Search results for "polyposis"

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

447 hits were found for 'polyposis'

# Family MCID Name MIFTS Score
1
P FML011 Familial Adenomatous Polyposis 85 12.449
2
P JVN014 Juvenile Polyposis Syndrome 69 8.059
3
PTZ001 Peutz-Jeghers Syndrome 76 5.636
4
MTY001 Mutyh-Associated Polyposis 51 5.501
5
P HRD069 Hereditary Mixed Polyposis Syndrome 2 26 4.611
6
P ATT003 Attenuated Familial Adenomatous Polyposis 52 4.594
7
CRN014 Cronkhite-Canada Syndrome 50 4.379
8
c FML254 Familial Adenomatous Polyposis Due to 5q22.2 Microdeletion 12 4.237
9
P TRC032 Turcot Syndrome 75 4.059
10
JVN012 Juvenile Polyposis/hereditary Hemorrhagic Telangiectasia Syndrome 22 3.895
11
c HRD101 Hereditary Mixed Polyposis Syndrome 1 10 3.868
12
HYP466 Hyperplastic Polyposis Syndrome 43 3.653
13
c JVN034 Juvenile Polyposis of Infancy 27 3.537
14
CPP003 Cap Polyposis 25 3.297
15
P ADN040 Adenomas, Multiple Colorectal 16 3.044
16
GST086 Gastric Adenocarcinoma and Proximal Polyposis of the Stomach 9 3.014
17
APC006 Apc-Associated Polyposis Conditions 5 3.014
18
BRN074 Brain Tumor-Polyposis Syndrome 2 10 2.996
19
c AXN008 Axin2-Related Attenuated Familial Adenomatous Polyposis 9 2.996
20
P LYN001 Lynch Syndrome 70 2.692
21
GRD002 Gardner Syndrome 33 2.601
22
c BMP001 Bmpr1a-Related Juvenile Polyposis 20 2.485
23
CLR065 Colorectal Adenomatous Polyposis, Autosomal Recessive, with Pilomatricomas 28 2.467
24
JVN023 Juvenile Polyposis Syndrome, Infantile Form 20 2.467
25
NSL012 Nasal Polyposis, Familial 2 2.467
26
c SMD006 Smad4-Related Juvenile Polyposis 8 2.446
27
PRS115 Prosthetic Joint Infection 48 1.757
28
P CLR023 Colorectal Cancer 73 0.453
29
ADN018 Adenoma 64 0.321
30
DDN006 Duodenitis 56 0.247
31
DSM004 Desmoid Tumor 67 0.216
32
P CLN016 Colon Cancer 78 0.208
33
c THY032 Thyroiditis 66 0.186
34
P ADN016 Adenocarcinoma 58 0.182
35
ULC004 Ulcerative Colitis 63 0.173
36
c CLR108 Colorectal Adenoma 44 0.153
37
P SNS014 Sinusitis 57 0.129
38
P AST005 Asthma 88 0.115
39
P RHN004 Rhinitis 65 0.115
40
HPT022 Hepatoblastoma 62 0.115
41
P HRD008 Hereditary Hemorrhagic Telangiectasia 81 0.111
42
THY028 Thyroid Cancer 73 0.105
43
c PNC044 Pancreatitis 69 0.105
44
P PPL020 Papillary Thyroid Carcinoma 58 0.105
45
PRT019 Protein-Losing Enteropathy 50 0.105
46
SYN053 Syndromic Diarrhea 32 0.105
47
HPT023 Hepatocellular Carcinoma 79 0.094
48
MNT001 Mantle Cell Lymphoma 64 0.094
49
GST050 Gastrointestinal System Disease 54 0.094
50
P INF037 Inflammatory Bowel Disease 45 0.094
51
P BRS047 Breast Cancer 100 0.088
52
c CWD001 Cowden Disease 71 0.088
53
ACN002 Acanthosis Nigricans 69 0.088
54
HPT067 Hepatocellular Adenoma 44 0.088
55
P LKM002 Leukemia 77 0.082
56
ART005 Arteriovenous Malformation 62 0.082
57
THR013 Thoracic Outlet Syndrome 52 0.082
58
MNN014 Mononeuritis 51 0.082
59
PCH007 Pouchitis 47 0.082
60
P ATX010 Ataxia Neuropathy Spectrum 41 0.082
61
GST040 Gastric Adenocarcinoma 40 0.082
62
SRC014 Sarcoma 69 0.075
63
ALL003 Allergic Rhinitis 64 0.075
64
P ESP024 Esophagitis 63 0.075
65
P STM004 Stomach Cancer 63 0.075
66
P ESN007 Eosinophilia 61 0.075
67
RTN023 Retinitis 53 0.075
68
BLN003 Blindness 52 0.075
69
GST060 Gastric Cancer, Somatic 50 0.075
70
NSP002 Nasopharyngitis 48 0.075
71
FBR019 Fibromatosis 47 0.075
72
GST039 Gastroduodenitis 30 0.075
73
c BNG076 Benign Exophthalmos Syndrome 22 0.075
74
P ATX002 Ataxia Telangiectasia 86 0.067
75
ANK002 Ankylosing Spondylitis 74 0.067
76
CRH001 Crohn's Disease 74 0.067
77
P ANG001 Angelman Syndrome 70 0.067
78
P HMN010 Hemangioma 70 0.067
79
P MRT001 Muir-Torre Syndrome 68 0.067
80
PPL022 Papilloma 65 0.067
81
c HPT021 Hepatitis 64 0.067
82
ART019 Aortic Valve Stenosis 64 0.067
83
c ACT027 Acute Pancreatitis 63 0.067
84
BNN001 Bannayan-Riley-Ruvalcaba Syndrome 62 0.067
85
c MLT074 Multiple Endocrine Neoplasia 59 0.067
86
PPL002 Papillary Carcinoma 59 0.067
87
INT051 Intussusception 58 0.067
88
MYC002 Mycobacterium Avium Complex Disease 58 0.067
89
ART001 Arterial Tortuosity Syndrome 54 0.067
90
VSM001 Vasomotor Rhinitis 53 0.067
91
AND003 Andersen-Tawil Syndrome 53 0.067
92
JVN033 Juvenile Nasopharyngeal Angiofibroma 51 0.067
93
END072 Endotheliitis 50 0.067
94
NRN002 Neuronitis 43 0.067
95
c FML053 Familial Colorectal Cancer 42 0.067
96
SCL017 Sclerosing Hemangioma 39 0.067
97
PLM018 Pulmonary Sclerosing Hemangioma 33 0.067
98
DDN007 Duodenal Disease 33 0.067
99
DDN010 Duodenum Cancer 23 0.067
100
AND005 Androgen Insensitivity Syndrome, Mild 21 0.067
101
P AMY001 Amyotrophic Lateral Sclerosis 98 0.058
102
P HYP075 Hypertension 85 0.058
103
P GST019 Gastrointestinal Stromal Tumor 82 0.058
104
AND002 Androgen Insensitivity Syndrome 80 0.058
105
P MDL005 Medulloblastoma 77 0.058
106
P LNG032 Lung Cancer 72 0.058
107
BRR003 Barrett's Esophagus 71 0.058
108
P GST044 Gastritis 66 0.058
109
c AXN002 Axenfeld-Rieger Syndrome 66 0.058
110
c INT070 Intestinal Obstruction 63 0.058
111
DFC004 Deficiency Anemia 62 0.058
112
P HST010 Histiocytosis 62 0.058
113
P HRD011 Hereditary Spherocytosis 62 0.058
114
P CWD006 Cowden Syndrome 1 58 0.058
115
P CLR070 Colorectal Cancer, Hereditary Nonpolyposis, Type 1 58 0.058
116
LNG024 Langerhans-Cell Histiocytosis 56 0.058
117
c ACR001 Aicardi-Goutieres Syndrome 53 0.058
118
PRN011 Pernicious Anemia 53 0.058
119
MNT147 Mental Retardation 51 0.058
120
CHL052 Choledochal Cyst 50 0.058
121
PNC019 Pancreatoblastoma 48 0.058
122
SCH016 Schimke Immunoosseous Dysplasia 46 0.058
123
TTR016 Tetra-Amelia Syndrome 41 0.058
124
RCT011 Rectal Prolapse 41 0.058
125
INV006 Inverted Papilloma 40 0.058
126
CRB009 Cerebritis 39 0.058
127
GST063 Gastric Cancer Risk After H. Pylori Infection 37 0.058
128
TFT003 Tufting Enteropathy 28 0.058
129
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.058
130
PRM190 Periampullary Adenoma 7 0.058
131
CYS001 Cystic Fibrosis 96 0.047
132
P PNC035 Pancreatic Cancer 91 0.047
133
P PRS040 Prostate Cancer 87 0.047
134
MTC003 Metachromatic Leukodystrophy 86 0.047
135
P OVR042 Ovarian Cancer 81 0.047
136
P RTN024 Retinoblastoma 81 0.047
137
SKN016 Skin Disease 75 0.047
138
c NNN003 Noonan Syndrome 73 0.047
139
GLN003 Glanzmann's Thrombasthenia 73 0.047
140
P END042 Endometrial Carcinoma 72 0.047
141
GLL008 Gilles De La Tourette Syndrome 70 0.047
142
PSD007 Pseudomyxoma Peritonei 67 0.047
143
P ART023 Arthropathy 63 0.047
144
CMM004 Common Variable Immunodeficiency 63 0.047
145
c MSC005 Muscular Dystrophy 62 0.047
146
BRN028 Brain Cancer 62 0.047
147
TTR011 Tetraploidy 61 0.047
148
PRS047 Prostatitis 60 0.047
149
HYP266 Hypoxia 57 0.047
150
SNS001 Sensorineural Hearing Loss 57 0.047
151
ETN001 Eating Disorder 57 0.047
152
ART017 Aortic Disease 56 0.047
153
ACN001 Acinar Cell Carcinoma 55 0.047
154
ADR008 Adrenal Adenoma 55 0.047
155
LPM005 Lipomatosis 54 0.047
156
c LYM026 Lymphoblastic Leukemia 54 0.047
157
PRT018 Portal Vein Thrombosis 54 0.047
158
ACH005 Achalasia 54 0.047
159
P EHL049 Ehlers–danlos Syndrome Classical Type 53 0.047
160
P ESN001 Eosinophilic Esophagitis 53 0.047
161
CLN019 Colonic Disease 53 0.047
162
LKD001 Leukodystrophy 52 0.047
163
EXS001 Exostosis 51 0.047
164
c TCL004 T-Cell Leukemia 50 0.047
165
CYS009 Cystadenoma 50 0.047
166
TLN003 Telangiectasis 49 0.047
167
P GRM009 Germ Cell Tumors 49 0.047
168
SKN023 Skin Tag 49 0.047
169
IMP002 Imperforate Anus 48 0.047
170
PLM026 Pilomatrixoma 48 0.047
171
URT010 Ureteral Obstruction 47 0.047
172
NNP001 Nonpapillary Renal Cell Carcinoma 46 0.047
173
EVN001 Evans' Syndrome 46 0.047
174
c ADL017 Adult T-Cell Leukemia 46 0.047
175
P PNB001 Pineoblastoma 46 0.047
176
MCP006 Mucoepidermoid Carcinoma 46 0.047
177
PLM052 Pulmonary Arteriovenous Malformation 45 0.047
178
FBR054 Fibroma 45 0.047
179
RVL002 Ruvalcaba Syndrome 45 0.047
180
P FCS001 Facioscapulohumeral Muscular Dystrophy 44 0.047
181
CRB022 Cerebellar Liponeurocytoma 43 0.047
182
LNG029 Lung Adenocarcinoma 42 0.047
183
CLR034 Colorectal Cancer, Somatic 42 0.047
184
P SRT002 Sertoli Cell Tumor 41 0.047
185
P CHR038 Chronic Maxillary Sinusitis 39 0.047
186
AMP009 Ampulla of Vater Adenocarcinoma 36 0.047
187
ORL015 Oral Squamous Cell Carcinoma 36 0.047
188
MDL012 Medulloblastoma, Desmoplastic 34 0.047
189
RCT018 Rectal Neoplasm 32 0.047
190
PNC073 Pancreatic Carcinoma, Somatic 31 0.047
191
RHN002 Rhinoscleroma 28 0.047
192
P ATS008 Autosomal Dominant Disease 28 0.047
193
c ATS021 Autosomal Recessive Juvenile Parkinson Disease 26 0.047
194
PNM003 Pneumatosis Cystoides Intestinalis 26 0.047
195
FLR003 Florid Cemento-Osseous Dysplasia 22 0.047
196
c FML143 Familial Papillary Thyroid Carcinoma 15 0.047
197
c TYP009 Type 2 Diabetes Mellitus 95 0.033
198
P RHM011 Rheumatoid Arthritis 93 0.033
199
P OBS005 Obesity 89 0.033
200
P LFR001 Li-Fraumeni Syndrome 87 0.033
201
P HNT001 Huntington's Disease 85 0.033
202
MRF001 Marfan Syndrome 83 0.033
203
P SCH015 Schizophrenia 82 0.033
204
P CSH001 Cushing's Syndrome 80 0.033
205
P HRS001 Hirschsprung's Disease 80 0.033
206
P ALG002 Alagille Syndrome 80 0.033
207
ESP021 Esophageal Cancer 80 0.033
208
c DBT009 Diabetes Mellitus 78 0.033
209
ACH004 Achondroplasia 78 0.033
210
P ACT074 Acute Lymphocytic Leukemia 75 0.033
211
TTR001 Tetralogy of Fallot 74 0.033
212
P LPR002 Leopard Syndrome 73 0.033
213
P THY014 Thyroid Medullary Carcinoma 73 0.033
214
HYP458 Hyper Ige Syndrome 71 0.033
215
PRT036 Peritonitis 71 0.033
216
P AST007 Astrocytoma 71 0.033
217
c CHR065 Chronic Myeloid Leukemia 71 0.033
218
CHR029 Choroid Plexus Papilloma 70 0.033
219
SCH014 Schistosomiasis 70 0.033
220
P MLT042 Multiple Endocrine Neoplasia Type 2a 70 0.033
221
P END044 Endometriosis 69 0.033
222
CHL065 Cholangiocarcinoma 69 0.033
223
c HYP086 Hypothyroidism 69 0.033
224
P RSP003 Respiratory Failure 68 0.033
225
P DRM010 Dermatomyositis 68 0.033
226
c HPT016 Hepatitis B 68 0.033
227
LMY002 Leiomyoma 67 0.033
228
GST023 Gastric Ulcer 67 0.033
229
P NNN008 Noonan Syndrome 1 66 0.033
230
NVD001 Nevoid Basal Cell Carcinoma Syndrome 66 0.033
231
GLL018 Gallbladder Cancer 66 0.033
232
P PRT013 Portal Hypertension 66 0.033
233
SHG001 Shigellosis 65 0.033
234
c MTR004 Maturity-Onset Diabetes of the Young 65 0.033
235
GST034 Gastroesophageal Reflux Disease 64 0.033
236
PLM033 Pulmonary Embolism 64 0.033
237
LPM004 Lipoma 64 0.033
238
P BSL007 Basal Cell Carcinoma 63 0.033
239
PRL009 Prolactinoma 63 0.033
240
CMM005 Common Cold 63 0.033
241
c HYP061 Hypertrophic Cardiomyopathy 63 0.033
242
TRN018 Transitional Cell Carcinoma 63 0.033
243
P MLN008 Melanoma 63 0.033
244
PTT006 Pituitary Adenoma 63 0.033
245
CYS005 Cysticercosis 63 0.033
246
FLL032 Follicular Thyroid Carcinoma 63 0.033
247
CRN036 Craniopharyngioma 63 0.033
248
CHG001 Chagas Disease 62 0.033
249
NSP001 Nasopharynx Carcinoma 62 0.033
250
PLM014 Pleomorphic Adenoma 62 0.033
251
PRT092 Partial Androgen Insensitivity Syndrome 62 0.033
252
P PRT010 Parathyroid Carcinoma 62 0.033
253
GLS001 Gliosarcoma 61 0.033
254
BRN022 Bronchiectasis 61 0.033
255
PLM032 Pulmonary Blastoma 61 0.033
256
CRC006 Carcinoid Syndrome 61 0.033
257
P DDN001 Duodenal Ulcer 60 0.033
258
ADR015 Adrenocortical Carcinoma 60 0.033
259
EYD002 Eye Disease 60 0.033
260
PRM027 Primitive Neuroectodermal Tumor 60 0.033
261
ISV001 Isovaleric Acidemia 60 0.033
262
SPN020 Spondylosis 59 0.033
263
CHR074 Choriocarcinoma 59 0.033
264
GLM008 Glomus Tumor 59 0.033
265
MGC001 Megacolon 59 0.033
266
P ATS007 Autism Spectrum Disorder 59 0.033
267
P LRY016 Laryngeal Carcinoma 59 0.033
268
P PTT014 Pitt-Hopkins Syndrome 59 0.033
269
TST014 Testicular Cancer 58 0.033
270
MYX005 Myxoid Liposarcoma 58 0.033
271
PLM020 Pleomorphic Xanthoastrocytoma 57 0.033
272
RHB003 Rhabdomyosarcoma 57 0.033
273
URN010 Urinary Tract Obstruction 57 0.033
274
MRG003 Marginal Zone B-Cell Lymphoma 57 0.033
275
GRW001 Growth Hormone Secreting Pituitary Adenoma 57 0.033
276
INS002 in Situ Carcinoma 57 0.033
277
CHR001 Churg-Strauss Syndrome 57 0.033
278
IRN001 Iron Deficiency Anemia 57 0.033
279
ALV005 Alveolar Soft Part Sarcoma 57 0.033
280
BRT002 Birt-Hogg-Dube Syndrome 56 0.033
281
ALP008 Alopecia 56 0.033
282
VLV044 Vulvar Intraepithelial Neoplasia 56 0.033
283
LRY018 Laryngeal Squamous Cell Carcinoma 56 0.033
284
c PRM011 Primary Ciliary Dyskinesia 56 0.033
285
HMM003 Hemimegalencephaly 55 0.033
286
HST009 Histiocytoma 55 0.033
287
GNT002 Giant Cell Glioblastoma 55 0.033
288
P HRD027 Hereditary Diffuse Gastric Cancer 55 0.033
289
c TRT010 Teratoma 55 0.033
290
FBR003 Fibrous Histiocytoma 54 0.033
291
NPH011 Nephroblastoma 54 0.033
292
ORL004 Oral Submucous Fibrosis 54 0.033
293
MCN001 Mucinous Adenocarcinoma 54 0.033
294
SRC002 Sarcomatoid Renal Cell Carcinoma 54 0.033
295
BRK001 Brooke-Spiegler Syndrome 54 0.033
296
LYS001 Loeys-Dietz Syndrome 54 0.033
297
BLS003 Blastoma 53 0.033
298
c ADN012 Adenocarcinoma in Situ 53 0.033
299
PLS025 Plasmablastic Lymphoma 53 0.033
300
c DFF019 Diffuse Gastric Cancer 53 0.033
301
P CNT005 Central Nervous System Lymphoma 52 0.033
302
ATP002 Atopy 52 0.033
303
RSD004 Rosai-Dorfman Disease 52 0.033
304
P STR020 Strabismus 51 0.033
305
c FML024 Familial Melanoma 51 0.033
306
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 51 0.033
307
HPT032 Hepatocellular Carcinoma, Somatic 51 0.033
308
c BRS049 Breast Carcinoma in Situ 51 0.033
309
c KRT005 Keratoacanthoma 51 0.033
310
c ATM024 Autoimmune Pancreatitis 50 0.033
311
ACR012 Aicardi Syndrome 50 0.033
312
c INT191 Intestinal Lymphangiectasia 50 0.033
313
FML027 Female Breast Carcinoma 50 0.033
314
MYP001 Myoepithelioma 50 0.033
315
c STS001 Sotos Syndrome 49 0.033
316
P PLM030 Pleomorphic Rhabdomyosarcoma 49 0.033
317
DBW001 Dubowitz Syndrome 49 0.033
318
DVR002 Diverticulitis 49 0.033
319
P PRK001 Porokeratosis 49 0.033
320
GNG002 Ganglioneuroma 49 0.033
321
EPT010 Epithelial-Myoepithelial Carcinoma 49 0.033
322
CRV038 Cervical Squamous Cell Carcinoma 49 0.033
323
SKN022 Skin Squamous Cell Carcinoma 49 0.033
324
P BCL006 B-Cell Lymphomas 49 0.033
325
ALC010 Alcoholic Cardiomyopathy 48 0.033
326
P BLD034 Bile Duct Carcinoma 48 0.033
327
c BRC032 Brachydactyly Type A2 48 0.033
328
IMM060 Immunodeficiency, Common Variable, 9 48 0.033
329
PNC033 Pancreas Adenocarcinoma 47 0.033
330
c GGN002 Gigantism 47 0.033
331
NNT016 Neonatal Hemochromatosis 47 0.033
332
CHN005 Choanal Atresia 47 0.033
333
CMM014 Common Variable Immune Deficiency 47 0.033
334
c CHR048 Chronic Rhinitis 47 0.033
335
LYM052 Lymphomatoid Papulosis 47 0.033
336
NRM004 Neuroma 47 0.033
337
GBL002 Goblet Cell Carcinoid 47 0.033
338
LBL001 Lobular Neoplasia 47 0.033
339
PNC013 Pancreatic Ductal Carcinoma 46 0.033
340
ASC002 Ascariasis 46 0.033
341
GST030 Gastrinoma 46 0.033
342
INT069 Intestinal Neoplasm 46 0.033
343
P ATR005 Atrophic Gastritis 46 0.033
344
LPD006 Lipoid Proteinosis 45 0.033
345
BWN003 Bowenoid Papulosis 45 0.033
346
P CNG390 Congenital Pulmonary Airway Malformation 45 0.033
347
SFT003 Soft Tissue Sarcoma 45 0.033
348
CRP018 Cor Pulmonale 44 0.033
349
c HRD004 Hereditary Breast Ovarian Cancer 44 0.033
350
MLG083 Male Germ Cell Tumor 44 0.033
351
OVR078 Ovarian Cancer, Somatic 44 0.033
352
HPY002 H. Pylori Infection 44 0.033
353
P CYS017 Cystic Teratoma 44 0.033
354
SML032 Small Bowel Adenocarcinoma 44 0.033
355
UTR024 Uterine Carcinosarcoma 44 0.033
356
CTN026 Cutaneous Neuroendocrine Carcinoma 43 0.033
357
MCR014 Microcystic Adenoma 43 0.033
358
SPR033 Superficial Spreading Melanoma 43 0.033
359
OVR054 Ovarian Mucinous Neoplasm 43 0.033
360
VLL006 Villous Adenoma 42 0.033
361
CRB002 Cerebral Primitive Neuroectodermal Tumor 42 0.033
362
OPT007 Optic Nerve Glioma 41 0.033
363
P THR027 Thoracic Aortic Aneurysms and Aortic Dissections 41 0.033
364
ESP028 Esophageal Squamous Cell Carcinoma 40 0.033
365
ATR013 Atrichia with Papular Lesions 40 0.033
366
BLD101 Bladder Cancer Susceptibility 40 0.033
367
c ACT115 Acute Myeloid Leukemia, Adult 40 0.033
368
c CHR208 Chromosome 17p Deletion 40 0.033
369
BRN015 Bronchiolo-Alveolar Adenocarcinoma 40 0.033
370
LMY003 Leiomyomatosis 39 0.033
371
THY042 Thymic Epithelial Tumor 39 0.033
372
CRB028 Cerebellar Medulloblastoma 39 0.033
373
c CHR253 Chromosome 5q Deletion 39 0.033
374
GRM004 Germinoma 39 0.033
375
INT040 Intrinsic Asthma 39 0.033
376
P MSC109 Mosaic Variegated Aneuploidy Syndrome 1 39 0.033
377
GST064 Gastric Outlet Obstruction 39 0.033
378
ANC001 Ancylostomiasis 39 0.033
379
c SPH018 Spherocytosis, Hereditary, Type 5 38 0.033
380
ANG037 Angiomatosis 38 0.033
381
c JVN024 Juvenile Hereditary Hemochromatosis 38 0.033
382
VCL001 Vacuolar Myopathy 38 0.033
383
AMP010 Ampulla of Vater Carcinoma 37 0.033
384
PTN006 Pten Hamartoma Tumor Syndrome 37 0.033
385
IPX001 Ipex Syndrome 37 0.033
386
ESN020 Eosinophilic Granulomatosis with Polyangiitis 36 0.033
387
OST111 Osteoporosis, Early-Onset Autosomal Dominant 36 0.033
388
UTR033 Uterine Corpus Cancer 35 0.033
389
MNP001 Monophasic Synovial Sarcoma 35 0.033
390
BLR005 Biliary Papillomatosis 35 0.033
391
ADS002 Adie Syndrome 35 0.033
392
CLC010 Calcifying Epithelial Odontogenic Tumor 34 0.033
393
c CHR243 Chromosome 3p Deletion 34 0.033
394
BNM001 Bone Marrow Cancer 34 0.033
395
OVR011 Ovarian Mucinous Adenocarcinoma 33 0.033
396
INT017 Intestinal Schistosomiasis 33 0.033
397
FCT013 Factor V Leiden Thrombophilia 33 0.033
398
ATY009 Atypical Polypoid Adenomyoma 33 0.033
399
SPR001 Superficial Urinary Bladder Cancer 32 0.033
400
BRS015 Breast Medullary Carcinoma 32 0.033
401
CLR109 Colorectal Adenocarcinoma 32 0.033
402
c CRN035 Cranial Nerve Palsy 31 0.033
403
BLD039 Bladder Adenocarcinoma 31 0.033
404
TST021 Testicular Germ Cell Tumor 31 0.033
405
MTR008 Mature B-Cell Neoplasm 31 0.033
406
c ADV001 Advanced Sleep Phase Syndrome 31 0.033
407
THY059 Thyroid Carcinoma, Follicular, Somatic 31 0.033
408
AMY016 Amyopathic Dermatomyositis 30 0.033
409
HPT033 Hepatoblastoma, Somatic 30 0.033
410
TXC001 Toxic Megacolon 29 0.033
411
FSC006 Fascioscapulohumeral Muscular Dystrophy 2, Digenic 29 0.033
412
PDT027 Pediatric Ulcerative Colitis 28 0.033
413
ANG004 Angioid Streaks 28 0.033
414
CLN030 Colon Cancer, Somatic 28 0.033
415
ADN034 Adenocarcinoma, Ovarian, Somatic 28 0.033
416
NNS020 Nonsmall Cell Lung Cancer, Somatic 28 0.033
417
TNS007 Taeniasis 28 0.033
418
DDN009 Duodenal Obstruction 28 0.033
419
STM006 Stomach Disease 28 0.033
420
HPT012 Hepatocellular Fibrolamellar Carcinoma 27 0.033
421
HNM002 Hinman Syndrome 27 0.033
422
END016 Endocervicitis 27 0.033
423
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 27 0.033
424
VNH006 Von Hippel-Lindau Syndrome, Modifier of 26 0.033
425
LNG061 Lung Cancer, Somatic 26 0.033
426
CHR034 Chromophobe Adenoma 26 0.033
427
CLN029 Colonic Adenoma Recurrence, Reduced Risk of 26 0.033
428
P HYP078 Hypertrophy of Breast 25 0.033
429
c CHR036 Chronic Cholangitis 25 0.033
430
c FRT001 Fourth Cranial Nerve Palsy 24 0.033
431
TST018 Testicular Yolk Sac Tumor 24 0.033
432
GST006 Gastric Leiomyoma 23 0.033
433
RNL068 Renal Cell Carcinoma, Clear Cell, Somatic 23 0.033
434
RSS008 Ras-Associated Autoimmune Leukoproliferative Disease 23 0.033
435
BLD063 Bile Duct Cysts 23 0.033
436
MLL004 Mallory-Weiss Syndrome 21 0.033
437
RCT017 Rectal Disease 20 0.033
438
RCT020 Rectum Adenocarcinoma 20 0.033
439
DSS008 Disease of Mental Health 20 0.033
440
GRN011 Granulomatous Gastritis 19 0.033
441
ESN014 Eosinophilic Enteropathy 16 0.033
442
JJN002 Jejunal Neoplasm 16 0.033
443
OTP003 Oto-Palatal-Digital Syndrome 16 0.033
444
10Q001 10q22.3q23.3 Microdeletion Syndrome 15 0.033
445
AST038 Asthma, Aspirin-Induced 11 0.033
446
CNT045 Central Nervous System Sarcoma 10 0.033
447
JNS001 Janus Kinase-3 Deficiency 8 0.033