Search results for "polyposis"

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

576 hits were found for 'polyposis'

# Family MCID Name MIFTS Score
1
ADN021 Adenomatous Polyposis Coli 76 11.069
2
PLY056 Polyposis, Juvenile Intestinal 55 8.287
3
MTY001 Mutyh-Associated Polyposis 47 5.510
4
P ATT003 Attenuated Familial Adenomatous Polyposis 45 4.957
5
PTZ001 Peutz-Jeghers Syndrome 70 4.819
6
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 36 4.144
7
c ADN040 Adenomas, Multiple Colorectal 28 3.876
8
MSM014 Mismatch Repair Cancer Syndrome 59 3.861
9
JVN012 Juvenile Polyposis/hereditary Hemorrhagic Telangiectasia Syndrome 26 3.861
10
c PLY066 Polyposis Syndrome, Hereditary Mixed, 2 17 3.836
11
c HRD101 Hereditary Mixed Polyposis Syndrome 1 37 3.687
12
FML299 Familial Adenomatous Polyposis 3 24 3.612
13
FML254 Familial Adenomatous Polyposis Due to 5q22.2 Microdeletion 8 3.471
14
CHR595 Chromosome 10q23 Deletion Syndrome Juvenile Polyposis of Infancy, Included 25 3.132
15
P CLR070 Colorectal Cancer, Hereditary Nonpolyposis, Type 1 55 3.121
16
P LYN001 Lynch Syndrome 69 2.981
17
c EPC004 Epcam-Related Lynch Syndrome 14 2.670
18
CPP003 Cap Polyposis 34 2.515
19
HYP466 Hyperplastic Polyposis Syndrome 31 2.412
20
GST086 Gastric Adenocarcinoma and Proximal Polyposis of the Stomach 10 2.265
21
APC006 Apc-Associated Polyposis Conditions 4 2.242
22
CLR065 Colorectal Adenomatous Polyposis, Autosomal Recessive, with Pilomatricomas 46 2.215
23
c CLR037 Colorectal Cancer, Hereditary Nonpolyposis, Type 5 27 2.215
24
c CLR039 Colorectal Cancer, Hereditary Nonpolyposis, Type 4 26 2.215
25
c CLR055 Colorectal Cancer, Hereditary Nonpolyposis, Type 6 25 2.215
26
c CLR100 Colorectal Cancer, Hereditary Nonpolyposis, Type 7 19 2.215
27
c AXN008 Axin2-Related Attenuated Familial Adenomatous Polyposis 8 2.215
28
P HRD144 Hereditary Mixed Polyposis Syndrome 24 1.750
29
c CLR041 Colorectal Cancer, Hereditary Nonpolyposis, Type 2 24 1.601
30
P BMP001 Bmpr1a-Related Juvenile Polyposis 15 1.601
31
NNP013 Non-Polyposis Turcot Syndrome 11 1.601
32
NSL012 Nasal Polyposis, Familial 4 1.601
33
c CLR089 Colorectal Cancer, Hereditary Nonpolyposis, Type 8 19 1.585
34
PLY138 Polymerase Proofreading-Related Adenomatous Polyposis 15 1.585
35
c SMD006 Smad4-Related Juvenile Polyposis 2 1.585
36
PRS115 Prosthetic Joint Infection 43 1.566
37
c MSH002 Msh2-Related Lynch Syndrome 8 1.541
38
c MSH005 Msh6-Related Lynch Syndrome 8 1.541
39
c PMS003 Pms2-Related Lynch Syndrome 8 1.541
40
c MLH002 Mlh1-Related Lynch Syndrome 8 1.541
41
c MLH005 Mlh3-Related Lynch Syndrome 8 1.541
42
c PMS002 Pms1-Related Lynch Syndrome 7 1.541
43
5Q2001 5q22 Deletion Syndrome 6 1.541
44
P CLR023 Colorectal Cancer 97 0.478
45
ADN018 Adenoma 59 0.356
46
DDN006 Duodenitis 44 0.247
47
P CLR108 Colorectal Adenoma 60 0.212
48
DSM004 Desmoid Tumor 51 0.201
49
CLN019 Colonic Disease 50 0.199
50
INT253 Intestinal Benign Neoplasm 50 0.192
51
RCT017 Rectal Disease 39 0.187
52
RCT018 Rectal Neoplasm 55 0.185
53
CLT003 Colitis 59 0.180
54
c HRD169 Hereditary Colorectal Cancer 43 0.180
55
P ADN016 Adenocarcinoma 69 0.178
56
P THY032 Thyroiditis 54 0.178
57
CLN044 Colon Adenoma 45 0.178
58
P NSP012 Nasopharyngeal Carcinoma 67 0.172
59
ALC007 Alcohol Dependence 65 0.172
60
PHR003 Pharyngitis 58 0.172
61
NSP003 Nasopharyngeal Disease 30 0.172
62
ULC004 Ulcerative Colitis 75 0.170
63
c FML053 Familial Colorectal Cancer 50 0.170
64
CRV068 Cervical Polyp 41 0.170
65
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 31 0.167
66
c CLR079 Colorectal Cancer 2 31 0.159
67
GST038 Gastrointestinal Adenoma 29 0.159
68
c INF067 Inflammatory Bowel Disease 10 51 0.147
69
P SNS014 Sinusitis 60 0.144
70
PRP021 Peripheral Nervous System Neoplasm 50 0.138
71
DDN007 Duodenal Disease 34 0.138
72
P AST005 Asthma 82 0.134
73
c CLR085 Colorectal Cancer 1 42 0.134
74
c CLR075 Colorectal Cancer 3 30 0.134
75
c INF078 Inflammatory Bowel Disease 2 24 0.131
76
P INT068 Intestinal Disease 61 0.124
77
DDN010 Duodenum Cancer 44 0.124
78
P LYM118 Lymphoma 70 0.120
79
NSD001 Nose Disease 52 0.120
80
P GST049 Gastrointestinal System Cancer 60 0.116
81
SNS023 Sensory System Cancer 46 0.116
82
HRD059 Hereditary Peripheral Nervous Disorder 14 0.116
83
DDN022 Duodenum Adenoma 12 0.116
84
P RHN004 Rhinitis 61 0.112
85
GST053 Gastric Cancer 77 0.108
86
P HRD008 Hereditary Hemorrhagic Telangiectasia 71 0.108
87
c INF071 Inflammatory Bowel Disease 1 51 0.108
88
PRT019 Protein-Losing Enteropathy 41 0.108
89
c INF086 Inflammatory Bowel Disease 3 21 0.108
90
THY028 Thyroid Cancer 68 0.100
91
P NRV006 Nervous System Cancer 62 0.100
92
P PNC044 Pancreatitis 60 0.100
93
PRN021 Paranasal Sinus Disease 50 0.100
94
NSL022 Nasal Cavity Disease 42 0.100
95
ORL014 Oral Pharyngeal Disorders 14 0.100
96
P BRS047 Breast Cancer 100 0.095
97
P CWD006 Cowden Syndrome 1 68 0.095
98
BNN001 Bannayan-Riley-Ruvalcaba Syndrome 54 0.095
99
HPT022 Hepatoblastoma 53 0.095
100
c INF087 Inflammatory Bowel Disease 4 27 0.095
101
c CLR080 Colorectal Cancer 5 35 0.090
102
HPT023 Hepatocellular Carcinoma 91 0.085
103
MNT001 Mantle Cell Lymphoma 70 0.085
104
GST040 Gastric Adenocarcinoma 52 0.085
105
PPL022 Papilloma 55 0.079
106
DSM003 Desmoid Disease, Hereditary 44 0.079
107
HPT067 Hepatocellular Adenoma 42 0.079
108
PCH007 Pouchitis 40 0.079
109
c CLR077 Colorectal Cancer 10 31 0.079
110
GST039 Gastroduodenitis 31 0.079
111
c CLR081 Colorectal Cancer 6 24 0.079
112
P LKM002 Leukemia 70 0.074
113
SRC014 Sarcoma 66 0.074
114
ALL003 Allergic Rhinitis 64 0.074
115
WST001 West Syndrome 61 0.074
116
P GLM045 Glioma 58 0.074
117
WLL006 Wells Syndrome 56 0.074
118
GST050 Gastrointestinal System Disease 54 0.074
119
RTN023 Retinitis 49 0.074
120
GDS001 Good Syndrome 45 0.074
121
P PRN020 Paranasal Sinus Cancer 41 0.074
122
P NSL008 Nasal Cavity Cancer 37 0.074
123
ALR002 Al-Raqad Syndrome 36 0.074
124
c CLR087 Colorectal Cancer 12 33 0.074
125
P SNS011 Sinus Cancer 25 0.074
126
c INF088 Inflammatory Bowel Disease 5 21 0.074
127
c PRN030 Paranasal Sinus Cancer, Adult 15 0.074
128
P ESP024 Esophagitis 62 0.067
129
P ESN007 Eosinophilia 61 0.067
130
ORL015 Oral Squamous Cell Carcinoma 56 0.067
131
P INT070 Intestinal Obstruction 56 0.067
132
c INH020 Inherited Metabolic Disorder 49 0.067
133
GNG002 Ganglioneuroma 48 0.067
134
ATN003 Autonomic Nervous System Neoplasm 43 0.067
135
END072 Endotheliitis 42 0.067
136
FBR019 Fibromatosis 42 0.067
137
NRN002 Neuronitis 42 0.067
138
c AST039 Asthma 2 31 0.067
139
FNC005 Functional Colonic Disease 30 0.067
140
c CLR083 Colorectal Cancer 8 27 0.067
141
AND005 Androgen Insensitivity Syndrome, Mild 16 0.067
142
P LNG032 Lung Cancer 94 0.060
143
CRH001 Crohn's Disease 76 0.060
144
P RTN024 Retinoblastoma 75 0.060
145
P HPT021 Hepatitis 70 0.060
146
ART005 Arteriovenous Malformation 65 0.060
147
P HMN010 Hemangioma 60 0.060
148
P SHR029 Short Syndrome 60 0.060
149
P MRT001 Muir-Torre Syndrome 58 0.060
150
ALL006 Allergic Asthma 58 0.060
151
PRS047 Prostatitis 56 0.060
152
P MLT074 Multiple Endocrine Neoplasia 55 0.060
153
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.060
154
P SML016 Small Intestine Cancer 54 0.060
155
CLR109 Colorectal Adenocarcinoma 50 0.060
156
STM006 Stomach Disease 50 0.060
157
CSY001 C Syndrome 49 0.060
158
P SHR001 Short Bowel Syndrome 48 0.060
159
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 46 0.060
160
AML029 Ameloblastoma 46 0.060
161
FBR054 Fibroma 43 0.060
162
NSP002 Nasopharyngitis 41 0.060
163
INV006 Inverted Papilloma 40 0.060
164
CRB009 Cerebritis 38 0.060
165
VSM001 Vasomotor Rhinitis 35 0.060
166
JJN003 Jejunal Cancer 30 0.060
167
AST038 Asthma, Aspirin-Induced 28 0.060
168
ILM001 Ileum Cancer 27 0.060
169
c CWD005 Cowden Syndrome 4 23 0.060
170
c INF073 Inflammatory Bowel Disease 12 21 0.060
171
c INF091 Inflammatory Bowel Disease 8 20 0.060
172
c INF075 Inflammatory Bowel Disease 16 20 0.060
173
RCT035 Rectum Adenoma 16 0.060
174
CYS001 Cystic Fibrosis 86 0.052
175
P SCH015 Schizophrenia 76 0.052
176
END057 Endometrial Cancer 75 0.052
177
P MTC003 Metachromatic Leukodystrophy 71 0.052
178
OCL009 Ocular Cancer 62 0.052
179
P GST044 Gastritis 58 0.052
180
P LKD001 Leukodystrophy 58 0.052
181
P ORL007 Oral Cavity Cancer 58 0.052
182
c ADL017 Adult T-Cell Leukemia 58 0.052
183
CND002 Conduct Disorder 56 0.052
184
c ACT027 Acute Pancreatitis 56 0.052
185
ORL011 Oral Cancer 55 0.052
186
HYP266 Hypoxia 55 0.052
187
HDN004 Head and Neck Carcinoma 55 0.052
188
P HST010 Histiocytosis 55 0.052
189
NRN004 Neuroendocrine Tumor 54 0.052
190
VSC006 Vascular Cancer 54 0.052
191
PPL002 Papillary Carcinoma 49 0.052
192
P TRC086 Trichohepatoenteric Syndrome 1 46 0.052
193
P TCL004 T-Cell Leukemia 46 0.052
194
RCT011 Rectal Prolapse 43 0.052
195
c PRM023 Pre-Malignant Neoplasm 43 0.052
196
ATS008 Autosomal Dominant Disease 42 0.052
197
GST071 Gastrointestinal Carcinoma 41 0.052
198
SCL017 Sclerosing Hemangioma 41 0.052
199
JVN033 Juvenile Nasopharyngeal Angiofibroma 39 0.052
200
PLM018 Pulmonary Sclerosing Hemangioma 39 0.052
201
P MXL015 Maxillary Sinusitis 38 0.052
202
TTR016 Tetra-Amelia Syndrome 36 0.052
203
c CHR038 Chronic Maxillary Sinusitis 35 0.052
204
c AST037 Asthma 1 31 0.052
205
c CLR082 Colorectal Cancer 7 23 0.052
206
c CLR084 Colorectal Cancer 9 20 0.052
207
c INF079 Inflammatory Bowel Disease 20 20 0.052
208
c INF089 Inflammatory Bowel Disease 6 20 0.052
209
c INF090 Inflammatory Bowel Disease 7 19 0.052
210
CLF045 Cleft, Median, of Upper Lip with Polyps of Facial Skin and Nasal Mucosa 19 0.052
211
c FML303 Familial/multiple Cancer 16 0.052
212
LRG015 Large Intestine Adenoma 15 0.052
213
P PRS040 Prostate Cancer 89 0.042
214
P PNC035 Pancreatic Cancer 85 0.042
215
P HNT016 Huntington Disease 80 0.042
216
P MDL005 Medulloblastoma 77 0.042
217
P OVR042 Ovarian Cancer 75 0.042
218
GST019 Gastrointestinal Stromal Tumor 72 0.042
219
PRP027 Peripheral Vascular Disease 69 0.042
220
PCK002 Pick Disease 67 0.042
221
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.042
222
c MLT024 Multiple Endocrine Neoplasia Iia 65 0.042
223
c BSL007 Basal Cell Carcinoma 64 0.042
224
c HPT016 Hepatitis B 64 0.042
225
P ATS007 Autism Spectrum Disorder 64 0.042
226
ATP002 Atopy 63 0.042
227
P PRT010 Parathyroid Carcinoma 62 0.042
228
PRT036 Peritonitis 62 0.042
229
GST092 Gastroesophageal Reflux 61 0.042
230
P LYM026 Lymphoblastic Leukemia 60 0.042
231
P MYP006 Myopia 59 0.042
232
P HRS035 Hirschsprung Disease 1 59 0.042
233
URT039 Urticaria 59 0.042
234
PLY023 Polycystic Liver Disease 57 0.042
235
ALP008 Alopecia 55 0.042
236
CHN016 Cohen Syndrome 55 0.042
237
THY103 Thyroid Cancer, Monmedullary, 1 54 0.042
238
P HRD011 Hereditary Spherocytosis 53 0.042
239
P LCH002 Lichen Planus 53 0.042
240
P INT063 Intellectual Disability 53 0.042
241
ALL026 Allergic Hypersensitivity Disease 53 0.042
242
PSD012 Pseudoachondroplasia 51 0.042
243
HNT002 Hantavirus Pulmonary Syndrome 51 0.042
244
HPT074 Hepatic Adenoma, Somatic 51 0.042
245
P DRR001 Diarrhea 51 0.042
246
ORL004 Oral Submucous Fibrosis 51 0.042
247
INT051 Intussusception 50 0.042
248
CLN015 Colon Adenocarcinoma 49 0.042
249
ILT001 Ileitis 49 0.042
250
URB001 Urbach-Wiethe Disease 48 0.042
251
c PRK024 Parkinson Disease, Juvenile, Type 2 48 0.042
252
ACD009 Acid-Labile Subunit, Deficiency of 48 0.042
253
ORL013 Oral Lichen Planus 47 0.042
254
LPM005 Lipomatosis 47 0.042
255
c CLR017 Clear Cell Sarcoma 46 0.042
256
CHR074 Choriocarcinoma 46 0.042
257
PRN011 Pernicious Anemia 46 0.042
258
SKN023 Skin Tag 46 0.042
259
P KRT005 Keratoacanthoma 45 0.042
260
ACR012 Aicardi Syndrome 45 0.042
261
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.042
262
ANS011 Anus Cancer 44 0.042
263
EXS001 Exostosis 44 0.042
264
P CRN035 Cranial Nerve Palsy 43 0.042
265
END080 Endometrial Disease 42 0.042
266
P MSC022 Mosaic Variegated Aneuploidy Syndrome 42 0.042
267
TST018 Testicular Yolk Sac Tumor 42 0.042
268
GST078 Gastrointestinal Allergy 41 0.042
269
BRL011 Bare Lymphocyte Syndrome, Type I 41 0.042
270
TTR011 Tetraploidy 41 0.042
271
INT040 Intrinsic Asthma 40 0.042
272
CHL052 Choledochal Cyst 40 0.042
273
BLD054 Blood Protein Disease 40 0.042
274
RDN001 Reading Disorder 39 0.042
275
c CHR048 Chronic Rhinitis 39 0.042
276
NSY001 N Syndrome 39 0.042
277
ADJ001 Adjustment Disorder 38 0.042
278
ESN020 Eosinophilic Granulomatosis with Polyangiitis 38 0.042
279
P BNG071 Benign Schwannoma 37 0.042
280
PLM052 Pulmonary Arteriovenous Malformation 34 0.042
281
RHN002 Rhinoscleroma 34 0.042
282
PTN006 Pten Hamartoma Tumor Syndrome 34 0.042
283
ANS012 Anus Disease 32 0.042
284
PNC019 Pancreatoblastoma 32 0.042
285
P FRT001 Fourth Cranial Nerve Palsy 31 0.042
286
RVL002 Ruvalcaba Syndrome 31 0.042
287
P ATX010 Ataxia Neuropathy Spectrum 28 0.042
288
PRM190 Periampullary Adenoma 28 0.042
289
FML143 Familial Papillary Thyroid Carcinoma 28 0.042
290
c CWD008 Cowden Syndrome 6 26 0.042
291
YNG002 Young Syndrome 26 0.042
292
c CWD004 Cowden Syndrome 5 24 0.042
293
c NSP014 Nasopharyngeal Carcinoma, 3 23 0.042
294
c NSP009 Nasopharyngeal Carcinoma 2 22 0.042
295
c INF083 Inflammatory Bowel Disease 24 19 0.042
296
ANL002 Anal Gland Neoplasm 16 0.042
297
CHR490 Chromosome 10q23 Deletion Syndrome 12 0.042
298
P OBS005 Obesity 93 0.030
299
P OST012 Osteoarthritis 82 0.030
300
P LFR001 Li-Fraumeni Syndrome 75 0.030
301
P INF038 Influenza 74 0.030
302
MRF001 Marfan Syndrome 73 0.030
303
P LVR013 Liver Disease 72 0.030
304
P ALG002 Alagille Syndrome 72 0.030
305
P RSP003 Respiratory Failure 70 0.030
306
TST021 Testicular Germ Cell Tumor 70 0.030
307
c NRF018 Neurofibromatosis, Type 1 68 0.030
308
c MLT136 Multiple Endocrine Neoplasia 1 68 0.030
309
SKN016 Skin Disease 68 0.030
310
CMM004 Common Variable Immunodeficiency 67 0.030
311
P KDN017 Kidney Cancer 67 0.030
312
ACH004 Achondroplasia 66 0.030
313
BRK010 Burkitt Lymphoma 66 0.030
314
P AST007 Astrocytoma 65 0.030
315
DWN001 Down Syndrome 65 0.030
316
DFC004 Deficiency Anemia 65 0.030
317
BSL036 Basal Cell Nevus Syndrome 65 0.030
318
P RBN001 Rubinstein-Taybi Syndrome 65 0.030
319
P MSC005 Muscular Dystrophy 64 0.030
320
P BCL006 B-Cell Lymphomas 64 0.030
321
P AGM001 Agammaglobulinemia 64 0.030
322
P CSH001 Cushing's Syndrome 64 0.030
323
P ART023 Arthropathy 63 0.030
324
CHG001 Chagas Disease 62 0.030
325
CNN005 Connective Tissue Disease 61 0.030
326
P INF032 Infertility 61 0.030
327
P ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 60 0.030
328
ETN001 Eating Disorder 60 0.030
329
P THY102 Thyroid Cancer, Nonmedullary, 2 60 0.030
330
GST045 Gastroenteritis 60 0.030
331
PLM033 Pulmonary Embolism 59 0.030
332
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.030
333
RBR001 Roberts Syndrome 59 0.030
334
P PRT013 Portal Hypertension 59 0.030
335
P CMR001 Camurati-Engelmann Disease 59 0.030
336
CMM005 Common Cold 58 0.030
337
CHL071 Child Syndrome 58 0.030
338
P PRM011 Primary Ciliary Dyskinesia 58 0.030
339
P DRM010 Dermatomyositis 58 0.030
340
ART017 Aortic Disease 58 0.030
341
MCC010 Mccune-Albright Syndrome, Somatic, Mosaic 58 0.030
342
SCH014 Schistosomiasis 58 0.030
343
RHB003 Rhabdomyosarcoma 58 0.030
344
LPM004 Lipoma 58 0.030
345
EPD016 Epidermolysis Bullosa 57 0.030
346
P MTR004 Maturity-Onset Diabetes of the Young 57 0.030
347
NRM005 Neuromuscular Disease 57 0.030
348
ACN002 Acanthosis Nigricans 57 0.030
349
SNS001 Sensorineural Hearing Loss 57 0.030
350
CNS004 Constipation 57 0.030
351
P HRD004 Hereditary Breast Ovarian Cancer 57 0.030
352
ADR005 Adrenal Carcinoma 56 0.030
353
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 56 0.030
354
SFT003 Soft Tissue Sarcoma 56 0.030
355
PTT006 Pituitary Adenoma 55 0.030
356
P PLY006 Polydactyly 55 0.030
357
BRN038 Bronchial Disease 54 0.030
358
HDC001 Headache 54 0.030
359
NWC001 Newcastle Disease 54 0.030
360
TRN018 Transitional Cell Carcinoma 54 0.030
361
ACH005 Achalasia 54 0.030
362
P END044 Endometriosis 53 0.030
363
OSS012 Osseous Heteroplasia, Progressive 53 0.030
364
P STR020 Strabismus 53 0.030
365
ADL002 Adult Syndrome 53 0.030
366
SHG001 Shigellosis 53 0.030
367
ESP023 Esophageal Disease 53 0.030
368
CNG008 Congenital Ichthyosiform Erythroderma 53 0.030
369
ALV010 Alveolar Soft-Part Sarcoma 53 0.030
370
KDS001 Kid Syndrome 53 0.030
371
P ANG015 Angioedema 53 0.030
372
TST014 Testicular Cancer 52 0.030
373
ANK001 Ankylosis 52 0.030
374
CRH005 Crohn's Colitis 52 0.030
375
TMR010 Tumor Predisposition Syndrome 52 0.030
376
P TRT010 Teratoma 52 0.030
377
IMP002 Imperforate Anus 52 0.030
378
P CRV031 Cervical Adenocarcinoma 52 0.030
379
P END033 Endocarditis 52 0.030
380
UTR024 Uterine Carcinosarcoma 52 0.030
381
CYS005 Cysticercosis 52 0.030
382
ART001 Arterial Tortuosity Syndrome 52 0.030
383
FRB001 Farber Lipogranulomatosis 51 0.030
384
IRN001 Iron Deficiency Anemia 51 0.030
385
P DDN001 Duodenal Ulcer 51 0.030
386
P EPD003 Epidermolysis Bullosa Simplex 51 0.030
387
FML038 Female Reproductive Organ Cancer 51 0.030
388
ADT003 Auditory System Disease 51 0.030
389
P DWL002 Dowling-Degos Disease 1 51 0.030
390
MGC001 Megacolon 50 0.030
391
UTR033 Uterine Corpus Cancer 50 0.030
392
MRG003 Marginal Zone B-Cell Lymphoma 50 0.030
393
KRT009 Keratosis 50 0.030
394
P EPD002 Epidermolytic Hyperkeratosis 49 0.030
395
CHR001 Churg-Strauss Syndrome 49 0.030
396
DYS073 Dysphagia 49 0.030
397
THR013 Thoracic Outlet Syndrome 49 0.030
398
P PCH015 Pachyonychia Congenita 1 49 0.030
399
PRT018 Portal Vein Thrombosis 49 0.030
400
FML039 Female Reproductive System Disease 48 0.030
401
ADR038 Adermatoglyphia 48 0.030
402
UPP004 Upper Respiratory Tract Disease 48 0.030
403
PLM102 Palmoplantar Keratoderma, Epidermolytic 48 0.030
404
P FBR025 Fibrochondrogenesis 48 0.030
405
P MYT002 Myotonic Dystrophy 47 0.030
406
DVR002 Diverticulitis 47 0.030
407
MCP006 Mucoepidermoid Carcinoma 47 0.030
408
CRD118 Cardiovascular Cancer 47 0.030
409
BRN022 Bronchiectasis 47 0.030
410
P SYM022 Symphalangism, Proximal, 1a 47 0.030
411
GST060 Gastric Cancer, Somatic 47 0.030
412
LKC003 Leukocyte Disease 47 0.030
413
HST009 Histiocytoma 47 0.030
414
P BRN120 Bronchus Cancer 46 0.030
415
ADR008 Adrenal Adenoma 46 0.030
416
P SKN013 Skin Benign Neoplasm 46 0.030
417
DBW001 Dubowitz Syndrome 46 0.030
418
INT017 Intestinal Schistosomiasis 46 0.030
419
BLD053 Blood Platelet Disease 46 0.030
420
HDR003 Hidradenitis 46 0.030
421
CVR006 Cavernous Hemangioma 46 0.030
422
c ATM024 Autoimmune Pancreatitis 46 0.030
423
VLV044 Vulvar Intraepithelial Neoplasia 46 0.030
424
KRT036 Keratosis, Seborrheic, Somatic 46 0.030
425
ALN001 Aland Island Eye Disease 45 0.030
426
PLS025 Plasmablastic Lymphoma 45 0.030
427
P BLD051 Blood Coagulation Disease 45 0.030
428
SML036 Small Intestinal Adenocarcinoma 45 0.030
429
VSC047 Vascular Malformation 45 0.030
430
URT010 Ureteral Obstruction 45 0.030
431
P CNN004 Connective Tissue Cancer 45 0.030
432
c BSL024 Basal Cell Carcinoma 1 45 0.030
433
BRC085 Brca2 Hereditary Breast and Ovarian Cancer Syndrome 44 0.030
434
P PNB001 Pineoblastoma 44 0.030
435
MLK006 Milk Allergy 44 0.030
436
c ADN012 Adenocarcinoma in Situ 44 0.030
437
BLL004 Bullous Keratopathy 44 0.030
438
P ICH001 Ichthyosis Vulgaris 44 0.030
439
P PRK001 Porokeratosis 44 0.030
440
EPD028 Epidermolysis Bullosa Simplex, Dowling-Meara Type 44 0.030
441
ICH002 Ichthyosis Bullosa of Siemens 43 0.030
442
OPT007 Optic Nerve Glioma 43 0.030
443
PRM025 Primary Bacterial Infectious Disease 43 0.030
444
UND005 Undifferentiated Pleomorphic Sarcoma 43 0.030
445
ANC001 Ancylostomiasis 43 0.030
446
SPN032 Spindle Cell Carcinoma 43 0.030
447
LMY002 Leiomyoma 42 0.030
448
BMF001 Bamforth-Lazarus Syndrome 42 0.030
449
FBR003 Fibrous Histiocytoma 42 0.030
450
CNV002 Conversion Disorder 42 0.030
451
TNS007 Taeniasis 42 0.030
452
EPD047 Epidermolysis Bullosa Simplex, Koebner Type 42 0.030
453
c BLD124 Bleeding Disorder, Platelet-Type, 11 42 0.030
454
STT007 Steatocystoma Multiplex 42 0.030
455
CPL007 Capillary Malformation-Arteriovenous Malformation 41 0.030
456
LMY003 Leiomyomatosis 41 0.030
457
LYM052 Lymphomatoid Papulosis 41 0.030
458
HYP458 Hyper Ige Syndrome 41 0.030
459
GST030 Gastrinoma 41 0.030
460
BSL006 Basaloid Squamous Cell Carcinoma 41 0.030
461
EPD041 Epidermolysis Bullosa Simplex, Weber-Cockayne Type 41 0.030
462
CHR034 Chromophobe Adenoma 41 0.030
463
WTH001 Withdrawal Disorder 41 0.030
464
ISC015 Ischemic Colitis 40 0.030
465
CLR096 Ciliary Dyskinesia, Primary, 1, with or Without Situs Inversus 40 0.030
466
PKL001 Poikiloderma with Neutropenia 40 0.030
467
CYS009 Cystadenoma 40 0.030
468
P UTR038 Uterine Disease 40 0.030
469
GST028 Gastric Squamous Cell Carcinoma 39 0.030
470
ATS009 Autosomal Genetic Disease 39 0.030
471
VSC012 Vesiculobullous Skin Disease 39 0.030
472
RSD004 Rosai-Dorfman Disease 39 0.030
473
P WHT013 White Sponge Nevus 1 38 0.030
474
ASC002 Ascariasis 38 0.030
475
GTR011 Goiter, Multinodular 1, with or Without Sertoli-Leydig Cell Tumors 38 0.030
476
OST032 Osteofibrous Dysplasia 38 0.030
477
LCH011 Lichen Planopilaris 37 0.030
478
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 37 0.030
479
PLM136 Palmoplantar Keratoderma, Nonepidermolytic 37 0.030
480
MYP002 Myoepithelial Carcinoma 37 0.030
481
EPS026 Epispadias 37 0.030
482
c OTP007 Otopalatodigital Syndrome, Type Ii 37 0.030
483
PLM030 Pleomorphic Rhabdomyosarcoma 37 0.030
484
c ALP005 Alpha Chain Disease 37 0.030
485
BRS063 Breast Squamous Cell Carcinoma 37 0.030
486
c FML311 Familial Colorectal Cancer Type X 36 0.030
487
c OTP006 Otopalatodigital Syndrome, Type I 36 0.030
488
P SRT002 Sertoli Cell Tumor 35 0.030
489
ATR013 Atrichia with Papular Lesions 35 0.030
490
HRF001 Hair Follicle Neoplasm 35 0.030
491
EPD065 Epidermolytic Ichthyosis 35 0.030
492
ANG037 Angiomatosis 34 0.030
493
SWL001 Swallowing Disorders 34 0.030
494
ALL007 Allergic Urticaria 34 0.030
495
ADP007 Adie Pupil 34 0.030
496
ODN006 Odontoma 34 0.030
497
c HMG004 Hemoglobin D Disease 33 0.030
498
ECC004 Eccrine Porocarcinoma 33 0.030
499
ETH009 Ethmoid Sinusitis 33 0.030
500
INT004 Intraneural Perineurioma 33 0.030
501
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 33 0.030
502
DYS011 Dyskinesia of Esophagus 33 0.030
503
EPD056 Epidermolysis Bullosa Simplex-Mp 33 0.030
504
RNL013 Renal Adenoma 32 0.030
505
VLL006 Villous Adenoma 32 0.030
506
MCN011 Mucinoses 32 0.030
507
DDN009 Duodenal Obstruction 32 0.030
508
GST006 Gastric Leiomyoma 32 0.030
509
c TRC078 Trichohepatoenteric Syndrome 2 31 0.030
510
PNM003 Pneumatosis Cystoides Intestinalis 31 0.030
511
PRS126 Prostate Cancer Susceptibility 31 0.030
512
BWN006 Bowen's Disease 31 0.030
513
ANG004 Angioid Streaks 31 0.030
514
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 31 0.030
515
FLM001 Filamentary Keratitis 30 0.030
516
EXS013 Exstrophy-Epispadias Complex 30 0.030
517
c EPD058 Epidermolysis Bullosa Simplex, Recessive 1 29 0.030
518
JJN007 Jejunal Adenocarcinoma 29 0.030
519
PLM135 Palmoplantar Keratoderma, Bothnian Type 29 0.030
520
c CLR066 Ciliary Dyskinesia, Primary, 2 29 0.030
521
LPD007 Lipoadenoma 28 0.030
522
P BRS017 Breast Adenomyoepithelioma 28 0.030
523
PDT027 Pediatric Ulcerative Colitis 28 0.030
524
TXC001 Toxic Megacolon 28 0.030
525
INF028 Infundibulocystic Basal Cell Carcinoma 27 0.030
526
GRN011 Granulomatous Gastritis 27 0.030
527
GGN002 Gigantism 27 0.030
528
SPN331 Spondyloocular Syndrome 27 0.030
529
PNG001 Pinguecula 27 0.030
530
MLK004 Malakoplakia 27 0.030
531
HMC038 Hemochromatosis, Neonatal 27 0.030
532
c CLR068 Ciliary Dyskinesia, Primary, 5 26 0.030
533
ECC008 Eccrine Sweat Gland Neoplasm 26 0.030
534
MLG011 Malignant Biphasic Mesothelioma 26 0.030
535
ICH031 Ichthyosis with Confetti 26 0.030
536
END016 Endocervicitis 26 0.030
537
MLL004 Mallory-Weiss Syndrome 25 0.030
538
c CLR114 Ciliary Dyskinesia, Primary, 30 25 0.030
539
HNM002 Hinman Syndrome 25 0.030
540
c CWD003 Cowden Syndrome 2 24 0.030
541
BCL011 Bacillary Angiomatosis 24 0.030
542
APC005 Apocrine Sweat Gland Neoplasm 24 0.030
543
c INF068 Inflammatory Bowel Disease 13 24 0.030
544
c LRG002 Large Cell Acanthoma 24 0.030
545
ICH036 Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis 24 0.030
546
c INF093 Inflammatory Bowel Disease 14 23 0.030
547
c CWD007 Cowden Syndrome 3 23 0.030
548
BRS058 Breast Myoepithelial Neoplasm 23 0.030
549
PRC021 Parc Syndrome 22 0.030
550
c CLR095 Ciliary Dyskinesia, Primary, 19 22 0.030
551
c CLR090 Ciliary Dyskinesia, Primary, 22 22 0.030
552
SKN011 Skin Pilomatrix Carcinoma 21 0.030
553
c INT282 Integumentary System Benign Neoplasm 20 0.030
554
STT009 Sutton Disease 2 20 0.030
555
EPD036 Epidermolysis Bullosa Simplex, Other Generalized 20 0.030
556
CNT045 Central Nervous System Sarcoma 19 0.030
557
c INF074 Inflammatory Bowel Disease 15 19 0.030
558
ESN014 Eosinophilic Enteropathy 19 0.030
559
OLG005 Oligodontia-Colorectal Cancer Syndrome 19 0.030
560
c INF092 Inflammatory Bowel Disease 9 19 0.030
561
c INF081 Inflammatory Bowel Disease 22 19 0.030
562
c CNG148 Congenital Heart Disease, Atrial Septal Defect 19 0.030
563
c INF082 Inflammatory Bowel Disease 23 18 0.030
564
BCH001 Beach Ear 18 0.030
565
EPD004 Epidermolytic Acanthoma 17 0.030
566
FLR003 Florid Cemento-Osseous Dysplasia 17 0.030
567
WSC001 Wisconsin Syndrome 17 0.030
568
P FML321 Familial Stomach Cancer 16 0.030
569
MLG028 Malignant Neoplasm of Acoustic Nerve 16 0.030
570
c DLT001 Delta Chain Disease 16 0.030
571
FXP001 Foxp2-Related Speech and Language Disorders 15 0.030
572
c RP1001 Rp1-Related Retinitis Pigmentosa 13 0.030
573
c CWD009 Cowden Syndrome 7 13 0.030
574
PRS059 Prostaglandin-Endoperoxide Synthase Deficiency 12 0.030
575
JNS001 Janus Kinase-3 Deficiency 9 0.030
576
10Q003 10q22.3q23 Microdeletion Syndrome 4 0.030