Search results for smad2

946 hits were found for smad2

# Family MCID Name MIFTS Score
1
P CLR023 Colorectal Cancer 100 27.523
2
P BRS047 Breast Cancer 98 24.429
3
P GST053 Gastric Cancer 83 24.259
4
P PNC035 Pancreatic Cancer 86 22.281
5
P LNG032 Lung Cancer 98 21.494
6
P HPT023 Hepatocellular Carcinoma 96 21.054
7
RNL077 Renal Fibrosis 46 20.827
8
END057 Endometrial Cancer 72 20.037
9
P OVR042 Ovarian Cancer 88 19.958
10
P PRS040 Prostate Cancer 95 19.309
11
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 18.571
12
P PLM037 Pulmonary Hypertension 72 15.639
13
P GLM007 Glomerulonephritis 60 14.364
14
P OST002 Osteoporosis 76 14.085
15
PLM134 Pulmonary Fibrosis, Idiopathic 76 14.064
16
P INF037 Inflammatory Bowel Disease 53 13.938
17
HYP457 Hypertrophic Scars 42 13.268
18
P RHB003 Rhabdomyosarcoma 66 13.126
19
PNC129 Pancreatic Adenocarcinoma 65 12.960
20
P LYS001 Loeys-Dietz Syndrome 65 12.917
21
CLR003 Clear Cell Adenocarcinoma 50 12.628
22
OBS082 Obstructive Nephropathy 41 12.359
23
P PLM036 Pulmonary Fibrosis 66 12.227
24
CHG001 Chagas Disease 66 12.128
25
c ART115 Aortic Valve Disease 1 74 11.693
26
BSC001 Buschke-Ollendorff Syndrome 56 10.952
27
MLR003 Melorheostosis 48 10.952
28
OST014 Osteopoikilosis 41 10.952
29
P HLP001 Holoprosencephaly 69 10.652
30
c HYP595 Hypertension, Essential 85 9.434
31
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 9.141
32
URN010 Urinary Tract Obstruction 55 8.343
33
c MCR130 Microvascular Complications of Diabetes 6 41 8.034
34
c MCR120 Microvascular Complications of Diabetes 7 47 8.034
35
c MCR113 Microvascular Complications of Diabetes 3 52 8.034
36
c MCR133 Microvascular Complications of Diabetes 4 41 8.034
37
P JVN014 Juvenile Polyposis Syndrome 64 7.769
38
P TTR001 Tetralogy of Fallot 69 7.769
39
URT010 Ureteral Obstruction 45 7.364
40
NPH018 Nephrogenic Systemic Fibrosis 49 7.245
41
PCM002 Pauci-Immune Glomerulonephritis 28 7.077
42
c SPN395 Spinal Muscular Atrophy, Type Ii 55 7.077
43
ALB025 Albinism, Ocular, with Late-Onset Sensorineural Deafness 49 6.671
44
c ATS417 Autosomal Dominant Non-Syndromic Intellectual Disability 19 29 6.671
45
P ORF002 Orofacial Cleft 43 6.671
46
c LYS017 Loeys-Dietz Syndrome 4 49 6.671
47
c LYS020 Loeys-Dietz Syndrome 5 49 6.671
48
c LYS021 Loeys-Dietz Syndrome 3 57 6.671
49
DYS160 Dyssegmental Dysplasia, Silverman-Handmaker Type 49 6.671
50
c SPS215 Spastic Paraplegia 3, Autosomal Dominant 62 6.671
51
DSS008 Disease of Mental Health 74 6.671
52
URT031 Ureteral Disease 41 6.671
53
VTR005 Vitreous Disease 40 6.671
54
SQM006 Squamous Cell Carcinoma 60 6.357
55
GLM045 Glioma 63 6.039
56
LNG099 Lung Disease 62 5.710
57
KLD004 Keloid Disorder 39 5.691
58
P LNG064 Lung Cancer Susceptibility 3 70 5.646
59
GLB002 Glioblastoma 67 5.603
60
P ADN016 Adenocarcinoma 63 5.179
61
GLL048 Glial Tumor 52 5.015
62
HYP266 Hypoxia 57 5.000
63
P BLD134 Bladder Cancer 79 4.919
64
c SML038 Small Cell Cancer of the Lung 69 4.828
65
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 4.781
66
ANR040 Aneurysm 61 4.581
67
CLN015 Colon Adenocarcinoma 65 4.555
68
c SCL052 Scleroderma, Familial Progressive 61 4.482
69
OST159 Osteogenic Sarcoma 66 4.423
70
CLF027 Cleft Palate, Isolated 64 4.418
71
PRT251 Proteinuria, Chronic Benign 57 4.348
72
CRV035 Cervical Cancer 73 4.293
73
GST103 Gastric Cancer, Hereditary Diffuse 68 4.290
74
SML009 Small Intestine Adenocarcinoma 57 4.196
75
c CHR684 Chronic Kidney Disease 69 4.184
76
ART016 Aortic Aneurysm 68 4.154
77
PNC041 Pancreatic Ductal Adenocarcinoma 51 4.138
78
P RTN024 Retinoblastoma 73 4.103
79
P MYC007 Myocardial Infarction 70 4.062
80
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 60 4.048
81
c CLR087 Colorectal Cancer 12 34 4.048
82
ORL015 Oral Squamous Cell Carcinoma 43 4.041
83
MRF001 Marfan Syndrome 76 4.038
84
P SYS005 Systemic Scleroderma 74 3.967
85
OST012 Osteoarthritis 77 3.944
86
c PLM164 Pulmonary Hypertension, Primary, 1 76 3.943
87
BNR002 Bone Resorption Disease 47 3.924
88
GST040 Gastric Adenocarcinoma 67 3.852
89
P ATR011 Atrial Fibrillation 66 3.834
90
RPD005 Rapidly Involuting Congenital Hemangioma 46 3.830
91
HYP066 Hyperglycemia 61 3.830
92
c PRC016 Pre-Eclampsia 65 3.830
93
MSC007 Muscle Hypertrophy 64 3.750
94
P PRD008 Periodontitis 64 3.705
95
ESP021 Esophageal Cancer 83 3.697
96
P BCL017 B-Cell Lymphoma 59 3.606
97
P KDN018 Kidney Disease 72 3.588
98
P AST005 Asthma 76 3.537
99
P MSC003 Muscular Atrophy 52 3.493
100
ISC004 Ischemia 61 3.478
101
RNL114 Renal Cell Carcinoma, Nonpapillary 80 3.353
102
PLM129 Pulmonary Disease, Chronic Obstructive 74 3.308
103
P INF032 Infertility 57 3.238
104
P SKN015 Skin Carcinoma 71 3.209
105
P NSP012 Nasopharyngeal Carcinoma 61 3.195
106
END086 End Stage Renal Disease 52 3.176
107
SVR004 Severe Combined Immunodeficiency 72 3.142
108
THY029 Thyroid Carcinoma 51 3.130
109
P END044 Endometriosis 62 3.130
110
HLX001 Helix Syndrome 48 3.107
111
CYT002 Cytokine Deficiency 43 3.080
112
INT066 Interstitial Lung Disease 60 3.072
113
c ATR087 Atrial Standstill 1 74 3.036
114
BRN056 Bronchopulmonary Dysplasia 56 2.976
115
P HRT032 Heart Disease 81 2.926
116
BRS099 Breast Ductal Carcinoma 61 2.893
117
CRB004 Cerebral Artery Occlusion 45 2.888
118
P SPP010 Suppressor of Tumorigenicity 3 51 2.849
119
ADN018 Adenoma 59 2.849
120
OVR094 Ovarian Epithelial Cancer 39 2.849
121
P OVR082 Overgrowth Syndrome 49 2.811
122
CLT003 Colitis 63 2.810
123
c BSL007 Basal Cell Carcinoma 68 2.794
125
KLD003 Keloid Formation 34 2.729
126
MYL069 Myeloma, Multiple 77 2.729
127
CHL065 Cholangiocarcinoma 58 2.722
128
INT079 Intrahepatic Cholangiocarcinoma 51 2.722
129
P VTR007 Vitreoretinopathy 46 2.692
130
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 2.692
131
P DBT009 Diabetes Mellitus 67 2.644
132
LVR012 Liver Cirrhosis 63 2.632
133
P VSC007 Vascular Disease 63 2.593
134
P PLY011 Polycystic Ovary Syndrome 57 2.593
135
LNG039 Lung Squamous Cell Carcinoma 57 2.564
136
ART074 Aortic Dissection 53 2.556
137
P BND020 Bone Disease 59 2.556
138
P ART022 Arthritis 71 2.553
139
P PLV020 Pelvic Organ Prolapse 58 2.529
140
ATM095 Autoimmune Disease 61 2.512
141
ORL011 Oral Cancer 60 2.510
142
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 2.479
143
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 2.479
144
AGN016 Aging 54 2.470
145
48X005 48,xyyy 39 2.469
146
P ADL010 Adult Respiratory Distress Syndrome 71 2.462
147
ULC004 Ulcerative Colitis 74 2.427
148
P MLN008 Melanoma 76 2.427
149
P ART021 Arteriosclerosis 54 2.427
150
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 2.414
151
IMP005 Impotence 52 2.401
152
SPN186 Spinal Cord Injury 61 2.383
153
ALL014 Allergic Encephalomyelitis 34 2.383
154
PYR010 Peyronie's Disease 50 2.366
155
ADN011 Adenoid Cystic Carcinoma 68 2.352
156
TLN003 Telangiectasis 51 2.339
157
CNG034 Congestive Heart Failure 69 2.339
158
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 2.293
159
NNL005 Non-Alcoholic Fatty Liver Disease 63 2.273
160
DGN001 Degenerative Disc Disease 49 2.259
161
SQM013 Squamous Cell Carcinoma, Head and Neck 73 2.245
162
SZR028 Seizures, Scoliosis, and Macrocephaly/microcephaly Syndrome 36 2.245
163
SLC006 Silicosis 56 2.245
164
KRT009 Keratosis 53 2.245
165
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.204
166
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.204
167
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.204
168
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 2.204
169
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 2.204
170
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 2.204
171
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.204
172
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 2.204
173
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.204
174
P GST044 Gastritis 55 2.204
175
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 2.204
176
THY121 Thyroid Gland Anaplastic Carcinoma 67 2.199
177
ATH013 Atherosclerosis Susceptibility 63 2.197
178
CHL068 Cholestasis 61 2.197
179
RHM028 Rheumatic Heart Disease 56 2.147
180
P PNC044 Pancreatitis 61 2.146
181
CRH001 Crohn's Disease 80 2.095
182
CHR074 Choriocarcinoma 46 2.095
183
c DLT002 Dilated Cardiomyopathy 78 2.095
184
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 2.087
185
ART001 Arterial Tortuosity Syndrome 65 2.087
186
c THY109 Thyroid Cancer, Nonmedullary, 1 55 2.087
187
HYP748 Hypertelorism 46 2.087
188
SKN016 Skin Disease 63 2.042
189
P MSC005 Muscular Dystrophy 67 2.029
190
P TRT010 Teratoma 51 2.024
191
P FML011 Familial Adenomatous Polyposis 71 1.987
192
c HPT001 Hepatitis C 62 1.987
193
LPD008 Lipid Metabolism Disorder 62 1.987
194
P PLY014 Polycystic Kidney Disease 69 1.946
195
HGH043 High Grade Glioma 45 1.946
196
END062 Endometrial Hyperplasia 48 1.930
197
P FCL005 Focal Segmental Glomerulosclerosis 57 1.930
198
P LTR001 Lateral Sclerosis 58 1.930
199
END041 Endometrial Adenocarcinoma 64 1.914
200
BCT022 Bacterial Infectious Disease 56 1.889
201
BRN028 Brain Cancer 74 1.889
202
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.870
203
c AMY091 Amyotrophic Lateral Sclerosis 1 88 1.870
204
PTT037 Pituitary Tumors 44 1.870
205
c MCR115 Microvascular Complications of Diabetes 5 65 1.860
206
NNL006 Non-Alcoholic Steatohepatitis 54 1.815
207
c ACT075 Acute Myocardial Infarction 56 1.815
208
P NRB001 Neuroblastoma 66 1.815
209
c ACT027 Acute Pancreatitis 60 1.814
210
c TYP008 Type 1 Diabetes Mellitus 70 1.807
211
ACT098 Acute Erythroid Leukemia 55 1.807
212
CLR108 Colorectal Adenoma 64 1.807
213
c ART101 Aortic Valve Disease 2 66 1.807
214
c PRD040 Periodontitis, Chronic 52 1.807
215
c TYP009 Type 2 Diabetes Mellitus 92 1.807
216
CRV002 Cervix Uteri Carcinoma in Situ 47 1.807
217
ART017 Aortic Disease 49 1.807
218
CRV045 Cervical Intraepithelial Neoplasia 39 1.807
219
SML031 Small Cell Carcinoma of the Bladder 46 1.797
220
FTT001 Fatty Liver Disease 62 1.769
221
PRM334 Primary Bone Dysplasia with Increased Bone Density 15 1.741
222
P CHN012 Chondrosarcoma 57 1.741
223
P ACT008 Actinic Keratosis 54 1.741
224
P INT070 Intestinal Obstruction 57 1.741
225
P ESP024 Esophagitis 60 1.741
226
GNG012 Gingival Overgrowth 49 1.741
227
P MYC008 Myocarditis 59 1.741
228
P BRS044 Breast Adenocarcinoma 58 1.735
229
P GLM040 Glioma Susceptibility 1 71 1.727
230
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.722
231
c PCH010 Pachyonychia Congenita 3 43 1.722
232
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 1.722
233
SCH014 Schistosomiasis 56 1.722
234
CRC021 Carcinosarcoma 64 1.675
235
CLR030 Clear Cell Renal Cell Carcinoma 54 1.675
236
c CHR711 Chronic Asthma 41 1.673
237
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 1.673
238
STR067 Stroke, Ischemic 80 1.672
240
HPT022 Hepatoblastoma 54 1.672
241
CRT017 Cartilage Disease 53 1.672
242
PRS021 Prostatic Adenoma 43 1.672
243
P TBR001 Tuberous Sclerosis 69 1.672
244
PRS045 Prostatic Hypertrophy 53 1.672
245
RHM001 Rheumatic Fever 59 1.672
246
HTR003 Heterotaxy 43 1.672
247
ALL006 Allergic Asthma 56 1.623
248
c HPT073 Hepatitis C Virus 71 1.606
249
SKN019 Skin Melanoma 71 1.606
250
INS024 Insulin-Like Growth Factor I 78 1.597
251
P DRM053 Dermatitis, Atopic 65 1.597
252
P PHC003 Pheochromocytoma 69 1.597
253
c WLM013 Wilms Tumor 1 66 1.597
254
DSS032 Disease by Infectious Agent 55 1.597
255
ADR040 Adrenal Gland Pheochromocytoma 46 1.597
256
P LVR013 Liver Disease 69 1.597
257
P FBR017 Fibrosarcoma 56 1.597
258
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 1.597
259
P DYS005 Dyslexia 41 1.597
260
PLM010 Pulmonary Edema 55 1.597
261
VSC006 Vascular Cancer 46 1.597
262
P INS002 in Situ Carcinoma 53 1.597
263
P RHM011 Rheumatoid Arthritis 82 1.572
264
MYL009 Myelodysplastic Syndrome 67 1.518
265
P ALP008 Alopecia 54 1.518
266
PRS129 Prostatic Hyperplasia, Benign 49 1.518
267
P ATX030 Ataxia-Telangiectasia 80 1.518
268
BRN032 Brain Glioma 45 1.518
269
P PLY041 Polymyositis 59 1.518
270
c CHR085 Chronic Cervicitis 32 1.518
271
P PTT006 Pituitary Adenoma 55 1.518
272
RCK004 Rickets 68 1.518
273
P MLN007 Male Infertility 56 1.518
274
KHN001 Kuhnt-Junius Degeneration 48 1.518
275
P CRV039 Cervicitis 52 1.518
276
FBR019 Fibromatosis 42 1.518
277
HYP114 Hypertensive Nephropathy 36 1.463
278
P ALZ034 Alzheimer Disease 87 1.431
279
P SLP006 Sleep Apnea 69 1.431
280
DFC004 Deficiency Anemia 74 1.431
281
CLR109 Colorectal Adenocarcinoma 50 1.431
282
MSN001 Mesangial Proliferative Glomerulonephritis 44 1.431
283
P VNT002 Ventricular Septal Defect 58 1.431
284
CHL004 Cholelithiasis 49 1.431
285
GTR002 Goiter 53 1.431
286
DRM006 Dermatitis 62 1.431
287
P OLG002 Oligodendroglioma 66 1.429
288
ADN089 Adenosquamous Lung Carcinoma 49 1.418
289
RTN017 Retinal Detachment 60 1.406
290
P HYD006 Hydrocephalus 61 1.406
291
GST019 Gastrointestinal Stromal Tumor 78 1.365
292
P TMR010 Tumor Predisposition Syndrome 67 1.358
293
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 1.358
294
c THY107 Thymoma, Familial 42 1.346
295
ALL003 Allergic Rhinitis 67 1.346
296
P HRD008 Hereditary Hemorrhagic Telangiectasia 65 1.346
297
P LPS004 Lupus Erythematosus 61 1.346
298
P LKM002 Leukemia 67 1.346
299
EXS001 Exostosis 49 1.346
300
P RHN004 Rhinitis 57 1.346
301
P THY023 Thymoma 64 1.346
302
c FBR084 Fibromatosis, Gingival, 1 49 1.335
303
P GNG025 Gingival Fibromatosis 47 1.335
304
P RRH023 Rare Hereditary Hemochromatosis 54 1.335
305
LNG031 Lung Benign Neoplasm 51 1.335
306
P MMB011 Membranous Nephropathy 50 1.335
307
CMM005 Common Cold 56 1.335
308
HMS001 Hemosiderosis 48 1.335
309
P ECL001 Eclampsia 52 1.335
310
DNT001 Dental Fluorosis 43 1.335
311
BCK006 Back Pain 47 1.335
314
P AMY004 Amyloidosis 70 1.315
315
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 1.283
316
PNM008 Pneumothorax 54 1.283
317
SPN035 Spindle Cell Sarcoma 54 1.283
318
SRC014 Sarcoma 65 1.283
319
ORL004 Oral Submucous Fibrosis 56 1.283
320
ATS010 Autosomal Recessive Disease 42 1.227
321
TTT001 Tatton-Brown-Rahman Syndrome 46 1.227
322
APN008 Apnea, Obstructive Sleep 67 1.227
323
LRY018 Laryngeal Squamous Cell Carcinoma 44 1.227
324
GST033 Gestational Diabetes 61 1.227
325
P PRL003 Proliferative Glomerulonephritis 43 1.227
326
AMN001 Amenorrhea 54 1.227
327
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 1.227
328
c SYS001 Systemic Lupus Erythematosus 87 1.217
329
P LYM118 Lymphoma 67 1.217
330
AND014 Androgenic Alopecia 47 1.217
331
ACT119 Acute Promyelocytic Leukemia 62 1.217
332
PNM010 Pneumothorax, Primary Spontaneous 58 1.217
333
P EST001 Estrogen-Receptor Positive Breast Cancer 49 1.217
334
URT037 Urethral Stricture 42 1.217
335
PRT013 Portal Hypertension 59 1.217
336
UTR024 Uterine Carcinosarcoma 59 1.217
337
P RTN018 Retinal Disease 53 1.217
338
P LKM062 Leukemia, Acute Lymphoblastic 69 1.184
339
MSC157 Muscular Dystrophy, Duchenne Type 79 1.148
340
OTT002 Otitis Media 71 1.148
341
LMB062 Limb Ischemia 55 1.148
342
c LKM061 Leukemia, Acute Myeloid 83 1.148
343
P ESP035 Esophagitis, Eosinophilic, 1 58 1.148
344
c HYP836 Hypercholesterolemia, Familial, 1 73 1.148
345
PRT037 Pertussis 65 1.148
346
c VRL010 Viral Hepatitis 53 1.148
347
P CTR002 Cataract 60 1.148
348
P CRN037 Craniosynostosis 68 1.148
349
P RSP003 Respiratory Failure 74 1.148
350
P BNG032 Benign Mesothelioma 53 1.148
351
P RCT021 Rectum Cancer 54 1.148
352
DWR001 Dwarfism 44 1.148
353
SKL017 Skeletal Dysplasias 41 1.098
354
c EXD008 Exudative Vitreoretinopathy 1 71 1.098
355
SYN036 Syncope 45 1.098
356
HMT002 Hematologic Cancer 61 1.098
357
P MNC007 Monocytic Leukemia 47 1.098
358
NSP002 Nasopharyngitis 45 1.098
359
DNT012 Dental Caries 53 1.098
360
P GLL018 Gallbladder Cancer 53 1.098
361
P KDN017 Kidney Cancer 61 1.098
362
SFT003 Soft Tissue Sarcoma 57 1.098
363
PLM173 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal 34 1.083
364
SKN022 Skin Squamous Cell Carcinoma 54 1.083
365
PSD011 Pseudovascular Skin Squamous Cell Carcinoma 16 1.083
366
CLR137 Clear Cell Adenocarcinoma of the Ovary 31 1.074
367
SPP011 Suppression of Tumorigenicity 12 61 1.074
368
CHR100 Chronic Ulcer of Skin 57 1.074
369
P ORT004 Orthostatic Intolerance 63 1.074
370
P MCR129 Microvascular Complications of Diabetes 1 68 1.074
371
P SRC025 Sarcoidosis 1 71 1.074
372
P CRC039 Coarctation of Aorta 46 1.074
373
ACR121 Acromelic Dysplasia 11 1.074
374
P MYL006 Myeloid Leukemia 61 1.074
375
47X002 47,xyy 48 1.074
376
P KRT007 Keratoconus 50 1.074
377
c MCR112 Microvascular Complications of Diabetes 2 42 1.074
378
PLM012 Pulmonary Sarcoidosis 53 1.074
379
P HPT021 Hepatitis 69 1.074
380
P MCR010 Microcephaly 60 1.074
381
OVR034 Ovarian Clear Cell Adenocarcinoma 39 1.074
382
EMB004 Embryonal Carcinoma 56 1.074
383
STT001 Status Epilepticus 59 1.074
384
P LMB006 Limb-Girdle Muscular Dystrophy 52 1.074
385
MYL005 Myelofibrosis 71 1.055
386
c GLM047 Glioma Susceptibility 3 33 1.024
387
c MSM022 Mismatch Repair Cancer Syndrome 1 70 1.024
388
c GLM025 Glioma Susceptibility 2 30 1.024
389
c GLM043 Glioma Susceptibility 9 30 1.024
390
MNN043 Meningioma, Familial 79 1.024
391
LBL001 Lobular Neoplasia 55 1.020
392
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 0.994
393
PRX085 Preaxial Hallucal Polydactyly 28 0.994
394
c MST023 Mesothelioma, Malignant 56 0.994
395
PRP080 Peripheral Artery Disease 54 0.994
396
FTL006 Fetal Alcohol Spectrum Disorder 43 0.994
397
KPS004 Kaposi Sarcoma 77 0.994
398
c BRN108 Branchiootic Syndrome 1 62 0.994
399
VRC005 Varicose Veins 60 0.994
400
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.994
401
P HYP098 Hypereosinophilic Syndrome 66 0.994
402
P KRT005 Keratoacanthoma 47 0.994
403
P GRF003 Graft-Versus-Host Disease 71 0.994
404
PPL022 Papilloma 53 0.994
405
SQM002 Squamous Cell Papilloma 46 0.994
406
P NPH012 Nephrotic Syndrome 60 0.994
407
BRN002 Bronchiolitis 57 0.994
408
P ART005 Arteriovenous Malformation 65 0.994
409
CRS001 Crescentic Glomerulonephritis 42 0.994
410
HRT015 Heritable Pulmonary Arterial Hypertension 46 0.994
411
c PRS097 Prostate Cancer, Hereditary, 1 39 0.982
412
c PRS070 Prostate Cancer, Hereditary, 12 22 0.982
413
c PRS071 Prostate Cancer, Hereditary, 13 25 0.982
414
c PRS117 Prostate Cancer, Hereditary, 11 24 0.982
415
c PRS114 Prostate Cancer, Hereditary, 2 33 0.982
416
PRS015 Prostate Signet Ring Cell Adenocarcinoma 25 0.982
417
P HRD084 Hereditary Cerebral Amyloid Angiopathy 30 0.930
418
c ANM042 Anemia, Congenital Dyserythropoietic, Type Ii 50 0.930
419
P PNC045 Pancreatic Agenesis 43 0.930
420
DBT081 Diabetic Encephalopathy 36 0.930
421
P CNG003 Congenital Dyserythropoietic Anemia 48 0.930
422
TTL012 Total Anomalous Pulmonary Venous Return 1 58 0.926
423
LYM133 Lymphoma, Hodgkin, Classic 74 0.907
424
P CRN300 Coronary Heart Disease 1 73 0.907
425
P KLZ004 Kala-Azar 1 41 0.907
426
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.907
427
c ACT249 Acute Asthma 40 0.907
428
LWG006 Low Grade Glioma 41 0.907
429
c DPH024 Diaphragmatic Hernia, Congenital 64 0.907
430
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.907
431
c ATS330 Autosomal Dominant Limb-Girdle Muscular Dystrophy 31 0.907
432
LMY002 Leiomyoma 51 0.907
433
CTN007 Cutaneous Leishmaniasis 62 0.907
434
URM002 Uremia 47 0.907
435
LSH001 Leishmaniasis 64 0.907
436
P ACN011 Acne 57 0.907
437
PRT036 Peritonitis 65 0.907
438
PST011 Pustulosis of Palm and Sole 52 0.907
439
PPT005 Peptic Ulcer Disease 58 0.907
440
GRN055 Granular Corneal Dystrophy 37 0.907
441
PRM236 Primary Biliary Cholangitis 60 0.907
442
P HYP069 Hyperparathyroidism 62 0.907
443
P EYD002 Eye Disease 57 0.907
444
P CRN025 Corneal Dystrophy 49 0.907
445
ENT004 Enthesopathy 51 0.907
446
c HPT016 Hepatitis B 62 0.907
447
HYP056 Hypoglycemia 65 0.907
448
LKP003 Leukoplakia 39 0.907
449
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.869
450
P BLD062 Bile Duct Cancer 67 0.869
451
P LNG021 Lung Occult Small Cell Carcinoma 20 0.869
452
LNG019 Lung Combined Type Small Cell Carcinoma 32 0.869
453
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.812
454
ADN027 Adenomyosis 57 0.812
455
INT146 Intervertebral Disc Disease 63 0.812
456
P SCH015 Schizophrenia 74 0.812
457
P MYS005 Myositis 56 0.812
458
PPL052 Papillomatosis, Confluent and Reticulated 34 0.812
459
PLY150 Polykaryocytosis Inducer 29 0.812
460
P MLT020 Multiple Sclerosis 79 0.812
461
GST092 Gastroesophageal Reflux 61 0.812
462
c LKM063 Leukemia, Chronic Myeloid 71 0.812
463
CHR005 Chorioamnionitis 50 0.812
464
P ANP001 Anaplastic Large Cell Lymphoma 61 0.812
465
P PRS049 Persistent Mullerian Duct Syndrome 52 0.812
466
LPP008 Lipoprotein Quantitative Trait Locus 65 0.812
467
HYP025 Hyperphosphatemia 48 0.812
468
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.812
469
P CMR001 Camurati-Engelmann Disease 59 0.812
470
P PYR039 Peyronie Disease 39 0.812
471
P SCL018 Scoliosis 57 0.812
472
P GLP001 Geleophysic Dysplasia 46 0.812
473
P CMM008 Communicating Hydrocephalus 45 0.812
474
P CYS018 Cystitis 59 0.812
475
P ART023 Arthropathy 61 0.812
476
CNN005 Connective Tissue Disease 67 0.812
477
NRM005 Neuromuscular Disease 63 0.812
478
TRC005 Tracheal Stenosis 43 0.812
479
BLR008 Bilirubin Metabolic Disorder 57 0.812
480
ECH003 Echinococcosis 53 0.812
481
P INT143 Interstitial Cystitis 60 0.812
482
END007 Endosalpingiosis 37 0.812
483
HYD002 Hydronephrosis 58 0.812
484
END011 Endometriosis of Ovary 39 0.812
485
P MTR012 Mitral Valve Disease 57 0.812
486
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.812
487
P SCK002 Sick Sinus Syndrome 55 0.812
488
P PTS002 Ptosis 52 0.812
489
AZS001 Azoospermia 45 0.812
490
c SVR005 Severe Pre-Eclampsia 50 0.812
491
KDN013 Kidney Hypertrophy 34 0.812
492
c LKM005 Leukemia, T-Cell, Chronic 34 0.812
493
CRD016 Cardiac Rupture 34 0.812
494
c LMB030 Limb-Girdle Muscular Dystrophy Type 1c 27 0.812
495
MLG163 Malignant Tumor of Penis 29 0.703
496
P SZR006 Seizure Disorder 70 0.703
497
P THL005 Thalassemia 56 0.703
498
P ALP061 Alopecia, Androgenetic, 1 49 0.703
499
SRC027 Sarcoma, Synovial 58 0.703
500
c TLN011 Telangiectasia, Hereditary Hemorrhagic, Type 2 45 0.703
501
BRT054 Brittle Bone Disorder 74 0.703
502
P LKM071 Leukemia, Chronic Lymphocytic 75 0.703
503
c OPT053 Optic Atrophy 1 62 0.703
504
BRK010 Burkitt Lymphoma 66 0.703
505
P VSC013 Visceral Heterotaxy 53 0.703
506
ILT001 Ileitis 48 0.703
507
c ATM022 Autoimmune Myocarditis 36 0.703
508
NRL016 Neural Tube Defects 81 0.703
509
P CRP001 Carpal Tunnel Syndrome 66 0.703
510
IGR001 Ige Responsiveness, Atopic 59 0.703
511
LMY014 Leiomyoma, Uterine 56 0.703
512
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.703
513
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.703
514
P SHW006 Shwachman-Diamond Syndrome 1 66 0.703
515
P PSD087 Pseudoxanthoma Elasticum 67 0.703
516
SHP005 Shprintzen-Goldberg Craniosynostosis Syndrome 46 0.703
517
c TBR025 Tuberous Sclerosis 1 84 0.703
518
FBR011 Fibrodysplasia Ossificans Progressiva 67 0.703
519
INC002 Inclusion Body Myositis 57 0.703
520
c GLC092 Glaucoma, Primary Open Angle 62 0.703
521
GLC003 Glucose Intolerance 54 0.703
522
CHL149 Childhood Acute Myeloid Leukemia 43 0.703
523
P OPN001 Open-Angle Glaucoma 55 0.703
524
P MYP004 Myopathy 67 0.703
525
OCL006 Ocular Hypertension 53 0.703
526
GST010 Gestational Trophoblastic Neoplasm 52 0.703
527
P PLM034 Pulmonary Emphysema 58 0.703
528
P ALC033 Alcohol Use Disorder 61 0.703
529
IGG001 Iga Glomerulonephritis 50 0.703
530
P LYN001 Lynch Syndrome 76 0.703
531
HRT012 Heart Valve Disease 53 0.703
532
THR016 Thrombophlebitis 50 0.703
533
P ESN008 Eosinophilic Pneumonia 50 0.703
534
P INF038 Influenza 68 0.703
535
MYF001 Myofibroma 42 0.703
536
P CRN024 Corneal Disease 44 0.703
537
OST003 Osteonecrosis 61 0.703
538
P UVT001 Uveitis 57 0.703
539
BRN012 Bronchiolitis Obliterans 56 0.703
540
RTN020 Retinal Vascular Disease 46 0.703
541
c ATM011 Autoimmune Hepatitis 63 0.703
542
MLG169 Malignant Astrocytoma 57 0.703
543
PPL002 Papillary Carcinoma 46 0.703
544
BRN024 Bronchitis 67 0.703
545
CRB039 Cerebrovascular Disease 66 0.703
546
BNN003 Bone Inflammation Disease 48 0.703
547
P MTR014 Motor Neuron Disease 65 0.703
548
PNL012 Penile Cancer 57 0.703
549
RCT020 Rectum Adenocarcinoma 48 0.703
550
HYP060 Hyperinsulinism 54 0.703
551
PLM035 Pulmonary Eosinophilia 49 0.703
552
UTR043 Uterine Sarcoma 40 0.703
553
DYS073 Dysphagia 53 0.703
554
c CHR417 Chronic Graft Versus Host Disease 55 0.703
555
PLM052 Pulmonary Arteriovenous Malformation 40 0.703
556
BRR014 Barrett Esophagus 66 0.681
557
P RTH006 Rothmund-Thomson Syndrome, Type 2 67 0.647
558
RMB001 Rombo Syndrome 30 0.647
559
P TRC095 Trichoepithelioma, Multiple Familial, 1 32 0.647
560
c BSL024 Basal Cell Carcinoma 1 55 0.647
561
BSL044 Basal Cell Carcinoma, Infundibulocystic 35 0.647
562
c BSL034 Basal Cell Carcinoma 7 26 0.647
563
CYS004 Cystic Basal Cell Carcinoma 36 0.647
564
SRC003 Sarcomatoid Basal Cell Carcinoma 28 0.647
565
NDL009 Nodular Basal Cell Carcinoma 40 0.647
566
MTT001 Metatypical Basal Cell Carcinoma 32 0.647
567
PGM002 Pigmented Basal Cell Carcinoma 31 0.647
568
MCR016 Micronodular Basal Cell Carcinoma 34 0.647
569
INF027 Infiltrative Basal Cell Carcinoma 32 0.647
570
ANL013 Anal Margin Basal Cell Carcinoma 18 0.647
571
SBC013 Sebaceous Basal Cell Carcinoma 13 0.647
572
ADM002 Adamantinoid Basal Cell Epithelioma 20 0.647
573
CLR015 Clear Cell Basal Cell Carcinoma 39 0.647
574
ADN015 Adenoid Basal Cell Carcinoma 31 0.647
575
SGN001 Signet Ring Basal Cell Carcinoma 32 0.647
576
9Q2001 9q22.3 Microdeletion 24 0.647
577
INF057 Inflammatory Linear Verrucous Epidermal Nevus 33 0.647
578
LNR004 Linear Porokeratosis 33 0.647
579
LNG012 Lung Occult Squamous Cell Carcinoma 20 0.614
580
LNG007 Lung Mixed Small Cell and Squamous Cell Carcinoma 21 0.614
581
PRQ002 Paraquat Poisoning 28 0.574
582
APN006 Apnea of Prematurity 24 0.574
583
GLM044 Glomerular Disease 35 0.574
584
PRM248 Primary Intrahepatic Lithiasis 13 0.574
585
c ACT134 Acute Liver Failure 59 0.574
586
ACR043 Acromicric Dysplasia 50 0.574
587
c ART068 Aortic Aneurysm, Familial Thoracic 2 33 0.574
588
c GLL024 Gallbladder Disease 1 52 0.574
589
CRT002 Cartilage-Hair Hypoplasia 60 0.574
590
c HTR021 Heterotaxy, Visceral, 5, Autosomal 38 0.574
591
c SPN398 Spinal Muscular Atrophy, Type Iv 44 0.574
592
CRC014 Carcinoid Tumors, Intestinal 46 0.574
593
CRD132 Cardiac Conduction Defect 60 0.574
594
FBR012 Fabry Disease 70 0.574
595
P SPR119 Spermatogenic Failure, X-Linked, 1 36 0.574
596
P CLC063 Celiac Disease 1 66 0.574
597
HMN044 Human Immunodeficiency Virus Type 1 78 0.574
598
ADR016 Adrenal Cortical Carcinoma 62 0.574
599
P WLL002 Weill-Marchesani Syndrome 55 0.574
600
P ADL017 Adult T-Cell Leukemia 56 0.574
601
c BTT014 Beta-Thalassemia 72 0.574
602
CRT069 Cortical Malformations, Occipital 30 0.574
604
P URN019 Urinary Tract Infection 49 0.574
605
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.574
606
P BRC006 Brachydactyly 51 0.574
607
HLC007 Helicobacter Pylori Infection 67 0.574
608
P EPD083 Epidermodysplasia Verruciformis 1 57 0.574
609
c GLP003 Geleophysic Dysplasia 1 44 0.574
610
IMM167 Immune Deficiency Disease 78 0.574
611
PNB004 Panbronchiolitis, Diffuse 34 0.574
612
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.574
613
GLC106 Glucocorticoid Resistance, Generalized 48 0.574
614
c RTN057 Retinitis Pigmentosa 29 33 0.574
615
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.574
616
P CLD001 Cleidocranial Dysplasia 64 0.574
617
c EXS019 Exostoses, Multiple, Type I 54 0.574
618
PCT003 Pectus Excavatum 46 0.574
619
MYH012 Myhre Syndrome 43 0.574
620
c HLP029 Holoprosencephaly 4 43 0.574
621
HRW001 Hair Whorl 35 0.574
622
MLD001 Melioidosis 67 0.574
623
c NMN014 Niemann-Pick Disease, Type C2 49 0.574
624
TNG009 Tongue Squamous Cell Carcinoma 43 0.574
625
P OVR106 Ovarian Clear Cell Carcinoma 44 0.574
626
BLP004 Blepharophimosis 36 0.574
627
HRD224 Hereditary Nonpolyposis Colon Cancer 51 0.574
628
ACT003 Acute Kidney Tubular Necrosis 46 0.574
629
TRM010 Traumatic Brain Injury 51 0.574
630
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.574
631
HPT009 Hepatopulmonary Syndrome 48 0.574
632
MCL003 Macular Holes 44 0.574
633
BRN004 Brain Edema 54 0.574
634
CLF001 Cleft Lip 53 0.574
635
IRD001 Iridocyclitis 53 0.574
636
P PSR002 Psoriasis 63 0.574
637
P ATR005 Atrophic Gastritis 50 0.574
638
DBT010 Diabetic Neuropathy 54 0.574
639
CLF056 Cleft Lip with or Without Cleft Palate 42 0.574
640
DFF036 Differentiated Thyroid Carcinoma 51 0.574
641
HRT011 Heart Septal Defect 49 0.574
642
ADR004 Adrenal Cortical Adenocarcinoma 38 0.574
643
FDL002 Food Allergy 47 0.574
644
PRC013 Pericarditis 53 0.574
645
P EPL164 Epilepsy 68 0.574
646
P OPT006 Optic Nerve Disease 58 0.574
647
INS001 Insulinoma 59 0.574
648
PLS011 Plasmacytoma 56 0.574
649
THY123 Thyroid Gland Follicular Carcinoma 55 0.574
650
ILS001 Ileus 50 0.574
651
SMN007 Seminoma 42 0.574
652
ANT024 Anthrax Disease 58 0.574
653
NPH009 Nephrolithiasis 54 0.574
654
PRP016 Paraplegia 52 0.574
655
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.574
656
ANG020 Angiosarcoma 64 0.574
657
PRL017 Prolymphocytic Leukemia 47 0.574
658
ALL029 Allergic Disease 59 0.574
659
ALV002 Alveolar Echinococcosis 57 0.574
660
c SCN007 Secondary Hyperparathyroidism 51 0.574
661
NRG002 Neurogenic Bladder 55 0.574
662
CNS004 Constipation 56 0.574
663
TXC005 Toxic Shock Syndrome 62 0.574
664
THY122 Thyroid Gland Cancer 59 0.574
665
FRZ001 Frozen Shoulder 55 0.574
666
c HRD010 Hereditary Spastic Paraplegia 66 0.574
667
FST001 Foster-Kennedy Syndrome 39 0.574
668
TST014 Testicular Cancer 52 0.574
669
P PYL005 Pyelonephritis 57 0.574
670
MTR002 Mitral Valve Insufficiency 52 0.574
671
PRM013 Premature Menopause 58 0.574
672
P ALP004 Alport Syndrome 69 0.574
673
CNS002 Constrictive Pericarditis 40 0.574
674
HYP006 Hypertensive Heart Disease 49 0.574
675
MCR013 Microphthalmia 60 0.574
676
PRG009 Progressive Multifocal Leukoencephalopathy 58 0.574
677
PLR006 Pleural Cancer 37 0.574
678
P TMP001 Temporal Lobe Epilepsy 49 0.574
679
DMY004 Demyelinating Disease 50 0.574
680
P SCL048 Sclerosteosis 58 0.574
681
DBT007 Diabetic Cataract 36 0.574
682
P EHL001 Ehlers-Danlos Syndrome 58 0.574
683
MCR017 Macrocytic Anemia 44 0.574
684
RNL011 Renal Osteodystrophy 49 0.574
685
VSC002 Vascular Dementia 60 0.574
686
MCN005 Mucinous Intrahepatic Cholangiocarcinoma 24 0.574
688
c CLD019 Cleidocranial Dysplasia Spectrum Disorder 20 0.574
689
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.574
690
DST006 Diastolic Heart Failure 45 0.574
691
SPL018 Splenomegaly 49 0.574
692
WLL004 Wallerian Degeneration 38 0.574
693
P SCK005 Sickle Cell Disease 56 0.574
694
TCL005 T-Cell Prolymphocytic Leukemia 48 0.574
695
BRN071 Brain Injury 50 0.574
696
BNT001 Banti's Syndrome 21 0.574
697
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.574
698
CHR178 Chromosomal Triplication 34 0.574
699
DXT001 Dextrocardia 55 0.524
700
CRN270 Coronary Artery Dissection, Spontaneous 32 0.524
701
CKT002 Cakut 47 0.482
702
IRN008 Iron Overload in Africa 51 0.458
703
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.458
704
PLM026 Pilomatrixoma 57 0.458
705
MLN065 Melanocytic Nevus Syndrome, Congenital 62 0.458
706
VNH007 Von Hippel-Lindau Syndrome 73 0.458
707
HPT079 Hepatoid Adenocarcinoma 39 0.458
708
RJS001 Ruijs-Aalfs Syndrome 47 0.458
709
c ALB010 Albinism, Oculocutaneous, Type Ib 52 0.458
710
PDT042 Pediatric Hepatocellular Carcinoma 49 0.458
711
MLT165 Multilocular Cystic Renal Neoplasm of Low Malignant Potential 28 0.458
712
MLT003 Multilocular Clear Cell Renal Cell Carcinoma 32 0.458
713
OVR062 Ovary Serous Adenocarcinoma 25 0.458
714
OVR011 Ovarian Mucinous Adenocarcinoma 34 0.458
715
MRK001 Merkel Cell Carcinoma 64 0.458
716
DST001 Distal Biliary Tract Carcinoma 24 0.458
717
FLL027 Fallopian Tube Carcinoma 67 0.458
718
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.458
719
ADL096 Adult Hepatocellular Carcinoma 60 0.458
720
PPL004 Papillary Squamous Carcinoma 39 0.458
721
FBR086 Fibrolamellar Carcinoma 59 0.458
722
HPT011 Hepatocellular Clear Cell Carcinoma 46 0.458
723
P LMY004 Leiomyosarcoma 62 0.458
724
KRK001 Krukenberg Carcinoma 39 0.458
725
RCS008 Recessive Dystrophic Epidermolysis Bullosa-Generalized Other 30 0.458
726
PTY007 Pityriasis Rotunda 26 0.458
727
LNG115 Lung Sarcomatoid Carcinoma 36 0.409
728
LNG091 Lung Mucoepidermoid Carcinoma 32 0.409
729
LNG003 Lung Carcinoma in Situ 36 0.409
730
BSL003 Basaloid Lung Carcinoma 35 0.409
731
P LNG035 Lung Large Cell Carcinoma 54 0.409
732
LNG011 Lung Adenoid Cystic Carcinoma 35 0.409
733
LNG020 Lung Oat Cell Carcinoma 51 0.409
734
END032 Endometrial Clear Cell Adenocarcinoma 34 0.409
735
LNG017 Lung Giant Cell Carcinoma 52 0.409
736
c LNG001 Lung Clear Cell Carcinoma 29 0.409
737
LNG006 Lung Occult Large Cell Carcinoma 14 0.409
738
LNG002 Lung Combined Large Cell Neuroendocrine Carcinoma 19 0.409
740
HLR002 Hilar Lung Carcinoma 24 0.409
741
LNG014 Lung Superior Sulcus Carcinoma 15 0.409
742
c HMC039 Hemochromatosis, Type 1 73 0.406
743
P PRM011 Primary Ciliary Dyskinesia 69 0.406
744
GRN022 Granulosa Cell Tumor of the Ovary 34 0.406
745
FNG016 Fungal Keratitis 39 0.406
746
MLG164 Malignant Epithelial Tumor of Ovary 24 0.406
747
SVR055 Severe Immune-Mediated Enteropathy 22 0.406
748
OST115 Osteonecrosis of the Jaw 41 0.406
749
SPS057 Spasticity 42 0.406
750
ART140 Arteries, Anomalies of 53 0.406
751
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.406
752
RTC012 Reticuloendotheliosis, X-Linked 35 0.406
753
P MYS003 Myasthenia Gravis 68 0.406
754
SDD001 Sudden Infant Death Syndrome 60 0.406
755
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 66 0.406
756
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.406
757
c BNM016 Bone Mineral Density Quantitative Trait Locus 1 24 0.406
758
P MTR004 Maturity-Onset Diabetes of the Young 68 0.406
759
MSC162 Muscular Dystrophy, Congenital Merosin-Deficient, 1a 55 0.406
760
CHR222 Chromosome 1p36 Deletion Syndrome 45 0.406
761
c OVR114 Ovarian Cancer 1 59 0.406
762
P MYC084 Mycobacterium Tuberculosis 1 68 0.406
763
OVR029 Ovarian Hyperstimulation Syndrome 63 0.406
764
P MLN069 Melanoma, Uveal 61 0.406
765
c SPN330 Spondylocostal Dysostosis 5 54 0.406
766
EPC005 Epicanthus 36 0.406
767
WLL001 Williams-Beuren Syndrome 61 0.406
768
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.406
769
c MGR028 Migraine with or Without Aura 1 64 0.406
770
P PRK057 Parkinson Disease, Late-Onset 80 0.406
771
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.406
772
CYS001 Cystic Fibrosis 78 0.406
773
c FNC027 Fanconi Anemia, Complementation Group a 81 0.406
774
GRN037 Granulomatosis with Polyangiitis 64 0.406
775
P CRN038 Carney Complex Variant 64 0.406
776
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 49 0.406
777
MTB004 Metabolic Acidosis 48 0.406
778
P EXN002 Exanthem 58 0.406
779
PRP036 Peripheral T-Cell Lymphoma 53 0.406
780
MLR004 Malaria 80 0.406
781
c HTR010 Heterotaxy, Visceral, 4, Autosomal 30 0.406
782
c GLP004 Geleophysic Dysplasia 2 39 0.406
783
c CLR055 Colorectal Cancer, Hereditary Nonpolyposis, Type 6 39 0.406
784
DFF005 Diffuse Large B-Cell Lymphoma 54 0.406
785
KSH004 Kashin-Beck Disease 38 0.406
786
BCT021 Bacterial Sepsis 43 0.406
787
RCK002 Rocky Mountain Spotted Fever 34 0.406
788
INF034 Infective Endocarditis 54 0.406
789
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.406
790
HMN047 Human Cytomegalovirus Infection 57 0.406
791
OST006 Osteoblastoma 38 0.406
792
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 0.406
793
INT029 Interleukin-7 Receptor Alpha Deficiency 28 0.406
794
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.406
795
TTH032 Tooth Size 35 0.406
796
c CHR647 Charcot-Marie-Tooth Disease, Demyelinating, Type 1c 46 0.406
797
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 52 0.406
798
P FNC044 Fanconi Anemia, Complementation Group C 56 0.406
799
LKC009 Leukocyte Adhesion Deficiency, Type I 70 0.406
800
PTZ001 Peutz-Jeghers Syndrome 70 0.406
801
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.406
802
KRT019 Keratitis, Hereditary 66 0.406
803
STF002 Stiff Skin Syndrome 53 0.406
804
c PRG020 Paragangliomas 3 39 0.406
805
LYM143 Lymphoma, Non-Hodgkin, Familial 75 0.406
806
AST006 Astigmatism 47 0.406
807
LPT014 Leptin Deficiency or Dysfunction 78 0.406
808
EST007 Estrogen Resistance 41 0.406
809
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 0.406
810
MRF021 Marfanoid-Progeroid-Lipodystrophy Syndrome 32 0.406
811
NRD037 Neurodevelopmental Disorder with Dysmorphic Facies and Distal Limb Anomalies 25 0.406
812
P CNG539 Congenital Disorder of Glycosylation with Defective Fucosylation 1 25 0.406
813
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.406
814
c GLP007 Geleophysic Dysplasia 3 33 0.406
816
c LYS018 Loeys-Dietz Syndrome 2 50 0.406
817
DRM014 Dermatofibrosarcoma Protuberans 65 0.406
818
c LYS019 Loeys-Dietz Syndrome 1 58 0.406
819
c SPN297 Spondylocostal Dysostosis 3, Autosomal Recessive 53 0.406
820
ENT011 Enterocolitis 55 0.406
821
P HRT035 Heart Block, Congenital 43 0.406
822
DWN001 Down Syndrome 70 0.406
823
PYC001 Pycnodysostosis 55 0.406
824
CHR619 Chromosome 2q35 Duplication Syndrome 64 0.406
825
PTR032 Peters-Plus Syndrome 63 0.406
826
P STR020 Strabismus 56 0.406
827
DGR001 Digeorge Syndrome 62 0.406
828
c EXS020 Exostoses, Multiple, Type Ii 38 0.406
829
P HNT016 Huntington Disease 73 0.406
830
CLB019 Clubfoot, Congenital, with or Without Deficiency of Long Bones and/or Mirror-Image Polydactyly 43 0.406
831
P MDL005 Medulloblastoma 75 0.406
832
HND015 Hand Skill, Relative 30 0.406
833
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.406
834
FBR054 Fibroma 44 0.406
835
P FLL037 Follicular Lymphoma 74 0.406
836
OST017 Osteomyelitis 63 0.406
837
RNL078 Renal Dysplasia 46 0.406
838
PRM329 Premature Aging 36 0.406
839
LRG008 Large Granular Lymphocyte Leukemia 34 0.406
840
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 55 0.406
841
P PRS062 Persistent Hyperplastic Primary Vitreous 48 0.406
842
P ISL078 Isolated Ectopia Lentis 58 0.406
843
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 62 0.406
844
OVR012 Ovarian Serous Cystadenocarcinoma 55 0.406
845
P DYS154 Dystonia 64 0.406
846
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.406
847
P EMB005 Embryonal Rhabdomyosarcoma 53 0.406
848
INT007 Intermediate Coronary Syndrome 54 0.406
849
MCC002 Mucocutaneous Leishmaniasis 47 0.406
850
MCH006 Mechanical Strabismus 40 0.406
851
KRT006 Keratoconjunctivitis 53 0.406
852
VRL011 Viral Infectious Disease 61 0.406
853
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 43 0.406
854
IDP092 Idiopathic/heritable Pulmonary Arterial Hypertension 41 0.406
855
P THR014 Thrombocytopenia 66 0.406
856
SVR001 Severe Acute Respiratory Syndrome 67 0.406
857
CHR001 Churg-Strauss Syndrome 61 0.406
858
DYS018 Dysostosis 44 0.406
859
TRT001 Teratocarcinoma 42 0.406
860
MTH009 Mouth Disease 57 0.406
861
P RST002 Restrictive Cardiomyopathy 54 0.406
862
SBC003 Subacute Bacterial Endocarditis 33 0.406
863
MLG079 Malignant Pleural Mesothelioma 42 0.406
864
c LCL006 Localized Scleroderma 65 0.406
865
SMT002 Smooth Muscle Tumor 39 0.406
866
ERD001 Erdheim-Chester Disease 53 0.406
867
P HRD001 Hereditary Multiple Exostoses 48 0.406
868
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.406
869
c MNT326 Mental Retardation, Autosomal Dominant 50 22 0.406
870
CMB007 Combined Immunodeficiency 57 0.406
871
TRY001 Trypanosomiasis 50 0.406
872
P DRM010 Dermatomyositis 61 0.406
873
SPP007 Suppression Amblyopia 38 0.406
874
AMB002 Amblyopia 50 0.406
875
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.406
876
P PLM006 Pulmonary Alveolar Proteinosis 53 0.406
877
P HYP061 Hypertrophic Cardiomyopathy 69 0.406
878
SYN005 Synostosis 43 0.406
879
P HMN010 Hemangioma 62 0.406
880
BLR001 Biliary Atresia 55 0.406
881
CLB002 Clubfoot 51 0.406
882
CLN044 Colon Adenoma 44 0.406
883
P HYP086 Hypothyroidism 69 0.406
884
CHL014 Cholera 62 0.406
885
P ECT006 Ectodermal Dysplasia 63 0.406
886
MYL031 Myeloproliferative Neoplasm 66 0.406
887
CYS014 Cystadenocarcinoma 51 0.406
888
NNS002 Nonspecific Interstitial Pneumonia 42 0.406
889
HYP041 Hypochondrogenesis 35 0.406
890
MCS002 Mucositis 56 0.406
891
P HYP040 Hypospadias 51 0.406
892
INT030 Intracranial Aneurysm 55 0.406
893
NPH010 Nephrosclerosis 50 0.406
894
SPT005 Spotted Fever 49 0.406
895
GST029 Gastric Cardia Adenocarcinoma 29 0.406
896
c INF023 Inflammatory Breast Carcinoma 49 0.406
897
THR012 Thoracic Cancer 44 0.406
898
P EPL003 Epulis 30 0.406
899
P OVR046 Ovarian Cyst 46 0.406
900
TCL001 T-Cell Adult Acute Lymphocytic Leukemia 43 0.406
901
GST050 Gastrointestinal System Disease 55 0.406
902
ANP009 Anaplastic Oligodendroglioma 41 0.406
903
P CYS039 Cystic Kidney Disease 53 0.406
904
SRS001 Serous Cystadenocarcinoma 52 0.406
905
ANP005 Anaplastic Astrocytoma 57 0.406
906
P CTS001 Cutis Laxa 65 0.406
907
P LRY044 Larynx Cancer 54 0.406
908
P EPD016 Epidermolysis Bullosa 53 0.406
909
MSN004 Mesenchymal Cell Neoplasm 42 0.406
910
PSD007 Pseudomyxoma Peritonei 53 0.406
911
EST004 Estrogen Excess 38 0.406
912
P OST001 Osteopetrosis 71 0.406
913
EXT006 Extrahepatic Cholestasis 40 0.406
914
CLN003 Clonorchiasis 43 0.406
915
HND002 Hand, Foot and Mouth Disease 50 0.406
916
P OVR049 Ovarian Disease 52 0.406
917
KRT008 Keratopathy 46 0.406
918
IRN002 Iron Metabolism Disease 57 0.406
919
OCL022 Ocular Melanoma 52 0.406
920
PLC007 Placental Abruption 47 0.406
921
MTY003 Mutyh Polyposis 30 0.406
922
1Q2003 1q21.1 Recurrent Microdeletion 22 0.406
923
c ACT135 Acute Graft Versus Host Disease 51 0.406
924
HRT036 Heritable Thoracic Aortic Disease 34 0.406
925
HYP706 Hypermobile Ehlers-Danlos Syndrome 55 0.406
926
FXG001 Foxg1 Syndrome 26 0.406
927
SYS003 Systolic Heart Failure 49 0.406
928
STM007 Stomatitis 54 0.406
929
MYH016 Myh-Associated Polyposis 36 0.406
930
ORL012 Oral Leukoplakia 36 0.406
931
VRN004 Vernal Keratoconjunctivitis 47 0.406
932
CMP083 Complete Plasminogen Activator Inhibitor 1 Deficiency 27 0.406
933
P CHR345 Chronic Pain 50 0.406
934
MCP033 Mucopolysaccharidoses 44 0.406
935
SRF006 Surfactant Dysfunction 33 0.406
936
RYN005 Raynaud Phenomenon 45 0.406
937
P ATM020 Autoimmune Enteropathy 34 0.406
938
BNG041 Benign Metastasizing Leiomyoma 29 0.406
939
CNG092 Congenital Extrahepatic Portosystemic Shunt 24 0.406
940
c CNG112 Congenital Muscular Dystrophy Type 1a 32 0.406
941
NNT024 Neonatal Stroke 33 0.406
942
PCT001 Pectus Carinatum 33 0.406
943
DFF035 Diffuse Cutaneous Systemic Sclerosis 46 0.406
944
LYM019 Lymphosarcoma 46 0.406
945
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.406
946
PRN019 Perinatal Necrotizing Enterocolitis 60 0.406
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