Search results for "polyposis"

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

581 hits were found for 'polyposis'

# Family MCID Name MIFTS Score
1
FML011 Familial Adenomatous Polyposis 68 9.716
2
PLY056 Polyposis, Juvenile Intestinal 54 8.440
3
ADN021 Adenomatous Polyposis Coli 71 7.275
4
MTY001 Mutyh-Associated Polyposis 48 5.522
5
P ATT003 Attenuated Familial Adenomatous Polyposis 47 4.971
6
PTZ001 Peutz-Jeghers Syndrome 71 4.833
7
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 39 4.144
8
MSM014 Mismatch Repair Cancer Syndrome 60 3.876
9
JVN012 Juvenile Polyposis/hereditary Hemorrhagic Telangiectasia Syndrome 27 3.861
10
c PLY066 Polyposis Syndrome, Hereditary Mixed, 2 18 3.837
11
c HRD101 Hereditary Mixed Polyposis Syndrome 1 24 3.692
12
c ADN040 Adenomas, Multiple Colorectal 26 3.574
13
FML254 Familial Adenomatous Polyposis Due to 5q22.2 Microdeletion 9 3.472
14
PLY073 Polyposis, Gastric 32 3.179
15
CHR595 Chromosome 10q23 Deletion Syndrome Juvenile Polyposis of Infancy, Included 18 3.110
16
P LYN001 Lynch Syndrome 69 2.990
17
P CLR070 Colorectal Cancer, Hereditary Nonpolyposis, Type 1 52 2.713
18
c EPC004 Epcam-Related Lynch Syndrome 14 2.670
19
CPP003 Cap Polyposis 30 2.506
20
GST086 Gastric Adenocarcinoma and Proximal Polyposis of the Stomach 11 2.285
21
CLR065 Colorectal Adenomatous Polyposis, Autosomal Recessive, with Pilomatricomas 46 2.242
22
APC006 Apc-Associated Polyposis Conditions 3 2.229
23
c CLR037 Colorectal Cancer, Hereditary Nonpolyposis, Type 5 26 2.215
24
c CLR039 Colorectal Cancer, Hereditary Nonpolyposis, Type 4 25 2.215
25
c CLR055 Colorectal Cancer, Hereditary Nonpolyposis, Type 6 23 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 25 1.756
29
c CLR041 Colorectal Cancer, Hereditary Nonpolyposis, Type 2 23 1.602
30
NNP013 Non-Polyposis Turcot Syndrome 12 1.602
31
NSL012 Nasal Polyposis, Familial 2 1.602
32
P BMP001 Bmpr1a-Related Juvenile Polyposis 16 1.602
33
c CLR089 Colorectal Cancer, Hereditary Nonpolyposis, Type 8 18 1.585
34
PRS115 Prosthetic Joint Infection 45 1.585
35
PLY138 Polymerase Proofreading-Related Adenomatous Polyposis 16 1.585
36
c SMD006 Smad4-Related Juvenile Polyposis 3 1.585
37
5Q2001 5q22 Deletion Syndrome 6 1.542
38
c MLH005 Mlh3-Related Lynch Syndrome 8 1.542
39
c PMS002 Pms1-Related Lynch Syndrome 7 1.542
40
c PMS003 Pms2-Related Lynch Syndrome 8 1.542
41
c MLH002 Mlh1-Related Lynch Syndrome 8 1.542
42
c MSH002 Msh2-Related Lynch Syndrome 8 1.542
43
c MSH005 Msh6-Related Lynch Syndrome 8 1.542
44
P CLR023 Colorectal Cancer 96 0.477
45
ADN018 Adenoma 59 0.360
46
DDN006 Duodenitis 44 0.256
47
P CLR108 Colorectal Adenoma 60 0.220
48
DSM004 Desmoid Tumor 55 0.203
49
CLN019 Colonic Disease 50 0.201
50
INT253 Intestinal Benign Neoplasm 48 0.196
51
RCT018 Rectal Neoplasm 53 0.192
52
P ADN016 Adenocarcinoma 69 0.189
53
P INT068 Intestinal Disease 60 0.187
54
CLT003 Colitis 56 0.187
55
P THY032 Thyroiditis 57 0.184
56
RCT017 Rectal Disease 35 0.184
57
c HRD169 Hereditary Colorectal Cancer 42 0.182
58
CLN044 Colon Adenoma 43 0.179
59
ULC004 Ulcerative Colitis 74 0.177
60
c FML053 Familial Colorectal Cancer 50 0.172
61
ALC007 Alcohol Dependence 66 0.169
62
PHR003 Pharyngitis 58 0.169
63
NSP001 Nasopharynx Carcinoma 54 0.169
64
NSP003 Nasopharyngeal Disease 25 0.169
65
CRV068 Cervical Polyp 40 0.167
66
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 35 0.164
67
c INF067 Inflammatory Bowel Disease 10 31 0.155
68
c CLR079 Colorectal Cancer 2 29 0.155
69
GST038 Gastrointestinal Adenoma 28 0.155
70
P SNS014 Sinusitis 66 0.143
71
DDN007 Duodenal Disease 34 0.140
72
P AST005 Asthma 80 0.137
73
P NRV006 Nervous System Cancer 62 0.137
74
c CLR085 Colorectal Cancer 1 39 0.137
75
PRP021 Peripheral Nervous System Neoplasm 49 0.137
76
c CLR075 Colorectal Cancer 3 37 0.130
77
c INF078 Inflammatory Bowel Disease 2 23 0.130
78
c INF071 Inflammatory Bowel Disease 1 51 0.127
79
DDN010 Duodenum Cancer 41 0.127
80
GST053 Gastric Cancer 52 0.127
81
P GST049 Gastrointestinal System Cancer 59 0.123
82
GST050 Gastrointestinal System Disease 58 0.120
83
P LYM118 Lymphoma 68 0.120
84
NSD001 Nose Disease 51 0.120
85
PRT019 Protein-Losing Enteropathy 42 0.120
86
SNS023 Sensory System Cancer 45 0.116
87
HRD059 Hereditary Peripheral Nervous Disorder 12 0.116
88
THY028 Thyroid Cancer 71 0.112
89
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.112
90
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.112
91
P RHN004 Rhinitis 59 0.112
92
P PNC044 Pancreatitis 62 0.112
93
ALR002 Al-Raqad Syndrome 36 0.112
94
DDN022 Duodenum Adenoma 11 0.112
95
P CWD001 Cowden Disease 63 0.108
96
HPT022 Hepatoblastoma 57 0.108
97
c INF086 Inflammatory Bowel Disease 3 20 0.108
98
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 46 0.104
99
P BRS047 Breast Cancer 100 0.099
100
HPT023 Hepatocellular Carcinoma 90 0.099
101
GST040 Gastric Adenocarcinoma 57 0.099
102
PRN021 Paranasal Sinus Disease 50 0.099
103
NSL022 Nasal Cavity Disease 41 0.099
104
ORL014 Oral Pharyngeal Disorders 13 0.099
105
P LKM002 Leukemia 70 0.095
106
PCH007 Pouchitis 40 0.095
107
GST039 Gastroduodenitis 32 0.095
108
HPT067 Hepatocellular Adenoma 41 0.095
109
c INF087 Inflammatory Bowel Disease 4 26 0.095
110
BNN001 Bannayan-Riley-Ruvalcaba Syndrome 56 0.090
111
SRC014 Sarcoma 66 0.090
112
c CLR080 Colorectal Cancer 5 32 0.090
113
c CWD006 Cowden Syndrome 1 43 0.085
114
P INT070 Intestinal Obstruction 55 0.085
115
MNT001 Mantle Cell Lymphoma 72 0.085
116
PPL022 Papilloma 54 0.085
117
RTN023 Retinitis 49 0.085
118
FBR019 Fibromatosis 40 0.085
119
P STM004 Stomach Cancer 73 0.079
120
P HPT021 Hepatitis 74 0.079
121
ART005 Arteriovenous Malformation 63 0.079
122
c CLR077 Colorectal Cancer 10 33 0.079
123
P SCH015 Schizophrenia 78 0.073
124
ALL003 Allergic Rhinitis 67 0.073
125
WST001 West Syndrome 61 0.073
126
DSM003 Desmoid Disease, Hereditary 43 0.073
127
c CLR087 Colorectal Cancer 12 32 0.073
128
P ESP024 Esophagitis 62 0.073
129
P PRN020 Paranasal Sinus Cancer 40 0.073
130
P NSL008 Nasal Cavity Cancer 34 0.073
131
P MLT074 Multiple Endocrine Neoplasia 55 0.073
132
AML029 Ameloblastoma 49 0.073
133
NSP002 Nasopharyngitis 39 0.073
134
JJN003 Jejunal Cancer 29 0.073
135
P GLM045 Glioma 53 0.073
136
c CLR081 Colorectal Cancer 6 23 0.073
137
ORL015 Oral Squamous Cell Carcinoma 55 0.073
138
c INF088 Inflammatory Bowel Disease 5 20 0.073
139
NRN002 Neuronitis 40 0.073
140
c PRN030 Paranasal Sinus Cancer, Adult 14 0.073
141
END072 Endotheliitis 41 0.073
142
P SNS011 Sinus Cancer 24 0.073
143
P LNG032 Lung Cancer 92 0.067
144
P RTN024 Retinoblastoma 75 0.067
145
MLN008 Melanoma 61 0.067
146
P MRT001 Muir-Torre Syndrome 59 0.067
147
P TRC086 Trichohepatoenteric Syndrome 1 46 0.067
148
CSY001 C Syndrome 49 0.067
149
THY103 Thyroid Cancer, Monmedullary, 1 55 0.067
150
P HMN010 Hemangioma 62 0.067
151
P ESN007 Eosinophilia 61 0.067
152
WLL006 Wells Syndrome 57 0.067
153
c AST039 Asthma 2 28 0.067
154
GDS001 Good Syndrome 46 0.067
155
c ACT027 Acute Pancreatitis 59 0.067
156
c CLR017 Clear Cell Sarcoma 48 0.067
157
c CLR083 Colorectal Cancer 8 26 0.067
158
c INH020 Inherited Metabolic Disorder 49 0.067
159
PRS047 Prostatitis 56 0.067
160
ORL011 Oral Cancer 53 0.067
161
PLM018 Pulmonary Sclerosing Hemangioma 39 0.067
162
PPL002 Papillary Carcinoma 50 0.067
163
ATN003 Autonomic Nervous System Neoplasm 43 0.067
164
FNC005 Functional Colonic Disease 32 0.067
165
SCL017 Sclerosing Hemangioma 41 0.067
166
FBR054 Fibroma 44 0.067
167
CRB009 Cerebritis 36 0.067
168
CLR109 Colorectal Adenocarcinoma 50 0.067
169
JVN033 Juvenile Nasopharyngeal Angiofibroma 38 0.067
170
ATS008 Autosomal Dominant Disease 41 0.067
171
FML143 Familial Papillary Thyroid Carcinoma 28 0.067
172
P PNC035 Pancreatic Cancer 86 0.060
173
P HNT016 Huntington Disease 80 0.060
174
P OVR042 Ovarian Cancer 73 0.060
175
c PRK024 Parkinson Disease, Juvenile, Type 2 49 0.060
176
GST019 Gastrointestinal Stromal Tumor 73 0.060
177
CRH001 Crohn's Disease 76 0.060
178
VHW001 Vohwinkel Syndrome 47 0.060
179
LNG024 Langerhans-Cell Histiocytosis 64 0.060
180
P SHR029 Short Syndrome 60 0.060
181
P HRD011 Hereditary Spherocytosis 51 0.060
182
P SML016 Small Intestine Cancer 54 0.060
183
P ORL007 Oral Cavity Cancer 58 0.060
184
P HST010 Histiocytosis 56 0.060
185
STM006 Stomach Disease 48 0.060
186
c ADL017 Adult T-Cell Leukemia 59 0.060
187
INT051 Intussusception 50 0.060
188
VSM001 Vasomotor Rhinitis 33 0.060
189
NRN004 Neuroendocrine Tumor 54 0.060
190
P DRR001 Diarrhea 60 0.060
191
RCT011 Rectal Prolapse 41 0.060
192
c CWD005 Cowden Syndrome 4 23 0.060
193
PRN011 Pernicious Anemia 41 0.060
194
ALL006 Allergic Asthma 59 0.060
195
P SHR001 Short Bowel Syndrome 51 0.060
196
INV006 Inverted Papilloma 43 0.060
197
HYP266 Hypoxia 55 0.060
198
CHL052 Choledochal Cyst 40 0.060
199
P TCL004 T-Cell Leukemia 44 0.060
200
c INF075 Inflammatory Bowel Disease 16 19 0.060
201
PRM190 Periampullary Adenoma 26 0.060
202
c INF073 Inflammatory Bowel Disease 12 20 0.060
203
c INF091 Inflammatory Bowel Disease 8 19 0.060
204
JNS001 Janus Kinase-3 Deficiency 7 0.060
205
RCT035 Rectum Adenoma 14 0.060
206
c PRM023 Pre-Malignant Neoplasm 42 0.060
207
CYS001 Cystic Fibrosis 87 0.052
208
P LFR001 Li-Fraumeni Syndrome 79 0.052
209
P MDL005 Medulloblastoma 76 0.052
210
P MTC003 Metachromatic Leukodystrophy 71 0.052
211
END057 Endometrial Cancer 75 0.052
212
P PRT010 Parathyroid Carcinoma 61 0.052
213
P NSP012 Nasopharyngeal Carcinoma 59 0.052
214
CMM004 Common Variable Immunodeficiency 68 0.052
215
P GST044 Gastritis 64 0.052
216
P ART023 Arthropathy 63 0.052
217
P MSC005 Muscular Dystrophy 64 0.052
218
c HPT016 Hepatitis B 61 0.052
219
AST038 Asthma, Aspirin-Induced 26 0.052
220
P LKD001 Leukodystrophy 58 0.052
221
P MYP006 Myopia 58 0.052
222
PLY023 Polycystic Liver Disease 57 0.052
223
IMP002 Imperforate Anus 54 0.052
224
P ATS007 Autism Spectrum Disorder 64 0.052
225
ALP008 Alopecia 56 0.052
226
ETN001 Eating Disorder 59 0.052
227
c BSL007 Basal Cell Carcinoma 66 0.052
228
HPT074 Hepatic Adenoma, Somatic 35 0.052
229
OCL009 Ocular Cancer 61 0.052
230
P LYM026 Lymphoblastic Leukemia 60 0.052
231
ILM001 Ileum Cancer 35 0.052
232
SNS001 Sensorineural Hearing Loss 52 0.052
233
CND002 Conduct Disorder 54 0.052
234
ORL004 Oral Submucous Fibrosis 52 0.052
235
P LCH002 Lichen Planus 61 0.052
236
P CRN035 Cranial Nerve Palsy 44 0.052
237
SKN023 Skin Tag 48 0.052
238
P INT063 Intellectual Disability 46 0.052
239
VSC006 Vascular Cancer 51 0.052
240
ADR008 Adrenal Adenoma 49 0.052
241
CLF045 Cleft, Median, of Upper Lip with Polyps of Facial Skin and Nasal Mucosa 19 0.052
242
PTN006 Pten Hamartoma Tumor Syndrome 35 0.052
243
c AST037 Asthma 1 35 0.052
244
CHR074 Choriocarcinoma 45 0.052
245
FLR003 Florid Cemento-Osseous Dysplasia 20 0.052
246
P PNB001 Pineoblastoma 35 0.052
247
MCP006 Mucoepidermoid Carcinoma 50 0.052
248
MYP002 Myoepithelial Carcinoma 38 0.052
249
ORL013 Oral Lichen Planus 53 0.052
250
GNG002 Ganglioneuroma 41 0.052
251
PRT018 Portal Vein Thrombosis 48 0.052
252
TST018 Testicular Yolk Sac Tumor 40 0.052
253
PNC019 Pancreatoblastoma 31 0.052
254
P FRT001 Fourth Cranial Nerve Palsy 29 0.052
255
HDN004 Head and Neck Carcinoma 54 0.052
256
ISC015 Ischemic Colitis 38 0.052
257
c CHR038 Chronic Maxillary Sinusitis 34 0.052
258
P KRT005 Keratoacanthoma 41 0.052
259
GST071 Gastrointestinal Carcinoma 37 0.052
260
c CLR082 Colorectal Cancer 7 22 0.052
261
c CLR084 Colorectal Cancer 9 19 0.052
262
PNM003 Pneumatosis Cystoides Intestinalis 32 0.052
263
P MXL015 Maxillary Sinusitis 36 0.052
264
LRG015 Large Intestine Adenoma 13 0.052
265
c INF079 Inflammatory Bowel Disease 20 19 0.052
266
c INF083 Inflammatory Bowel Disease 24 18 0.052
267
c INF089 Inflammatory Bowel Disease 6 19 0.052
268
c INF090 Inflammatory Bowel Disease 7 18 0.052
269
P SRT002 Sertoli Cell Tumor 35 0.052
270
JJN007 Jejunal Adenocarcinoma 29 0.052
271
URT010 Ureteral Obstruction 45 0.052
272
CHR490 Chromosome 10q23 Deletion Syndrome 13 0.052
273
c FML303 Familial/multiple Cancer 15 0.052
274
P PRS040 Prostate Cancer 89 0.042
275
P HRS035 Hirschsprung Disease 1 58 0.042
276
BRN028 Brain Cancer 69 0.042
277
P RBN001 Rubinstein-Taybi Syndrome 65 0.042
278
c MLT024 Multiple Endocrine Neoplasia Iia 64 0.042
279
ICH002 Ichthyosis Bullosa of Siemens 44 0.042
280
P EPD002 Epidermolytic Hyperkeratosis 51 0.042
281
GST092 Gastroesophageal Reflux 62 0.042
282
PSD012 Pseudoachondroplasia 53 0.042
283
ADR016 Adrenal Cortical Carcinoma 60 0.042
284
PCK002 Pick Disease 66 0.042
285
URT039 Urticaria 58 0.042
286
P ICH001 Ichthyosis Vulgaris 44 0.042
287
FCS012 Facioscapulohumeral Muscular Dystrophy 1 50 0.042
288
PLM102 Palmoplantar Keratoderma, Epidermolytic 46 0.042
289
c ART101 Aortic Valve Disease 2 56 0.042
290
CHN016 Cohen Syndrome 55 0.042
291
EPD047 Epidermolysis Bullosa Simplex, Koebner Type 37 0.042
292
P WHT013 White Sponge Nevus 1 40 0.042
293
URB001 Urbach-Wiethe Disease 48 0.042
294
EPD028 Epidermolysis Bullosa Simplex, Dowling-Meara Type 41 0.042
295
EPD056 Epidermolysis Bullosa Simplex-Mp 34 0.042
296
CHL071 Child Syndrome 58 0.042
297
P PCH001 Pachyonychia Congenita 54 0.042
298
CLV009 Clove Syndrome, Somatic 41 0.042
299
LPM004 Lipoma 59 0.042
300
EPD016 Epidermolysis Bullosa 59 0.042
301
ACR012 Aicardi Syndrome 45 0.042
302
PRP019 Peripheral Nervous System Disease 52 0.042
303
STT007 Steatocystoma Multiplex 45 0.042
304
THR013 Thoracic Outlet Syndrome 48 0.042
305
PKL001 Poikiloderma with Neutropenia 43 0.042
306
CNG008 Congenital Ichthyosiform Erythroderma 52 0.042
307
ALL026 Allergic Hypersensitivity Disease 53 0.042
308
ATP002 Atopy 62 0.042
309
PRP027 Peripheral Vascular Disease 69 0.042
310
HNT002 Hantavirus Pulmonary Syndrome 51 0.042
311
PRT036 Peritonitis 65 0.042
312
P PLY006 Polydactyly 56 0.042
313
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 37 0.042
314
c MYP080 Myopathy, Myofibrillar, 4 32 0.042
315
EPD065 Epidermolytic Ichthyosis 38 0.042
316
ANS011 Anus Cancer 44 0.042
317
ADR038 Adermatoglyphia 39 0.042
318
BRL011 Bare Lymphocyte Syndrome, Type I 40 0.042
319
P PRX021 Proximal Symphalangism 49 0.042
320
KDS001 Kid Syndrome 53 0.042
321
P LNG064 Lung Cancer Susceptibility 3 62 0.042
322
EPD041 Epidermolysis Bullosa Simplex, Weber-Cockayne Type 38 0.042
323
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 32 0.042
324
ICH036 Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis 29 0.042
325
P PRM001 Primary Cutaneous Amyloidosis 54 0.042
326
c BLD124 Bleeding Disorder, Platelet-Type, 11 37 0.042
327
ICH031 Ichthyosis with Confetti 27 0.042
328
ESN020 Eosinophilic Granulomatosis with Polyangiitis 38 0.042
329
P FBR025 Fibrochondrogenesis 49 0.042
330
P EPD003 Epidermolysis Bullosa Simplex 50 0.042
331
CRD201 Cardiomyopathy, Dilated, 1c, with or Without Lvnc 22 0.042
332
ANS012 Anus Disease 32 0.042
333
46X010 46xy Partial Gonadal Dysgenesis, with Minifascicular Neuropathy 27 0.042
334
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 42 0.042
335
c BSL024 Basal Cell Carcinoma 1 44 0.042
336
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.042
337
BMF001 Bamforth-Lazarus Syndrome 43 0.042
338
CNS004 Constipation 57 0.042
339
P MSC022 Mosaic Variegated Aneuploidy Syndrome 42 0.042
340
c EPD058 Epidermolysis Bullosa Simplex, Recessive 1 28 0.042
341
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 29 0.042
342
c CWD004 Cowden Syndrome 5 28 0.042
343
c CWD008 Cowden Syndrome 6 26 0.042
344
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 32 0.042
345
HDR002 Hidradenitis Suppurativa 53 0.042
346
P MYT002 Myotonic Dystrophy 46 0.042
347
CRC014 Carcinoid Tumors, Intestinal 30 0.042
348
RDN001 Reading Disorder 39 0.042
349
LCH011 Lichen Planopilaris 40 0.042
350
EXS001 Exostosis 42 0.042
351
CLN045 Colonic Benign Neoplasm 38 0.042
352
EPD066 Epidermoid Brain Tumor 17 0.042
353
SPN331 Spondyloocular Syndrome 27 0.042
354
OST032 Osteofibrous Dysplasia 39 0.042
355
c CHR048 Chronic Rhinitis 39 0.042
356
PLM052 Pulmonary Arteriovenous Malformation 36 0.042
357
P BNG071 Benign Schwannoma 38 0.042
358
ILT001 Ileitis 48 0.042
359
ANK001 Ankylosis 52 0.042
360
ECC004 Eccrine Porocarcinoma 33 0.042
361
ADJ001 Adjustment Disorder 38 0.042
362
LPM005 Lipomatosis 46 0.042
363
VRR004 Verrucous Carcinoma 54 0.042
364
YNG002 Young Syndrome 25 0.042
365
P BRS017 Breast Adenomyoepithelioma 27 0.042
366
GST028 Gastric Squamous Cell Carcinoma 39 0.042
367
ECC008 Eccrine Sweat Gland Neoplasm 24 0.042
368
HDR003 Hidradenitis 46 0.042
369
P SKN013 Skin Benign Neoplasm 38 0.042
370
c NSP009 Nasopharyngeal Carcinoma 2 20 0.042
371
RVL002 Ruvalcaba Syndrome 32 0.042
372
VLV044 Vulvar Intraepithelial Neoplasia 44 0.042
373
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 34 0.042
374
AND005 Androgen Insensitivity Syndrome, Mild 14 0.042
375
BRS058 Breast Myoepithelial Neoplasm 23 0.042
376
BLL004 Bullous Keratopathy 45 0.042
377
PPL009 Papillary Craniopharyngioma 37 0.042
378
BRS063 Breast Squamous Cell Carcinoma 36 0.042
379
CLN015 Colon Adenocarcinoma 55 0.042
380
SKN011 Skin Pilomatrix Carcinoma 21 0.042
381
VSC012 Vesiculobullous Skin Disease 38 0.042
382
BRN032 Brain Glioma 46 0.042
383
TTR011 Tetraploidy 41 0.042
384
ODN006 Odontoma 34 0.042
385
P ATX010 Ataxia Neuropathy Spectrum 24 0.042
386
c FML321 Familial Stomach Cancer 17 0.042
387
INF028 Infundibulocystic Basal Cell Carcinoma 28 0.042
388
INT004 Intraneural Perineurioma 33 0.042
389
RHN002 Rhinoscleroma 34 0.042
390
BLD054 Blood Protein Disease 38 0.042
391
FXP001 Foxp2-Related Speech and Language Disorders 15 0.042
392
ANL002 Anal Gland Neoplasm 15 0.042
393
APC005 Apocrine Sweat Gland Neoplasm 20 0.042
394
END080 Endometrial Disease 42 0.042
395
10Q001 10q22.3q23.3 Microdeletion Syndrome 14 0.042
396
BSL006 Basaloid Squamous Cell Carcinoma 40 0.042
397
HRF001 Hair Follicle Neoplasm 34 0.042
398
MLG011 Malignant Biphasic Mesothelioma 26 0.042
399
INT040 Intrinsic Asthma 40 0.042
400
OTP003 Oto-Palatal-Digital Syndrome 14 0.042
401
EPD004 Epidermolytic Acanthoma 18 0.042
402
LPD007 Lipoadenoma 29 0.042
403
c LRG002 Large Cell Acanthoma 25 0.042
404
FLM001 Filamentary Keratitis 30 0.042
405
c BNG076 Benign Exophthalmos Syndrome 15 0.042
406
c CNG148 Congenital Heart Disease, Atrial Septal Defect 17 0.042
407
GST078 Gastrointestinal Allergy 41 0.042
408
c RP1001 Rp1-Related Retinitis Pigmentosa 13 0.042
409
VSC047 Vascular Malformation 45 0.042
410
P OBS005 Obesity 91 0.030
411
c MCL042 Macular Degeneration, Age-Related, 1 71 0.030
412
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 60 0.030
413
P KDN017 Kidney Cancer 67 0.030
414
P RSP003 Respiratory Failure 68 0.030
415
MCC010 Mccune-Albright Syndrome, Somatic, Mosaic 58 0.030
416
P ALG002 Alagille Syndrome 70 0.030
417
P CMR001 Camurati-Engelmann Disease 63 0.030
418
P LVR013 Liver Disease 76 0.030
419
P CSH001 Cushing's Syndrome 65 0.030
420
c MLT136 Multiple Endocrine Neoplasia 1 68 0.030
421
P OST012 Osteoarthritis 81 0.030
422
P TBR001 Tuberous Sclerosis 68 0.030
423
ACH004 Achondroplasia 64 0.030
424
FRB001 Farber Lipogranulomatosis 54 0.030
425
PLM033 Pulmonary Embolism 59 0.030
426
MRF001 Marfan Syndrome 73 0.030
427
P THY102 Thyroid Cancer, Nonmedullary, 2 60 0.030
428
BSL036 Basal Cell Nevus Syndrome 65 0.030
429
P STR020 Strabismus 55 0.030
430
TST014 Testicular Cancer 55 0.030
431
ADT003 Auditory System Disease 49 0.030
432
DFC004 Deficiency Anemia 64 0.030
433
DWN001 Down Syndrome 65 0.030
434
P PRM011 Primary Ciliary Dyskinesia 56 0.030
435
TST021 Testicular Germ Cell Tumor 67 0.030
436
c NRF018 Neurofibromatosis, Type 1 69 0.030
437
CMM005 Common Cold 58 0.030
438
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.030
439
P INF032 Infertility 61 0.030
440
SHG001 Shigellosis 52 0.030
441
ADL002 Adult Syndrome 53 0.030
442
P DRM010 Dermatomyositis 59 0.030
443
ACH005 Achalasia 55 0.030
444
c MTB001 Metabolic Syndrome X 61 0.030
445
BRN022 Bronchiectasis 55 0.030
446
P AST007 Astrocytoma 66 0.030
447
P INF038 Influenza 71 0.030
448
BRN038 Bronchial Disease 54 0.030
449
ESP023 Esophageal Disease 52 0.030
450
ANC001 Ancylostomiasis 43 0.030
451
ADR005 Adrenal Carcinoma 57 0.030
452
TMR010 Tumor Predisposition Syndrome 58 0.030
453
SCH014 Schistosomiasis 59 0.030
454
CYS005 Cysticercosis 52 0.030
455
ACN002 Acanthosis Nigricans 59 0.030
456
P END044 Endometriosis 53 0.030
457
ALV010 Alveolar Soft-Part Sarcoma 53 0.030
458
c CLR066 Ciliary Dyskinesia, Primary, 2 26 0.030
459
OLG005 Oligodontia-Colorectal Cancer Syndrome 20 0.030
460
P MTR004 Maturity-Onset Diabetes of the Young 58 0.030
461
DYS073 Dysphagia 51 0.030
462
c CLR095 Ciliary Dyskinesia, Primary, 19 21 0.030
463
CHG001 Chagas Disease 62 0.030
464
DYS011 Dyskinesia of Esophagus 31 0.030
465
RHB003 Rhabdomyosarcoma 55 0.030
466
IRN001 Iron Deficiency Anemia 51 0.030
467
CNV002 Conversion Disorder 45 0.030
468
P HRD004 Hereditary Breast Ovarian Cancer 57 0.030
469
DBW001 Dubowitz Syndrome 48 0.030
470
P DDN001 Duodenal Ulcer 51 0.030
471
ALN001 Aland Island Eye Disease 45 0.030
472
P PRK001 Porokeratosis 45 0.030
473
PRL009 Prolactinoma 63 0.030
474
ATR013 Atrichia with Papular Lesions 36 0.030
475
NRM005 Neuromuscular Disease 56 0.030
476
GST060 Gastric Cancer, Somatic 44 0.030
477
P PRT013 Portal Hypertension 61 0.030
478
RPR002 Reproductive System Disease 45 0.030
479
ASC002 Ascariasis 38 0.030
480
c TRC078 Trichohepatoenteric Syndrome 2 30 0.030
481
c CLR090 Ciliary Dyskinesia, Primary, 22 23 0.030
482
ACD009 Acid-Labile Subunit, Deficiency of 37 0.030
483
c CWD003 Cowden Syndrome 2 34 0.030
484
c CLR068 Ciliary Dyskinesia, Primary, 5 22 0.030
485
c CWD007 Cowden Syndrome 3 23 0.030
486
P CHN005 Choanal Atresia 42 0.030
487
CLR096 Ciliary Dyskinesia, Primary, 1, with or Without Situs Inversus 35 0.030
488
ART017 Aortic Disease 57 0.030
489
c CLR114 Ciliary Dyskinesia, Primary, 30 21 0.030
490
P ANG015 Angioedema 53 0.030
491
GST045 Gastroenteritis 59 0.030
492
P BCL006 B-Cell Lymphomas 64 0.030
493
NSY001 N Syndrome 42 0.030
494
EXS013 Exstrophy-Epispadias Complex 33 0.030
495
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 31 0.030
496
LRN003 Learning Disability 49 0.030
497
LMY002 Leiomyoma 56 0.030
498
CNN005 Connective Tissue Disease 60 0.030
499
P UTR038 Uterine Disease 38 0.030
500
NWC001 Newcastle Disease 51 0.030
501
MGC001 Megacolon 50 0.030
502
SFT003 Soft Tissue Sarcoma 55 0.030
503
FML039 Female Reproductive System Disease 49 0.030
504
TRN018 Transitional Cell Carcinoma 56 0.030
505
RSD004 Rosai-Dorfman Disease 40 0.030
506
INT017 Intestinal Schistosomiasis 45 0.030
507
c INF068 Inflammatory Bowel Disease 13 23 0.030
508
LYM052 Lymphomatoid Papulosis 45 0.030
509
TNS007 Taeniasis 41 0.030
510
UTR024 Uterine Carcinosarcoma 52 0.030
511
MLL004 Mallory-Weiss Syndrome 25 0.030
512
ESN014 Eosinophilic Enteropathy 21 0.030
513
STT009 Sutton Disease 2 21 0.030
514
HDC001 Headache 52 0.030
515
PRC021 Parc Syndrome 22 0.030
516
SWL001 Swallowing Disorders 33 0.030
517
DVR002 Diverticulitis 47 0.030
518
c INF093 Inflammatory Bowel Disease 14 22 0.030
519
P TRT010 Teratoma 49 0.030
520
CHR001 Churg-Strauss Syndrome 48 0.030
521
CRH005 Crohn's Colitis 50 0.030
522
FML038 Female Reproductive Organ Cancer 50 0.030
523
PTT006 Pituitary Adenoma 54 0.030
524
HYP458 Hyper Ige Syndrome 43 0.030
525
SML036 Small Intestinal Adenocarcinoma 46 0.030
526
UTR033 Uterine Corpus Cancer 50 0.030
527
c ATM024 Autoimmune Pancreatitis 46 0.030
528
FBR003 Fibrous Histiocytoma 46 0.030
529
BLD053 Blood Platelet Disease 44 0.030
530
MLK006 Milk Allergy 50 0.030
531
CYS009 Cystadenoma 40 0.030
532
GST030 Gastrinoma 39 0.030
533
MLK004 Malakoplakia 28 0.030
534
LKC003 Leukocyte Disease 45 0.030
535
P CRV031 Cervical Adenocarcinoma 52 0.030
536
P CNN004 Connective Tissue Cancer 44 0.030
537
PLS025 Plasmablastic Lymphoma 46 0.030
538
PLM030 Pleomorphic Rhabdomyosarcoma 37 0.030
539
c CWD009 Cowden Syndrome 7 14 0.030
540
BCH001 Beach Ear 16 0.030
541
ALL007 Allergic Urticaria 31 0.030
542
MLG028 Malignant Neoplasm of Acoustic Nerve 14 0.030
543
PRS059 Prostaglandin-Endoperoxide Synthase Deficiency 12 0.030
544
P BLD051 Blood Coagulation Disease 44 0.030
545
ETH009 Ethmoid Sinusitis 32 0.030
546
BRN039 Bronchial Neoplasm 35 0.030
547
BCL011 Bacillary Angiomatosis 25 0.030
548
c ALP005 Alpha Chain Disease 36 0.030
549
HST009 Histiocytoma 47 0.030
550
EPS026 Epispadias 36 0.030
551
CHR034 Chromophobe Adenoma 41 0.030
552
UPP004 Upper Respiratory Tract Disease 48 0.030
553
LMY003 Leiomyomatosis 42 0.030
554
c INF081 Inflammatory Bowel Disease 22 18 0.030
555
OPT007 Optic Nerve Glioma 43 0.030
556
TXC001 Toxic Megacolon 26 0.030
557
c HMG004 Hemoglobin D Disease 32 0.030
558
GGN002 Gigantism 29 0.030
559
c INF074 Inflammatory Bowel Disease 15 18 0.030
560
c INF082 Inflammatory Bowel Disease 23 17 0.030
561
c INF092 Inflammatory Bowel Disease 9 18 0.030
562
MRG003 Marginal Zone B-Cell Lymphoma 50 0.030
563
VLL006 Villous Adenoma 32 0.030
564
GST006 Gastric Leiomyoma 31 0.030
565
ANG004 Angioid Streaks 29 0.030
566
CNT045 Central Nervous System Sarcoma 18 0.030
567
RNL013 Renal Adenoma 32 0.030
568
DDN009 Duodenal Obstruction 35 0.030
569
ATS009 Autosomal Genetic Disease 38 0.030
570
GRN011 Granulomatous Gastritis 28 0.030
571
ANG037 Angiomatosis 33 0.030
572
c ADN012 Adenocarcinoma in Situ 44 0.030
573
PDT027 Pediatric Ulcerative Colitis 26 0.030
574
WSC001 Wisconsin Syndrome 16 0.030
575
WTH001 Withdrawal Disorder 36 0.030
576
END016 Endocervicitis 27 0.030
577
MCN011 Mucinoses 31 0.030
578
c DLT001 Delta Chain Disease 14 0.030
579
c FML311 Familial Colorectal Cancer Type X 32 0.030
580
PRM025 Primary Bacterial Infectious Disease 42 0.030
581
PRS126 Prostate Cancer Susceptibility 30 0.030