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

635 hits were found for 'polyposis'

# Family MCID Name MIFTS Score
1
P FML011 Familial Adenomatous Polyposis 93 11.782
2
P JVN014 Juvenile Polyposis Syndrome 73 8.192
3
MTY001 Mutyh-Associated Polyposis 46 5.424
4
PTZ001 Peutz-Jeghers Syndrome 83 5.305
5
P HRD069 Hereditary Mixed Polyposis Syndrome 2 24 4.592
6
CRN014 Cronkhite-Canada Syndrome 46 4.347
7
ATT003 Attenuated Familial Adenomatous Polyposis 41 4.317
8
c FML254 Familial Adenomatous Polyposis Due to 5q22.2 Microdeletion 14 4.208
9
P TRC032 Turcot Syndrome 70 4.056
10
JVN012 Juvenile Polyposis/hereditary Hemorrhagic Telangiectasia Syndrome 21 3.875
11
c HRD101 Hereditary Mixed Polyposis Syndrome 1 7 3.841
12
HYP466 Hyperplastic Polyposis Syndrome 36 3.449
13
c JVN034 Juvenile Polyposis of Infancy 21 3.449
14
ADN040 Adenomas, Multiple Colorectal 21 3.038
15
APC006 Apc-Associated Polyposis Conditions 4 2.991
16
CPP003 Cap Polyposis 18 2.975
17
BRN074 Brain Tumor-Polyposis Syndrome 2 11 2.975
18
GST086 Gastric Adenocarcinoma and Proximal Polyposis of the Stomach 9 2.975
19
GRD002 Gardner Syndrome 41 2.656
20
P LYN001 Lynch Syndrome 70 2.634
21
CLR065 Colorectal Adenomatous Polyposis, Autosomal Recessive, with Pilomatricomas 31 2.510
22
c BMP001 Bmpr1a-Related Juvenile Polyposis 13 2.488
23
NSL012 Nasal Polyposis, Familial 1 2.447
24
JVN023 Juvenile Polyposis Syndrome, Infantile Form 8 2.429
25
c SMD006 Smad4-Related Juvenile Polyposis 3 2.429
26
PRS115 Prosthetic Joint Infection 27 1.988
27
PTZ002 Peutz–jeghers Syndrome 3 1.718
28
P CLR023 Colorectal Cancer 73 0.397
29
c XP2001 Xp22.3 Microdeletion Syndrome 21 0.307
30
ADN018 Adenoma 67 0.281
31
DDN006 Duodenitis 62 0.215
32
P CLN016 Colon Cancer 67 0.208
33
GRF006 Grfoma 26 0.198
34
DSM004 Desmoid Tumor 58 0.187
35
MLN020 Melanoma, Malignant, Somatic 51 0.176
36
CLR034 Colorectal Cancer, Somatic 40 0.171
37
14Q004 14q22q23 Microdeletion Syndrome 29 0.169
38
3Q2005 3q26q27 Microdeletion Syndrome 14 0.166
39
CNC006 Cancer: Lynch Syndrome Multi-Gene Panels 9 0.161
40
c THY032 Thyroiditis 67 0.159
41
ULC004 Ulcerative Colitis 72 0.154
42
P ADN016 Adenocarcinoma 60 0.154
43
IDP042 Idiopathic Recurrent Stupor 15 0.151
44
P CNG390 Congenital Pulmonary Airway Malformation 39 0.137
45
c MLH005 Mlh3-Related Lynch Syndrome 11 0.134
46
BNN001 Bannayan-Riley-Ruvalcaba Syndrome 68 0.131
47
DST056 Distal 22q11.2 Microdeletion Syndrome 37 0.128
48
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 43 0.121
49
P MGS003 Meigs Syndrome 35 0.118
50
PRX070 Proximal 16p11.2 Microduplication Syndrome 18 0.118
51
ANK002 Ankylosing Spondylitis 75 0.110
52
THR013 Thoracic Outlet Syndrome 54 0.110
53
MNN014 Mononeuritis 48 0.110
54
14Q001 14q12 Microdeletion Syndrome 23 0.110
55
TFT003 Tufting Enteropathy 21 0.110
56
c FML259 Familial Renal Amyloidosis Due to Fibrinogen a Alpha-Chain Variant 14 0.110
57
GLL008 Gilles De La Tourette Syndrome 73 0.107
58
P ICH047 Ichthyosis, Congenital, Autosomal Recessive 1 45 0.107
59
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 43 0.107
60
P MLR006 Male Reproductive Organ Cancer 23 0.107
61
MNS013 Monosomy 13q34 17 0.107
62
c DST058 Distal Monosomy 12p 17 0.107
63
c CLR098 Ciliary Dyskinesia, Primary, 27 13 0.107
64
P PPL020 Papillary Thyroid Carcinoma 59 0.103
65
MCR071 Microdeletion 15q11.2 25 0.103
66
c CHR226 Chromosome 1q41-Q42 Deletion Syndrome 24 0.103
67
P AST005 Asthma 88 0.099
68
P RHN004 Rhinitis 65 0.099
69
HPT022 Hepatoblastoma 65 0.099
70
PPL002 Papillary Carcinoma 61 0.099
71
MCR014 Microcystic Adenoma 40 0.099
72
GST063 Gastric Cancer Risk After H. Pylori Infection 36 0.099
73
17Q002 17q23.1q23.2 Microdeletion Syndrome 34 0.099
74
c CHR243 Chromosome 3p Deletion 23 0.099
75
10P002 10p11.21p12.31 Microdeletion Syndrome 15 0.099
76
P HRD008 Hereditary Hemorrhagic Telangiectasia 86 0.095
77
THY028 Thyroid Cancer 76 0.095
78
ACN002 Acanthosis Nigricans 73 0.095
79
c CWD001 Cowden Disease 69 0.095
80
INT051 Intussusception 59 0.095
81
SPS019 Spastic Paraparesis 35 0.095
82
17Q007 17q11 Microdeletion Syndrome 26 0.095
83
c 2Q3005 2q31.1 Microdeletion Syndrome 26 0.095
84
OVR101 Ovarian Malignant Sertoli-Leydig Cell Tumor 18 0.095
85
ODN006 Odontoma 16 0.095
86
HPT023 Hepatocellular Carcinoma 89 0.090
87
c PNC044 Pancreatitis 67 0.090
88
IMP002 Imperforate Anus 47 0.090
89
RVL002 Ruvalcaba Syndrome 41 0.090
90
PCH007 Pouchitis 40 0.090
91
c FML053 Familial Colorectal Cancer 39 0.090
92
CTN026 Cutaneous Neuroendocrine Carcinoma 35 0.090
93
BLD087 Bladder Cancer, Somatic 34 0.090
94
CRK001 Cork-Handlers' Disease 32 0.090
95
ESP010 Esophageal Basaloid Squamous Cell Carcinoma 26 0.090
96
CHL109 Childhood Apraxia of Speech 24 0.090
97
P MLG002 Malignant Peritoneal Mesothelioma 55 0.086
98
PRT019 Protein-Losing Enteropathy 48 0.086
99
GST039 Gastroduodenitis 46 0.086
100
MXL004 Maxillary Sinus Squamous Cell Carcinoma 43 0.086
101
INT052 Intestinal Volvulus 42 0.086
102
PRL008 Paralytic Ileus 39 0.086
103
BRS015 Breast Medullary Carcinoma 32 0.086
104
19Q001 19q13.11 Microdeletion Syndrome 25 0.086
105
P BRS047 Breast Cancer 105 0.081
106
P ATX002 Ataxia Telangiectasia 93 0.081
107
P LKM002 Leukemia 79 0.081
108
GST023 Gastric Ulcer 72 0.081
109
c LCL006 Localized Scleroderma 68 0.081
110
MNT001 Mantle Cell Lymphoma 67 0.081
111
MYC002 Mycobacterium Avium Complex Disease 57 0.081
112
SCN006 Secondary Syphilis 55 0.081
113
P INF037 Inflammatory Bowel Disease 50 0.081
114
DDF001 Dedifferentiated Liposarcoma 42 0.081
115
OST006 Osteoblastoma 41 0.081
116
c HRD045 Hereditary Hemorrhagic Telangiectasia Type 2 38 0.081
117
FCT013 Factor V Leiden Thrombophilia 35 0.081
118
TNF006 Tnfrsf13b-Related Common Variable Immune Deficiency 14 0.081
119
P PNC035 Pancreatic Cancer 95 0.075
120
P LNG032 Lung Cancer 74 0.075
121
P STM004 Stomach Cancer 65 0.075
122
ART005 Arteriovenous Malformation 63 0.075
123
CNG008 Congenital Ichthyosiform Erythroderma 53 0.075
124
IMM060 Immunodeficiency, Common Variable, 9 46 0.075
125
PLS016 Plasma Cell Leukemia 42 0.075
126
SYN053 Syndromic Diarrhea 42 0.075
127
JVN033 Juvenile Nasopharyngeal Angiofibroma 39 0.075
128
c SPH018 Spherocytosis, Hereditary, Type 5 36 0.075
129
17Q004 17q12 Microdeletion Syndrome 33 0.075
130
c OVR069 Ovarian Germ Cell Tumor 32 0.075
131
NNS020 Nonsmall Cell Lung Cancer, Somatic 27 0.075
132
c CHR459 Chromosome Xp Deletion 12 0.075
133
P HMP004 Hemophilia B 80 0.070
134
LNG024 Langerhans-Cell Histiocytosis 75 0.070
135
TRN018 Transitional Cell Carcinoma 64 0.070
136
WST001 West Syndrome 64 0.070
137
SRC014 Sarcoma 63 0.070
138
ATX019 Ataxia with Vitamin E Deficiency 55 0.070
139
EVN001 Evans' Syndrome 54 0.070
140
P THR090 Thrombocythemia 1 54 0.070
141
SCL017 Sclerosing Hemangioma 54 0.070
142
c ACR001 Aicardi-Goutieres Syndrome 49 0.070
143
1P3001 1p36 Deletion Syndrome 48 0.070
144
GST040 Gastric Adenocarcinoma 48 0.070
145
SML009 Small Intestine Adenocarcinoma 47 0.070
146
TLN003 Telangiectasis 46 0.070
147
CHL079 Children's Interstitial Lung Disease 46 0.070
148
LBL001 Lobular Neoplasia 44 0.070
149
DDN007 Duodenal Disease 38 0.070
150
IMG001 Image Syndrome 34 0.070
151
LKP003 Leukoplakia 32 0.070
152
OVR011 Ovarian Mucinous Adenocarcinoma 31 0.070
153
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.070
154
TRP008 Tropical Calcific Pancreatitis 27 0.070
155
DST051 Distal 7q11.23 Microdeletion Syndrome 21 0.070
156
RPD005 Rapidly Involuting Congenital Hemangioma 16 0.070
157
12Q001 12q15q21.1 Microdeletion Syndrome 15 0.070
158
c ENG003 Eng-Related Hereditary Hemorrhagic Telangiectasia 11 0.070
159
P HMN010 Hemangioma 68 0.064
160
ALL003 Allergic Rhinitis 66 0.064
161
P HRD011 Hereditary Spherocytosis 66 0.064
162
ADR008 Adrenal Adenoma 62 0.064
163
RTN023 Retinitis 61 0.064
164
P CWD006 Cowden Syndrome 1 61 0.064
165
SQM006 Squamous Cell Carcinoma 61 0.064
166
P ESN007 Eosinophilia 60 0.064
167
P ESP024 Esophagitis 60 0.064
168
c FML024 Familial Melanoma 51 0.064
169
NSP002 Nasopharyngitis 49 0.064
170
PLM018 Pulmonary Sclerosing Hemangioma 48 0.064
171
PNC019 Pancreatoblastoma 46 0.064
172
P ATX010 Ataxia Neuropathy Spectrum 44 0.064
173
PRL042 Proliferating Trichilemmal Cyst 38 0.064
174
c 3Q2003 3q29 Microdeletion Syndrome 36 0.064
175
MSM004 Mesomelia-Synostoses Syndrome 32 0.064
176
12Q002 12q14 Microdeletion Syndrome 31 0.064
177
CRB006 Cribriform Carcinoma 29 0.064
178
2Q3003 2q32q33 Microdeletion Syndrome 27 0.064
179
c 2Q2001 2q23.1 Microdeletion Syndrome 27 0.064
180
CLF029 Cleft Palate and Mental Retardation 25 0.064
181
CLD014 Cole Disease 24 0.064
182
c 4Q2001 4q21 Microdeletion Syndrome 23 0.064
183
c CHR260 Chromosome 7p Deletion 15 0.064
184
c CHR255 Chromosome 6p Deletion 13 0.064
185
c EPC004 Epcam-Related Lynch Syndrome 11 0.064
186
CRH001 Crohn's Disease 83 0.057
187
P END042 Endometrial Carcinoma 78 0.057
188
PRC016 Pre-Eclampsia 75 0.057
189
c HPT021 Hepatitis 75 0.057
190
c LPR002 Leopard Syndrome 72 0.057
191
RLP001 Relapsing Polychondritis 69 0.057
192
P GST044 Gastritis 68 0.057
193
TRP002 Tropical Spastic Paraparesis 67 0.057
194
PPL022 Papilloma 64 0.057
195
NRN002 Neuronitis 64 0.057
196
c ACT027 Acute Pancreatitis 63 0.057
197
NNS005 Non-Small Cell Lung Carcinoma 58 0.057
198
c INT070 Intestinal Obstruction 54 0.057
199
CHL056 Cheilitis 54 0.057
200
FML026 Familial Lipoprotein Lipase Deficiency 52 0.057
201
GST060 Gastric Cancer, Somatic 52 0.057
202
INV006 Inverted Papilloma 52 0.057
203
HRD004 Hereditary Breast Ovarian Cancer 50 0.057
204
HMH002 Hemihypertrophy 50 0.057
205
VSM001 Vasomotor Rhinitis 49 0.057
206
GST014 Gastrointestinal Lymphoma 49 0.057
207
CRC006 Carcinoid Syndrome 46 0.057
208
P ATS008 Autosomal Dominant Disease 46 0.057
209
LYM014 Lymphangitis 46 0.057
210
RCR004 Recurrent Respiratory Papillomatosis 45 0.057
211
c BRC032 Brachydactyly Type A2 42 0.057
212
P STR021 Struma Ovarii 42 0.057
213
ANP009 Anaplastic Oligodendroglioma 38 0.057
214
OST111 Osteoporosis, Early-Onset Autosomal Dominant 36 0.057
215
BRN015 Bronchiolo-Alveolar Adenocarcinoma 35 0.057
216
c ATS021 Autosomal Recessive Juvenile Parkinson Disease 30 0.057
217
PNC073 Pancreatic Carcinoma, Somatic 28 0.057
218
PNM003 Pneumatosis Cystoides Intestinalis 26 0.057
219
P FML252 Familial Advanced Sleep Phase Syndrome 1 24 0.057
220
HNM002 Hinman Syndrome 24 0.057
221
c FML253 Familial Cold Autoinflammatory Syndrome 3 23 0.057
222
AND005 Androgen Insensitivity Syndrome, Mild 18 0.057
223
c 9P1001 9p13 Microdeletion Syndrome 15 0.057
224
c 5Q3002 5q31.3 Microdeletion Syndrome 15 0.057
225
FLR003 Florid Cemento-Osseous Dysplasia 13 0.057
226
c MLH002 Mlh1-Related Lynch Syndrome 12 0.057
227
c CHR237 Chromosome 2p Deletion 12 0.057
228
P AMY001 Amyotrophic Lateral Sclerosis 100 0.049
229
AND002 Androgen Insensitivity Syndrome 88 0.049
230
P HYP075 Hypertension 86 0.049
231
P GST019 Gastrointestinal Stromal Tumor 83 0.049
232
P MDL005 Medulloblastoma 82 0.049
233
P HST010 Histiocytosis 71 0.049
234
P ANG001 Angelman Syndrome 70 0.049
235
ART019 Aortic Valve Stenosis 68 0.049
236
BRN028 Brain Cancer 67 0.049
237
DFC004 Deficiency Anemia 66 0.049
238
P MRT001 Muir-Torre Syndrome 65 0.049
239
c AXN002 Axenfeld-Rieger Syndrome 60 0.049
240
CRB009 Cerebritis 56 0.049
241
P SRT002 Sertoli Cell Tumor 54 0.049
242
CLN019 Colonic Disease 54 0.049
243
PRN011 Pernicious Anemia 52 0.049
244
THY089 Thymic Epithelial Neoplasm 52 0.049
245
PLM009 Pleomorphic Adenoma Carcinoma 51 0.049
246
HPT032 Hepatocellular Carcinoma, Somatic 50 0.049
247
SCH016 Schimke Immunoosseous Dysplasia 49 0.049
248
LNG029 Lung Adenocarcinoma 49 0.049
249
c ADN012 Adenocarcinoma in Situ 48 0.049
250
FML027 Female Breast Carcinoma 48 0.049
251
CHL052 Choledochal Cyst 46 0.049
252
PLM026 Pilomatrixoma 46 0.049
253
EPT010 Epithelial-Myoepithelial Carcinoma 46 0.049
254
HPR003 Heparin-Induced Thrombocytopenia 45 0.049
255
c EPN002 Ependymoma 44 0.049
256
END016 Endocervicitis 44 0.049
257
TTR016 Tetra-Amelia Syndrome 43 0.049
258
RHB017 Rhabdoid Tumor 38 0.049
259
c LNG063 Lung Cancer Susceptibility 38 0.049
260
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 38 0.049
261
15Q001 15q13.3 Microdeletion 37 0.049
262
ACT093 Actinic Cheilitis 37 0.049
263
PLM070 Pulmonic Stenosis 37 0.049
264
P JVN024 Juvenile Hereditary Hemochromatosis 35 0.049
265
PRN049 Paraneoplastic Pemphigus 35 0.049
266
ANL022 Anal Fistula 34 0.049
267
ERL004 Early Yaws 33 0.049
268
BLD039 Bladder Adenocarcinoma 33 0.049
269
SML032 Small Bowel Adenocarcinoma 31 0.049
270
MTG002 Mutagen Sensitivity 31 0.049
271
VCL001 Vacuolar Myopathy 30 0.049
272
c CHR253 Chromosome 5q Deletion 28 0.049
273
RCT020 Rectum Adenocarcinoma 26 0.049
274
16Q001 16q24.3 Microdeletion Syndrome 25 0.049
275
DDN008 Duodenal Neoplasm 22 0.049
276
c FML251 Familial Partial Lipodystrophy Type 4 22 0.049
277
c BNG076 Benign Exophthalmos Syndrome 21 0.049
278
c MNS010 Monosomy Xp21 20 0.049
279
CHR457 Chromosome 17p13.1 Deletion Syndrome 19 0.049
280
c TTL001 Total Internal Ophthalmoplegia 17 0.049
281
P ISC010 Isochromosome Yp 14 0.049
282
c FML255 Familial Syringomyelia 11 0.049
283
CYS001 Cystic Fibrosis 103 0.040
284
P TYP009 Type 2 Diabetes Mellitus 93 0.040
285
P LFR001 Li-Fraumeni Syndrome 93 0.040
286
MRF001 Marfan Syndrome 92 0.040
287
P PRS040 Prostate Cancer 91 0.040
288
VNH001 Von Hippel-Lindau Disease 89 0.040
289
MTC003 Metachromatic Leukodystrophy 87 0.040
290
P HNT001 Huntington's Disease 87 0.040
291
P RTN024 Retinoblastoma 86 0.040
292
GLN003 Glanzmann's Thrombasthenia 80 0.040
293
P OVR042 Ovarian Cancer 79 0.040
294
PRT036 Peritonitis 78 0.040
295
P CRN008 Carney Complex 78 0.040
296
P ACT074 Acute Lymphocytic Leukemia 77 0.040
297
c NNN003 Noonan Syndrome 77 0.040
298
BRN024 Bronchitis 76 0.040
299
FBR011 Fibrodysplasia Ossificans Progressiva 75 0.040
300
c CHR065 Chronic Myeloid Leukemia 74 0.040
301
P AST007 Astrocytoma 72 0.040
302
IRR002 Irritable Bowel Syndrome 68 0.040
303
BRR003 Barrett's Esophagus 68 0.040
304
CMM004 Common Variable Immunodeficiency 66 0.040
305
P ART023 Arthropathy 66 0.040
306
PTT006 Pituitary Adenoma 64 0.040
307
ETN001 Eating Disorder 63 0.040
308
P LRY019 Laryngitis 62 0.040
309
P EHL033 Ehlers-Danlos Syndrome, Classic Type 62 0.040
310
PSD007 Pseudomyxoma Peritonei 62 0.040
311
SMT015 Smith Magenis Syndrome 62 0.040
312
PRS047 Prostatitis 62 0.040
313
ART001 Arterial Tortuosity Syndrome 62 0.040
314
c MSC005 Muscular Dystrophy 62 0.040
315
PPT003 Peptic Ulcer 61 0.040
316
P LPS002 Liposarcoma 61 0.040
317
CLR003 Clear Cell Adenocarcinoma 60 0.040
318
HYP003 Hypermethioninemia 60 0.040
319
WLF002 Wolf-Hirschhorn Syndrome 60 0.040
320
MLT001 Multiple Chemical Sensitivity 59 0.040
321
ACH005 Achalasia 59 0.040
322
BRT002 Birt-Hogg-Dube Syndrome 59 0.040
323
P CLF002 Cleft Palate 59 0.040
324
c FML035 Familial Hyperlipidemia 59 0.040
325
P ESN001 Eosinophilic Esophagitis 58 0.040
326
INS002 in Situ Carcinoma 58 0.040
327
LKD001 Leukodystrophy 58 0.040
328
ORL004 Oral Submucous Fibrosis 57 0.040
329
PRT018 Portal Vein Thrombosis 57 0.040
330
P LYM026 Lymphoblastic Leukemia 56 0.040
331
SNS001 Sensorineural Hearing Loss 56 0.040
332
CRV031 Cervical Adenocarcinoma 56 0.040
333
ATY005 Atypical Teratoid Rhabdoid Tumor 55 0.040
334
URN010 Urinary Tract Obstruction 55 0.040
335
PLM020 Pleomorphic Xanthoastrocytoma 55 0.040
336
EXS001 Exostosis 54 0.040
337
c DRR001 Diarrhea 54 0.040
338
P CLR070 Colorectal Cancer, Hereditary Nonpolyposis, Type 1 54 0.040
339
ART017 Aortic Disease 54 0.040
340
SPN020 Spondylosis 54 0.040
341
GST050 Gastrointestinal System Disease 54 0.040
342
GNT002 Giant Cell Glioblastoma 54 0.040
343
RFR003 Refractive Error 53 0.040
344
c ADL017 Adult T-Cell Leukemia 53 0.040
345
c KRT005 Keratoacanthoma 53 0.040
346
INT007 Intermediate Coronary Syndrome 53 0.040
347
BSL006 Basaloid Squamous Cell Carcinoma 53 0.040
348
P CLR017 Clear Cell Sarcoma 52 0.040
349
LPM005 Lipomatosis 52 0.040
350
P ALV004 Alveolar Rhabdomyosarcoma 51 0.040
351
ESP025 Esophagus Adenocarcinoma 51 0.040
352
ACN001 Acinar Cell Carcinoma 51 0.040
353
CYS009 Cystadenoma 51 0.040
354
SKN023 Skin Tag 50 0.040
355
HMN012 Hemangioma of Lung 50 0.040
356
BLT006 Bilateral Breast Cancer 50 0.040
357
P PND001 Pain Disorder 49 0.040
358
URT010 Ureteral Obstruction 49 0.040
359
UTR024 Uterine Carcinosarcoma 49 0.040
360
c TCL004 T-Cell Leukemia 49 0.040
361
JCB001 Jacobsen Syndrome 48 0.040
362
MCP006 Mucoepidermoid Carcinoma 48 0.040
363
CLN015 Colon Adenocarcinoma 48 0.040
364
P FCS001 Facioscapulohumeral Muscular Dystrophy 47 0.040
365
OVR034 Ovarian Clear Cell Adenocarcinoma 45 0.040
366
INV004 Invasive Bladder Transitional Cell Carcinoma 45 0.040
367
INT069 Intestinal Neoplasm 45 0.040
368
SYR002 Syringocystadenoma Papilliferum 45 0.040
369
RCR001 Recurrent Corneal Erosion 44 0.040
370
c CHR048 Chronic Rhinitis 43 0.040
371
AND003 Andersen-Tawil Syndrome 43 0.040
372
ACR014 Acral Lentiginous Melanoma 42 0.040
373
BLD049 Bladder Transitional Cell Papilloma 42 0.040
374
RCT011 Rectal Prolapse 42 0.040
375
DFF019 Diffuse Gastric Cancer 42 0.040
376
CRB022 Cerebellar Liponeurocytoma 41 0.040
377
P PNB001 Pineoblastoma 40 0.040
378
ESP027 Esophagus Squamous Cell Carcinoma 39 0.040
379
IPX001 Ipex Syndrome 39 0.040
380
MTN001 Metanephric Adenoma 38 0.040
381
HTL002 Htlv-1 Associated Myelopathy 38 0.040
382
TXC012 Toxic Epidermal Necrolysis 38 0.040
383
SPP002 Sipple Syndrome 37 0.040
384
P CHR038 Chronic Maxillary Sinusitis 37 0.040
385
c RSM001 Rasmussen Encephalitis 37 0.040
386
EMN001 Emanuel Syndrome 36 0.040
387
CRY008 Cryopyrin-Associated Periodic Syndrome 36 0.040
388
BPH002 Biphasic Synovial Sarcoma 35 0.040
389
FBR019 Fibromatosis 34 0.040
390
EMB007 Embryonal Sarcoma 34 0.040
391
PTN006 Pten Hamartoma Tumor Syndrome 33 0.040
392
INT017 Intestinal Schistosomiasis 32 0.040
393
RCT018 Rectal Neoplasm 31 0.040
394
c HNT004 Huntington Disease-Like 2 30 0.040
395
PTL001 Patulous Eustachian Tube 30 0.040
396
FSC006 Fascioscapulohumeral Muscular Dystrophy 2, Digenic 29 0.040
397
RHN002 Rhinoscleroma 29 0.040
398
THY059 Thyroid Carcinoma, Follicular, Somatic 28 0.040
399
P HYP078 Hypertrophy of Breast 26 0.040
400
MNS009 Monosomy 13q14 26 0.040
401
LNG061 Lung Cancer, Somatic 25 0.040
402
P ADL001 Adult Lymphoma 24 0.040
403
6Q1001 6q16 Deletion Syndrome 24 0.040
404
c HMP017 Hemophilia a, Congenital 21 0.040
405
c CHR271 Chromosome 9q Deletion 19 0.040
406
JJN002 Jejunal Neoplasm 17 0.040
407
21Q002 21q22.13q22.2 Microdeletion Syndrome 15 0.040
408
BLD063 Bile Duct Cysts 13 0.040
409
c FML143 Familial Papillary Thyroid Carcinoma 10 0.040
410
P OBS005 Obesity 93 0.029
411
P RHM011 Rheumatoid Arthritis 91 0.029
412
P WSK001 Wiskott-Aldrich Syndrome 87 0.029
413
P HRS001 Hirschsprung's Disease 84 0.029
414
ACH004 Achondroplasia 83 0.029
415
P ALG002 Alagille Syndrome 83 0.029
416
AGR001 Age Related Macular Degeneration 83 0.029
417
P CSH001 Cushing's Syndrome 83 0.029
418
P THY014 Thyroid Medullary Carcinoma 81 0.029
419
ESP021 Esophageal Cancer 81 0.029
420
P RTN008 Retinitis Pigmentosa 81 0.029
421
c DBT009 Diabetes Mellitus 80 0.029
422
P MNN012 Meningioma 79 0.029
423
CST001 Costello Syndrome 79 0.029
424
P SCH015 Schizophrenia 77 0.029
425
RNL002 Renal Agenesis 77 0.029
426
TTR001 Tetralogy of Fallot 76 0.029
427
NVD001 Nevoid Basal Cell Carcinoma Syndrome 75 0.029
428
P CRD013 Cardiofaciocutaneous Syndrome 74 0.029
429
CHL065 Cholangiocarcinoma 73 0.029
430
SCH014 Schistosomiasis 72 0.029
431
PRL009 Prolactinoma 71 0.029
432
P DRM010 Dermatomyositis 70 0.029
433
P RSP003 Respiratory Failure 70 0.029
434
P PRT010 Parathyroid Carcinoma 69 0.029
435
PSY004 Psychotic Disorder 69 0.029
436
P END044 Endometriosis 69 0.029
437
P NNN008 Noonan Syndrome 1 69 0.029
438
P FML032 Familial Hypertrophic Cardiomyopathy 69 0.029
439
CHR029 Choroid Plexus Papilloma 68 0.029
440
LMY002 Leiomyoma 68 0.029
441
PLM033 Pulmonary Embolism 68 0.029
442
c HYP086 Hypothyroidism 68 0.029
443
P DDN001 Duodenal Ulcer 68 0.029
444
GST034 Gastroesophageal Reflux Disease 67 0.029
445
P OLG002 Oligodendroglioma 67 0.029
446
P PRT013 Portal Hypertension 67 0.029
447
DSS009 Disseminated Intravascular Coagulation 66 0.029
448
CHG001 Chagas Disease 66 0.029
449
c HPT016 Hepatitis B 65 0.029
450
P MLN008 Melanoma 65 0.029
451
HMT002 Hematologic Cancer 64 0.029
452
c SML001 Small Cell Carcinoma 64 0.029
453
FLL032 Follicular Thyroid Carcinoma 64 0.029
454
CYS005 Cysticercosis 64 0.029
455
BRN022 Bronchiectasis 64 0.029
456
GLL018 Gallbladder Cancer 64 0.029
457
P BSL007 Basal Cell Carcinoma 64 0.029
458
SHG001 Shigellosis 63 0.029
459
c MTR004 Maturity-Onset Diabetes of the Young 63 0.029
460
c LRY016 Laryngeal Carcinoma 63 0.029
461
ADR015 Adrenocortical Carcinoma 63 0.029
462
GRW001 Growth Hormone Secreting Pituitary Adenoma 63 0.029
463
c ACT073 Acute Leukemia 62 0.029
464
GLB001 Gilbert Syndrome 62 0.029
465
BRN029 Brain Disease 62 0.029
466
c VRL010 Viral Hepatitis 61 0.029
467
P ORL007 Oral Cavity Cancer 61 0.029
468
P INT068 Intestinal Disease 61 0.029
469
c HYP061 Hypertrophic Cardiomyopathy 61 0.029
470
IRN001 Iron Deficiency Anemia 61 0.029
471
ADN002 Adenoiditis 60 0.029
472
THR009 Thrombocytopenia-Absent Radius Syndrome 60 0.029
473
ALL006 Allergic Asthma 60 0.029
474
P VLC001 Velocardiofacial Syndrome 60 0.029
475
LPM004 Lipoma 60 0.029
476
ALP008 Alopecia 60 0.029
477
c HPT003 Hepatitis a 60 0.029
478
GLS001 Gliosarcoma 60 0.029
479
ISV001 Isovaleric Acidemia 60 0.029
480
P PNM006 Pneumoconiosis 59 0.029
481
P PTT014 Pitt-Hopkins Syndrome 59 0.029
482
P RNL014 Renal Cell Carcinoma 59 0.029
483
CHR001 Churg-Strauss Syndrome 59 0.029
484
ACR008 Acrocallosal Syndrome 59 0.029
485
ALV005 Alveolar Soft Part Sarcoma 59 0.029
486
CMM005 Common Cold 59 0.029
487
CHR074 Choriocarcinoma 59 0.029
488
PRM027 Primitive Neuroectodermal Tumor 59 0.029
489
P HMN013 Hemangiopericytoma 58 0.029
490
TST014 Testicular Cancer 58 0.029
491
VRR004 Verrucous Carcinoma 58 0.029
492
PLM032 Pulmonary Blastoma 58 0.029
493
P ATS007 Autism Spectrum Disorder 57 0.029
494
GNG002 Ganglioneuroma 57 0.029
495
MYP001 Myoepithelioma 57 0.029
496
LRY018 Laryngeal Squamous Cell Carcinoma 57 0.029
497
MGC001 Megacolon 56 0.029
498
HST009 Histiocytoma 56 0.029
499
P THR012 Thoracic Cancer 56 0.029
500
P STR020 Strabismus 56 0.029
501
GLM004 Gliomatosis Cerebri 56 0.029
502
SWT001 Sweat Gland Carcinoma 56 0.029
503
HRD027 Hereditary Diffuse Gastric Cancer 56 0.029
504
MCN001 Mucinous Adenocarcinoma 56 0.029
505
GLM008 Glomus Tumor 56 0.029
506
NPH011 Nephroblastoma 56 0.029
507
c HYP060 Hyperinsulinism 56 0.029
508
BRS051 Breast Disease 56 0.029
509
GST030 Gastrinoma 55 0.029
510
FBR003 Fibrous Histiocytoma 55 0.029
511
EMB003 Embryonal Cancer 55 0.029
512
LPC002 Lip Cancer 55 0.029
513
P PLY006 Polydactyly 54 0.029
514
RHB003 Rhabdomyosarcoma 54 0.029
515
CRV038 Cervical Squamous Cell Carcinoma 54 0.029
516
c PRM011 Primary Ciliary Dyskinesia 53 0.029
517
ACR012 Aicardi Syndrome 53 0.029
518
P EXN002 Exanthem 53 0.029
519
LYM006 Lymphoepithelioma-Like Carcinoma 53 0.029
520
MRG003 Marginal Zone B-Cell Lymphoma 53 0.029
521
CRD005 Cardia Cancer 53 0.029
522
ASB001 Asbestosis 52 0.029
523
PNC013 Pancreatic Ductal Carcinoma 52 0.029
524
SRC002 Sarcomatoid Renal Cell Carcinoma 52 0.029
525
CYS014 Cystadenocarcinoma 52 0.029
526
PLM016 Pleomorphic Carcinoma 52 0.029
527
EXF001 Exfoliation Syndrome 51 0.029
528
ART002 Arts Syndrome 51 0.029
529
CHL004 Cholelithiasis 51 0.029
530
BRK001 Brooke-Spiegler Syndrome 51 0.029
531
DBW001 Dubowitz Syndrome 51 0.029
532
BLS003 Blastoma 50 0.029
533
CNV002 Conversion Disorder 50 0.029
534
KLT001 Klatskin's Tumor 50 0.029
535
LMY003 Leiomyomatosis 49 0.029
536
P CHN005 Choanal Atresia 49 0.029
537
DRG002 Drug-Induced Hepatitis 49 0.029
538
P CYS017 Cystic Teratoma 48 0.029
539
ALC010 Alcoholic Cardiomyopathy 48 0.029
540
GLL017 Gallbladder Adenocarcinoma 47 0.029
541
CLD007 Cold Agglutinin Disease 47 0.029
542
P PLM030 Pleomorphic Rhabdomyosarcoma 47 0.029
543
ASC002 Ascariasis 47 0.029
544
LPD006 Lipoid Proteinosis 45 0.029
545
c STS001 Sotos Syndrome 45 0.029
546
HMM003 Hemimegalencephaly 45 0.029
547
MNN006 Meninges Hemangiopericytoma 45 0.029
548
CMM014 Common Variable Immune Deficiency 45 0.029
549
P PRK001 Porokeratosis 45 0.029
550
RTR010 Retroperitoneal Sarcoma 45 0.029
551
GMS001 Gemistocytic Astrocytoma 45 0.029
552
P PLC011 Pilocytic Astrocytoma 45 0.029
553
DVR002 Diverticulitis 45 0.029
554
CNG041 Congenital Cataracts, Facial Dysmorphism, and Neuropathy 44 0.029
555
NNP001 Nonpapillary Renal Cell Carcinoma 44 0.029
556
P PRG017 Paraganglioma and Gastric Stromal Sarcoma 44 0.029
557
c MLT074 Multiple Endocrine Neoplasia 43 0.029
558
P LNG038 Lung Small Cell Carcinoma 43 0.029
559
ANC001 Ancylostomiasis 43 0.029
560
INT040 Intrinsic Asthma 43 0.029
561
END043 Endometrial Stromal Tumor 41 0.029
562
CRB002 Cerebral Primitive Neuroectodermal Tumor 41 0.029
563
c CRN035 Cranial Nerve Palsy 41 0.029
564
HPT006 Hepatic Angiomyolipoma 41 0.029
565
SCH063 Schimmelpenning-Feuerstein-Mims Syndrome, Somatic Mosaic 41 0.029
566
OVR048 Ovarian Cystadenoma 41 0.029
567
ESP023 Esophageal Disease 40 0.029
568
URT031 Ureteral Disease 40 0.029
569
P MSC109 Mosaic Variegated Aneuploidy Syndrome 1 40 0.029
570
P PRG003 Progesterone-Receptor Negative Breast Cancer 40 0.029
571
HPT067 Hepatocellular Adenoma 40 0.029
572
NXS001 Naxos Disease 40 0.029
573
HYP030 Hypoactive Sexual Desire Disorder 39 0.029
574
P 2Q3002 2q37 Microdeletion Syndrome 39 0.029
575
ORL011 Oral Cancer 38 0.029
576
P BRN035 Brain Stem Glioma 38 0.029
577
ATR008 Atrophy of Prostate 38 0.029
578
CRB028 Cerebellar Medulloblastoma 38 0.029
579
PRM014 Periampullary Adenocarcinoma 37 0.029
580
OPT007 Optic Nerve Glioma 37 0.029
581
c BLN003 Blindness 37 0.029
582
AMP009 Ampulla of Vater Adenocarcinoma 37 0.029
583
PLY040 Polymorphous Low-Grade Adenocarcinoma 36 0.029
584
ANP006 Anaplastic Ependymoma 36 0.029
585
HDR006 Hidradenocarcinoma 35 0.029
586
SCR001 Secretory Meningioma 35 0.029
587
MNT147 Mental Retardation 35 0.029
588
SPR033 Superficial Spreading Melanoma 35 0.029
589
SPT007 Spitz Nevus 35 0.029
590
MTR001 Mature Cataract 34 0.029
591
MNP001 Monophasic Synovial Sarcoma 33 0.029
592
ADS002 Adie Syndrome 33 0.029
593
BLR005 Biliary Papillomatosis 33 0.029
594
ANG004 Angioid Streaks 33 0.029
595
MNT053 Mental Retardation, Stereotypic Movements, Epilepsy, and/or Cerebral Malformations 33 0.029
596
CRB026 Cerebellar Astrocytoma 32 0.029
597
SPR001 Superficial Urinary Bladder Cancer 31 0.029
598
P SLP004 Salpingo-Oophoritis 31 0.029
599
KDN019 Kidney Sarcoma 31 0.029
600
ATY019 Atypical Mole Syndrome 31 0.029
601
ESN020 Eosinophilic Granulomatosis with Polyangiitis 30 0.029
602
c FRT001 Fourth Cranial Nerve Palsy 30 0.029
603
TXC001 Toxic Megacolon 29 0.029
604
c 2P2001 2p21 Microdeletion Syndrome 29 0.029
605
P KLN006 Koolen-De Vries Syndrome 29 0.029
606
DYS036 Dysequilibrium Syndrome 28 0.029
607
c SKN013 Skin Benign Neoplasm 28 0.029
608
c CHR036 Chronic Cholangitis 28 0.029
609
DDN009 Duodenal Obstruction 27 0.029
610
CHR034 Chromophobe Adenoma 26 0.029
611
DSS008 Disease of Mental Health 25 0.029
612
TNS007 Taeniasis 25 0.029
613
SML008 Small Intestine Lymphoma 25 0.029
614
c PNC094 Pancreatic Cancer 1 25 0.029
615
GST006 Gastric Leiomyoma 24 0.029
616
KDN007 Kidney Clear Cell Sarcoma 24 0.029
617
RNL013 Renal Adenoma 24 0.029
618
10Q001 10q22.3q23.3 Microdeletion Syndrome 23 0.029
619
TST018 Testicular Yolk Sac Tumor 23 0.029
620
RCT017 Rectal Disease 22 0.029
621
MDN003 Median Cleft of Upper Lip with Polyps of Facial Skin and Nasal Mucosa 22 0.029
622
END058 Endometrial Carcinoma, Somatic 20 0.029
623
CLN005 Colon Lymphoma 20 0.029
624
GRN011 Granulomatous Gastritis 20 0.029
625
END029 Endocervical Carcinoma 17 0.029
626
ILL001 Ileal Neoplasm 17 0.029
627
ESN014 Eosinophilic Enteropathy 15 0.029
628
SGM001 Sigmoid Disease 14 0.029
629
CNT045 Central Nervous System Sarcoma 14 0.029
630
OTP003 Oto-Palatal-Digital Syndrome 13 0.029
631
ESP015 Esophagus Lymphoma 13 0.029
632
c CTR006 Cataract Anterior Polar Dominant 13 0.029
633
AST038 Asthma, Aspirin-Induced 12 0.029
634
c LNG001 Lung Clear Cell Carcinoma 11 0.029
635
JNS001 Janus Kinase-3 Deficiency 6 0.029