Search results for mycn

483 hits were found for mycn

# Family MCID Name MIFTS Score
1
P NRB001 Neuroblastoma 66 85.872
2
P FNG006 Feingold Syndrome 1 62 50.124
3
P RTN024 Retinoblastoma 73 33.767
4
P MDL005 Medulloblastoma 75 26.301
5
P LNG032 Lung Cancer 98 22.812
6
GLB002 Glioblastoma 67 20.322
7
P RHB003 Rhabdomyosarcoma 66 19.049
8
GNG008 Ganglioneuroblastoma 47 16.055
9
P PRS040 Prostate Cancer 95 15.596
10
GNG002 Ganglioneuroma 52 15.155
11
RHB024 Rhabdomyosarcoma 2 67 14.608
12
P OVR042 Ovarian Cancer 88 14.429
13
EWN003 Ewing Sarcoma 70 14.307
14
P EMB005 Embryonal Rhabdomyosarcoma 53 14.107
15
P MCR010 Microcephaly 60 13.721
16
CHL018 Childhood Medulloblastoma 48 13.710
17
BRN028 Brain Cancer 74 12.642
18
P LKM062 Leukemia, Acute Lymphoblastic 69 12.364
19
P VNT002 Ventricular Septal Defect 58 12.082
20
c WLM013 Wilms Tumor 1 66 11.954
21
LRN003 Learning Disability 49 11.605
22
HPT022 Hepatoblastoma 54 11.470
23
SRC027 Sarcoma, Synovial 58 11.060
24
ESP020 Esophageal Atresia 60 10.778
25
LYM143 Lymphoma, Non-Hodgkin, Familial 75 10.211
26
c BSL007 Basal Cell Carcinoma 68 10.171
27
NDL011 Nodular Ganglioneuroblastoma 26 9.977
28
BLT001 Bilateral Retinoblastoma 35 9.737
29
RCH001 Richter's Syndrome 45 9.336
30
c LKM061 Leukemia, Acute Myeloid 83 9.285
31
DFF012 Differentiating Neuroblastoma 27 9.181
32
P PLR004 Pleuropulmonary Blastoma 65 9.134
33
GNG004 Ganglioglioma 53 9.134
34
TST014 Testicular Cancer 52 9.134
35
CRB002 Cerebral Primitive Neuroectodermal Tumor 27 9.134
36
SPP011 Suppression of Tumorigenicity 12 61 8.245
37
ADR003 Adrenal Neuroblastoma 27 8.063
38
P EPN001 Ependymoblastoma 44 7.898
39
RTN015 Retinal Cancer 49 7.655
40
UNL002 Unilateral Retinoblastoma 37 7.655
41
DBL002 Double Outlet Right Ventricle 57 7.626
42
ATY005 Atypical Teratoid Rhabdoid Tumor 69 7.404
43
P LFR001 Li-Fraumeni Syndrome 73 7.393
44
DFF039 Diffuse Midline Glioma, H3 K27m-Mutant 47 7.204
45
CRV067 Cervical Neuroblastoma 20 7.089
46
BSL036 Basal Cell Nevus Syndrome 73 6.958
47
ADL023 Adult Medulloblastoma 42 6.958
48
NDL005 Nodular Medulloblastoma 38 6.958
49
P HRN001 Horner's Syndrome 46 6.804
50
c MSM022 Mismatch Repair Cancer Syndrome 1 70 6.686
51
P PRP019 Peripheral Nervous System Disease 58 6.602
52
DSM006 Desmoplastic Infantile Ganglioglioma 22 6.602
53
CNT097 Central Hypoventilation Syndrome, Congenital 70 6.114
54
P RTN008 Retinitis Pigmentosa 80 6.114
55
PRP105 Peripheral Nervous System Benign Neoplasm 25 6.114
56
ATN017 Autonomic Nervous System Benign Neoplasm 25 6.114
57
CNT109 Central Nervous System Benign Neoplasm 30 6.114
58
P CNT044 Central Nervous System Primitive Neuroectodermal Neoplasm 28 6.114
59
c CHR376 Charcot-Marie-Tooth Disease, Type 4d 47 6.114
60
SWN003 Sweeney-Cox Syndrome 39 6.114
61
c MCR241 Microphthalmia, Syndromic 3 55 6.114
62
INF039 Infratentorial Cancer 38 6.114
63
SPR008 Supratentorial Primitive Neuroectodermal Tumor 42 6.114
64
SPR024 Supratentorial Cancer 39 6.114
65
CRB038 Cerebral Ventricle Cancer 29 6.114
66
CNT033 Central Nervous System Cancer 47 6.114
67
CRB040 Cerebrum Cancer 27 6.114
68
CRB030 Cerebellum Cancer 39 6.114
69
SKL003 Skeletal Muscle Cancer 28 6.114
70
MSC072 Muscle Cancer 48 6.114
71
EXT024 Extracranial Neuroblastoma 19 6.114
72
ADL041 Adult Spinal Cord Ependymoma 10 6.114
73
FRN007 Frontal Lobe Neoplasm 29 6.114
74
RTR023 Retroperitoneal Neuroblastoma 18 6.114
75
PRS017 Prostate Neuroendocrine Neoplasm 24 6.114
76
P ATN003 Autonomic Nervous System Neoplasm 26 6.114
77
INT082 Intraocular Retinoblastoma 29 6.114
78
ORB011 Orbit Rhabdomyosarcoma 32 6.114
79
P NRV006 Nervous System Cancer 48 6.114
80
P PRP021 Peripheral Nervous System Neoplasm 38 6.114
81
P NRV007 Nervous System Disease 67 6.114
82
GNG005 Gangliocytoma 55 6.068
83
c SML038 Small Cell Cancer of the Lung 69 5.916
84
c NRB010 Neuroblastoma 1 59 5.381
85
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 5.078
86
TTR011 Tetraploidy 43 4.749
87
CHR178 Chromosomal Triplication 34 4.659
88
HLX001 Helix Syndrome 48 4.408
89
GLM045 Glioma 63 4.327
90
P GLM040 Glioma Susceptibility 1 71 4.262
91
SVR004 Severe Combined Immunodeficiency 72 4.245
92
GLL048 Glial Tumor 52 3.706
93
MLG169 Malignant Astrocytoma 57 3.690
94
P LKM002 Leukemia 67 3.590
95
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 3.547
96
END057 Endometrial Cancer 72 3.468
97
47X002 47,xyy 48 3.431
98
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 3.319
99
CHR220 Chromosome 1p Deletion 15 3.270
100
CLL010 Cellular Ependymoma 57 3.254
101
P BNG030 Benign Ependymoma 51 3.254
102
P HPT023 Hepatocellular Carcinoma 96 3.221
103
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 3.171
104
MNN043 Meningioma, Familial 79 3.049
105
P ATX030 Ataxia-Telangiectasia 80 3.013
106
CHR619 Chromosome 2q35 Duplication Syndrome 64 3.013
107
TLN003 Telangiectasis 51 3.013
108
SFT003 Soft Tissue Sarcoma 57 3.013
109
P LYM118 Lymphoma 67 2.971
110
END041 Endometrial Adenocarcinoma 64 2.938
111
OST159 Osteogenic Sarcoma 66 2.909
112
NRN001 Neuroendocrine Carcinoma 47 2.901
113
HYP266 Hypoxia 57 2.875
114
P PLY006 Polydactyly 59 2.843
115
BRK010 Burkitt Lymphoma 66 2.783
116
P RTT002 Rett Syndrome 79 2.657
117
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 2.657
118
P LKM071 Leukemia, Chronic Lymphocytic 75 2.638
119
P MYL006 Myeloid Leukemia 61 2.539
120
SPN035 Spindle Cell Sarcoma 54 2.539
121
SRC014 Sarcoma 65 2.539
122
SCR001 Secretory Meningioma 40 2.477
123
LYM002 Lymphoplasmacyte-Rich Meningioma 35 2.477
124
SPN021 Spinal Meningioma 50 2.477
125
P OVR082 Overgrowth Syndrome 49 2.450
126
P BCL017 B-Cell Lymphoma 59 2.450
127
P HYD006 Hydrocephalus 61 2.413
128
TRP014 Triploidy 38 2.413
129
RPD005 Rapidly Involuting Congenital Hemangioma 46 2.347
130
P SPN042 Spinal Cord Ependymoma 29 2.296
131
AGN016 Aging 54 2.289
132
ACT098 Acute Erythroid Leukemia 55 2.206
133
P SML001 Small Cell Carcinoma 52 2.206
134
P MGL030 Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1 46 2.206
135
MCR237 Macrocephaly/megalencephaly Syndrome, Autosomal Recessive 40 2.206
136
PLY183 Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome 41 2.206
137
MLG077 Malignant Peripheral Nerve Sheath Tumor 54 2.206
138
PLY024 Polymicrogyria 47 2.206
139
P MGL013 Megalencephaly 45 2.206
140
EMB007 Embryonal Sarcoma 40 2.206
141
ADN018 Adenoma 59 2.131
142
P ADN016 Adenocarcinoma 63 2.052
143
PTT037 Pituitary Tumors 44 2.052
144
HRT011 Heart Septal Defect 49 2.028
145
NRN046 Neuronal Tumor 19 1.968
146
HGH043 High Grade Glioma 45 1.968
147
P KDN017 Kidney Cancer 61 1.968
148
ANP006 Anaplastic Ependymoma 44 1.968
149
DFF005 Diffuse Large B-Cell Lymphoma 54 1.879
150
HYP748 Hypertelorism 46 1.879
151
CHL065 Cholangiocarcinoma 58 1.879
152
INT079 Intrahepatic Cholangiocarcinoma 51 1.879
153
NRL008 Neural Crest Tumor 25 1.879
154
PLY100 Polyploidy 36 1.809
155
MNT001 Mantle Cell Lymphoma 67 1.809
156
SMT018 Smith-Mccort Dysplasia 2 34 1.783
157
TNG007 Tongue Carcinoma 52 1.783
158
HMT002 Hematologic Cancer 61 1.783
160
CHR238 Chromosome 2p Duplication 14 1.783
161
RNL114 Renal Cell Carcinoma, Nonpapillary 80 1.764
162
CLR030 Clear Cell Renal Cell Carcinoma 54 1.764
163
NRN004 Neuroendocrine Tumor 59 1.688
164
P LNG064 Lung Cancer Susceptibility 3 70 1.680
165
CSP005 Caspase 8 Deficiency 58 1.679
166
P CLR023 Colorectal Cancer 100 1.679
167
PHL006 Phelan-Mcdermid Syndrome 60 1.679
168
LNG039 Lung Squamous Cell Carcinoma 57 1.631
169
PNL012 Penile Cancer 57 1.619
170
c MNS014 Monosomy 22 35 1.616
171
P GST053 Gastric Cancer 83 1.582
172
c HYD064 Hydrocephalus, Congenital, 1 51 1.564
173
P RDL002 Radioulnar Synostosis 47 1.564
174
SYN005 Synostosis 43 1.564
175
FML008 Familial Retinoblastoma 50 1.541
176
OVR094 Ovarian Epithelial Cancer 39 1.541
177
CNT061 Conotruncal Heart Malformations 66 1.512
178
GLL036 Gallbladder, Agenesis of 18 1.512
179
DSS008 Disease of Mental Health 74 1.512
180
P PHC003 Pheochromocytoma 69 1.462
181
RHB001 Rhabdoid Cancer 68 1.462
182
P ERL057 Early Infantile Epileptic Encephalopathy 60 1.434
183
WST001 West Syndrome 59 1.434
184
CRP035 Corpus Callosum, Partial Agenesis of, X-Linked 38 1.434
185
c UNP011 Uniparental Disomy of Chromosome 14 15 1.434
186
P PNB001 Pineoblastoma 49 1.434
187
PNC008 Pancreatic Endocrine Carcinoma 39 1.434
188
P ENC018 Encephalopathy 62 1.434
189
P BLD134 Bladder Cancer 79 1.350
190
CNT019 Central Neurocytoma 46 1.299
191
MLG163 Malignant Tumor of Penis 29 1.289
192
ADR040 Adrenal Gland Pheochromocytoma 46 1.289
193
BRN049 Brain Tumor, Childhood 28 1.289
194
MLT173 Multiple Congenital Anomalies/dysmorphic Syndrome-Intellectual Disability 20 1.279
195
FNG009 Feingold Syndrome 2 27 1.279
196
c LFR007 Li-Fraumeni Syndrome 2 46 1.279
197
P OLG002 Oligodendroglioma 66 1.261
198
ESP021 Esophageal Cancer 83 1.226
199
P THL005 Thalassemia 56 1.194
200
HPT046 Hepatic Veno-Occlusive Disease 62 1.194
201
P MYC033 Myoclonus 47 1.194
202
SML031 Small Cell Carcinoma of the Bladder 46 1.191
203
P BRS047 Breast Cancer 98 1.119
204
GST103 Gastric Cancer, Hereditary Diffuse 68 1.095
205
ADN011 Adenoid Cystic Carcinoma 68 1.095
206
SML009 Small Intestine Adenocarcinoma 57 1.095
207
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 1.090
208
MYL069 Myeloma, Multiple 77 1.090
209
ULC004 Ulcerative Colitis 74 1.090
210
CNT115 Central Nervous System Embryonal Tumor 21 1.090
211
CMB007 Combined Immunodeficiency 57 1.090
212
P TRT010 Teratoma 51 1.090
213
ANP005 Anaplastic Astrocytoma 57 1.090
214
SPL018 Splenomegaly 49 1.090
215
NDL020 Nodal Marginal Zone B-Cell Lymphoma 29 1.077
216
MRG003 Marginal Zone B-Cell Lymphoma 52 1.077
217
JCB001 Jacobsen Syndrome 50 1.077
218
P FLL037 Follicular Lymphoma 74 1.077
219
PRL017 Prolymphocytic Leukemia 47 1.077
220
CHR223 Chromosome 1q Deletion 13 1.077
221
MRK001 Merkel Cell Carcinoma 64 1.019
222
P TMR010 Tumor Predisposition Syndrome 67 0.991
223
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 60 0.991
224
c CLR087 Colorectal Cancer 12 34 0.991
225
GST040 Gastric Adenocarcinoma 67 0.991
226
ADN089 Adenosquamous Lung Carcinoma 49 0.991
227
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 0.991
228
P RRT020 Rare Tumor 39 0.975
229
DDN011 Duodenal Atresia 48 0.975
231
P NTR004 Neutropenia 63 0.975
232
P HYP086 Hypothyroidism 69 0.975
233
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.975
234
P TCD001 Tic Disorder 49 0.975
235
DSM007 Desmoplastic Small Round Cell Tumor 54 0.975
236
MYL009 Myelodysplastic Syndrome 67 0.964
237
P URN019 Urinary Tract Infection 49 0.844
238
ALV005 Alveolar Soft Part Sarcoma 61 0.844
239
P PRS062 Persistent Hyperplastic Primary Vitreous 48 0.844
240
c ACT073 Acute Leukemia 58 0.844
241
MDL002 Medulloepithelioma 39 0.844
242
CRC021 Carcinosarcoma 64 0.844
243
P THR014 Thrombocytopenia 66 0.844
244
P SKN015 Skin Carcinoma 71 0.844
245
OLF005 Olfactory Neuroblastoma 46 0.844
246
ANT024 Anthrax Disease 58 0.844
247
CHR055 Chordoid Meningioma 28 0.844
248
P GRF003 Graft-Versus-Host Disease 71 0.844
249
MCS002 Mucositis 56 0.844
250
P HYP040 Hypospadias 51 0.844
251
P NRF002 Neurofibromatosis 57 0.844
252
STM007 Stomatitis 54 0.844
253
c LKM005 Leukemia, T-Cell, Chronic 34 0.844
254
OPS006 Opsoclonus-Myoclonus Syndrome 48 0.844
255
SQM006 Squamous Cell Carcinoma 60 0.817
256
CLN015 Colon Adenocarcinoma 65 0.809
257
PNC129 Pancreatic Adenocarcinoma 65 0.724
258
GLS001 Gliosarcoma 64 0.724
259
GNT002 Giant Cell Glioblastoma 57 0.724
260
ALP100 Alpha-Thalassemia/mental Retardation Syndrome, X-Linked 64 0.689
261
CRD223 Cardiac Arrhythmia 63 0.689
262
c ALP101 Alpha-Thalassemia 62 0.689
263
P PLM037 Pulmonary Hypertension 72 0.689
264
P ANP001 Anaplastic Large Cell Lymphoma 61 0.689
265
HMR023 Hemorrhagic Cystitis 43 0.689
266
c FNC028 Fanconi Anemia, Complementation Group L 46 0.689
267
NPH113 Nephroma 37 0.689
268
c ATS007 Autism Spectrum Disorder 72 0.689
269
P CHN012 Chondrosarcoma 57 0.689
270
c NRB014 Neuroblastoma 3 28 0.689
271
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.689
272
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 54 0.689
273
P SPP010 Suppressor of Tumorigenicity 3 51 0.689
274
P RBL001 Rubella 58 0.689
275
P DBT009 Diabetes Mellitus 67 0.689
276
CHC001 Chickenpox 57 0.689
277
P CYS018 Cystitis 59 0.689
278
P FBR017 Fibrosarcoma 56 0.689
279
P PLM036 Pulmonary Fibrosis 66 0.689
280
CHL061 Childhood Leukemia 47 0.689
281
P PLC011 Pilocytic Astrocytoma 57 0.689
282
SLP001 Sleeping Sickness 56 0.689
283
P MMP001 Mumps 57 0.689
284
c PRC016 Pre-Eclampsia 65 0.689
285
c ACT068 Acute Cystitis 61 0.689
286
GST020 Gastric Antral Vascular Ectasia 40 0.689
287
OCL009 Ocular Cancer 55 0.689
288
MYL031 Myeloproliferative Neoplasm 66 0.689
289
PPL018 Papillary Adenocarcinoma 44 0.689
290
P ECL001 Eclampsia 52 0.689
291
DSS009 Disseminated Intravascular Coagulation 57 0.689
292
CNG034 Congestive Heart Failure 69 0.689
293
UTR024 Uterine Carcinosarcoma 59 0.689
294
c INF023 Inflammatory Breast Carcinoma 49 0.689
295
MYX001 Myxopapillary Ependymoma 39 0.689
296
c MLG081 Malignant Teratoma 38 0.689
297
P LPS002 Liposarcoma 64 0.689
298
CPL003 Capillary Leak Syndrome 54 0.689
299
P ADL010 Adult Respiratory Distress Syndrome 71 0.689
300
P HYP265 Hypotonia 42 0.689
301
PRN039 Paraneoplastic Syndromes 37 0.689
302
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 30 0.689
303
MSL001 Measles 61 0.689
304
PLM173 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal 34 0.660
305
SKN022 Skin Squamous Cell Carcinoma 54 0.660
306
PSD011 Pseudovascular Skin Squamous Cell Carcinoma 16 0.660
307
BRS099 Breast Ductal Carcinoma 61 0.660
308
P PNC035 Pancreatic Cancer 86 0.644
309
STR094 Stromme Syndrome 45 0.590
310
INT060 Intestinal Atresia 41 0.590
311
MCR013 Microphthalmia 60 0.590
312
c GLM047 Glioma Susceptibility 3 33 0.572
313
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.572
314
c GLM025 Glioma Susceptibility 2 30 0.572
315
c GLM043 Glioma Susceptibility 9 30 0.572
316
P BLD062 Bile Duct Cancer 67 0.572
317
P LNG021 Lung Occult Small Cell Carcinoma 20 0.572
318
LNG019 Lung Combined Type Small Cell Carcinoma 32 0.572
319
LNG012 Lung Occult Squamous Cell Carcinoma 20 0.572
320
LNG007 Lung Mixed Small Cell and Squamous Cell Carcinoma 21 0.572
321
SHR044 Short Rib-Polydactyly Syndrome 46 0.487
322
c INH030 Inherited Retinal Disorder 28 0.487
323
SBP004 Subependymoma 40 0.487
324
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.487
325
CTS003 Coats Disease 53 0.487
326
FRY006 Fryns Microphthalmia Syndrome 52 0.487
327
P TRC072 Treacher Collins Syndrome 1 62 0.487
328
HMF006 Hemifacial Microsomia 55 0.487
329
PPL052 Papillomatosis, Confluent and Reticulated 34 0.487
330
PLY150 Polykaryocytosis Inducer 29 0.487
331
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.487
332
P SHR074 Short-Rib Thoracic Dysplasia 1 with or Without Polydactyly 60 0.487
333
c FNC027 Fanconi Anemia, Complementation Group a 81 0.487
334
c LKM063 Leukemia, Chronic Myeloid 71 0.487
335
CHN065 Choanal Atresia, Posterior 48 0.487
336
P ADL017 Adult T-Cell Leukemia 56 0.487
337
ATS010 Autosomal Recessive Disease 42 0.487
338
P PRG013 Paraganglioma 57 0.487
339
c NRB011 Neuroblastoma 4 13 0.487
340
c NRB012 Neuroblastoma 5 15 0.487
341
CLT003 Colitis 63 0.487
342
MYL020 Myelomeningocele 51 0.487
343
ASP005 Asphyxiating Thoracic Dystrophy 47 0.487
344
MDL030 Medulloblastoma Wnt Activated 6 0.487
345
CHR103 Charge Syndrome 66 0.487
346
ELL001 Ellis-Van Creveld Syndrome 62 0.487
347
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.487
348
HYP212 Hypomandibular Faciocranial Dysostosis 23 0.487
349
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.487
350
c MLT160 Multiple Endocrine Neoplasia, Type Iia 67 0.487
351
LMY014 Leiomyoma, Uterine 56 0.487
352
MND020 Mandibulofacial Dysostosis, Guion-Almeida Type 51 0.487
353
BRN133 Bronchomalacia 32 0.487
354
MYL005 Myelofibrosis 71 0.487
355
VTR016 Vater/vacterl Association 49 0.487
356
P STR020 Strabismus 56 0.487
357
THY111 Thyroid Carcinoma, Familial Medullary 67 0.487
358
c NRF024 Neurofibromatosis, Type I 72 0.487
359
c SHR064 Short-Rib Thoracic Dysplasia 10 with or Without Polydactyly 42 0.487
360
c NRB016 Neuroblastoma 7 15 0.487
361
CLR109 Colorectal Adenocarcinoma 50 0.487
362
ORL015 Oral Squamous Cell Carcinoma 43 0.487
363
P LKD001 Leukodystrophy 59 0.487
364
CRD137 Cardiogenic Shock 56 0.487
365
THY029 Thyroid Carcinoma 51 0.487
366
c HPT003 Hepatitis a 63 0.487
367
LMY002 Leiomyoma 51 0.487
368
CHL149 Childhood Acute Myeloid Leukemia 43 0.487
369
MTR008 Mature B-Cell Neoplasm 35 0.487
370
EMB002 Embryoma 37 0.487
371
EXT065 Extraosseous Ewing Sarcoma 29 0.487
372
WLL039 Well-Differentiated Liposarcoma 40 0.487
373
MCH006 Mechanical Strabismus 40 0.487
374
P NRP001 Neuropathy 60 0.487
375
HGH030 High-Grade Neuroendocrine Carcinoma of the Cervix Uteri 16 0.487
376
MLN001 Melanotic Neuroectodermal Tumor 33 0.487
377
P PTT006 Pituitary Adenoma 55 0.487
378
P LVR013 Liver Disease 69 0.487
379
DYS018 Dysostosis 44 0.487
380
THY022 Thymic Carcinoma 57 0.487
381
TRT001 Teratocarcinoma 42 0.487
382
P CRV031 Cervical Adenocarcinoma 48 0.487
383
CRV038 Cervical Squamous Cell Carcinoma 58 0.487
384
INS001 Insulinoma 59 0.487
385
CHL022 Childhood Central Nervous System Primitive Neuroectodermal Neoplasm 15 0.487
386
THY125 Thyroid Gland Medullary Carcinoma 48 0.487
387
FLL031 Follicular Adenoma 40 0.487
388
ILS001 Ileus 50 0.487
389
SMN007 Seminoma 42 0.487
390
P CTR002 Cataract 60 0.487
391
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.487
392
c FTL071 Fetal Akinesia Deformation Sequence 3 30 0.487
393
CHL004 Cholelithiasis 49 0.487
394
P MLN007 Male Infertility 56 0.487
395
TST004 Testicular Lymphoma 39 0.487
396
CNS004 Constipation 56 0.487
397
P HMN010 Hemangioma 62 0.487
398
PPL022 Papilloma 53 0.487
399
BLR008 Bilirubin Metabolic Disorder 57 0.487
400
SQM002 Squamous Cell Papilloma 46 0.487
401
P ATR010 Atrial Heart Septal Defect 58 0.487
402
END075 Endocervical Adenocarcinoma 37 0.487
403
FCL014 Focal Epilepsy 53 0.487
404
HYD002 Hydronephrosis 58 0.487
405
P BND020 Bone Disease 59 0.487
406
P RSP003 Respiratory Failure 74 0.487
407
HMP001 Hemopericardium 47 0.487
408
c MLG069 Malignant Hypertension 46 0.487
409
P PRC012 Pericardial Effusion 50 0.487
410
THY020 Thyroid Hyalinizing Trabecular Adenoma 20 0.487
411
PNL002 Pineal Parenchymal Tumor of Intermediate Differentiation 22 0.487
412
P INF032 Infertility 57 0.487
413
ANP009 Anaplastic Oligodendroglioma 41 0.487
414
EMB004 Embryonal Carcinoma 56 0.487
415
GRM005 Germ Cell Cancer 46 0.487
416
P CHR573 Choroid Plexus Cancer 48 0.487
417
P BNG032 Benign Mesothelioma 53 0.487
418
BRN002 Bronchiolitis 57 0.487
419
PTN001 Patent Foramen Ovale 62 0.487
420
P PTS002 Ptosis 52 0.487
421
VCT001 Vacterl Association 47 0.487
422
P URT039 Urticaria 58 0.487
423
IRN002 Iron Metabolism Disease 57 0.487
424
P LMY004 Leiomyosarcoma 62 0.487
425
P INS002 in Situ Carcinoma 53 0.487
426
CHL062 Childhood Pilocytic Astrocytoma 24 0.487
427
c ACT135 Acute Graft Versus Host Disease 51 0.487
428
PTH003 Pathologic Nystagmus 52 0.487
429
HRL002 Harlequin Syndrome 22 0.487
430
MYX011 Myxozoa 18 0.487
431
HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 60 0.487
432
CHR183 Chromosome 10q Deletion 13 0.487
433
PNS014 Penis Agenesis 36 0.487
434
SCR024 Sacrococcygeal Teratoma 28 0.487
435
CRN051 Craniofacial Microsomia 28 0.487
436
NRN006 Neuroendocrine Carcinoma of the Cervix 19 0.487
437
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.487
438
MLN065 Melanocytic Nevus Syndrome, Congenital 62 0.467
439
P ATS364 Autism 69 0.455
440
BRR014 Barrett Esophagus 66 0.455
441
CRC045 Carcinoma of Gallbladder and Extrahepatic Biliary Tract 21 0.330
442
SQM016 Squamous Cell Carcinoma of Gallbladder and Extrahepatic Biliary Tract 16 0.330
443
SQM013 Squamous Cell Carcinoma, Head and Neck 73 0.330
444
P RTH006 Rothmund-Thomson Syndrome, Type 2 67 0.330
445
RMB001 Rombo Syndrome 30 0.330
446
PLM026 Pilomatrixoma 57 0.330
447
VNH007 Von Hippel-Lindau Syndrome 73 0.330
448
PGT003 Paget Disease, Extramammary 47 0.330
449
LMN016 Luminal Breast Carcinoma B 28 0.330
450
P LMN015 Luminal Breast Carcinoma a 35 0.330
451
P TRC095 Trichoepithelioma, Multiple Familial, 1 32 0.330
452
c BSL024 Basal Cell Carcinoma 1 55 0.330
453
BSL044 Basal Cell Carcinoma, Infundibulocystic 35 0.330
454
c BSL034 Basal Cell Carcinoma 7 26 0.330
455
c CWD006 Cowden Syndrome 1 78 0.330
456
c ALB010 Albinism, Oculocutaneous, Type Ib 52 0.330
457
MLT165 Multilocular Cystic Renal Neoplasm of Low Malignant Potential 28 0.330
458
MLT003 Multilocular Clear Cell Renal Cell Carcinoma 32 0.330
459
CYS004 Cystic Basal Cell Carcinoma 36 0.330
460
SRC003 Sarcomatoid Basal Cell Carcinoma 28 0.330
461
NDL009 Nodular Basal Cell Carcinoma 40 0.330
462
MTT001 Metatypical Basal Cell Carcinoma 32 0.330
463
PGM002 Pigmented Basal Cell Carcinoma 31 0.330
464
MCR016 Micronodular Basal Cell Carcinoma 34 0.330
465
INF027 Infiltrative Basal Cell Carcinoma 32 0.330
466
PNS002 Penis Carcinoma in Situ 21 0.330
467
SKN019 Skin Melanoma 71 0.330
468
ESP027 Esophagus Squamous Cell Carcinoma 45 0.330
469
THY124 Thyroid Gland Papillary Carcinoma 39 0.330
470
ANL013 Anal Margin Basal Cell Carcinoma 18 0.330
471
SBC013 Sebaceous Basal Cell Carcinoma 13 0.330
472
ADM002 Adamantinoid Basal Cell Epithelioma 20 0.330
473
CLR015 Clear Cell Basal Cell Carcinoma 39 0.330
474
ADN015 Adenoid Basal Cell Carcinoma 31 0.330
475
SGN001 Signet Ring Basal Cell Carcinoma 32 0.330
476
CRV013 Cervical Adenoid Cystic Carcinoma 33 0.330
477
PNS010 Penis Squamous Cell Carcinoma 45 0.330
478
PNS005 Penis Mixed Squamous Cell Carcinoma 12 0.330
479
ORL011 Oral Cancer 60 0.330
480
9Q2001 9q22.3 Microdeletion 24 0.330
481
RCS008 Recessive Dystrophic Epidermolysis Bullosa-Generalized Other 30 0.330
482
INF057 Inflammatory Linear Verrucous Epidermal Nevus 33 0.330
483
LNR004 Linear Porokeratosis 33 0.330
Content
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