Search results for "INS"

9697 hits were found for 'INS'

# Family MCID Name MIFTS Score
1
P MTR004 Maturity-Onset Diabetes of the Young 69 7.173
2
P NNT009 Neonatal Diabetes Mellitus 51 6.808
3
P OBS005 Obesity 98 6.727
4
SPN027 Spinal Stenosis 61 4.959
5
c SKN012 Skin Carcinoma in Situ 21 4.842
6
c INS012 Ins-Related Permanent Neonatal Diabetes Mellitus 7 4.474
7
P MYL006 Myeloid Leukemia 74 3.673
8
P DBT083 Diabetes Mellitus, Permanent Neonatal 58 3.625
9
P HYP110 Hyperproinsulinemia 39 3.612
10
LCK001 Locked-in Syndrome 41 3.567
11
CRV002 Cervix Uteri Carcinoma in Situ 25 3.414
12
P PLY011 Polycystic Ovary Syndrome 67 3.340
13
BHC001 Behcet's Syndrome Arthropathy 9 3.236
14
HYP056 Hypoglycemia 62 3.214
15
HYP066 Hyperglycemia 60 3.202
16
LPD010 Lipodystrophy 57 3.156
17
GLC003 Glucose Intolerance 59 3.144
18
DBT001 Diabetic Ketoacidosis 57 3.115
19
P HYP060 Hyperinsulinism 55 3.106
20
ACN002 Acanthosis Nigricans 63 3.072
21
c STM003 Stomach Carcinoma in Situ 15 3.058
22
ANL008 Anal Carcinoma in Situ 8 3.051
23
FTL021 Fetal Macrosomia 43 3.001
24
HYP026 Hypoglycemic Coma 47 2.987
25
LPR018 Leprechaunism 70 2.980
26
c MTB001 Metabolic Syndrome X 67 2.976
27
BRT037 Brittle Diabetes 26 2.964
28
P FML035 Familial Hyperlipidemia 55 2.962
29
RBS003 Rabson-Mendenhall Syndrome 69 2.961
30
P DBT085 Diabetes Mellitus, Insulin-Dependent 85 2.960
31
OLG010 Oligomenorrhea 42 2.957
32
c MTR044 Maturity-Onset Diabetes of the Young, Type 10 22 2.932
33
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 17 2.932
34
CLN004 Colon Carcinoma in Situ 14 2.864
35
LVR003 Liver Carcinoma in Situ 11 2.859
36
TRC002 Trachea Carcinoma in Situ 9 2.859
37
c NSL007 Nasal Cavity Carcinoma in Situ 8 2.854
38
P LNG032 Lung Cancer 95 2.795
39
c BLD008 Bladder Carcinoma in Situ 25 2.691
40
c LNG003 Lung Carcinoma in Situ 13 2.648
41
LRY009 Larynx Carcinoma in Situ 9 2.648
42
END018 Endometrium Carcinoma in Situ 8 2.648
43
OST013 Osteosarcoma Arising in Bone Paget's Disease 7 2.642
44
P MTH008 Methylmalonic Acidemia 72 2.518
45
DCT002 Ductal Carcinoma in Situ 40 2.481
46
P BRS047 Breast Cancer 91 2.452
47
DDN006 Duodenitis 55 2.437
48
c PRS031 Prostate Carcinoma in Situ 18 2.418
49
ESP005 Esophagus Carcinoma in Situ 9 2.418
50
DCN001 Dic in Newborn 6 2.416
51
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 13 2.412
52
c BRS033 Breast Apocrine Carcinoma in Situ 6 2.412
53
STN004 Stone in Bladder Diverticulum 5 2.412
54
c ADN012 Adenocarcinoma in Situ 52 2.322
55
END030 End Stage Renal Failure 57 2.276
56
NNL002 Nonalcoholic Steatohepatitis 51 2.274
57
P RNV001 Renovascular Hypertension 60 2.256
58
FSC002 Fascioliasis 61 2.255
59
END040 Endogenous Depression 52 2.234
60
P OVR049 Ovarian Disease 64 2.231
61
DBT006 Diabetic Macular Edema 52 2.227
62
c BRS049 Breast Carcinoma in Situ 51 2.221
63
P ALT001 Alternating Hemiplegia of Childhood 61 2.220
64
P GLL020 Gallbladder Disease 64 2.216
65
CLC001 Calciphylaxis 54 2.212
66
P AST005 Asthma 91 2.207
67
NCR007 Necrotizing Fasciitis 44 2.207
68
ASP004 Asphyxia Neonatorum 29 2.204
69
ASH001 Asherman's Syndrome 22 2.195
70
P HYP263 Hypersomnia 43 2.193
71
DBT002 Diabetic Autonomic Neuropathy 47 2.191
72
PST055 Postural Hypotension 44 2.188
73
GSG001 Gas Gangrene 66 2.186
74
BLR006 Biliary Tract Disease 49 2.186
75
FBR064 Febrile Infection-Related Epilepsy Syndrome 31 2.185
76
DMP001 Dumping Syndrome 48 2.184
77
OVR063 Overnutrition 47 2.181
78
P HYP120 Hypoaldosteronism 48 2.179
79
HTC002 Hutchinson-Gilford Progeria 55 2.170
80
NCR002 Necrobiosis Lipoidica 42 2.168
81
c EYC001 Eye Carcinoma in Situ 9 2.168
82
PTT004 Pituitary Apoplexy 53 2.167
83
c TRS005 Torsion Dystonia with Onset in Infancy 13 2.166
84
PNS002 Penis Carcinoma in Situ 10 2.164
85
RCT010 Rectum Carcinoma in Situ 9 2.164
86
LPP001 Lipoprotein Lipase Deficiency 69 2.158
87
PLY002 Polyneuropathy in Collagen Vascular Disease 5 2.157
88
STF001 Stiff-Person Syndrome 60 2.156
89
EMP001 Empty Sella Syndrome 50 2.151
90
P FML012 Familial Partial Lipodystrophy 60 2.150
91
NRG005 Neurogenic Hypertension 30 2.149
92
c CNG012 Congenital Generalized Lipodystrophy 50 2.144
93
ALP001 Alopecia Universalis 66 2.138
94
P ATM019 Autoimmune Polyendocrine Syndrome 46 2.136
95
MDL009 Medullary Sponge Kidney 55 2.133
96
HYP231 Hypothalamic Hamartomas 47 2.133
97
MNG006 Monogenic Diabetes 41 2.131
98
DBT008 Diabetic Angiopathy 55 2.130
99
ACT088 Acute Insulin Response 43 2.130
100
ARM001 Aromatase Deficiency 67 2.128
101
PNC053 Pancreatic Islet Cell Tumors 51 2.126
102
GRN022 Granulosa Cell Tumor of the Ovary 43 2.124
103
HYP226 Hyporeninemic Hypoaldosteronism 37 2.123
104
c ADL027 Adult Dermatomyositis 46 2.122
105
INS006 Insulin Autoimmune Syndrome 46 2.122
106
MND007 Mandibuloacral Dysplasia 66 2.119
107
MTR046 Maternally Inherited Diabetes and Deafness 58 2.115
108
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 2.114
109
SLN001 Silent Myocardial Infarction 30 2.113
110
FST010 Fasting Hypoglycemia 44 2.111
111
ALS001 Alstrom Syndrome 67 2.108
112
BRR012 Berardinelli-Seip Congenital Lipodystrophy 50 2.107
113
JHN001 Johanson-Blizzard Syndrome 54 2.106
114
PTT052 Pituitary Gigantism 45 2.105
115
SKN023 Skin Tag 47 2.103
116
ACR013 Acrodysostosis 57 2.100
117
P PNC045 Pancreatic Agenesis 56 2.099
118
P SHR029 Short Syndrome 57 2.098
119
LPD008 Lipid Metabolism Disorder 47 2.098
120
SXL003 Sexual Disorder 37 2.095
121
P FML187 Familial Hypertension 34 2.094
122
P ATM025 Autoimmune Polyglandular Syndrome Type 2 37 2.091
123
CRB025 Carbohydrate Metabolic Disorder 23 2.091
124
c HRN019 Hair-an Syndrome 18 2.085
125
P ACQ022 Acquired Generalized Lipodystrophy 46 2.083
126
FBR065 Fibrocalculous Pancreatopathy 26 2.081
127
c ATM001 Autoimmune Polyendocrine Syndrome Type 2 21 2.079
128
EXR005 Exercise-Induced Hyperinsulinism 19 2.076
129
c HYP512 Hyperproinsulinemia, Familial 9 2.070
130
c INS002 in Situ Carcinoma 58 1.993
131
ART035 Arterial Calcification of Infancy 50 1.908
132
RFR007 Refractory Anemia with Excess Blasts in Transformation 19 1.903
133
MTH056 Methylmalonic Aciduria and Homocystinuria, Cblf Type 38 1.884
134
c MTH034 Methylmalonic Aciduria, Vitamin B12-Responsive, Due to Defect in Synthesis of Adenosylcobalamin, Cblb Complementation Type 19 1.883
135
STN011 Sting-Associated Vasculopathy with Onset in Infancy 9 1.883
136
PRN019 Perinatal Necrotizing Enterocolitis 35 1.880
137
c FML067 Familial Hyperthyroidism Due to Mutations in Tsh Receptor 15 1.878
138
c CNG411 Congenital Disorder of Glycosylation, Type in 38 1.876
139
c KDN012 Kidney Carcinoma in Situ 9 1.876
140
c INT019 Intestine Carcinoma in Situ 7 1.876
141
GRP002 Group B Strep Disease in Newborns 2 1.874
142
HRN007 Hearing Problems in Children 1 1.874
143
c LPC001 Lip Carcinoma in Situ 8 1.871
144
INT145 Intracranial Hemorrhage in Brain Cerebrovascular Malformations 30 1.868
145
c RCK006 Rickets Due to Defect in Vitamin D 25-Hydroxylation 19 1.868
146
IMM029 Immunodeficiency Due to Defect in Mapbp-Interacting Protein 12 1.868
147
RSP017 Response to Antiviral Treatment in Hepatitis C 11 1.868
148
INF009 Inflammatory Spondylopathy 7 1.868
149
UTR009 Uterus Carcinoma in Situ 6 1.868
150
IMM008 Immunodeficiency Due to Defect in Cd3-Gamma 6 1.868
151
MYC061 Myoclonic Epilepsy in Non-Progressive Encephalopathies 5 1.868
152
c ORL001 Oral Cavity Carcinoma in Situ 4 1.868
153
TBS007 T+b+ Severe Combined Deficiency of Adaptive Immunity Due to Mutation in the Ctps1 Gene 4 1.868
154
CRC002 Carcinoma Arising in Nasal Papillomatosis 4 1.868
155
c PHR001 Pharynx Carcinoma in Situ 3 1.868
156
P ECL001 Eclampsia 61 1.852
157
EST005 Esotropia 41 1.681
158
DBT004 Diabetic Polyneuropathy 51 1.663
159
ACT017 Acute Chest Syndrome 55 1.649
160
P DRV001 Dravet Syndrome 74 1.633
161
PYR004 Pyuria 28 1.629
162
P CNV004 Canavan Disease 67 1.617
163
BLP005 Blepharitis 47 1.616
164
LRY027 Laryngeal Papillomatosis 24 1.608
165
MYL003 Myeloid Sarcoma 55 1.600
166
BRR002 Barrett's Adenocarcinoma 32 1.600
167
TRD003 Taurodontism 34 1.593
168
CYS001 Cystic Fibrosis 100 1.592
169
NNT008 Neonatal Abstinence Syndrome 39 1.592
170
PLR001 Pleural Tuberculosis 54 1.591
171
TTR005 Tetrahydrobiopterin Deficiency 49 1.584
172
LBL001 Lobular Neoplasia 49 1.576
173
HJD001 Hajdu-Cheney Syndrome 48 1.576
174
P PRS049 Persistent Mullerian Duct Syndrome 48 1.564
175
P MYC023 Myoclonic Astatic Epilepsy 35 1.564
176
P NNN008 Noonan Syndrome 1 75 1.563
177
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 42 1.561
178
CHY002 Chylomicron Retention Disease 54 1.554
179
IRN004 Iron-Refractory Iron Deficiency Anemia 40 1.554
180
c EXD008 Exudative Vitreoretinopathy 1 45 1.550
181
ESP002 Esophageal Varix 41 1.550
182
PRG097 Paragangliomas 1, with or Without Deafness 40 1.550
183
BNT002 Bantu Siderosis 22 1.548
184
UVN001 Uv-Induced Skin Damage 21 1.545
185
PLM013 Pulmonary Immaturity 14 1.543
186
HMC023 Homocystinuria-Megaloblastic Anemia, Cbl E Type 27 1.542
187
ESN009 Eosinophil Peroxidase Deficiency 35 1.540
188
KYR001 Kyrle Disease 13 1.540
189
LRY022 Laryngoonychocutaneous Syndrome 34 1.538
190
c HMC035 Hemochromatosis, Type 4 34 1.538
191
ULC001 Ulceration of Vulva 16 1.536
192
c ALB017 Albinism, Oculocutaneous, Type Vi 22 1.534
193
PRN018 Paraneoplastic Polyneuropathy 17 1.534
194
SRC006 Sarcoid Meningitis 11 1.534
195
INT188 Intestinal Obstruction in the Newborn Due to Guanylate Cyclase 2c Deficiency 8 1.534
196
SNW001 Snowflake Vitreoretinal Degeneration 37 1.531
197
c MLN043 Melanoma, Cutaneous Malignant 8 36 1.531
198
PLM009 Pleomorphic Adenoma Carcinoma 14 1.531
199
ACT186 Acute Megakaryoblastic Leukemia in Down Syndrome 12 1.531
200
CMP052 Complication in Hemodialysis 7 1.531
201
BLD001 Bile Duct Carcinoma in Situ 7 1.531
202
c HYP488 Hypothyroidism Due to Deficient Transcription Factors Involved in Pituitary Development or Function 35 1.529
203
GLY058 Glycogen Storage Disease 0, Liver 20 1.529
204
INF021 Infant Gynecomastia 8 1.529
205
ICH027 Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin 7 1.529
206
PRM033 Paraomphalocele 7 1.529
207
ACH016 Achard Thiers Syndrome 6 1.529
208
BLR014 Bilirubin Induced Brain Injury in the Newborn 3 1.529
209
FCL024 Focal or Multifocal Malformations in Neuronal Migration 2 1.529
210
DNS002 Dens in Dente and Palatal Invaginations 1 1.529
211
c HMC017 Homocystinuria Due to Defect in Methylation Cbl E 1 1.529
212
c HMC018 Homocystinuria Due to Defect in Methylation Cbl G 1 1.529
213
BLC009 Bile Acid Synthesis Defect, Congenital, 4 28 1.526
214
SLC025 Selection of Therapeutic Option in Non-Small Cell Lung Carcinoma 23 1.526
215
BLM005 Bulimia Nervosa, Age of Onset of Weight Loss in 14 1.526
216
PLM015 Pulmonary Systemic Sclerosis 12 1.526
217
SYM015 Symptomatic Form of Coffin-Lowry Syndrome in Female Carriers 11 1.526
218
END012 Endometriosis in Scar of Skin 11 1.526
219
LMY009 Leiomyomatosis, Esophageal and Vulval, with Nephropathy 9 1.526
220
DFC003 Deficiency in Anterior Pituitary Function-Variable Immunodeficiency Syndrome 8 1.526
221
PSD098 Pseudohyperaldosteronism Type 2 8 1.526
222
PLZ009 Pelizaeus-Merzbacher Disease in Female Carriers 8 1.526
223
c SCN015 Scn1a-Related Severe Myoclonic Epilepsy in Infancy 7 1.526
224
SYM016 Symptomatic Form of Muscular Dystrophy of Duchenne and Becker in Female Carriers 7 1.526
225
P SYM020 Symptomatic Form of Hemophilia a in Female Carriers 6 1.526
226
c SYM021 Symptomatic Form of Hemophilia B in Female Carriers 6 1.526
227
RSS021 Resistance to Bleomycine in the Treatment of Testicular Cancer 6 1.526
228
c ANG059 Angelman Syndrome Due to Imprinting Defect in 15q11-Q13 5 1.526
229
INS022 in Situ Pulmonary Adenocarcinoma 5 1.526
230
SLC026 Selection of Therapeutic Option in Colorectal Cancer 5 1.526
231
ADN063 Adenovirus Infection in Immunocompromised Patients 4 1.526
232
BNG063 Benign Partial Epilepsy with Secondarily Generalized Seizures in Infancy 4 1.526
233
RCR023 Recurrent Hepatitis C Virus Induced Liver Disease in Liver Transplant Recipients 4 1.526
234
SCR032 Scarring in Glaucoma Filtration Surgical Procedures 4 1.526
235
CNG229 Congenital Deficiency in Alpha-Fetoprotein 3 1.526
236
GLL001 Gall Bladder Carcinoma in Situ 3 1.526
237
PLM110 Poliomyelitis in Patients with Immunodeficiencies Deemed at Risk 3 1.526
238
RTN007 Retinal Dystrophy in Systemic or Cerebroretinal Lipidoses 3 1.526
239
HGH022 High-Grade Dysplasia in Patients with Barrett Esophagus 2 1.526
240
PLM107 Pulmonary Fungal Infections in Patients Deemed at Risk 2 1.526
241
APP014 Appendix: About Genomic Databases Listed in Genereviews 1 1.526
242
P DND019 Dend Syndrome 35 1.509
243
MTR048 Maturity-Onset Diabetes of the Young Type10 4 1.464
244
PRP016 Paraplegia 46 1.323
245
AVN001 Avian Influenza 50 1.282
246
P QFV001 Q Fever 56 1.270
247
PCK002 Pick Disease 72 1.268
248
P SDD001 Sudden Infant Death Syndrome 71 1.258
249
DXT001 Dextrocardia 43 1.243
250
c VRL007 Viral Encephalitis 64 1.196
251
P ALX003 Alexander Disease 76 1.185
252
P FCS002 Fucosidosis 68 1.179
253
STS003 Sitosterolemia 65 1.150
254
CNG105 Congenital Lobar Emphysema 39 1.145
255
KSH001 Keshan Disease 42 1.137
256
VLV042 Vulvar Vestibulitis Syndrome 46 1.128
257
PLV001 Pelvic Lipomatosis 34 1.124
258
P HYP607 Hypercholesterolemia, Familial 80 1.114
259
P JRV003 Jervell and Lange-Nielsen Syndrome 52 1.114
260
c NML015 Nemaline Myopathy 3, Autosomal Dominant or Recessive 36 1.112
261
URT011 Urethral Calculus 21 1.112
262
P STS008 Sotos Syndrome 1 53 1.110
263
c USH032 Usher Syndrome, Type 2a 53 1.109
264
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 44 1.108
265
c GRS013 Griscelli Syndrome, Type 1 32 1.108
266
CRN239 Carnitine Deficiency, Systemic Primary 45 1.107
267
MTC056 Mitochondrial Dna Depletion Syndrome 4a 42 1.105
268
GRS011 Gerstmann-Straussler Disease 34 1.104
269
YCH001 Y Chromosome Infertility 30 1.104
270
LCH008 Lichen Planus Pigmentosus 25 1.104
271
BHR001 Behr Syndrome 28 1.102
272
HMC033 Homocystinuria-Megaloblastic Anemia, Cblg Complementation Type 24 1.101
273
c LKM061 Leukemia, Acute Myeloid 75 1.099
274
HMG006 Hmg-Coa Lyase Deficiency 41 1.099
275
HYP322 Hypoaldosteronism, Congenital, Due to Cmo I Deficiency 30 1.099
276
HTR005 Heterochromia Iridis 18 1.099
277
BRT013 Baritosis 16 1.099
278
c HMC010 Hemochromatosis, Type 3 42 1.097
279
NRD015 Neurodegeneration with Brain Iron Accululation 5 29 1.095
280
SCH027 Schizotaxia 8 1.093
281
c RTN058 Retinitis Pigmentosa 3 44 1.091
282
c NML014 Nemaline Myopathy 1, Autosomal Dominant or Recessive 32 1.091
283
MLG120 Malignant Migrating Partial Seizures of Infancy 23 1.091
284
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 37 1.089
285
MTH021 Methylmalonic Acidemia with Homocystinuria 30 1.089
286
c MLG132 Malignant Hyperthermia Susceptibility 1 32 1.086
287
ANS012 Anus Disease 23 1.086
288
GRW003 Growth Hormone Insensitivity with Immunodeficiency 23 1.086
289
RST020 Restless Legs Syndrome 6 13 1.086
290
PLM129 Pulmonary Disease, Chronic Obstructive 54 1.083
291
c NML009 Nemaline Myopathy 2, Autosomal Recessive 29 1.083
292
c NML017 Nemaline Myopathy 4, Autosomal Dominant 27 1.083
293
MTH024 Methylmalonicacidemia with Homocystinuria Cbl D 24 1.083
294
CRM007 Crome Syndrome 18 1.083
295
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 15 1.083
296
KCH001 Kocher-Debre-Semelaigne Syndrome 12 1.083
297
ARN001 Arena Syndrome 5 1.083
298
c CTR025 Cataract, Total Congenital 30 1.079
299
NML020 Nemaline Myopathy 5, Amish Type 27 1.079
300
FBR026 Fibromatosis Multiple Non Ossifying 21 1.079
301
KRT023 Keratoderma Palmoplantaris Transgrediens 19 1.079
302
STR032 Steroid Dehydrogenase Deficiency Dental Anomalies 18 1.079
303
P HYP211 Hypomagnesemia Primary 16 1.079
304
TRC057 Trichoodontoonychial Dysplasia 13 1.079
305
IMM085 Immunodeficiency 25 12 1.079
306
ECT009 Ectopia Pupillae 10 1.079
307
MTH057 Methylmalonic Acidemia with Homocystinuria, Type Cblj 10 1.079
308
HYP500 Hyperphalangy, Unilateral 8 1.079
309
BNG074 Benign Familial Nocturnal Alternating Hemiplegia of Childhood 8 1.079
310
MTH058 Methylmalonic Acidemia with Homocystinuria, Type Cblx 8 1.079
311
KRN006 Karandikar Maria Kamble Syndrome 6 1.079
312
BSN001 Basan Syndrome 6 1.079
313
RVL001 Ruvalcaba Churesigaew Myhre Syndrome 5 1.079
314
c RDL013 Radio-Ulnar Synostosis Type 2 4 1.079
315
THL008 Thalamic Degeneration, Symmetric Infantile 4 1.079
316
CRD031 Cardiomyopathy, Fatal Fetal, Due to Myocardial Calcification 3 1.079
317
INF051 Infantile Recurrent Chronic Multifocal Osteomyolitis 3 1.079
318
PRM053 Primary Release Disorder of Platelets 3 1.079
319
P LKM002 Leukemia 76 0.687
320
END072 Endotheliitis 51 0.650
321
P HPT021 Hepatitis 63 0.629
322
PRS047 Prostatitis 58 0.587
323
NRN002 Neuronitis 42 0.553
324
P PNC044 Pancreatitis 68 0.498
325
P THY032 Thyroiditis 65 0.491
326
P ART022 Arthritis 74 0.488
327
CRB009 Cerebritis 37 0.476
328
P PRS040 Prostate Cancer 97 0.463
329
P ADN016 Adenocarcinoma 57 0.463
330
MLN008 Melanoma 63 0.424
331
RTN023 Retinitis 51 0.415
332
P CLR023 Colorectal Cancer 95 0.410
333
P RHM011 Rheumatoid Arthritis 96 0.409
334
P CRV039 Cervicitis 56 0.388
335
HPT023 Hepatocellular Carcinoma 100 0.371
336
P SCH015 Schizophrenia 88 0.364
337
P ESP024 Esophagitis 62 0.351
338
P MYC007 Myocardial Infarction 93 0.347
339
TBR010 Tuberculosis 84 0.336
340
P LPS004 Lupus Erythematosus 76 0.335
341
ISC004 Ischemia 61 0.330
342
P NRP001 Neuropathy 60 0.324
343
c HPT001 Hepatitis C 65 0.322
344
P BLN003 Blindness 54 0.316
345
HYP266 Hypoxia 57 0.315
346
c SYS001 Systemic Lupus Erythematosus 92 0.309
347
SRC014 Sarcoma 68 0.307
348
ADN018 Adenoma 64 0.305
349
ATH003 Atherosclerosis 65 0.298
350
P NRB001 Neuroblastoma 72 0.295
351
P PNM007 Pneumonia 76 0.290
352
ART111 Artery Disease 62 0.282
353
P MNN013 Meningitis 67 0.280
354
DMN002 Dementia 65 0.279
355
ANR040 Aneurysm 45 0.278
356
P MYL007 Myeloma 59 0.277
357
P RNL014 Renal Cell Carcinoma 83 0.275
358
PRT036 Peritonitis 71 0.272
359
DRM006 Dermatitis 67 0.270
360
P ENC004 Encephalitis 64 0.270
361
c HPT016 Hepatitis B 68 0.269
362
CLT003 Colitis 62 0.266
363
P PRD008 Periodontitis 68 0.260
364
MLR004 Malaria 84 0.259
365
HV1006 Hiv-1 79 0.256
366
P ATX004 Ataxia 58 0.256
367
P KDN018 Kidney Disease 64 0.255
368
P MSC005 Muscular Dystrophy 62 0.255
369
P PNC035 Pancreatic Cancer 95 0.254
370
P LVR013 Liver Disease 71 0.253
371
P LYM026 Lymphoblastic Leukemia 56 0.250
372
P CRN211 Coronary Artery Disease 77 0.249
373
c MLT019 Multiple Myeloma 85 0.244
374
P GLM007 Glomerulonephritis 67 0.241
375
P GLB002 Glioblastoma 67 0.237
376
P INF038 Influenza 68 0.236
377
SPS057 Spasticity 37 0.228
378
P INF037 Inflammatory Bowel Disease 44 0.227
379
c ACT075 Acute Myocardial Infarction 59 0.226
380
P BCL006 B-Cell Lymphomas 54 0.226
381
P CHR090 Chronic Lymphocytic Leukemia 81 0.226
382
INS024 Insulin-Like Growth Factor I 65 0.225
383
P LRY019 Laryngitis 63 0.221
384
CRH001 Crohn's Disease 75 0.219
385
c HPT073 Hepatitis C Virus 59 0.219
386
GNG013 Gingivitis 60 0.219
387
P PSR002 Psoriasis 62 0.217
388
ULC004 Ulcerative Colitis 63 0.214
389
P THL005 Thalassemia 73 0.211
390
P INF032 Infertility 53 0.206
391
P END044 Endometriosis 68 0.203
392
P CTR002 Cataract 58 0.203
393
P RHN004 Rhinitis 62 0.203
394
P LTR001 Lateral Sclerosis 50 0.202
395
P MYP004 Myopathy 61 0.202
396
MYL009 Myelodysplastic Syndrome 75 0.200
397
P OST012 Osteoarthritis 79 0.197
398
P HYP086 Hypothyroidism 68 0.197
399
P ATP001 Atopic Dermatitis 66 0.196
400
P OST002 Osteoporosis 81 0.195
401
P PLM037 Pulmonary Hypertension 92 0.194
402
ORL015 Oral Squamous Cell Carcinoma 37 0.193
403
P AMY004 Amyloidosis 73 0.192
404
P DRR001 Diarrhea 50 0.190
405
PRP030 Purpura 63 0.189
406
URT001 Urethritis 54 0.189
407
LSH001 Leishmaniasis 72 0.186
408
P DYS154 Dystonia 60 0.186
409
P HRP006 Herpes Simplex 66 0.186
410
P RTN024 Retinoblastoma 86 0.186
411
P ATR011 Atrial Fibrillation 62 0.183
412
EPD016 Epidermolysis Bullosa 57 0.183
413
LVR012 Liver Cirrhosis 75 0.183
414
P THR014 Thrombocytopenia 69 0.183
415
P LPR003 Leprosy 81 0.182
416
CHR008 Choroiditis 52 0.181
417
MGR002 Migraine 75 0.180
418
P AST007 Astrocytoma 72 0.180
419
DWN001 Down Syndrome 59 0.180
420
P NPH012 Nephrotic Syndrome 68 0.180
421
P BPL003 Bipolar Disorder 75 0.179
422
P MST018 Mesothelioma 58 0.179
423
c ACT073 Acute Leukemia 55 0.179
424
BRN106 Burns 48 0.178
425
P PRP029 Porphyria 66 0.178
426
THY028 Thyroid Cancer 74 0.176
427
P HMP007 Hemophilia 64 0.175
428
P HYP069 Hyperparathyroidism 66 0.175
429
P CNJ013 Conjunctivitis 61 0.175
430
P HYD006 Hydrocephalus 65 0.174
431
P UVT001 Uveitis 64 0.174
432
NPH051 Nephritis 53 0.174
433
NSP002 Nasopharyngitis 46 0.174
434
VSC011 Vasculitis 65 0.174
435
ART016 Aortic Aneurysm 71 0.173
436
VGN023 Vaginitis 59 0.171
437
P SYP003 Syphilis 56 0.170
438
P PLY019 Polyneuropathy 60 0.169
439
P HYP061 Hypertrophic Cardiomyopathy 68 0.169
440
P MNT147 Mental Retardation 56 0.169
441
P DLT002 Dilated Cardiomyopathy 86 0.168
442
P NTR004 Neutropenia 65 0.168
443
P HMR012 Hemorrhagic Fever 56 0.167
444
CNG034 Congestive Heart Failure 77 0.166
445
P SCL016 Scleroderma 72 0.166
446
VSC007 Vascular Disease 67 0.165
447
SPN051 Spondylitis 56 0.165
448
BRN071 Brain Injury 57 0.164
449
P NRF002 Neurofibromatosis 79 0.164
450
P CND004 Candidiasis 61 0.164
451
PMP001 Pemphigus 59 0.164
452
P PRS038 Personality Disorder 57 0.164
453
ASP006 Aspergillosis 72 0.163
454
KRT004 Keratitis 69 0.163
455
HDG012 Hodgkin Lymphoma 86 0.162
456
P ALZ034 Alzheimer Disease 99 0.162
457
c PRC016 Pre-Eclampsia 67 0.162
458
CRB037 Cerebral Palsy 63 0.162
459
ACR007 Acromegaly 79 0.162
460
RHB003 Rhabdomyosarcoma 59 0.162
461
P GST044 Gastritis 65 0.162
462
P RTN008 Retinitis Pigmentosa 83 0.162
463
DFF005 Diffuse Large B-Cell Lymphoma 56 0.161
464
ALL003 Allergic Rhinitis 72 0.161
465
GRV001 Graves' Disease 63 0.161
466
SCH014 Schistosomiasis 68 0.161
467
P PLM036 Pulmonary Fibrosis 67 0.160
468
ESP021 Esophageal Cancer 76 0.160
469
GTR002 Goiter 61 0.159
470
P MYC008 Myocarditis 56 0.158
471
ALP008 Alopecia 58 0.157
472
ANR007 Anorexia Nervosa 71 0.156
473
SCK005 Sickle Cell Disease 61 0.156
474
P PYL005 Pyelonephritis 50 0.156
475
P TCL004 T-Cell Leukemia 50 0.155
476
PRT039 Proteinuria 50 0.155
477
P SLP006 Sleep Apnea 57 0.155
478
OTT002 Otitis Media 58 0.154
479
P TRT010 Teratoma 57 0.154
480
c ACT027 Acute Pancreatitis 63 0.154
481
END057 Endometrial Cancer 80 0.154
482
PLM001 Pulmonary Tuberculosis 59 0.153
483
PTT006 Pituitary Adenoma 60 0.153
484
P CLC005 Celiac Disease 79 0.152
485
CHL068 Cholestasis 58 0.152
486
P TXP001 Toxoplasmosis 65 0.151
487
P OPN001 Open-Angle Glaucoma 59 0.151
488
P TBR001 Tuberous Sclerosis 78 0.150
489
P MYT002 Myotonic Dystrophy 65 0.150
490
P ESN007 Eosinophilia 62 0.150
491
P MDL005 Medulloblastoma 81 0.150
492
HDC001 Headache 57 0.149
493
ATT013 Attention Deficit-Hyperactivity Disorder 62 0.149
494
NSP012 Nasopharyngeal Carcinoma 48 0.148
495
GRW007 Growth Hormone Deficiency 52 0.147
496
CHL065 Cholangiocarcinoma 68 0.147
497
c BSL007 Basal Cell Carcinoma 66 0.147
498
P END033 Endocarditis 55 0.145
499
FTT001 Fatty Liver Disease 45 0.144
500
P PNC025 Panic Disorder 72 0.144
501
P HMC003 Hemochromatosis 86 0.143
502
HMT018 Hematopoietic Stem Cell Transplantation 41 0.143
503
P MYS005 Myositis 71 0.143
504
P PHC003 Pheochromocytoma 88 0.143
505
P PRM006 Primary Biliary Cirrhosis 66 0.143
506
P MYS003 Myasthenia Gravis 72 0.143
507
ANX002 Anxiety Disorder 67 0.142
508
P WLM002 Wilms Tumor 71 0.141
509
SPN186 Spinal Cord Injury 62 0.141
510
P OST005 Osteogenesis Imperfecta 85 0.141
511
ACQ007 Acquired Immunodeficiency Syndrome 51 0.141
512
P MSC003 Muscular Atrophy 51 0.140
513
P MCP010 Mucopolysaccharidosis 64 0.140
514
PPL022 Papilloma 64 0.140
515
P PLY014 Polycystic Kidney Disease 61 0.139
516
BRN002 Bronchiolitis 59 0.139
517
MSL001 Measles 67 0.139
518
TRN018 Transitional Cell Carcinoma 62 0.138
519
P HYP080 Hypogonadism 58 0.138
520
ECH003 Echinococcosis 58 0.137
521
P CHL066 Cholangitis 52 0.137
522
c VRL010 Viral Hepatitis 63 0.137
523
TRM010 Traumatic Brain Injury 54 0.136
524
P ANT006 Antiphospholipid Syndrome 64 0.136
525
TMP001 Temporal Lobe Epilepsy 56 0.136
526
P TRM003 Tremor 56 0.136
527
P SNS014 Sinusitis 56 0.135
528
c MLG068 Malignant Glioma 67 0.135
529
CYT008 Cytomegalovirus Infection 43 0.135
530
ORL011 Oral Cancer 53 0.135
531
P HYP076 Hyperthyroidism 62 0.134
532
LCH002 Lichen Planus 60 0.134
533
KWS002 Kawasaki Disease 75 0.134
534
c ATM003 Autoimmune Thyroiditis 64 0.133
535
LMY002 Leiomyoma 68 0.133
536
P HYP004 Hypercalcemia 66 0.133
537
P ABD003 Abdominal Aortic Aneurysm 67 0.133
538
P MLT074 Multiple Endocrine Neoplasia 61 0.132
539
ALC007 Alcohol Dependence 68 0.132
540
SPT005 Spotted Fever 52 0.132
541
P PLY018 Polycythemia 59 0.132
542
DCH001 Duchenne Muscular Dystrophy 80 0.132
543
P HML002 Hemolytic Anemia 65 0.131
544
URT039 Urticaria 63 0.131
545
P RBL001 Rubella 62 0.131
546
ATP002 Atopy 63 0.131
547
P PSR001 Psoriatic Arthritis 58 0.131
548
OBS061 Obstructive Sleep Apnea 56 0.131
549
OBS002 Obsessive-Compulsive Disorder 77 0.130
550
P SPN049 Spinocerebellar Ataxia 55 0.130
551
P APL001 Aplastic Anemia 86 0.130
552
ART021 Arteriosclerosis 66 0.130
553
P DRM010 Dermatomyositis 71 0.129
554
ISC006 Ischemic Heart Disease 59 0.129
555
CNN005 Connective Tissue Disease 58 0.129
556
P ATS007 Autism Spectrum Disorder 59 0.129
557
GST019 Gastrointestinal Stromal Tumor 84 0.129
558
P DBT005 Diabetes Insipidus 57 0.128
559
P SPN046 Spinal Muscular Atrophy 66 0.128
560
PRT037 Pertussis 61 0.127
561
KRT006 Keratoconjunctivitis 56 0.127
562
MRF001 Marfan Syndrome 86 0.127
563
GST045 Gastroenteritis 52 0.127
564
CLF001 Cleft Lip 59 0.127
565
PLM074 Pulmonary Function 35 0.127
566
LPS007 Lupus Nephritis 51 0.126
567
PHN003 Phenylketonuria 83 0.126
568
P RSP003 Respiratory Failure 68 0.126
569
HYP037 Hyperhomocysteinemia 51 0.125
570
SCK003 Sickle Cell Anemia 79 0.125
571
PRD007 Periodontal Disease 54 0.125
572
PRP023 Peripheral Neuropathy 51 0.124
573
GST040 Gastric Adenocarcinoma 39 0.124
574
P LNG028 Long Qt Syndrome 71 0.124
575
MDS022 Mediastinitis 45 0.124
576
P PRD006 Prader-Willi Syndrome 73 0.124
577
MNT001 Mantle Cell Lymphoma 63 0.124
578
STM007 Stomatitis 49 0.124
579
PLS007 Plasmodium Falciparum Malaria 56 0.124
580
P RTT002 Rett Syndrome 84 0.124
581
GLM011 Glomerulosclerosis 46 0.124
582
P HMN010 Hemangioma 69 0.123
583
P CHR071 Charcot-Marie-Tooth Disease 69 0.123
584
PLM033 Pulmonary Embolism 66 0.123
585
BCT015 Bacteremia 53 0.123
586
P HST010 Histiocytosis 62 0.123
587
SYN007 Synovitis 58 0.123
588
P MYL005 Myelofibrosis 78 0.123
589
P PRT013 Portal Hypertension 66 0.123
590
MLT021 Multiple System Atrophy 80 0.123
591
VSC003 Visceral Leishmaniasis 58 0.123
592
TTH006 Tooth Disease 53 0.122
593
P CYS018 Cystitis 50 0.122
594
P GLY013 Glycogen Storage Disease 59 0.122
595
SFT003 Soft Tissue Sarcoma 48 0.122
596
AZS001 Azoospermia 47 0.122
597
RHM027 Rheumatic Disease 48 0.122
598
SVR004 Severe Combined Immunodeficiency 77 0.122
599
ALL006 Allergic Asthma 53 0.121
600
c PRM005 Primary Hyperparathyroidism 66 0.121
601
CHR012 Chronic Granulomatous Disease 74 0.121
602
ATN004 Autonomic Neuropathy 48 0.121
603
P HYP117 Hypertriglyceridemia 71 0.120
604
TYP011 Typhus 55 0.120
605
ANG054 Angina Pectoris 44 0.120
606
P MYP006 Myopia 47 0.120
607
RLP002 Relapsing-Remitting Multiple Sclerosis 45 0.120
608
P CSH001 Cushing's Syndrome 85 0.119
609
IRR002 Irritable Bowel Syndrome 64 0.119
610
P TRN020 Turner Syndrome 67 0.119
611
TTN003 Tetanus 64 0.119
612
P EHL001 Ehlers-Danlos Syndrome 64 0.119
613
URM002 Uremia 55 0.119
614
NRT004 Neuritis 48 0.119
615
NRL016 Neural Tube Defects 79 0.118
616
P MST009 Mastocytosis 70 0.118
617
c HPT003 Hepatitis a 58 0.118
618
FSC004 Fasciitis 45 0.118
619
MYC033 Myoclonus 45 0.118
620
P FRG001 Fragile X Syndrome 75 0.118
621
CTN007 Cutaneous Leishmaniasis 55 0.118
622
BRN024 Bronchitis 66 0.118
623
P RTN022 Retinal Vein Occlusion 55 0.117
624
PLM031 Poliomyelitis 52 0.117
625
FLL037 Follicular Lymphoma 57 0.117
626
FBR047 Fibromyalgia 49 0.117
627
APH002 Aphasia 41 0.117
628
P ATX030 Ataxia-Telangiectasia 86 0.117
629
PHR003 Pharyngitis 65 0.117
630
P RTN016 Retinal Degeneration 44 0.117
631
P DDN001 Duodenal Ulcer 60 0.117
632
PNM008 Pneumothorax 48 0.117
633
CRB004 Cerebral Artery Occlusion 42 0.117
634
P THR015 Thrombophilia 66 0.117
635
P LKD001 Leukodystrophy 52 0.116
636
TNS005 Tonsillitis 56 0.116
637
CLN015 Colon Adenocarcinoma 50 0.116
638
ACN011 Acne 61 0.116
639
CHR074 Choriocarcinoma 59 0.116
640
PLY001 Polycythemia Vera 85 0.115
641
CHG001 Chagas Disease 62 0.115
642
RTN017 Retinal Detachment 55 0.115
643
CMM004 Common Variable Immunodeficiency 77 0.115
644
c HMP029 Hemophilia a 68 0.115
645
c ACT004 Acute Diarrhea 43 0.115
646
P CHN012 Chondrosarcoma 63 0.115
647
P CRT072 Creutzfeldt-Jakob Disease 74 0.115
648
ETN001 Eating Disorder 56 0.115
649
INT066 Interstitial Lung Disease 51 0.115
650
P PRC019 Precocious Puberty 60 0.115
651
HRP004 Herpes Zoster 56 0.115
652
P RCK004 Rickets 67 0.115
653
P ESS003 Essential Thrombocythemia 75 0.114
654
CHL014 Cholera 64 0.114
655
DFC004 Deficiency Anemia 61 0.114
656
OST017 Osteomyelitis 57 0.114
657
DNT012 Dental Caries 48 0.114
658
CRN025 Corneal Dystrophy 45 0.114
659
NRN004 Neuroendocrine Tumor 58 0.114
660
TTR001 Tetralogy of Fallot 76 0.114
661
CHL067 Cholecystitis 59 0.114
662
LRY018 Laryngeal Squamous Cell Carcinoma 56 0.114
663
NPH017 Nephrosis 42 0.114
664
ATN005 Autonomic Dysfunction 45 0.114
665
CHR066 Chronic Fatigue Syndrome 65 0.113
666
ALB002 Albinism 50 0.113
667
MTH009 Mouth Disease 49 0.113
668
FBR012 Fabry Disease 86 0.113
669
CRB039 Cerebrovascular Disease 66 0.113
670
BCK006 Back Pain 38 0.113
671
SNS001 Sensorineural Hearing Loss 55 0.113
672
SCR011 Scrapie 43 0.112
673
IRN001 Iron Deficiency Anemia 55 0.112
674
PRS039 Prostate Adenocarcinoma 40 0.112
675
DSS009 Disseminated Intravascular Coagulation 60 0.112
676
BRN056 Bronchopulmonary Dysplasia 57 0.112
677
c BCT007 Bacterial Meningitis 49 0.112
678
c NRF018 Neurofibromatosis, Type 1 73 0.112
679
STT001 Status Epilepticus 64 0.112
680
GST023 Gastric Ulcer 65 0.112
681
P ANG015 Angioedema 60 0.112
682
P GT001 Gout 65 0.111
683
SYS003 Systolic Heart Failure 36 0.111
684
P LRY016 Laryngeal Carcinoma 59 0.111
685
P SCL009 Sclerosing Cholangitis 47 0.111
686
WST005 West Nile Virus 47 0.111
687
GST092 Gastroesophageal Reflux 60 0.111
688
P PMP005 Pemphigus Vulgaris 54 0.111
689
BRC012 Brucellosis 60 0.111
690
BLR001 Biliary Atresia 58 0.111
691
c ATM011 Autoimmune Hepatitis 59 0.111
692
c CNG006 Congenital Hypothyroidism 69 0.111
693
c HPT007 Hepatitis E 52 0.111
694
PLR008 Pleurisy 46 0.111
695
DBT010 Diabetic Neuropathy 59 0.110
696
CRY003 Cryptosporidiosis 63 0.110
697
c BPL002 Bipolar I Disorder 38 0.110
698
PNC041 Pancreatic Ductal Adenocarcinoma 34 0.110
699
PTT037 Pituitary Tumors 53 0.110
700
VSC002 Vascular Dementia 55 0.110
701
CNS004 Constipation 52 0.110
702
MDD011 Mood Disorder 52 0.110
703
P CNG401 Congenital Heart Disease 70 0.110
704
P STM004 Stomach Cancer 68 0.110
705
HPT022 Hepatoblastoma 61 0.109
706
APP008 Appendicitis 55 0.109
707
P CNG368 Congenital Adrenal Hyperplasia 74 0.109
708
CHL069 Cholesteatoma 52 0.109
709
CNT047 Contact Dermatitis 54 0.109
710
END041 Endometrial Adenocarcinoma 49 0.109
711
HYP043 Hyperandrogenism 48 0.109
712
CRV045 Cervical Intraepithelial Neoplasia 45 0.109
713
ANX004 Anoxia 36 0.109
714
P DYS005 Dyslexia 36 0.109
715
c ACT134 Acute Liver Failure 55 0.109
716
P LYN001 Lynch Syndrome 76 0.109
717
OCL006 Ocular Hypertension 54 0.109
718
HMG002 Hemoglobinuria 50 0.109
719
PRT038 Protein-Energy Malnutrition 46 0.109
720
ECT006 Ectodermal Dysplasia 56 0.109
721
LMB062 Limb Ischemia 45 0.109
722
BCT004 Bacteriuria 58 0.108
723
P NRC002 Narcolepsy 78 0.108
724
INS001 Insulinoma 57 0.108
725
c ADL017 Adult T-Cell Leukemia 46 0.108
726
P ANP001 Anaplastic Large Cell Lymphoma 62 0.108
727
SKN016 Skin Disease 73 0.108
728
P ART023 Arthropathy 62 0.108
729
FLR002 Filariasis 57 0.108
730
ORL013 Oral Lichen Planus 41 0.108
731
BLL006 Bullous Pemphigoid 69 0.108
732
RNL015 Renal Hypertension 58 0.108
733
CRY002 Cryptorchidism 65 0.108
734
P CNG015 Congenital Diaphragmatic Hernia 65 0.108
735
TST014 Testicular Cancer 60 0.108
736
CRY004 Cryoglobulinemia 57 0.107
737
GLB015 Glioblastoma Multiforme 56 0.107
738
DYS014 Dyspepsia 52 0.107
739
P CTN015 Cutaneous T Cell Lymphoma 51 0.107
740
KWS001 Kwashiorkor 47 0.107
741
BRN022 Bronchiectasis 61 0.107
742
LPT001 Leptospirosis 52 0.107
743
BLM002 Bulimia Nervosa 56 0.107
744
CCC002 Coccidiosis 32 0.107
745
PLG002 Plague 54 0.107
746
ADN002 Adenoiditis 36 0.107
747
ONC002 Onchocerciasis 51 0.107
748
MST005 Mastitis 48 0.107
749
HDN002 Head Injury 48 0.107
750
RST001 Restless Legs Syndrome 57 0.106
751
HPT019 Hepatic Encephalopathy 55 0.106
752
OBS006 Obstructive Lung Disease 51 0.106
753
BRN080 Brain Ischemia 50 0.106
754
c JVN010 Juvenile Rheumatoid Arthritis 60 0.106
755
SPS019 Spastic Paraparesis 41 0.106
756
EYD002 Eye Disease 61 0.106
757
MLG056 Malignant Hyperthermia 69 0.106
758
P FBR017 Fibrosarcoma 60 0.106
759
HMP005 Hemiplegia 51 0.106
760
P KRT007 Keratoconus 52 0.106
761
P CHR345 Chronic Pain 46 0.106
762
P VNT002 Ventricular Septal Defect 55 0.106
763
LKP003 Leukoplakia 46 0.106
764
CLR030 Clear Cell Renal Cell Carcinoma 44 0.105
765
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.105
766
MLN007 Male Infertility 52 0.105
767
FCL014 Focal Epilepsy 44 0.105
768
HST011 Histoplasmosis 73 0.105
769
P HYP014 Hyperuricemia 54 0.105
770
FDL002 Food Allergy 51 0.105
771
P NRM001 Neuromyelitis Optica 59 0.105
772
P HML001 Hemolytic-Uremic Syndrome 50 0.105
773
ALL014 Allergic Encephalomyelitis 41 0.105
774
P BRG001 Brugada Syndrome 64 0.104
775
OST003 Osteonecrosis 57 0.104
776
STS002 Situs Inversus 53 0.104
777
SLC006 Silicosis 57 0.104
778
ART005 Arteriovenous Malformation 61 0.104
779
PNM013 Pneumococcal Meningitis 54 0.104
780
BRD004 Borderline Personality Disorder 46 0.104
781
CRY005 Cryptococcosis 67 0.104
782
TYP007 Typhoid Fever 61 0.104
783
P MMP001 Mumps 58 0.104
784
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 58 0.104
785
TCK001 Tick-Borne Encephalitis 52 0.104
786
PRC013 Pericarditis 52 0.104
787
c ACT042 Acute Pyelonephritis 41 0.104
788
P NRN021 Neuronal Ceroid Lipofuscinosis 63 0.103
789
RBS001 Rabies 57 0.103
790
DPH001 Diphtheria 56 0.103
791
P VSC005 Vesicoureteral Reflux 53 0.103
792
TRN044 Transposition of the Great Arteries 48 0.103
793
KLD001 Keloids 36 0.103
794
P HRD008 Hereditary Hemorrhagic Telangiectasia 79 0.103
795
ACH004 Achondroplasia 78 0.103
796
MCR004 Macroglobulinemia 53 0.103
797
AMB002 Amblyopia 46 0.103
798
WLS001 Wilson Disease 82 0.103
799
P LPS002 Liposarcoma 64 0.103
800
P INT001 Intrahepatic Cholestasis 63 0.103
801
DYS073 Dysphagia 51 0.103
802
PLY041 Polymyositis 59 0.103
803
P MYM002 Moyamoya Disease 59 0.103
804
GNR004 Generalized Anxiety Disorder 56 0.102
805
BRN004 Brain Edema 52 0.102
806
MTR014 Motor Neuron Disease 61 0.102
807
KRT009 Keratosis 48 0.102
808
P ALP009 Alopecia Areata 63 0.102
809
MRB003 Morbid Obesity 55 0.102
810
P PRG013 Paraganglioma 54 0.102
811
TNC002 Tinea Capitis 48 0.102
812
P CRN037 Craniosynostosis 69 0.102
813
P LCT001 Lactic Acidosis 48 0.102
814
P MTR012 Mitral Valve Disease 60 0.102
815
INV001 Invasive Aspergillosis 51 0.101
816
P SHR001 Short Bowel Syndrome 52 0.101
817
AND015 Androgen Insensitivity 78 0.101
818
P THY023 Thymoma 66 0.101
819
P HRD011 Hereditary Spherocytosis 64 0.101
820
PLM012 Pulmonary Sarcoidosis 52 0.101
821
ADR007 Adrenoleukodystrophy 81 0.101
822
c HMP004 Hemophilia B 80 0.101
823
DRM011 Dermatophytosis 46 0.101
824
P HYP040 Hypospadias 62 0.101
825
THR035 Thrombasthenia 43 0.101
826
THR004 Thrombocytosis 59 0.101
827
MYC006 Mycosis Fungoides 72 0.101
828
MNN009 Meningoencephalitis 45 0.101
829
P FCL005 Focal Segmental Glomerulosclerosis 68 0.101
830
PST028 Post-Traumatic Stress Disorder 66 0.101
831
MTB004 Metabolic Acidosis 44 0.101
832
CRT049 Critical Limb Ischemia 50 0.100
833
BTL001 Botulism 59 0.100
834
VRC001 Varicocele 48 0.100
835
CDS001 Cadasil 81 0.100
836
RHM001 Rheumatic Fever 66 0.100
837
MYL020 Myelomeningocele 62 0.100
838
OPT009 Optic Neuritis 49 0.100
839
c ESS001 Essential Tremor 70 0.100
840
TRC008 Trachoma 68 0.100
841
LYM019 Lymphosarcoma 57 0.100
842
P PNM006 Pneumoconiosis 49 0.100
843
LPR001 Lepromatous Leprosy 49 0.100
844
LYM021 Lymphadenitis 45 0.100
845
P ALP004 Alport Syndrome 69 0.099
846
PTN002 Patent Ductus Arteriosus 57 0.099
847
WLF001 Wolff-Parkinson-White Syndrome 74 0.099
848
SHG001 Shigellosis 65 0.099
849
NWC001 Newcastle Disease 53 0.099
850
WLL004 Wallerian Degeneration 45 0.099
851
c MLG079 Malignant Pleural Mesothelioma 44 0.099
852
CYT005 Cytomegalovirus Retinitis 56 0.099
853
CHR005 Chorioamnionitis 49 0.099
854
SLP001 Sleeping Sickness 56 0.099
855
PRG009 Progressive Multifocal Leukoencephalopathy 52 0.099
856
P GND004 Gonadal Dysgenesis 49 0.099
857
JPN002 Japanese Encephalitis 54 0.099
858
P HYP020 Hyperprolactinemia 66 0.099
859
HPR003 Heparin-Induced Thrombocytopenia 53 0.099
860
SYN036 Syncope 43 0.099
861
SMN007 Seminoma 47 0.098
862
VCC001 Vaccinia 47 0.098
863
RFR003 Refractive Error 47 0.098
864
NRM002 Normal Pressure Hydrocephalus 64 0.098
865
P LMY004 Leiomyosarcoma 61 0.098
866
P OPH004 Ophthalmoplegia 54 0.098
867
CHL004 Cholelithiasis 47 0.098
868
P AGG001 Aggressive Periodontitis 45 0.098
869
CLR109 Colorectal Adenocarcinoma 32 0.098
870
P ALC004 Alcohol Abuse 51 0.098
871
INT075 Intracranial Hypertension 50 0.098
872
P PRM019 Premature Ovarian Failure 69 0.098
873
PPL002 Papillary Carcinoma 56 0.098
874
HYP024 Hypoparathyroidism 56 0.098
875
P LYM025 Lymphedema 52 0.098
876
NRM005 Neuromuscular Disease 50 0.098
877
URT010 Ureteral Obstruction 45 0.098
878
PLM034 Pulmonary Emphysema 55 0.098
879
P STR020 Strabismus 51 0.098
880
CYS008 Cystic Echinococcosis 73 0.098
881
CRD137 Cardiogenic Shock 48 0.098
882
P CMP010 Complex Regional Pain Syndrome 60 0.098
883
P ANG001 Angelman Syndrome 76 0.097
884
P NMN002 Niemann-Pick Disease 72 0.097
885
OVR029 Ovarian Hyperstimulation Syndrome 67 0.097
886
BBS001 Babesiosis 63 0.097
887
ALX002 Alexithymia 50 0.097
888
CND006 Candida Glabrata 43 0.097
889
P WSK001 Wiskott-Aldrich Syndrome 79 0.097
890
INT002 Intermittent Claudication 53 0.097
891
NPH003 Nephrocalcinosis 48 0.097
892
GRD001 Giardiasis 55 0.097
893
DWR001 Dwarfism 54 0.097
894
SBS003 Substance Abuse 48 0.097
895
TBR011 Tuberculous Meningitis 58 0.097
896
TRN015 Transient Cerebral Ischemia 51 0.097
897
BRN012 Bronchiolitis Obliterans 58 0.097
898
CYS010 Cystinosis 65 0.097
899
RFT001 Rift Valley Fever 55 0.097
900
P SCL018 Scoliosis 51 0.097
901
P DYS021 Dysautonomia 51 0.097
902
P NRL007 Neurologic Diseases 44 0.097
903
P END046 Endometritis 39 0.097
904
P AGM001 Agammaglobulinemia 60 0.096
905
CRP018 Cor Pulmonale 43 0.096
906
P MTC003 Metachromatic Leukodystrophy 87 0.096
907
SCL003 Social Phobia 60 0.096
908
NRC020 Neuroectodermal Tumor 58 0.096
909
ALL009 Allergic Conjunctivitis 46 0.096
910
P ATR005 Atrophic Gastritis 45 0.096
911
PTZ001 Peutz-Jeghers Syndrome 78 0.096
912
P HMP002 Hemophagocytic Lymphohistiocytosis 62 0.096
913
LYM027 Lymphopenia 50 0.096
914
CYS005 Cysticercosis 62 0.096
915
SCR008 Scrub Typhus 68 0.096
916
ALC006 Alcoholic Hepatitis 57 0.096
917
WBR001 Weber Syndrome 50 0.096
918
VNW001 Von Willebrand's Disease 76 0.096
919
APR001 Apraxia 44 0.096
920
BRN018 Borna Disease 49 0.096
921
P CLR108 Colorectal Adenoma 45 0.096
922
SPS007 Spastic Cerebral Palsy 43 0.096
923
P HYD002 Hydronephrosis 52 0.095
924
MXD005 Mixed Connective Tissue Disease 64 0.095
925
BCK001 Becker Muscular Dystrophy 62 0.095
926
AMN001 Amenorrhea 57 0.095
927
PRC002 Paracoccidioidomycosis 67 0.095
928
PRP027 Peripheral Vascular Disease 66 0.095
929
NRG002 Neurogenic Bladder 53 0.095
930
SPN019 Spondylolisthesis 52 0.095
931
DYS015 Dysentery 49 0.095
932
PYL006 Pyloric Stenosis 49 0.095
933
PRN023 Prion Disease 56 0.095
934
SBC001 Subacute Sclerosing Panencephalitis 54 0.095
935
P PRM002 Primary Hyperoxaluria 78 0.095
936
P HMC002 Homocystinuria 58 0.095
937
DNG002 Dengue Hemorrhagic Fever 47 0.095
938
P SPN052 Spondyloarthropathy 45 0.095
939
GNR005 Gonorrhea 58 0.094
940
GLC006 Galactosemia 85 0.094
941
CND002 Conduct Disorder 57 0.094
942
LST001 Listeriosis 56 0.094
943
DNT001 Dental Fluorosis 48 0.094
944
TRT001 Teratocarcinoma 41 0.094
945
P ADL010 Adult Respiratory Distress Syndrome 59 0.094
946
SCB001 Scabies 59 0.094
947
MLT006 Multidrug-Resistant Tuberculosis 53 0.094
948
PLY013 Polymyalgia Rheumatica 52 0.094
949
PLM010 Pulmonary Edema 47 0.094
950
SWN001 Swine Influenza 40 0.094
951
P CRB042 Cerebellar Ataxia 63 0.094
952
ILS001 Ileus 44 0.094
953
EPD046 Epididymitis 28 0.094
954
P NPH009 Nephrolithiasis 59 0.093
955
EHR002 Ehrlichiosis 52 0.093
956
BCT002 Bacterial Vaginosis 52 0.093
957
ADD001 Addison's Disease 73 0.093
958
BRS051 Breast Disease 50 0.093
959
ADN027 Adenomyosis 43 0.093
960
TRD006 Tardive Dyskinesia 54 0.093
961
CHL061 Childhood Leukemia 37 0.093
962
INT051 Intussusception 61 0.093
963
LNG024 Langerhans-Cell Histiocytosis 57 0.093
964
P FBR031 Febrile Seizures 54 0.093
965
TRY001 Trypanosomiasis 48 0.093
966
HYP017 Hypophosphatemia 47 0.093
967
P PSD015 Pseudohypoparathyroidism 54 0.093
968
ECT026 Ectopic Pregnancy 45 0.093
969
VLV010 Vulvovaginitis 45 0.093
970
P BCK002 Beckwith-Wiedemann Syndrome 71 0.092
971
LYM017 Lyme Disease 65 0.092
972
MYL001 Myelitis 53 0.092
973
OBS001 Obstructive Jaundice 49 0.092
974
MYT011 Myotonia 43 0.092
975
P OST001 Osteopetrosis 74 0.092
976
MLD001 Melioidosis 62 0.092
977
URN003 Urinary Schistosomiasis 58 0.092
978
RNL011 Renal Osteodystrophy 49 0.092
979
SPL018 Splenomegaly 46 0.092
980
STR008 Strongyloidiasis 65 0.092
981
RNL007 Renal Tubular Acidosis 56 0.092
982
PRP003 Porphyria Cutanea Tarda 78 0.092
983
MRK001 Merkel Cell Carcinoma 55 0.092
984
INC002 Inclusion Body Myositis 80 0.092
985
ARC002 Arachnoiditis 43 0.092
986
TRC003 Trichomoniasis 41 0.092
987
PRT018 Portal Vein Thrombosis 54 0.091
988
P HYP083 Hypopituitarism 54 0.091
989
c HYP163 Hyperlipidemia Type 3 28 0.091
990
MYS004 Myiasis 36 0.091
991
GST009 Gastroschisis 64 0.091
992
CLL003 Cellulitis 57 0.091
993
THY033 Thyrotoxicosis 57 0.091
994
P DMY001 Demyelinating Polyneuropathy 46 0.091
995
INF034 Infective Endocarditis 43 0.091
996
CRN030 Coronary Stenosis 42 0.091
997
ADG002 Audiogenic Seizures 32 0.091
998
SPT004 Septic Arthritis 52 0.091
999
KRT008 Keratopathy 49 0.091
1000
c CHR417 Chronic Graft Versus Host Disease 43 0.091
1001
P CRB019 Cerebral Amyloid Angiopathy 67 0.091
1002
PRT014 Protein S Deficiency 63 0.091
1003
STT002 Status Asthmaticus 60 0.091
1004
NRF007 Neurofibroma 57 0.091
1005
NCR004 Nocardiosis 54 0.091
1006
CHK001 Chikungunya 47 0.091
1007
PRT011 Protein C Deficiency 63 0.091
1008
P EPN002 Ependymoma 62 0.091
1009
P HYP055 Hypoplastic Left Heart Syndrome 68 0.090
1010
PLM014 Pleomorphic Adenoma 61 0.090
1011
GNG012 Gingival Overgrowth 51 0.090
1012
NRM004 Neuroma 46 0.090
1013
P OLG002 Oligodendroglioma 62 0.090
1014
PRL009 Prolactinoma 58 0.090
1015
END028 Endemic Goiter 46 0.090
1016
CHN015 Chondrodysplasia 43 0.090
1017
CRS001 Crescentic Glomerulonephritis 41 0.090
1018
MCR013 Microphthalmia 60 0.090
1019
PRS045 Prostatic Hypertrophy 35 0.090
1020
P INT030 Intracranial Aneurysm 55 0.090
1021
PRN011 Pernicious Anemia 53 0.090
1022
AGR002 Agoraphobia 50 0.090
1023
ASP003 Aseptic Meningitis 60 0.090
1024
P VNS003 Venous Insufficiency 46 0.090
1025
SPP008 Suppurative Otitis Media 40 0.090
1026
PLS006 Plasmodium Vivax Malaria 66 0.090
1027
P HYP065 Hyperaldosteronism 57 0.090
1028
P OTS001 Otosclerosis 53 0.090
1029
TLR001 Tularemia 52 0.090
1030
c MLG069 Malignant Hypertension 62 0.089
1031
YLL002 Yellow Fever 58 0.089
1032
P SYR001 Syringomyelia 57 0.089
1033
XNT003 Xanthomatosis 48 0.089
1034
HLL004 Hellp Syndrome 53 0.089
1035
ZLL002 Zollinger-Ellison Syndrome 65 0.089
1036
P DRM007 Dermatitis Herpetiformis 64 0.089
1037
ADR015 Adrenocortical Carcinoma 57 0.089
1038
P CRV043 Cervical Dystonia 54 0.089
1039
CLC006 Calcinosis 51 0.089
1040
PRP080 Peripheral Artery Disease 34 0.089
1041
RLP003 Relapsing Fever 48 0.089
1042
P TYS001 Tay-Sachs Disease 84 0.089
1043
ANR002 Aniridia 71 0.089
1044
ALL008 Allergic Bronchopulmonary Aspergillosis 66 0.089
1045
P RTN025 Retinoschisis 58 0.089
1046
P MCR010 Microcephaly 56 0.089
1047
TRP002 Tropical Spastic Paraparesis 53 0.089
1048
CRT016 Carotid Artery Disease 44 0.089
1049
ZYG002 Zygomycosis 44 0.089
1050
TKY001 Takayasu's Arteritis 69 0.089
1051
CHC001 Chickenpox 59 0.089
1052
OST016 Osteochondrosis 57 0.089
1053
P SCK002 Sick Sinus Syndrome 58 0.088
1054
FCL044 Fecal Incontinence 27 0.088
1055
P FRD001 Friedreich Ataxia 71 0.088
1056
CRN036 Craniopharyngioma 62 0.088
1057
P UVL004 Uveal Melanoma 61 0.088
1058
HYP025 Hyperphosphatemia 42 0.088
1059
CCC001 Coccidioidomycosis 71 0.088
1060
SLP005 Sleep Disorder 54 0.088
1061
VTM002 Vitamin B12 Deficiency 46 0.088
1062
BRS090 Breast Reconstruction 44 0.088
1063
ATS001 Autistic Disorder 69 0.088
1064
GLC085 Glucose-6-Phosphate Dehydrogenase Deficiency 65 0.088
1065
c SVR001 Severe Acute Respiratory Syndrome 58 0.088
1066
INT079 Intrahepatic Cholangiocarcinoma 38 0.088
1067
CRM001 Crimean-Congo Hemorrhagic Fever 54 0.088
1068
PRP036 Peripheral T-Cell Lymphoma 48 0.088
1069
CRT013 Carotid Stenosis 46 0.088
1070
PHC013 Phaeochromocytoma 40 0.088
1071
c HRD010 Hereditary Spastic Paraplegia 62 0.087
1072
CHR001 Churg-Strauss Syndrome 56 0.087
1073
c ANT034 Anterior Uveitis 51 0.087
1074
LCH009 Lichen Sclerosus 48 0.087
1075
c SYS004 Systemic Mastocytosis 65 0.087
1076
KLN001 Klinefelter's Syndrome 54 0.087
1077
P SPN183 Spontaneous Pneumothorax 52 0.087
1078
QDR001 Quadriplegia 42 0.087
1079
AST006 Astigmatism 41 0.087
1080
P GCH001 Gaucher's Disease 80 0.087
1081
P LYM007 Lymphangioleiomyomatosis 75 0.087
1082
P HLP001 Holoprosencephaly 75 0.087
1083
ANK001 Ankylosis 55 0.087
1084
P CYS017 Cystic Teratoma 42 0.087
1085
PLR005 Pleuropneumonia 42 0.087
1086
SMT004 Smith-Lemli-Opitz Syndrome 85 0.087
1087
c ATM010 Autoimmune Hemolytic Anemia 66 0.087
1088
ADL030 Adult-Onset Still's Disease 62 0.087
1089
AMB001 Amebiasis 59 0.087
1090
CCN001 Cocaine Dependence 53 0.087
1091
ALL010 Allergic Contact Dermatitis 53 0.087
1092
P CNT005 Central Nervous System Lymphoma 52 0.087
1093
TRC023 Trichinosis 39 0.087
1094
PTN001 Patent Foramen Ovale 60 0.087
1095
P KDN017 Kidney Cancer 59 0.087
1096
c CNG021 Congenital Toxoplasmosis 57 0.087
1097
c CNT016 Central Retinal Vein Occlusion 56 0.087
1098
ASB001 Asbestosis 49 0.087
1099
HMP009 Haemophilus Influenzae 41 0.087
1100
TPT001 Tauopathy 34 0.087
1101
P CYS013 Cystinuria 76 0.087
1102
MLT022 Malt Lymphoma 63 0.087
1103
ACH005 Achalasia 61 0.087
1104
RCT015 Reactive Arthritis 57 0.087
1105
PRC012 Pericardial Effusion 56 0.087
1106
c CNG124 Congenital Rubella 58 0.087
1107
P CRB059 Cerebellar Degeneration 33 0.087
1108
P MTH007 Methemoglobinemia 59 0.086
1109
ORL004 Oral Submucous Fibrosis 55 0.086
1110
DBT062 Diabetic Foot Ulcers 46 0.086
1111
CRT015 Carotid Artery Occlusion 43 0.086
1112
HPT004 Hepatic Coma 41 0.086
1113
CNT060 Central Serous Chorioretinopathy 40 0.086
1114
ART031 Aortic Coarctation 60 0.086
1115
CLS010 Cluster Headache 50 0.086
1116
c FML108 Familial Breast Cancer 34 0.086
1117
LKM006 Leukomalacia 31 0.086
1118
P PLM006 Pulmonary Alveolar Proteinosis 54 0.086
1119
ORC001 Orchitis 49 0.086
1120
P CRB088 Cerebral Atrophy 47 0.086
1121
RHN001 Rhinotracheitis 30 0.086
1122
LRN003 Learning Disability 61 0.086
1123
PTH002 Pathological Gambling 57 0.086
1124
P ACT135 Acute Graft Versus Host Disease 50 0.086
1125
RGH001 Right Bundle Branch Block 35 0.086
1126
c CHR285 Chronic Myelomonocytic Leukemia 55 0.086
1127
TXC011 Toxocariasis 49 0.086
1128
MMB001 Membranoproliferative Glomerulonephritis 48 0.086
1129
P CTN003 Cutaneous Lupus Erythematosus 47 0.086
1130
LKP004 Leukopenia 44 0.086
1131
LYM011 Lymphogranuloma Venereum 43 0.086
1132
P LMB006 Limb-Girdle Muscular Dystrophy 60 0.085
1133
DVL001 Developmental Coordination Disorder 29 0.085
1134
TXC005 Toxic Shock Syndrome 60 0.085
1135
PST041 Posterior Urethral Valves 56 0.085
1136
PRG004 Progeria 70 0.085
1137
ASP001 Asperger Syndrome 52 0.085
1138
HYP005 Hypokalemia 48 0.085
1139
CRB086 Cerebral Aneurysms 39 0.085
1140
RFR010 Refractory Anemia 50 0.085
1141
P PNC001 Pancytopenia 47 0.085
1142
WHP002 Whiplash 41 0.084
1143
c ALM001 Al Amyloidosis 65 0.084
1144
LYM040 Lymphoblastic Lymphoma 53 0.084
1145
ESP020 Esophageal Atresia 53 0.084
1146
EPG003 Epiglottitis 40 0.084
1147
RCK002 Rocky Mountain Spotted Fever 36 0.084
1148
LYM009 Lymphocytic Choriomeningitis 62 0.084
1149
P RTN014 Retinal Artery Occlusion 55 0.084
1150
P MNC007 Monocytic Leukemia 55 0.084
1151
HYP068 Hyperostosis 49 0.084
1152
ERY004 Erysipelas 49 0.084
1153
PMP004 Pemphigus Foliaceus 47 0.084
1154
c ACT076 Acute Myocarditis 46 0.084
1155
PRV004 Periventricular Leukomalacia 45 0.084
1156
KRT012 Keratoderma 45 0.084
1157
BLL003 Bell's Palsy 63 0.084
1158
HMR004 Hemorrhagic Fever with Renal Syndrome 60 0.084
1159
P HYP009 Hypertrophic Pyloric Stenosis 49 0.084
1160
MNN032 Meningococcal Meningitis 37 0.084
1161
P HYP035 Hypophosphatasia 74 0.083
1162
P END047 Endophthalmitis 59 0.083
1163
GST037 Gastroparesis 55 0.083
1164
MLL001 Molluscum Contagiosum 51 0.083
1165
STL001 St. Louis Encephalitis 50 0.083
1166
SCR002 Scurvy 59 0.083
1167
STN007 Stenotrophomonas Maltophilia 52 0.083
1168
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 51 0.083
1169
DVL002 Developmental Disabilities 39 0.083
1170
P OVR046 Ovarian Cyst 45 0.083
1171
HPT014 Hepatorenal Syndrome 55 0.083
1172
DRG011 Drug Addiction 51 0.083
1173
TND004 Tendinopathy 38 0.083
1174
TRP004 Tropical Sprue 36 0.083
1175
WRN001 Werner Syndrome 72 0.082
1176
ANN002 Anencephaly 65 0.082
1177
P HRP009 Herpes Simplex Encephalitis 64 0.082
1178
BRN029 Brain Disease 56 0.082
1179
BRN016 Bronchogenic Carcinoma 37 0.082
1180
P MCH002 Machado-Joseph Disease 70 0.082
1181
GLL018 Gallbladder Cancer 66 0.082
1182
P PRM011 Primary Ciliary Dyskinesia 59 0.082
1183
P HYP098 Hypereosinophilic Syndrome 58 0.082
1184
OST011 Osteomalacia 51 0.082
1185
SPN020 Spondylosis 58 0.082
1186
c CNG033 Congenital Syphilis 40 0.082
1187
ORL012 Oral Leukoplakia 33 0.082
1188
LPM004 Lipoma 64 0.082
1189
P FTL001 Fetal Alcohol Syndrome 62 0.082
1190
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 53 0.082
1191
CHL039 Choledocholithiasis 45 0.082
1192
INF013 Inferior Myocardial Infarction 39 0.082
1193
BLS002 Blastomycosis 55 0.082
1194
PYM001 Pyomyositis 48 0.082
1195
P USH001 Usher Syndrome 64 0.082
1196
P INT070 Intestinal Obstruction 61 0.082
1197
MGC001 Megacolon 59 0.082
1198
GYN001 Gynecomastia 43 0.082
1199
ORL005 Oral Candidiasis 56 0.081
1200
MMB002 Membranous Glomerulonephritis 47 0.081
1201
ASC002 Ascariasis 45 0.081
1202
GNT003 Genital Herpes 68 0.081
1203
c SML001 Small Cell Carcinoma 63 0.081
1204
P EPD003 Epidermolysis Bullosa Simplex 61 0.081
1205
EXT022 Exotropia 38 0.081
1206
PLV003 Pelvic Inflammatory Disease 50 0.081
1207
P CLB002 Clubfoot 48 0.081
1208
HRS011 Horseshoe Kidney 44 0.081
1209
SLP010 Slipped Capital Femoral Epiphysis 27 0.081
1210
OLG003 Oligohydramnios 59 0.081
1211
CNG069 Congenital Cytomegalovirus 48 0.081
1212
P OTT001 Otitis Externa 37 0.081