Search results for "polyposis"

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

583 hits were found for 'polyposis'

# Family MCID Name MIFTS Score
1
P FML011 Familial Adenomatous Polyposis 68 9.759
2
PLY056 Polyposis, Juvenile Intestinal 54 8.305
3
ADN021 Adenomatous Polyposis Coli 70 7.308
4
MTY001 Mutyh-Associated Polyposis 49 5.542
5
P ATT003 Attenuated Familial Adenomatous Polyposis 47 4.983
6
PTZ001 Peutz-Jeghers Syndrome 71 4.831
7
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 34 4.163
8
c ADN040 Adenomas, Multiple Colorectal 27 3.886
9
JVN012 Juvenile Polyposis/hereditary Hemorrhagic Telangiectasia Syndrome 26 3.871
10
MSM014 Mismatch Repair Cancer Syndrome 57 3.855
11
c PLY066 Polyposis Syndrome, Hereditary Mixed, 2 18 3.847
12
c HRD101 Hereditary Mixed Polyposis Syndrome 1 37 3.711
13
c FML299 Familial Adenomatous Polyposis 3 25 3.633
14
FML254 Familial Adenomatous Polyposis Due to 5q22.2 Microdeletion 8 3.480
15
CHR595 Chromosome 10q23 Deletion Syndrome Juvenile Polyposis of Infancy, Included 26 3.141
16
P CLR070 Colorectal Cancer, Hereditary Nonpolyposis, Type 1 55 3.130
17
P LYN001 Lynch Syndrome 69 2.997
18
c EPC004 Epcam-Related Lynch Syndrome 14 2.677
19
CPP003 Cap Polyposis 35 2.529
20
HYP466 Hyperplastic Polyposis Syndrome 32 2.418
21
GST086 Gastric Adenocarcinoma and Proximal Polyposis of the Stomach 10 2.281
22
APC006 Apc-Associated Polyposis Conditions 4 2.248
23
CLR065 Colorectal Adenomatous Polyposis, Autosomal Recessive, with Pilomatricomas 45 2.221
24
c CLR039 Colorectal Cancer, Hereditary Nonpolyposis, Type 4 27 2.221
25
c CLR037 Colorectal Cancer, Hereditary Nonpolyposis, Type 5 27 2.221
26
c CLR055 Colorectal Cancer, Hereditary Nonpolyposis, Type 6 25 2.221
27
c CLR100 Colorectal Cancer, Hereditary Nonpolyposis, Type 7 18 2.221
28
c AXN008 Axin2-Related Attenuated Familial Adenomatous Polyposis 8 2.221
29
P HRD144 Hereditary Mixed Polyposis Syndrome 29 1.747
30
c CLR041 Colorectal Cancer, Hereditary Nonpolyposis, Type 2 23 1.605
31
P BMP001 Bmpr1a-Related Juvenile Polyposis 15 1.605
32
NSL012 Nasal Polyposis, Familial 4 1.605
33
c CLR089 Colorectal Cancer, Hereditary Nonpolyposis, Type 8 19 1.589
34
PLY138 Polymerase Proofreading-Related Adenomatous Polyposis 16 1.589
35
c MSH007 Msh3-Related Attenuated Familial Adenomatous Polyposis 5 1.589
36
c SMD006 Smad4-Related Juvenile Polyposis 2 1.589
37
c MLH005 Mlh3-Related Lynch Syndrome 8 1.545
38
c PMS002 Pms1-Related Lynch Syndrome 7 1.545
39
c PMS003 Pms2-Related Lynch Syndrome 7 1.545
40
c MLH002 Mlh1-Related Lynch Syndrome 7 1.545
41
c MSH002 Msh2-Related Lynch Syndrome 7 1.545
42
c MSH005 Msh6-Related Lynch Syndrome 7 1.545
43
5Q2001 5q22 Deletion Syndrome 6 1.545
44
P CLR023 Colorectal Cancer 97 0.482
45
ADN018 Adenoma 58 0.360
46
DDN006 Duodenitis 42 0.249
47
P CLR108 Colorectal Adenoma 60 0.218
48
DSM004 Desmoid Tumor 56 0.206
49
CLN019 Colonic Disease 51 0.206
50
INT253 Intestinal Benign Neoplasm 47 0.199
51
RCT018 Rectal Neoplasm 54 0.192
52
RCT017 Rectal Disease 40 0.192
53
c HRD169 Hereditary Colorectal Cancer 42 0.187
54
CLN044 Colon Adenoma 44 0.185
55
CLT003 Colitis 60 0.183
56
P ADN016 Adenocarcinoma 69 0.180
57
P THY032 Thyroiditis 54 0.180
58
P NSP012 Nasopharyngeal Carcinoma 66 0.178
59
ALC007 Alcohol Dependence 63 0.178
60
PHR003 Pharyngitis 56 0.178
61
c FML053 Familial Colorectal Cancer 51 0.178
62
NSP003 Nasopharyngeal Disease 26 0.178
63
P INF037 Inflammatory Bowel Disease 63 0.175
64
CRV068 Cervical Polyp 30 0.175
65
ULC004 Ulcerative Colitis 76 0.172
66
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 29 0.172
67
c CLR079 Colorectal Cancer 2 29 0.164
68
GST038 Gastrointestinal Adenoma 27 0.164
69
P SNS014 Sinusitis 60 0.144
70
DDN007 Duodenal Disease 33 0.144
71
P GST049 Gastrointestinal System Cancer 60 0.141
72
PRP021 Peripheral Nervous System Neoplasm 46 0.141
73
c CLR085 Colorectal Cancer 1 45 0.141
74
c CLR075 Colorectal Cancer 3 28 0.141
75
c INF078 Inflammatory Bowel Disease 2 31 0.134
76
P AST005 Asthma 82 0.131
77
DDN010 Duodenum Cancer 43 0.131
78
P LYM118 Lymphoma 69 0.124
79
P INT068 Intestinal Disease 60 0.120
80
NSD001 Nose Disease 48 0.120
81
SNS023 Sensory System Cancer 43 0.120
82
HRD059 Hereditary Peripheral Nervous Disorder 11 0.120
83
DDN022 Duodenum Adenoma 10 0.120
84
GST053 Gastric Cancer 78 0.116
85
P RHN004 Rhinitis 60 0.112
86
PRT019 Protein-Losing Enteropathy 42 0.112
87
c INF086 Inflammatory Bowel Disease 3 38 0.112
88
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.108
89
P CWD001 Cowden Disease 64 0.108
90
THY028 Thyroid Cancer 69 0.104
91
P PNC044 Pancreatitis 61 0.104
92
HPT022 Hepatoblastoma 55 0.104
93
c INF071 Inflammatory Bowel Disease 1 51 0.104
94
ORL014 Oral Pharyngeal Disorders 11 0.104
95
P NRV006 Nervous System Cancer 60 0.100
96
MCS002 Mucositis 55 0.100
97
BNN001 Bannayan-Riley-Ruvalcaba Syndrome 54 0.100
98
PRN021 Paranasal Sinus Disease 49 0.100
99
c INF087 Inflammatory Bowel Disease 4 40 0.100
100
NSL022 Nasal Cavity Disease 38 0.100
101
P BRS047 Breast Cancer 100 0.095
102
P HPT023 Hepatocellular Carcinoma 92 0.095
103
c CLR080 Colorectal Cancer 5 32 0.095
104
MNT001 Mantle Cell Lymphoma 72 0.090
105
GST040 Gastric Adenocarcinoma 52 0.090
106
HPT067 Hepatocellular Adenoma 42 0.085
107
PCH007 Pouchitis 38 0.085
108
GST039 Gastroduodenitis 31 0.085
109
c CLR081 Colorectal Cancer 6 22 0.085
110
P LKM002 Leukemia 71 0.079
111
SQM006 Squamous Cell Carcinoma 70 0.079
112
SRC014 Sarcoma 66 0.079
113
GST050 Gastrointestinal System Disease 56 0.079
114
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.079
115
RTN023 Retinitis 50 0.079
116
GNG002 Ganglioneuroma 47 0.079
117
ALR002 Al-Raqad Syndrome 36 0.079
118
c CLR077 Colorectal Cancer 10 29 0.079
119
c CLR083 Colorectal Cancer 8 24 0.079
120
AND005 Androgen Insensitivity Syndrome, Mild 16 0.079
121
P HPT021 Hepatitis 69 0.074
122
ALL003 Allergic Rhinitis 63 0.074
123
P GLM045 Glioma 60 0.074
124
WLL006 Wells Syndrome 59 0.074
125
WST001 West Syndrome 57 0.074
126
P INT070 Intestinal Obstruction 57 0.074
127
PPL022 Papilloma 55 0.074
128
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 46 0.074
129
GDS001 Good Syndrome 44 0.074
130
DSM003 Desmoid Disease, Hereditary 44 0.074
131
FBR019 Fibromatosis 43 0.074
132
P PRN020 Paranasal Sinus Cancer 40 0.074
133
P NSL008 Nasal Cavity Cancer 33 0.074
134
c INF088 Inflammatory Bowel Disease 5 31 0.074
135
P SNS011 Sinus Cancer 31 0.074
136
c CLR087 Colorectal Cancer 12 30 0.074
137
c PRN030 Paranasal Sinus Cancer, Adult 12 0.074
138
P LNG032 Lung Cancer 95 0.067
139
ART005 Arteriovenous Malformation 66 0.067
140
P ESP024 Esophagitis 61 0.067
141
P HMN010 Hemangioma 59 0.067
142
P MRT001 Muir-Torre Syndrome 59 0.067
143
c CWD006 Cowden Syndrome 1 57 0.067
144
ORL015 Oral Squamous Cell Carcinoma 57 0.067
145
P MLT074 Multiple Endocrine Neoplasia 56 0.067
146
CSY001 C Syndrome 50 0.067
147
c INH020 Inherited Metabolic Disorder 49 0.067
148
END072 Endotheliitis 42 0.067
149
NRN002 Neuronitis 41 0.067
150
NSP002 Nasopharyngitis 40 0.067
151
ATN003 Autonomic Nervous System Neoplasm 40 0.067
152
JJN003 Jejunal Cancer 29 0.067
153
c AST039 Asthma 2 28 0.067
154
FNC005 Functional Colonic Disease 27 0.067
155
c INF091 Inflammatory Bowel Disease 8 22 0.067
156
P SCH015 Schizophrenia 77 0.060
157
CRH001 Crohn's Disease 75 0.060
158
P RTN024 Retinoblastoma 74 0.060
159
ALL006 Allergic Asthma 58 0.060
160
P SHR029 Short Syndrome 58 0.060
161
THR024 Thrombosis 57 0.060
162
c ACT027 Acute Pancreatitis 57 0.060
163
PRS047 Prostatitis 56 0.060
164
P SML016 Small Intestine Cancer 52 0.060
165
PPL002 Papillary Carcinoma 51 0.060
166
CLR109 Colorectal Adenocarcinoma 51 0.060
167
PSD012 Pseudoachondroplasia 51 0.060
168
STM006 Stomach Disease 50 0.060
169
P SHR001 Short Bowel Syndrome 49 0.060
170
FBR054 Fibroma 46 0.060
171
INV006 Inverted Papilloma 41 0.060
172
SCL017 Sclerosing Hemangioma 41 0.060
173
CRB009 Cerebritis 39 0.060
174
JVN033 Juvenile Nasopharyngeal Angiofibroma 39 0.060
175
PLM018 Pulmonary Sclerosing Hemangioma 39 0.060
176
P BNG071 Benign Schwannoma 38 0.060
177
VSM001 Vasomotor Rhinitis 34 0.060
178
P ATX010 Ataxia Neuropathy Spectrum 30 0.060
179
c INF075 Inflammatory Bowel Disease 16 30 0.060
180
c AST037 Asthma 1 29 0.060
181
AST038 Asthma, Aspirin-Induced 27 0.060
182
ILM001 Ileum Cancer 25 0.060
183
c CWD005 Cowden Syndrome 4 23 0.060
184
c INF073 Inflammatory Bowel Disease 12 21 0.060
185
c CLR082 Colorectal Cancer 7 20 0.060
186
RCT035 Rectum Adenoma 14 0.060
187
P PNC035 Pancreatic Cancer 87 0.052
188
CYS001 Cystic Fibrosis 83 0.052
189
P HNT016 Huntington Disease 80 0.052
190
P OVR042 Ovarian Cancer 76 0.052
191
END057 Endometrial Cancer 75 0.052
192
GST019 Gastrointestinal Stromal Tumor 73 0.052
193
P MTC003 Metachromatic Leukodystrophy 70 0.052
194
MLN008 Melanoma 62 0.052
195
c ADL017 Adult T-Cell Leukemia 60 0.052
196
P ORL007 Oral Cavity Cancer 59 0.052
197
OCL009 Ocular Cancer 59 0.052
198
P LKD001 Leukodystrophy 59 0.052
199
P HST010 Histiocytosis 58 0.052
200
ORL011 Oral Cancer 56 0.052
201
HYP266 Hypoxia 56 0.052
202
P GST044 Gastritis 56 0.052
203
NRN004 Neuroendocrine Tumor 56 0.052
204
P FNC043 Fanconi Anemia, Complementation Group E 55 0.052
205
P HRD011 Hereditary Spherocytosis 54 0.052
206
CND002 Conduct Disorder 54 0.052
207
THY103 Thyroid Cancer, Monmedullary, 1 53 0.052
208
VSC006 Vascular Cancer 51 0.052
209
INT051 Intussusception 50 0.052
210
P TRC086 Trichohepatoenteric Syndrome 1 48 0.052
211
P TCL004 T-Cell Leukemia 47 0.052
212
c CLR017 Clear Cell Sarcoma 46 0.052
213
AML029 Ameloblastoma 46 0.052
214
PRN011 Pernicious Anemia 44 0.052
215
RCT011 Rectal Prolapse 43 0.052
216
GST071 Gastrointestinal Carcinoma 42 0.052
217
CHL052 Choledochal Cyst 41 0.052
218
ATS008 Autosomal Dominant Disease 39 0.052
219
P MXL015 Maxillary Sinusitis 38 0.052
220
ADJ001 Adjustment Disorder 38 0.052
221
TTR016 Tetra-Amelia Syndrome 36 0.052
222
c CHR038 Chronic Maxillary Sinusitis 36 0.052
223
c INF089 Inflammatory Bowel Disease 6 34 0.052
224
PNC019 Pancreatoblastoma 32 0.052
225
FML143 Familial Papillary Thyroid Carcinoma 28 0.052
226
PRM190 Periampullary Adenoma 28 0.052
227
c INF090 Inflammatory Bowel Disease 7 26 0.052
228
c INF079 Inflammatory Bowel Disease 20 21 0.052
229
CLF045 Cleft, Median, of Upper Lip with Polyps of Facial Skin and Nasal Mucosa 19 0.052
230
c INF083 Inflammatory Bowel Disease 24 19 0.052
231
c CLR084 Colorectal Cancer 9 17 0.052
232
c FML303 Familial/multiple Cancer 14 0.052
233
LRG015 Large Intestine Adenoma 13 0.052
234
P PRS040 Prostate Cancer 90 0.042
235
P MDL005 Medulloblastoma 77 0.042
236
P LFR001 Li-Fraumeni Syndrome 75 0.042
237
c HPT073 Hepatitis C Virus 73 0.042
238
PRP027 Peripheral Vascular Disease 69 0.042
239
c HPT001 Hepatitis C 68 0.042
240
CMM004 Common Variable Immunodeficiency 68 0.042
241
PCK002 Pick Disease 68 0.042
242
ATP002 Atopy 66 0.042
243
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.042
244
P ATS007 Autism Spectrum Disorder 65 0.042
245
P MSC005 Muscular Dystrophy 65 0.042
246
c BSL007 Basal Cell Carcinoma 65 0.042
247
c HPT016 Hepatitis B 65 0.042
248
P ART023 Arthropathy 64 0.042
249
c MLT024 Multiple Endocrine Neoplasia Iia 64 0.042
250
P PRT010 Parathyroid Carcinoma 63 0.042
251
PRT036 Peritonitis 63 0.042
252
GST092 Gastroesophageal Reflux 62 0.042
253
P LYM026 Lymphoblastic Leukemia 62 0.042
254
P DRR001 Diarrhea 60 0.042
255
ETN001 Eating Disorder 58 0.042
256
P HRS035 Hirschsprung Disease 1 58 0.042
257
ALP008 Alopecia 57 0.042
258
URT039 Urticaria 57 0.042
259
SNS001 Sensorineural Hearing Loss 57 0.042
260
P MYP006 Myopia 56 0.042
261
CHN016 Cohen Syndrome 54 0.042
262
P END033 Endocarditis 54 0.042
263
P LCH002 Lichen Planus 53 0.042
264
IMP002 Imperforate Anus 52 0.042
265
ALL026 Allergic Hypersensitivity Disease 52 0.042
266
HNT002 Hantavirus Pulmonary Syndrome 51 0.042
267
ORL004 Oral Submucous Fibrosis 51 0.042
268
ART001 Arterial Tortuosity Syndrome 50 0.042
269
CLN015 Colon Adenocarcinoma 50 0.042
270
HPT074 Hepatic Adenoma, Somatic 50 0.042
271
URB001 Urbach-Wiethe Disease 49 0.042
272
P INT063 Intellectual Disability 49 0.042
273
ILT001 Ileitis 49 0.042
274
PRT018 Portal Vein Thrombosis 49 0.042
275
MCP006 Mucoepidermoid Carcinoma 48 0.042
276
c PRK024 Parkinson Disease, Juvenile, Type 2 48 0.042
277
ORL013 Oral Lichen Planus 47 0.042
278
ADR008 Adrenal Adenoma 47 0.042
279
LPM005 Lipomatosis 47 0.042
280
P CRN035 Cranial Nerve Palsy 46 0.042
281
CHR074 Choriocarcinoma 46 0.042
282
CVR006 Cavernous Hemangioma 46 0.042
283
ACR012 Aicardi Syndrome 46 0.042
284
URT010 Ureteral Obstruction 45 0.042
285
ACD009 Acid-Labile Subunit, Deficiency of 45 0.042
286
P PNB001 Pineoblastoma 44 0.042
287
P MSC022 Mosaic Variegated Aneuploidy Syndrome 44 0.042
288
SKN023 Skin Tag 44 0.042
289
ANS011 Anus Cancer 42 0.042
290
EXS001 Exostosis 42 0.042
291
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.042
292
c PRM023 Pre-Malignant Neoplasm 41 0.042
293
TTR011 Tetraploidy 41 0.042
294
GST078 Gastrointestinal Allergy 40 0.042
295
INT040 Intrinsic Asthma 40 0.042
296
TST018 Testicular Yolk Sac Tumor 40 0.042
297
ISC015 Ischemic Colitis 39 0.042
298
ESN020 Eosinophilic Granulomatosis with Polyangiitis 39 0.042
299
RVL002 Ruvalcaba Syndrome 39 0.042
300
c CHR048 Chronic Rhinitis 38 0.042
301
MYP002 Myoepithelial Carcinoma 38 0.042
302
BLD054 Blood Protein Disease 37 0.042
303
GTR011 Goiter, Multinodular 1, with or Without Sertoli-Leydig Cell Tumors 37 0.042
304
BRL011 Bare Lymphocyte Syndrome, Type I 37 0.042
305
NSY001 N Syndrome 36 0.042
306
P SRT002 Sertoli Cell Tumor 36 0.042
307
PLM052 Pulmonary Arteriovenous Malformation 34 0.042
308
RDN001 Reading Disorder 34 0.042
309
RHN002 Rhinoscleroma 34 0.042
310
ANS012 Anus Disease 32 0.042
311
P FRT001 Fourth Cranial Nerve Palsy 31 0.042
312
JJN007 Jejunal Adenocarcinoma 30 0.042
313
PNM003 Pneumatosis Cystoides Intestinalis 29 0.042
314
END080 Endometrial Disease 27 0.042
315
c CWD008 Cowden Syndrome 6 27 0.042
316
YNG002 Young Syndrome 26 0.042
317
c CWD004 Cowden Syndrome 5 24 0.042
318
c NSP014 Nasopharyngeal Carcinoma, 3 21 0.042
319
c INF074 Inflammatory Bowel Disease 15 19 0.042
320
c NSP009 Nasopharyngeal Carcinoma 2 19 0.042
321
FLR003 Florid Cemento-Osseous Dysplasia 18 0.042
322
P FML321 Familial Stomach Cancer 13 0.042
323
ANL002 Anal Gland Neoplasm 13 0.042
324
CHR490 Chromosome 10q23 Deletion Syndrome 13 0.042
325
JNS001 Janus Kinase-3 Deficiency 9 0.042
326
P OBS005 Obesity 92 0.030
327
P OST012 Osteoarthritis 83 0.030
328
P LVR013 Liver Disease 75 0.030
329
MRF001 Marfan Syndrome 73 0.030
330
P ALG002 Alagille Syndrome 72 0.030
331
P INF038 Influenza 72 0.030
332
P RSP003 Respiratory Failure 71 0.030
333
TST021 Testicular Germ Cell Tumor 69 0.030
334
c MLT136 Multiple Endocrine Neoplasia 1 69 0.030
335
BRK010 Burkitt Lymphoma 69 0.030
336
c NRF018 Neurofibromatosis, Type 1 67 0.030
337
P TBR001 Tuberous Sclerosis 67 0.030
338
CHG001 Chagas Disease 67 0.030
339
P END044 Endometriosis 66 0.030
340
SKN016 Skin Disease 66 0.030
341
ACH004 Achondroplasia 66 0.030
342
DWN001 Down Syndrome 66 0.030
343
P BCL006 B-Cell Lymphomas 65 0.030
344
P CSH001 Cushing's Syndrome 65 0.030
345
P KDN017 Kidney Cancer 65 0.030
346
P AST007 Astrocytoma 65 0.030
347
P AGM001 Agammaglobulinemia 64 0.030
348
DFC004 Deficiency Anemia 64 0.030
349
P RBN001 Rubinstein-Taybi Syndrome 64 0.030
350
P LNG064 Lung Cancer Susceptibility 3 62 0.030
351
CNN005 Connective Tissue Disease 62 0.030
352
P DRM010 Dermatomyositis 62 0.030
353
ADR016 Adrenal Cortical Carcinoma 61 0.030
354
P PRT013 Portal Hypertension 60 0.030
355
PLM033 Pulmonary Embolism 60 0.030
356
LPM004 Lipoma 60 0.030
357
RBR001 Roberts Syndrome 60 0.030
358
GST045 Gastroenteritis 59 0.030
359
P INF032 Infertility 59 0.030
360
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.030
361
CMM005 Common Cold 59 0.030
362
MCC010 Mccune-Albright Syndrome, Somatic, Mosaic 58 0.030
363
P CMR001 Camurati-Engelmann Disease 58 0.030
364
P MTR004 Maturity-Onset Diabetes of the Young 58 0.030
365
P THY102 Thyroid Cancer, Nonmedullary, 2 58 0.030
366
SCH014 Schistosomiasis 58 0.030
367
RHB003 Rhabdomyosarcoma 57 0.030
368
ART017 Aortic Disease 57 0.030
369
ADR005 Adrenal Carcinoma 57 0.030
370
CNS004 Constipation 57 0.030
371
P HRD004 Hereditary Breast Ovarian Cancer 57 0.030
372
SFT003 Soft Tissue Sarcoma 57 0.030
373
P PRM011 Primary Ciliary Dyskinesia 57 0.030
374
ACN002 Acanthosis Nigricans 57 0.030
375
PLY023 Polycystic Liver Disease 56 0.030
376
NRM005 Neuromuscular Disease 56 0.030
377
PTT006 Pituitary Adenoma 56 0.030
378
P PLY006 Polydactyly 56 0.030
379
HDC001 Headache 54 0.030
380
SHG001 Shigellosis 54 0.030
381
LMY002 Leiomyoma 54 0.030
382
ESP023 Esophageal Disease 54 0.030
383
P ACR001 Aicardi-Goutieres Syndrome 54 0.030
384
NWC001 Newcastle Disease 54 0.030
385
ALV010 Alveolar Soft-Part Sarcoma 54 0.030
386
CYS005 Cysticercosis 54 0.030
387
KDS001 Kid Syndrome 53 0.030
388
TST014 Testicular Cancer 53 0.030
389
FRB001 Farber Lipogranulomatosis 53 0.030
390
TRN018 Transitional Cell Carcinoma 53 0.030
391
P CRV031 Cervical Adenocarcinoma 53 0.030
392
P EPD003 Epidermolysis Bullosa Simplex 53 0.030
393
ACH005 Achalasia 52 0.030
394
ADL002 Adult Syndrome 52 0.030
395
BRT005 Barth Syndrome 52 0.030
396
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.030
397
UTR024 Uterine Carcinosarcoma 52 0.030
398
P ANG015 Angioedema 52 0.030
399
P ICH004 Ichthyosis 52 0.030
400
SLM003 Salmonellosis 52 0.030
401
MRG003 Marginal Zone B-Cell Lymphoma 52 0.030
402
P TRT010 Teratoma 52 0.030
403
CRH005 Crohn's Colitis 52 0.030
404
IRN001 Iron Deficiency Anemia 52 0.030
405
BRN038 Bronchial Disease 51 0.030
406
HDR002 Hidradenitis Suppurativa 51 0.030
407
P STR020 Strabismus 51 0.030
408
P LFT003 Left Ventricular Noncompaction 50 0.030
409
P EPD002 Epidermolytic Hyperkeratosis 50 0.030
410
P DDN001 Duodenal Ulcer 50 0.030
411
FML038 Female Reproductive Organ Cancer 50 0.030
412
BRN022 Bronchiectasis 50 0.030
413
P PRM001 Primary Cutaneous Amyloidosis 50 0.030
414
FCS012 Facioscapulohumeral Muscular Dystrophy 1 50 0.030
415
THR013 Thoracic Outlet Syndrome 50 0.030
416
P PCH015 Pachyonychia Congenita 1 49 0.030
417
UTR033 Uterine Corpus Cancer 49 0.030
418
c INF067 Inflammatory Bowel Disease 10 49 0.030
419
CHR001 Churg-Strauss Syndrome 49 0.030
420
P MYT002 Myotonic Dystrophy 48 0.030
421
P FBR025 Fibrochondrogenesis 48 0.030
422
DYS073 Dysphagia 48 0.030
423
FML039 Female Reproductive System Disease 48 0.030
424
HST009 Histiocytoma 47 0.030
425
GST060 Gastric Cancer, Somatic 47 0.030
426
PLM102 Palmoplantar Keratoderma, Epidermolytic 47 0.030
427
MLK006 Milk Allergy 47 0.030
428
TMR010 Tumor Predisposition Syndrome 47 0.030
429
c ATM024 Autoimmune Pancreatitis 47 0.030
430
UPP004 Upper Respiratory Tract Disease 46 0.030
431
BRC084 Brca1 Hereditary Breast and Ovarian Cancer Syndrome 46 0.030
432
BLD053 Blood Platelet Disease 46 0.030
433
ADR038 Adermatoglyphia 46 0.030
434
PLS025 Plasmablastic Lymphoma 46 0.030
435
SML036 Small Intestinal Adenocarcinoma 46 0.030
436
P ICH001 Ichthyosis Vulgaris 46 0.030
437
P KRT005 Keratoacanthoma 46 0.030
438
MGC001 Megacolon 45 0.030
439
INT017 Intestinal Schistosomiasis 45 0.030
440
P PRK001 Porokeratosis 45 0.030
441
VSC047 Vascular Malformation 45 0.030
442
DVR002 Diverticulitis 45 0.030
443
ICH002 Ichthyosis Bullosa of Siemens 45 0.030
444
HDR003 Hidradenitis 45 0.030
445
EPD028 Epidermolysis Bullosa Simplex, Dowling-Meara Type 45 0.030
446
c ADN012 Adenocarcinoma in Situ 45 0.030
447
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.030
448
CRD118 Cardiovascular Cancer 44 0.030
449
P BRN120 Bronchus Cancer 44 0.030
450
ANC001 Ancylostomiasis 44 0.030
451
PRS115 Prosthetic Joint Infection 44 0.030
452
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.030
453
P SKN013 Skin Benign Neoplasm 43 0.030
454
PLM029 Palmoplantar Keratosis 43 0.030
455
LKC003 Leukocyte Disease 43 0.030
456
FBR003 Fibrous Histiocytoma 43 0.030
457
GST030 Gastrinoma 42 0.030
458
LMY003 Leiomyomatosis 42 0.030
459
STT007 Steatocystoma Multiplex 42 0.030
460
BMF001 Bamforth-Lazarus Syndrome 42 0.030
461
c BSL024 Basal Cell Carcinoma 1 42 0.030
462
BLD130 Bladder Exstrophy 42 0.030
463
HYP458 Hyper Ige Syndrome 42 0.030
464
P MYF003 Myofibrillar Myopathy 42 0.030
465
P BLD051 Blood Coagulation Disease 42 0.030
466
PRM025 Primary Bacterial Infectious Disease 41 0.030
467
RSD004 Rosai-Dorfman Disease 41 0.030
468
DBW001 Dubowitz Syndrome 41 0.030
469
OPT007 Optic Nerve Glioma 41 0.030
470
CNV002 Conversion Disorder 41 0.030
471
OSS014 Ossification of the Posterior Longitudinal Ligament of Spine 41 0.030
472
TNS007 Taeniasis 41 0.030
473
LYM052 Lymphomatoid Papulosis 41 0.030
474
CLV009 Clove Syndrome, Somatic 41 0.030
475
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.030
476
P CNN004 Connective Tissue Cancer 40 0.030
477
CHR034 Chromophobe Adenoma 40 0.030
478
CLR096 Ciliary Dyskinesia, Primary, 1, with or Without Situs Inversus 40 0.030
479
ADT003 Auditory System Disease 40 0.030
480
CYS009 Cystadenoma 40 0.030
481
EPS026 Epispadias 40 0.030
482
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.030
483
c MYP082 Myopathy, Myofibrillar, 2 39 0.030
484
c MYP072 Myopathy, Myofibrillar, 1 39 0.030
485
ASC002 Ascariasis 39 0.030
486
PLM136 Palmoplantar Keratoderma, Nonepidermolytic 39 0.030
487
P WHT013 White Sponge Nevus 1 39 0.030
488
MYP094 Myopathy, Spheroid Body 38 0.030
489
P UTR038 Uterine Disease 37 0.030
490
WTH001 Withdrawal Disorder 37 0.030
491
CHR073 Choreatic Disease 37 0.030
492
PLM030 Pleomorphic Rhabdomyosarcoma 37 0.030
493
c ALP005 Alpha Chain Disease 37 0.030
494
ANG037 Angiomatosis 37 0.030
495
PTN006 Pten Hamartoma Tumor Syndrome 37 0.030
496
EPD065 Epidermolytic Ichthyosis 37 0.030
497
c OTP007 Otopalatodigital Syndrome, Type Ii 36 0.030
498
MLD003 Meleda Disease 36 0.030
499
ECC004 Eccrine Porocarcinoma 36 0.030
500
c OTP006 Otopalatodigital Syndrome, Type I 36 0.030
501
c FML311 Familial Colorectal Cancer Type X 36 0.030
502
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.030
503
ATS009 Autosomal Genetic Disease 35 0.030
504
c MSC063 Muscular Dystrophy, Limb-Girdle, Type 2j 35 0.030
505
ATR013 Atrichia with Papular Lesions 35 0.030
506
ADP007 Adie Pupil 34 0.030
507
c MYP078 Myopathy, Myofibrillar, 3 34 0.030
508
ETH009 Ethmoid Sinusitis 34 0.030
509
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.030
510
BWN006 Bowen's Disease 33 0.030
511
CLN045 Colonic Benign Neoplasm 33 0.030
512
c INF092 Inflammatory Bowel Disease 9 33 0.030
513
SWL001 Swallowing Disorders 33 0.030
514
DDN009 Duodenal Obstruction 32 0.030
515
GGN002 Gigantism 32 0.030
516
HRF001 Hair Follicle Neoplasm 32 0.030
517
VLL006 Villous Adenoma 32 0.030
518
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 32 0.030
519
PRS126 Prostate Cancer Susceptibility 32 0.030
520
FLM001 Filamentary Keratitis 32 0.030
521
RNL013 Renal Adenoma 32 0.030
522
GST006 Gastric Leiomyoma 32 0.030
523
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 31 0.030
524
DYS001 Dyskinetic Cerebral Palsy 31 0.030
525
ACN010 Acanthoma 31 0.030
526
c HMG004 Hemoglobin D Disease 31 0.030
527
FML304 Familial Isolated Dilated Cardiomyopathy 31 0.030
528
ALL007 Allergic Urticaria 31 0.030
529
ICH031 Ichthyosis with Confetti 31 0.030
530
PLM135 Palmoplantar Keratoderma, Bothnian Type 30 0.030
531
ANG004 Angioid Streaks 30 0.030
532
MCN011 Mucinoses 29 0.030
533
HMC038 Hemochromatosis, Neonatal 29 0.030
534
c TRC078 Trichohepatoenteric Syndrome 2 29 0.030
535
PDT027 Pediatric Ulcerative Colitis 29 0.030
536
DYS011 Dyskinesia of Esophagus 28 0.030
537
c CLR068 Ciliary Dyskinesia, Primary, 5 28 0.030
538
MLK004 Malakoplakia 28 0.030
539
ICH036 Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis 28 0.030
540
GRN011 Granulomatous Gastritis 28 0.030
541
TXC001 Toxic Megacolon 28 0.030
542
INF028 Infundibulocystic Basal Cell Carcinoma 27 0.030
543
SPN331 Spondyloocular Syndrome 27 0.030
544
c CLR066 Ciliary Dyskinesia, Primary, 2 27 0.030
545
46X010 46xy Partial Gonadal Dysgenesis, with Minifascicular Neuropathy 27 0.030
546
ATH004 Athetosis 26 0.030
547
c MYP080 Myopathy, Myofibrillar, 4 26 0.030
548
c CLR114 Ciliary Dyskinesia, Primary, 30 26 0.030
549
END016 Endocervicitis 26 0.030
550
ULC006 Ulceroglandular Tularemia 25 0.030
551
HNM002 Hinman Syndrome 25 0.030
552
c CWD003 Cowden Syndrome 2 25 0.030
553
c INF068 Inflammatory Bowel Disease 13 25 0.030
554
P GST100 Gastric Neuroendocrine Tumor 25 0.030
555
c LRG002 Large Cell Acanthoma 25 0.030
556
BCL011 Bacillary Angiomatosis 24 0.030
557
c INF093 Inflammatory Bowel Disease 14 23 0.030
558
c CWD007 Cowden Syndrome 3 23 0.030
559
MLL004 Mallory-Weiss Syndrome 23 0.030
560
c CLR090 Ciliary Dyskinesia, Primary, 22 22 0.030
561
c CLR095 Ciliary Dyskinesia, Primary, 19 22 0.030
562
c DFN278 Deafness, Autosomal Dominant 65 22 0.030
563
SKN011 Skin Pilomatrix Carcinoma 21 0.030
564
ESN014 Eosinophilic Enteropathy 21 0.030
565
EPD004 Epidermolytic Acanthoma 20 0.030
566
c DFN275 Deafness , Autosomal Recessive 86 20 0.030
567
OLG005 Oligodontia-Colorectal Cancer Syndrome 19 0.030
568
PRC021 Parc Syndrome 19 0.030
569
c INF081 Inflammatory Bowel Disease 22 18 0.030
570
c INF082 Inflammatory Bowel Disease 23 18 0.030
571
STT009 Sutton Disease 2 18 0.030
572
c CNG148 Congenital Heart Disease, Atrial Septal Defect 18 0.030
573
CNT045 Central Nervous System Sarcoma 16 0.030
574
BCH001 Beach Ear 15 0.030
575
c BNG076 Benign Exophthalmos Syndrome 15 0.030
576
MLG028 Malignant Neoplasm of Acoustic Nerve 15 0.030
577
WSC001 Wisconsin Syndrome 14 0.030
578
c RP1001 Rp1-Related Retinitis Pigmentosa 13 0.030
579
c CWD009 Cowden Syndrome 7 13 0.030
580
c DLT001 Delta Chain Disease 13 0.030
581
PRS059 Prostaglandin-Endoperoxide Synthase Deficiency 12 0.030
582
GLN001 Glandular Tularemia 12 0.030
583
10Q003 10q22.3q23 Microdeletion Syndrome 5 0.030