Search results for gnas

759 hits were found for gnas

# Family MCID Name MIFTS Score
1
P PSD015 Pseudohypoparathyroidism 55 53.845
2
c PSD108 Pseudohypoparathyroidism, Type Ia 65 51.613
3
MCC012 Mccune-Albright Syndrome 70 49.747
4
PSD014 Pseudopseudohypoparathyroidism 54 46.443
5
c PSD066 Pseudohypoparathyroidism, Type Ib 52 43.715
6
OSS012 Osseous Heteroplasia, Progressive 61 41.041
7
c PSD117 Pseudohypoparathyroidism, Type Ic 37 33.519
8
P ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 56 30.677
9
P BRC006 Brachydactyly 51 27.731
10
DSR013 Disorders of Gnas Inactivation 15 26.649
11
CNN003 Conn's Syndrome 79 25.428
12
FBR009 Fibrous Dysplasia 48 24.903
13
c PTT061 Pituitary Adenoma 3, Multiple Types 31 24.150
14
P CLR023 Colorectal Cancer 100 22.939
15
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 21.163
16
ADN018 Adenoma 59 19.902
17
HYP025 Hyperphosphatemia 48 18.885
18
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 18.396
19
P LNG032 Lung Cancer 98 18.348
20
P HPT023 Hepatocellular Carcinoma 96 17.742
21
GST040 Gastric Adenocarcinoma 67 16.843
22
ACR007 Acromegaly 70 16.500
23
P ADN016 Adenocarcinoma 63 16.368
24
P HYP086 Hypothyroidism 69 15.607
25
P BRS047 Breast Cancer 98 15.602
26
P PTT006 Pituitary Adenoma 55 15.528
27
P HYP076 Hyperthyroidism 53 14.733
28
SXC001 Sex Cord-Gonadal Stromal Tumor 47 14.650
29
P PRC019 Precocious Puberty 47 14.641
30
c HYP374 Hypothyroidism, Congenital, Nongoitrous, 1 51 14.527
31
MZB001 Mazabraud Syndrome 19 14.377
32
PNC129 Pancreatic Adenocarcinoma 65 14.108
33
P MLN008 Melanoma 76 13.972
34
PTT037 Pituitary Tumors 44 13.960
35
P LNG064 Lung Cancer Susceptibility 3 70 13.675
36
MNS012 Monostotic Fibrous Dysplasia 19 13.590
37
c CNG006 Congenital Hypothyroidism 63 13.567
38
P GRV001 Graves' Disease 55 13.384
39
ADL096 Adult Hepatocellular Carcinoma 60 12.827
40
SQM006 Squamous Cell Carcinoma 60 12.790
41
CHL014 Cholera 62 12.727
42
PSD007 Pseudomyxoma Peritonei 53 12.662
43
GTR002 Goiter 53 12.575
44
P HYP024 Hypoparathyroidism 55 12.262
45
SKN019 Skin Melanoma 71 12.206
46
ADR005 Adrenal Carcinoma 62 11.966
47
P MLT008 Multinodular Goiter 42 11.777
48
P GRW001 Growth Hormone Secreting Pituitary Adenoma 47 11.493
49
P MLT074 Multiple Endocrine Neoplasia 59 11.487
50
SQM013 Squamous Cell Carcinoma, Head and Neck 73 11.040
51
ADR008 Adrenal Adenoma 55 10.808
52
CRV035 Cervical Cancer 73 10.796
53
ADR016 Adrenal Cortical Carcinoma 62 10.796
54
VLL006 Villous Adenoma 41 10.778
55
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 10.755
56
P OSS001 Ossifying Fibroma 42 10.708
57
CYS009 Cystadenoma 43 10.660
58
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 55 10.608
59
c HYP595 Hypertension, Essential 85 10.496
60
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 10.362
61
FBR083 Fibrous Dysplasia/mccune-Albright Syndrome 26 10.212
62
HYP020 Hyperprolactinemia 63 10.177
63
P OST002 Osteoporosis 76 9.901
64
CLC006 Calcinosis 47 9.824
65
PTZ001 Peutz-Jeghers Syndrome 70 9.755
66
c CHR684 Chronic Kidney Disease 69 9.740
67
c PRM005 Primary Hyperparathyroidism 59 9.675
68
c MLT156 Multiple Endocrine Neoplasia, Type I 72 9.263
69
P OVR046 Ovarian Cyst 46 9.263
70
OST032 Osteofibrous Dysplasia 52 9.240
71
DSS008 Disease of Mental Health 74 9.238
72
PTR034 Paternal Uniparental Disomy 19 9.144
73
P ACT244 Acth-Independent Cushing Syndrome 38 8.929
74
c ACT247 Acth-Independent Macronodular Adrenal Hyperplasia 1 16 8.763
75
P CRN038 Carney Complex Variant 64 8.661
76
P BCK002 Beckwith-Wiedemann Syndrome 62 8.520
77
LYD001 Leydig Cell Tumor 45 8.519
78
OBS067 Obesity Due to Melanocortin 4 Receptor Deficiency 36 8.495
79
PRT029 Parathyroid Adenoma 51 8.389
80
JXT003 Juxtacortical Osteosarcoma 29 8.353
81
ACR013 Acrodysostosis 51 8.309
82
OVR012 Ovarian Serous Cystadenocarcinoma 55 8.094
83
APP010 Appendix Cancer 45 8.094
84
DFC004 Deficiency Anemia 74 7.953
85
ODN023 Odontochondrodysplasia 67 7.953
86
PTT008 Pituitary Carcinoma 46 7.953
87
FLL031 Follicular Adenoma 40 7.953
88
P PLC011 Pilocytic Astrocytoma 57 7.953
89
PLY012 Polyhydramnios 46 7.953
90
OST004 Osteitis Fibrosa 38 7.953
91
END035 Endocrine Gland Cancer 43 7.953
92
APP009 Appendix Adenocarcinoma 45 7.825
93
HRM003 Hormone Producing Pituitary Cancer 33 7.825
94
c DWL002 Dowling-Degos Disease 1 58 7.581
95
P ACT010 Acth-Secreting Pituitary Adenoma 61 7.295
96
MDL024 Madelung Deformity 16 7.260
97
c TRN032 Transient Neonatal Diabetes Mellitus 47 7.064
98
URC003 Urachal Adenocarcinoma 30 7.042
99
PTT009 Pituitary Gland Disease 53 6.947
100
PRC038 Precocious Puberty, Male-Limited 61 6.744
101
P SLV027 Silver-Russell Syndrome 1 52 6.600
102
TMP012 Temple Syndrome 38 6.497
103
CHR543 Chromosome 2q37 Deletion Syndrome 44 6.307
104
MTL002 Metal Metabolism Disorder 30 6.307
105
SCH078 Schimmelpenning-Feuerstein-Mims Syndrome 61 6.060
106
NVS017 Nevus, Epidermal 66 6.060
107
PRS029 Periosteal Osteogenic Sarcoma 30 6.060
108
BRS025 Breast Juvenile Papillomatosis 32 6.060
109
THY030 Thyroid Gland Disease 50 6.060
110
BNS001 Bone Osteosarcoma 40 6.060
111
APP003 Appendiceal Neoplasm 36 6.060
112
P BRS060 Breast Papillomatosis 34 6.060
113
SGL002 Sagliker Syndrome 22 5.623
114
ENC044 Enchondromatosis, Multiple, Ollier Type 56 5.623
115
BNB001 Bone Benign Neoplasm 25 5.623
116
P PRT008 Proteus Syndrome 63 5.623
117
MLT145 Multiple Enchondromatosis, Maffucci Type 49 5.623
118
DVL051 Developmental and Epileptic Encephalopathy 25, with Amelogenesis Imperfecta 38 5.623
119
CHN054 Chondrodysplasia, Blomstrand Type 52 5.623
120
c HYP210 Hypomagnesemia 2, Renal 40 5.623
121
c SHR083 Short-Rib Thoracic Dysplasia 13 with or Without Polydactyly 34 5.623
122
MLG168 Malignant Exocrine Pancreas Neoplasm 30 5.623
123
OVR059 Ovary Adenocarcinoma 49 5.623
124
APP018 Appendix Disease 31 5.623
125
BRT015 Bartholin's Gland Adenocarcinoma 29 5.623
126
OVR047 Ovarian Cystadenocarcinoma 38 5.623
127
PHS001 Phosphorus Metabolism Disease 38 5.623
128
HYP070 Hyperpituitarism 36 5.623
129
c JVN002 Juvenile Type Testicular Granulosa Cell Tumor 35 5.623
130
VLL001 Villous Adenocarcinoma 24 5.623
131
P TST016 Testicular Granulosa Cell Tumor 28 5.623
132
FRN003 Frontal Convexity Meningioma 30 5.623
133
PRP024 Peripheral Osteosarcoma 27 5.623
134
MND001 Mandibular Cancer 36 5.623
135
PNC041 Pancreatic Ductal Adenocarcinoma 51 5.432
136
OST159 Osteogenic Sarcoma 66 4.943
137
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 4.365
138
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 4.365
139
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 4.365
140
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 4.365
141
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 4.365
142
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 4.365
143
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 4.365
144
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 4.365
145
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 4.365
146
P PNC035 Pancreatic Cancer 86 4.060
147
P GST053 Gastric Cancer 83 3.836
148
GST103 Gastric Cancer, Hereditary Diffuse 68 3.774
149
P HYP069 Hyperparathyroidism 62 3.644
150
P BND020 Bone Disease 59 3.643
151
c PTT056 Pituitary Adenoma 1, Multiple Types 53 3.617
152
END057 Endometrial Cancer 72 3.566
153
P BLD134 Bladder Cancer 79 3.397
154
c SML038 Small Cell Cancer of the Lung 69 3.194
155
P OVR082 Overgrowth Syndrome 49 3.183
156
c HPT073 Hepatitis C Virus 71 3.176
157
SML031 Small Cell Carcinoma of the Bladder 46 3.166
158
FBR054 Fibroma 44 3.077
159
THY029 Thyroid Carcinoma 51 3.072
160
P PRS040 Prostate Cancer 95 3.041
161
SML009 Small Intestine Adenocarcinoma 57 3.033
162
GRW007 Growth Hormone Deficiency 46 2.999
163
P MDL005 Medulloblastoma 75 2.960
164
CLN015 Colon Adenocarcinoma 65 2.915
165
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 60 2.893
166
c CLR087 Colorectal Cancer 12 34 2.893
167
LNG039 Lung Squamous Cell Carcinoma 57 2.779
168
LPT014 Leptin Deficiency or Dysfunction 78 2.700
169
ESP021 Esophageal Cancer 83 2.692
170
P OVR042 Ovarian Cancer 88 2.673
171
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.673
172
P CTR002 Cataract 60 2.662
173
47X002 47,xyy 48 2.603
174
THY123 Thyroid Gland Follicular Carcinoma 55 2.599
175
MYX013 Myxofibrosarcoma 44 2.549
176
P TRT010 Teratoma 51 2.549
177
P FML011 Familial Adenomatous Polyposis 71 2.529
178
P NSP012 Nasopharyngeal Carcinoma 61 2.521
179
SPN035 Spindle Cell Sarcoma 54 2.494
180
CHL065 Cholangiocarcinoma 58 2.420
181
INT079 Intrahepatic Cholangiocarcinoma 51 2.420
182
ADN011 Adenoid Cystic Carcinoma 68 2.420
183
SRC014 Sarcoma 65 2.377
184
ADN089 Adenosquamous Lung Carcinoma 49 2.342
185
OCL022 Ocular Melanoma 52 2.314
186
HLX001 Helix Syndrome 48 2.270
187
P TMR010 Tumor Predisposition Syndrome 67 2.261
188
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 2.261
189
HPT067 Hepatocellular Adenoma 43 2.201
190
MCN001 Mucinous Adenocarcinoma 49 2.201
191
c HPT001 Hepatitis C 62 2.201
192
P INF032 Infertility 57 2.201
193
CLR109 Colorectal Adenocarcinoma 50 2.183
194
GLM045 Glioma 63 2.149
195
GGN002 Gigantism 33 2.142
196
SPN027 Spinal Stenosis 59 2.125
197
MLR004 Malaria 80 2.112
198
P NRF002 Neurofibromatosis 57 2.112
199
PRT037 Pertussis 65 2.095
200
CLR030 Clear Cell Renal Cell Carcinoma 54 2.092
201
c SCN007 Secondary Hyperparathyroidism 51 2.080
202
TBL003 Tubular Adenocarcinoma 40 2.080
203
P BLD062 Bile Duct Cancer 67 2.061
204
BNR002 Bone Resorption Disease 47 2.016
205
CLR108 Colorectal Adenoma 64 2.016
206
NRL016 Neural Tube Defects 81 2.016
207
EWN003 Ewing Sarcoma 70 2.016
208
RCK004 Rickets 68 2.016
209
P MLN007 Male Infertility 56 2.016
210
NPH013 Nephrogenic Syndrome of Inappropriate Antidiuresis 37 1.948
211
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.948
212
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.948
213
MST005 Mastitis 53 1.948
214
OVR094 Ovarian Epithelial Cancer 39 1.948
215
END041 Endometrial Adenocarcinoma 64 1.929
216
P FNC044 Fanconi Anemia, Complementation Group C 56 1.877
217
P HMN010 Hemangioma 62 1.877
218
P INF038 Influenza 68 1.872
219
P HYP265 Hypotonia 42 1.872
220
PRS063 Paresthesia 39 1.872
221
P GLM040 Glioma Susceptibility 1 71 1.829
222
MNN043 Meningioma, Familial 79 1.829
223
P MLN069 Melanoma, Uveal 61 1.803
224
HYP249 Hyperthyroidism, Nonautoimmune 36 1.803
225
MST020 Mast Cell Activation Syndrome 28 1.803
226
MYL069 Myeloma, Multiple 77 1.801
227
MCR037 Macroglossia 44 1.723
228
OST011 Osteomalacia 52 1.723
229
P CRN037 Craniosynostosis 68 1.723
230
GST033 Gestational Diabetes 61 1.723
231
P NNT058 Neonatal Diabetes 52 1.723
232
P INS002 in Situ Carcinoma 53 1.723
233
c MSM022 Mismatch Repair Cancer Syndrome 1 70 1.637
234
IMM167 Immune Deficiency Disease 78 1.575
235
HMN044 Human Immunodeficiency Virus Type 1 78 1.513
236
GNR004 Generalized Anxiety Disorder 55 1.513
237
HYP017 Hypophosphatemia 49 1.449
238
P PHC014 Phocomelia 23 1.449
239
CRD132 Cardiac Conduction Defect 60 1.441
240
P ANG001 Angelman Syndrome 65 1.441
241
INS001 Insulinoma 59 1.441
242
c PRC016 Pre-Eclampsia 65 1.441
243
PLS006 Plasmodium Vivax Malaria 51 1.441
244
PLM033 Pulmonary Embolism 58 1.441
245
P CRP001 Carpal Tunnel Syndrome 66 1.441
246
c GLM047 Glioma Susceptibility 3 33 1.392
247
c GLM025 Glioma Susceptibility 2 30 1.392
248
c GLM043 Glioma Susceptibility 9 30 1.392
249
P OLG002 Oligodendroglioma 66 1.392
250
MTH071 Methane Production 25 1.381
251
PTT058 Pituitary Adenoma 2, Growth Hormone-Secreting 31 1.362
252
c PRS097 Prostate Cancer, Hereditary, 1 39 1.362
253
c PTT060 Pituitary Adenoma 5, Multiple Types 39 1.362
254
c PRS070 Prostate Cancer, Hereditary, 12 22 1.362
255
c PRS071 Prostate Cancer, Hereditary, 13 25 1.362
256
c PRS117 Prostate Cancer, Hereditary, 11 24 1.362
257
c PRS114 Prostate Cancer, Hereditary, 2 33 1.362
258
PRS015 Prostate Signet Ring Cell Adenocarcinoma 25 1.362
259
RST023 Resting Heart Rate, Variation in 40 1.324
260
BNG091 Benign Chronic Pemphigus 57 1.324
261
P PRD006 Prader-Willi Syndrome 61 1.324
262
P TRN020 Turner Syndrome 67 1.324
263
P GND004 Gonadal Dysgenesis 47 1.324
264
HYP080 Hypogonadism 50 1.324
265
c SVR005 Severe Pre-Eclampsia 50 1.324
266
c CNT075 Central Precocious Puberty 53 1.324
267
CYS021 Cystic Adenomatoid Malformation of Lung 32 1.324
268
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 1.311
269
P NRB001 Neuroblastoma 66 1.311
270
P FBR017 Fibrosarcoma 56 1.311
271
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.298
272
INT381 Intraductal Tubulopapillary Neoplasm of Pancreas 13 1.236
273
P ALZ034 Alzheimer Disease 87 1.236
274
MLD018 Mild Cognitive Impairment 48 1.236
275
c ALZ045 Alzheimer Disease 9 45 1.236
276
P GST044 Gastritis 55 1.236
277
FML168 Familial Isolated Pituitary Adenoma 32 1.236
278
P PHC003 Pheochromocytoma 69 1.227
279
P PRG013 Paraganglioma 57 1.227
280
ADR040 Adrenal Gland Pheochromocytoma 46 1.227
281
VNH007 Von Hippel-Lindau Syndrome 73 1.218
282
MLT165 Multilocular Cystic Renal Neoplasm of Low Malignant Potential 28 1.218
283
MLT003 Multilocular Clear Cell Renal Cell Carcinoma 32 1.218
284
c HYD064 Hydrocephalus, Congenital, 1 51 1.185
285
ORL015 Oral Squamous Cell Carcinoma 43 1.185
286
AML029 Ameloblastoma 47 1.185
287
SYN005 Synostosis 43 1.185
288
P BRS053 Breast Fibroadenoma 49 1.185
289
DSS009 Disseminated Intravascular Coagulation 57 1.185
290
PRG010 Pregnancy Adenoma 21 1.185
291
P PTT014 Pitt-Hopkins Syndrome 64 1.184
292
CHR525 Chromosome Xq26.3 Duplication Syndrome 37 1.156
293
P URN019 Urinary Tract Infection 49 1.156
294
c UNP009 Uniparental Disomy of Chromosome 20 9 1.156
295
CHL123 Chlamydia 58 1.156
296
THY121 Thyroid Gland Anaplastic Carcinoma 67 1.140
297
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.121
298
P VSC007 Vascular Disease 63 1.121
299
BRS099 Breast Ductal Carcinoma 61 1.094
300
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 1.090
301
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 1.070
302
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 1.070
303
P SCH015 Schizophrenia 74 1.070
304
CYS001 Cystic Fibrosis 78 1.070
305
INT072 Intestinal Pseudo-Obstruction 62 1.070
306
P HYP760 Hypothyroidism, Congenital, Nongoitrous, 2 55 1.070
307
VRG001 Variegate Porphyria 56 1.070
308
PRP083 Porphyria, Acute Intermittent 65 1.070
309
c MLT086 Multiple Endocrine Neoplasia, Type Iv 50 1.070
310
P HNT016 Huntington Disease 73 1.070
311
SKN016 Skin Disease 63 1.070
312
GLB002 Glioblastoma 67 1.070
313
P ACN011 Acne 57 1.070
314
ILS001 Ileus 50 1.070
315
c ACT027 Acute Pancreatitis 60 1.070
316
ACT078 Acute Porphyria 49 1.070
317
P PRP029 Porphyria 60 1.070
318
HYP056 Hypoglycemia 65 1.070
319
48X005 48,xyyy 39 1.070
320
DST001 Distal Biliary Tract Carcinoma 24 1.055
321
CLC064 Calcifying Aponeurotic Fibroma 22 1.004
322
P THY032 Thyroiditis 57 1.004
323
c MLG084 Malignant Fibrous Histiocytoma 62 1.004
324
ODN006 Odontoma 29 1.004
325
MTR087 Maternal Uniparental Disomy 28 0.977
326
c PTR020 Paternal Uniparental Disomy of Chromosome 20 6 0.977
327
SVR001 Severe Acute Respiratory Syndrome 67 0.977
328
P LYN001 Lynch Syndrome 76 0.977
329
P DNG005 Dengue Virus 56 0.977
330
DNC004 Diencephalic Syndrome 36 0.977
331
LBL001 Lobular Neoplasia 55 0.953
332
P RRT020 Rare Tumor 39 0.874
333
MYC006 Mycosis Fungoides 65 0.874
334
P AST005 Asthma 76 0.874
335
ANX010 Anxiety 70 0.874
336
PLY150 Polykaryocytosis Inducer 29 0.874
337
UMB002 Umbilical Hernia 47 0.874
338
P ASP001 Asperger Syndrome 48 0.874
339
c LKM061 Leukemia, Acute Myeloid 83 0.874
340
BLD063 Bile Duct Cysts 42 0.874
341
FBR011 Fibrodysplasia Ossificans Progressiva 67 0.874
342
P MYC007 Myocardial Infarction 70 0.874
343
HYP066 Hyperglycemia 61 0.874
344
CRB004 Cerebral Artery Occlusion 45 0.874
345
CHL068 Cholestasis 61 0.874
346
P OVR049 Ovarian Disease 52 0.874
347
VSC002 Vascular Dementia 60 0.874
348
DCR010 Dicer1 Tumor Predisposition 30 0.874
349
PNS014 Penis Agenesis 36 0.874
351
IRN008 Iron Overload in Africa 51 0.862
352
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.862
353
MLN065 Melanocytic Nevus Syndrome, Congenital 62 0.862
354
P JVN014 Juvenile Polyposis Syndrome 64 0.862
355
c CLR085 Colorectal Cancer 1 42 0.862
356
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.862
357
HPT079 Hepatoid Adenocarcinoma 39 0.862
358
PTT057 Pituitary Adenoma 4, Acth-Secreting 48 0.862
359
RJS001 Ruijs-Aalfs Syndrome 47 0.862
360
c CLR075 Colorectal Cancer 3 31 0.862
361
PLM173 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal 34 0.862
362
c EXS020 Exostoses, Multiple, Type Ii 38 0.862
363
c EXS019 Exostoses, Multiple, Type I 54 0.862
364
c CLR077 Colorectal Cancer 10 33 0.862
365
PDT042 Pediatric Hepatocellular Carcinoma 49 0.862
366
P LNG021 Lung Occult Small Cell Carcinoma 20 0.862
367
LNG019 Lung Combined Type Small Cell Carcinoma 32 0.862
368
SKN022 Skin Squamous Cell Carcinoma 54 0.862
369
THY124 Thyroid Gland Papillary Carcinoma 39 0.862
370
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.862
371
LNG012 Lung Occult Squamous Cell Carcinoma 20 0.862
372
PPL004 Papillary Squamous Carcinoma 39 0.862
373
FBR086 Fibrolamellar Carcinoma 59 0.862
374
HPT011 Hepatocellular Clear Cell Carcinoma 46 0.862
375
LNG007 Lung Mixed Small Cell and Squamous Cell Carcinoma 21 0.862
376
PSD011 Pseudovascular Skin Squamous Cell Carcinoma 16 0.862
377
ORL011 Oral Cancer 60 0.862
378
PTY007 Pityriasis Rotunda 26 0.862
379
P THL005 Thalassemia 56 0.757
380
c CNG578 Congenital Hemangioma 18 0.757
381
HYP854 Hypopigmentation of the Skin 22 0.757
382
THY128 Thyroid Tumor 35 0.757
383
P RTT002 Rett Syndrome 79 0.757
384
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 0.757
385
c GLL024 Gallbladder Disease 1 52 0.757
386
c THY107 Thymoma, Familial 42 0.757
387
ART002 Arts Syndrome 66 0.757
388
c SPR086 Spermatogenic Failure 3 46 0.757
389
c ALP101 Alpha-Thalassemia 62 0.757
390
PPL052 Papillomatosis, Confluent and Reticulated 34 0.757
391
DNL003 Dna, Low-Repetitive Sequences of 9 0.757
392
P ATX030 Ataxia-Telangiectasia 80 0.757
393
MYL009 Myelodysplastic Syndrome 67 0.757
394
c ATM101 Autoimmune Gastritis 40 0.757
395
P CHN012 Chondrosarcoma 57 0.757
396
c LNG048 Long Qt Syndrome 3 53 0.757
397
c ACT202 Acth-Independent Macronodular Adrenal Hyperplasia 2 33 0.757
398
P RTN024 Retinoblastoma 73 0.757
399
FLR007 Failure of Tooth Eruption, Primary 34 0.757
400
P HRS035 Hirschsprung Disease 1 66 0.757
401
P SCL018 Scoliosis 57 0.757
402
ALL006 Allergic Asthma 56 0.757
403
P ATR005 Atrophic Gastritis 50 0.757
404
P DBT009 Diabetes Mellitus 67 0.757
405
P MYL006 Myeloid Leukemia 61 0.757
406
P MVM001 Movement Disease 61 0.757
407
PST092 Posttransplant Acute Limbic Encephalitis 28 0.757
408
GLL048 Glial Tumor 52 0.757
409
P HYP098 Hypereosinophilic Syndrome 66 0.757
410
NRN001 Neuroendocrine Carcinoma 47 0.757
411
VCC001 Vaccinia 47 0.757
412
PRT036 Peritonitis 65 0.757
413
NPH009 Nephrolithiasis 54 0.757
414
LNG099 Lung Disease 62 0.757
415
c FML297 Familial Thyroid Dyshormonogenesis 47 0.757
416
TLN003 Telangiectasis 51 0.757
417
P DMN002 Dementia 66 0.757
418
P LKM002 Leukemia 67 0.757
419
c BSL007 Basal Cell Carcinoma 68 0.757
420
HYP068 Hyperostosis 47 0.757
421
RPR002 Reproductive System Disease 36 0.757
422
ACN001 Acinar Cell Carcinoma 45 0.757
423
c ACT071 Acute Kidney Failure 60 0.757
424
P THY023 Thymoma 64 0.757
425
SGN002 Signet Ring Cell Adenocarcinoma 46 0.757
426
P GLM007 Glomerulonephritis 60 0.757
427
MGC001 Megacolon 48 0.757
428
VSC006 Vascular Cancer 46 0.757
429
NRN004 Neuroendocrine Tumor 59 0.757
430
BLN010 Balanitis 36 0.757
431
BNS003 Binswanger's Disease 41 0.757
432
ATM060 Autoimmune Atrophic Gastritis 19 0.757
433
ONC003 Oncogenic Osteomalacia 42 0.757
435
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 0.684
436
P SLP006 Sleep Apnea 69 0.684
437
OBS015 Obesity, Hyperphagia, and Developmental Delay 35 0.684
438
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.684
439
LPT006 Leptin Receptor Deficiency 50 0.684
440
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.684
441
END081 Endosteal Hyperostosis, Autosomal Dominant 54 0.684
442
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.684
443
ART016 Aortic Aneurysm 68 0.684
444
c DRR009 Diarrhea 6 45 0.684
445
CRT017 Cartilage Disease 53 0.684
446
P DRR001 Diarrhea 55 0.684
447
ANR040 Aneurysm 61 0.684
448
c BRD010 Bardet-Biedl Syndrome 1 64 0.618
449
MCK005 Mckusick-Kaufman Syndrome 61 0.618
450
GLY081 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency 47 0.618
451
ANX004 Anoxia 40 0.618
452
SLP010 Slipped Capital Femoral Epiphysis 38 0.618
453
SKL017 Skeletal Dysplasias 41 0.618
454
ONC007 Oncocytoma 50 0.618
455
KGM001 Kagami-Ogata Syndrome 53 0.618
456
OVR029 Ovarian Hyperstimulation Syndrome 63 0.618
457
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 56 0.618
458
GGN006 Gigantiform Cementoma, Familial 15 0.618
459
GST092 Gastroesophageal Reflux 61 0.618
460
c MJR022 Major Affective Disorder 8 38 0.618
461
P PLY014 Polycystic Kidney Disease 69 0.618
462
SPN221 Spina Bifida Occulta 40 0.618
463
MNC002 Munchausen by Proxy 29 0.618
464
IGR001 Ige Responsiveness, Atopic 59 0.618
465
P LKM062 Leukemia, Acute Lymphoblastic 69 0.618
466
c PGM022 Pigmented Nodular Adrenocortical Disease, Primary, 4 24 0.618
467
c MJR024 Major Affective Disorder 9 41 0.618
468
MTP004 Metaphyseal Acroscyphodysplasia 23 0.618
469
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.618
470
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.618
471
c GLY060 Glycogen Storage Disease Ia 63 0.618
472
VRC005 Varicose Veins 60 0.618
473
MYL005 Myelofibrosis 71 0.618
474
c TRC092 Trichorhinophalangeal Syndrome, Type I 54 0.618
475
DGR001 Digeorge Syndrome 62 0.618
476
c BRD021 Bardet-Biedl Syndrome 9 40 0.618
477
ADR041 Adrenal Cortical Adenoma 49 0.618
478
GLC003 Glucose Intolerance 54 0.618
479
P GLL020 Gallbladder Disease 56 0.618
480
P MTP001 Metaphyseal Dysplasia 38 0.618
481
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.618
482
CRH001 Crohn's Disease 80 0.618
483
P HYP083 Hypopituitarism 52 0.618
484
LTM002 Luteoma 31 0.618
485
P RPD001 Rapidly Progressive Glomerulonephritis 44 0.618
486
P KDN018 Kidney Disease 72 0.618
487
P DYS154 Dystonia 64 0.618
488
INT075 Intracranial Hypertension 53 0.618
489
GST010 Gestational Trophoblastic Neoplasm 52 0.618
490
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 0.618
491
ADR004 Adrenal Cortical Adenocarcinoma 38 0.618
492
P LVR013 Liver Disease 69 0.618
493
FCT008 Factitious Disorder 34 0.618
494
P BPL003 Bipolar Disorder 56 0.618
495
END086 End Stage Renal Disease 52 0.618
496
MYP002 Myoepithelial Carcinoma 46 0.618
497
P END046 Endometritis 46 0.618
498
PPL022 Papilloma 53 0.618
499
SKN005 Skin Atrophy 41 0.618
500
CLN044 Colon Adenoma 44 0.618
501
P CYS017 Cystic Teratoma 41 0.618
502
P GLY013 Glycogen Storage Disease 60 0.618
503
P HYD006 Hydrocephalus 61 0.618
504
PRT013 Portal Hypertension 59 0.618
505
DDN003 Duodenum Adenocarcinoma 38 0.618
506
ESP002 Esophageal Varix 51 0.618
507
LVR012 Liver Cirrhosis 63 0.618
508
LMY003 Leiomyomatosis 44 0.618
509
EPT010 Epithelial-Myoepithelial Carcinoma 55 0.618
510
MTR010 Mature Teratoma 40 0.618
511
INT020 Intravenous Leiomyomatosis 36 0.618
512
ISC004 Ischemia 61 0.618
513
P CYS039 Cystic Kidney Disease 53 0.618
514
GNG013 Gingivitis 59 0.618
515
P KDN017 Kidney Cancer 61 0.618
516
MMM001 Mammary Paget's Disease 53 0.618
517
P OST001 Osteopetrosis 71 0.618
518
EXT006 Extrahepatic Cholestasis 40 0.618
519
PST028 Post-Traumatic Stress Disorder 59 0.618
520
HYP060 Hyperinsulinism 54 0.618
521
NSS002 Neisseria Meningitidis Infection 47 0.618
522
FHT001 Fh Tumor Predisposition Syndrome 27 0.618
523
FBR019 Fibromatosis 42 0.618
524
RNL119 Renal Cell Carcinoma, Xp11-Associated 42 0.609
525
LNG115 Lung Sarcomatoid Carcinoma 36 0.609
526
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.609
527
LNG091 Lung Mucoepidermoid Carcinoma 32 0.609
528
MLG159 Malignant Pediatric Adrenal Gland Pheochromocytoma 12 0.609
529
LNG003 Lung Carcinoma in Situ 36 0.609
530
OVR011 Ovarian Mucinous Adenocarcinoma 34 0.609
531
BSL003 Basaloid Lung Carcinoma 35 0.609
532
ESP027 Esophagus Squamous Cell Carcinoma 45 0.609
533
MRK001 Merkel Cell Carcinoma 64 0.609
534
P LNG035 Lung Large Cell Carcinoma 54 0.609
535
MTN001 Metanephric Adenoma 40 0.609
536
LNG011 Lung Adenoid Cystic Carcinoma 35 0.609
537
LNG020 Lung Oat Cell Carcinoma 51 0.609
538
LNG017 Lung Giant Cell Carcinoma 52 0.609
539
c LNG001 Lung Clear Cell Carcinoma 29 0.609
540
LNG006 Lung Occult Large Cell Carcinoma 14 0.609
541
LNG002 Lung Combined Large Cell Neuroendocrine Carcinoma 19 0.609
543
HLR002 Hilar Lung Carcinoma 24 0.609
544
LNG014 Lung Superior Sulcus Carcinoma 15 0.609
545
CRC045 Carcinoma of Gallbladder and Extrahepatic Biliary Tract 21 0.574
546
SQM016 Squamous Cell Carcinoma of Gallbladder and Extrahepatic Biliary Tract 16 0.574
547
P FRG001 Fragile X Syndrome 70 0.567
548
HSH003 Hashimoto Thyroiditis 60 0.567
549
GYN001 Gynecomastia 47 0.567
550
IMP005 Impotence 52 0.567
551
INF021 Infant Gynecomastia 30 0.567
552
P PLY011 Polycystic Ovary Syndrome 57 0.567
553
HYP043 Hyperandrogenism 48 0.567
554
P MYT002 Myotonic Dystrophy 51 0.567
555
c TYP008 Type 1 Diabetes Mellitus 70 0.437
556
PRX035 Paroxysmal Dyskinesia 30 0.437
557
VLV044 Vulvar Intraepithelial Neoplasia 43 0.437
558
CMP097 Complex Chromosomal Rearrangement 23 0.437
559
ACR079 Acrodysostosis with Multiple Hormone Resistance 32 0.437
560
P PHC019 Pheochromocytoma-Paraganglioma 35 0.437
561
c MTR067 Maternal Uniparental Disomy of Chromosome 16 16 0.437
562
P SZR006 Seizure Disorder 70 0.437
563
ALD013 Aldosterone-Producing Adenoma 36 0.437
564
P ACR110 Acrodysostosis 1 with or Without Hormone Resistance 34 0.437
565
P CRN300 Coronary Heart Disease 1 73 0.437
566
PRS129 Prostatic Hyperplasia, Benign 49 0.437
567
c FNC032 Fanconi Anemia, Complementation Group B 48 0.437
568
P TST021 Testicular Germ Cell Tumor 61 0.437
569
P SHR029 Short Syndrome 58 0.437
570
DRR016 Diarrhea 2, with Microvillus Atrophy 54 0.437
571
BRT054 Brittle Bone Disorder 74 0.437
572
c PLM164 Pulmonary Hypertension, Primary, 1 76 0.437
573
P LFR001 Li-Fraumeni Syndrome 73 0.437
574
TRT017 Teratoma, Ovarian 28 0.437
575
P LKM071 Leukemia, Chronic Lymphocytic 75 0.437
576
FLT006 Floating-Harbor Syndrome 52 0.437
577
P SPR041 Spermatogenic Failure 6 47 0.437
578
c ATR087 Atrial Standstill 1 74 0.437
579
ATM095 Autoimmune Disease 61 0.437
580
PLM026 Pilomatrixoma 57 0.437
581
ALC007 Alcohol Dependence 66 0.437
582
FML345 Familial Expansile Osteolysis 46 0.437
583
c LKM063 Leukemia, Chronic Myeloid 71 0.437
584
CHN065 Choanal Atresia, Posterior 48 0.437
585
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 0.437
586
FML037 Female Breast Cancer 51 0.437
587
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.437
588
c FNC028 Fanconi Anemia, Complementation Group L 46 0.437
589
MSC007 Muscle Hypertrophy 64 0.437
590
c ATM024 Autoimmune Pancreatitis 52 0.437
591
MLG157 Malignant Pheochromocytoma 36 0.437
593
GST105 Gastroesophageal Adenocarcinoma 42 0.437
594
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.437
595
c ACT249 Acute Asthma 40 0.437
596
P CTN015 Cutaneous T Cell Lymphoma 48 0.437
597
OST006 Osteoblastoma 38 0.437
598
MST019 Mastoiditis 41 0.437
599
P SML001 Small Cell Carcinoma 52 0.437
600
c RTN041 Retinitis Pigmentosa 11 42 0.437
601
HLC007 Helicobacter Pylori Infection 67 0.437
602
c DBT064 Diabetes Mellitus, Transient Neonatal, 1 31 0.437
603
CHR103 Charge Syndrome 66 0.437
604
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.437
605
TRD006 Tardive Dyskinesia 53 0.437
606
c GRV008 Graves Disease 1 54 0.437
607
c CHR320 Chiari Malformation Type I 46 0.437
608
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.437
609
LCR013 Lacrimal Duct Defect 40 0.437
610
ANR009 Aneurysmal Bone Cysts 43 0.437
611
P PLY006 Polydactyly 59 0.437
612
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.437
613
LNG108 Langerhans Cell Histiocytosis 58 0.437
614
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 0.437
615
HRN029 Hearing Loss, Noise-Induced 37 0.437
616
c LVR030 Liver Failure, Infantile, Transient 34 0.437
617
c BRC060 Brachydactyly, Type E2 34 0.437
618
c PGM011 Pigmented Nodular Adrenocortical Disease, Primary, 2 25 0.437
619
c HYP355 Hypothyroidism, Congenital, Nongoitrous, 3 20 0.437
620
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 65 0.437
621
c LFR007 Li-Fraumeni Syndrome 2 46 0.437
622
c WLM013 Wilms Tumor 1 66 0.437
623
OST160 Osteoid Osteoma 37 0.437
624
PLY001 Polycythemia Vera 69 0.437
625
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.437
626
P SRC025 Sarcoidosis 1 71 0.437
627
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 66 0.437
628
P STR020 Strabismus 56 0.437
629
HYP748 Hypertelorism 46 0.437
630
c TYP009 Type 2 Diabetes Mellitus 92 0.437
631
P HYP726 Hypercalcemia, Infantile, 1 58 0.437
632
HYP741 Hyperparathyroidism 2 with Jaw Tumors 51 0.437
633
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.437
634
P EPS030 Episodic Kinesigenic Dyskinesia 1 55 0.437
635
THY111 Thyroid Carcinoma, Familial Medullary 67 0.437
636
P NNN008 Noonan Syndrome 1 77 0.437
637
ACR112 Acroleukopathy, Symmetric 14 0.437
638
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.437
639
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 51 0.437
640
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 53 0.437
641
c ATR085 Atrial Fibrillation, Familial, 18 21 0.437
642
GST071 Gastrointestinal Carcinoma 46 0.437
643
P OVR106 Ovarian Clear Cell Carcinoma 44 0.437
644
ACN026 Acinar Cell Carcinoma of Pancreas 27 0.437
645
c PRM340 Primary Adrenal Insufficiency 38 0.437
646
NPH003 Nephrocalcinosis 49 0.437
647
P PRK039 Parkinsonism 55 0.437
648
P MYP006 Myopia 56 0.437
649
FML211 Familial Papillary or Follicular Thyroid Carcinoma 25 0.437
650
P BCL017 B-Cell Lymphoma 59 0.437
651
CHR177 Chromophobe Renal Cell Carcinoma 54 0.437
652
EMB002 Embryoma 37 0.437
653
PNC015 Pancreatic Acinar Cell Adenocarcinoma 39 0.437
654
FNC007 Functioning Pituitary Adenoma 42 0.437
655
CMD001 Comedo Carcinoma 37 0.437
656
OCL006 Ocular Hypertension 53 0.437
657
CLF001 Cleft Lip 53 0.437
658
MCH006 Mechanical Strabismus 40 0.437
659
VRL011 Viral Infectious Disease 61 0.437
660
PNC019 Pancreatoblastoma 38 0.437
661
HPT022 Hepatoblastoma 54 0.437
662
CHR066 Chronic Fatigue Syndrome 60 0.437
663
c PRM301 Primary Cutaneous T-Cell Lymphoma 36 0.437
664
c UNP012 Uniparental Disomy of Chromosome 7 14 0.437
665
ACT162 Acute Sensory Ataxic Neuropathy 24 0.437
666
IDP034 Idiopathic Central Precocious Puberty 27 0.437
667
DFF036 Differentiated Thyroid Carcinoma 51 0.437
668
FDL002 Food Allergy 47 0.437
669
P EPL164 Epilepsy 68 0.437
670
HST010 Histiocytosis 49 0.437
671
END040 Endogenous Depression 55 0.437
672
MNT002 Mental Depression 57 0.437
673
P CNG001 Congenital Myasthenic Syndrome 68 0.437
674
VRR004 Verrucous Carcinoma 48 0.437
675
THY125 Thyroid Gland Medullary Carcinoma 48 0.437
676
SRC030 Sarcomatoid Carcinoma 42 0.437
677
BLD039 Bladder Adenocarcinoma 32 0.437
678
P RNL017 Renal Oncocytoma 54 0.437
679
SCR001 Secretory Meningioma 40 0.437
680
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.437
681
ACT084 Acute Stress Disorder 54 0.437
682
P PLY018 Polycythemia 56 0.437
683
ADN009 Adenosquamous Carcinoma 48 0.437
684
HMT002 Hematologic Cancer 61 0.437
685
ERD001 Erdheim-Chester Disease 53 0.437
686
NNL001 Non-Langerhans-Cell Histiocytosis 35 0.437
687
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.437
688
P KRT007 Keratoconus 50 0.437
689
P HMP002 Hemophagocytic Lymphohistiocytosis 61 0.437
690
c DLT002 Dilated Cardiomyopathy 78 0.437
691
DNG003 Dengue Disease 65 0.437
692
PLC002 Plica Syndrome 35 0.437
693
P NTR004 Neutropenia 63 0.437
694
ALL029 Allergic Disease 59 0.437
695
TRN003 Transverse Colon Cancer 38 0.437
696
PRS021 Prostatic Adenoma 43 0.437
697
SQM002 Squamous Cell Papilloma 46 0.437
698
THY122 Thyroid Gland Cancer 59 0.437
699
PSY004 Psychotic Disorder 66 0.437
700
END075 Endocervical Adenocarcinoma 37 0.437
701
P NPH012 Nephrotic Syndrome 60 0.437
702
RTR008 Root Resorption 44 0.437
703
P ESS003 Essential Thrombocythemia 69 0.437
704
P HPT021 Hepatitis 69 0.437
705
MLG169 Malignant Astrocytoma 57 0.437
706
HGH043 High Grade Glioma 45 0.437
707
PPL018 Papillary Adenocarcinoma 44 0.437
708
P ECL001 Eclampsia 52 0.437
709
P END044 Endometriosis 62 0.437
710
P HRT032 Heart Disease 81 0.437
711
QFV001 Q Fever 62 0.437
712
PRS045 Prostatic Hypertrophy 53 0.437
713
CNG034 Congestive Heart Failure 69 0.437
714
BRN024 Bronchitis 67 0.437
715
CRB039 Cerebrovascular Disease 66 0.437
716
P PGT001 Paget's Disease of Bone 61 0.437
717
P PNC044 Pancreatitis 61 0.437
718
OVR109 Ovarian Germ Cell Teratoma 32 0.437
719
P EYD002 Eye Disease 57 0.437
720
PLC008 Placenta Disease 49 0.437
721
GST049 Gastrointestinal System Cancer 49 0.437
722
LPD008 Lipid Metabolism Disorder 62 0.437
723
SYN007 Synovitis 55 0.437
724
MDD011 Mood Disorder 62 0.437
725
P LPS002 Liposarcoma 64 0.437
726
GST045 Gastroenteritis 58 0.437
727
CHN004 Chondroblastoma 41 0.437
728
BRS051 Breast Disease 58 0.437
729
OBS004 Obstructive Hydrocephalus 45 0.437
730
PLS007 Plasmodium Falciparum Malaria 52 0.437
731
SPN021 Spinal Meningioma 50 0.437
732
RCT020 Rectum Adenocarcinoma 48 0.437
733
P RCT021 Rectum Cancer 54 0.437
734
ADN020 Adenosarcoma 42 0.437
735
HLL004 Hellp Syndrome 53 0.437
736
KLD004 Keloid Disorder 39 0.437
737
P MNN013 Meningitis 65 0.437
739
P TRC031 Trichorhinophalangeal Syndrome 38 0.437
740
GRM010 Germ Cells Tumors 33 0.437
741
OPT032 Optic Pathway Glioma 33 0.437
742
c PSD047 Pseudo-Turner Syndrome 52 0.437
743
RSD004 Rosai-Dorfman Disease 49 0.437
744
SPL018 Splenomegaly 49 0.437
745
URC004 Urachal Cancer 24 0.437
746
BNN005 Bunion 31 0.437
747
P HDC001 Headache 57 0.437
748
UTR043 Uterine Sarcoma 40 0.437
749
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 30 0.437
750
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.437
751
P MYC033 Myoclonus 47 0.437
752
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.437
753
c FML094 Familial Wilms Tumor 2 25 0.437
754
GYN003 Gynandroblastoma 24 0.437
755
P CHR342 Chiari Malformation 41 0.437
756
NRN006 Neuroendocrine Carcinoma of the Cervix 19 0.437
757
ODN005 Odontogenic Myxoma 31 0.437
758
JVN045 Juvenile Ossifying Fibroma 16 0.437
759
GBL002 Goblet Cell Carcinoid 32 0.437
Content
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