Search results for smad4

869 hits were found for smad4

# Family MCID Name MIFTS Score
1
P TMR010 Tumor Predisposition Syndrome 69 102.535
2
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 99.869
3
INH023 Inherited Cancer-Predisposing Syndrome 53 99.869
4
P JVN014 Juvenile Polyposis Syndrome 65 80.363
5
GNR035 Generalized Juvenile Polyposis/juvenile Polyposis Coli 41 57.019
6
MYH012 Myhre Syndrome 43 51.803
7
JVN012 Juvenile Polyposis/hereditary Hemorrhagic Telangiectasia Syndrome 48 50.311
8
P PNC035 Pancreatic Cancer 86 47.673
9
P CLR023 Colorectal Cancer 100 41.307
10
P HRD008 Hereditary Hemorrhagic Telangiectasia 65 33.970
11
P LNG032 Lung Cancer 98 24.828
12
P BRS047 Breast Cancer 97 23.233
13
GST040 Gastric Adenocarcinoma 66 21.165
14
PNC129 Pancreatic Adenocarcinoma 65 20.840
15
P GST053 Gastric Cancer 82 20.777
16
ESP021 Esophageal Cancer 84 19.840
17
P ADN016 Adenocarcinoma 63 19.480
18
P LNG064 Lung Cancer Susceptibility 3 70 18.734
19
P PRS040 Prostate Cancer 95 18.578
20
P THR014 Thrombocytopenia 66 18.253
21
END057 Endometrial Cancer 71 17.492
22
P FML364 Familial Thoracic Aortic Aneurysm and Aortic Dissection 71 17.373
23
P OVR042 Ovarian Cancer 88 16.858
24
CRV035 Cervical Cancer 72 16.656
25
CLN015 Colon Adenocarcinoma 64 16.107
26
P HPT023 Hepatocellular Carcinoma 95 15.860
27
SQM006 Squamous Cell Carcinoma 59 15.280
28
SQM013 Squamous Cell Carcinoma, Head and Neck 75 15.095
29
ADN018 Adenoma 58 15.044
30
P BLD062 Bile Duct Cancer 68 14.739
31
DSS008 Disease of Mental Health 74 14.477
32
PNC041 Pancreatic Ductal Adenocarcinoma 51 14.348
33
BRS099 Breast Ductal Carcinoma 61 13.569
34
P FML011 Familial Adenomatous Polyposis 71 13.511
35
P PLM037 Pulmonary Hypertension 69 13.383
36
TLN003 Telangiectasis 51 13.169
37
GST103 Gastric Cancer, Hereditary Diffuse 68 13.167
38
CLT003 Colitis 63 12.941
39
ART016 Aortic Aneurysm 69 12.033
40
P ART005 Arteriovenous Malformation 65 11.652
41
PNC013 Pancreatic Ductal Carcinoma 48 11.582
42
ART074 Aortic Dissection 53 11.573
43
ART017 Aortic Disease 49 11.563
44
P RHB003 Rhabdomyosarcoma 66 11.362
45
SPP011 Suppression of Tumorigenicity 12 61 11.350
46
P PNC044 Pancreatitis 61 11.215
47
ULC004 Ulcerative Colitis 74 11.152
48
P CWD010 Cowden Syndrome 71 11.019
49
P NSP012 Nasopharyngeal Carcinoma 60 11.019
50
P HRT032 Heart Disease 84 10.973
51
HRT036 Heritable Thoracic Aortic Disease 36 10.519
52
CLR003 Clear Cell Adenocarcinoma 50 10.413
53
CHL065 Cholangiocarcinoma 58 10.250
54
INT079 Intrahepatic Cholangiocarcinoma 51 10.250
55
ANR040 Aneurysm 60 10.130
56
BRR014 Barrett Esophagus 66 10.044
57
DFC004 Deficiency Anemia 74 9.651
58
PTZ001 Peutz-Jeghers Syndrome 69 9.579
59
BLR013 Biliary Tract Cancer 43 9.570
60
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 9.566
61
P BRC006 Brachydactyly 52 9.291
62
P HMR003 Hemorrhagic Disease 59 9.261
63
c ART115 Aortic Valve Disease 1 72 9.248
64
CLN044 Colon Adenoma 44 9.172
65
c CWD006 Cowden Syndrome 1 79 9.158
66
ACT119 Acute Promyelocytic Leukemia 62 9.038
67
VPM001 Vipoma 49 8.889
68
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 56 8.820
69
ACN001 Acinar Cell Carcinoma 44 8.571
70
PYR010 Peyronie's Disease 50 8.553
71
P MLN069 Melanoma, Uveal 59 8.510
72
ADN009 Adenosquamous Carcinoma 49 8.510
73
AMP013 Ampulla of Vater Cancer 41 8.486
74
c LCL006 Localized Scleroderma 64 8.458
75
P TTR001 Tetralogy of Fallot 69 8.425
76
OCL022 Ocular Melanoma 54 8.425
77
P SML016 Small Intestine Cancer 47 8.383
78
P LRG016 Large Intestine Adenocarcinoma 34 8.280
79
P MCR010 Microcephaly 59 8.280
80
MCN008 Mucinous Cystadenocarcinoma 39 8.280
81
c PLM164 Pulmonary Hypertension, Primary, 1 80 8.133
82
c ART067 Aortic Aneurysm, Familial Thoracic 1 61 7.362
83
P LYN001 Lynch Syndrome 76 7.154
84
PLM134 Pulmonary Fibrosis, Idiopathic 76 7.126
85
P LYS001 Loeys-Dietz Syndrome 65 6.956
86
OVR059 Ovary Adenocarcinoma 49 6.928
87
APP009 Appendix Adenocarcinoma 47 6.747
88
SML009 Small Intestine Adenocarcinoma 57 6.732
89
P HRD144 Hereditary Mixed Polyposis Syndrome 54 6.703
90
P LFR001 Li-Fraumeni Syndrome 73 6.634
91
c CLR087 Colorectal Cancer 12 34 6.419
92
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 60 6.419
93
APP010 Appendix Cancer 44 6.000
94
c FML311 Familial Colorectal Cancer Type X 37 6.000
95
NPH018 Nephrogenic Systemic Fibrosis 49 6.000
96
c SPN395 Spinal Muscular Atrophy, Type Ii 55 5.958
97
c SPN398 Spinal Muscular Atrophy, Type Iv 44 5.958
98
URT024 Urethra Clear Cell Adenocarcinoma 26 5.958
99
MCN005 Mucinous Intrahepatic Cholangiocarcinoma 23 5.958
100
DDN010 Duodenum Cancer 52 5.855
101
CLL012 Cell Type Benign Neoplasm 21 5.855
102
CRD007 Cardiovascular Organ Benign Neoplasm 25 5.855
103
ALB025 Albinism, Ocular, with Late-Onset Sensorineural Deafness 49 5.855
104
c HMC009 Hemochromatosis Type 2 58 5.855
105
c ATS417 Autosomal Dominant Non-Syndromic Intellectual Disability 19 28 5.855
106
APP018 Appendix Disease 31 5.855
107
MLG168 Malignant Exocrine Pancreas Neoplasm 30 5.855
108
BRT013 Baritosis 32 5.855
109
OVR047 Ovarian Cystadenocarcinoma 38 5.855
110
GST038 Gastrointestinal Adenoma 21 5.855
111
DDN027 Duodenum Disease 36 5.855
112
INT253 Intestinal Benign Neoplasm 46 5.855
113
P ART028 Aortic Aneurysm, Familial Thoracic 4 61 4.190
114
ADN011 Adenoid Cystic Carcinoma 68 3.699
115
LNG039 Lung Squamous Cell Carcinoma 57 3.625
116
P BLD134 Bladder Cancer 79 3.367
117
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 3.019
118
BLD173 Bladder Small Cell Carcinoma 44 2.999
119
P SKN015 Skin Carcinoma 71 2.897
120
GLM045 Glioma 62 2.617
121
ADN089 Adenosquamous Lung Carcinoma 49 2.611
122
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 2.611
123
c SML038 Small Cell Cancer of the Lung 69 2.487
124
ORL015 Oral Squamous Cell Carcinoma 43 2.447
125
DST001 Distal Biliary Tract Carcinoma 24 2.379
126
P SPP010 Suppressor of Tumorigenicity 3 51 2.270
127
RNL077 Renal Fibrosis 46 2.268
128
P PLM036 Pulmonary Fibrosis 65 2.143
129
IDP092 Idiopathic/heritable Pulmonary Arterial Hypertension 43 2.060
130
c MCR133 Microvascular Complications of Diabetes 4 41 1.998
131
c MCR113 Microvascular Complications of Diabetes 3 52 1.998
132
c MCR130 Microvascular Complications of Diabetes 6 41 1.998
133
c MCR120 Microvascular Complications of Diabetes 7 47 1.998
134
THY029 Thyroid Carcinoma 54 1.962
135
GLL048 Glial Tumor 52 1.957
136
c BSL007 Basal Cell Carcinoma 68 1.921
137
SKN022 Skin Squamous Cell Carcinoma 54 1.910
138
c BRN108 Branchiootic Syndrome 1 63 1.884
139
HYP266 Hypoxia 56 1.861
140
c THY109 Thyroid Cancer, Nonmedullary, 1 55 1.751
141
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.748
142
IRN002 Iron Metabolism Disease 56 1.716
143
OST159 Osteogenic Sarcoma 66 1.716
144
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.697
145
P RCT021 Rectum Cancer 54 1.614
146
MRF001 Marfan Syndrome 76 1.538
147
HLX001 Helix Syndrome 47 1.513
148
URT010 Ureteral Obstruction 45 1.513
149
P INF037 Inflammatory Bowel Disease 53 1.504
150
CRH001 Crohn's Disease 80 1.478
151
c HPT073 Hepatitis C Virus 71 1.475
152
OVR011 Ovarian Mucinous Adenocarcinoma 34 1.475
153
CLF027 Cleft Palate, Isolated 64 1.470
154
OVR094 Ovarian Epithelial Cancer 39 1.460
155
MNN043 Meningioma, Familial 79 1.419
156
P ALP008 Alopecia 53 1.403
157
c WLM013 Wilms Tumor 1 65 1.396
158
CLR109 Colorectal Adenocarcinoma 50 1.385
159
HMS001 Hemosiderosis 48 1.352
160
P RRH023 Rare Hereditary Hemochromatosis 53 1.352
161
ORL011 Oral Cancer 60 1.337
162
HRD224 Hereditary Nonpolyposis Colon Cancer 51 1.326
163
c TLN010 Telangiectasia, Hereditary Hemorrhagic, Type 4 21 1.321
164
HRW001 Hair Whorl 35 1.315
165
MCR013 Microphthalmia 60 1.302
166
THY123 Thyroid Gland Follicular Carcinoma 53 1.298
167
c WLM018 Wilms Tumor 5 54 1.293
168
P MYM016 Moyamoya Angiopathy 22 1.293
169
PRS129 Prostatic Hyperplasia, Benign 48 1.289
170
PRS045 Prostatic Hypertrophy 52 1.289
171
THY124 Thyroid Gland Papillary Carcinoma 38 1.263
172
SQM016 Squamous Cell Carcinoma of Gallbladder and Extrahepatic Biliary Tract 16 1.263
173
CRC045 Carcinoma of Gallbladder and Extrahepatic Biliary Tract 20 1.263
174
P NRB001 Neuroblastoma 66 1.252
175
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.232
176
LKP003 Leukoplakia 39 1.232
177
SRR001 Serrated Polyposis Syndrome 42 1.220
178
ORL012 Oral Leukoplakia 35 1.211
179
P BND020 Bone Disease 60 1.203
180
P END044 Endometriosis 62 1.200
181
c LKM061 Leukemia, Acute Myeloid 83 1.200
182
P RRT020 Rare Tumor 39 1.200
183
BNR002 Bone Resorption Disease 47 1.189
184
c PNC103 Pancreatic Cancer 4 25 1.177
185
PLM151 Pulmonary Arteriovenous Fistulas 35 1.169
186
P MLN008 Melanoma 75 1.166
187
TRM010 Traumatic Brain Injury 50 1.166
188
47X002 47,xyy 48 1.166
189
THR100 Thrombocytopenic Purpura, Autoimmune 60 1.154
190
P INF032 Infertility 60 1.115
191
TRN018 Transitional Cell Carcinoma 56 1.115
192
P INS002 in Situ Carcinoma 53 1.115
193
c PRC016 Pre-Eclampsia 64 1.102
194
PPL052 Papillomatosis, Confluent and Reticulated 34 1.102
195
PRS047 Prostatitis 58 1.102
196
CHR074 Choriocarcinoma 46 1.102
197
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.088
198
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 1.088
199
END041 Endometrial Adenocarcinoma 63 1.079
200
PLM173 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal 34 1.077
201
PSD011 Pseudovascular Skin Squamous Cell Carcinoma 16 1.077
202
c TLN011 Telangiectasia, Hereditary Hemorrhagic, Type 2 45 1.071
203
ISC004 Ischemia 61 1.058
204
c BSL024 Basal Cell Carcinoma 1 54 1.058
205
SKN013 Skin Benign Neoplasm 49 1.058
206
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 1.058
207
MCR011 Microinvasive Gastric Cancer 41 1.042
208
PRS021 Prostatic Adenoma 43 1.042
209
PPL002 Papillary Carcinoma 46 1.042
210
LNG099 Lung Disease 62 1.032
211
SHP005 Shprintzen-Goldberg Craniosynostosis Syndrome 46 1.025
212
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.025
213
P EMB005 Embryonal Rhabdomyosarcoma 53 1.025
214
IRN001 Iron Deficiency Anemia 58 1.025
215
c FML053 Familial Colorectal Cancer 47 1.009
216
LBL001 Lobular Neoplasia 55 1.008
217
P SCH015 Schizophrenia 74 1.008
218
LPD008 Lipid Metabolism Disorder 61 1.008
219
SGN002 Signet Ring Cell Adenocarcinoma 46 1.008
220
HYP457 Hypertrophic Scars 42 1.001
221
KLD004 Keloid Disorder 39 0.990
222
P RTN024 Retinoblastoma 72 0.979
223
GLB002 Glioblastoma 67 0.979
224
P ART023 Arthropathy 60 0.979
225
THR004 Thrombocytosis 52 0.969
226
PRP030 Purpura 54 0.969
227
PLM052 Pulmonary Arteriovenous Malformation 42 0.969
228
P LKM062 Leukemia, Acute Lymphoblastic 69 0.947
229
P OST002 Osteoporosis 77 0.944
230
SVR004 Severe Combined Immunodeficiency 71 0.944
231
c MSM022 Mismatch Repair Cancer Syndrome 1 69 0.933
232
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.932
233
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.932
234
PRC013 Pericarditis 53 0.932
235
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.919
236
NRN004 Neuroendocrine Tumor 55 0.919
237
CNS004 Constipation 56 0.919
238
SKN019 Skin Melanoma 70 0.913
239
c PRG020 Paragangliomas 3 39 0.906
240
CLR030 Clear Cell Renal Cell Carcinoma 54 0.906
241
MCN001 Mucinous Adenocarcinoma 49 0.892
242
P PLY011 Polycystic Ovary Syndrome 57 0.892
243
MTY003 Mutyh Polyposis 38 0.892
244
c PCH010 Pachyonychia Congenita 3 43 0.878
245
c FNC027 Fanconi Anemia, Complementation Group a 81 0.878
246
GST071 Gastrointestinal Carcinoma 46 0.878
247
P GLL018 Gallbladder Cancer 53 0.878
248
c CLR077 Colorectal Cancer 10 32 0.865
249
HLC007 Helicobacter Pylori Infection 67 0.864
250
HYD002 Hydronephrosis 58 0.864
251
c HPT016 Hepatitis B 62 0.864
252
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.864
253
P ART022 Arthritis 70 0.864
254
FTT001 Fatty Liver Disease 61 0.864
255
P NRF002 Neurofibromatosis 60 0.864
256
INT358 Intestinal Polyposis Syndrome 25 0.864
257
LNG012 Lung Occult Squamous Cell Carcinoma 20 0.852
258
PPL004 Papillary Squamous Carcinoma 39 0.852
259
LNG007 Lung Mixed Small Cell and Squamous Cell Carcinoma 20 0.852
260
c ACT027 Acute Pancreatitis 60 0.851
261
c HMC039 Hemochromatosis, Type 1 73 0.848
262
END062 Endometrial Hyperplasia 48 0.848
263
RVL002 Ruvalcaba Syndrome 42 0.848
264
P HPT021 Hepatitis 68 0.848
265
FRZ001 Frozen Shoulder 54 0.848
266
SFT003 Soft Tissue Sarcoma 57 0.848
267
THY128 Thyroid Tumor 33 0.848
268
P ANT088 Anterior Segment Dysgenesis 53 0.832
269
c VRL010 Viral Hepatitis 52 0.832
270
KRT009 Keratosis 52 0.832
271
GST033 Gestational Diabetes 61 0.832
272
PTR032 Peters-Plus Syndrome 63 0.832
273
P CTR002 Cataract 59 0.832
274
MYH016 Myh-Associated Polyposis 38 0.832
275
ECH003 Echinococcosis 52 0.819
276
NNL006 Non-Alcoholic Steatohepatitis 54 0.816
277
P CLD001 Cleidocranial Dysplasia 64 0.816
278
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.816
279
c HPT001 Hepatitis C 61 0.816
280
P VSC007 Vascular Disease 62 0.816
281
P TRT010 Teratoma 50 0.816
282
CRV002 Cervix Uteri Carcinoma in Situ 48 0.816
283
CRV045 Cervical Intraepithelial Neoplasia 38 0.816
284
ANT024 Anthrax Disease 58 0.816
285
c CLD019 Cleidocranial Dysplasia Spectrum Disorder 20 0.816
286
DWR001 Dwarfism 45 0.816
287
P ACT008 Actinic Keratosis 54 0.816
288
MCN019 Mucinous Adenocarcinoma of Ovary 16 0.816
289
WRN001 Werner Syndrome 69 0.798
290
MSC007 Muscle Hypertrophy 64 0.798
291
GLC003 Glucose Intolerance 53 0.798
292
c FML347 Familial Adenomatous Polyposis 2 56 0.798
293
P MYC007 Myocardial Infarction 69 0.798
294
BRT054 Brittle Bone Disorder 74 0.798
295
OSS012 Osseous Heteroplasia, Progressive 61 0.798
296
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.798
297
P CRN300 Coronary Heart Disease 1 73 0.798
298
P ATT003 Attenuated Familial Adenomatous Polyposis 57 0.798
299
P NRP001 Neuropathy 59 0.798
300
P PRG139 Progeroid Syndrome 29 0.798
301
PRM013 Premature Menopause 57 0.779
302
RTN017 Retinal Detachment 60 0.779
303
TNG009 Tongue Squamous Cell Carcinoma 43 0.779
304
TRT017 Teratoma, Ovarian 28 0.779
305
IGG001 Iga Glomerulonephritis 50 0.779
306
P HML002 Hemolytic Anemia 62 0.779
307
OVR109 Ovarian Germ Cell Teratoma 32 0.779
308
HRT011 Heart Septal Defect 49 0.779
309
P HYP086 Hypothyroidism 69 0.779
310
HYP066 Hyperglycemia 60 0.779
311
CRV038 Cervical Squamous Cell Carcinoma 56 0.779
312
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 47 0.779
313
BRN056 Bronchopulmonary Dysplasia 57 0.779
314
P GLM040 Glioma Susceptibility 1 70 0.763
315
P OLG002 Oligodendroglioma 66 0.763
316
c CLR085 Colorectal Cancer 1 42 0.762
317
c CLR075 Colorectal Cancer 3 31 0.762
318
MLN065 Melanocytic Nevus Syndrome, Congenital 61 0.762
319
MYP002 Myoepithelial Carcinoma 46 0.762
320
EPT010 Epithelial-Myoepithelial Carcinoma 55 0.762
321
P SNS001 Sensorineural Hearing Loss 59 0.759
322
P PNM006 Pneumoconiosis 55 0.759
323
INT395 Intracranial Meningioma 48 0.759
324
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.759
325
ERM002 Ear Malformation 35 0.759
326
P VNT002 Ventricular Septal Defect 58 0.759
327
P NPH012 Nephrotic Syndrome 62 0.759
328
ANT018 Anthracosis 51 0.759
329
P RST002 Restrictive Cardiomyopathy 54 0.759
330
P FBR017 Fibrosarcoma 55 0.759
331
VLV034 Vulva Squamous Cell Carcinoma 49 0.759
332
P MYP004 Myopathy 67 0.759
333
SCR001 Secretory Meningioma 40 0.759
334
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.759
335
P ADT009 Auditory Neuropathy Spectrum Disorder 33 0.759
336
THR123 Thrombotic Microangiopathy 40 0.759
337
VLL006 Villous Adenoma 40 0.737
338
P CRC039 Coarctation of Aorta 46 0.737
339
c PNC108 Pancreatitis, Hereditary 68 0.737
340
RTN020 Retinal Vascular Disease 45 0.737
341
P GLM007 Glomerulonephritis 59 0.737
342
PLS011 Plasmacytoma 56 0.737
343
SMN007 Seminoma 42 0.737
344
ALL006 Allergic Asthma 56 0.737
345
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.713
346
IMM167 Immune Deficiency Disease 77 0.713
347
P EXN002 Exanthem 58 0.713
348
c LFR007 Li-Fraumeni Syndrome 2 44 0.713
349
P DFF019 Diffuse Gastric Cancer 50 0.713
350
ACT098 Acute Erythroid Leukemia 55 0.713
351
DBL002 Double Outlet Right Ventricle 57 0.713
352
DFF002 Diffuse Pulmonary Fibrosis 27 0.713
353
SNS003 Sensory Peripheral Neuropathy 51 0.713
354
P KDN017 Kidney Cancer 60 0.713
355
SLC006 Silicosis 55 0.713
356
LNG031 Lung Benign Neoplasm 51 0.713
357
P BRS044 Breast Adenocarcinoma 58 0.713
358
NNS035 Nonsyndromic 46,xx Testicular Disorders of Sex Development 10 0.713
359
P HYP730 Hypogonadotropic Hypogonadism 54 0.685
360
PRT019 Protein-Losing Enteropathy 44 0.685
361
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.685
362
c DWL002 Dowling-Degos Disease 1 58 0.685
363
GRG001 Greig Cephalopolysyndactyly Syndrome 64 0.685
364
HYP060 Hyperinsulinism 53 0.685
365
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.685
366
LYM027 Lymphopenia 56 0.685
367
GNG002 Ganglioneuroma 52 0.685
368
HYP080 Hypogonadism 49 0.685
369
GNG005 Gangliocytoma 54 0.685
370
P PLY006 Polydactyly 58 0.685
371
P HRP006 Herpes Simplex 65 0.685
372
c JVN010 Juvenile Rheumatoid Arthritis 66 0.685
373
P PRC019 Precocious Puberty 49 0.685
374
MCR004 Macroglobulinemia 48 0.685
375
IRN008 Iron Overload in Africa 51 0.660
376
RJS001 Ruijs-Aalfs Syndrome 47 0.660
377
LMN016 Luminal Breast Carcinoma B 28 0.660
378
P LMN015 Luminal Breast Carcinoma a 34 0.660
379
HPT079 Hepatoid Adenocarcinoma 39 0.660
380
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.660
381
c PRS070 Prostate Cancer, Hereditary, 12 22 0.660
382
c PRS071 Prostate Cancer, Hereditary, 13 25 0.660
383
c PRS117 Prostate Cancer, Hereditary, 11 24 0.660
384
c PRS114 Prostate Cancer, Hereditary, 2 33 0.660
385
c PRS097 Prostate Cancer, Hereditary, 1 38 0.660
386
ADL096 Adult Hepatocellular Carcinoma 60 0.660
387
PRS015 Prostate Signet Ring Cell Adenocarcinoma 25 0.660
388
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.660
389
PDT042 Pediatric Hepatocellular Carcinoma 50 0.660
390
PTY007 Pityriasis Rotunda 26 0.660
391
FBR086 Fibrolamellar Carcinoma 59 0.660
392
HPT011 Hepatocellular Clear Cell Carcinoma 45 0.660
393
OVR062 Ovary Serous Adenocarcinoma 25 0.660
394
MCP006 Mucoepidermoid Carcinoma 48 0.654
395
P DRM010 Dermatomyositis 61 0.652
396
HNC001 Henoch-Schoenlein Purpura 56 0.652
397
PLC006 Placental Choriocarcinoma 38 0.652
398
ALL029 Allergic Disease 61 0.652
399
PNC034 Pancreas Disease 49 0.652
400
CRN006 Coronary Aneurysm 41 0.652
401
P MSC003 Muscular Atrophy 52 0.652
402
CHL078 Childhood-Onset Schizophrenia 29 0.652
403
P CRN074 Coronary Artery Aneurysm 41 0.652
404
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.652
405
MRK001 Merkel Cell Carcinoma 65 0.642
406
CRC021 Carcinosarcoma 62 0.634
407
CYN002 Cyanosis, Transient Neonatal 43 0.609
408
P ASP006 Aspergillosis 71 0.609
409
P ALL008 Allergic Bronchopulmonary Aspergillosis 53 0.609
410
CYS008 Cystic Echinococcosis 57 0.609
411
INS001 Insulinoma 59 0.609
412
VCC001 Vaccinia 49 0.609
413
c PNC106 Pancreatic Agenesis 1 51 0.609
414
GST030 Gastrinoma 45 0.609
415
EXT034 Extrinsic Allergic Alveolitis 56 0.609
416
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.560
417
CHR072 Chordoma 57 0.544
418
MYL005 Myelofibrosis 70 0.544
419
P LKM071 Leukemia, Chronic Lymphocytic 74 0.544
420
c GLM043 Glioma Susceptibility 9 30 0.539
421
c GLM047 Glioma Susceptibility 3 32 0.539
422
c GLM025 Glioma Susceptibility 2 29 0.539
423
THY127 Thyroid Gland Hurthle Cell Carcinoma 19 0.539
424
THY027 Thymus Squamous Cell Carcinoma 24 0.539
425
PRM126 Primary Peritoneal Carcinoma 61 0.539
426
P SLV026 Salivary Gland Carcinoma 60 0.527
427
ALV002 Alveolar Echinococcosis 56 0.506
428
48X005 48,xyyy 39 0.506
429
P FLL037 Follicular Lymphoma 73 0.484
430
THY022 Thymic Carcinoma 56 0.484
431
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.441
432
P LKM002 Leukemia 66 0.413
433
CLR108 Colorectal Adenoma 63 0.400
434
P SYS005 Systemic Scleroderma 73 0.386
435
LYM143 Lymphoma, Non-Hodgkin, Familial 79 0.381
436
PLS025 Plasmablastic Lymphoma 56 0.381
437
END032 Endometrial Clear Cell Adenocarcinoma 33 0.381
438
FLL027 Fallopian Tube Carcinoma 66 0.381
439
THY025 Thymus Cancer 56 0.381
440
KRK001 Krukenberg Carcinoma 39 0.381
441
PNS010 Penis Squamous Cell Carcinoma 45 0.381
442
P LNG035 Lung Large Cell Carcinoma 53 0.381
443
c TYP010 Type C Thymoma 25 0.381
444
SCL043 Sclerosing Mucoepidermoid Carcinoma with Eosinophilia 18 0.381
445
LNG006 Lung Occult Large Cell Carcinoma 14 0.381
446
PNS005 Penis Mixed Squamous Cell Carcinoma 12 0.381
447
LYM018 Lymphoepithelioma-Like Thymic Carcinoma 26 0.381
448
P LYM118 Lymphoma 69 0.358
449
NRN001 Neuroendocrine Carcinoma 47 0.358
450
ATM095 Autoimmune Disease 61 0.342
451
TRC005 Tracheal Stenosis 43 0.326
452
OST003 Osteonecrosis 61 0.310
453
LYN004 Lynch Syndrome I 60 0.310
454
KLD003 Keloid Formation 34 0.310
455
c FML346 Familial Adenomatous Polyposis 1 65 0.310
456
LVR012 Liver Cirrhosis 62 0.310
457
END086 End Stage Renal Disease 54 0.310
458
HRT015 Heritable Pulmonary Arterial Hypertension 46 0.310
459
SZR028 Seizures, Scoliosis, and Macrocephaly/microcephaly Syndrome 36 0.292
460
P ANP001 Anaplastic Large Cell Lymphoma 61 0.292
461
c SCL052 Scleroderma, Familial Progressive 60 0.292
462
GST029 Gastric Cardia Adenocarcinoma 29 0.292
463
P BCL017 B-Cell Lymphoma 57 0.292
464
c 46X071 46,xy Disorder of Sexual Development Due to Dihydrotestosterone Backdoor Pathway Biosynthesis Defect 42 0.292
465
c LKM063 Leukemia, Chronic Myeloid 71 0.273
466
TNG007 Tongue Carcinoma 55 0.273
467
c SPN225 Spondyloarthropathy 1 70 0.273
468
GST086 Gastric Adenocarcinoma and Proximal Polyposis of the Stomach 30 0.273
469
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 42 0.273
470
SPN051 Spondylitis 51 0.273
471
INF009 Inflammatory Spondylopathy 30 0.273
472
SKN016 Skin Disease 62 0.273
473
P MLT074 Multiple Endocrine Neoplasia 58 0.273
474
P GST044 Gastritis 55 0.273
475
P KDN018 Kidney Disease 72 0.273
476
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 68 0.273
477
GRN022 Granulosa Cell Tumor of the Ovary 34 0.273
478
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.253
480
P MLT020 Multiple Sclerosis 79 0.253
481
BRN032 Brain Glioma 45 0.253
482
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 42 0.253
483
KPS004 Kaposi Sarcoma 76 0.253
484
PNM010 Pneumothorax, Primary Spontaneous 58 0.253
485
LMY002 Leiomyoma 51 0.253
486
PLM009 Pleomorphic Adenoma Carcinoma 33 0.253
487
PNM008 Pneumothorax 54 0.253
488
P OBS001 Obstructive Jaundice 49 0.253
489
INT066 Interstitial Lung Disease 60 0.253
490
PSD007 Pseudomyxoma Peritonei 52 0.253
491
c TLN009 Telangiectasia, Hereditary Hemorrhagic, Type 3 18 0.253
492
HRT012 Heart Valve Disease 53 0.253
494
P MYL006 Myeloid Leukemia 60 0.253
495
PLM014 Pleomorphic Adenoma 51 0.253
496
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 0.253
497
ACR121 Acromelic Dysplasia 11 0.253
498
P AST005 Asthma 76 0.231
499
OSS014 Ossification of the Posterior Longitudinal Ligament of Spine 48 0.231
500
PRT251 Proteinuria, Chronic Benign 58 0.231
501
P GLP001 Geleophysic Dysplasia 46 0.231
502
ACR043 Acromicric Dysplasia 49 0.231
503
P RHM011 Rheumatoid Arthritis 81 0.231
504
P WLL002 Weill-Marchesani Syndrome 55 0.231
505
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.231
506
c VSC019 Vesicoureteral Reflux 1 56 0.231
507
SVR001 Severe Acute Respiratory Syndrome 68 0.231
508
UTR024 Uterine Carcinosarcoma 58 0.231
509
PPL022 Papilloma 53 0.231
510
SQM002 Squamous Cell Papilloma 45 0.231
511
KHN001 Kuhnt-Junius Degeneration 48 0.231
512
P LPS002 Liposarcoma 64 0.231
513
P DNT011 Dentinogenesis Imperfecta 52 0.231
514
SPN035 Spindle Cell Sarcoma 51 0.231
515
ACT058 Active Peptic Ulcer Disease 55 0.231
516
c CHR684 Chronic Kidney Disease 74 0.231
517
BRN071 Brain Injury 50 0.231
518
APC006 Apc-Associated Polyposis Conditions 22 0.231
519
PRQ002 Paraquat Poisoning 28 0.231
520
CLR137 Clear Cell Adenocarcinoma of the Ovary 31 0.231
521
AGN016 Aging 54 0.206
522
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.206
523
CRT069 Cortical Malformations, Occipital 31 0.206
524
P MLT008 Multinodular Goiter 42 0.206
525
PRT013 Portal Hypertension 59 0.206
526
DST033 Distichiasis 35 0.206
527
P SCL057 Scoliosis, Isolated 1 40 0.206
528
P SCL018 Scoliosis 57 0.206
529
IDP070 Idiopathic Scoliosis 41 0.206
530
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 52 0.206
531
LYM029 Lymphedema-Distichiasis Syndrome 52 0.206
532
P PYR039 Peyronie Disease 39 0.206
533
P HMN032 Human Herpesvirus 8 47 0.206
534
SRC014 Sarcoma 64 0.206
535
c HRD202 Hereditary Lymphedema I 55 0.206
536
OPS001 Opisthorchiasis 41 0.206
537
FLL031 Follicular Adenoma 40 0.206
538
PRG009 Progressive Multifocal Leukoencephalopathy 58 0.206
539
TBL003 Tubular Adenocarcinoma 40 0.206
540
OVR034 Ovarian Clear Cell Adenocarcinoma 39 0.206
541
PNC015 Pancreatic Acinar Cell Adenocarcinoma 39 0.206
542
GTR002 Goiter 52 0.206
543
PLM010 Pulmonary Edema 54 0.206
544
P THY023 Thymoma 64 0.206
545
c THY107 Thymoma, Familial 42 0.206
546
P MSC005 Muscular Dystrophy 66 0.206
547
c ACT075 Acute Myocardial Infarction 55 0.206
548
P ATR005 Atrophic Gastritis 50 0.206
549
ACN026 Acinar Cell Carcinoma of Pancreas 27 0.206
550
PRM334 Primary Bone Dysplasia with Increased Bone Density 15 0.206
551
RNL078 Renal Dysplasia 46 0.206
552
INT381 Intraductal Tubulopapillary Neoplasm of Pancreas 12 0.206
553
ART140 Arteries, Anomalies of 52 0.179
554
c FRS014 Fraser Syndrome 1 56 0.179
555
MYL069 Myeloma, Multiple 77 0.179
556
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.179
557
P RTN008 Retinitis Pigmentosa 79 0.179
558
c MCR115 Microvascular Complications of Diabetes 5 65 0.179
559
LPP008 Lipoprotein Quantitative Trait Locus 65 0.179
561
P SML001 Small Cell Carcinoma 52 0.179
562
DSS032 Disease by Infectious Agent 55 0.179
563
NRR001 Neuroretinitis 42 0.179
564
P OPN001 Open-Angle Glaucoma 55 0.179
565
P CRB045 Cerebellar Hypoplasia 40 0.179
566
GST105 Gastroesophageal Adenocarcinoma 42 0.179
567
CKT002 Cakut 48 0.179
568
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.179
569
ATH013 Atherosclerosis Susceptibility 63 0.179
570
BRK010 Burkitt Lymphoma 66 0.179
571
c ATS007 Autism Spectrum Disorder 72 0.179
572
ADR040 Adrenal Gland Pheochromocytoma 45 0.179
573
P APL001 Aplastic Anemia 73 0.179
574
CHD004 Chudley-Mccullough Syndrome 47 0.179
575
ALL003 Allergic Rhinitis 66 0.179
576
P CPL014 Capillary Malformation-Arteriovenous Malformation 1 53 0.179
577
P PHC003 Pheochromocytoma 70 0.179
578
c TLN008 Telangiectasia, Hereditary Hemorrhagic, Type 5 24 0.179
579
c GLC092 Glaucoma, Primary Open Angle 61 0.179
580
P ATS364 Autism 72 0.179
581
BRN012 Bronchiolitis Obliterans 56 0.179
582
BRN002 Bronchiolitis 57 0.179
583
DNT012 Dental Caries 53 0.179
584
CYS009 Cystadenoma 43 0.179
585
ISL001 Islet Cell Tumor 55 0.179
586
P CRV031 Cervical Adenocarcinoma 48 0.179
587
RTN023 Retinitis 45 0.179
588
BLD039 Bladder Adenocarcinoma 32 0.179
589
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.179
590
STR067 Stroke, Ischemic 79 0.179
591
GST019 Gastrointestinal Stromal Tumor 78 0.179
592
URC003 Urachal Adenocarcinoma 30 0.179
593
OBS082 Obstructive Nephropathy 41 0.179
594
CYT002 Cytokine Deficiency 43 0.179
595
FRS019 Farsightedness 35 0.179
596
PTT037 Pituitary Tumors 44 0.179
597
ANL017 Anal Squamous Cell Carcinoma 44 0.179
598
SPL018 Splenomegaly 47 0.179
599
PNC019 Pancreatoblastoma 39 0.179
600
P INT070 Intestinal Obstruction 57 0.179
601
P DBT009 Diabetes Mellitus 67 0.179
602
c MNS014 Monosomy 22 34 0.179
603
P VTR007 Vitreoretinopathy 45 0.179
604
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.146
605
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.146
606
ADN027 Adenomyosis 59 0.146
607
RHB024 Rhabdomyosarcoma 2 65 0.146
608
P ATX030 Ataxia-Telangiectasia 80 0.146
609
INS024 Insulin-Like Growth Factor I 77 0.146
610
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.146
611
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.146
612
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.146
613
c HMP013 Hemophagocytic Lymphohistiocytosis, Familial, 3 47 0.146
614
c FNC025 Fanconi Anemia, Complementation Group J 52 0.146
615
WST005 West Nile Virus 55 0.146
616
c BRS098 Breast-Ovarian Cancer, Familial 4 29 0.146
617
c ATM024 Autoimmune Pancreatitis 52 0.146
618
c NPH096 Nephrotic Syndrome, Type 12 28 0.146
619
CMB007 Combined Immunodeficiency 56 0.146
620
CRB004 Cerebral Artery Occlusion 46 0.146
621
OTT002 Otitis Media 71 0.146
622
c ATR087 Atrial Standstill 1 74 0.146
623
c MCR247 Microcephaly 1, Primary, Autosomal Recessive 42 0.146
624
c TYP008 Type 1 Diabetes Mellitus 77 0.146
625
CNT061 Conotruncal Heart Malformations 66 0.146
626
CRH005 Crohn's Colitis 53 0.146
627
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.146
628
c NPH093 Nephrotic Syndrome, Type 13 21 0.146
629
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.146
630
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.146
631
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.146
632
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.146
633
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.146
634
ECT009 Ectopia Pupillae 13 0.146
635
P CMR001 Camurati-Engelmann Disease 59 0.146
636
c NRF024 Neurofibromatosis, Type I 76 0.146
637
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.146
638
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.146
639
HND015 Hand Skill, Relative 29 0.146
640
CRC014 Carcinoid Tumors, Intestinal 46 0.146
641
WTS001 Watson Syndrome 30 0.146
642
PYL006 Pyloric Stenosis 48 0.146
643
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.146
644
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.146
645
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 49 0.146
646
CHL068 Cholestasis 61 0.146
647
CNG034 Congestive Heart Failure 69 0.146
648
P ACN011 Acne 55 0.146
649
PNC127 Pancreatic Adenosquamous Carcinoma 34 0.146
650
P PRP019 Peripheral Nervous System Disease 57 0.146
651
P ATR010 Atrial Heart Septal Defect 58 0.146
652
RCT020 Rectum Adenocarcinoma 48 0.146
653
ANG011 Angiodysplasia 42 0.146
654
P HMN010 Hemangioma 61 0.146
655
P FCL005 Focal Segmental Glomerulosclerosis 57 0.146
656
P HYP069 Hyperparathyroidism 62 0.146
657
DDN003 Duodenum Adenocarcinoma 37 0.146
658
END011 Endometriosis of Ovary 40 0.146
659
CNS002 Constrictive Pericarditis 39 0.146
660
HMP001 Hemopericardium 47 0.146
661
P PRC012 Pericardial Effusion 50 0.146
662
P ADL010 Adult Respiratory Distress Syndrome 71 0.146
663
P LVR013 Liver Disease 68 0.146
664
OLF005 Olfactory Neuroblastoma 46 0.146
665
HGH043 High Grade Glioma 46 0.146
666
P PTT006 Pituitary Adenoma 55 0.146
667
P RHN004 Rhinitis 57 0.146
668
ASC004 Ascending Colon Cancer 42 0.146
669
P AML002 Amelogenesis Imperfecta 56 0.146
670
P ART021 Arteriosclerosis 53 0.146
671
GST049 Gastrointestinal System Cancer 49 0.146
672
BLD063 Bile Duct Cysts 42 0.146
673
THY042 Thymic Epithelial Tumor 26 0.146
674
BNG036 Bone Giant Cell Tumor 48 0.146
675
c CLR039 Colorectal Cancer, Hereditary Nonpolyposis, Type 4 40 0.146
676
GBL002 Goblet Cell Carcinoid 32 0.146
677
P THL005 Thalassemia 56 0.146
678
WBR001 Weber Syndrome 38 0.146
679
DYS073 Dysphagia 53 0.146
680
DGN001 Degenerative Disc Disease 48 0.146
681
CLF001 Cleft Lip 54 0.146
682
OVR012 Ovarian Serous Cystadenocarcinoma 55 0.146
683
ORL004 Oral Submucous Fibrosis 56 0.146
684
VNF001 Vein of Galen Aneurysm 18 0.146
685
PPT005 Peptic Ulcer Disease 58 0.146
686
CHL040 Cholangiolocellular Carcinoma 30 0.146
687
c SPR009 Sporadic Breast Cancer 42 0.146
688
PLC008 Placenta Disease 49 0.146
689
PST021 Postpartum Depression 50 0.146
690
DFF035 Diffuse Cutaneous Systemic Sclerosis 45 0.146
691
GNT179 Genetic Steroid-Resistant Nephrotic Syndrome 40 0.146
692
GRM010 Germ Cells Tumors 33 0.146
693
PRT009 Parotid Gland Cancer 32 0.146
694
P HYP658 Hypoplastic Amelogenesis Imperfecta 30 0.146
695
DFF036 Differentiated Thyroid Carcinoma 51 0.146
696
THY089 Thymic Epithelial Neoplasm 27 0.146
697
PLY100 Polyploidy 36 0.146
698
P ALZ034 Alzheimer Disease 87 0.103
699
c TYP009 Type 2 Diabetes Mellitus 92 0.103
700
CYS001 Cystic Fibrosis 77 0.103
701
P FNC044 Fanconi Anemia, Complementation Group C 56 0.103
702
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.103
703
c GLL024 Gallbladder Disease 1 53 0.103
704
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.103
705
P MYS003 Myasthenia Gravis 68 0.103
706
P PRS083 Prostate Cancer, Hereditary, X-Linked 1 12 0.103
707
AST006 Astigmatism 46 0.103
708
ANX010 Anxiety 70 0.103
709
MYL009 Myelodysplastic Syndrome 67 0.103
710
ADR016 Adrenal Cortical Carcinoma 61 0.103
711
P CLR037 Colorectal Cancer, Hereditary Nonpolyposis, Type 5 48 0.103
712
c DVL078 Developmental and Epileptic Encephalopathy 54 26 0.103
713
CPL015 Capillary Malformation-Arteriovenous Malformation 2 29 0.103
714
KSH004 Kashin-Beck Disease 37 0.103
715
HYP020 Hyperprolactinemia 63 0.103
716
ZLL002 Zollinger-Ellison Syndrome 55 0.103
717
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.103
718
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.103
719
DSM004 Desmoid Tumor 65 0.103
720
THY111 Thyroid Carcinoma, Familial Medullary 67 0.103
721
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 64 0.103
722
PLY150 Polykaryocytosis Inducer 29 0.103
723
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.103
724
P EPD083 Epidermodysplasia Verruciformis 1 57 0.103
725
P CLC063 Celiac Disease 1 66 0.103
726
ENT011 Enterocolitis 55 0.103
727
VNH007 Von Hippel-Lindau Syndrome 73 0.103
728
P OVR106 Ovarian Clear Cell Carcinoma 43 0.103
729
P SLP006 Sleep Apnea 69 0.103
730
MTR088 Mature T-Cell and Nk-Cell Lymphoma 42 0.103
731
CHL147 Chlamydia Pneumonia 47 0.103
732
P SCL048 Sclerosteosis 58 0.103
733
PLL012 Pollen Allergy 44 0.103
734
LRG014 Large Cell Neuroendocrine Carcinoma 44 0.103
735
HYP114 Hypertensive Nephropathy 35 0.103
736
P DRM053 Dermatitis, Atopic 65 0.103
737
OVR112 Ovarian Germ Cell Cancer 41 0.103
738
HMN044 Human Immunodeficiency Virus Type 1 76 0.103
739
MND020 Mandibulofacial Dysostosis, Guion-Almeida Type 50 0.103
740
c BNM016 Bone Mineral Density Quantitative Trait Locus 1 24 0.103
741
PKL001 Poikiloderma with Neutropenia 43 0.103
742
P KLZ004 Kala-Azar 1 41 0.103
743
c MLT086 Multiple Endocrine Neoplasia, Type Iv 50 0.103
744
c HYP595 Hypertension, Essential 84 0.103
745
c HYP836 Hypercholesterolemia, Familial, 1 73 0.103
746
INT051 Intussusception 53 0.103
747
EPC005 Epicanthus 36 0.103
748
NRL016 Neural Tube Defects 81 0.103
749
c CHL119 Cholangitis, Primary Sclerosing 57 0.103
750
P CNG436 Congenital Disorder of Deglycosylation 51 0.103
751
P WSK001 Wiskott-Aldrich Syndrome 72 0.103
752
CHR610 Chromosome 10q22.3-Q23.2 Deletion Syndrome 22 0.103
753
P RTH006 Rothmund-Thomson Syndrome, Type 2 67 0.103
754
c CLR041 Colorectal Cancer, Hereditary Nonpolyposis, Type 2 36 0.103
755
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.103
756
P CRD224 Cardiofaciocutaneous Syndrome 1 71 0.103
757
CRD223 Cardiac Arrhythmia 63 0.103
758
DGR001 Digeorge Syndrome 62 0.103
759
c DPH024 Diaphragmatic Hernia, Congenital 64 0.103
760
c TBR025 Tuberous Sclerosis 1 84 0.103
761
APP003 Appendiceal Neoplasm 36 0.103
762
P ALC033 Alcohol Use Disorder 67 0.103
763
P PTS002 Ptosis 52 0.103
764
P PRG013 Paraganglioma 57 0.103
765
RHM028 Rheumatic Heart Disease 56 0.103
766
CMP034 Complete Androgen Insensitivity Syndrome 55 0.103
767
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 0.103
768
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.103
769
c ACT073 Acute Leukemia 59 0.103
770
PTN001 Patent Foramen Ovale 62 0.103
771
P MYP006 Myopia 55 0.103
772
CLN003 Clonorchiasis 42 0.103
773
P TBR001 Tuberous Sclerosis 69 0.103
774
MLG169 Malignant Astrocytoma 57 0.103
775
OVR015 Ovarian Mixed Germ Cell Neoplasm 35 0.103
776
CRB039 Cerebrovascular Disease 65 0.103
777
BLD050 Bladder Urachal Carcinoma 24 0.103
778
ACR014 Acral Lentiginous Melanoma 52 0.103
779
ANP006 Anaplastic Ependymoma 46 0.103
780
BRN024 Bronchitis 67 0.103
781
P BNG030 Benign Ependymoma 51 0.103
782
P INT068 Intestinal Disease 53 0.103
783
GST041 Gastric Cardia Carcinoma 20 0.103
784
c INF023 Inflammatory Breast Carcinoma 48 0.103
785
THY030 Thyroid Gland Disease 50 0.103
786
CMD001 Comedo Carcinoma 37 0.103
787
P HYP040 Hypospadias 51 0.103
788
KRT002 Keratomalacia 54 0.103
789
P LTR001 Lateral Sclerosis 58 0.103
790
URT037 Urethral Stricture 42 0.103
791
IMP005 Impotence 52 0.103
792
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.103
793
TST015 Testicular Disease 42 0.103
794
THY122 Thyroid Gland Cancer 59 0.103
795
AZS001 Azoospermia 45 0.103
796
P SCL009 Sclerosing Cholangitis 46 0.103
797
P GND004 Gonadal Dysgenesis 46 0.103
798
c DLT002 Dilated Cardiomyopathy 79 0.103
799
P DMN001 Diamond-Blackfan Anemia 73 0.103
800
P HYD006 Hydrocephalus 63 0.103
801
c PRM005 Primary Hyperparathyroidism 59 0.103
802
CHL123 Chlamydia 58 0.103
803
P ESP024 Esophagitis 60 0.103
804
P PLM006 Pulmonary Alveolar Proteinosis 53 0.103
805
LYM009 Lymphocytic Choriomeningitis 46 0.103
806
P NTR004 Neutropenia 62 0.103
807
CRT017 Cartilage Disease 52 0.103
808
BLP004 Blepharophimosis 36 0.103
809
PNL012 Penile Cancer 57 0.103
810
PLC005 Placental Insufficiency 56 0.103
811
P TCD001 Tic Disorder 50 0.103
812
TST014 Testicular Cancer 51 0.103
813
AMP009 Ampulla of Vater Adenocarcinoma 36 0.103
814
ADR004 Adrenal Cortical Adenocarcinoma 38 0.103
815
EMB004 Embryonal Carcinoma 55 0.103
816
MMM001 Mammary Paget's Disease 53 0.103
817
PPL018 Papillary Adenocarcinoma 44 0.103
818
DMY004 Demyelinating Disease 50 0.103
819
MCN003 Mucinous Ovarian Cystadenoma 21 0.103
820
THY125 Thyroid Gland Medullary Carcinoma 48 0.103
821
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.103
822
P PTN014 Patent Ductus Arteriosus 1 59 0.103
823
PRM014 Periampullary Adenocarcinoma 39 0.103
824
P MYC008 Myocarditis 59 0.103
825
NRM005 Neuromuscular Disease 63 0.103
826
DRM006 Dermatitis 62 0.103
827
CNG608 Congenital Hypopituitarism 29 0.103
828
P INH011 Inherited Bone Marrow Failure Syndromes 34 0.103
829
NRN006 Neuroendocrine Carcinoma of the Cervix 19 0.103
830
BCK006 Back Pain 43 0.103
831
P ENC018 Encephalopathy 62 0.103
832
TST043 Testicular Seminoma 31 0.103
833
SRF006 Surfactant Dysfunction 33 0.103
834
P HYP265 Hypotonia 42 0.103
835
VSC003 Visceral Leishmaniasis 54 0.103
837
CLL010 Cellular Ependymoma 58 0.103
838
AVN001 Avian Influenza 61 0.103
839
c LRG001 Large Cell Carcinoma 48 0.103
840
WST010 West Nile Virus Infection 32 0.103
841
ALL014 Allergic Encephalomyelitis 34 0.103
842
HPT022 Hepatoblastoma 54 0.103
843
LSH001 Leishmaniasis 63 0.103
844
OST012 Osteoarthritis 77 0.103
845
P INF038 Influenza 68 0.103
846
DVR002 Diverticulitis 46 0.103
847
PTT001 Pituitary Hypoplasia 34 0.103
848
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.103
849
PRT029 Parathyroid Adenoma 51 0.103
850
GST050 Gastrointestinal System Disease 55 0.103
852
DST006 Diastolic Heart Failure 45 0.103
853
P CHL066 Cholangitis 51 0.103
854
NRF007 Neurofibroma 64 0.103
855
PRN019 Perinatal Necrotizing Enterocolitis 60 0.103
856
GRW007 Growth Hormone Deficiency 47 0.103
857
FXG001 Foxg1 Syndrome 27 0.103
858
P HYP083 Hypopituitarism 52 0.103
859
ERY069 Erythrokeratoderma ''en Cocardes'' 26 0.103
860
NTH004 Nthl1 Tumor Syndrome 9 0.103
861
PRT063 Proteus-Like Syndrome 27 0.103
862
CLF056 Cleft Lip with or Without Cleft Palate 43 0.103
863
MXD032 Mixed Germ Cell Tumor 24 0.103
864
CLF004 Cleft Lip/palate 57 0.103
865
MLG163 Malignant Tumor of Penis 29 0.103
866
SLD011 Solid Pseudopapillary Carcinoma of Pancreas 29 0.103
867
HRD215 Hereditary Gastric Cancer 21 0.103
868
EXT062 Extracranial Carotid Artery Aneurysm 19 0.103
869
ATR055 Atrial Septal Aneurysm 22 0.103
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