The MalaCard for "polyposis" has been retired.
Searching MalaCards for entries containing "polyposis"

702 hits were found for 'polyposis'

# ++ Fam MCID Name MIFTS Score
1
P FML011 Familial Adenomatous Polyposis 80 11.711
2
P JVN014 Juvenile Polyposis Syndrome 60 8.179
3
PTZ001 Peutz-Jeghers Syndrome 73 5.574
4
MTY001 Mutyh-Associated Polyposis 35 5.224
5
P HRD069 Hereditary Mixed Polyposis Syndrome 2 21 4.586
6
ATT003 Attenuated Familial Adenomatous Polyposis 44 4.518
7
CRN014 Cronkhite-Canada Syndrome 40 4.339
8
c FML253 Familial Adenomatous Polyposis Due to 5q22.2 Microdeletion 9 4.205
9
TRC032 Turcot Syndrome 66 4.129
10
JVN012 Juvenile Polyposis/hereditary Hemorrhagic Telangiectasia Syndrome 20 3.906
11
c HRD101 Hereditary Mixed Polyposis Syndrome 1 7 3.850
12
c JVN034 Juvenile Polyposis of Infancy 14 3.446
13
HYP466 Hyperplastic Polyposis Syndrome 33 3.157
14
ADN040 Adenomas, Multiple Colorectal 19 3.083
15
BRN074 Brain Tumor-Polyposis Syndrome 2 4 2.973
16
GST086 Gastric Adenocarcinoma and Proximal Polyposis of the Stomach 3 2.973
17
APC006 Apc-Associated Polyposis Conditions 2 2.973
18
GRD002 Gardner Syndrome 44 2.763
19
LYN001 Lynch Syndrome 63 2.634
20
CPP003 Cap Polyposis 20 2.555
21
BMP001 Bmpr1a-Related Juvenile Polyposis 10 2.514
22
CLR065 Colorectal Adenomatous Polyposis, Autosomal Recessive, with Pilomatricomas 19 2.505
23
SMD006 Smad4-Related Juvenile Polyposis 3 2.445
24
NSL012 Nasal Polyposis, Familial 0 2.445
25
JVN023 Juvenile Polyposis Syndrome, Infantile Form 4 2.428
26
PRS115 Prosthetic Joint Infection 36 2.012
27
PTZ002 Peutz–jeghers Syndrome 17 1.912
28
ADN018 Adenoma 67 0.886
29
P CLR023 Colorectal Cancer 66 0.381
30
c XP2001 Xp22.3 Microdeletion Syndrome 17 0.294
31
CNC006 Cancer: Lynch Syndrome Multi-Gene Panels 7 0.267
32
DSM004 Desmoid Tumor 63 0.241
33
14Q004 14q22q23 Microdeletion Syndrome 25 0.228
34
3Q2005 3q26q27 Microdeletion Syndrome 14 0.228
35
MLH005 Mlh3-Related Lynch Syndrome 9 0.222
36
CLN016 Colon Cancer 66 0.187
37
c FML053 Familial Colorectal Cancer 47 0.179
38
IDP042 Idiopathic Recurrent Stupor 15 0.177
39
CLR034 Colorectal Cancer, Somatic 41 0.173
40
MLN020 Melanoma, Malignant, Somatic 46 0.168
41
c CLR098 Ciliary Dyskinesia, Primary, 27 11 0.164
42
PRX070 Proximal 16p11.2 Microduplication Syndrome 11 0.161
43
14Q001 14q12 Microdeletion Syndrome 23 0.149
44
ULC004 Ulcerative Colitis 71 0.147
45
P ADN016 Adenocarcinoma 60 0.147
46
c DST058 Distal Monosomy 12p 16 0.144
47
MNS013 Monosomy 13q34 14 0.144
48
THY035 Thyroid Adenoma 44 0.139
49
c CHR226 Chromosome 1q41-Q42 Deletion Syndrome 23 0.139
50
MCR071 Microdeletion 15q11.2 21 0.139
51
NSY001 N Syndrome 57 0.134
52
MNN014 Mononeuritis 40 0.134
53
10P002 10p11.21p12.31 Microdeletion Syndrome 14 0.134
54
P CNG389 Congenital Pulmonary Airway Malformation 38 0.131
55
c 2Q3005 2q31.1 Microdeletion Syndrome 22 0.128
56
17Q007 17q11 Microdeletion Syndrome 21 0.128
57
BNN001 Bannayan-Riley-Ruvalcaba Syndrome 57 0.125
58
DST056 Distal 22q11.2 Microdeletion Syndrome 33 0.122
59
21Q001 21q22.11q22.12 Microdeletion Syndrome 13 0.119
60
JCB001 Jacobsen Syndrome 49 0.116
61
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 46 0.116
62
GST063 Gastric Cancer Risk After H. Pylori Infection 26 0.116
63
19Q001 19q13.11 Microdeletion Syndrome 21 0.116
64
P MGS003 Meigs Syndrome 41 0.113
65
P AST005 Asthma 86 0.109
66
ANK002 Ankylosing Spondylitis 75 0.106
67
P SNS014 Sinusitis 54 0.106
68
THR013 Thoracic Outlet Syndrome 53 0.106
69
PCH007 Pouchitis 50 0.106
70
c 2P1003 2p13.2 Microdeletion Syndrome 11 0.106
71
EPC004 Epcam-Related Lynch Syndrome 9 0.106
72
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 35 0.102
73
P ICH047 Ichthyosis, Congenital, Autosomal Recessive 1 34 0.102
74
17Q004 17q12 Microdeletion Syndrome 32 0.102
75
MLR006 Male Reproductive Organ Cancer 21 0.102
76
PPL001 Papillary Adenoma 37 0.098
77
17Q001 17q21.31 Microdeletion Syndrome 29 0.098
78
ATX002 Ataxia Telangiectasia 81 0.095
79
PPL002 Papillary Carcinoma 60 0.095
80
P RHN004 Rhinitis 59 0.095
81
HPT022 Hepatoblastoma 56 0.095
82
PPL020 Papillary Thyroid Carcinoma 49 0.095
83
HPT067 Hepatocellular Adenoma 46 0.095
84
1P3001 1p36 Deletion Syndrome 44 0.095
85
MCR014 Microcystic Adenoma 38 0.095
86
c CHR243 Chromosome 3p Deletion 29 0.095
87
17Q002 17q23.1q23.2 Microdeletion Syndrome 28 0.095
88
PNC049 Pancreatic Adenoma 21 0.095
89
GRF006 Grfoma 20 0.095
90
12Q001 12q15q21.1 Microdeletion Syndrome 14 0.095
91
FML259 Familial Renal Amyloidosis Due to Apolipoprotein Ai Variant 9 0.095
92
MLH002 Mlh1-Related Lynch Syndrome 9 0.095
93
HRD008 Hereditary Hemorrhagic Telangiectasia 74 0.091
94
ACN002 Acanthosis Nigricans 70 0.091
95
c CWD001 Cowden Disease 63 0.091
96
SPS019 Spastic Paraparesis 49 0.091
97
RVL002 Ruvalcaba Syndrome 42 0.091
98
ODN006 Odontoma 26 0.091
99
12P001 12p12.1 Microdeletion Syndrome 15 0.091
100
OVR101 Ovarian Malignant Sertoli-Leydig Cell Tumor 14 0.091
101
GST038 Gastrointestinal Adenoma 13 0.091
102
THY028 Thyroid Cancer 73 0.086
103
LKM002 Leukemia 70 0.086
104
HPT023 Hepatocellular Carcinoma 69 0.086
105
c LCL006 Localized Scleroderma 64 0.086
106
MYC002 Mycobacterium Avium Complex Disease 56 0.086
107
IMP002 Imperforate Anus 47 0.086
108
JVN033 Juvenile Nasopharyngeal Angiofibroma 46 0.086
109
c 3Q2003 3q29 Microdeletion Syndrome 37 0.086
110
CTN026 Cutaneous Neuroendocrine Carcinoma 35 0.086
111
CRK001 Cork-Handlers' Disease 28 0.086
112
12Q002 12q14 Microdeletion Syndrome 28 0.086
113
TFT003 Tufting Enteropathy 26 0.086
114
2Q3003 2q32q33 Microdeletion Syndrome 25 0.086
115
c 2Q2001 2q23.1 Microdeletion Syndrome 25 0.086
116
c 4Q2001 4q21 Microdeletion Syndrome 24 0.086
117
ESP010 Esophageal Basaloid Squamous Cell Carcinoma 21 0.086
118
FML143 Familial Papillary Thyroid Carcinoma 13 0.086
119
P STM004 Stomach Cancer 62 0.082
120
INT051 Intussusception 57 0.082
121
ADR008 Adrenal Adenoma 57 0.082
122
P MLG002 Malignant Peritoneal Mesothelioma 51 0.082
123
PRT019 Protein-Losing Enteropathy 46 0.082
124
CHL079 Children's Interstitial Lung Disease 39 0.082
125
MXL004 Maxillary Sinus Squamous Cell Carcinoma 38 0.082
126
BRS045 Breast Adenoma 27 0.082
127
BRS015 Breast Medullary Carcinoma 25 0.082
128
P BRS047 Breast Cancer 85 0.077
129
GST023 Gastric Ulcer 67 0.077
130
WST001 West Syndrome 64 0.077
131
MNT001 Mantle Cell Lymphoma 63 0.077
132
SCN006 Secondary Syphilis 53 0.077
133
DDF001 Dedifferentiated Liposarcoma 48 0.077
134
P INF037 Inflammatory Bowel Disease 44 0.077
135
SML009 Small Intestine Adenocarcinoma 41 0.077
136
OST006 Osteoblastoma 35 0.077
137
LNG030 Lung Adenoma 33 0.077
138
FCT013 Factor V Leiden Thrombophilia 31 0.077
139
HRD045 Hereditary Hemorrhagic Telangiectasia Type 2 29 0.077
140
MNT053 Mental Retardation, Stereotypic Movements, Epilepsy, and/or Cerebral Malformations 29 0.077
141
BLD087 Bladder Cancer, Somatic 24 0.077
142
c CHR266 Chromosome 8p23.1 Deletion 21 0.077
143
c 9P1001 9p13 Microdeletion Syndrome 13 0.077
144
c 5Q3002 5q31.3 Microdeletion Syndrome 13 0.077
145
TNF006 Tnfrsf13b-Related Common Variable Immune Deficiency 12 0.077
146
P PNC035 Pancreatic Cancer 82 0.072
147
ART005 Arteriovenous Malformation 62 0.072
148
LNG032 Lung Cancer 61 0.072
149
GLL008 Gilles De La Tourette Syndrome 60 0.072
150
c PNC044 Pancreatitis 58 0.072
151
CNG008 Congenital Ichthyosiform Erythroderma 51 0.072
152
PLS016 Plasma Cell Leukemia 49 0.072
153
SCL017 Sclerosing Hemangioma 46 0.072
154
INT052 Intestinal Volvulus 40 0.072
155
c OVR069 Ovarian Germ Cell Tumor 40 0.072
156
PRL008 Paralytic Ileus 37 0.072
157
c SPH018 Spherocytosis, Hereditary, Type 5 31 0.072
158
NNS020 Nonsmall Cell Lung Cancer, Somatic 19 0.072
159
c CHR459 Chromosome Xp Deletion 16 0.072
160
P HMP004 Hemophilia B 66 0.067
161
RLP001 Relapsing Polychondritis 66 0.067
162
TRN018 Transitional Cell Carcinoma 61 0.067
163
SRC014 Sarcoma 54 0.067
164
P THR090 Thrombocythemia 1 48 0.067
165
FBR019 Fibromatosis 47 0.067
166
P CWD006 Cowden Syndrome 1 46 0.067
167
c ACR001 Aicardi-Goutieres Syndrome 46 0.067
168
TLN003 Telangiectasis 46 0.067
169
LKP003 Leukoplakia 45 0.067
170
LBL001 Lobular Neoplasia 41 0.067
171
GST040 Gastric Adenocarcinoma 41 0.067
172
ATX019 Ataxia with Vitamin E Deficiency 40 0.067
173
DDN007 Duodenal Disease 31 0.067
174
TRP008 Tropical Calcific Pancreatitis 30 0.067
175
15Q001 15q13.3 Microdeletion 29 0.067
176
OVR011 Ovarian Mucinous Adenocarcinoma 26 0.067
177
RCT021 Rectum Cancer 25 0.067
178
16Q001 16q24.3 Microdeletion Syndrome 23 0.067
179
JJN003 Jejunal Cancer 22 0.067
180
RPD005 Rapidly Involuting Congenital Hemangioma 19 0.067
181
DST051 Distal 7q11.23 Microdeletion Syndrome 19 0.067
182
10Q001 10q22.3q23.3 Microdeletion Syndrome 19 0.067
183
c TTL001 Total Internal Ophthalmoplegia 17 0.067
184
ENG003 Eng-Related Hereditary Hemorrhagic Telangiectasia 10 0.067
185
ALL003 Allergic Rhinitis 62 0.061
186
HMN010 Hemangioma 62 0.061
187
PPL022 Papilloma 60 0.061
188
P HRD011 Hereditary Spherocytosis 59 0.061
189
SQM006 Squamous Cell Carcinoma 58 0.061
190
CRC006 Carcinoid Syndrome 55 0.061
191
P ESN007 Eosinophilia 54 0.061
192
GST060 Gastric Cancer, Somatic 47 0.061
193
c INT070 Intestinal Obstruction 46 0.061
194
c FML024 Familial Melanoma 45 0.061
195
PLM018 Pulmonary Sclerosing Hemangioma 44 0.061
196
NNT016 Neonatal Hemochromatosis 41 0.061
197
PRL042 Proliferating Trichilemmal Cyst 40 0.061
198
PNC019 Pancreatoblastoma 39 0.061
199
c ATX010 Ataxia Neuropathy Spectrum 33 0.061
200
MSM004 Mesomelia-Synostoses Syndrome 29 0.061
201
HNM001 Hinman's Syndrome 28 0.061
202
CRB006 Cribriform Carcinoma 27 0.061
203
CLD014 Cole Disease 23 0.061
204
CLF029 Cleft Palate and Mental Retardation 21 0.061
205
FLR003 Florid Cemento-Osseous Dysplasia 19 0.061
206
AND005 Androgen Insensitivity Syndrome, Mild 19 0.061
207
c CHR255 Chromosome 6p Deletion 16 0.061
208
c CHR260 Chromosome 7p Deletion 15 0.061
209
END042 Endometrial Carcinoma 69 0.055
210
P LPR002 Leopard Syndrome 66 0.055
211
PRC016 Pre-Eclampsia 64 0.055
212
c ACT027 Acute Pancreatitis 60 0.055
213
P GST044 Gastritis 59 0.055
214
MRT001 Muir-Torre Syndrome 59 0.055
215
MLT074 Multiple Endocrine Neoplasia 58 0.055
216
HMH002 Hemihypertrophy 57 0.055
217
P ALV004 Alveolar Rhabdomyosarcoma 51 0.055
218
RCR004 Recurrent Respiratory Papillomatosis 51 0.055
219
FML026 Familial Lipoprotein Lipase Deficiency 50 0.055
220
CHL056 Cheilitis 49 0.055
221
HRD004 Hereditary Breast Ovarian Cancer 48 0.055
222
VSM001 Vasomotor Rhinitis 46 0.055
223
MYP002 Myoepithelial Carcinoma 46 0.055
224
P ATS008 Autosomal Dominant Disease 45 0.055
225
INV006 Inverted Papilloma 45 0.055
226
GST014 Gastrointestinal Lymphoma 44 0.055
227
BLR013 Biliary Tract Cancer 44 0.055
228
ANP009 Anaplastic Oligodendroglioma 44 0.055
229
LYM014 Lymphangitis 42 0.055
230
P CLR070 Colorectal Cancer, Hereditary Nonpolyposis, Type 1 41 0.055
231
P STR021 Struma Ovarii 40 0.055
232
c BRC032 Brachydactyly Type A2 34 0.055
233
DDN010 Duodenum Cancer 33 0.055
234
c ATS021 Autosomal Recessive Juvenile Parkinson Disease 31 0.055
235
OST111 Osteoporosis, Early-Onset Autosomal Dominant 29 0.055
236
6Q1001 6q16 Deletion Syndrome 24 0.055
237
PNM003 Pneumatosis Cystoides Intestinalis 24 0.055
238
PNC073 Pancreatic Carcinoma, Somatic 24 0.055
239
P DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 23 0.055
240
MNS009 Monosomy 13q14 22 0.055
241
P FML251 Familial Advanced Sleep Phase Syndrome 1 17 0.055
242
c BNG076 Benign Exophthalmos Syndrome 17 0.055
243
c CHR237 Chromosome 2p Deletion 15 0.055
244
c FML252 Familial Cold Autoinflammatory Syndrome 3 15 0.055
245
21Q002 21q22.13q22.2 Microdeletion Syndrome 14 0.055
246
P AMY001 Amyotrophic Lateral Sclerosis 87 0.047
247
P HYP075 Hypertension 76 0.047
248
P GST019 Gastrointestinal Stromal Tumor 75 0.047
249
AND002 Androgen Insensitivity Syndrome 75 0.047
250
ACT074 Acute Lymphocytic Leukemia 69 0.047
251
P ANG001 Angelman Syndrome 67 0.047
252
P MDL005 Medulloblastoma 66 0.047
253
DFC004 Deficiency Anemia 65 0.047
254
BRN028 Brain Cancer 65 0.047
255
ART019 Aortic Valve Stenosis 64 0.047
256
c AXN002 Axenfeld-Rieger Syndrome 57 0.047
257
HPR003 Heparin-Induced Thrombocytopenia 55 0.047
258
c EPN002 Ependymoma 54 0.047
259
THY089 Thymic Epithelial Neoplasm 53 0.047
260
ART001 Arterial Tortuosity Syndrome 52 0.047
261
PRN011 Pernicious Anemia 52 0.047
262
LPM004 Lipoma 51 0.047
263
c MNT147 Mental Retardation 51 0.047
264
CLN020 Colonic Neoplasm 51 0.047
265
P SRT002 Sertoli Cell Tumor 50 0.047
266
EVN001 Evans' Syndrome 50 0.047
267
LYM026 Lymphoblastic Leukemia 49 0.047
268
RHB017 Rhabdoid Tumor 49 0.047
269
PLM070 Pulmonic Stenosis 48 0.047
270
PLM009 Pleomorphic Adenoma Carcinoma 47 0.047
271
PLM026 Pilomatrixoma 45 0.047
272
EPT010 Epithelial-Myoepithelial Carcinoma 44 0.047
273
PRN049 Paraneoplastic Pemphigus 43 0.047
274
RCR001 Recurrent Corneal Erosion 43 0.047
275
CHL052 Choledochal Cyst 43 0.047
276
ACT093 Actinic Cheilitis 43 0.047
277
c LNG063 Lung Cancer Susceptibility 42 0.047
278
LNG029 Lung Adenocarcinoma 42 0.047
279
FML027 Female Breast Carcinoma 42 0.047
280
ORL015 Oral Squamous Cell Carcinoma 40 0.047
281
MTG002 Mutagen Sensitivity 40 0.047
282
ANL022 Anal Fistula 40 0.047
283
SCH016 Schimke Immunoosseous Dysplasia 40 0.047
284
GST039 Gastroduodenitis 39 0.047
285
AND003 Andersen-Tawil Syndrome 39 0.047
286
VCL001 Vacuolar Myopathy 37 0.047
287
TTR016 Tetra-Amelia Syndrome 36 0.047
288
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 36 0.047
289
SML032 Small Bowel Adenocarcinoma 36 0.047
290
c CHR253 Chromosome 5q Deletion 31 0.047
291
BLD039 Bladder Adenocarcinoma 31 0.047
292
c ERL004 Early Yaws 29 0.047
293
JVN024 Juvenile Hereditary Hemochromatosis 28 0.047
294
BRS082 Breast Cancer, Lobular 23 0.047
295
FML255 Familial Cervical Artery Dissections 19 0.047
296
c CLR085 Colorectal Cancer 1 17 0.047
297
CHR457 Chromosome 17p13.1 Deletion Syndrome 17 0.047
298
c FML254 Familial Syringomyelia 9 0.047
299
CYS001 Cystic Fibrosis 91 0.039
300
P HNT001 Huntington's Disease 81 0.039
301
MRF001 Marfan Syndrome 78 0.039
302
CRH001 Crohn's Disease 78 0.039
303
P PRS040 Prostate Cancer 76 0.039
304
MTC003 Metachromatic Leukodystrophy 75 0.039
305
c NNN003 Noonan Syndrome 73 0.039
306
OVR042 Ovarian Cancer 73 0.039
307
BRN024 Bronchitis 71 0.039
308
AGR001 Age Related Macular Degeneration 71 0.039
309
P AST007 Astrocytoma 70 0.039
310
P RTN024 Retinoblastoma 70 0.039
311
P CRN008 Carney Complex 68 0.039
312
P MNN012 Meningioma 67 0.039
313
PRT036 Peritonitis 67 0.039
314
CHR065 Chronic Myeloid Leukemia 67 0.039
315
FBR011 Fibrodysplasia Ossificans Progressiva 66 0.039
316
IRR002 Irritable Bowel Syndrome 65 0.039
317
c HPT021 Hepatitis 65 0.039
318
CMM004 Common Variable Immunodeficiency 64 0.039
319
VNH001 Von Hippel-Lindau Disease 63 0.039
320
LNG024 Langerhans-Cell Histiocytosis 63 0.039
321
c THY032 Thyroiditis 61 0.039
322
P HST010 Histiocytosis 61 0.039
323
HYP266 Hypoxia 60 0.039
324
P CLF002 Cleft Palate 60 0.039
325
CLR003 Clear Cell Adenocarcinoma 58 0.039
326
SMT015 Smith Magenis Syndrome 58 0.039
327
PSD007 Pseudomyxoma Peritonei 58 0.039
328
MLT001 Multiple Chemical Sensitivity 58 0.039
329
ACH005 Achalasia 57 0.039
330
PTT006 Pituitary Adenoma 56 0.039
331
ETN001 Eating Disorder 55 0.039
332
PPT003 Peptic Ulcer 55 0.039
333
THR009 Thrombocytopenia-Absent Radius Syndrome 55 0.039
334
SNS001 Sensorineural Hearing Loss 55 0.039
335
DDN006 Duodenitis 54 0.039
336
P LPS002 Liposarcoma 54 0.039
337
c MSC005 Muscular Dystrophy 54 0.039
338
PRT018 Portal Vein Thrombosis 54 0.039
339
TTR011 Tetraploidy 54 0.039
340
P LRY019 Laryngitis 53 0.039
341
c FML035 Familial Hyperlipidemia 53 0.039
342
EHL033 Ehlers-Danlos Syndrome, Classic Type 53 0.039
343
SPN020 Spondylosis 53 0.039
344
P LKD001 Leukodystrophy 53 0.039
345
HYP003 Hypermethioninemia 52 0.039
346
P ESN001 Eosinophilic Esophagitis 52 0.039
347
URN010 Urinary Tract Obstruction 52 0.039
348
WLF002 Wolf-Hirschhorn Syndrome 51 0.039
349
BRT002 Birt-Hogg-Dube Syndrome 51 0.039
350
P ESP024 Esophagitis 51 0.039
351
ORL004 Oral Submucous Fibrosis 51 0.039
352
ART017 Aortic Disease 51 0.039
353
CYS009 Cystadenoma 50 0.039
354
ATY005 Atypical Teratoid Rhabdoid Tumor 50 0.039
355
GST050 Gastrointestinal System Disease 50 0.039
356
P PND001 Pain Disorder 49 0.039
357
BSL006 Basaloid Squamous Cell Carcinoma 49 0.039
358
TXC012 Toxic Epidermal Necrolysis 49 0.039
359
EXS001 Exostosis 49 0.039
360
c DRR001 Diarrhea 49 0.039
361
ACT115 Acute Myeloid Leukemia, Adult 49 0.039
362
P CLR017 Clear Cell Sarcoma 48 0.039
363
PLM020 Pleomorphic Xanthoastrocytoma 48 0.039
364
RFR003 Refractive Error 48 0.039
365
INS002 in Situ Carcinoma 48 0.039
366
ACN001 Acinar Cell Carcinoma 48 0.039
367
P DFF019 Diffuse Gastric Cancer 47 0.039
368
EXF001 Exfoliation Syndrome 47 0.039
369
SKN023 Skin Tag 47 0.039
370
c KRT005 Keratoacanthoma 47 0.039
371
c BLT006 Bilateral Breast Cancer 47 0.039
372
MCP006 Mucoepidermoid Carcinoma 46 0.039
373
GNT002 Giant Cell Glioblastoma 46 0.039
374
CRV031 Cervical Adenocarcinoma 46 0.039
375
P FCS001 Facioscapulohumeral Muscular Dystrophy 46 0.039
376
c RSM001 Rasmussen Encephalitis 46 0.039
377
PLM052 Pulmonary Arteriovenous Malformation 45 0.039
378
LPM005 Lipomatosis 45 0.039
379
P GRM009 Germ Cell Tumors 45 0.039
380
CLN019 Colonic Disease 44 0.039
381
UTR024 Uterine Carcinosarcoma 44 0.039
382
ESP025 Esophagus Adenocarcinoma 44 0.039
383
c ADN012 Adenocarcinoma in Situ 43 0.039
384
HPT032 Hepatocellular Carcinoma, Somatic 43 0.039
385
EMB007 Embryonal Sarcoma 43 0.039
386
OVR034 Ovarian Clear Cell Adenocarcinoma 43 0.039
387
CHR101 Char Syndrome 42 0.039
388
CLN015 Colon Adenocarcinoma 41 0.039
389
RCT011 Rectal Prolapse 40 0.039
390
c CHR048 Chronic Rhinitis 39 0.039
391
ACR014 Acral Lentiginous Melanoma 39 0.039
392
SYR002 Syringocystadenoma Papilliferum 39 0.039
393
SPP002 Sipple Syndrome 39 0.039
394
INV004 Invasive Bladder Transitional Cell Carcinoma 38 0.039
395
BLD101 Bladder Cancer Susceptibility 38 0.039
396
BLD049 Bladder Transitional Cell Papilloma 38 0.039
397
MSS002 Mass Syndrome 37 0.039
398
HTL002 Htlv-1 Associated Myelopathy 36 0.039
399
END016 Endocervicitis 36 0.039
400
INT069 Intestinal Neoplasm 36 0.039
401
MTN001 Metanephric Adenoma 36 0.039
402
IPX001 Ipex Syndrome 35 0.039
403
CRY008 Cryopyrin-Associated Periodic Syndrome 35 0.039
404
P CHR038 Chronic Maxillary Sinusitis 35 0.039
405
P 2Q3002 2q37 Microdeletion Syndrome 34 0.039
406
ESP027 Esophagus Squamous Cell Carcinoma 34 0.039
407
CRB022 Cerebellar Liponeurocytoma 33 0.039
408
MTR001 Mature Cataract 32 0.039
409
HMN012 Hemangioma of Lung 32 0.039
410
P PNB001 Pineoblastoma 32 0.039
411
BRN015 Bronchiolo-Alveolar Adenocarcinoma 31 0.039
412
BPH002 Biphasic Synovial Sarcoma 31 0.039
413
MCR029 Micro Syndrome 31 0.039
414
LNG061 Lung Cancer, Somatic 30 0.039
415
PTN006 Pten Hamartoma Tumor Syndrome 30 0.039
416
INT017 Intestinal Schistosomiasis 30 0.039
417
PTL001 Patulous Eustachian Tube 28 0.039
418
CLR014 Clear Cell Adenoma 28 0.039
419
RHN002 Rhinoscleroma 27 0.039
420
c HMP017 Hemophilia a, Congenital 26 0.039
421
AMP009 Ampulla of Vater Adenocarcinoma 25 0.039
422
c 2P2001 2p21 Microdeletion Syndrome 25 0.039
423
CCM003 Cecum Cancer 25 0.039
424
NNS006 Non-Suppurative Otitis Media 24 0.039
425
c HNT004 Huntington Disease-Like 2 23 0.039
426
P ADL001 Adult Lymphoma 23 0.039
427
c CHR271 Chromosome 9q Deletion 23 0.039
428
THY059 Thyroid Carcinoma, Follicular, Somatic 22 0.039
429
FSC006 Fascioscapulohumeral Muscular Dystrophy 2, Digenic 21 0.039
430
P HYP078 Hypertrophy of Breast 20 0.039
431
IMG001 Image Syndrome 20 0.039
432
BLD063 Bile Duct Cysts 20 0.039
433
P 19P001 19p13.12 Microdeletion Syndrome 19 0.039
434
CLN005 Colon Lymphoma 19 0.039
435
RNL013 Renal Adenoma 18 0.039
436
P ISC010 Isochromosome Yp 14 0.039
437
c GST089 Gastrointestinal Stromal Tumor, Familial 9 0.039
438
FML158 Familial Hemangioma 6 0.039
439
P RHM011 Rheumatoid Arthritis 83 0.027
440
P CSH001 Cushing's Syndrome 78 0.027
441
ACH004 Achondroplasia 77 0.027
442
P WSK001 Wiskott-Aldrich Syndrome 76 0.027
443
P LFR001 Li-Fraumeni Syndrome 75 0.027
444
P HRS001 Hirschsprung's Disease 72 0.027
445
CST001 Costello Syndrome 71 0.027
446
P SCH015 Schizophrenia 69 0.027
447
P ALG002 Alagille Syndrome 68 0.027
448
c DBT009 Diabetes Mellitus 68 0.027
449
RNL002 Renal Agenesis 68 0.027
450
THY014 Thyroid Medullary Carcinoma 68 0.027
451
GLN003 Glanzmann's Thrombasthenia 68 0.027
452
ESP021 Esophageal Cancer 68 0.027
453
PRT014 Protein S Deficiency 67 0.027
454
P HPT001 Hepatitis C 66 0.027
455
NVD001 Nevoid Basal Cell Carcinoma Syndrome 66 0.027
456
P PRT013 Portal Hypertension 65 0.027
457
GST034 Gastroesophageal Reflux Disease 65 0.027
458
P ART023 Arthropathy 65 0.027
459
PRL009 Prolactinoma 64 0.027
460
PRT010 Parathyroid Carcinoma 63 0.027
461
P DDN001 Duodenal Ulcer 63 0.027
462
ACT073 Acute Leukemia 62 0.027
463
PSY004 Psychotic Disorder 62 0.027
464
SML001 Small Cell Carcinoma 62 0.027
465
P BRN022 Bronchiectasis 62 0.027
466
BSL007 Basal Cell Carcinoma 62 0.027
467
BRR003 Barrett's Esophagus 62 0.027
468
CHR029 Choroid Plexus Papilloma 61 0.027
469
P CRD013 Cardiofaciocutaneous Syndrome 61 0.027
470
LMY002 Leiomyoma 61 0.027
471
CHL065 Cholangiocarcinoma 61 0.027
472
P END044 Endometriosis 61 0.027
473
BRN029 Brain Disease 60 0.027
474
P RSP003 Respiratory Failure 60 0.027
475
PLM033 Pulmonary Embolism 60 0.027
476
P DRM010 Dermatomyositis 59 0.027
477
P ATS007 Autism Spectrum Disorder 59 0.027
478
c HYP061 Hypertrophic Cardiomyopathy 59 0.027
479
SCH014 Schistosomiasis 59 0.027
480
ALP008 Alopecia 59 0.027
481
DSS009 Disseminated Intravascular Coagulation 59 0.027
482
c HYP086 Hypothyroidism 59 0.027
483
GLB001 Gilbert Syndrome 59 0.027
484
PRT011 Protein C Deficiency 59 0.027
485
CYS005 Cysticercosis 59 0.027
486
SKN014 Skin Cancer 58 0.027
487
CHG001 Chagas Disease 58 0.027
488
IRN001 Iron Deficiency Anemia 58 0.027
489
ALL006 Allergic Asthma 58 0.027
490
LRY016 Laryngeal Carcinoma 58 0.027
491
GRW001 Growth Hormone Secreting Pituitary Adenoma 58 0.027
492
c VRL010 Viral Hepatitis 57 0.027
493
SHG001 Shigellosis 57 0.027
494
P VLC001 Velocardiofacial Syndrome 57 0.027
495
c HPT003 Hepatitis a 57 0.027
496
ADR015 Adrenocortical Carcinoma 57 0.027
497
CHR001 Churg-Strauss Syndrome 56 0.027
498
P FML032 Familial Hypertrophic Cardiomyopathy 56 0.027
499
P OLG002 Oligodendroglioma 56 0.027
500
P MLN008 Melanoma 56 0.027
501
HMT002 Hematologic Cancer 56 0.027
502
P NNN008 Noonan Syndrome 1 56 0.027
503
c EMR001 Emery-Dreifuss Muscular Dystrophy 56 0.027
504
ALV005 Alveolar Soft Part Sarcoma 56 0.027
505
VRR004 Verrucous Carcinoma 56 0.027
506
TST014 Testicular Cancer 55 0.027
507
TTR001 Tetralogy of Fallot 55 0.027
508
P PLY006 Polydactyly 55 0.027
509
c HYP060 Hyperinsulinism 55 0.027
510
CMM005 Common Cold 55 0.027
511
THR012 Thoracic Cancer 54 0.027
512
FBR003 Fibrous Histiocytoma 54 0.027
513
c BLN003 Blindness 54 0.027
514
c PRM011 Primary Ciliary Dyskinesia 54 0.027
515
MCN001 Mucinous Adenocarcinoma 54 0.027
516
FLL032 Follicular Thyroid Carcinoma 53 0.027
517
GLS001 Gliosarcoma 53 0.027
518
GLL018 Gallbladder Cancer 53 0.027
519
RTN023 Retinitis 53 0.027
520
c TRT010 Teratoma 53 0.027
521
P STR020 Strabismus 53 0.027
522
ACR008 Acrocallosal Syndrome 53 0.027
523
CHR074 Choriocarcinoma 52 0.027
524
HPY002 H. Pylori Infection 52 0.027
525
ATP002 Atopy 52 0.027
526
ISV001 Isovaleric Acidemia 51 0.027
527
GNG002 Ganglioneuroma 51 0.027
528
c GGN002 Gigantism 51 0.027
529
GST030 Gastrinoma 51 0.027
530
RNL014 Renal Cell Carcinoma 51 0.027
531
P HMN013 Hemangiopericytoma 51 0.027
532
c ATM024 Autoimmune Pancreatitis 51 0.027
533
P INT068 Intestinal Disease 51 0.027
534
P PLC011 Pilocytic Astrocytoma 51 0.027
535
LPC002 Lip Cancer 50 0.027
536
ORL007 Oral Cavity Cancer 50 0.027
537
CHL004 Cholelithiasis 50 0.027
538
HMM003 Hemimegalencephaly 50 0.027
539
P EXN002 Exanthem 50 0.027
540
P PNM006 Pneumoconiosis 50 0.027
541
GLM004 Gliomatosis Cerebri 50 0.027
542
MGC001 Megacolon 50 0.027
543
ORL011 Oral Cancer 50 0.027
544
LYM052 Lymphomatoid Papulosis 50 0.027
545
PRM027 Primitive Neuroectodermal Tumor 50 0.027
546
HST009 Histiocytoma 49 0.027
547
ASB001 Asbestosis 49 0.027
548
SWT001 Sweat Gland Carcinoma 49 0.027
549
P PTT014 Pitt-Hopkins Syndrome 49 0.027
550
ADN002 Adenoiditis 49 0.027
551
P PRT029 Parathyroid Adenoma 49 0.027
552
BLS003 Blastoma 49 0.027
553
NPH011 Nephroblastoma 49 0.027
554
URT010 Ureteral Obstruction 48 0.027
555
BRS051 Breast Disease 48 0.027
556
RHB003 Rhabdomyosarcoma 48 0.027
557
CRD005 Cardia Cancer 48 0.027
558
BRK001 Brooke-Spiegler Syndrome 48 0.027
559
CNV002 Conversion Disorder 48 0.027
560
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.027
561
ACR012 Aicardi Syndrome 47 0.027
562
P PNL012 Penile Cancer 47 0.027
563
PLM016 Pleomorphic Carcinoma 47 0.027
564
PLM032 Pulmonary Blastoma 47 0.027
565
GLM008 Glomus Tumor 46 0.027
566
PNC013 Pancreatic Ductal Carcinoma 46 0.027
567
SFT003 Soft Tissue Sarcoma 46 0.027
568
SRC002 Sarcomatoid Renal Cell Carcinoma 46 0.027
569
DRG002 Drug-Induced Hepatitis 46 0.027
570
HRD027 Hereditary Diffuse Gastric Cancer 46 0.027
571
P STS001 Sotos Syndrome 46 0.027
572
CRV038 Cervical Squamous Cell Carcinoma 46 0.027
573
CYS014 Cystadenocarcinoma 45 0.027
574
PLS025 Plasmablastic Lymphoma 45 0.027
575
P PRK001 Porokeratosis 44 0.027
576
RSD004 Rosai-Dorfman Disease 44 0.027
577
P OVR046 Ovarian Cyst 44 0.027
578
EMB003 Embryonal Cancer 44 0.027
579
ASC002 Ascariasis 44 0.027
580
ALC010 Alcoholic Cardiomyopathy 44 0.027
581
INT191 Intestinal Lymphangiectasia 43 0.027
582
GRM004 Germinoma 43 0.027
583
LMY003 Leiomyomatosis 43 0.027
584
FLL031 Follicular Adenoma 43 0.027
585
P CHN005 Choanal Atresia 43 0.027
586
CMM014 Common Variable Immune Deficiency 43 0.027
587
GLL017 Gallbladder Adenocarcinoma 43 0.027
588
KLT001 Klatskin's Tumor 42 0.027
589
SPT007 Spitz Nevus 42 0.027
590
LPD006 Lipoid Proteinosis 42 0.027
591
DBW001 Dubowitz Syndrome 42 0.027
592
P CYS017 Cystic Teratoma 41 0.027
593
ANC001 Ancylostomiasis 41 0.027
594
NXS001 Naxos Disease 41 0.027
595
ART002 Arts Syndrome 40 0.027
596
INT040 Intrinsic Asthma 40 0.027
597
DVR002 Diverticulitis 39 0.027
598
HYP030 Hypoactive Sexual Desire Disorder 39 0.027
599
ESP028 Esophageal Squamous Cell Carcinoma 39 0.027
600
PRG017 Paraganglioma and Gastric Stromal Sarcoma 39 0.027
601
IMM034 Immunodeficiency, Common Variable, 2 39 0.027
602
HDR006 Hidradenocarcinoma 38 0.027
603
P PLM030 Pleomorphic Rhabdomyosarcoma 38 0.027
604
RTR010 Retroperitoneal Sarcoma 38 0.027
605
NSP002 Nasopharyngitis 38 0.027
606
NNP001 Nonpapillary Renal Cell Carcinoma 38 0.027
607
CNG041 Congenital Cataracts, Facial Dysmorphism, and Neuropathy 37 0.027
608
ANG037 Angiomatosis 37 0.027
609
GMS001 Gemistocytic Astrocytoma 37 0.027
610
RCT009 Rectosigmoid Cancer 37 0.027
611
AMP010 Ampulla of Vater Carcinoma 37 0.027
612
SPR033 Superficial Spreading Melanoma 37 0.027
613
HPT006 Hepatic Angiomyolipoma 37 0.027
614
ATY019 Atypical Mole Syndrome 36 0.027
615
P PRG003 Progesterone-Receptor Negative Breast Cancer 36 0.027
616
ANP006 Anaplastic Ependymoma 35 0.027
617
GST064 Gastric Outlet Obstruction 35 0.027
618
c CRN035 Cranial Nerve Palsy 35 0.027
619
CRB002 Cerebral Primitive Neuroectodermal Tumor 34 0.027
620
EMN001 Emanuel Syndrome 34 0.027
621
PLY040 Polymorphous Low-Grade Adenocarcinoma 34 0.027
622
LYM006 Lymphoepithelioma-Like Carcinoma 34 0.027
623
ESP023 Esophageal Disease 34 0.027
624
TMR010 Tumor Predisposition Syndrome 34 0.027
625
TST021 Testicular Germ Cell Tumor 34 0.027
626
PRM014 Periampullary Adenocarcinoma 34 0.027
627
OVR048 Ovarian Cystadenoma 34 0.027
628
P BRN035 Brain Stem Glioma 34 0.027
629
END043 Endometrial Stromal Tumor 33 0.027
630
FML087 Familial Renal Cell Carcinoma 33 0.027
631
MNN006 Meninges Hemangiopericytoma 33 0.027
632
LNG038 Lung Small Cell Carcinoma 33 0.027
633
DYS036 Dysequilibrium Syndrome 32 0.027
634
OPT007 Optic Nerve Glioma 32 0.027
635
ADS002 Adie Syndrome 32 0.027
636
SBC009 Sebaceous Adenoma 32 0.027
637
ANG004 Angioid Streaks 31 0.027
638
CRB028 Cerebellar Medulloblastoma 31 0.027
639
SCH062 Schimmelpenning-Feuerstein-Mims Syndrome, Somatic Mosaic 31 0.027
640
c PNC094 Pancreatic Cancer 1 31 0.027
641
P SLP004 Salpingo-Oophoritis 30 0.027
642
SCR001 Secretory Meningioma 29 0.027
643
BLR005 Biliary Papillomatosis 29 0.027
644
MNP001 Monophasic Synovial Sarcoma 29 0.027
645
c FML187 Familial Hypertension 29 0.027
646
P MSC109 Mosaic Variegated Aneuploidy Syndrome 1 28 0.027
647
TXC001 Toxic Megacolon 28 0.027
648
c CHR036 Chronic Cholangitis 27 0.027
649
CRB026 Cerebellar Astrocytoma 26 0.027
650
c FRT001 Fourth Cranial Nerve Palsy 26 0.027
651
AMY016 Amyopathic Dermatomyositis 25 0.027
652
ATR008 Atrophy of Prostate 25 0.027
653
KDN019 Kidney Sarcoma 25 0.027
654
P KLN006 Koolen-De Vries Syndrome 25 0.027
655
SPR001 Superficial Urinary Bladder Cancer 25 0.027
656
PDT027 Pediatric Ulcerative Colitis 24 0.027
657
CHR034 Chromophobe Adenoma 24 0.027
658
SBC018 Sebaceous Gland Neoplasm 24 0.027
659
TNS007 Taeniasis 23 0.027
660
GST006 Gastric Leiomyoma 23 0.027
661
NVS002 Nevo Syndrome 23 0.027
662
RCT020 Rectum Adenocarcinoma 23 0.027
663
DDN009 Duodenal Obstruction 22 0.027
664
P CHR259 Chromosome 6q25 Microdeletion Syndrome 22 0.027
665
KDN007 Kidney Clear Cell Sarcoma 21 0.027
666
ESN020 Eosinophilic Granulomatosis with Polyangiitis 21 0.027
667
PNC077 Pancreatitis, Idiopathic 21 0.027
668
HRT003 Heart Lymphoma 20 0.027
669
BRT042 Birt-Hogg-Dub� Syndrome 19 0.027
670
ESN014 Eosinophilic Enteropathy 18 0.027
671
ILL001 Ileal Neoplasm 18 0.027
672
MLL004 Mallory-Weiss Syndrome 18 0.027
673
c CLR079 Colorectal Cancer 2 18 0.027
674
RCT017 Rectal Disease 18 0.027
675
END058 Endometrial Carcinoma, Somatic 17 0.027
676
GRN011 Granulomatous Gastritis 17 0.027
677
DSS008 Disease of Mental Health 17 0.027
678
MDN003 Median Cleft of Upper Lip with Polyps of Facial Skin and Nasal Mucosa 16 0.027
679
AST038 Asthma, Aspirin-Induced 16 0.027
680
c AST037 Asthma 1 15 0.027
681
c BLT015 Bilateral Choanal Atresia 15 0.027
682
DCR005 Decr Deficiency 15 0.027
683
SGM001 Sigmoid Disease 14 0.027
684
END029 Endocervical Carcinoma 14 0.027
685
CRC014 Carcinoid Tumors, Intestinal 14 0.027
686
c CTR006 Cataract Anterior Polar Dominant 14 0.027
687
OTP003 Oto-Palatal-Digital Syndrome 13 0.027
688
c CLR075 Colorectal Cancer 3 13 0.027
689
DDN008 Duodenal Neoplasm 13 0.027
690
ESP015 Esophagus Lymphoma 12 0.027
691
c CLR077 Colorectal Cancer 10 12 0.027
692
BRT018 Birt–hogg–dubé Syndrome 11 0.027
693
c CLR078 Colorectal Cancer 11 11 0.027
694
c UNL004 Unilateral Choanal Atresia 11 0.027
695
ANL023 Anal Endocrine Tumor 10 0.027
696
c CHR183 Chromosome 10q Deletion 10 0.027
697
CNT045 Central Nervous System Sarcoma 10 0.027
698
LNG001 Lung Clear Cell Carcinoma 9 0.027
699
JNS001 Janus Kinase-3 Deficiency 9 0.027
700
HPT033 Hepatoblastoma, Somatic 7 0.027
701
c CSH002 Cushing Syndrome, Familial 5 0.027
702
HMN024 Hemangioma, Hereditary 3 0.027