Search results for "INS"

9697 hits were found for 'INS'

# Family MCID Name MIFTS Score
1
P MTR004 Maturity-Onset Diabetes of the Young 54 7.172
2
P OBS005 Obesity 94 6.725
3
P NNT009 Neonatal Diabetes Mellitus 44 6.141
4
SPN027 Spinal Stenosis 53 4.957
5
c SKN012 Skin Carcinoma in Situ 18 4.714
6
c INS012 Ins-Related Permanent Neonatal Diabetes Mellitus 5 4.475
7
P DBT083 Diabetes Mellitus, Permanent Neonatal 52 3.625
8
P HYP110 Hyperproinsulinemia 34 3.612
9
LCK001 Locked-in Syndrome 35 3.563
10
P PLY011 Polycystic Ovary Syndrome 59 3.340
11
P MYL006 Myeloid Leukemia 64 3.264
12
BHC001 Behcet's Syndrome Arthropathy 8 3.231
13
HYP056 Hypoglycemia 53 3.215
14
HYP066 Hyperglycemia 52 3.203
15
LPD010 Lipodystrophy 49 3.156
16
GLC003 Glucose Intolerance 50 3.145
17
DBT001 Diabetic Ketoacidosis 52 3.116
18
P HYP060 Hyperinsulinism 47 3.107
19
ACN002 Acanthosis Nigricans 55 3.073
20
CRV002 Cervix Uteri Carcinoma in Situ 21 3.051
21
FTL021 Fetal Macrosomia 37 3.002
22
HYP026 Hypoglycemic Coma 41 2.987
23
LPR018 Leprechaunism 62 2.980
24
c MTB001 Metabolic Syndrome X 58 2.977
25
BRT037 Brittle Diabetes 23 2.964
26
P FML035 Familial Hyperlipidemia 48 2.963
27
RBS003 Rabson-Mendenhall Syndrome 60 2.962
28
P DBT085 Diabetes Mellitus, Insulin-Dependent 83 2.961
29
OLG010 Oligomenorrhea 37 2.958
30
c MTR044 Maturity-Onset Diabetes of the Young, Type 10 18 2.933
31
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 14 2.933
32
c STM003 Stomach Carcinoma in Situ 12 2.858
33
LVR003 Liver Carcinoma in Situ 10 2.857
34
ANL008 Anal Carcinoma in Situ 8 2.852
35
P LNG032 Lung Cancer 94 2.792
36
c BLD008 Bladder Carcinoma in Situ 21 2.688
37
c LNG003 Lung Carcinoma in Situ 11 2.646
38
P MTH008 Methylmalonic Acidemia 63 2.515
39
P BRS047 Breast Cancer 90 2.450
40
DDN006 Duodenitis 48 2.437
41
CLN004 Colon Carcinoma in Situ 11 2.421
42
c PRS031 Prostate Carcinoma in Situ 15 2.416
43
ESP005 Esophagus Carcinoma in Situ 8 2.416
44
LRY009 Larynx Carcinoma in Situ 8 2.416
45
TRC002 Trachea Carcinoma in Situ 8 2.416
46
END018 Endometrium Carcinoma in Situ 7 2.416
47
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 11 2.411
48
c NSL007 Nasal Cavity Carcinoma in Situ 7 2.411
49
OST013 Osteosarcoma Arising in Bone Paget's Disease 6 2.411
50
c ADN012 Adenocarcinoma in Situ 45 2.319
51
END030 End Stage Renal Failure 56 2.276
52
NNL002 Nonalcoholic Steatohepatitis 45 2.274
53
P RNV001 Renovascular Hypertension 52 2.256
54
FSC002 Fascioliasis 53 2.255
55
END040 Endogenous Depression 45 2.234
56
P OVR049 Ovarian Disease 56 2.231
57
DBT006 Diabetic Macular Edema 45 2.228
58
P ALT001 Alternating Hemiplegia of Childhood 54 2.216
59
P GLL020 Gallbladder Disease 56 2.216
60
CLC001 Calciphylaxis 47 2.212
61
NCR007 Necrotizing Fasciitis 38 2.207
62
P AST005 Asthma 84 2.205
63
ASP004 Asphyxia Neonatorum 25 2.201
64
P HYP263 Hypersomnia 37 2.193
65
DCT002 Ductal Carcinoma in Situ 36 2.192
66
DBT002 Diabetic Autonomic Neuropathy 41 2.192
67
ASH001 Asherman's Syndrome 20 2.191
68
PST055 Postural Hypotension 37 2.189
69
GSG001 Gas Gangrene 58 2.186
70
BLR006 Biliary Tract Disease 43 2.186
71
DMP001 Dumping Syndrome 42 2.184
72
FBR064 Febrile Infection-Related Epilepsy Syndrome 27 2.182
73
OVR063 Overnutrition 41 2.181
74
P HYP120 Hypoaldosteronism 42 2.179
75
HTC002 Hutchinson-Gilford Progeria 49 2.170
76
NCR002 Necrobiosis Lipoidica 36 2.168
77
PTT004 Pituitary Apoplexy 46 2.167
78
c EYC001 Eye Carcinoma in Situ 8 2.166
79
c TRS005 Torsion Dystonia with Onset in Infancy 11 2.164
80
PNS002 Penis Carcinoma in Situ 9 2.163
81
RCT010 Rectum Carcinoma in Situ 8 2.163
82
DCN001 Dic in Newborn 5 2.161
83
LPP001 Lipoprotein Lipase Deficiency 61 2.158
84
c BRS033 Breast Apocrine Carcinoma in Situ 6 2.157
85
PLY002 Polyneuropathy in Collagen Vascular Disease 5 2.157
86
STN004 Stone in Bladder Diverticulum 4 2.157
87
STF001 Stiff-Person Syndrome 52 2.156
88
EMP001 Empty Sella Syndrome 44 2.151
89
P FML012 Familial Partial Lipodystrophy 52 2.150
90
NRG005 Neurogenic Hypertension 26 2.149
91
c CNG012 Congenital Generalized Lipodystrophy 43 2.144
92
ALP001 Alopecia Universalis 57 2.139
93
P ATM019 Autoimmune Polyendocrine Syndrome 40 2.136
94
MDL009 Medullary Sponge Kidney 48 2.134
95
HYP231 Hypothalamic Hamartomas 40 2.134
96
MNG006 Monogenic Diabetes 35 2.131
97
DBT008 Diabetic Angiopathy 47 2.130
98
ACT088 Acute Insulin Response 37 2.130
99
ARM001 Aromatase Deficiency 58 2.128
100
PNC053 Pancreatic Islet Cell Tumors 46 2.126
101
GRN022 Granulosa Cell Tumor of the Ovary 36 2.124
102
HYP226 Hyporeninemic Hypoaldosteronism 32 2.124
103
INS006 Insulin Autoimmune Syndrome 39 2.122
104
c ADL027 Adult Dermatomyositis 39 2.122
105
MND007 Mandibuloacral Dysplasia 57 2.119
106
MTR046 Maternally Inherited Diabetes and Deafness 44 2.115
107
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 55 2.115
108
SLN001 Silent Myocardial Infarction 25 2.114
109
FST010 Fasting Hypoglycemia 38 2.111
110
ALS001 Alstrom Syndrome 58 2.108
111
BRR012 Berardinelli-Seip Congenital Lipodystrophy 43 2.107
112
JHN001 Johanson-Blizzard Syndrome 48 2.106
113
PTT052 Pituitary Gigantism 40 2.105
114
SKN023 Skin Tag 41 2.103
115
ACR013 Acrodysostosis 49 2.100
116
P PNC045 Pancreatic Agenesis 49 2.099
117
P SHR029 Short Syndrome 49 2.098
118
LPD008 Lipid Metabolism Disorder 41 2.098
119
SXL003 Sexual Disorder 32 2.096
120
P FML187 Familial Hypertension 29 2.094
121
P ATM025 Autoimmune Polyglandular Syndrome Type 2 32 2.091
122
CRB025 Carbohydrate Metabolic Disorder 20 2.091
123
c HRN019 Hair-an Syndrome 15 2.085
124
P ACQ022 Acquired Generalized Lipodystrophy 40 2.083
125
FBR065 Fibrocalculous Pancreatopathy 22 2.081
126
c ATM001 Autoimmune Polyendocrine Syndrome Type 2 18 2.079
127
EXR005 Exercise-Induced Hyperinsulinism 17 2.077
128
c HYP512 Hyperproinsulinemia, Familial 7 2.071
129
c INS002 in Situ Carcinoma 50 1.991
130
c BRS049 Breast Carcinoma in Situ 44 1.932
131
RFR007 Refractory Anemia with Excess Blasts in Transformation 15 1.901
132
MTH056 Methylmalonic Aciduria and Homocystinuria, Cblf Type 33 1.882
133
c MTH034 Methylmalonic Aciduria, Vitamin B12-Responsive, Due to Defect in Synthesis of Adenosylcobalamin, Cblb Complementation Type 16 1.882
134
STN011 Sting-Associated Vasculopathy with Onset in Infancy 7 1.882
135
c FML067 Familial Hyperthyroidism Due to Mutations in Tsh Receptor 13 1.877
136
c CNG411 Congenital Disorder of Glycosylation, Type in 33 1.875
137
c KDN012 Kidney Carcinoma in Situ 8 1.875
138
c INT019 Intestine Carcinoma in Situ 7 1.875
139
GRP002 Group B Strep Disease in Newborns 2 1.873
140
HRN007 Hearing Problems in Children 1 1.873
141
INT145 Intracranial Hemorrhage in Brain Cerebrovascular Malformations 25 1.868
142
c RCK006 Rickets Due to Defect in Vitamin D 25-Hydroxylation 16 1.868
143
IMM029 Immunodeficiency Due to Defect in Mapbp-Interacting Protein 10 1.868
144
RSP017 Response to Antiviral Treatment in Hepatitis C 9 1.868
145
UTR009 Uterus Carcinoma in Situ 6 1.868
146
IMM008 Immunodeficiency Due to Defect in Cd3-Gamma 4 1.868
147
END012 Endometriosis in Scar of Skin 4 1.868
148
MYC061 Myoclonic Epilepsy in Non-Progressive Encephalopathies 4 1.868
149
c ORL001 Oral Cavity Carcinoma in Situ 4 1.868
150
TBS007 T+b+ Severe Combined Deficiency of Adaptive Immunity Due to Mutation in the Ctps1 Gene 4 1.868
151
CRC002 Carcinoma Arising in Nasal Papillomatosis 3 1.868
152
INF009 Inflammatory Spondylopathy 7 1.866
153
P ECL001 Eclampsia 53 1.849
154
P CNV004 Canavan Disease 59 1.615
155
BLP005 Blepharitis 40 1.614
156
MYL003 Myeloid Sarcoma 48 1.598
157
CYS001 Cystic Fibrosis 92 1.591
158
PLR001 Pleural Tuberculosis 47 1.589
159
TTR005 Tetrahydrobiopterin Deficiency 43 1.582
160
LBL001 Lobular Neoplasia 43 1.574
161
HJD001 Hajdu-Cheney Syndrome 42 1.574
162
ART035 Arterial Calcification of Infancy 43 1.565
163
P NNN008 Noonan Syndrome 1 66 1.564
164
P MYC023 Myoclonic Astatic Epilepsy 30 1.562
165
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 38 1.559
166
CHY002 Chylomicron Retention Disease 48 1.552
167
IRN004 Iron-Refractory Iron Deficiency Anemia 34 1.552
168
c EXD008 Exudative Vitreoretinopathy 1 39 1.548
169
ESP002 Esophageal Varix 35 1.548
170
PRG097 Paragangliomas 1, with or Without Deafness 34 1.548
171
UVN001 Uv-Induced Skin Damage 17 1.543
172
PLM013 Pulmonary Immaturity 12 1.541
173
HMC023 Homocystinuria-Megaloblastic Anemia, Cbl E Type 23 1.539
174
ESN009 Eosinophil Peroxidase Deficiency 30 1.538
175
PRN019 Perinatal Necrotizing Enterocolitis 31 1.536
176
LRY022 Laryngoonychocutaneous Syndrome 29 1.536
177
c HMC035 Hemochromatosis, Type 4 30 1.536
178
ULC001 Ulceration of Vulva 14 1.534
179
INT188 Intestinal Obstruction in the Newborn Due to Guanylate Cyclase 2c Deficiency 7 1.534
180
c ALB017 Albinism, Oculocutaneous, Type Vi 20 1.532
181
ACT186 Acute Megakaryoblastic Leukemia in Down Syndrome 10 1.532
182
CMP052 Complication in Hemodialysis 5 1.532
183
BLD001 Bile Duct Carcinoma in Situ 6 1.532
184
c MLG132 Malignant Hyperthermia Susceptibility 1 33 1.529
185
c MLN043 Melanoma, Cutaneous Malignant 8 31 1.529
186
c HYP488 Hypothyroidism Due to Deficient Transcription Factors Involved in Pituitary Development or Function 30 1.529
187
c LPC001 Lip Carcinoma in Situ 8 1.529
188
ICH027 Ichthyosis-Mental Retardation Syndrome with Large Keratohyalin Granules in the Skin 6 1.529
189
BLR014 Bilirubin Induced Brain Injury in the Newborn 3 1.529
190
FCL024 Focal or Multifocal Malformations in Neuronal Migration 2 1.529
191
DNS002 Dens in Dente and Palatal Invaginations 1 1.529
192
c HMC017 Homocystinuria Due to Defect in Methylation Cbl E 1 1.529
193
c HMC018 Homocystinuria Due to Defect in Methylation Cbl G 1 1.529
194
SLC025 Selection of Therapeutic Option in Non-Small Cell Lung Carcinoma 20 1.526
195
GLY058 Glycogen Storage Disease 0, Liver 18 1.526
196
BLM005 Bulimia Nervosa, Age of Onset of Weight Loss in 12 1.526
197
SYM015 Symptomatic Form of Coffin-Lowry Syndrome in Female Carriers 10 1.526
198
DFC003 Deficiency in Anterior Pituitary Function-Variable Immunodeficiency Syndrome 7 1.526
199
PLZ009 Pelizaeus-Merzbacher Disease in Female Carriers 6 1.526
200
c SCN015 Scn1a-Related Severe Myoclonic Epilepsy in Infancy 7 1.526
201
SYM016 Symptomatic Form of Muscular Dystrophy of Duchenne and Becker in Female Carriers 5 1.526
202
INS022 in Situ Pulmonary Adenocarcinoma 5 1.526
203
P SYM020 Symptomatic Form of Hemophilia a in Female Carriers 4 1.526
204
c SYM021 Symptomatic Form of Hemophilia B in Female Carriers 4 1.526
205
RSS021 Resistance to Bleomycine in the Treatment of Testicular Cancer 4 1.526
206
c ANG059 Angelman Syndrome Due to Imprinting Defect in 15q11-Q13 5 1.526
207
SLC026 Selection of Therapeutic Option in Colorectal Cancer 4 1.526
208
ADN063 Adenovirus Infection in Immunocompromised Patients 4 1.526
209
BNG063 Benign Partial Epilepsy with Secondarily Generalized Seizures in Infancy 4 1.526
210
c PHR001 Pharynx Carcinoma in Situ 4 1.526
211
PRM033 Paraomphalocele 4 1.526
212
RCR023 Recurrent Hepatitis C Virus Induced Liver Disease in Liver Transplant Recipients 4 1.526
213
SCR032 Scarring in Glaucoma Filtration Surgical Procedures 4 1.526
214
CNG229 Congenital Deficiency in Alpha-Fetoprotein 3 1.526
215
GLL001 Gall Bladder Carcinoma in Situ 3 1.526
216
PLM110 Poliomyelitis in Patients with Immunodeficiencies Deemed at Risk 3 1.526
217
RTN007 Retinal Dystrophy in Systemic or Cerebroretinal Lipidoses 2 1.526
218
HGH022 High-Grade Dysplasia in Patients with Barrett Esophagus 2 1.526
219
PLM107 Pulmonary Fungal Infections in Patients Deemed at Risk 2 1.526
220
APP014 Appendix: About Genomic Databases Listed in Genereviews 1 1.526
221
PSD098 Pseudohyperaldosteronism Type 2 7 1.523
222
P DND019 Dend Syndrome 31 1.510
223
MTR048 Maturity-Onset Diabetes of the Young Type10 3 1.464
224
PRP016 Paraplegia 40 1.322
225
AVN001 Avian Influenza 43 1.280
226
P QFV001 Q Fever 49 1.268
227
PCK002 Pick Disease 64 1.266
228
P SDD001 Sudden Infant Death Syndrome 62 1.256
229
DXT001 Dextrocardia 37 1.242
230
EST005 Esotropia 34 1.237
231
DBT004 Diabetic Polyneuropathy 44 1.219
232
ACT017 Acute Chest Syndrome 48 1.204
233
c VRL007 Viral Encephalitis 55 1.194
234
P DRV001 Dravet Syndrome 64 1.189
235
PYR004 Pyuria 24 1.184
236
P ALX003 Alexander Disease 66 1.183
237
P FCS002 Fucosidosis 59 1.178
238
LRY027 Laryngeal Papillomatosis 20 1.163
239
BRR002 Barrett's Adenocarcinoma 27 1.155
240
STS003 Sitosterolemia 56 1.149
241
TRD003 Taurodontism 29 1.148
242
NNT008 Neonatal Abstinence Syndrome 35 1.147
243
KSH001 Keshan Disease 36 1.136
244
VLV042 Vulvar Vestibulitis Syndrome 40 1.126
245
PLV001 Pelvic Lipomatosis 29 1.123
246
P PRS049 Persistent Mullerian Duct Syndrome 42 1.119
247
P HYP607 Hypercholesterolemia, Familial 81 1.113
248
P JRV003 Jervell and Lange-Nielsen Syndrome 46 1.112
249
c NML015 Nemaline Myopathy 3, Autosomal Dominant or Recessive 30 1.110
250
URT011 Urethral Calculus 19 1.110
251
P STS008 Sotos Syndrome 1 46 1.109
252
c USH032 Usher Syndrome, Type 2a 47 1.108
253
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 39 1.106
254
c GRS013 Griscelli Syndrome, Type 1 28 1.106
255
CRN239 Carnitine Deficiency, Systemic Primary 39 1.105
256
MTC056 Mitochondrial Dna Depletion Syndrome 4a 37 1.104
257
GRS011 Gerstmann-Straussler Disease 29 1.102
258
YCH001 Y Chromosome Infertility 26 1.102
259
LCH008 Lichen Planus Pigmentosus 21 1.102
260
BNT002 Bantu Siderosis 19 1.102
261
BHR001 Behr Syndrome 24 1.101
262
HMC033 Homocystinuria-Megaloblastic Anemia, Cblg Complementation Type 21 1.099
263
c LKM061 Leukemia, Acute Myeloid 69 1.097
264
HMG006 Hmg-Coa Lyase Deficiency 37 1.097
265
HYP322 Hypoaldosteronism, Congenital, Due to Cmo I Deficiency 25 1.097
266
HTR005 Heterochromia Iridis 16 1.097
267
BRT013 Baritosis 14 1.097
268
c HMC010 Hemochromatosis, Type 3 36 1.096
269
NRD015 Neurodegeneration with Brain Iron Accululation 5 24 1.094
270
KYR001 Kyrle Disease 12 1.094
271
SCH027 Schizotaxia 7 1.092
272
c RTN058 Retinitis Pigmentosa 3 38 1.090
273
c NML014 Nemaline Myopathy 1, Autosomal Dominant or Recessive 26 1.090
274
MLG120 Malignant Migrating Partial Seizures of Infancy 20 1.090
275
CMD001 Comedo Carcinoma 11 1.090
276
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 34 1.087
277
MTH021 Methylmalonic Acidemia with Homocystinuria 26 1.087
278
PRN018 Paraneoplastic Polyneuropathy 15 1.087
279
SRC006 Sarcoid Meningitis 9 1.087
280
SNW001 Snowflake Vitreoretinal Degeneration 32 1.085
281
ANS012 Anus Disease 20 1.085
282
GRW003 Growth Hormone Insensitivity with Immunodeficiency 19 1.085
283
RST020 Restless Legs Syndrome 6 12 1.085
284
PLM009 Pleomorphic Adenoma Carcinoma 12 1.085
285
PLM129 Pulmonary Disease, Chronic Obstructive 53 1.081
286
c NML009 Nemaline Myopathy 2, Autosomal Recessive 25 1.081
287
c NML017 Nemaline Myopathy 4, Autosomal Dominant 23 1.081
288
MTH024 Methylmalonicacidemia with Homocystinuria Cbl D 20 1.081
289
CRM007 Crome Syndrome 15 1.081
290
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 13 1.081
291
KCH001 Kocher-Debre-Semelaigne Syndrome 11 1.081
292
INF021 Infant Gynecomastia 7 1.081
293
ACH016 Achard Thiers Syndrome 5 1.081
294
ARN001 Arena Syndrome 4 1.081
295
c CTR025 Cataract, Total Congenital 27 1.077
296
BLC009 Bile Acid Synthesis Defect, Congenital, 4 24 1.077
297
NML020 Nemaline Myopathy 5, Amish Type 23 1.077
298
c MTR072 Maturity-Onset Diabetes of the Young, Type Ix 23 1.077
299
FBR026 Fibromatosis Multiple Non Ossifying 18 1.077
300
KRT023 Keratoderma Palmoplantaris Transgrediens 16 1.077
301
STR032 Steroid Dehydrogenase Deficiency Dental Anomalies 16 1.077
302
P HYP211 Hypomagnesemia Primary 13 1.077
303
TRC057 Trichoodontoonychial Dysplasia 12 1.077
304
IMM085 Immunodeficiency 25 10 1.077
305
PLM015 Pulmonary Systemic Sclerosis 16 1.077
306
MTH057 Methylmalonic Acidemia with Homocystinuria, Type Cblj 9 1.077
307
ECT009 Ectopia Pupillae 8 1.077
308
LMY009 Leiomyomatosis, Esophageal and Vulval, with Nephropathy 8 1.077
309
HYP500 Hyperphalangy, Unilateral 7 1.077
310
BNG074 Benign Familial Nocturnal Alternating Hemiplegia of Childhood 7 1.077
311
MTH058 Methylmalonic Acidemia with Homocystinuria, Type Cblx 7 1.077
312
KRN006 Karandikar Maria Kamble Syndrome 5 1.077
313
BSN001 Basan Syndrome 5 1.077
314
RVL001 Ruvalcaba Churesigaew Myhre Syndrome 4 1.077
315
THL008 Thalamic Degeneration, Symmetric Infantile 4 1.077
316
c RDL013 Radio-Ulnar Synostosis Type 2 4 1.077
317
CRD031 Cardiomyopathy, Fatal Fetal, Due to Myocardial Calcification 3 1.077
318
INF051 Infantile Recurrent Chronic Multifocal Osteomyolitis 3 1.077
319
PRM053 Primary Release Disorder of Platelets 3 1.077
320
P LKM002 Leukemia 66 0.687
321
END072 Endotheliitis 44 0.650
322
P HPT021 Hepatitis 55 0.629
323
PRS047 Prostatitis 51 0.587
324
NRN002 Neuronitis 36 0.553
325
P PNC044 Pancreatitis 59 0.498
326
P THY032 Thyroiditis 56 0.491
327
P ART022 Arthritis 65 0.488
328
CRB009 Cerebritis 33 0.476
329
P PRS040 Prostate Cancer 84 0.463
330
P ADN016 Adenocarcinoma 49 0.463
331
MLN008 Melanoma 55 0.425
332
RTN023 Retinitis 44 0.415
333
P CLR023 Colorectal Cancer 96 0.410
334
P RHM011 Rheumatoid Arthritis 94 0.409
335
P CRV039 Cervicitis 49 0.388
336
HPT023 Hepatocellular Carcinoma 95 0.371
337
P SCH015 Schizophrenia 79 0.364
338
P ESP024 Esophagitis 54 0.351
339
P MYC007 Myocardial Infarction 81 0.347
340
TBR010 Tuberculosis 73 0.336
341
P LPS004 Lupus Erythematosus 67 0.335
342
ISC004 Ischemia 53 0.330
343
P NRP001 Neuropathy 52 0.324
344
c HPT001 Hepatitis C 57 0.322
345
P BLN003 Blindness 47 0.316
346
HYP266 Hypoxia 49 0.315
347
c SYS001 Systemic Lupus Erythematosus 91 0.309
348
SRC014 Sarcoma 61 0.307
349
ADN018 Adenoma 55 0.305
350
ATH003 Atherosclerosis 56 0.298
351
P NRB001 Neuroblastoma 68 0.295
352
P PNM007 Pneumonia 64 0.290
353
ART111 Artery Disease 55 0.282
354
P MNN013 Meningitis 58 0.280
355
DMN002 Dementia 58 0.279
356
ANR040 Aneurysm 35 0.278
357
P MYL007 Myeloma 53 0.277
358
P RNL014 Renal Cell Carcinoma 83 0.275
359
PRT036 Peritonitis 61 0.272
360
DRM006 Dermatitis 58 0.270
361
P ENC004 Encephalitis 56 0.270
362
c HPT016 Hepatitis B 60 0.269
363
CLT003 Colitis 54 0.266
364
P PRD008 Periodontitis 59 0.260
365
MLR004 Malaria 81 0.259
366
HV1006 Hiv-1 83 0.256
367
P ATX004 Ataxia 50 0.256
368
P KDN018 Kidney Disease 57 0.255
369
P MSC005 Muscular Dystrophy 54 0.255
370
P PNC035 Pancreatic Cancer 82 0.254
371
P LVR013 Liver Disease 62 0.253
372
P LYM026 Lymphoblastic Leukemia 55 0.250
373
P CRN211 Coronary Artery Disease 73 0.249
374
c MLT019 Multiple Myeloma 75 0.244
375
P GLM007 Glomerulonephritis 59 0.241
376
P GLB002 Glioblastoma 59 0.237
377
P INF038 Influenza 67 0.236
378
SPS057 Spasticity 32 0.228
379
P INF037 Inflammatory Bowel Disease 39 0.227
380
c ACT075 Acute Myocardial Infarction 57 0.226
381
P BCL006 B-Cell Lymphomas 47 0.226
382
P CHR090 Chronic Lymphocytic Leukemia 74 0.226
383
INS024 Insulin-Like Growth Factor I 58 0.225
384
P LRY019 Laryngitis 56 0.221
385
CRH001 Crohn's Disease 71 0.219
386
c HPT073 Hepatitis C Virus 51 0.219
387
GNG013 Gingivitis 52 0.219
388
P PSR002 Psoriasis 54 0.217
389
ULC004 Ulcerative Colitis 63 0.215
390
P THL005 Thalassemia 64 0.211
391
P INF032 Infertility 46 0.206
392
P END044 Endometriosis 59 0.203
393
P CTR002 Cataract 50 0.203
394
P RHN004 Rhinitis 54 0.203
395
P LTR001 Lateral Sclerosis 43 0.202
396
P MYP004 Myopathy 53 0.202
397
MYL009 Myelodysplastic Syndrome 67 0.200
398
P OST012 Osteoarthritis 80 0.197
399
P HYP086 Hypothyroidism 59 0.197
400
P ATP001 Atopic Dermatitis 56 0.196
401
P OST002 Osteoporosis 71 0.195
402
P PLM037 Pulmonary Hypertension 85 0.194
403
ORL015 Oral Squamous Cell Carcinoma 33 0.193
404
P AMY004 Amyloidosis 63 0.192
405
P DRR001 Diarrhea 44 0.190
406
PRP030 Purpura 54 0.189
407
URT001 Urethritis 48 0.189
408
LSH001 Leishmaniasis 63 0.186
409
P DYS154 Dystonia 55 0.186
410
P HRP006 Herpes Simplex 63 0.186
411
P RTN024 Retinoblastoma 75 0.186
412
P ATR011 Atrial Fibrillation 62 0.183
413
EPD016 Epidermolysis Bullosa 49 0.183
414
LVR012 Liver Cirrhosis 66 0.183
415
P THR014 Thrombocytopenia 56 0.183
416
P LPR003 Leprosy 71 0.182
417
CHR008 Choroiditis 45 0.181
418
MGR002 Migraine 64 0.180
419
P AST007 Astrocytoma 63 0.180
420
DWN001 Down Syndrome 51 0.180
421
P NPH012 Nephrotic Syndrome 60 0.180
422
P BPL003 Bipolar Disorder 65 0.179
423
P MST018 Mesothelioma 51 0.179
424
c ACT073 Acute Leukemia 48 0.179
425
BRN106 Burns 42 0.178
426
P PRP029 Porphyria 57 0.178
427
THY028 Thyroid Cancer 63 0.176
428
P HMP007 Hemophilia 59 0.175
429
P HYP069 Hyperparathyroidism 57 0.175
430
P CNJ013 Conjunctivitis 53 0.175
431
P HYD006 Hydrocephalus 56 0.174
432
P UVT001 Uveitis 57 0.174
433
NPH051 Nephritis 46 0.174
434
NSP002 Nasopharyngitis 40 0.174
435
VSC011 Vasculitis 57 0.174
436
ART016 Aortic Aneurysm 62 0.173
437
VGN023 Vaginitis 51 0.171
438
P SYP003 Syphilis 48 0.170
439
P PLY019 Polyneuropathy 52 0.169
440
P HYP061 Hypertrophic Cardiomyopathy 59 0.169
441
P MNT147 Mental Retardation 46 0.169
442
P DLT002 Dilated Cardiomyopathy 77 0.168
443
P NTR004 Neutropenia 56 0.168
444
P HMR012 Hemorrhagic Fever 52 0.167
445
CNG034 Congestive Heart Failure 69 0.166
446
P SCL016 Scleroderma 76 0.166
447
VSC007 Vascular Disease 59 0.165
448
SPN051 Spondylitis 48 0.165
449
BRN071 Brain Injury 49 0.164
450
P NRF002 Neurofibromatosis 69 0.164
451
P CND004 Candidiasis 54 0.164
452
PMP001 Pemphigus 51 0.164
453
P PRS038 Personality Disorder 50 0.164
454
ASP006 Aspergillosis 63 0.163
455
P ALZ034 Alzheimer Disease 100 0.163
456
KRT004 Keratitis 60 0.163
457
HDG012 Hodgkin Lymphoma 79 0.162
458
c PRC016 Pre-Eclampsia 58 0.162
459
CRB037 Cerebral Palsy 55 0.162
460
ACR007 Acromegaly 69 0.162
461
RHB003 Rhabdomyosarcoma 49 0.162
462
P GST044 Gastritis 56 0.162
463
P RTN008 Retinitis Pigmentosa 72 0.162
464
DFF005 Diffuse Large B-Cell Lymphoma 50 0.161
465
ALL003 Allergic Rhinitis 63 0.161
466
GRV001 Graves' Disease 54 0.161
467
SCH014 Schistosomiasis 60 0.161
468
P PLM036 Pulmonary Fibrosis 64 0.160
469
ESP021 Esophageal Cancer 67 0.160
470
GTR002 Goiter 53 0.159
471
P MYC008 Myocarditis 50 0.158
472
ALP008 Alopecia 51 0.157
473
ANR007 Anorexia Nervosa 62 0.156
474
SCK005 Sickle Cell Disease 54 0.156
475
P PYL005 Pyelonephritis 43 0.156
476
P TCL004 T-Cell Leukemia 43 0.155
477
PRT039 Proteinuria 43 0.155
478
P SLP006 Sleep Apnea 50 0.155
479
OTT002 Otitis Media 56 0.155
480
P TRT010 Teratoma 50 0.154
481
c ACT027 Acute Pancreatitis 55 0.154
482
END057 Endometrial Cancer 71 0.154
483
PLM001 Pulmonary Tuberculosis 60 0.153
484
PTT006 Pituitary Adenoma 52 0.153
485
P CLC005 Celiac Disease 69 0.152
486
CHL068 Cholestasis 50 0.152
487
P TXP001 Toxoplasmosis 56 0.151
488
P OPN001 Open-Angle Glaucoma 51 0.151
489
P TBR001 Tuberous Sclerosis 68 0.150
490
P MYT002 Myotonic Dystrophy 57 0.150
491
P ESN007 Eosinophilia 54 0.150
492
P MDL005 Medulloblastoma 71 0.150
493
HDC001 Headache 50 0.149
494
ATT013 Attention Deficit-Hyperactivity Disorder 63 0.149
495
NSP012 Nasopharyngeal Carcinoma 44 0.148
496
GRW007 Growth Hormone Deficiency 46 0.147
497
CHL065 Cholangiocarcinoma 59 0.147
498
c BSL007 Basal Cell Carcinoma 56 0.147
499
P END033 Endocarditis 48 0.145
500
FTT001 Fatty Liver Disease 39 0.144
501
P PNC025 Panic Disorder 64 0.144
502
P HMC003 Hemochromatosis 75 0.143
503
HMT018 Hematopoietic Stem Cell Transplantation 36 0.143
504
P MYS005 Myositis 63 0.143
505
P PHC003 Pheochromocytoma 79 0.143
506
P PRM006 Primary Biliary Cirrhosis 56 0.143
507
P MYS003 Myasthenia Gravis 64 0.143
508
ANX002 Anxiety Disorder 60 0.142
509
P WLM002 Wilms Tumor 70 0.141
510
SPN186 Spinal Cord Injury 54 0.141
511
P OST005 Osteogenesis Imperfecta 77 0.141
512
ACQ007 Acquired Immunodeficiency Syndrome 46 0.141
513
P MSC003 Muscular Atrophy 44 0.140
514
P MCP010 Mucopolysaccharidosis 56 0.140
515
PPL022 Papilloma 55 0.140
516
P PLY014 Polycystic Kidney Disease 53 0.139
517
BRN002 Bronchiolitis 52 0.139
518
MSL001 Measles 58 0.139
519
TRN018 Transitional Cell Carcinoma 54 0.138
520
P HYP080 Hypogonadism 51 0.138
521
ECH003 Echinococcosis 51 0.137
522
P CHL066 Cholangitis 45 0.137
523
c VRL010 Viral Hepatitis 54 0.137
524
TRM010 Traumatic Brain Injury 46 0.136
525
P ANT006 Antiphospholipid Syndrome 55 0.136
526
TMP001 Temporal Lobe Epilepsy 50 0.136
527
P TRM003 Tremor 48 0.136
528
P SNS014 Sinusitis 56 0.135
529
c MLG068 Malignant Glioma 58 0.135
530
CYT008 Cytomegalovirus Infection 39 0.135
531
ORL011 Oral Cancer 47 0.135
532
P HYP076 Hyperthyroidism 54 0.134
533
LCH002 Lichen Planus 52 0.134
534
KWS002 Kawasaki Disease 66 0.134
535
c ATM003 Autoimmune Thyroiditis 58 0.133
536
LMY002 Leiomyoma 59 0.133
537
P HYP004 Hypercalcemia 57 0.133
538
P ABD003 Abdominal Aortic Aneurysm 58 0.133
539
P MLT074 Multiple Endocrine Neoplasia 53 0.132
540
ALC007 Alcohol Dependence 60 0.132
541
SPT005 Spotted Fever 45 0.132
542
P PLY018 Polycythemia 58 0.132
543
DCH001 Duchenne Muscular Dystrophy 78 0.132
544
P HML002 Hemolytic Anemia 56 0.131
545
URT039 Urticaria 55 0.131
546
P RBL001 Rubella 53 0.131
547
ATP002 Atopy 55 0.131
548
P PSR001 Psoriatic Arthritis 50 0.131
549
OBS061 Obstructive Sleep Apnea 48 0.131
550
OBS002 Obsessive-Compulsive Disorder 69 0.130
551
P SPN049 Spinocerebellar Ataxia 53 0.130
552
P APL001 Aplastic Anemia 76 0.130
553
ART021 Arteriosclerosis 58 0.130
554
P DRM010 Dermatomyositis 62 0.129
555
ISC006 Ischemic Heart Disease 51 0.129
556
CNN005 Connective Tissue Disease 50 0.129
557
P ATS007 Autism Spectrum Disorder 56 0.129
558
GST019 Gastrointestinal Stromal Tumor 74 0.129
559
P DBT005 Diabetes Insipidus 53 0.128
560
P SPN046 Spinal Muscular Atrophy 57 0.128
561
PRT037 Pertussis 54 0.127
562
KRT006 Keratoconjunctivitis 48 0.127
563
MRF001 Marfan Syndrome 75 0.127
564
GST045 Gastroenteritis 45 0.127
565
CLF001 Cleft Lip 51 0.127
566
PLM074 Pulmonary Function 30 0.127
567
LPS007 Lupus Nephritis 44 0.126
568
PHN003 Phenylketonuria 73 0.126
569
P RSP003 Respiratory Failure 62 0.126
570
HYP037 Hyperhomocysteinemia 45 0.125
571
SCK003 Sickle Cell Anemia 70 0.125
572
PRD007 Periodontal Disease 47 0.125
573
PRP023 Peripheral Neuropathy 44 0.124
574
GST040 Gastric Adenocarcinoma 34 0.124
575
P LNG028 Long Qt Syndrome 62 0.124
576
MDS022 Mediastinitis 39 0.124
577
P PRD006 Prader-Willi Syndrome 64 0.124
578
MNT001 Mantle Cell Lymphoma 55 0.124
579
STM007 Stomatitis 43 0.124
580
PLS007 Plasmodium Falciparum Malaria 48 0.124
581
P RTT002 Rett Syndrome 73 0.124
582
GLM011 Glomerulosclerosis 40 0.124
583
P HMN010 Hemangioma 60 0.123
584
P CHR071 Charcot-Marie-Tooth Disease 60 0.123
585
PLM033 Pulmonary Embolism 56 0.123
586
BCT015 Bacteremia 45 0.123
587
P HST010 Histiocytosis 55 0.123
588
SYN007 Synovitis 51 0.123
589
P MYL005 Myelofibrosis 68 0.123
590
P PRT013 Portal Hypertension 49 0.123
591
MLT021 Multiple System Atrophy 70 0.123
592
VSC003 Visceral Leishmaniasis 50 0.123
593
TTH006 Tooth Disease 46 0.122
594
P CYS018 Cystitis 43 0.122
595
P GLY013 Glycogen Storage Disease 51 0.122
596
SFT003 Soft Tissue Sarcoma 44 0.122
597
AZS001 Azoospermia 41 0.122
598
RHM027 Rheumatic Disease 42 0.122
599
SVR004 Severe Combined Immunodeficiency 68 0.122
600
ALL006 Allergic Asthma 46 0.121
601
c PRM005 Primary Hyperparathyroidism 58 0.121
602
CHR012 Chronic Granulomatous Disease 64 0.121
603
ATN004 Autonomic Neuropathy 41 0.121
604
P HYP117 Hypertriglyceridemia 61 0.120
605
TYP011 Typhus 47 0.120
606
ANG054 Angina Pectoris 43 0.120
607
P MYP006 Myopia 41 0.120
608
RLP002 Relapsing-Remitting Multiple Sclerosis 39 0.120
609
P CSH001 Cushing's Syndrome 76 0.119
610
IRR002 Irritable Bowel Syndrome 56 0.119
611
P TRN020 Turner Syndrome 58 0.119
612
TTN003 Tetanus 54 0.119
613
P EHL001 Ehlers-Danlos Syndrome 56 0.119
614
URM002 Uremia 47 0.119
615
NRT004 Neuritis 40 0.119
616
NRL016 Neural Tube Defects 78 0.118
617
P MST009 Mastocytosis 61 0.118
618
c HPT003 Hepatitis a 51 0.118
619
FSC004 Fasciitis 39 0.118
620
MYC033 Myoclonus 39 0.118
621
P FRG001 Fragile X Syndrome 66 0.118
622
CTN007 Cutaneous Leishmaniasis 57 0.118
623
BRN024 Bronchitis 62 0.118
624
P RTN022 Retinal Vein Occlusion 48 0.117
625
PLM031 Poliomyelitis 45 0.117
626
FLL037 Follicular Lymphoma 50 0.117
627
FBR047 Fibromyalgia 42 0.117
628
APH002 Aphasia 35 0.117
629
P ATX030 Ataxia-Telangiectasia 76 0.117
630
PHR003 Pharyngitis 56 0.117
631
P RTN016 Retinal Degeneration 38 0.117
632
P DDN001 Duodenal Ulcer 53 0.117
633
PNM008 Pneumothorax 43 0.117
634
CRB004 Cerebral Artery Occlusion 36 0.117
635
P THR015 Thrombophilia 57 0.117
636
P LKD001 Leukodystrophy 45 0.116
637
TNS005 Tonsillitis 48 0.116
638
CLN015 Colon Adenocarcinoma 43 0.116
639
ACN011 Acne 58 0.116
640
CHR074 Choriocarcinoma 50 0.116
641
PLY001 Polycythemia Vera 75 0.115
642
CHG001 Chagas Disease 54 0.115
643
RTN017 Retinal Detachment 48 0.115
644
CMM004 Common Variable Immunodeficiency 67 0.115
645
c HMP029 Hemophilia a 66 0.115
646
c ACT004 Acute Diarrhea 37 0.115
647
P CHN012 Chondrosarcoma 56 0.115
648
P CRT072 Creutzfeldt-Jakob Disease 64 0.115
649
ETN001 Eating Disorder 49 0.115
650
INT066 Interstitial Lung Disease 44 0.115
651
P PRC019 Precocious Puberty 53 0.115
652
HRP004 Herpes Zoster 49 0.115
653
P RCK004 Rickets 58 0.115
654
P ESS003 Essential Thrombocythemia 66 0.114
655
CHL014 Cholera 56 0.114
656
DFC004 Deficiency Anemia 54 0.114
657
OST017 Osteomyelitis 50 0.114
658
DNT012 Dental Caries 42 0.114
659
CRN025 Corneal Dystrophy 38 0.114
660
NRN004 Neuroendocrine Tumor 50 0.114
661
TTR001 Tetralogy of Fallot 67 0.114
662
CHL067 Cholecystitis 53 0.114
663
LRY018 Laryngeal Squamous Cell Carcinoma 49 0.114
664
NPH017 Nephrosis 36 0.114
665
ATN005 Autonomic Dysfunction 39 0.114
666
CHR066 Chronic Fatigue Syndrome 55 0.113
667
ALB002 Albinism 43 0.113
668
MTH009 Mouth Disease 43 0.113
669
FBR012 Fabry Disease 76 0.113
670
CRB039 Cerebrovascular Disease 59 0.113
671
BCK006 Back Pain 33 0.113
672
SNS001 Sensorineural Hearing Loss 48 0.113
673
SCR011 Scrapie 37 0.112
674
IRN001 Iron Deficiency Anemia 48 0.112
675
PRS039 Prostate Adenocarcinoma 35 0.112
676
DSS009 Disseminated Intravascular Coagulation 52 0.112
677
BRN056 Bronchopulmonary Dysplasia 49 0.112
678
c BCT007 Bacterial Meningitis 42 0.112
679
c NRF018 Neurofibromatosis, Type 1 65 0.112
680
STT001 Status Epilepticus 56 0.112
681
GST023 Gastric Ulcer 57 0.112
682
P ANG015 Angioedema 51 0.112
683
P GT001 Gout 56 0.111
684
SYS003 Systolic Heart Failure 31 0.111
685
P LRY016 Laryngeal Carcinoma 51 0.111
686
P SCL009 Sclerosing Cholangitis 41 0.111
687
WST005 West Nile Virus 40 0.111
688
GST092 Gastroesophageal Reflux 60 0.111
689
P PMP005 Pemphigus Vulgaris 47 0.111
690
BRC012 Brucellosis 53 0.111
691
BLR001 Biliary Atresia 51 0.111
692
c ATM011 Autoimmune Hepatitis 51 0.111
693
c CNG006 Congenital Hypothyroidism 61 0.111
694
c HPT007 Hepatitis E 45 0.111
695
PLR008 Pleurisy 41 0.111
696
DBT010 Diabetic Neuropathy 52 0.110
697
CRY003 Cryptosporidiosis 53 0.110
698
c BPL002 Bipolar I Disorder 33 0.110
699
PNC041 Pancreatic Ductal Adenocarcinoma 38 0.110
700
PTT037 Pituitary Tumors 46 0.110
701
VSC002 Vascular Dementia 48 0.110
702
MDD011 Mood Disorder 48 0.110
703
CNS004 Constipation 45 0.110
704
P CNG401 Congenital Heart Disease 62 0.110
705
P STM004 Stomach Cancer 59 0.110
706
HPT022 Hepatoblastoma 53 0.109
707
APP008 Appendicitis 48 0.109
708
P CNG368 Congenital Adrenal Hyperplasia 66 0.109
709
CHL069 Cholesteatoma 45 0.109
710
CNT047 Contact Dermatitis 46 0.109
711
END041 Endometrial Adenocarcinoma 43 0.109
712
HYP043 Hyperandrogenism 40 0.109
713
CRV045 Cervical Intraepithelial Neoplasia 39 0.109
714
ANX004 Anoxia 31 0.109
715
P DYS005 Dyslexia 30 0.109
716
c ACT134 Acute Liver Failure 48 0.109
717
P LYN001 Lynch Syndrome 66 0.109
718
OCL006 Ocular Hypertension 47 0.109
719
HMG002 Hemoglobinuria 43 0.109
720
PRT038 Protein-Energy Malnutrition 40 0.109
721
ECT006 Ectodermal Dysplasia 48 0.109
722
LMB062 Limb Ischemia 38 0.109
723
BCT004 Bacteriuria 50 0.108
724
P NRC002 Narcolepsy 67 0.108
725
INS001 Insulinoma 49 0.108
726
c ADL017 Adult T-Cell Leukemia 40 0.108
727
P ANP001 Anaplastic Large Cell Lymphoma 53 0.108
728
SKN016 Skin Disease 64 0.108
729
P ART023 Arthropathy 54 0.108
730
FLR002 Filariasis 50 0.108
731
ORL013 Oral Lichen Planus 35 0.108
732
BLL006 Bullous Pemphigoid 60 0.108
733
RNL015 Renal Hypertension 42 0.108
734
CRY002 Cryptorchidism 57 0.108
735
P CNG015 Congenital Diaphragmatic Hernia 56 0.108
736
TST014 Testicular Cancer 53 0.108
737
GLB015 Glioblastoma Multiforme 51 0.107
738
CRY004 Cryoglobulinemia 49 0.107
739
DYS014 Dyspepsia 45 0.107
740
P CTN015 Cutaneous T Cell Lymphoma 45 0.107
741
KWS001 Kwashiorkor 41 0.107
742
BRN022 Bronchiectasis 54 0.107
743
LPT001 Leptospirosis 46 0.107
744
BLM002 Bulimia Nervosa 49 0.107
745
CCC002 Coccidiosis 28 0.107
746
PLG002 Plague 47 0.107
747
ADN002 Adenoiditis 31 0.107
748
MST005 Mastitis 43 0.107
749
ONC002 Onchocerciasis 43 0.107
750
HDN002 Head Injury 41 0.107
751
RST001 Restless Legs Syndrome 50 0.106
752
HPT019 Hepatic Encephalopathy 51 0.106
753
BRN080 Brain Ischemia 43 0.106
754
OBS006 Obstructive Lung Disease 43 0.106
755
c JVN010 Juvenile Rheumatoid Arthritis 59 0.106
756
SPS019 Spastic Paraparesis 35 0.106
757
EYD002 Eye Disease 54 0.106
758
MLG056 Malignant Hyperthermia 62 0.106
759
P FBR017 Fibrosarcoma 52 0.106
760
HMP005 Hemiplegia 44 0.106
761
P KRT007 Keratoconus 45 0.106
762
P CHR345 Chronic Pain 39 0.106
763
P VNT002 Ventricular Septal Defect 47 0.106
764
LKP003 Leukoplakia 39 0.106
765
CLR030 Clear Cell Renal Cell Carcinoma 38 0.105
766
P THR005 Thrombotic Thrombocytopenic Purpura 53 0.105
767
MLN007 Male Infertility 46 0.105
768
FCL014 Focal Epilepsy 37 0.105
769
HST011 Histoplasmosis 64 0.105
770
P HYP014 Hyperuricemia 47 0.105
771
FDL002 Food Allergy 41 0.105
772
P NRM001 Neuromyelitis Optica 52 0.105
773
P HML001 Hemolytic-Uremic Syndrome 43 0.105
774
ALL014 Allergic Encephalomyelitis 35 0.105
775
P BRG001 Brugada Syndrome 56 0.104
776
OST003 Osteonecrosis 49 0.104
777
STS002 Situs Inversus 46 0.104
778
SLC006 Silicosis 49 0.104
779
ART005 Arteriovenous Malformation 53 0.104
780
PNM013 Pneumococcal Meningitis 47 0.104
781
BRD004 Borderline Personality Disorder 39 0.104
782
CRY005 Cryptococcosis 58 0.104
783
TYP007 Typhoid Fever 53 0.104
784
P MMP001 Mumps 51 0.104
785
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 51 0.104
786
TCK001 Tick-Borne Encephalitis 45 0.104
787
PRC013 Pericarditis 45 0.104
788
c ACT042 Acute Pyelonephritis 36 0.104
789
P NRN021 Neuronal Ceroid Lipofuscinosis 55 0.103
790
RBS001 Rabies 50 0.103
791
DPH001 Diphtheria 47 0.103
792
P VSC005 Vesicoureteral Reflux 46 0.103
793
TRN044 Transposition of the Great Arteries 41 0.103
794
KLD001 Keloids 31 0.103
795
P HRD008 Hereditary Hemorrhagic Telangiectasia 75 0.103
796
ACH004 Achondroplasia 68 0.103
797
MCR004 Macroglobulinemia 48 0.103
798
AMB002 Amblyopia 39 0.103
799
WLS001 Wilson Disease 74 0.103
800
P LPS002 Liposarcoma 56 0.103
801
P INT001 Intrahepatic Cholestasis 55 0.103
802
DYS073 Dysphagia 45 0.103
803
PLY041 Polymyositis 51 0.103
804
P MYM002 Moyamoya Disease 51 0.103
805
GNR004 Generalized Anxiety Disorder 49 0.102
806
BRN004 Brain Edema 46 0.102
807
MTR014 Motor Neuron Disease 53 0.102
808
KRT009 Keratosis 45 0.102
809
P ALP009 Alopecia Areata 56 0.102
810
MRB003 Morbid Obesity 52 0.102
811
P PRG013 Paraganglioma 46 0.102
812
TNC002 Tinea Capitis 41 0.102
813
P CRN037 Craniosynostosis 60 0.102
814
P LCT001 Lactic Acidosis 42 0.102
815
P MTR012 Mitral Valve Disease 52 0.102
816
INV001 Invasive Aspergillosis 44 0.101
817
P SHR001 Short Bowel Syndrome 45 0.101
818
AND015 Androgen Insensitivity 69 0.101
819
P THY023 Thymoma 57 0.101
820
P HRD011 Hereditary Spherocytosis 56 0.101
821
PLM012 Pulmonary Sarcoidosis 45 0.101
822
ADR007 Adrenoleukodystrophy 76 0.101
823
c HMP004 Hemophilia B 72 0.101
824
DRM011 Dermatophytosis 40 0.101
825
P HYP040 Hypospadias 54 0.101
826
THR035 Thrombasthenia 37 0.101
827
THR004 Thrombocytosis 50 0.101
828
MYC006 Mycosis Fungoides 62 0.101
829
MNN009 Meningoencephalitis 39 0.101
830
PST028 Post-Traumatic Stress Disorder 59 0.101
831
P FCL005 Focal Segmental Glomerulosclerosis 58 0.101
832
MTB004 Metabolic Acidosis 38 0.101
833
CRT049 Critical Limb Ischemia 43 0.100
834
BTL001 Botulism 52 0.100
835
VRC001 Varicocele 42 0.100
836
CDS001 Cadasil 73 0.100
837
RHM001 Rheumatic Fever 55 0.100
838
MYL020 Myelomeningocele 54 0.100
839
OPT009 Optic Neuritis 42 0.100
840
c ESS001 Essential Tremor 61 0.100
841
TRC008 Trachoma 58 0.100
842
LYM019 Lymphosarcoma 50 0.100
843
P PNM006 Pneumoconiosis 43 0.100
844
LPR001 Lepromatous Leprosy 42 0.100
845
LYM021 Lymphadenitis 39 0.100
846
P ALP004 Alport Syndrome 60 0.099
847
PTN002 Patent Ductus Arteriosus 49 0.099
848
WLF001 Wolff-Parkinson-White Syndrome 65 0.099
849
SHG001 Shigellosis 56 0.099
850
NWC001 Newcastle Disease 46 0.099
851
WLL004 Wallerian Degeneration 39 0.099
852
c MLG079 Malignant Pleural Mesothelioma 38 0.099
853
CYT005 Cytomegalovirus Retinitis 48 0.099
854
CHR005 Chorioamnionitis 42 0.099
855
SLP001 Sleeping Sickness 49 0.099
856
PRG009 Progressive Multifocal Leukoencephalopathy 45 0.099
857
P GND004 Gonadal Dysgenesis 43 0.099
858
JPN002 Japanese Encephalitis 46 0.099
859
P HYP020 Hyperprolactinemia 58 0.099
860
HPR003 Heparin-Induced Thrombocytopenia 46 0.099
861
SYN036 Syncope 37 0.099
862
SMN007 Seminoma 42 0.098
863
VCC001 Vaccinia 41 0.098
864
RFR003 Refractive Error 40 0.098
865
NRM002 Normal Pressure Hydrocephalus 56 0.098
866
P LMY004 Leiomyosarcoma 53 0.098
867
P OPH004 Ophthalmoplegia 47 0.098
868
CHL004 Cholelithiasis 40 0.098
869
P AGG001 Aggressive Periodontitis 39 0.098
870
CLR109 Colorectal Adenocarcinoma 29 0.098
871
P ALC004 Alcohol Abuse 48 0.098
872
INT075 Intracranial Hypertension 43 0.098
873
P PRM019 Premature Ovarian Failure 63 0.098
874
PPL002 Papillary Carcinoma 49 0.098
875
HYP024 Hypoparathyroidism 48 0.098
876
P LYM025 Lymphedema 45 0.098
877
NRM005 Neuromuscular Disease 43 0.098
878
URT010 Ureteral Obstruction 39 0.098
879
P STR020 Strabismus 44 0.098
880
CYS008 Cystic Echinococcosis 64 0.098
881
CRD137 Cardiogenic Shock 42 0.098
882
P CMP010 Complex Regional Pain Syndrome 53 0.098
883
PLM034 Pulmonary Emphysema 53 0.098
884
P ANG001 Angelman Syndrome 66 0.097
885
P NMN002 Niemann-Pick Disease 63 0.097
886
OVR029 Ovarian Hyperstimulation Syndrome 60 0.097
887
BBS001 Babesiosis 54 0.097
888
ALX002 Alexithymia 43 0.097
889
CND006 Candida Glabrata 36 0.097
890
P WSK001 Wiskott-Aldrich Syndrome 69 0.097
891
INT002 Intermittent Claudication 47 0.097
892
NPH003 Nephrocalcinosis 41 0.097
893
DWR001 Dwarfism 48 0.097
894
GRD001 Giardiasis 47 0.097
895
SBS003 Substance Abuse 41 0.097
896
TBR011 Tuberculous Meningitis 50 0.097
897
TRN015 Transient Cerebral Ischemia 44 0.097
898
BRN012 Bronchiolitis Obliterans 50 0.097
899
CYS010 Cystinosis 57 0.097
900
RFT001 Rift Valley Fever 47 0.097
901
P SCL018 Scoliosis 45 0.097
902
P DYS021 Dysautonomia 44 0.097
903
P NRL007 Neurologic Diseases 39 0.097
904
P END046 Endometritis 34 0.097
905
P AGM001 Agammaglobulinemia 59 0.096
906
CRP018 Cor Pulmonale 37 0.096
907
P MTC003 Metachromatic Leukodystrophy 76 0.096
908
NRC020 Neuroectodermal Tumor 51 0.096
909
SCL003 Social Phobia 48 0.096
910
ALL009 Allergic Conjunctivitis 40 0.096
911
P ATR005 Atrophic Gastritis 39 0.096
912
PTZ001 Peutz-Jeghers Syndrome 68 0.096
913
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.096
914
LYM027 Lymphopenia 43 0.096
915
CYS005 Cysticercosis 54 0.096
916
SCR008 Scrub Typhus 59 0.096
917
WBR001 Weber Syndrome 44 0.096
918
VNW001 Von Willebrand's Disease 67 0.096
919
APR001 Apraxia 38 0.096
920
ALC006 Alcoholic Hepatitis 58 0.096
921
BRN018 Borna Disease 42 0.096
922
SPS007 Spastic Cerebral Palsy 38 0.096
923
BCK001 Becker Muscular Dystrophy 61 0.095
924
P HYD002 Hydronephrosis 45 0.095
925
P CLR108 Colorectal Adenoma 49 0.095
926
MXD005 Mixed Connective Tissue Disease 56 0.095
927
AMN001 Amenorrhea 49 0.095
928
PRP027 Peripheral Vascular Disease 60 0.095
929
PRC002 Paracoccidioidomycosis 56 0.095
930
SPN019 Spondylolisthesis 45 0.095
931
NRG002 Neurogenic Bladder 44 0.095
932
DYS015 Dysentery 41 0.095
933
PYL006 Pyloric Stenosis 41 0.095
934
PRN023 Prion Disease 49 0.095
935
SBC001 Subacute Sclerosing Panencephalitis 47 0.095
936
P PRM002 Primary Hyperoxaluria 68 0.095
937
P HMC002 Homocystinuria 52 0.095
938
P SPN052 Spondyloarthropathy 39 0.095
939
GNR005 Gonorrhea 50 0.094
940
DNG002 Dengue Hemorrhagic Fever 50 0.094
941
GLC006 Galactosemia 75 0.094
942
CND002 Conduct Disorder 50 0.094
943
LST001 Listeriosis 49 0.094
944
DNT001 Dental Fluorosis 41 0.094
945
TRT001 Teratocarcinoma 36 0.094
946
P ADL010 Adult Respiratory Distress Syndrome 53 0.094
947
SCB001 Scabies 50 0.094
948
MLT006 Multidrug-Resistant Tuberculosis 46 0.094
949
PLY013 Polymyalgia Rheumatica 45 0.094
950
PLM010 Pulmonary Edema 41 0.094
951
SWN001 Swine Influenza 35 0.094
952
P CRB042 Cerebellar Ataxia 54 0.094
953
ILS001 Ileus 38 0.094
954
EPD046 Epididymitis 24 0.094
955
P NPH009 Nephrolithiasis 51 0.093
956
EHR002 Ehrlichiosis 45 0.093
957
BCT002 Bacterial Vaginosis 44 0.093
958
ADD001 Addison's Disease 65 0.093
959
BRS051 Breast Disease 43 0.093
960
ADN027 Adenomyosis 37 0.093
961
TRD006 Tardive Dyskinesia 47 0.093
962
CHL061 Childhood Leukemia 31 0.093
963
INT051 Intussusception 53 0.093
964
LNG024 Langerhans-Cell Histiocytosis 51 0.093
965
P FBR031 Febrile Seizures 47 0.093
966
HYP017 Hypophosphatemia 42 0.093
967
TRY001 Trypanosomiasis 42 0.093
968
P PSD015 Pseudohypoparathyroidism 47 0.093
969
ECT026 Ectopic Pregnancy 39 0.093
970
VLV010 Vulvovaginitis 38 0.093
971
P BCK002 Beckwith-Wiedemann Syndrome 61 0.092
972
LYM017 Lyme Disease 56 0.092
973
MYL001 Myelitis 46 0.092
974
OBS001 Obstructive Jaundice 42 0.092
975
MYT011 Myotonia 37 0.092
976
P OST001 Osteopetrosis 65 0.092
977
URN003 Urinary Schistosomiasis 50 0.092
978
RNL011 Renal Osteodystrophy 43 0.092
979
SPL018 Splenomegaly 40 0.092
980
STR008 Strongyloidiasis 58 0.092
981
MLD001 Melioidosis 62 0.092
982
RNL007 Renal Tubular Acidosis 48 0.092
983
PRP003 Porphyria Cutanea Tarda 69 0.092
984
MRK001 Merkel Cell Carcinoma 48 0.092
985
INC002 Inclusion Body Myositis 71 0.092
986
ARC002 Arachnoiditis 39 0.092
987
TRC003 Trichomoniasis 35 0.092
988
PRT018 Portal Vein Thrombosis 47 0.091
989
P HYP083 Hypopituitarism 47 0.091
990
c HYP163 Hyperlipidemia Type 3 23 0.091
991
MYS004 Myiasis 31 0.091
992
GST009 Gastroschisis 55 0.091
993
CLL003 Cellulitis 50 0.091
994
THY033 Thyrotoxicosis 49 0.091
995
P DMY001 Demyelinating Polyneuropathy 39 0.091
996
INF034 Infective Endocarditis 38 0.091
997
CRN030 Coronary Stenosis 36 0.091
998
ADG002 Audiogenic Seizures 27 0.091
999
SPT004 Septic Arthritis 45 0.091
1000
KRT008 Keratopathy 42 0.091
1001
c CHR417 Chronic Graft Versus Host Disease 37 0.091
1002
P CRB019 Cerebral Amyloid Angiopathy 59 0.091
1003
PRT014 Protein S Deficiency 55 0.091
1004
STT002 Status Asthmaticus 52 0.091
1005
NRF007 Neurofibroma 49 0.091
1006
NCR004 Nocardiosis 47 0.091
1007
CHK001 Chikungunya 41 0.091
1008
P EPN002 Ependymoma 55 0.091
1009
PRT011 Protein C Deficiency 54 0.091
1010
P HYP055 Hypoplastic Left Heart Syndrome 61 0.090
1011
PLM014 Pleomorphic Adenoma 53 0.090
1012
GNG012 Gingival Overgrowth 44 0.090
1013
NRM004 Neuroma 39 0.090
1014
P OLG002 Oligodendroglioma 55 0.090
1015
PRL009 Prolactinoma 50 0.090
1016
END028 Endemic Goiter 41 0.090
1017
CHN015 Chondrodysplasia 37 0.090
1018
CRS001 Crescentic Glomerulonephritis 35 0.090
1019
MCR013 Microphthalmia 52 0.090
1020
PRS045 Prostatic Hypertrophy 35 0.090
1021
P INT030 Intracranial Aneurysm 48 0.090
1022
PRN011 Pernicious Anemia 46 0.090
1023
AGR002 Agoraphobia 42 0.090
1024
ASP003 Aseptic Meningitis 52 0.090
1025
P VNS003 Venous Insufficiency 39 0.090
1026
SPP008 Suppurative Otitis Media 34 0.090
1027
PLS006 Plasmodium Vivax Malaria 57 0.090
1028
P HYP065 Hyperaldosteronism 49 0.090
1029
P OTS001 Otosclerosis 46 0.090
1030
TLR001 Tularemia 45 0.090
1031
c MLG069 Malignant Hypertension 54 0.089
1032
YLL002 Yellow Fever 50 0.089
1033
P SYR001 Syringomyelia 49 0.089
1034
XNT003 Xanthomatosis 41 0.089
1035
HLL004 Hellp Syndrome 46 0.089
1036
ZLL002 Zollinger-Ellison Syndrome 57 0.089
1037
P DRM007 Dermatitis Herpetiformis 56 0.089
1038
ADR015 Adrenocortical Carcinoma 49 0.089
1039
P CRV043 Cervical Dystonia 45 0.089
1040
CLC006 Calcinosis 44 0.089
1041
PRP080 Peripheral Artery Disease 30 0.089
1042
RLP003 Relapsing Fever 42 0.089
1043
P TYS001 Tay-Sachs Disease 73 0.089
1044
ANR002 Aniridia 61 0.089
1045
ALL008 Allergic Bronchopulmonary Aspergillosis 57 0.089
1046
P RTN025 Retinoschisis 50 0.089
1047
P MCR010 Microcephaly 49 0.089
1048
TRP002 Tropical Spastic Paraparesis 46 0.089
1049
ZYG002 Zygomycosis 39 0.089
1050
CRT016 Carotid Artery Disease 38 0.089
1051
TKY001 Takayasu's Arteritis 60 0.089
1052
CHC001 Chickenpox 51 0.089
1053
OST016 Osteochondrosis 49 0.089
1054
P SCK002 Sick Sinus Syndrome 50 0.088
1055
FCL044 Fecal Incontinence 24 0.088
1056
P FRD001 Friedreich Ataxia 61 0.088
1057
CRN036 Craniopharyngioma 54 0.088
1058
P UVL004 Uveal Melanoma 53 0.088
1059
HYP025 Hyperphosphatemia 36 0.088
1060
CCC001 Coccidioidomycosis 63 0.088
1061
SLP005 Sleep Disorder 48 0.088
1062
VTM002 Vitamin B12 Deficiency 40 0.088
1063
BRS090 Breast Reconstruction 38 0.088
1064
ATS001 Autistic Disorder 61 0.088
1065
GLC085 Glucose-6-Phosphate Dehydrogenase Deficiency 57 0.088
1066