Search results for ret

480 hits were found for ret

# Family MCID Name MIFTS Score
1
INH023 Inherited Cancer-Predisposing Syndrome 46 7.928
2
c MLT160 Multiple Endocrine Neoplasia, Type Iia 70 6.483
3
P HRS035 Hirschsprung Disease 1 65 5.833
4
P PHC003 Pheochromocytoma 71 5.000
5
THY111 Thyroid Carcinoma, Familial Medullary 67 4.999
6
THY029 Thyroid Carcinoma 59 4.905
7
P MLT074 Multiple Endocrine Neoplasia 56 4.553
8
c MLT159 Multiple Endocrine Neoplasia, Type Iib 60 3.846
9
CNT097 Central Hypoventilation Syndrome, Congenital 71 3.649
10
P RNL100 Renal Hypodysplasia/aplasia 1 63 3.474
11
P CLR023 Colorectal Cancer 99 3.231
12
THY122 Thyroid Gland Cancer 57 3.051
13
P LNG032 Lung Cancer 98 2.853
14
P HYP069 Hyperparathyroidism 63 2.849
15
THY125 Thyroid Gland Medullary Carcinoma 50 2.796
16
P ADN016 Adenocarcinoma 64 2.748
17
CNS004 Constipation 58 2.738
18
P PNC035 Pancreatic Cancer 84 2.713
19
ADN018 Adenoma 59 2.690
20
P HYP086 Hypothyroidism 69 2.571
21
PPL002 Papillary Carcinoma 47 2.492
22
END057 Endometrial Cancer 74 2.356
23
c MLT156 Multiple Endocrine Neoplasia, Type I 72 2.320
24
MGC001 Megacolon 46 2.297
25
c PRM005 Primary Hyperparathyroidism 58 2.285
26
FLL031 Follicular Adenoma 39 2.218
27
P PRG013 Paraganglioma 52 2.187
28
PRT029 Parathyroid Adenoma 50 2.170
29
P AMY004 Amyloidosis 70 2.161
30
VNH007 Von Hippel-Lindau Syndrome 73 2.143
31
HSH003 Hashimoto Thyroiditis 62 2.143
32
P NRF002 Neurofibromatosis 56 2.143
33
P NRB001 Neuroblastoma 72 2.107
34
SRC014 Sarcoma 65 2.089
35
P WRD001 Waardenburg's Syndrome 59 2.089
36
P SNS001 Sensorineural Hearing Loss 60 2.063
37
c CWD006 Cowden Syndrome 1 78 2.032
38
SDD001 Sudden Infant Death Syndrome 61 2.032
39
c MLT086 Multiple Endocrine Neoplasia, Type Iv 51 1.931
40
THY128 Thyroid Tumor 47 1.918
41
P THY032 Thyroiditis 52 1.912
42
NRN004 Neuroendocrine Tumor 55 1.898
43
GTR002 Goiter 53 1.898
44
c HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 59 1.892
45
P INT070 Intestinal Obstruction 58 1.892
46
END035 Endocrine Gland Cancer 45 1.805
47
CKT002 Cakut 48 1.786
48
NDL007 Nodular Goiter 47 1.786
49
THY121 Thyroid Gland Anaplastic Carcinoma 66 1.775
50
LNG099 Lung Disease 60 1.742
51
NRM004 Neuroma 51 1.742
52
P HYP024 Hypoparathyroidism 56 1.729
53
RNL114 Renal Cell Carcinoma, Nonpapillary 78 1.716
54
P MDL005 Medulloblastoma 77 1.716
55
P TTR001 Tetralogy of Fallot 70 1.701
56
EWN003 Ewing Sarcoma 69 1.701
57
c INT072 Intestinal Pseudo-Obstruction 56 1.701
58
GNG012 Gingival Overgrowth 51 1.701
59
HYP748 Hypertelorism 50 1.701
60
c NRF024 Neurofibromatosis, Type I 77 1.685
61
PRT010 Parathyroid Carcinoma 67 1.685
62
LNG039 Lung Squamous Cell Carcinoma 66 1.685
63
GNG002 Ganglioneuroma 52 1.685
64
c WRD020 Waardenburg Syndrome, Type 4a 48 1.685
65
PYL006 Pyloric Stenosis 48 1.685
66
PRT030 Parathyroid Gland Disease 45 1.685
67
P HYP009 Hypertrophic Pyloric Stenosis 41 1.685
68
P PRM002 Primary Hyperoxaluria 62 1.666
69
ISL001 Islet Cell Tumor 56 1.666
70
c MNN043 Meningioma, Familial 74 1.644
71
P MTR014 Motor Neuron Disease 65 1.644
72
ALV005 Alveolar Soft Part Sarcoma 61 1.644
73
P HMN010 Hemangioma 61 1.644
74
P MCR010 Microcephaly 59 1.644
75
P RTN016 Retinal Degeneration 53 1.644
76
ACH005 Achalasia 51 1.644
77
GLD006 Goldberg-Shprintzen Syndrome 47 1.644
78
ECT093 Ectopic Cushing Syndrome 42 1.644
79
P STR021 Struma Ovarii 38 1.644
80
P LNG064 Lung Cancer Susceptibility 3 78 1.582
81
THY030 Thyroid Gland Disease 52 1.402
82
LCH014 Lichen Amyloidosis 31 1.333
83
DFF036 Differentiated Thyroid Carcinoma 52 1.301
84
P MLT008 Multinodular Goiter 42 1.289
85
HYP572 Hypoganglionosis 28 1.276
86
P RTN008 Retinitis Pigmentosa 79 1.248
87
c VSC019 Vesicoureteral Reflux 1 57 1.248
88
c PRG018 Paragangliomas 1 58 1.232
89
HYP706 Hypermobile Ehlers-Danlos Syndrome 53 1.232
90
c AMY060 Amyloidosis, Primary Localized Cutaneous, 1 41 1.232
91
P PHC019 Pheochromocytoma-Paraganglioma 36 1.232
92
c RRH009 Rare Hypothyroidism 24 1.232
93
P RRT020 Rare Tumor 41 1.213
94
MDL009 Medullary Sponge Kidney 40 1.213
95
BLY005 B-Lymphoblastic Leukemia/lymphoma with Hyperdiploidy 31 1.213
96
BLY006 B-Lymphoblastic Leukemia/lymphoma with Hypodiploidy 26 1.213
97
RNL065 Renal Cell Carcinoma, Papillary, 1 73 1.191
98
PRM126 Primary Peritoneal Carcinoma 62 1.191
99
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 1.191
100
HYP741 Hyperparathyroidism 2 with Jaw Tumors 53 1.191
101
c RNL122 Renal Hypodysplasia/aplasia 3 44 1.191
102
SPR068 Sporadic Pheochromocytoma/secreting Paraganglioma 29 1.191
103
P RNL123 Renal Agenesis, Bilateral 26 1.191
104
c HRS027 Hirschsprung Disease 5 18 1.191
105
P CWD010 Cowden Syndrome 67 1.163
106
P CHR071 Charcot-Marie-Tooth Disease 65 1.163
107
P CRN038 Carney Complex Variant 61 1.163
108
PRG017 Paraganglioma and Gastric Stromal Sarcoma 61 1.163
109
P FML068 Familial Hypocalciuric Hypercalcemia 54 1.163
110
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 1.163
111
THY123 Thyroid Gland Follicular Carcinoma 48 1.163
112
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 1.163
113
LYM116 Lymph Node Disease 41 1.163
114
PRS123 Persistent Generalized Lymphadenopathy 37 1.163
115
SPT022 Spitzoid Melanoma 36 1.163
116
EXT054 Extra-Adrenal Pheochromocytoma 34 1.163
117
TST010 Testicular Spermatocytic Seminoma 33 1.163
118
OVR109 Ovarian Germ Cell Teratoma 32 1.163
119
PST014 Postsurgical Hypothyroidism 32 1.163
120
ESP014 Esophagus Leiomyoma 29 1.163
121
c MLG059 Malignant Struma Ovarii 29 1.163
122
ADR014 Adrenal Medulla Cancer 29 1.163
123
CNT109 Central Nervous System Benign Neoplasm 28 1.163
124
CRD007 Cardiovascular Organ Benign Neoplasm 27 1.163
125
SKN002 Skin Lipoma 27 1.163
126
TLL001 Tall Cell Variant Papillary Carcinoma 27 1.163
127
c ATN017 Autonomic Nervous System Benign Neoplasm 26 1.163
128
CNT023 Central Nervous System Hemangioma 25 1.163
129
NNN001 Nonencapsulated Sclerosing Carcinoma 25 1.163
130
c ATS009 Autosomal Genetic Disease 25 1.163
131
c ATM014 Autoimmune Disease of Endocrine System 25 1.163
132
c PRP105 Peripheral Nervous System Benign Neoplasm 24 1.163
133
c BNG029 Benign Struma Ovarii 24 1.163
134
MLT011 Multiple Mucosal Neuroma 23 1.163
135
END036 Endocrine Organ Benign Neoplasm 22 1.163
136
SLD013 Solid Adenocarcinoma with Mucin Production 21 1.163
137
ATY007 Atypical Follicular Adenoma 20 1.163
138
MLT005 Multicentric Papillary Thyroid Carcinoma 17 1.163
139
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.562
140
ADR040 Adrenal Gland Pheochromocytoma 46 0.498
141
c SML038 Small Cell Cancer of the Lung 65 0.291
142
LNG031 Lung Benign Neoplasm 51 0.154
143
IRN002 Iron Metabolism Disease 57 0.146
144
P BRS047 Breast Cancer 97 0.129
145
DFC004 Deficiency Anemia 70 0.114
146
P MLN008 Melanoma 69 0.109
147
IRN001 Iron Deficiency Anemia 59 0.109
148
NRN001 Neuroendocrine Carcinoma 47 0.103
149
P PRK057 Parkinson Disease, Late-Onset 78 0.098
150
SKN019 Skin Melanoma 68 0.098
151
c THY102 Thyroid Cancer, Nonmedullary, 2 58 0.098
152
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.098
153
c LKM061 Leukemia, Acute Myeloid 84 0.091
154
P RSP003 Respiratory Failure 74 0.091
155
P LKM002 Leukemia 68 0.091
156
P MYL006 Myeloid Leukemia 60 0.091
157
RNL025 Renal Hypoplasia 42 0.091
158
IRR002 Irritable Bowel Syndrome 65 0.085
159
P PLR004 Pleuropulmonary Blastoma 65 0.085
160
P BNG030 Benign Ependymoma 60 0.085
161
P EXN002 Exanthem 57 0.085
162
CLL010 Cellular Ependymoma 54 0.085
163
RSP006 Respiratory System Disease 50 0.085
164
P BRN120 Bronchus Cancer 45 0.085
165
THR012 Thoracic Cancer 44 0.085
166
THY124 Thyroid Gland Papillary Carcinoma 38 0.085
167
c HRS034 Hirschsprung Disease 3 26 0.085
168
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.077
169
P OVR042 Ovarian Cancer 88 0.077
170
OST159 Osteogenic Sarcoma 66 0.077
171
c BRN108 Branchiootic Syndrome 1 62 0.077
172
P FBR017 Fibrosarcoma 56 0.077
173
P PTT006 Pituitary Adenoma 55 0.077
174
P LTR001 Lateral Sclerosis 54 0.077
175
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.077
176
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.077
177
RTN023 Retinitis 46 0.077
178
CLN045 Colonic Benign Neoplasm 46 0.077
179
P END084 Endocrine System Disease 45 0.077
180
NRR001 Neuroretinitis 42 0.077
181
48X005 48,xyyy 39 0.077
182
CHR178 Chromosomal Triplication 35 0.077
183
BRN148 Bronchial Benign Neoplasm 23 0.077
184
GLB015 Glioblastoma Multiforme 75 0.069
185
DWN001 Down Syndrome 70 0.069
186
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.069
187
SQM006 Squamous Cell Carcinoma 60 0.069
188
P NRP001 Neuropathy 56 0.069
189
P MNC007 Monocytic Leukemia 53 0.069
190
SPN035 Spindle Cell Sarcoma 53 0.069
191
P TRT010 Teratoma 52 0.069
192
GRM005 Germ Cell Cancer 47 0.069
193
c CNG023 Congenital Fibrosarcoma 42 0.069
194
P HPT023 Hepatocellular Carcinoma 100 0.060
195
P PRS040 Prostate Cancer 97 0.060
196
P GST053 Gastric Cancer 83 0.060
197
P RTN024 Retinoblastoma 73 0.060
198
P KDN018 Kidney Disease 72 0.060
199
P LYM118 Lymphoma 68 0.060
200
P GLM045 Glioma 63 0.060
201
P THL005 Thalassemia 60 0.060
202
ERY029 Erythermalgia, Primary 58 0.060
203
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.060
204
SFT003 Soft Tissue Sarcoma 56 0.060
205
c FML008 Familial Retinoblastoma 53 0.060
206
PNG002 Pain Agnosia 51 0.060
207
ENT011 Enterocolitis 51 0.060
208
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.060
209
RNL078 Renal Dysplasia 50 0.060
210
HLX001 Helix Syndrome 47 0.060
211
GLL048 Glial Tumor 45 0.060
212
P MLG074 Malignant Mesenchymoma 40 0.060
213
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.060
214
GST019 Gastrointestinal Stromal Tumor 78 0.049
215
SVR004 Severe Combined Immunodeficiency 73 0.049
216
P FML011 Familial Adenomatous Polyposis 72 0.049
217
ACR007 Acromegaly 71 0.049
218
P EPL164 Epilepsy 71 0.049
219
ADL002 Adult Syndrome 70 0.049
220
PNC129 Pancreatic Adenocarcinoma 68 0.049
221
P PLM037 Pulmonary Hypertension 67 0.049
222
c RHB024 Rhabdomyosarcoma 2 67 0.049
223
P SKN015 Skin Carcinoma 66 0.049
224
P LPS002 Liposarcoma 65 0.049
225
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.049
226
ANG020 Angiosarcoma 64 0.049
227
P RHB003 Rhabdomyosarcoma 63 0.049
228
P VSC007 Vascular Disease 63 0.049
229
ALL026 Allergic Hypersensitivity Disease 62 0.049
230
HYP066 Hyperglycemia 61 0.049
231
HYD002 Hydronephrosis 60 0.049
232
P MLN069 Melanoma, Uveal 59 0.049
233
P SZR006 Seizure Disorder 56 0.049
234
HMG005 Hemoglobinopathy 56 0.049
235
P INF049 Infantile Myofibromatosis 56 0.049
236
JVN009 Juvenile Pilocytic Astrocytoma 55 0.049
237
P INS002 in Situ Carcinoma 53 0.049
238
P INT068 Intestinal Disease 53 0.049
239
CYS014 Cystadenocarcinoma 51 0.049
240
P OVR082 Overgrowth Syndrome 50 0.049
241
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.049
242
CRC014 Carcinoid Tumors, Intestinal 47 0.049
243
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.049
244
CNT033 Central Nervous System Cancer 47 0.049
245
c OPT051 Opitz Gbbb Syndrome, Type I 47 0.049
246
LYM019 Lymphosarcoma 46 0.049
247
P BNG032 Benign Mesothelioma 46 0.049
248
PTT037 Pituitary Tumors 44 0.049
249
PPL001 Papillary Adenoma 44 0.049
250
P EPN001 Ependymoblastoma 44 0.049
251
ORL015 Oral Squamous Cell Carcinoma 43 0.049
252
c MYF007 Myofibromatosis, Infantile, 1 43 0.049
254
ATX019 Ataxia with Vitamin E Deficiency 42 0.049
255
MLT084 Multicystic Dysplastic Kidney 42 0.049
256
c OVR114 Ovarian Cancer 1 38 0.049
257
c MLG157 Malignant Pheochromocytoma 38 0.049
258
HYP001 Hypochromic Microcytic Anemia 38 0.049
259
OVR094 Ovarian Epithelial Cancer 38 0.049
260
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 38 0.049
261
BRN048 Brain Stem Cancer 37 0.049
262
c HRS036 Hirschsprung Disease 2 36 0.049
263
c PYL018 Pyloric Stenosis, Infantile Hypertrophic, 1 33 0.049
264
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.049
265
c HRS024 Hirschsprung Disease 9 14 0.049
266
c HYP595 Hypertension, Essential 84 0.034
267
P GLM040 Glioma Susceptibility 1 81 0.034
268
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.034
269
STR067 Stroke, Ischemic 81 0.034
270
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.034
271
CNN003 Conn's Syndrome 79 0.034
272
INS024 Insulin-Like Growth Factor I 79 0.034
273
AST005 Asthma 76 0.034
274
P HRT032 Heart Disease 75 0.034
275
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.034
276
c BTT014 Beta-Thalassemia 74 0.034
277
c HYP836 Hypercholesterolemia, Familial, 1 73 0.034
278
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.034
279
P CNR004 Cone-Rod Dystrophy 2 73 0.034
280
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.034
281
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.034
282
SCH036 Scheie Syndrome 72 0.034
283
P HNT016 Huntington Disease 72 0.034
284
c LKM063 Leukemia, Chronic Myeloid 72 0.034
285
GST040 Gastric Adenocarcinoma 70 0.034
286
PTZ001 Peutz-Jeghers Syndrome 70 0.034
287
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.034
288
SMT004 Smith-Lemli-Opitz Syndrome 70 0.034
289
P MYP004 Myopathy 70 0.034
290
CNG034 Congestive Heart Failure 69 0.034
291
P PNM007 Pneumonia 68 0.034
292
RCK004 Rickets 68 0.034
293
P CRD119 Cardiac Arrest 67 0.034
294
CRB039 Cerebrovascular Disease 67 0.034
295
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.034
296
ANG054 Angina Pectoris 66 0.034
297
P MSC005 Muscular Dystrophy 66 0.034
298
MYX005 Myxoid Liposarcoma 66 0.034
299
LBR036 Leber Plus Disease 66 0.034
300
P HYD006 Hydrocephalus 66 0.034
301
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.034
302
ATH013 Atherosclerosis Susceptibility 65 0.034
303
c WLM013 Wilms Tumor 1 65 0.034
304
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.034
305
P THY023 Thymoma 65 0.034
306
P DBT009 Diabetes Mellitus 64 0.034
307
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.034
308
PLL001 Pallister-Hall Syndrome 64 0.034
309
NRF007 Neurofibroma 64 0.034
310
P CMP005 Campomelic Dysplasia 64 0.034
311
P NTR004 Neutropenia 63 0.034
312
c HYP794 Hyperoxaluria, Primary, Type I 63 0.034
313
P CRN300 Coronary Heart Disease 1 63 0.034
314
ACT119 Acute Promyelocytic Leukemia 63 0.034
315
RHB001 Rhabdoid Cancer 63 0.034
316
c GLC092 Glaucoma, Primary Open Angle 62 0.034
317
c ALP101 Alpha-Thalassemia 62 0.034
318
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.034
319
HMT002 Hematologic Cancer 62 0.034
320
c SVR001 Severe Acute Respiratory Syndrome 62 0.034
321
LPP008 Lipoprotein Quantitative Trait Locus 62 0.034
322
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 62 0.034
323
c SCL052 Scleroderma, Familial Progressive 61 0.034
324
P ENC018 Encephalopathy 61 0.034
325
c WLM018 Wilms Tumor 5 61 0.034
326
NRL005 Neurilemmoma 60 0.034
327
SPN186 Spinal Cord Injury 60 0.034
328
P TST021 Testicular Germ Cell Tumor 60 0.034
329
DPH001 Diphtheria 60 0.034
330
c LPM012 Lipomatosis, Multiple 60 0.034
331
STR039 Sturge-Weber Syndrome 60 0.034
332
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.034
333
ORL011 Oral Cancer 60 0.034
334
INS001 Insulinoma 60 0.034
335
STT001 Status Epilepticus 60 0.034
336
P CHR285 Chronic Myelomonocytic Leukemia 60 0.034
337
CRT002 Cartilage-Hair Hypoplasia 59 0.034
338
VSL002 Visual Epilepsy 59 0.034
339
c LTN004 Late-Onset Retinal Degeneration 59 0.034
340
DCT002 Ductal Carcinoma in Situ 59 0.034
341
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.034
342
ANR040 Aneurysm 59 0.034
343
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.034
344
P BCL017 B-Cell Lymphoma 58 0.034
345
c PTT056 Pituitary Adenoma 1, Multiple Types 58 0.034
346
LNG108 Langerhans Cell Histiocytosis 58 0.034
347
MCR013 Microphthalmia 57 0.034
348
c MST023 Mesothelioma, Malignant 57 0.034
349
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.034
350
P FCL005 Focal Segmental Glomerulosclerosis 57 0.034
351
P CRD246 Cardiovascular System Disease 57 0.034
352
HYP266 Hypoxia 57 0.034
353
PLS011 Plasmacytoma 56 0.034
354
BCT022 Bacterial Infectious Disease 56 0.034
355
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 56 0.034
356
EMB004 Embryonal Carcinoma 56 0.034
357
GST050 Gastrointestinal System Disease 56 0.034
358
P LBR014 Leber Congenital Amaurosis 4 56 0.034
359
c WRD030 Waardenburg Syndrome, Type 1 56 0.034
360
HPT022 Hepatoblastoma 56 0.034
361
ZLL002 Zollinger-Ellison Syndrome 55 0.034
362
P MLN007 Male Infertility 55 0.034
363
P DRR001 Diarrhea 55 0.034
364
GNG005 Gangliocytoma 55 0.034
365
CRC006 Carcinoid Syndrome 55 0.034
366
MWT001 Mowat-Wilson Syndrome 54 0.034
367
c MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.034
368
PLM010 Pulmonary Edema 54 0.034
369
PPL022 Papilloma 54 0.034
370
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.034
371
P TRM003 Tremor 54 0.034
372
BRN038 Bronchial Disease 53 0.034
373
P SHR001 Short Bowel Syndrome 53 0.034
374
P PTS002 Ptosis 53 0.034
375
DRM011 Dermatophytosis 52 0.034
376
P SML001 Small Cell Carcinoma 52 0.034
377
c THY107 Thymoma, Familial 52 0.034
378
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 52 0.034
379
NPH003 Nephrocalcinosis 51 0.034
380
c HYP243 Hyperparathyroidism 1 51 0.034
381
VSC044 Visceral Myopathy 51 0.034
382
ILS001 Ileus 51 0.034
383
CLR109 Colorectal Adenocarcinoma 51 0.034
384
CLB002 Clubfoot 51 0.034
385
P RNL007 Renal Tubular Acidosis 51 0.034
386
HYP081 Hypolipoproteinemia 51 0.034
387
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.034
388
FSC004 Fasciitis 50 0.034
389
c LRG001 Large Cell Carcinoma 50 0.034
390
HYP017 Hypophosphatemia 50 0.034
391
AMB002 Amblyopia 49 0.034
392
c NRB010 Neuroblastoma 1 49 0.034
393
47X002 47,xyy 49 0.034
394
P OPN001 Open-Angle Glaucoma 49 0.034
395
GST049 Gastrointestinal System Cancer 49 0.034
396
SCT005 Scott Syndrome 49 0.034
397
P SDR003 Sideroblastic Anemia 49 0.034
398
URM002 Uremia 49 0.034
399
HST010 Histiocytosis 48 0.034
400
c ACT150 Acute Adrenal Insufficiency 48 0.034
401
c NPH049 Nephrotic Syndrome, Type 2 48 0.034
402
END062 Endometrial Hyperplasia 48 0.034
403
ADN009 Adenosquamous Carcinoma 47 0.034
404
ANH002 Anhidrosis 47 0.034
405
CLN019 Colonic Disease 47 0.034
406
KRT002 Keratomalacia 47 0.034
407
GST071 Gastrointestinal Carcinoma 47 0.034
408
CHR074 Choriocarcinoma 47 0.034
409
c PRM093 Premature Ovarian Failure 7 47 0.034
410
MCS004 Mucosal Melanoma 46 0.034
411
ANP006 Anaplastic Ependymoma 46 0.034
412
SQM002 Squamous Cell Papilloma 46 0.034
413
c MLG068 Malignant Glioma 46 0.034
414
GST030 Gastrinoma 45 0.034
415
c LYM145 Lymphatic Malformation 5 45 0.034
416
MXD026 Mixed Glioma 45 0.034
417
PPL018 Papillary Adenocarcinoma 45 0.034
418
TRT001 Teratocarcinoma 45 0.034
419
INT253 Intestinal Benign Neoplasm 45 0.034
420
DST006 Diastolic Heart Failure 45 0.034
421
CRB004 Cerebral Artery Occlusion 45 0.034
422
CHR466 Chronic Thromboembolic Pulmonary Hypertension 45 0.034
423
P CHR345 Chronic Pain 44 0.034
424
c PCH010 Pachyonychia Congenita 3 44 0.034
425
P END039 Endodermal Sinus Tumor 44 0.034
426
ACN001 Acinar Cell Carcinoma 44 0.034
427
c HYP272 Hypercholesterolemia, Familial, 3 44 0.034
428
SPN032 Spindle Cell Carcinoma 44 0.034
429
c PRM038 Primary Agammaglobulinemia 44 0.034
430
SMN007 Seminoma 43 0.034
431
P TST026 Testicular Germ Cell Cancer 43 0.034
432
c MLG079 Malignant Pleural Mesothelioma 42 0.034
433
GTR011 Goiter, Multinodular 1, with or Without Sertoli-Leydig Cell Tumors 42 0.034
434
PLM005 Pleomorphic Lipoma 40 0.034
435
PNC015 Pancreatic Acinar Cell Adenocarcinoma 39 0.034
436
PPL035 Papillary Thyroid Microcarcinoma 39 0.034
437
c ERL056 Early-Onset Parkinson's Disease 39 0.034
438
SPP007 Suppression Amblyopia 39 0.034
439
TST018 Testicular Yolk Sac Tumor 39 0.034
440
CVT001 Cavitary Optic Disc Anomalies 38 0.034
441
PTT002 Potter's Syndrome 38 0.034
442
TNC002 Tinea Capitis 38 0.034
443
TRP005 Trophoblastic Neoplasm 38 0.034
444
PSD016 Pseudosarcomatous Fibromatosis 37 0.034
445
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 0.034
446
c WLM011 Wilms Tumor 6 37 0.034
447
c PRG021 Paragangliomas 4 37 0.034
448
TST043 Testicular Seminoma 35 0.034
449
WBR001 Weber Syndrome 35 0.034
451
OLG021 Oligomeganephronia 33 0.034
452
NNS011 Nonseminomatous Germ Cell Tumor 33 0.034
453
c PRS136 Prostate Cancer, Hereditary, 6 33 0.034
454
LTT002 Letterer-Siwe Disease 33 0.034
455
c PRS130 Prostate Cancer, Hereditary, 8 32 0.034
456
TQP001 Taqi Polymorphism 32 0.034
457
CLL004 Cellular Myxoid Liposarcoma 31 0.034
458
SNG003 Single Ventricular Heart 30 0.034
459
ACT228 Acute Radiation Syndrome 29 0.034
460
c NNS018 Nonsyndromic Paraganglioma 29 0.034
461
PST092 Posttransplant Acute Limbic Encephalitis 29 0.034
462
BYS001 Byssinosis 28 0.034
463
ACN026 Acinar Cell Carcinoma of Pancreas 28 0.034
464
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.034
465
NRL008 Neural Crest Tumor 27 0.034
466
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.034
467
THY027 Thymus Squamous Cell Carcinoma 25 0.034
468
HYP693 Hyperparathyroidism, Primary, Caused by Water Clear Cell Hyperplasia 25 0.034
469
PNC038 Pancreatic Cystadenocarcinoma 25 0.034
470
CHR176 Chromophil Renal Cell Carcinoma 23 0.034
471
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 0.034
472
MCL047 Macular Amyloidosis 21 0.034
473
UNL014 Unilateral Multicystic Dysplastic Kidney 18 0.034
474
c VSC054 Visceral Neuropathy, Familial, Autosomal Recessive 18 0.034
475
P NRN038 Neuronal Intestinal Dysplasia, Type B 18 0.034
476
ACR112 Acroleukopathy, Symmetric 16 0.034
477
P FML354 Familial Nonmedullary Thyroid Carcinoma 15 0.034
478
SRC029 Sarcoma of Cervix Uteri 14 0.034
479
c HRS025 Hirschsprung Disease 8 14 0.034
480
APF001 Aip Familial Isolated Pituitary Adenomas 13 0.034
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