL009 Sclerosing Cholangitis 49 0.080
158
CNG039 Congenital Absence of the Vas Deferens 42 0.080
159
P DLT002 Dilated Cardiomyopathy 82 0.078
160
CNG034 Congestive Heart Failure 81 0.078
161
P ART022 Arthritis 75 0.078
162
P ESN007 Eosinophilia 60 0.078
163
HYP006 Hypertensive Heart Disease 56 0.078
164
MDS022 Mediastinitis 56 0.078
165
SCN006 Secondary Syphilis 55 0.078
166
INT066 Interstitial Lung Disease 53 0.078
167
ALB002 Albinism 50 0.078
168
ENT015 Enthesitis-Related Arthritis 48 0.078
169
P SYS005 Systemic Scleroderma 69 0.077
170
EXT034 Extrinsic Allergic Alveolitis 65 0.077
171
CHL068 Cholestasis 63 0.077
172
BRN002 Bronchiolitis 61 0.077
173
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 41 0.077
174
P OBS005 Obesity 93 0.075
175
c DBT009 Diabetes Mellitus 80 0.075
176
P LKM002 Leukemia 79 0.075
177
VSC007 Vascular Disease 72 0.075
178
P PNM006 Pneumoconiosis 59 0.075
179
SPS019 Spastic Paraparesis 35 0.075
180
MYC006 Mycosis Fungoides 71 0.073
181
P ADN016 Adenocarcinoma 60 0.073
182
ALC006 Alcoholic Hepatitis 57 0.073
183
EGG001 Egg Allergy 54 0.073
184
ATP002 Atopy 38 0.073
185
P MLR006 Male Reproductive Organ Cancer 23 0.073
186
RHM009 Rheumatoid Lung Disease 23 0.073
187
GNR028 Generalized Essential Telangiectasia 16 0.073
188
NKC001 Nk-Cell Enteropathy 12 0.073
189
c MSC005 Muscular Dystrophy 62 0.072
190
BRN012 Bronchiolitis Obliterans 59 0.072
191
CNN005 Connective Tissue Disease 57 0.072
192
c INT070 Intestinal Obstruction 54 0.072
193
c OST080 Osteogenesis Imperfecta, Type Ii 51 0.072
194
THR079 Thromboembolism 50 0.072
195
ART031 Aortic Coarctation 47 0.072
196
CHL109 Childhood Apraxia of Speech 24 0.072
197
CRN131 Coronary Artery Disease, Modifier of 15 0.072
198
CRH001 Crohn's Disease 83 0.070
199
P INF038 Influenza 69 0.070
200
P GLM007 Glomerulonephritis 66 0.070
201
CRB009 Cerebritis 56 0.070
202
P DYS142 Dyskeratosis Congenita, Autosomal Recessive 4 52 0.070
203
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 33 0.070
204
P TRN034 Transverse Myelitis 27 0.070
205
P SPR035 Superior Vena Cava Syndrome 19 0.070
206
P RHM011 Rheumatoid Arthritis 91 0.068
207
ACN002 Acanthosis Nigricans 73 0.068
208
ART019 Aortic Valve Stenosis 68 0.068
209
LCH002 Lichen Planus 63 0.068
210
APH001 Aphthous Stomatitis 59 0.068
211
MYC002 Mycobacterium Avium Complex Disease 57 0.068
212
P RNL028 Renal Tubular Dysgenesis 51 0.068
213
P THR045 Thrombotic Thrombocytopenic Purpura, Congenital 43 0.068
214
ACT105 Acute Mountain Sickness 40 0.068
215
INT103 Intrauterine Infections 36 0.068
216
RDT013 Radiation Proctitis 33 0.068
217
P SRF004 Surfactant Metabolism Dysfunction, Pulmonary, 1 32 0.068
218
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.068
219
P PRM006 Primary Biliary Cirrhosis 74 0.066
220
P DDN001 Duodenal Ulcer 68 0.066
221
GST034 Gastroesophageal Reflux Disease 67 0.066
222
c NPH005 Nephronophthisis 53 0.066
223
DST006 Diastolic Heart Failure 52 0.066
224
CRS001 Crescentic Glomerulonephritis 51 0.066
225
P AVS004 Avascular Necrosis of the Femoral Head 49 0.066
226
CRY001 Cryptogenic Organizing Pneumonia 44 0.066
227
CLC008 Colchicine Resistance 26 0.066
228
P HMC003 Hemochromatosis 80 0.064
229
P HMP004 Hemophilia B 80 0.064
230
c CYS016 Cystic Kidney 56 0.064
231
DRM004 Dermatofibrosarcoma 53 0.064
232
DDF001 Dedifferentiated Liposarcoma 42 0.064
233
DFF024 Diffuse Panbronchiolitis 38 0.064
234
CLR005 Clear Cell Chondrosarcoma 36 0.064
235
c SPN183 Spontaneous Pneumothorax 31 0.064
236
PRS115 Prosthetic Joint Infection 27 0.064
237
HSL001 House Allergic Alveolitis 11 0.064
238
GST023 Gastric Ulcer 72 0.062
239
P MLN007 Male Infertility 62 0.062
240
c SBC007 Subacute Thyroiditis 58 0.062
241
P END033 Endocarditis 48 0.062
242
P HYP090 Hyperalphalipoproteinemia 47 0.062
243
GRN037 Granulomatosis with Polyangiitis 39 0.062
244
STN007 Stenotrophomonas Maltophilia 35 0.062
245
ERL004 Early Yaws 33 0.062
246
AML009 Amelogenesis Imperfecta Nephrocalcinosis 13 0.062
247
LNG024 Langerhans-Cell Histiocytosis 75 0.060
248
P ATM003 Autoimmune Thyroiditis 70 0.060
249
P ANG001 Angelman Syndrome 70 0.060
250
CCT002 Cicatricial Pemphigoid 64 0.060
251
c ACT027 Acute Pancreatitis 63 0.060
252
PRC013 Pericarditis 57 0.060
253
DRM014 Dermatofibrosarcoma Protuberans 52 0.060
254
INV001 Invasive Aspergillosis 49 0.060
255
c ACR001 Aicardi-Goutieres Syndrome 49 0.060
256
LKS001 Leukostasis 48 0.060
257
c PLY026 Polycystic Kidney Disease, Autosomal Dominant 46 0.060
258
P ATS008 Autosomal Dominant Disease 46 0.060
259
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 43 0.060
260
PNM013 Pneumococcal Meningitis 39 0.060
261
JVN033 Juvenile Nasopharyngeal Angiofibroma 39 0.060
262
P ENC008 Encephalocele 34 0.060
263
HYP114 Hypertensive Nephropathy 34 0.060
264
LWR010 Low Renin Hypertension 34 0.060
265
CYT008 Cytomegalovirus Infection 34 0.060
266
ALB014 Alobar Holoprosencephaly 32 0.060
267
BNZ002 Benzene Toxicity 26 0.060
268
NNS006 Non-Suppurative Otitis Media 26 0.060
269
SBL004 Sea-Blue Histiocytosis 17 0.060
270
VRS002 Virus-Associated Trichodysplasia Spinulosa 14 0.060
271
SKN016 Skin Disease 75 0.058
272
ATH003 Atherosclerosis 71 0.058
273
RLP001 Relapsing Polychondritis 69 0.058
274
c THL005 Thalassemia 68 0.058
275
ART016 Aortic Aneurysm 62 0.058
276
P INT068 Intestinal Disease 61 0.058
277
OBS006 Obstructive Lung Disease 57 0.058
278
P HYP117 Hypertriglyceridemia 54 0.058
279
c PRM011 Primary Ciliary Dyskinesia 53 0.058
280
FBR032 Fibromuscular Dysplasia 47 0.058
281
ESN005 Eosinophilic Gastroenteritis 47 0.058
282
EPT020 Epithelioid Hemangioendothelioma 44 0.058
283
c CHR048 Chronic Rhinitis 43 0.058
284
WRN005 Wrinkles 37 0.058
285
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 35 0.058
286
WST001 West Syndrome 64 0.055
287
GLC003 Glucose Intolerance 63 0.055
288
PRT002 Paratyphoid Fever 62 0.055
289
P ESP024 Esophagitis 60 0.055
290
STF001 Stiff-Person Syndrome 60 0.055
291
P RNV001 Renovascular Hypertension 58 0.055
292
P MYC008 Myocarditis 56 0.055
293
P CRP001 Carpal Tunnel Syndrome 55 0.055
294
CHL056 Cheilitis 54 0.055
295
c EHL021 Ehlers-Danlos Syndrome Type Viib 53 0.055
296
P JBR004 Joubert Syndrome 2 52 0.055
297
P PMP005 Pemphigus Vulgaris 47 0.055
298
CHL079 Children's Interstitial Lung Disease 46 0.055
299
P CRT033 Corticobasal Degeneration 45 0.055
300
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 44 0.055
301
ENT001 Enterocele 42 0.055
302
VLV044 Vulvar Intraepithelial Neoplasia 42 0.055
303
LFT013 Left Ventricular Noncompaction 1, with or Without Congenital Heart Defects 41 0.055
304
c TWN006 Twin Twin Transfusion Syndrome 40 0.055
305
FCL041 Focal Myositis 40 0.055
306
MCR014 Microcystic Adenoma 40 0.055
307
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 40 0.055
308
c ATS010 Autosomal Recessive Disease 39 0.055
309
P PLY027 Polycystic Kidney Disease, Autosomal Recessive 38 0.055
310
PRT082 Preterm Premature Rupture of the Membranes 38 0.055
311
SPN119 Spondylarthropathy 35 0.055
312
FCT013 Factor V Leiden Thrombophilia 35 0.055
313
c HRM011 Hermansky-Pudlak Syndrome 8 31 0.055
314
SPR034 Superior Limbic Keratoconjunctivitis 31 0.055
315
PST041 Posterior Urethral Valves 31 0.055
316
ESN020 Eosinophilic Granulomatosis with Polyangiitis 30 0.055
317
BWN003 Bowenoid Papulosis 29 0.055
318
EMP007 Emphysema Due to Aat Deficiency 28 0.055
319
c DYS055 Dystonia 10 19 0.055
320
CNG069 Congenital Cytomegalovirus 18 0.055
321
CPD002 Copd, Rate of Decline of Lung Function in 18 0.055
322
c TTL001 Total Internal Ophthalmoplegia 17 0.055
323
CYT018 Cytochrome P450 2d6 Variant 13 0.055
324
ACR022 Acardia 6 0.055
325
P PNC035 Pancreatic Cancer 95 0.053
326
WLS001 Wilson Disease 89 0.053
327
c LPS004 Lupus Erythematosus 73 0.053
328
ULC004 Ulcerative Colitis 72 0.053
329
P RHN004 Rhinitis 65 0.053
330
ACR003 Acrodermatitis Enteropathica 63 0.053
331
DDN006 Duodenitis 62 0.053
332
c OCL002 Oculocutaneous Albinism 60 0.053
333
CHR001 Churg-Strauss Syndrome 59 0.053
334
P CLL015 Collagen Disease 59 0.053
335
PNM008 Pneumothorax 55 0.053
336
PRC012 Pericardial Effusion 54 0.053
337
c JBR001 Joubert Syndrome 51 0.053
338
ACR005 Acrodermatitis 45 0.053
339
HYP026 Hypoglycemic Coma 45 0.053
340
c JBR026 Joubert Syndrome 15 43 0.053
341
BRN013 Bronchiolitis Obliterans Organizing Pneumonia 42 0.053
342
WRD002 Werdnig-Hoffmann Disease 41 0.053
343
P PNC102 Pancreatitis, Chronic 39 0.053
344
P CNG071 Congenital Disorder of Glycosylation Type 1b 35 0.053
345
TLY002 T-Lymphocytopenia 34 0.053
346
CLL005 Cellular Leiomyoma 33 0.053
347
HYP319 Hypereosinophilic Syndrome, Idiopathic, Resistant to Imatinib 31 0.053
348
c FRS006 Fraser Like Syndrome 4 0.053
349
AND002 Androgen Insensitivity Syndrome 88 0.051
350
P SYS001 Systemic Lupus Erythematosus 87 0.051
351
TBR010 Tuberculosis 84 0.051
352
P ALP006 Alpha Thalassemia 75 0.051
353
P ADL010 Adult Respiratory Distress Syndrome 71 0.051
354
DSS009 Disseminated Intravascular Coagulation 66 0.051
355
P CNG368 Congenital Adrenal Hyperplasia 66 0.051
356
ERD001 Erdheim-Chester Disease 64 0.051
357
RTN023 Retinitis 61 0.051
358
STR008 Strongyloidiasis 61 0.051
359
c AXN002 Axenfeld-Rieger Syndrome 60 0.051
360
c MLG069 Malignant Hypertension 60 0.051
361
P PLM006 Pulmonary Alveolar Proteinosis 56 0.051
362
P STR020 Strabismus 56 0.051
363
BCT002 Bacterial Vaginosis 56 0.051
364
MLT006 Multidrug-Resistant Tuberculosis 56 0.051
365
CYC004 Cyclic Hematopoiesis 52 0.051
366
P MSC003 Muscular Atrophy 52 0.051
367
MST002 Mast-Cell Leukemia 50 0.051
368
STT004 Steatorrhea 50 0.051
369
SPT013 Septic Shock 48 0.051
370
ALC005 Alcoholic Pancreatitis 47 0.051
371
PLM019 Pleomorphic Liposarcoma 45 0.051
372
P AZS001 Azoospermia 44 0.051
373
BRN105 Burn Scar 44 0.051
374
THR035 Thrombasthenia 37 0.051
375
c RSM001 Rasmussen Encephalitis 37 0.051
376
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 36 0.051
377
RHM014 Rheumatoid Vasculitis 35 0.051
378
DSQ001 Desquamative Interstitial Pneumonia 35 0.051
379
PST055 Postural Hypotension 33 0.051
380
PRN029 Parainfluenza Virus Type 3 33 0.051
381
ECT006 Ectodermal Dysplasia 32 0.051
382
P VNT028 Ventricular Septal Defect 1 31 0.051
383
MYC065 Myocardial Infarction, Decreased 30 0.051
384
ZYG002 Zygomycosis 28 0.051
385
BRG002 Berger Disease 27 0.051
386
P CRD132 Cardiac Conduction Defect 27 0.051
387
c MCK009 Meckel Syndrome Type 3 18 0.051
388
SCN044 Secondary Ciliary Dyskinesia 17 0.051
389
PLM048 Pleomorphic Malignant Fibrous Histiocytoma 17 0.051
390
PRR008 Periarteritis Nodosa 13 0.051
391
P BRS047 Breast Cancer 105 0.048
392
DCH001 Duchenne Muscular Dystrophy 78 0.048
393
LRN002 Laron Syndrome 76 0.048
394
PCK001 Pick's Disease 74 0.048
395
c THR014 Thrombocytopenia 67 0.048
396
VSC011 Vasculitis 67 0.048
397
P FNC001 Fanconi's Anemia 67 0.048
398
PMP001 Pemphigus 63 0.048
399
CRY004 Cryoglobulinemia 61 0.048
400
IRN001 Iron Deficiency Anemia 61 0.048
401
RNL015 Renal Hypertension 60 0.048
402
PRT011 Protein C Deficiency 60 0.048
403
CNT047 Contact Dermatitis 59 0.048
404
INT075 Intracranial Hypertension 59 0.048
405
P ESN001 Eosinophilic Esophagitis 58 0.048
406
SNG010 Single Median Maxillary Central Incisor 57 0.048
407
PGM001 Pigmented Villonodular Synovitis 57 0.048
408
CHR008 Choroiditis 57 0.048
409
P RPD001 Rapidly Progressive Glomerulonephritis 55 0.048
410
CVR006 Cavernous Hemangioma 54 0.048
411
NCR004 Nocardiosis 54 0.048
412
HMS001 Hemosiderosis 52 0.048
413
c PRL003 Proliferative Glomerulonephritis 52 0.048
414
WLL006 Wells Syndrome 49 0.048
415
c MLR021 Malaria, Severe 49 0.048
416
P AXN003 Axenfeld-Rieger Syndrome Type 1 49 0.048
417
PRT019 Protein-Losing Enteropathy 48 0.048
418
MYL020 Myelomeningocele 47 0.048
419
P ATX010 Ataxia Neuropathy Spectrum 44 0.048
420
LPS007 Lupus Nephritis 43 0.048
421
GRW007 Growth Hormone Deficiency 39 0.048
422
c ATX004 Ataxia 38 0.048
423
PRP034 Purpura Fulminans 38 0.048
424
USL001 Usual Interstitial Pneumonia 38 0.048
425
GBL002 Goblet Cell Carcinoid 37 0.048
426
P JVN024 Juvenile Hereditary Hemochromatosis 35 0.048
427
PPT001 Peptic Esophagitis 34 0.048
428
P INF069 Infantile Neuroaxonal Dystrophy 1 32 0.048
429
FTL021 Fetal Macrosomia 32 0.048
430
P SLP004 Salpingo-Oophoritis 31 0.048
431
AML006 Amelogenesis Imperfecta Hypoplastic Type, Ig 28 0.048
432
HYP226 Hyporeninemic Hypoaldosteronism 27 0.048
433
c HRM006 Hermansky-Pudlak Syndrome 3 25 0.048
434
MCL055 Mcleod Syndrome with or Without Chronic Granulomatous Disease 22 0.048
435
c BNG076 Benign Exophthalmos Syndrome 21 0.048
436
AND005 Androgen Insensitivity Syndrome, Mild 18 0.048
437
P PRM021 Primary Pulmonary Hypertension 82 0.045
438
TTR001 Tetralogy of Fallot 76 0.045
439
CHL065 Cholangiocarcinoma 73 0.045
440
P MLR004 Malaria 73 0.045
441
P ABD003 Abdominal Aortic Aneurysm 71 0.045
442
P TRC032 Turcot Syndrome 70 0.045
443
P DRM010 Dermatomyositis 70 0.045
444
ADL030 Adult-Onset Still's Disease 68 0.045
445
PMS001 Poems Syndrome 67 0.045
446
P GRF002 Graft Versus Host Disease 65 0.045
447
BRN106 Burns 64 0.045
448
ISC004 Ischemia 64 0.045
449
ALL006 Allergic Asthma 60 0.045
450
P NPH009 Nephrolithiasis 59 0.045
451
P SYN007 Synovitis 59 0.045
452
CHL069 Cholesteatoma 58 0.045
453
APP008 Appendicitis 57 0.045
454
PLY013 Polymyalgia Rheumatica 56 0.045
455
NTR003 Natural Killer Cell Leukemia 56 0.045
456
P BRN009 Burning Mouth Syndrome 56 0.045
457
NRM005 Neuromuscular Disease 55 0.045
458
P THR090 Thrombocythemia 1 54 0.045
459
P GND004 Gonadal Dysgenesis 52 0.045
460
P CRV039 Cervicitis 52 0.045
461
CRD003 Cardiac Sarcoidosis 49 0.045
462
PLY012 Polyhydramnios 49 0.045
463
P INS005 Insulin Resistance 48 0.045
464
c CPL003 Capillary Leak Syndrome 47 0.045
465
c RST002 Restrictive Cardiomyopathy 47 0.045
466
INT146 Intervertebral Disc Disease 47 0.045
467
CHL052 Choledochal Cyst 46 0.045
468
P MCK022 Meckel Syndrome 1 46 0.045
469
XLN005 X-Linked Hyper Igm Syndrome 45 0.045
470
BGS001 Bagassosis 45 0.045
471
CNS002 Constrictive Pericarditis 43 0.045
472
VND002 Van Der Woude Syndrome 43 0.045
473
FML089 Familial Thoracic Aortic Aneurysm and Dissection 43 0.045
474
OST006 Osteoblastoma 41 0.045
475
BST001 Bestrophinopathy 40 0.045
476
P ORT004 Orthostatic Intolerance 39 0.045
477
c CMP058 Complex Regional Pain Syndrome Type 1 38 0.045
478
SPL018 Splenomegaly 37 0.045
479
SMT019 Somatostatin Analog 37 0.045
480
STP004 Staphylococcal Toxic Shock Syndrome 34 0.045
481
DXR001 Doxorubicin Induced Cardiomyopathy 32 0.045
482
c ICH041 Ichthyosis, Autosomal Recessive 4b 31 0.045
483
c WRD010 Waardenburg Syndrome Type 4 28 0.045
484
MLD012 Melioidosis, Susceptibilty to 21 0.045
485
c CTR105 Cataract 12, Multiple Types 19 0.045
486
TNF006 Tnfrsf13b-Related Common Variable Immune Deficiency 14 0.045
487
P ISC010 Isochromosome Yp 14 0.045
488
MTH028 Mthfr Thermolabile Variant 13 0.045
489
CRN197 Coronary Arterial Fistulas 12 0.045
490
BLR009 Biliary Atresia Extrahepatic 11 0.045
491
MDL007 Medial Medullary Syndrome 10 0.045
492
LBR003 Labrador Lung 8 0.045
493
P MYC007 Myocardial Infarction 88 0.042
494
P OST002 Osteoporosis 77 0.042
495
P WGN002 Wegener's Granulomatosis 75 0.042
496
P LYM007 Lymphangioleiomyomatosis 74 0.042
497
PRC002 Paracoccidioidomycosis 70 0.042
498
PLY017 Polyarteritis Nodosa 68 0.042
499
P ATP001 Atopic Dermatitis 68 0.042
500
P PLY011 Polycystic Ovary Syndrome 68 0.042
501
GNG013 Gingivitis 67 0.042
502
c JVN010 Juvenile Rheumatoid Arthritis 67 0.042
503
MXD005 Mixed Connective Tissue Disease 65 0.042
504
P MLN008 Melanoma 65 0.042
505
PLM001 Pulmonary Tuberculosis 63 0.042
506
URT001 Urethritis 62 0.042
507
ART001 Arterial Tortuosity Syndrome 62 0.042
508
DWN001 Down Syndrome 62 0.042
509
URT039 Urticaria 61 0.042
510
FLR002 Filariasis 60 0.042
511
CMM005 Common Cold 59 0.042
512
c HYP065 Hyperaldosteronism 59 0.042
513
INT067 Interstitial Nephritis 57 0.042
514
c ACT134 Acute Liver Failure 57 0.042
515
ANR008 Aneurysm Disease 57 0.042
516
PRT039 Proteinuria 57 0.042
517
PYR010 Peyronie's Disease 56 0.042
518
STS002 Situs Inversus 56 0.042
519
P MTR012 Mitral Valve Disease 56 0.042
520
MLR002 Miliary Tuberculosis 55 0.042
521
MLT016 Multicentric Reticulohistiocytosis 55 0.042
522
c DRR001 Diarrhea 54 0.042
523
DFF003 Diffuse Scleroderma 54 0.042
524
SCL017 Sclerosing Hemangioma 54 0.042
525
SLD003 Sialadenitis 53 0.042
526
P NGH001 Night Blindness 53 0.042
527
CHR031 Chromoblastomycosis 52 0.042
528
PLM035 Pulmonary Eosinophilia 51 0.042
529
ANK001 Ankylosis 50 0.042
530
c HPT007 Hepatitis E 50 0.042
531
P PST022 Posterior Uveal Melanoma 49 0.042
532
PST046 Post-Transplant Lymphoproliferative Disease 49 0.042
533
c HYD002 Hydronephrosis 48 0.042
534
c AFB001 Afibrinogenemia 48 0.042
535
KRT002 Keratomalacia 47 0.042
536
IMM060 Immunodeficiency, Common Variable, 9 46 0.042
537
AND003 Andersen-Tawil Syndrome 43 0.042
538
LDP002 Lead Poisoning 43 0.042
539
c INT099 Intrahepatic Cholestasis of Pregnancy 41 0.042
540
ADS004 Aids Dementia Complex 38 0.042
541
RPP001 Rapp-Hodgkin Syndrome 34 0.042
542
ADS002 Adie Syndrome 33 0.042
543
c MLG033 Malignant Ovarian Cyst 31 0.042
544
RTR009 Retroperitoneal Cancer 29 0.042
545
MRC002 Marcus Gunn Phenomenon 22 0.042
546
PTS008 Ptosis, Congenital 21 0.042
547
SLR005 Solar Urticaria 12 0.042
548
MTR030 Mitral Valve Prolapse, Familial, X-Linked 12 0.042
549
CLF021 Cleft Palate X-Linked 11 0.042
550
P PRK002 Parkinson's Disease 92 0.039
551
P TYS001 Tay-Sachs Disease 82 0.039
552
P ACT074 Acute Lymphocytic Leukemia 77 0.039
553
THR006 Thromboangiitis Obliterans 75 0.039
554
KWS002 Kawasaki Disease 74 0.039
555
LSH001 Leishmaniasis 74 0.039
556
ABT001 Abetalipoproteinemia 73 0.039
557
c MNN013 Meningitis 71 0.039
558
c OST005 Osteogenesis Imperfecta 70 0.039
559
c HYP086 Hypothyroidism 68 0.039
560
P OST025 Osteogenesis Imperfecta Type Iii 66 0.039
561
P AMY004 Amyloidosis 65 0.039
562
ART021 Arteriosclerosis 65 0.039
563
HYP066 Hyperglycemia 65 0.039
564
HYP458 Hyper Ige Syndrome 65 0.039
565
P DYS007 Dyskeratosis Congenita 64 0.039
566
NRN002 Neuronitis 64 0.039
567
P DNT039 Dent's Disease 64 0.039
568
PRS047 Prostatitis 62 0.039
569
ALP007 Alpha 1-Antitrypsin Deficiency 61 0.039
570
EPD006 Epidermolysis Bullosa Acquisita 61 0.039
571
SPN051 Spondylitis 60 0.039
572
c MLG054 Malignant Histiocytosis 60 0.039
573
INT051 Intussusception 59 0.039
574
CRB021 Cerebral Malaria 59 0.039
575
c GLL020 Gallbladder Disease 59 0.039
576
P FML052 Familial Cold Autoinflammatory Syndrome 58 0.039
577
NNS005 Non-Small Cell Lung Carcinoma 58 0.039
578
CRY005 Cryptococcosis 57 0.039
579
P DND001 Dandy-Walker Syndrome 56 0.039
580
c THR003 Thoracic Aortic Aneurysm 56 0.039
581
URN010 Urinary Tract Obstruction 55 0.039
582
P MTR005 Mitral Valve Prolapse 55 0.039
583
PLY041 Polymyositis 54 0.039
584
DBT061 Diabetic Nephropathy 54 0.039
585
NPH003 Nephrocalcinosis 53 0.039
586
c PST005 Posterior Uveitis 53 0.039
587
MCR088 Microscopic Polyangiitis 53 0.039
588
ART008 Arteriosclerosis Obliterans 53 0.039
589
PLR008 Pleurisy 53 0.039
590
DNG001 Dengue Shock Syndrome 53 0.039
591
c OPH004 Ophthalmoplegia 52 0.039
592
BLL004 Bullous Keratopathy 51 0.039
593
BRN018 Borna Disease 51 0.039
594
IMM001 Immune-Complex Glomerulonephritis 50 0.039
595
OTS002 Otospondylomegaepiphyseal Dysplasia 50 0.039
596
PST010 Pasteurellosis 50 0.039
597
HPT032 Hepatocellular Carcinoma, Somatic 50 0.039
598
MYX004 Myxedema 50 0.039
599
P PND001 Pain Disorder 49 0.039
600
SCH016 Schimke Immunoosseous Dysplasia 49 0.039
601
BLR006 Biliary Tract Disease 49 0.039
602
HYP457 Hypertrophic Scars 48 0.039
603
PYM001 Pyomyositis 47 0.039
604
ACT095 Acute Biphenotypic Leukemia 47 0.039
605
PRM024 Primary Angle-Closure Glaucoma 46 0.039
606
CHR078 Chorioretinitis 45 0.039
607
RNL022 Renal Vascular Disease 45 0.039
608
PRN021 Paranasal Sinus Disease 45 0.039
609
NNT016 Neonatal Hemochromatosis 44 0.039
610
P LSS005 Lissencephaly 1 44 0.039
611
RCR001 Recurrent Corneal Erosion 44 0.039
612
ETH009 Ethmoid Sinusitis 44 0.039
613
MYX013 Myxofibrosarcoma 43 0.039
614
TTR016 Tetra-Amelia Syndrome 43 0.039
615
KLD001 Keloids 42 0.039
616
SPR017 Spermatocele 42 0.039
617
SKL017 Skeletal Dysplasias 42 0.039
618
HYP121 Hypoalphalipoproteinemia 41 0.039
619
VRN004 Vernal Keratoconjunctivitis 40 0.039
620
URT031 Ureteral Disease 40 0.039
621
HPY002 H. Pylori Infection 39 0.039
622
RYN001 Raynaud Disease 39 0.039
623
c CRB126 Cerebral Cavernous Malformation 39 0.039
624
KSH001 Keshan Disease 39 0.039
625
NNL002 Nonalcoholic Steatohepatitis 39 0.039
626
CNG116 Congenital Nephrotic Syndrome Finnish Type 39 0.039
627
IPX001 Ipex Syndrome 39 0.039
628
PRG060 Pregnancy Loss 38 0.039
629
P FBR045 Fibromatosis, Gingival 38 0.039
630
ART012 Aortitis 38 0.039
631
ACT093 Actinic Cheilitis 37 0.039
632
c PSD080 Pseudohypoaldosteronism Type 1 37 0.039
633
LMB051 Lumbar Disc Disease 36 0.039
634
CRY008 Cryopyrin-Associated Periodic Syndrome 36 0.039
635
ATP013 Atopic Keratoconjunctivitis 36 0.039
636
GST063 Gastric Cancer Risk After H. Pylori Infection 36 0.039
637
LKM006 Leukomalacia 35 0.039
638
PRN049 Paraneoplastic Pemphigus 35 0.039
639
FBR019 Fibromatosis 34 0.039
640
c TRN032 Transient Neonatal Diabetes Mellitus 33 0.039
641
FST010 Fasting Hypoglycemia 32 0.039
642
LKP003 Leukoplakia 32 0.039
643
MNN021 Meningococcemia 32 0.039
644
HGH023 High Bone Mass Osteogenesis Imperfecta 31 0.039
645
SML020 Small Patella Syndrome 30 0.039
646
ACT164 Actinic Prurigo 30 0.039
647
c PLM071 Pulmonary Surfactant Metabolism Dysfunction 28 0.039
648
TRP008 Tropical Calcific Pancreatitis 27 0.039
649
ENC017 Encephaloceles 26 0.039
650
GRF006 Grfoma 26 0.039
651
ELS002 Elastosis Perforans Serpiginosa 25 0.039
652
ADM001 Adamantinous Craniopharyngioma 25 0.039
653
INH011 Inherited Bone Marrow Failure Syndromes 24 0.039
654
MNB001 Main Bronchus Cancer 18 0.039
655
c DYS040 Dyskeratosis Congenita Autosomal Recessive 17 0.039
656
RDT005 Radiation Induced Cancer 17 0.039
657
RSP001 Respiratory Bronchiolitis-Associated Interstitial Lung Disease 16 0.039
658
RTR005 Retroperitoneal Lymphoma 15 0.039
659
c PRM041 Primary Cortisol Resistance 13 0.039
660
DND010 Dandy-Walker Malformation with Mental Retardation Basal Ganglia Disease and Seizures 13 0.039
661
EHL006 Ehlers–danlos Syndrome 11 0.039
662
c FML109 Familial Cerebral Cavernous Malformation 1 9 0.039
663
PRT049 Partial Deletion of Y 9 0.039
664
THM003 Thompson Baraitser Syndrome 1 0.039
665
P ALZ001 Alzheimer's Disease 103 0.036
666
P NRF002 Neurofibromatosis 100 0.036
667
P GCH001 Gaucher's Disease 79 0.036
668
c NNN003 Noonan Syndrome 77 0.036
669
P TRN020 Turner Syndrome 77 0.036
670
DBT011 Diabetic Retinopathy 73 0.036
671
P CNG026 Congenital Heart Defect 73 0.036
672
OVR029 Ovarian Hyperstimulation Syndrome 70 0.036
673
c BTT002 Beta Thalassemia 70 0.036
674
DRM006 Dermatitis 68 0.036
675
P ANR007 Anorexia Nervosa 67 0.036
676
ANT006 Antiphospholipid Syndrome 67 0.036
677
P CLN016 Colon Cancer 67 0.036
678
ALL003 Allergic Rhinitis 66 0.036
679
P PRD008 Periodontitis 66 0.036
680
c NPH012 Nephrotic Syndrome 66 0.036
681
CHG001 Chagas Disease 66 0.036
682
MLD001 Melioidosis 65 0.036
683
P CND004 Candidiasis 63 0.036
684
P OVR049 Ovarian Disease 63 0.036
685
CLB001 Coloboma 63 0.036
686
FLT001 Felty's Syndrome 62 0.036
687
P RNL014 Renal Cell Carcinoma 59 0.036
688
PLY023 Polycystic Liver Disease 59 0.036
689
LMT001 Limited Scleroderma 58 0.036
690
VRR004 Verrucous Carcinoma 58 0.036
691
GNG012 Gingival Overgrowth 57 0.036
692
OCC006 Occipital Horn Syndrome 57 0.036
693
P PYL005 Pyelonephritis 57 0.036
694
DBT004 Diabetic Polyneuropathy 57 0.036
695
SRS001 Serous Cystadenocarcinoma 57 0.036
696
PRL007 Proliferative Diabetic Retinopathy 57 0.036
697
MGC001 Megacolon 56 0.036
698
P LYM026 Lymphoblastic Leukemia 56 0.036
699
HYP063 Hypersplenism 56 0.036
700
MMM001 Mammary Paget's Disease 56 0.036
701
URN003 Urinary Schistosomiasis 56 0.036
702
ATX019 Ataxia with Vitamin E Deficiency 55 0.036
703
ART004 Aortic Atherosclerosis 54 0.036
704
CLN019 Colonic Disease 54 0.036
705
PNN001 Panniculitis 53 0.036
706
GST045 Gastroenteritis 53 0.036
707
CRN030 Coronary Stenosis 53 0.036
708
P HRD057 Hereditary Pancreatitis 53 0.036
709
ADL002 Adult Syndrome 52 0.036
710
CLC001 Calciphylaxis 52 0.036
711
c ACT042 Acute Pyelonephritis 52 0.036
712
P EXP004 Exophthalmos 51 0.036
713
CYS006 Cystoid Macular Edema 50 0.036
714
CNG064 Congenital Chloride Diarrhea 50 0.036
715
P INF037 Inflammatory Bowel Disease 50 0.036
716
LNG029 Lung Adenocarcinoma 49 0.036
717
HPT009 Hepatopulmonary Syndrome 49 0.036
718
DSM007 Desmoplastic Small Round Cell Tumor 48 0.036
719
c KBK001 Kabuki Syndrome 48 0.036
720
KWS001 Kwashiorkor 47 0.036
721
PGT004 Paget Disease, Juvenile 46 0.036
722
GST039 Gastroduodenitis 46 0.036
723
c CHR037 Chronic Eosinophilic Pneumonia 43 0.036
724
DBT007 Diabetic Cataract 42 0.036
725
P BRT034 Bartter Syndrome, Type 2 42 0.036
726
P HYP058 Hypervitaminosis a 42 0.036
727
ISL003 Isolated Growth Hormone Deficiency 39 0.036
728
HYP030 Hypoactive Sexual Desire Disorder 39 0.036
729
PNC041 Pancreatic Ductal Adenocarcinoma 38 0.036
730
EMN001 Emanuel Syndrome 36 0.036
731
SYN036 Syncope 35 0.036
732
HMC014 Homocysteinemia 35 0.036
733
BCK006 Back Pain 33 0.036
734
CHR276 Chronic Active Epstein-Barr Virus Infection 32 0.036
735
CRB077 Cerebro-Costo-Mandibular Syndrome 31 0.036
736
ANT018 Anthracosis 31 0.036
737
PLM007 Pulmonary Aspergilloma 28 0.036
738
c ANT034 Anterior Uveitis 28 0.036
739
DDN009 Duodenal Obstruction 27 0.036
740
EHL039 Ehlers-Danlos Syndrome, Periodontitis Type 26 0.036
741
CLF029 Cleft Palate and Mental Retardation 25 0.036
742
CLD014 Cole Disease 24 0.036
743
ATR015 Atresia of Small Intestine 23 0.036
744
c HMP017 Hemophilia a, Congenital 21 0.036
745
OST008 Osteosclerotic Myeloma 19 0.036
746
HYP159 Hyperinsulinism, Focal 17 0.036
747
BNM007 Bone Marrow Failure, Telomere-Related, 1 16 0.036
748
RSP016 Respiratory Bronchiolitis - Interstitial Lung Disease 13 0.036
749
SPS044 Spastic Paraplegia Epilepsy Mental Retardation 12 0.036
750
c EHL016 Ehlers-Danlos Syndrome Type 5 11 0.036
751
EHL008 Ehlers–danlos Syndrome, Vascular Type 8 0.036
752
P AMY001 Amyotrophic Lateral Sclerosis 100 0.032
753
P TYP009 Type 2 Diabetes Mellitus 93 0.032
754
MRF001 Marfan Syndrome 92 0.032
755
P PRS040 Prostate Cancer 91 0.032
756
21H001 21-Hydroxylase Deficiency 87 0.032
757
GLN003 Glanzmann's Thrombasthenia 80 0.032
758
PRC016 Pre-Eclampsia 75 0.032
759
P FML018 Familial Mediterranean Fever 74 0.032
760
P FRD001 Friedreich Ataxia 72 0.032
761
P BRD002 Bardet-Biedl Syndrome 71 0.032
762
P HST010 Histiocytosis 71 0.032
763
c ESS002 Essential Hypertension 71 0.032
764
SHW002 Shwachman-Diamond Syndrome 68 0.032
765
P HMN010 Hemangioma 68 0.032
766
c PRM002 Primary Hyperoxaluria 68 0.032
767
PLM033 Pulmonary Embolism 68 0.032
768
TRP002 Tropical Spastic Paraparesis 67 0.032
769
CRB042 Cerebellar Ataxia 66 0.032
770
P DRM007 Dermatitis Herpetiformis 66 0.032
771
HPT002 Hepatic Vein Thrombosis 65 0.032
772
ZLL002 Zollinger-Ellison Syndrome 64 0.032
773
TXC005 Toxic Shock Syndrome 63 0.032
774
TYP007 Typhoid Fever 63 0.032
775
c SPN046 Spinal Muscular Atrophy 63 0.032
776
GNT003 Genital Herpes 62 0.032
777
c ACT073 Acute Leukemia 62 0.032
778
HRY003 Hairy Cell Leukemia 62 0.032
779
SCK005 Sickle Cell Disease 62 0.032
780
TNS005 Tonsillitis 62 0.032
781
HYP014 Hyperuricemia 61 0.032
782
NRP001 Neuropathy 61 0.032
783
PPT003 Peptic Ulcer 61 0.032
784
CRY003 Cryptosporidiosis 60 0.032
785
VTL002 Vitiligo 60 0.032
786
c ATM011 Autoimmune Hepatitis 60 0.032
787
FCL008 Focal Glomerulosclerosis 60 0.032
788
MLT001 Multiple Chemical Sensitivity 59 0.032
789
SCR008 Scrub Typhus 59 0.032
790
ACR008 Acrocallosal Syndrome 59 0.032
791
P CLF002 Cleft Palate 59 0.032
792
LPD010 Lipodystrophy 59 0.032
793
INS002 in Situ Carcinoma 58 0.032
794
c RNL003 Renal Clear Cell Carcinoma 58 0.032
795
P MYP004 Myopathy 58 0.032
796
STT002 Status Asthmaticus 57 0.032
797
ALV002 Alveolar Echinococcosis 57 0.032
798
ARM001 Aromatase Deficiency 57 0.032
799
P SCL015 Scleritis 57 0.032
800
ARC002 Arachnoiditis 57 0.032
801
URM002 Uremia 56 0.032
802
OST019 Osteosclerosis 56 0.032
803
NPH010 Nephrosclerosis 56 0.032
804
RTN003 Retinal Ischemia 56 0.032
805
RNL011 Renal Osteodystrophy 56 0.032
806
CLL003 Cellulitis 56 0.032
807
HYP068 Hyperostosis 56 0.032
808
CNS004 Constipation 55 0.032
809
AVN001 Avian Influenza 55 0.032
810
HYP037 Hyperhomocysteinemia 55 0.032
811
P PNC001 Pancytopenia 55 0.032
812
SHR001 Short Bowel Syndrome 55 0.032
813
ACT017 Acute Chest Syndrome 55 0.032
814
PRP007 Priapism 55 0.032
815
LPC002 Lip Cancer 55 0.032
816
P ESN008 Eosinophilic Pneumonia 54 0.032
817
PPL006 Papillon-Lefevre Disease 54 0.032
818
ART017 Aortic Disease 54 0.032
819
SPN020 Spondylosis 54 0.032
820
GST050 Gastrointestinal System Disease 54 0.032
821
FSC002 Fascioliasis 54 0.032
822
BCL002 B Cell Deficiency 53 0.032
823
P CYS010 Cystinosis 53 0.032
824
c RTN014 Retinal Artery Occlusion 53 0.032
825
P BLD034 Bile Duct Carcinoma 52 0.032
826
c CNG018 Congenital Heart Block 52 0.032
827
EHL034 Ehlers-Danlos Syndrome, Hypermobility Type 52 0.032
828
CRD001 Cardiac Tamponade 52 0.032
829
SYS003 Systolic Heart Failure 51 0.032
830
PRC003 Proctitis 51 0.032
831
c NMN004 Niemann-Pick Disease Type C1 51 0.032
832
c MCK006 Meckel Syndrome 51 0.032
833
NPH004 Nephropathia Epidemica 51 0.032
834
SYM002 Sympathetic Ophthalmia 51 0.032
835
ANG002 Angiostrongyliasis 50 0.032
836
P LCT002 Lactose Intolerance 50 0.032
837
ANG011 Angiodysplasia 50 0.032
838
CHR370 Chronic Granulomatous Disease, Autosomal, Due to Deficiency of Cyba 50 0.032
839
CTS003 Coats Disease 50 0.032
840
IRN002 Iron Metabolism Disease 50 0.032
841
c INT064 Intermediate Uveitis 50 0.032
842
PLM010 Pulmonary Edema 50 0.032
843
FRZ001 Frozen Shoulder 49 0.032
844
c WRD015 Waardenburg Syndrome Type Iva 49 0.032
845
NDL007 Nodular Goiter 49 0.032
846
PLM018 Pulmonary Sclerosing Hemangioma 48 0.032
847
GST029 Gastric Cardia Adenocarcinoma 48 0.032
848
MLK003 Melkersson-Rosenthal Syndrome 48 0.032
849
c ART084 Arteriovenous Fistula 47 0.032
850
c PSD003 Pseudohypoaldosteronism 47 0.032
851
ESN015 Eosinophilic Fasciitis 47 0.032
852
PLP001 Pulpitis 46 0.032
853
ACT040 Acute Poststreptococcal Glomerulonephritis 46 0.032
854
HYD005 Hydrocele 46 0.032
855
LYM014 Lymphangitis 46 0.032
856
PNC033 Pancreas Adenocarcinoma 46 0.032
857
P PRK001 Porokeratosis 45 0.032
858
CHR415 Chronic Venous Leg Ulcers 45 0.032
859
PRT058 Pure Autonomic Failure 44 0.032
860
BNG016 Benign Migratory Glossitis 44 0.032
861
PRL011 Proliferative Vitreoretinopathy 44 0.032
862
PRL019 Prolidase Deficiency 44 0.032
863
PLR007 Pleural Empyema 44 0.032
864
BRN014 Bronchopneumonia 44 0.032
865
CHR466 Chronic Thromboembolic Pulmonary Hypertension 43 0.032
866
HYD028 Hydrops, Ectopic Calcification, Moth-Eaten Skeletal Dysplasia 43 0.032
867
LYM052 Lymphomatoid Papulosis 43 0.032
868
CNJ007 Conjunctivochalasis 43 0.032
869
PNC053 Pancreatic Islet Cell Tumors 43 0.032
870
HYP266 Hypoxia 43 0.032
871
CHL039 Choledocholithiasis 43 0.032
872
SCT002 Scotoma 42 0.032
873
HTS001 Hiatus Hernia 42 0.032
874
BLD054 Blood Protein Disease 41 0.032
875
PST087 Posterior Urethral Valve 40 0.032
876
EXT006 Extrahepatic Cholestasis 39 0.032
877
NPH051 Nephritis 39 0.032
878
OVR054 Ovarian Mucinous Neoplasm 39 0.032
879
HTL002 Htlv-1 Associated Myelopathy 38 0.032
880
PLM052 Pulmonary Arteriovenous Malformation 38 0.032
881
TXC012 Toxic Epidermal Necrolysis 38 0.032
882
c BLN003 Blindness 37 0.032
883
KLB001 Klebsiella 37 0.032
884
CRR001 Carrion's Disease 37 0.032
885
c SVR056 Severe Hemophilia a 37 0.032
886
OST032 Osteofibrous Dysplasia 37 0.032
887
VRL011 Viral Infectious Disease 37 0.032
888
WRT003 Warthin Tumor 36 0.032
889
SCR003 Secretory Diarrhea 36 0.032
890
HYP231 Hypothalamic Hamartomas 36 0.032
891
XRP001 Xerophthalmia 35 0.032
892
IMG001 Image Syndrome 34 0.032
893
PNC028 Pancreatic Steatorrhea 34 0.032
894
MTR001 Mature Cataract 34 0.032
895
MYC013 Mycobacterium Abscessus 33 0.032
896
ILS001 Ileus 33 0.032
897
EHL010 Ehlers-Danlos Syndrome Arthrochalasia Type 33 0.032
898
BRN078 Bronchiectasis with or Without Elevated Sweat Chloride 1, Modifier of 33 0.032
899
STC004 Stachybotrys Chartarum 32 0.032
900
GRN003 Granulomatous Dermatitis 32 0.032
901
PNC002 Pancreatic Mucinous Cystadenoma 32 0.032
902
SCL025 Scleromyxedema 32 0.032
903
ORB013 Orbital Disease 32 0.032
904
URT036 Urethral Obstruction 31 0.032
905
CL1004 Col1a1/2-Related Osteogenesis Imperfecta 31 0.032
906
c HMP006 Hemiplegic Migraine 31 0.032
907
END048 Endotoxin Hyporesponsiveness 31 0.032
908
PTL001 Patulous Eustachian Tube 30 0.032
909
ACT022 Acute Retinal Necrosis Syndrome 30 0.032
910
ENC011 Encephalomyopathy 29 0.032
911
CSC001 Cascade Stomach 29 0.032
912
c CHR036 Chronic Cholangitis 28 0.032
913
NRT005 North Carolina Macular Dystrophy 28 0.032
914
CRD016 Cardiac Rupture 27 0.032
915
ENT007 Enteropathica 27 0.032
916
INT011 Interstitial Emphysema 26 0.032
917
PRT015 Partial Third-Nerve Palsy 26 0.032
918
DBT042 Diabetes, Permanent Neonatal 25 0.032
919
YCH001 Y Chromosome Infertility 25 0.032
920
PTY004 Pityriasis Lichenoides 25 0.032
921
PLM074 Pulmonary Function 24 0.032
922
STR015 Stereotypic Movement Disorder 24 0.032
923
DFF031 Diffuse Alveolar Hemorrhage 23 0.032
924
BDN001 Bednar's Tumor 23 0.032
925
HRL001 Harlequin Type Ichthyosis 22 0.032
926
CFT001 Cftr-Related Disorders 21 0.032
927
c PDT025 Pediatric Multiple Sclerosis 21 0.032
928
EPT021 Epithelial Recurrent Erosion Dystrophy 19 0.032
929
JJN004 Jejunal Atresia 17 0.032
930
THY020 Thyroid Hyalinizing Trabecular Adenoma 17 0.032
931
AMY016 Amyopathic Dermatomyositis 17 0.032
932
SPS082 Spastic Paraplegia - Epilepsy - Intellectual Deficit 16 0.032
933
ISL075 Isolated Pierre Robin Sequence 15 0.032
934
GNT018 Gianotti Crosti Syndrome 15 0.032
935
NNT025 Neonatal Systemic Lupus Erythematosus 14 0.032
936
c EHL019 Ehlers-Danlos Syndrome Type Via 13 0.032
937
BLD063 Bile Duct Cysts 13 0.032
938
CMV001 Cmv Antenatal Infection 13 0.032
939
GLC006 Galactosemia 93 0.028
940
FBR012 Fabry Disease 88 0.028
941
P NMN002 Niemann-Pick Disease 87 0.028
942
P RTT002 Rett Syndrome 85 0.028
943
P APL001 Aplastic Anemia 83 0.028
944
AGR001 Age Related Macular Degeneration 83 0.028
945
P PRP003 Porphyria Cutanea Tarda 81 0.028
946
c MCP002 Mucopolysaccharidosis I 80 0.028
947
PRP027 Peripheral Vascular Disease 75 0.028
948
SCK003 Sickle Cell Anemia 73 0.028
949
P CLC005 Celiac Disease 73 0.028
950
P CNG030 Congenital Muscular Dystrophy 72 0.028
951
P PRM005 Primary Hyperparathyroidism 72 0.028
952
PLL001 Pallister-Hall Syndrome 71 0.028
953
ANR002 Aniridia 71 0.028
954
c HYD006 Hydrocephalus 70 0.028
955
P TMP003 Temporal Arteritis 69 0.028
956
PSY004 Psychotic Disorder 69 0.028
957
DBT001 Diabetic Ketoacidosis 69 0.028
958
ISC006 Ischemic Heart Disease 69 0.028
959
LMY002 Leiomyoma 68 0.028
960
c HMP007 Hemophilia 68 0.028
961
MRB003 Morbid Obesity 68 0.028
962
BRR003 Barrett's Esophagus 68 0.028
963
P RTH001 Rothmund-Thomson Syndrome 67 0.028
964
MYS005 Myositis 67 0.028
965
P MTB001 Metabolic Syndrome X 67 0.028
966
P LNG044 Long Qt Syndrome 1 66 0.028
967
ACT010 Acth-Secreting Pituitary Adenoma 66 0.028
968
HYP056 Hypoglycemia 66 0.028
969
CHR066 Chronic Fatigue Syndrome 65 0.028
970
HPT022 Hepatoblastoma 65 0.028
971
P CMP010 Complex Regional Pain Syndrome 65 0.028
972
THR016 Thrombophlebitis 65 0.028
973
PPL022 Papilloma 64 0.028
974
CHR282 Chronic Infantile Neurological Cutaneous Articular Syndrome 63 0.028
975
ACQ007 Acquired Immunodeficiency Syndrome 63 0.028
976
P GRV001 Graves' Disease 63 0.028
977
c HYP069 Hyperparathyroidism 63 0.028
978
SRC014 Sarcoma 63 0.028
979
SPT014 Septo-Optic Dysplasia 63 0.028
980
PHR003 Pharyngitis 62 0.028
981
P QFV001 Q Fever 62 0.028
982
PSD007 Pseudomyxoma Peritonei 62 0.028
983
PLS006 Plasmodium Vivax Malaria 62 0.028
984
PPL002 Papillary Carcinoma 61 0.028
985
P AGM001 Agammaglobulinemia 61 0.028
986
P ANP001 Anaplastic Large Cell Lymphoma 61 0.028
987
c ACT075 Acute Myocardial Infarction 61 0.028
988
P HMC002 Homocystinuria 61 0.028
989
PRD007 Periodontal Disease 61 0.028
990
CHL014 Cholera 61 0.028
991
P HLP001 Holoprosencephaly 61 0.028
992
MCK007 Muckle-Wells Syndrome 60 0.028
993
CRT049 Critical Limb Ischemia 60 0.028
994
FDL002 Food Allergy 60 0.028
995
KRT006 Keratoconjunctivitis 60 0.028
996
SPT004 Septic Arthritis 60 0.028
997
P PTT014 Pitt-Hopkins Syndrome 59 0.028
998
P RTN022 Retinal Vein Occlusion 59 0.028
999
ALL009 Allergic Conjunctivitis 59 0.028
1000
CHR074 Choriocarcinoma 59 0.028
1001
CMP002 Campylobacteriosis 59 0.028
1002
PRV004 Periventricular Leukomalacia 58 0.028
1003
ERY003 Erythema Multiforme 58 0.028
1004
ALL010 Allergic Contact Dermatitis 58 0.028
1005
P GLC007 Glaucoma 58 0.028
1006
P TWN001 Twin-to-Twin Transfusion Syndrome 58 0.028
1007
CRT016 Carotid Artery Disease 58 0.028
1008
ASP003 Aseptic Meningitis 58 0.028
1009
INT054 Intraocular Lymphoma 58 0.028
1010
OST011 Osteomalacia 57 0.028
1011
P DBT005 Diabetes Insipidus 57 0.028
1012
LYM022 Lymphangioma 57 0.028
1013
P ISC002 Ischemic Optic Neuropathy 57 0.028
1014
P LYM025 Lymphedema 56 0.028
1015
P END047 Endophthalmitis 56 0.028
1016
TCL002 T-Cell Large Granular Lymphocyte Leukemia 56 0.028
1017
ACN011 Acne 56 0.028
1018
CHR005 Chorioamnionitis 56 0.028
1019
FBR003 Fibrous Histiocytoma 55 0.028
1020
c CNG015 Congenital Diaphragmatic Hernia 55 0.028
1021
ANR004 Anuria 55 0.028
1022
ALC009 Alcoholic Liver Cirrhosis 55 0.028
1023
BRN016 Bronchogenic Carcinoma 55 0.028
1024
P HYP098 Hypereosinophilic Syndrome 54 0.028
1025
c VNT002 Ventricular Septal Defect 53 0.028
1026
MMB001 Membranoproliferative Glomerulonephritis 53 0.028
1027
c CTR002 Cataract 53 0.028
1028
TRN007 Transsexualism 53 0.028
1029
HMG005 Hemoglobinopathy 53 0.028
1030
PRT038 Protein-Energy Malnutrition 53 0.028
1031
VLV010 Vulvovaginitis 53 0.028
1032
SPN035 Spindle Cell Sarcoma 53 0.028
1033
c CNT016 Central Retinal Vein Occlusion 53 0.028
1034
PRP023 Peripheral Neuropathy 53 0.028
1035
c ATM019 Autoimmune Polyendocrine Syndrome 52 0.028
1036
EXT033 Extrapulmonary Tuberculosis 52 0.028
1037
KRT008 Keratopathy 52 0.028
1038
PLY020 Polyradiculoneuropathy 52 0.028
1039
CRN024 Corneal Disease 52 0.028
1040
MCN007 Meconium Aspiration Syndrome 52 0.028
1041
SRC002 Sarcomatoid Renal Cell Carcinoma 52 0.028
1042
NRR001 Neuroretinitis 52 0.028
1043
LPM005 Lipomatosis 52 0.028
1044
THY089 Thymic Epithelial Neoplasm 52 0.028
1045
DNT012 Dental Caries 51 0.028
1046
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 51 0.028
1047
OBS001 Obstructive Jaundice 51 0.028
1048
HRD004 Hereditary Breast Ovarian Cancer 50 0.028
1049
DBT006 Diabetic Macular Edema 50 0.028
1050
CNV002 Conversion Disorder 50 0.028
1051
SCN036 Secondary Progressive Multiple Sclerosis 50 0.028
1052
VLL003 Villonodular Synovitis 50 0.028
1053
IDP064 Idiopathic Neutropenia 50 0.028
1054
INF034 Infective Endocarditis 50 0.028
1055
PRP002 Periapical Granuloma 50 0.028
1056
VSM001 Vasomotor Rhinitis 49 0.028
1057
PYL006 Pyloric Stenosis 49 0.028
1058
c TRP001 Triple-a Syndrome 49 0.028
1059
TND004 Tendinopathy 48 0.028
1060
ALC010 Alcoholic Cardiomyopathy 48 0.028
1061
ART006 Arthus Reaction 48 0.028
1062
LGN001 Legionnaires' Disease 48 0.028
1063
CLS007 Classic Kaposi Sarcoma 48 0.028
1064
MNN014 Mononeuritis 48 0.028
1065
MCR020 Microsporidiosis 47 0.028
1066
CMP009 Complement Deficiency 47 0.028
1067
P PRM100 Primary Spontaneous Pneumothorax 46 0.028
1068
HRT012 Heart Valve Disease 46 0.028
1069
NNT012 Neonatal Jaundice 46 0.028
1070
TLN003 Telangiectasis 46 0.028
1071
MCN008 Mucinous Cystadenocarcinoma 46 0.028
1072
HPR003 Heparin-Induced Thrombocytopenia 45 0.028
1073
P PLM129 Pulmonary Disease, Chronic Obstructive 45 0.028
1074
MRS001 Marasmus 44 0.028
1075
c MLG086 Malignant Hyperthermia Susceptibility 44 0.028
1076
c SLP006 Sleep Apnea 44 0.028
1077
c CHR098 Chronic Pyelonephritis 44 0.028
1078
PST062 Pustulosis Palmaris Et Plantaris 43 0.028
1079
INT079 Intrahepatic Cholangiocarcinoma 43 0.028
1080
PRX015 Paroxysmal Extreme Pain Disorder 43 0.028
1081
VNS009 Venous Thrombosis 43 0.028
1082
BRN038 Bronchial Disease 42 0.028
1083
ACT055 Actinomycosis 42 0.028
1084
CYT005 Cytomegalovirus Retinitis 42 0.028
1085
SKL007 Skeletal Muscle Regeneration 42 0.028
1086
PMP004 Pemphigus Foliaceus 42 0.028
1087
FNS001 Funisitis 41 0.028
1088
LFT009 Left Ventricular Outflow Tract Obstruction 41 0.028
1089
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 41 0.028
1090
OLG015 Oligoarticular Juvenile Arthritis 40 0.028
1091
TND006 Tendinosis 40 0.028
1092
c CHR417 Chronic Graft Versus Host Disease 40 0.028
1093
LRG008 Large Granular Lymphocyte Leukemia 40 0.028
1094
RFR010 Refractory Anemia 39 0.028
1095
c LNG063 Lung Cancer Susceptibility 38 0.028
1096
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 38 0.028
1097
DDN007 Duodenal Disease 38 0.028
1098
c RNL078 Renal Dysplasia 37 0.028
1099
DFF016 Diffuse Astrocytoma 37 0.028
1100
c ACQ022 Acquired Generalized Lipodystrophy 37 0.028
1101
ACL001 Acalculous Cholecystitis 37 0.028
1102
MYC012 Mycetoma 37 0.028
1103
CRB086 Cerebral Aneurysms 37 0.028
1104
PLM070 Pulmonic Stenosis 37 0.028
1105
ERY017 Erythema Elevatum Diutinum 37 0.028
1106
c PLY084 Polycystic Kidney Disease, Type 2 36 0.028
1107
P DPH016 Diaphragmatic Hernia 3 36 0.028
1108
CRP018 Cor Pulmonale 36 0.028
1109
P TYP024 Type Ii Mixed Cryoglobulinemia 36 0.028
1110
RTC003 Root Caries 36 0.028
1111
GRD005 Geroderma Osteodysplasticum 36 0.028
1112
VLV042 Vulvar Vestibulitis Syndrome 36 0.028
1113
c ACQ014 Acquired Hemophilia 35 0.028
1114
MNT147 Mental Retardation 35 0.028
1115
P INF131 Infant Acute Respiratory Distress Syndrome 35 0.028
1116
CLT002 Cluttering 33 0.028
1117
ODN005 Odontogenic Myxoma 33 0.028
1118
SLL001 Sialolithiasis 33 0.028
1119
PYR026 Peyronies Disease 32 0.028
1120
SML032 Small Bowel Adenocarcinoma 31 0.028
1121
EHL012 Ehlers-Danlos Syndrome Dermatosparaxis Type 31 0.028
1122
KRT012 Keratoderma 31 0.028
1123
c CHR013 Chronic Apical Periodontitis 30 0.028
1124
HLM001 Helminthiasis 30 0.028
1125
SRF006 Surfactant Dysfunction 30 0.028
1126
MYT011 Myotonia 29 0.028
1127
BRW003 Brown Induration 29 0.028
1128
DYS036 Dysequilibrium Syndrome 28 0.028
1129
MNN034 Mannose-Binding Lectin Deficiency 28 0.028
1130
DFN039 Deafness-Infertility Syndrome 27 0.028
1131
c DYS039 Dyskeratosis Congenita Autosomal Dominant 26 0.028
1132
P PLM103 Pulmonary Capillary Hemangiomatosis 26 0.028
1133
c EHL047 Ehlers-Danlos Syndrome, Musculocontractural Type 1 25 0.028
1134
c FML060 Familial Eosinophilia 25 0.028
1135
c MTP005 Metaphyseal Anadysplasia 25 0.028
1136
PSD059 Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency 23 0.028
1137
NNH002 Non-a-E Hepatitis 23 0.028
1138
HPT066 Hepatoportal Sclerosis 23 0.028
1139
c CNG372 Congenital Stationary Night Blindness, Type 1f 22 0.028
1140
NTL001 Nut Allergic Reaction 22 0.028
1141
CRY006 Cryofibrinogenemia 22 0.028
1142
ESN009 Eosinophil Peroxidase Deficiency 22 0.028
1143
INT093 Interferon Gamma, Receptor 1, Deficiency 21 0.028
1144
P KRN003 Kernicterus Due to Isoimmunization 21 0.028
1145
HRD009 Hereditary Wilms' Tumor 21 0.028
1146
c MNS010 Monosomy Xp21 20 0.028
1147
TRC038 Tracheobronchomegaly 18 0.028
1148
BFD003 Bifid Uvula 16 0.028
1149
AMY010 Amyloidosis Beta2m 16 0.028
1150
ISL072 Isolated Levocardia 14 0.028
1151
OTP003 Oto-Palatal-Digital Syndrome 13 0.028
1152
c LCT011 Lactose Intolerance, Adult Type 9 0.028
1153
MLD005 Meliodosis 8 0.028
1154
TMP006 Temporomandibular Ankylosis 8 0.028
1155
PHN003 Phenylketonuria 93 0.023
1156
P LFR001 Li-Fraumeni Syndrome 93 0.023
1157
P HNT001 Huntington's Disease 87 0.023
1158
P CSH001 Cushing's Syndrome 83 0.023
1159
PLY001 Polycythemia Vera 83 0.023
1160
P MLT020 Multiple Sclerosis 82 0.023
1161
P MYS003 Myasthenia Gravis 79 0.023
1162
CLD001 Cleidocranial Dysplasia 78 0.023
1163
INC002 Inclusion Body Myositis 78 0.023
1164
P LPR003 Leprosy 78 0.023
1165
FCT007 Factor Vii Deficiency 78 0.023
1166
BRK003 Burkitt's Lymphoma 78 0.023
1167
P CHR089 Chronic Kidney Failure 76 0.023
1168
P OST012 Osteoarthritis 73 0.023
1169
BLS001 Blau Syndrome 73 0.023
1170
P JVN014 Juvenile Polyposis Syndrome 73 0.023
1171
c MYL006 Myeloid Leukemia 72 0.023
1172
CHR012 Chronic Granulomatous Disease 72 0.023
1173
c CNG006 Congenital Hypothyroidism 72 0.023
1174
XLN002 X-Linked Hypophosphatemia 72 0.023
1175
FCT001 Factor Viii Deficiency 71 0.023
1176
P MGR002 Migraine 71 0.023
1177
LKC001 Leukocyte Adhesion Deficiency 70 0.023
1178
ALP004 Alport Syndrome 69 0.023
1179
BCK001 Becker Muscular Dystrophy 69 0.023
1180
P END044 Endometriosis 69 0.023
1181
P FML032 Familial Hypertrophic Cardiomyopathy 69 0.023
1182
CCC001 Coccidioidomycosis 68 0.023
1183
IRR002 Irritable Bowel Syndrome 68 0.023
1184
ATM004 Autoimmune Thrombocytopenic Purpura 68 0.023
1185
P HML002 Hemolytic Anemia 68 0.023
1186
GTL001 Gitelman Syndrome 67 0.023
1187
P RCK004 Rickets 67 0.023
1188
CHR072 Chordoma 67 0.023
1189
ADN018 Adenoma 67 0.023
1190
CMM004 Common Variable Immunodeficiency 66 0.023
1191
PRT014 Protein S Deficiency 66 0.023
1192
P THR015 Thrombophilia 66 0.023
1193
P PSD087 Pseudoxanthoma Elasticum 66 0.023
1194
GSG001 Gas Gangrene 66 0.023
1195
P VTL001 Vitelliform Macular Dystrophy 66 0.023
1196
P ART023 Arthropathy 66 0.023
1197
P HMP002 Hemophagocytic Lymphohistiocytosis 66 0.023
1198
MLG056 Malignant Hyperthermia 65 0.023
1199
HST011 Histoplasmosis 65 0.023
1200
c NTR004 Neutropenia 65 0.023
1201
PTN002 Patent Ductus Arteriosus 65 0.023
1202
RHM001 Rheumatic Fever 65 0.023
1203
P MLG077