Search results for "polyposis"

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

783 hits were found for 'polyposis'

# Family MCID Name MIFTS Score
1
P FML011 Familial Adenomatous Polyposis 65 9.871
2
PLY056 Polyposis, Juvenile Intestinal 55 7.378
3
ADN021 Adenomatous Polyposis Coli 71 5.613
4
PTZ001 Peutz-Jeghers Syndrome 67 5.391
5
MTY001 Mutyh-Associated Polyposis 44 5.127
6
P ATT003 Attenuated Familial Adenomatous Polyposis 41 4.827
7
CRN014 Cronkhite-Canada Syndrome 46 3.807
8
MSM014 Mismatch Repair Cancer Syndrome 58 3.788
9
JVN012 Juvenile Polyposis/hereditary Hemorrhagic Telangiectasia Syndrome 30 3.775
10
c PLY066 Polyposis Syndrome, Hereditary Mixed, 2 18 3.434
11
FML254 Familial Adenomatous Polyposis Due to 5q22.2 Microdeletion 10 3.399
12
P LYN001 Lynch Syndrome 64 3.254
13
P JVN034 Juvenile Polyposis of Infancy 18 2.715
14
c HRD101 Hereditary Mixed Polyposis Syndrome 1 17 2.654
15
CPP003 Cap Polyposis 26 2.420
16
HYP466 Hyperplastic Polyposis Syndrome 29 2.346
17
c FML299 Familial Adenomatous Polyposis 3 17 2.298
18
c ADN040 Adenomas, Multiple Colorectal 21 2.252
19
P CLR070 Colorectal Cancer, Hereditary Nonpolyposis, Type 1 44 2.211
20
GNR035 Generalized Juvenile Polyposis/juvenile Polyposis Coli 19 2.191
21
CLR065 Colorectal Adenomatous Polyposis, Autosomal Recessive, with Pilomatricomas 46 2.179
22
c BMP001 Bmpr1a-Related Juvenile Polyposis 15 2.179
23
GST086 Gastric Adenocarcinoma and Proximal Polyposis of the Stomach 11 2.179
24
APC006 Apc-Associated Polyposis Conditions 5 2.179
25
c APC008 Apc-Related Attenuated Familial Adenomatous Polyposis 9 2.167
26
c AXN008 Axin2-Related Attenuated Familial Adenomatous Polyposis 9 2.167
27
c MTY002 Mutyh-Related Attenuated Familial Adenomatous Polyposis 9 2.167
28
c SMD006 Smad4-Related Juvenile Polyposis 5 2.167
29
c EPC004 Epcam-Related Lynch Syndrome 10 2.136
30
P HRD144 Hereditary Mixed Polyposis Syndrome 25 1.688
31
NNP013 Non-Polyposis Turcot Syndrome 30 1.563
32
c CLR041 Colorectal Cancer, Hereditary Nonpolyposis, Type 2 22 1.563
33
NSL012 Nasal Polyposis, Familial 2 1.563
34
c CLR037 Colorectal Cancer, Hereditary Nonpolyposis, Type 5 24 1.549
35
c CLR089 Colorectal Cancer, Hereditary Nonpolyposis, Type 8 23 1.549
36
c CLR039 Colorectal Cancer, Hereditary Nonpolyposis, Type 4 23 1.549
37
c CLR100 Colorectal Cancer, Hereditary Nonpolyposis, Type 7 22 1.549
38
c CLR055 Colorectal Cancer, Hereditary Nonpolyposis, Type 6 21 1.549
39
TRC098 Turcot Syndrome with Polyposis 7 1.549
40
PRS115 Prosthetic Joint Infection 35 1.532
41
c PMS002 Pms1-Related Lynch Syndrome 8 1.510
42
c PMS003 Pms2-Related Lynch Syndrome 8 1.510
43
c MLH002 Mlh1-Related Lynch Syndrome 8 1.510
44
c MLH005 Mlh3-Related Lynch Syndrome 8 1.510
45
c MSH002 Msh2-Related Lynch Syndrome 8 1.510
46
c MSH005 Msh6-Related Lynch Syndrome 8 1.510
47
5Q2001 5q22 Deletion Syndrome 8 1.510
48
P CLR023 Colorectal Cancer 95 0.413
49
ADN018 Adenoma 54 0.306
50
DDN006 Duodenitis 40 0.213
51
P CLR108 Colorectal Adenoma 49 0.181
52
CLN045 Colonic Benign Neoplasm 38 0.179
53
DSM004 Desmoid Tumor 50 0.173
54
GST050 Gastrointestinal System Disease 43 0.167
55
CLT003 Colitis 47 0.161
56
CLN019 Colonic Disease 41 0.157
57
c HRD169 Hereditary Colorectal Cancer 34 0.157
58
P THY032 Thyroiditis 48 0.154
59
CLN044 Colon Adenoma 35 0.154
60
P ADN016 Adenocarcinoma 56 0.152
61
ULC004 Ulcerative Colitis 75 0.150
62
c FML053 Familial Colorectal Cancer 40 0.150
63
INT253 Intestinal Benign Neoplasm 33 0.147
64
P INT068 Intestinal Disease 44 0.142
65
P GST049 Gastrointestinal System Cancer 43 0.142
66
GST038 Gastrointestinal Adenoma 19 0.132
67
P SNS014 Sinusitis 49 0.127
68
P AST005 Asthma 77 0.121
69
DDN007 Duodenal Disease 25 0.118
70
c CLR079 Colorectal Cancer 2 14 0.118
71
P LRG017 Large Intestine Cancer 37 0.112
72
P TRC086 Trichohepatoenteric Syndrome 1 42 0.109
73
RCT018 Rectal Neoplasm 43 0.106
74
GST053 Gastric Cancer 41 0.106
75
c CNT033 Central Nervous System Cancer 45 0.102
76
P NRV006 Nervous System Cancer 44 0.102
77
PRP021 Peripheral Nervous System Neoplasm 34 0.102
78
DDN023 Duodenal Benign Neoplasm 33 0.102
79
NSD001 Nose Disease 28 0.102
80
c INF078 Inflammatory Bowel Disease 2 15 0.102
81
HRD059 Hereditary Peripheral Nervous Disorder 2 0.102
82
P PNC044 Pancreatitis 51 0.099
83
c CLR085 Colorectal Cancer 1 23 0.099
84
P RHN004 Rhinitis 47 0.095
85
c CLR075 Colorectal Cancer 3 26 0.095
86
RCT017 Rectal Disease 23 0.095
87
DDN022 Duodenum Adenoma 3 0.095
88
P HRD008 Hereditary Hemorrhagic Telangiectasia 74 0.092
89
P CWD001 Cowden Disease 64 0.092
90
THY028 Thyroid Cancer 60 0.092
91
HPT022 Hepatoblastoma 49 0.092
92
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 46 0.092
93
PRT019 Protein-Losing Enteropathy 40 0.092
94
P HMR005 Hemorrhoid 35 0.092
95
THR013 Thoracic Outlet Syndrome 47 0.088
96
MNN014 Mononeuritis 39 0.088
97
PRN021 Paranasal Sinus Disease 38 0.088
98
NSL022 Nasal Cavity Disease 28 0.088
99
HPT023 Hepatocellular Carcinoma 90 0.084
100
ACN002 Acanthosis Nigricans 53 0.084
101
c INF071 Inflammatory Bowel Disease 1 48 0.084
102
P BRS047 Breast Cancer 100 0.079
103
ANR002 Aniridia 72 0.079
104
MNT001 Mantle Cell Lymphoma 60 0.079
105
c PNC108 Pancreatitis, Hereditary 59 0.079
106
CHL071 Child Syndrome 51 0.079
107
KDS001 Kid Syndrome 44 0.079
108
PPL001 Papillary Adenoma 36 0.079
109
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 34 0.079
110
P ATX010 Ataxia Neuropathy Spectrum 31 0.079
111
c INF086 Inflammatory Bowel Disease 3 9 0.079
112
P HRM001 Hermansky-Pudlak Syndrome 62 0.075
113
P HMP002 Hemophagocytic Lymphohistiocytosis 59 0.075
114
BNN001 Bannayan-Riley-Ruvalcaba Syndrome 57 0.075
115
SRC014 Sarcoma 57 0.075
116
HNT002 Hantavirus Pulmonary Syndrome 52 0.075
117
RTN023 Retinitis 43 0.075
118
HPT067 Hepatocellular Adenoma 36 0.075
119
GST039 Gastroduodenitis 30 0.075
120
P ATX030 Ataxia-Telangiectasia 76 0.070
121
AND015 Androgen Insensitivity 65 0.070
122
P LKM002 Leukemia 61 0.070
123
ALL003 Allergic Rhinitis 61 0.070
124
P AXN010 Axenfeld-Rieger Syndrome, Type 3 60 0.070
125
ART001 Arterial Tortuosity Syndrome 59 0.070
126
P HPT021 Hepatitis 58 0.070
127
P AND016 Andersen Syndrome 58 0.070
128
GST060 Gastric Cancer, Somatic 48 0.070
129
MYC002 Mycobacterium Avium Complex Disease 46 0.070
130
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 46 0.070
131
GST040 Gastric Adenocarcinoma 44 0.070
132
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 43 0.070
133
NRN002 Neuronitis 40 0.070
134
c CWD006 Cowden Syndrome 1 39 0.070
135
FBR019 Fibromatosis 36 0.070
136
PCH007 Pouchitis 35 0.070
137
ALR002 Al-Raqad Syndrome 23 0.070
138
c BNG076 Benign Exophthalmos Syndrome 21 0.070
139
AND005 Androgen Insensitivity Syndrome, Mild 19 0.070
140
c INF087 Inflammatory Bowel Disease 4 15 0.070
141
P PNC035 Pancreatic Cancer 78 0.065
142
c SPN225 Spondyloarthropathy 1 66 0.065
143
P ANG001 Angelman Syndrome 66 0.065
144
WST001 West Syndrome 54 0.065
145
P ACR001 Aicardi-Goutieres Syndrome 53 0.065
146
SCH016 Schimke Immunoosseous Dysplasia 51 0.065
147
PRS047 Prostatitis 50 0.065
148
PPL022 Papilloma 49 0.065
149
P ESN007 Eosinophilia 48 0.065
150
c ART101 Aortic Valve Disease 2 46 0.065
151
TTR016 Tetra-Amelia Syndrome 38 0.065
152
DSM003 Desmoid Disease, Hereditary 27 0.065
153
GRN008 Granular Cell Carcinoma 23 0.065
154
c CLR077 Colorectal Cancer 10 22 0.065
155
c CLR087 Colorectal Cancer 12 19 0.065
156
c CLR080 Colorectal Cancer 5 16 0.065
157
c CLR081 Colorectal Cancer 6 13 0.065
158
P PRS040 Prostate Cancer 90 0.059
159
c AMY091 Amyotrophic Lateral Sclerosis 1 83 0.059
160
CRH001 Crohn's Disease 80 0.059
161
ART005 Arteriovenous Malformation 56 0.059
162
P HMN010 Hemangioma 54 0.059
163
DFC004 Deficiency Anemia 52 0.059
164
P ESP024 Esophagitis 51 0.059
165
KRT002 Keratomalacia 49 0.059
166
WLL006 Wells Syndrome 48 0.059
167
ALL006 Allergic Asthma 46 0.059
168
ORL015 Oral Squamous Cell Carcinoma 45 0.059
169
CSY001 C Syndrome 44 0.059
170
FCT013 Factor V Leiden Thrombophilia 43 0.059
171
P MLT074 Multiple Endocrine Neoplasia 43 0.059
172
END072 Endotheliitis 39 0.059
173
NSP002 Nasopharyngitis 38 0.059
174
CRB009 Cerebritis 37 0.059
175
GDS001 Good Syndrome 37 0.059
176
STM006 Stomach Disease 36 0.059
177
UND005 Undifferentiated Pleomorphic Sarcoma 31 0.059
178
c AST039 Asthma 2 23 0.059
179
P LNG032 Lung Cancer 91 0.053
180
P SCH015 Schizophrenia 79 0.053
181
P LFR001 Li-Fraumeni Syndrome 79 0.053
182
P OVR042 Ovarian Cancer 69 0.053
183
END057 Endometrial Cancer 67 0.053
184
P STM004 Stomach Cancer 63 0.053
185
IMG001 Image Syndrome 56 0.053
186
IRR002 Irritable Bowel Syndrome 53 0.053
187
P SHR029 Short Syndrome 49 0.053
188
P PTT050 Pituitary Adenoma, Growth Hormone-Secreting 47 0.053
189
c ACT027 Acute Pancreatitis 47 0.053
190
THY103 Thyroid Cancer, Monmedullary, 1 46 0.053
191
P INT070 Intestinal Obstruction 45 0.053
192
ORL011 Oral Cancer 43 0.053
193
PPL002 Papillary Carcinoma 43 0.053
194
P SHR001 Short Bowel Syndrome 42 0.053
195
INT051 Intussusception 41 0.053
196
NTR005 Nutritional Deficiency Disease 41 0.053
197
CLR109 Colorectal Adenocarcinoma 40 0.053
198
c SML016 Small Intestine Cancer 39 0.053
199
JVN033 Juvenile Nasopharyngeal Angiofibroma 37 0.053
200
FBR054 Fibroma 36 0.053
201
AML029 Ameloblastoma 36 0.053
202
SCL017 Sclerosing Hemangioma 36 0.053
203
INV006 Inverted Papilloma 35 0.053
204
RCT011 Rectal Prolapse 34 0.053
205
PRP019 Peripheral Nervous System Disease 31 0.053
206
GST071 Gastrointestinal Carcinoma 31 0.053
207
PLM018 Pulmonary Sclerosing Hemangioma 30 0.053
208
c PRM023 Pre-Malignant Neoplasm 29 0.053
209
c CWD005 Cowden Syndrome 4 21 0.053
210
c INF088 Inflammatory Bowel Disease 5 19 0.053
211
DDN003 Duodenum Adenocarcinoma 18 0.053
212
RCT035 Rectum Adenoma 9 0.053
213
c INF073 Inflammatory Bowel Disease 12 9 0.053
214
P HNT016 Huntington Disease 78 0.046
215
P RTN024 Retinoblastoma 74 0.046
216
P MTC003 Metachromatic Leukodystrophy 72 0.046
217
TTR001 Tetralogy of Fallot 68 0.046
218
BSL036 Basal Cell Nevus Syndrome 64 0.046
219
LNG024 Langerhans-Cell Histiocytosis 63 0.046
220
BRN028 Brain Cancer 59 0.046
221
PRT036 Peritonitis 58 0.046
222
P MRT001 Muir-Torre Syndrome 58 0.046
223
CHR001 Churg-Strauss Syndrome 53 0.046
224
P HRD011 Hereditary Spherocytosis 52 0.046
225
P HST010 Histiocytosis 51 0.046
226
VHW001 Vohwinkel Syndrome 50 0.046
227
P GST044 Gastritis 49 0.046
228
c ADL017 Adult T-Cell Leukemia 48 0.046
229
P ORL007 Oral Cavity Cancer 47 0.046
230
CND002 Conduct Disorder 45 0.046
231
P LKD001 Leukodystrophy 45 0.046
232
PRN011 Pernicious Anemia 44 0.046
233
ADR008 Adrenal Adenoma 44 0.046
234
NRN004 Neuroendocrine Tumor 44 0.046
235
c PND001 Pain Disorder 43 0.046
236
c CLR017 Clear Cell Sarcoma 43 0.046
237
HYP266 Hypoxia 42 0.046
238
SPN035 Spindle Cell Sarcoma 41 0.046
239
VSC006 Vascular Cancer 40 0.046
240
P TCL004 T-Cell Leukemia 40 0.046
241
CRP017 Carpal Tunnel Syndrome, Familial 39 0.046
242
GRM004 Germinoma 36 0.046
243
VSM001 Vasomotor Rhinitis 35 0.046
244
CHL052 Choledochal Cyst 34 0.046
245
ILL001 Ileal Neoplasm 32 0.046
246
c CHR038 Chronic Maxillary Sinusitis 32 0.046
247
ATS008 Autosomal Dominant Disease 31 0.046
248
CRV068 Cervical Polyp 29 0.046
249
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 28 0.046
250
PLM052 Pulmonary Arteriovenous Malformation 28 0.046
251
TFT003 Tufting Enteropathy 27 0.046
252
FNC005 Functional Colonic Disease 24 0.046
253
AST038 Asthma, Aspirin-Induced 24 0.046
254
FML143 Familial Papillary Thyroid Carcinoma 22 0.046
255
c AST037 Asthma 1 20 0.046
256
PRM190 Periampullary Adenoma 19 0.046
257
MDN003 Median Cleft of Upper Lip with Polyps of Facial Skin and Nasal Mucosa 19 0.046
258
ILM001 Ileum Cancer 13 0.046
259
c INF089 Inflammatory Bowel Disease 6 10 0.046
260
c INF075 Inflammatory Bowel Disease 16 9 0.046
261
c INF083 Inflammatory Bowel Disease 24 9 0.046
262
c FML303 Familial/multiple Cancer 6 0.046
263
LRG015 Large Intestine Adenoma 5 0.046
264
CYS001 Cystic Fibrosis 90 0.037
265
P RHM011 Rheumatoid Arthritis 88 0.037
266
CDS001 Cadasil 70 0.037
267
P MDL005 Medulloblastoma 69 0.037
268
c HYP595 Hypertension, Essential 68 0.037
269
GST019 Gastrointestinal Stromal Tumor 68 0.037
270
GLL008 Gilles De La Tourette Syndrome 67 0.037
271
GLN010 Glanzmann Thrombasthenia 65 0.037
272
P INF038 Influenza 64 0.037
273
CMM004 Common Variable Immunodeficiency 64 0.037
274
PRP027 Peripheral Vascular Disease 62 0.037
275
c MLT024 Multiple Endocrine Neoplasia Iia 61 0.037
276
PCK002 Pick Disease 61 0.037
277
SKN016 Skin Disease 61 0.037
278
P ATS007 Autism Spectrum Disorder 60 0.037
279
P EHL033 Ehlers-Danlos Syndrome, Classic Type 60 0.037
280
TST021 Testicular Germ Cell Tumor 60 0.037
281
P HRS035 Hirschsprung Disease 1 59 0.037
282
c HPT016 Hepatitis B 59 0.037
283
GST092 Gastroesophageal Reflux 58 0.037
284
P LYM026 Lymphoblastic Leukemia 57 0.037
285
c BSL007 Basal Cell Carcinoma 57 0.037
286
P BCL006 B-Cell Lymphomas 57 0.037
287
P AST007 Astrocytoma 55 0.037
288
SMT008 Smith-Magenis Syndrome 54 0.037
289
MLN008 Melanoma 54 0.037
290
P PRT010 Parathyroid Carcinoma 53 0.037
291
P MSC005 Muscular Dystrophy 52 0.037
292
ETN001 Eating Disorder 52 0.037
293
CLF027 Cleft Palate, Isolated 52 0.037
294
c MTB001 Metabolic Syndrome X 52 0.037
295
P ART023 Arthropathy 50 0.037
296
P LCH002 Lichen Planus 50 0.037
297
URT039 Urticaria 50 0.037
298
CHN016 Cohen Syndrome 49 0.037
299
SNS001 Sensorineural Hearing Loss 49 0.037
300
P THY102 Thyroid Cancer, Nonmedullary, 2 49 0.037
301
GLC003 Glucose Intolerance 49 0.037
302
LPM004 Lipoma 48 0.037
303
SFT003 Soft Tissue Sarcoma 48 0.037
304
ADR015 Adrenocortical Carcinoma 48 0.037
305
ORL004 Oral Submucous Fibrosis 46 0.037
306
URB001 Urbach-Wiethe Disease 46 0.037
307
ACR012 Aicardi Syndrome 46 0.037
308
EVN001 Evans' Syndrome 46 0.037
309
P MYP006 Myopia 46 0.037
310
IMP002 Imperforate Anus 45 0.037
311
P DRR001 Diarrhea 45 0.037
312
MTH009 Mouth Disease 44 0.037
313
CNS004 Constipation 44 0.037
314
CRC006 Carcinoid Syndrome 44 0.037
315
P HRD004 Hereditary Breast Ovarian Cancer 44 0.037
316
MCP006 Mucoepidermoid Carcinoma 43 0.037
317
CHR074 Choriocarcinoma 43 0.037
318
MSM001 Meesmann Corneal Dystrophy 42 0.037
319
P MSC022 Mosaic Variegated Aneuploidy Syndrome 42 0.037
320
TLN003 Telangiectasis 41 0.037
321
DCT002 Ductal Carcinoma in Situ 41 0.037
322
PRT018 Portal Vein Thrombosis 41 0.037
323
P TRT010 Teratoma 40 0.037
324
P BRS053 Breast Fibroadenoma 40 0.037
325
CLN015 Colon Adenocarcinoma 40 0.037
326
VLV044 Vulvar Intraepithelial Neoplasia 40 0.037
327
MNT002 Mental Depression 39 0.037
328
EXS001 Exostosis 39 0.037
329
P SKN013 Skin Benign Neoplasm 39 0.037
330
LPM005 Lipomatosis 39 0.037
331
URT010 Ureteral Obstruction 38 0.037
332
NRR001 Neuroretinitis 38 0.037
333
ORL013 Oral Lichen Planus 38 0.037
334
TTR011 Tetraploidy 37 0.037
335
CHR010 Chorioangioma 37 0.037
336
P INT063 Intellectual Disability 36 0.037
337
PLM005 Pleomorphic Lipoma 36 0.037
338
ADR041 Adrenal Cortical Adenoma 36 0.037
339
INT276 Interatrial Communication 36 0.037
340
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 34 0.037
341
PTN006 Pten Hamartoma Tumor Syndrome 34 0.037
342
P PNB001 Pineoblastoma 34 0.037
343
ANS011 Anus Cancer 34 0.037
344
STT004 Steatorrhea 33 0.037
345
ISC015 Ischemic Colitis 33 0.037
346
c PRK024 Parkinson Disease, Juvenile, Type 2 33 0.037
347
SKN023 Skin Tag 33 0.037
348
P SRT002 Sertoli Cell Tumor 33 0.037
349
P CRN035 Cranial Nerve Palsy 33 0.037
350
PNM003 Pneumatosis Cystoides Intestinalis 32 0.037
351
INT040 Intrinsic Asthma 31 0.037
352
TST018 Testicular Yolk Sac Tumor 31 0.037
353
ODN006 Odontoma 30 0.037
354
HPT074 Hepatic Adenoma, Somatic 30 0.037
355
BRL011 Bare Lymphocyte Syndrome, Type I 30 0.037
356
PNC019 Pancreatoblastoma 30 0.037
357
AMP009 Ampulla of Vater Adenocarcinoma 27 0.037
358
P FRT001 Fourth Cranial Nerve Palsy 27 0.037
359
c CWD004 Cowden Syndrome 5 27 0.037
360
JJN007 Jejunal Adenocarcinoma 26 0.037
361
RDN001 Reading Disorder 25 0.037
362
CRC014 Carcinoid Tumors, Intestinal 25 0.037
363
BLD054 Blood Protein Disease 24 0.037
364
c CWD008 Cowden Syndrome 6 24 0.037
365
ANS012 Anus Disease 23 0.037
366
FLR003 Florid Cemento-Osseous Dysplasia 23 0.037
367
c CLR083 Colorectal Cancer 8 17 0.037
368
YNG002 Young Syndrome 16 0.037
369
10Q001 10q22.3q23.3 Microdeletion Syndrome 15 0.037
370
c CLR084 Colorectal Cancer 9 11 0.037
371
JNS001 Janus Kinase-3 Deficiency 8 0.037
372
ANL002 Anal Gland Neoplasm 6 0.037
373
P OBS005 Obesity 89 0.026
374
P DBT085 Diabetes Mellitus, Insulin-Dependent 82 0.026
375
P OST012 Osteoarthritis 79 0.026
376
GLC006 Galactosemia 76 0.026
377
c MCL042 Macular Degeneration, Age-Related, 1 74 0.026
378
P NRB001 Neuroblastoma 73 0.026
379
MRF001 Marfan Syndrome 72 0.026
380
SQM013 Squamous Cell Carcinoma, Head and Neck 71 0.026
381
ESP021 Esophageal Cancer 69 0.026
382
c MCP037 Mucopolysaccharidosis is 68 0.026
383
STR067 Stroke, Ischemic 68 0.026
384
BRK010 Burkitt Lymphoma 68 0.026
385
P CSH001 Cushing's Syndrome 67 0.026
386
P RBN001 Rubinstein-Taybi Syndrome 66 0.026
387
P ALG002 Alagille Syndrome 66 0.026
388
P TBR001 Tuberous Sclerosis 65 0.026
389
ACH004 Achondroplasia 65 0.026
390
P EPD002 Epidermolytic Hyperkeratosis 64 0.026
391
c LKM062 Leukemia, Acute Lymphoblastic 63 0.026
392
BLM001 Bloom Syndrome 63 0.026
393
c NRF018 Neurofibromatosis, Type 1 63 0.026
394
c MLT136 Multiple Endocrine Neoplasia 1 62 0.026
395
ATS001 Autistic Disorder 62 0.026
396
LYM115 Lymphoma, Non-Hodgkin 62 0.026
397
DWN001 Down Syndrome 62 0.026
398
P LKM068 Leukemia, Chronic Myeloid, Somatic 62 0.026
399
WLM007 Wilms Tumor Susceptibility-5 61 0.026
400
P END044 Endometriosis 61 0.026
401
P KDN017 Kidney Cancer 60 0.026
402
TNG009 Tongue Squamous Cell Carcinoma 60 0.026
403
P LVR013 Liver Disease 59 0.026
404
TYP007 Typhoid Fever 59 0.026
405
WLL001 Williams-Beuren Syndrome 59 0.026
406
P RSP003 Respiratory Failure 58 0.026
407
CRB039 Cerebrovascular Disease 58 0.026
408
c MYT021 Myotonic Dystrophy 1 58 0.026
409
P DRM010 Dermatomyositis 57 0.026
410
OVR078 Ovarian Cancer, Somatic 56 0.026
411
ISV001 Isovaleric Acidemia 56 0.026
412
P RCK004 Rickets 55 0.026
413
c MNN043 Meningioma, Familial 55 0.026
414
SCH014 Schistosomiasis 55 0.026
415
P ORT004 Orthostatic Intolerance 55 0.026
416
MCC010 Mccune-Albright Syndrome, Somatic, Mosaic 55 0.026
417
P CMR001 Camurati-Engelmann Disease 54 0.026
418
P HYD006 Hydrocephalus 54 0.026
419
P PRM011 Primary Ciliary Dyskinesia 54 0.026
420
RBR001 Roberts Syndrome 54 0.026
421
P EPL002 Epilepsy Syndrome 54 0.026
422
EYD002 Eye Disease 54 0.026
423
FRB001 Farber Lipogranulomatosis 53 0.026
424
DMN002 Dementia 53 0.026
425
CHG001 Chagas Disease 53 0.026
426
P GLB002 Glioblastoma 53 0.026
427
PLM033 Pulmonary Embolism 53 0.026
428
P HYP086 Hypothyroidism 52 0.026
429
OSS012 Osseous Heteroplasia, Progressive 52 0.026
430
CMM005 Common Cold 52 0.026
431
P INF032 Infertility 52 0.026
432
P PCH001 Pachyonychia Congenita 52 0.026
433
CRY002 Cryptorchidism 52 0.026
434
SHG001 Shigellosis 52 0.026
435
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 52 0.026
436
RHB003 Rhabdomyosarcoma 51 0.026
437
STT001 Status Epilepticus 51 0.026
438
P ICH001 Ichthyosis Vulgaris 51 0.026
439
FCS012 Facioscapulohumeral Muscular Dystrophy 1 51 0.026
440
TST014 Testicular Cancer 51 0.026
441
P CHL002 Childhood Absence Epilepsy 51 0.026
442
GLL018 Gallbladder Cancer 51 0.026
443
HST011 Histoplasmosis 51 0.026
444
EPD001 Epidermodysplasia Verruciformis 50 0.026
445
ATP002 Atopy 50 0.026
446
HPY002 H. Pylori Infection 50 0.026
447
TNG003 Tongue Cancer 50 0.026
448
P EPD003 Epidermolysis Bullosa Simplex 50 0.026
449
MYM001 Myoma 49 0.026
450
BRN022 Bronchiectasis 49 0.026
451
P MTR004 Maturity-Onset Diabetes of the Young 49 0.026
452
PRL009 Prolactinoma 49 0.026
453
CMP002 Campylobacteriosis 49 0.026
454
P PLY006 Polydactyly 49 0.026
455
EPD016 Epidermolysis Bullosa 49 0.026
456
P LPS002 Liposarcoma 49 0.026
457
BRK001 Brooke-Spiegler Syndrome 49 0.026
458
CYS005 Cysticercosis 49 0.026
459
LMY002 Leiomyoma 49 0.026
460
FLL026 Fallopian Tube Cancer 49 0.026
461
MGR028 Migraine with or Without Aura 1 49 0.026
462
P SZR006 Seizure Disorder 48 0.026
463
P LNG064 Lung Cancer Susceptibility 3 48 0.026
464
PHR003 Pharyngitis 48 0.026
465
HDR002 Hidradenitis Suppurativa 48 0.026
466
P MYT002 Myotonic Dystrophy 48 0.026
467
P LYM025 Lymphedema 48 0.026
468
c SCN006 Secondary Syphilis 48 0.026
469
P ACT074 Acute Lymphocytic Leukemia 48 0.026
470
THR100 Thrombocytopenic Purpura, Autoimmune 47 0.026
471
P CRN038 Carney Complex Variant 47 0.026
472
ALP008 Alopecia 47 0.026
473
LRN003 Learning Disability 47 0.026
474
P PRX021 Proximal Symphalangism 47 0.026
475
IRN001 Iron Deficiency Anemia 47 0.026
476
ALV010 Alveolar Soft-Part Sarcoma 47 0.026
477
P STR020 Strabismus 47 0.026
478
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 46 0.026
479
PTN002 Patent Ductus Arteriosus 46 0.026
480
DBW001 Dubowitz Syndrome 46 0.026
481
P SLP006 Sleep Apnea 46 0.026
482
P SPR013 Spiradenoma 46 0.026
483
OBS061 Obstructive Sleep Apnea 46 0.026
484
P FML035 Familial Hyperlipidemia 46 0.026
485
ACH005 Achalasia 46 0.026
486
P ANG015 Angioedema 46 0.026
487
STF001 Stiff-Person Syndrome 46 0.026
488
P DDN001 Duodenal Ulcer 46 0.026
489
P AGN002 Agnosia 46 0.026
490
P CPL006 Capillary Hemangioma 46 0.026
491
OBS006 Obstructive Lung Disease 45 0.026
492
P PRT013 Portal Hypertension 45 0.026
493
NWC001 Newcastle Disease 45 0.026
494
GST045 Gastroenteritis 45 0.026
495
BLD034 Bile Duct Carcinoma 45 0.026
496
PTT006 Pituitary Adenoma 45 0.026
497
PLM136 Palmoplantar Keratoderma, Nonepidermolytic 45 0.026
498
c OTP007 Otopalatodigital Syndrome, Type Ii 45 0.026
499
MGC001 Megacolon 45 0.026
500
P UTR038 Uterine Disease 44 0.026
501
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.026
502
ART031 Aortic Coarctation 44 0.026
503
ANC001 Ancylostomiasis 44 0.026
504
PRK001 Porokeratosis 44 0.026
505
TRN018 Transitional Cell Carcinoma 44 0.026
506
INT079 Intrahepatic Cholangiocarcinoma 44 0.026
507
CHN005 Choanal Atresia 44 0.026
508
CRN036 Craniopharyngioma 44 0.026
509
ESP023 Esophageal Disease 44 0.026
510
EPD028 Epidermolysis Bullosa Simplex, Dowling-Meara Type 44 0.026
511
BMF001 Bamforth-Lazarus Syndrome 44 0.026
512
SCT005 Scott Syndrome 43 0.026
513
SML033 Small Cell Cancer of the Lung, Somatic 43 0.026
514
ADR016 Adrenal Cortical Carcinoma 43 0.026
515
NSP001 Nasopharynx Carcinoma 43 0.026
516
P OTS001 Otosclerosis 43 0.026
517
P GLM040 Glioma Susceptibility 1 43 0.026
518
CLD007 Cold Agglutinin Disease 43 0.026
519
IPX001 Ipex Syndrome 43 0.026
520
CHL069 Cholesteatoma 43 0.026
521
ADL002 Adult Syndrome 43 0.026
522
P FBR025 Fibrochondrogenesis 43 0.026
523
HMP005 Hemiplegia 43 0.026
524
GNT002 Giant Cell Glioblastoma 43 0.026
525
ANK001 Ankylosis 43 0.026
526
NNC002 Nance-Horan Syndrome 42 0.026
527
P WHT013 White Sponge Nevus 1 42 0.026
528
MYP001 Myoepithelioma 42 0.026
529
HDC001 Headache 42 0.026
530
UTR024 Uterine Carcinosarcoma 42 0.026
531
URN010 Urinary Tract Obstruction 42 0.026
532
PLM019 Pleomorphic Liposarcoma 42 0.026
533
ART017 Aortic Disease 42 0.026
534
KLD001 Keloids 42 0.026
535
ADT003 Auditory System Disease 42 0.026
536
SWT001 Sweat Gland Carcinoma 41 0.026
537
MRG003 Marginal Zone B-Cell Lymphoma 41 0.026
538
ICH054 Ichthyosis, X-Linked 41 0.026
539
ILT001 Ileitis 41 0.026
540
RSD004 Rosai-Dorfman Disease 41 0.026
541
BRN038 Bronchial Disease 41 0.026
542
c MLG081 Malignant Teratoma 41 0.026
543
P DWL001 Dowling-Degos Disease 41 0.026
544
c INF023 Inflammatory Breast Carcinoma 41 0.026
545
DSC009 Discoid Lupus Erythematosus 41 0.026
546
EPD041 Epidermolysis Bullosa Simplex, Weber-Cockayne Type 41 0.026
547
c RTN172 Retinitis Pigmentosa 1 41 0.026
548
BRS099 Breast Ductal Carcinoma 41 0.026
549
APH002 Aphasia 40 0.026
550
APR001 Apraxia 40 0.026
551
c OTP006 Otopalatodigital Syndrome, Type I 40 0.026
552
URT001 Urethritis 40 0.026
553
MLR002 Miliary Tuberculosis 40 0.026
554
LYM052 Lymphomatoid Papulosis 40 0.026
555
P PRM001 Primary Cutaneous Amyloidosis 40 0.026
556
DVR002 Diverticulitis 40 0.026
557
SPN032 Spindle Cell Carcinoma 40 0.026
558
CRK001 Cork-Handlers' Disease 40 0.026
559
EPS026 Epispadias 40 0.026
560
CYS009 Cystadenoma 40 0.026
561
CHL018 Childhood Medulloblastoma 40 0.026
562
EPD047 Epidermolysis Bullosa Simplex, Koebner Type 40 0.026
563
LCH011 Lichen Planopilaris 40 0.026
564
ATR013 Atrichia with Papular Lesions 39 0.026
565
EPT010 Epithelial-Myoepithelial Carcinoma 39 0.026
566
TBR008 Tuberculous Peritonitis 39 0.026
567
ASC002 Ascariasis 39 0.026
568
P INT191 Intestinal Lymphangiectasia 39 0.026
569
P KRT005 Keratoacanthoma 39 0.026
570
c ATM024 Autoimmune Pancreatitis 39 0.026
571
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 39 0.026
572
HYP005 Hypokalemia 39 0.026
573
INT017 Intestinal Schistosomiasis 39 0.026
574
SPN021 Spinal Meningioma 39 0.026
575
HMM003 Hemimegalencephaly 39 0.026
576
BRN032 Brain Glioma 39 0.026
577
SYN031 Synovial Chondromatosis 38 0.026
578
ACN010 Acanthoma 38 0.026
579
PLN010 Pili Annulati 38 0.026
580
HDR003 Hidradenitis 38 0.026
581
HST009 Histiocytoma 38 0.026
582
GNG002 Ganglioneuroma 38 0.026
583
KRT036 Keratosis, Seborrheic, Somatic 38 0.026
584
LYM006 Lymphoepithelioma-Like Carcinoma 38 0.026
585
HYP458 Hyper Ige Syndrome 38 0.026
586
EMN001 Emanuel Syndrome 38 0.026
587
c EYC002 Eye Carcinoma 38 0.026
588
MYS001 Myositis Ossificans 38 0.026
589
MRT007 Martsolf Syndrome 38 0.026
590
UTR033 Uterine Corpus Cancer 38 0.026
591
PLS025 Plasmablastic Lymphoma 38 0.026
592
P TMR010 Tumor Predisposition Syndrome 38 0.026
593
P END039 Endodermal Sinus Tumor 37 0.026
594
RTN015 Retinal Cancer 37 0.026
595
ANL017 Anal Squamous Cell Carcinoma 37 0.026
596
CLR096 Ciliary Dyskinesia, Primary, 1, with or Without Situs Inversus 37 0.026
597
GST030 Gastrinoma 37 0.026
598
NNT016 Neonatal Hemochromatosis 37 0.026
599
P SPS003 Spastic Diplegia 37 0.026
600
BSL006 Basaloid Squamous Cell Carcinoma 37 0.026
601
CNV002 Conversion Disorder 37 0.026
602
SCT002 Scotoma 37 0.026
603
CHR034 Chromophobe Adenoma 37 0.026
604
GMS001 Gemistocytic Astrocytoma 37 0.026
605
FML038 Female Reproductive Organ Cancer 37 0.026
606
c ADN012 Adenocarcinoma in Situ 37 0.026
607
SML020 Small Patella Syndrome 37 0.026
608
FBR003 Fibrous Histiocytoma 37 0.026
609
PNC033 Pancreas Adenocarcinoma 36 0.026
610
c BSL024 Basal Cell Carcinoma 1 36 0.026
611
LMY003 Leiomyomatosis 36 0.026
612
ALX001 Alexia 36 0.026
613
ESP027 Esophagus Squamous Cell Carcinoma 36 0.026
614
P CMM008 Communicating Hydrocephalus 36 0.026
615
AMP010 Ampulla of Vater Carcinoma 36 0.026
616
DYS003 Dysgraphia 36 0.026
617
VSC047 Vascular Malformation 35 0.026
618
EMB007 Embryonal Sarcoma 35 0.026
619
CRH005 Crohn's Colitis 35 0.026
620
OBS004 Obstructive Hydrocephalus 35 0.026
621
P HYP265 Hypotonia 35 0.026
622
HRT011 Heart Septal Defect 35 0.026
623
AMB002 Amblyopia 35 0.026
624
OPT007 Optic Nerve Glioma 35 0.026
625
THY030 Thyroid Gland Disease 35 0.026
626
PLM016 Pleomorphic Carcinoma 35 0.026
627
ADS002 Adie Syndrome 34 0.026
628
NSY001 N Syndrome 34 0.026
629
EPD056 Epidermolysis Bullosa Simplex-Mp 34 0.026
630
UPP004 Upper Respiratory Tract Disease 34 0.026
631
P ATR010 Atrial Heart Septal Defect 34 0.026
632
MTS001 Mutism 34 0.026
633
INF039 Infratentorial Cancer 34 0.026
634
RHN002 Rhinoscleroma 33 0.026
635
c CLL013 Cell Type Cancer 33 0.026
636
DYS073 Dysphagia 33 0.026
637
P OTP001 Otopalatodigital Syndrome 33 0.026
638
INT004 Intraneural Perineurioma 33 0.026
639
AGR018 Agraphia 33 0.026
640
RVL002 Ruvalcaba Syndrome 33 0.026
641
OST032 Osteofibrous Dysplasia 33 0.026
642
DSS008 Disease of Mental Health 33 0.026
643
ARS002 Arsacs 33 0.026
644
BLD053 Blood Platelet Disease 32 0.026
645
P PLM030 Pleomorphic Rhabdomyosarcoma 32 0.026
646
c FML008 Familial Retinoblastoma 32 0.026
647
c MTR002 Mitral Valve Insufficiency 32 0.026
648
P PHR004 Pharynx Cancer 32 0.026
649
PRC005 Pericardial Tuberculosis 32 0.026
650
AMN003 Amnestic Disorder 32 0.026
651
CPL011 Capillary Malformations, Congenital, 1, Somatic, Mosaic 32 0.026
652
EXS013 Exstrophy-Epispadias Complex 32 0.026
653
P WRB001 Warburg Micro Syndrome 31 0.026
654
ECH002 Echolalia 31 0.026
655
MTR008 Mature B-Cell Neoplasm 31 0.026
656
GST006 Gastric Leiomyoma 31 0.026
657
PPL009 Papillary Craniopharyngioma 31 0.026
658
MVM001 Movement Disease 31 0.026
659
VSL002 Visual Epilepsy 31 0.026
660
SPS057 Spasticity 30 0.026
661
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 30 0.026
662
MLK004 Malakoplakia 30 0.026
663
SPN331 Spondyloocular Syndrome 30 0.026
664
P BLD051 Blood Coagulation Disease 30 0.026
665
ADJ001 Adjustment Disorder 30 0.026
666
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 30 0.026
667
TNS007 Taeniasis 30 0.026
668
c CHR048 Chronic Rhinitis 30 0.026
669
ANG037 Angiomatosis 30 0.026
670
c JVN024 Juvenile Hereditary Hemochromatosis 30 0.026
671
LPD007 Lipoadenoma 30 0.026
672
ATY002 Atypical Choroid Plexus Papilloma 30 0.026
673
ESP010 Esophageal Basaloid Squamous Cell Carcinoma 30 0.026
674
DDN009 Duodenal Obstruction 30 0.026
675
BWN002 Bowen Syndrome 30 0.026
676
c CLL012 Cell Type Benign Neoplasm 30 0.026
677
ETH009 Ethmoid Sinusitis 30 0.026
678
HYP264 Hypertonia 30 0.026
679
DSS002 Dissociative Amnesia 30 0.026
680
PTN008 Patent Arterial Duct 29 0.026
681
BRN015 Bronchiolo-Alveolar Adenocarcinoma 29 0.026
682
BCL011 Bacillary Angiomatosis 29 0.026
683
CRB028 Cerebellar Medulloblastoma 29 0.026
684
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 29 0.026
685
P BRS017 Breast Adenomyoepithelioma 29 0.026
686
CRV026 Cervical Clear Cell Adenocarcinoma 28 0.026
687
P GGN002 Gigantism 28 0.026
688
LKC003 Leukocyte Disease 28 0.026
689
SPP007 Suppression Amblyopia 28 0.026
690
c ALP005 Alpha Chain Disease 28 0.026
691
GRN011 Granulomatous Gastritis 28 0.026
692
ATS009 Autosomal Genetic Disease 28 0.026
693
P EXT032 Extraosseous Osteosarcoma 28 0.026
694
FML039 Female Reproductive System Disease 28 0.026
695
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 27 0.026
696
c GST048 Gastrointestinal System Benign Neoplasm 27 0.026
697
CHL109 Childhood Apraxia of Speech 27 0.026
698
VLL006 Villous Adenoma 27 0.026
699
c EPD058 Epidermolysis Bullosa Simplex, Recessive 1 27 0.026
700
END016 Endocervicitis 27 0.026
701
WTH001 Withdrawal Disorder 27 0.026
702
HNM002 Hinman Syndrome 27 0.026
703
BRS063 Breast Squamous Cell Carcinoma 27 0.026
704
PRM025 Primary Bacterial Infectious Disease 27 0.026
705
P SML009 Small Intestine Adenocarcinoma 27 0.026
706
RNL013 Renal Adenoma 27 0.026
707
INF028 Infundibulocystic Basal Cell Carcinoma 26 0.026
708
c CWD003 Cowden Syndrome 2 26 0.026
709
RCT020 Rectum Adenocarcinoma 26 0.026
710
ANG004 Angioid Streaks 26 0.026
711
P PRT063 Proteus-Like Syndrome 26 0.026
712
FLM001 Filamentary Keratitis 26 0.026
713
RPR002 Reproductive System Disease 26 0.026
714
LNG015 Lingual-Facial-Buccal Dyskinesia 26 0.026
715
VSC012 Vesiculobullous Skin Disease 26 0.026
716
PRS004 Prostate Squamous Cell Carcinoma 25 0.026
717
c HYD047 Hydrocephalus, Nonsyndromic, Autosomal Recessive 25 0.026
718
TXC001 Toxic Megacolon 25 0.026
719
c HYD043 Hydrocephalus, Nonsyndromic, Autosomal Recessive 2 25 0.026
720
BRS029 Breast Myoepithelial Carcinoma 25 0.026
721
c ICH014 Ichthyosis Lamellar 1 25 0.026
722
TBR009 Tuberculous Empyema 25 0.026
723
GNT018 Gianotti Crosti Syndrome 25 0.026
724
AMY016 Amyopathic Dermatomyositis 25 0.026
725
P BRS060 Breast Papillomatosis 25 0.026
726
HRF001 Hair Follicle Neoplasm 25 0.026
727
MLG070 Malignant Iris Melanoma 24 0.026
728
ECC007 Eccrine Sweat Gland Cancer 24 0.026
729
CRB032 Cerebral Convexity Meningioma 24 0.026
730
46X010 46xy Partial Gonadal Dysgenesis, with Minifascicular Neuropathy 23 0.026
731
c CLR066 Ciliary Dyskinesia, Primary, 2 23 0.026
732
c LRG002 Large Cell Acanthoma 23 0.026
733
DYS011 Dyskinesia of Esophagus 23 0.026
734
CTR147 Cataract - Intellectual Disability - Hypogonadism 23 0.026
735
MLG011 Malignant Biphasic Mesothelioma 23 0.026
736
UTR030 Uterine Adnexa Cancer 22 0.026
737
c CLR090 Ciliary Dyskinesia, Primary, 22 22 0.026
738
c HMG004 Hemoglobin D Disease 22 0.026
739
ART030 Aortic Arch Interruption 22 0.026
740
JJN002 Jejunal Neoplasm 22 0.026
741
c CWD007 Cowden Syndrome 3 22 0.026
742
ALL007 Allergic Urticaria 21 0.026
743
BLB005 Beaulieu-Boycott-Innes Syndrome 21 0.026
744
c CLR095 Ciliary Dyskinesia, Primary, 19 21 0.026
745
SRC007 Sarcomatoid Transitional Cell Carcinoma 21 0.026
746
PRS063 Paresthesia 20 0.026
747
SWL001 Swallowing Disorders 20 0.026
748
c TRC078 Trichohepatoenteric Syndrome 2 20 0.026
749
MLL004 Mallory-Weiss Syndrome 19 0.026
750
SKN011 Skin Pilomatrix Carcinoma 19 0.026
751
c CLR068 Ciliary Dyskinesia, Primary, 5 19 0.026
752
OLG005 Oligodontia-Colorectal Cancer Syndrome 19 0.026
753
c FML311 Familial Colorectal Cancer Type X 18 0.026
754
MCN004 Mucinous Tubular and Spindle Renal Cell Carcinoma 18 0.026
755
PDT027 Pediatric Ulcerative Colitis 18 0.026
756
BLD063 Bile Duct Cysts 18 0.026
757
c CLR114 Ciliary Dyskinesia, Primary, 30 18 0.026
758
c LKM005 Leukemia, T-Cell, Chronic 18 0.026
759
EPD036 Epidermolysis Bullosa Simplex, Other Generalized 17 0.026
760
ADN025 Adenoameloblastoma 17 0.026
761
NVF002 Nevi Flammei 17 0.026
762
PRC021 Parc Syndrome 17 0.026
763
c RP1001 Rp1-Related Retinitis Pigmentosa 15 0.026
764
TCT002 Tactile Agnosia 15 0.026
765
SBC016 Subacute Delirium 15 0.026
766
c INF068 Inflammatory Bowel Disease 13 14 0.026
767
c CNG148 Congenital Heart Disease, Atrial Septal Defect 13 0.026
768
c INF093 Inflammatory Bowel Disease 14 13 0.026
769
c CLR082 Colorectal Cancer 7 13 0.026
770
c INF067 Inflammatory Bowel Disease 10 13 0.026
771
BCH001 Beach Ear 10 0.026
772
c INF091 Inflammatory Bowel Disease 8 9 0.026
773
TXC021 Toxicity or Absent Response to Clozapine 9 0.026
774
CNT045 Central Nervous System Sarcoma 9 0.026
775
c INF079 Inflammatory Bowel Disease 20 9 0.026
776
c INF090 Inflammatory Bowel Disease 7 9 0.026
777
c INF092 Inflammatory Bowel Disease 9 9 0.026
778
c STM012 Stomach Cancer, Familial 9 0.026
779
STT009 Sutton Disease 2 7 0.026
780
FCT015 Factor 2 Deficiency 7 0.026
781
c DLT001 Delta Chain Disease 5 0.026
782
PRS059 Prostaglandin-Endoperoxide Synthase Deficiency 5 0.026
783
WSC001 Wisconsin Syndrome 4 0.026