Search results for digestive diseases

1174 hits were found for digestive diseases

# Family MCID Name MIFTS Score
1
GST050 Gastrointestinal System Disease 56 3.651
2
CHG001 Chagas Disease 67 2.490
3
P LVR013 Liver Disease 75 0.138
4
P INT068 Intestinal Disease 60 0.125
5
P PNC044 Pancreatitis 61 0.117
6
P KDN018 Kidney Disease 66 0.117
7
CRH001 Crohn's Disease 75 0.115
8
P GST049 Gastrointestinal System Cancer 60 0.114
9
P INF037 Inflammatory Bowel Disease 63 0.110
10
P HRT032 Heart Disease 75 0.110
11
STM006 Stomach Disease 50 0.108
12
P CLC005 Celiac Disease 68 0.098
13
LNG099 Lung Disease 64 0.096
14
CLN019 Colonic Disease 51 0.095
15
PNC034 Pancreas Disease 58 0.094
16
P CRN211 Coronary Artery Disease 74 0.092
17
P HPT021 Hepatitis 69 0.090
18
P CLR023 Colorectal Cancer 97 0.090
19
P OBS005 Obesity 92 0.089
20
GST053 Gastric Cancer 78 0.088
21
P ADN016 Adenocarcinoma 69 0.086
22
P HPT023 Hepatocellular Carcinoma 92 0.082
23
NTR005 Nutritional Deficiency Disease 36 0.082
24
CYS001 Cystic Fibrosis 83 0.080
25
MTH009 Mouth Disease 61 0.079
26
P PNC035 Pancreatic Cancer 87 0.079
27
ESP023 Esophageal Disease 54 0.078
28
GST045 Gastroenteritis 59 0.077
29
NRN002 Neuronitis 41 0.076
30
P DRR001 Diarrhea 60 0.076
31
c PNC106 Pancreatic Agenesis 1 37 0.075
32
VSC007 Vascular Disease 67 0.075
33
ESP021 Esophageal Cancer 76 0.073
34
CLT003 Colitis 60 0.073
35
PHY002 Physical Disorder 43 0.072
36
FTT001 Fatty Liver Disease 59 0.071
37
P ESP024 Esophagitis 61 0.071
38
DYS073 Dysphagia 48 0.070
39
INT253 Intestinal Benign Neoplasm 47 0.070
40
P PNM007 Pneumonia 68 0.069
41
PCK002 Pick Disease 68 0.069
42
GST092 Gastroesophageal Reflux 62 0.069
43
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.067
44
CNS004 Constipation 57 0.066
45
CHY002 Chylomicron Retention Disease 57 0.066
46
IRR002 Irritable Bowel Syndrome 58 0.066
47
ULC004 Ulcerative Colitis 76 0.065
48
LPD008 Lipid Metabolism Disorder 58 0.065
49
RCT017 Rectal Disease 40 0.064
50
PRP027 Peripheral Vascular Disease 68 0.064
51
RSP006 Respiratory System Disease 58 0.064
52
GST023 Gastric Ulcer 56 0.063
53
MVM001 Movement Disease 49 0.063
54
P LKM002 Leukemia 71 0.063
55
P ENC018 Encephalopathy 59 0.062
56
P MYP004 Myopathy 67 0.062
57
END072 Endotheliitis 42 0.062
58
P INF038 Influenza 72 0.062
59
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.061
60
MCS002 Mucositis 55 0.061
61
P PRD008 Periodontitis 63 0.061
62
GST078 Gastrointestinal Allergy 40 0.060
63
DDN006 Duodenitis 42 0.060
64
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.060
65
TTH006 Tooth Disease 52 0.059
66
RHM027 Rheumatic Disease 58 0.059
67
PRD007 Periodontal Disease 60 0.059
68
P GLL020 Gallbladder Disease 59 0.059
69
CNN005 Connective Tissue Disease 62 0.059
70
GLC008 Glucose Metabolism Disease 42 0.059
71
CRB025 Carbohydrate Metabolic Disorder 46 0.059
72
c INF071 Inflammatory Bowel Disease 1 51 0.059
73
EXC002 Exocrine Pancreatic Insufficiency 43 0.059
74
MSC004 Muscle Tissue Disease 34 0.058
75
P RHM011 Rheumatoid Arthritis 89 0.058
76
PPT005 Peptic Ulcer Disease 58 0.058
77
P ART022 Arthritis 75 0.058
78
P LYM118 Lymphoma 69 0.058
79
BLR006 Biliary Tract Disease 52 0.058
80
P NRV007 Nervous System Disease 71 0.058
81
c PND001 Pain Disorder 54 0.057
82
P PRK057 Parkinson Disease, Late-Onset 70 0.056
83
SQM006 Squamous Cell Carcinoma 70 0.056
84
LCT002 Lactose Intolerance 46 0.056
85
WLS001 Wilson Disease 72 0.056
86
BSL008 Basal Ganglia Disease 40 0.056
87
FBR012 Fabry Disease 69 0.055
88
FDL002 Food Allergy 53 0.055
89
SWL001 Swallowing Disorders 33 0.055
90
LRN003 Learning Disability 49 0.055
91
CHL067 Cholecystitis 57 0.055
92
GST013 Gastrojejunal Ulcer 25 0.055
93
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.055
94
P MSC033 Muscle Disorders 52 0.054
95
P AST005 Asthma 82 0.054
96
KWS002 Kawasaki Disease 70 0.054
97
GNG013 Gingivitis 61 0.054
98
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 54 0.054
99
RCT018 Rectal Neoplasm 54 0.054
100
c INH020 Inherited Metabolic Disorder 49 0.054
101
P RSP003 Respiratory Failure 71 0.053
102
c CLR079 Colorectal Cancer 2 29 0.053
103
NRM005 Neuromuscular Disease 56 0.053
104
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 54 0.053
105
ALR002 Al-Raqad Syndrome 36 0.053
106
LVR012 Liver Cirrhosis 67 0.053
107
SKN016 Skin Disease 66 0.053
108
P BRS047 Breast Cancer 100 0.053
109
ANR040 Aneurysm 57 0.052
110
ART021 Arteriosclerosis 58 0.052
111
P GLY013 Glycogen Storage Disease 60 0.052
112
GST019 Gastrointestinal Stromal Tumor 73 0.052
113
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.052
114
CLN009 Colon Squamous Cell Carcinoma 26 0.052
115
CSY001 C Syndrome 50 0.051
116
PRM025 Primary Bacterial Infectious Disease 41 0.051
117
DYS014 Dyspepsia 50 0.051
118
ISC004 Ischemia 61 0.051
119
c CHR089 Chronic Kidney Failure 66 0.051
120
FNC006 Functional Gastric Disease 32 0.051
121
CRB009 Cerebritis 39 0.050
122
ATH003 Atherosclerosis 65 0.050
123
PRP019 Peripheral Nervous System Disease 55 0.050
124
FNC005 Functional Colonic Disease 27 0.050
125
P PRT013 Portal Hypertension 60 0.050
126
GST071 Gastrointestinal Carcinoma 42 0.050
127
ING001 Inguinal Hernia 58 0.049
128
ETN001 Eating Disorder 58 0.049
129
RTN023 Retinitis 50 0.049
130
ACR041 Acromelic Frontonasal Dysostosis 45 0.049
131
BRT030 Birth Defects 43 0.049
132
c HPT001 Hepatitis C 68 0.049
133
P PLM036 Pulmonary Fibrosis 71 0.049
134
PLY023 Polycystic Liver Disease 56 0.048
135
P SML016 Small Intestine Cancer 52 0.048
136
c FML311 Familial Colorectal Cancer Type X 36 0.048
137
c INF086 Inflammatory Bowel Disease 3 38 0.048
138
c CLR085 Colorectal Cancer 1 45 0.048
139
NRN004 Neuroendocrine Tumor 56 0.048
140
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.048
141
BLN006 Blind Loop Syndrome 28 0.048
142
END035 Endocrine Gland Cancer 49 0.047
143
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 33 0.047
144
P NRV006 Nervous System Cancer 60 0.047
145
GST028 Gastric Squamous Cell Carcinoma 37 0.047
146
c INF078 Inflammatory Bowel Disease 2 31 0.047
147
PRT036 Peritonitis 63 0.047
148
END038 Endocrine Pancreas Disease 41 0.047
149
THR024 Thrombosis 57 0.047
150
NNL002 Nonalcoholic Steatohepatitis 50 0.047
151
P LPS004 Lupus Erythematosus 64 0.047
152
BLD054 Blood Protein Disease 37 0.047
153
BNS002 Bone Structure Disease 37 0.046
154
APP008 Appendicitis 60 0.046
155
VSC006 Vascular Cancer 51 0.046
156
c GLL024 Gallbladder Disease 1 34 0.046
157
UND009 Undifferentiated Carcinoma of Stomach 15 0.046
158
CRC038 Carcinoma of Stomach, Salivary Gland Type 13 0.046
159
ACD009 Acid-Labile Subunit, Deficiency of 45 0.046
160
NWC001 Newcastle Disease 54 0.046
161
INC022 Inclusion-Cell Disease 46 0.046
162
ANS012 Anus Disease 32 0.046
163
ALL026 Allergic Hypersensitivity Disease 52 0.046
164
ATN002 Autonomic Nervous System Disease 48 0.045
165
c ACT027 Acute Pancreatitis 57 0.045
166
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.045
167
ABD010 Abdominal Wall Defect 38 0.045
168
P MYC007 Myocardial Infarction 79 0.045
169
c SYS001 Systemic Lupus Erythematosus 86 0.045
170
IMM136 Immune System Disease 51 0.045
171
CTS003 Coats Disease 57 0.045
172
P ALG002 Alagille Syndrome 72 0.045
173
P HYP607 Hypercholesterolemia, Familial 76 0.045
174
ANX002 Anxiety Disorder 67 0.044
175
DFC004 Deficiency Anemia 64 0.044
176
P CNG015 Congenital Diaphragmatic Hernia 60 0.044
177
c RCR022 Recurrent Acute Pancreatitis 41 0.044
178
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.044
179
C3D001 C3 Deficiency 53 0.044
180
c CLR075 Colorectal Cancer 3 28 0.044
181
c PRK031 Parkinson Disease 1 51 0.044
182
P ADD001 Addison's Disease 62 0.044
183
CHL071 Child Syndrome 58 0.044
184
P HST010 Histiocytosis 58 0.044
185
c CRN174 Coronary Heart Disease 2 20 0.044
186
KDS001 Kid Syndrome 53 0.044
187
CRD118 Cardiovascular Cancer 44 0.044
188
MCR094 Microvillus Inclusion Disease 50 0.043
189
c PNC094 Pancreatic Cancer 1 27 0.043
190
DGS008 Digestive System Melanoma 17 0.043
191
P LNG032 Lung Cancer 95 0.043
192
CHL127 Cholangiocarcinoma, Susceptibility to 54 0.043
193
P GST044 Gastritis 56 0.043
194
DDN007 Duodenal Disease 33 0.043
195
PLV003 Pelvic Inflammatory Disease 54 0.043
196
P CRD011 Cardiomyopathy 68 0.043
197
CND002 Conduct Disorder 54 0.043
198
SKN023 Skin Tag 44 0.043
199
c HPT003 Hepatitis a 59 0.043
200
UND008 Undifferentiated Carcinoma of Esophagus 13 0.043
201
CRC037 Carcinoma of Esophagus, Salivary Gland Type 13 0.043
202
c PNC095 Pancreatic Cancer 3 30 0.043
203
VND001 Vein Disease 47 0.043
204
RSD004 Rosai-Dorfman Disease 41 0.043
205
P HRS035 Hirschsprung Disease 1 58 0.043
206
CRY003 Cryptosporidiosis 46 0.043
207
DGS007 Digestive Duplication 7 0.043
208
DYS011 Dyskinesia of Esophagus 28 0.043
209
ACT058 Active Peptic Ulcer Disease 43 0.042
210
c INF088 Inflammatory Bowel Disease 5 31 0.042
211
P ALP004 Alport Syndrome 69 0.042
212
GLT021 Glutaricaciduria, Type I 46 0.042
213
PHR003 Pharyngitis 56 0.042
214
P NRP001 Neuropathy 59 0.042
215
PYL007 Pylorus Cancer 18 0.042
216
ADM013 Adamantinoma of Long Bones 57 0.042
217
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.042
218
HYP066 Hyperglycemia 61 0.042
219
NSD001 Nose Disease 48 0.041
220
PNC048 Pancreatic Lipase Deficiency 27 0.041
221
c INF087 Inflammatory Bowel Disease 4 40 0.041
222
PST035 Postgastrectomy Syndrome 34 0.041
223
c CRN175 Coronary Heart Disease 4 19 0.041
224
c CHR096 Chronic Pulmonary Heart Disease 40 0.041
225
DSS008 Disease of Mental Health 52 0.041
226
c CLR080 Colorectal Cancer 5 32 0.041
227
GLL018 Gallbladder Cancer 63 0.041
228
PNC118 Pancreas, Annular 36 0.041
229
c HPT016 Hepatitis B 64 0.041
230
GST037 Gastroparesis 54 0.041
231
PST030 Postcholecystectomy Syndrome 32 0.041
232
ENT006 Enterokinase Deficiency 23 0.041
233
P HYP086 Hypothyroidism 64 0.041
234
SPC003 Specific Developmental Disorder 38 0.041
235
c ACT004 Acute Diarrhea 39 0.040
236
P AMY004 Amyloidosis 65 0.040
237
c ATM011 Autoimmune Hepatitis 60 0.040
238
SQM013 Squamous Cell Carcinoma, Head and Neck 70 0.040
239
MLT021 Multiple System Atrophy 70 0.040
240
SPL011 Spleen Cancer 36 0.040
241
LYS002 Lysosomal Storage Disease 52 0.040
242
BLD036 Bile Duct Disease 48 0.040
243
SQM014 Squamous Cell Carcinoma of Pancreas 16 0.040
244
c PNC111 Pancreatic Cancer 2 28 0.040
245
c INF089 Inflammatory Bowel Disease 6 34 0.040
246
ATM052 Autoimmune Disease 1 25 0.040
247
P INF032 Infertility 59 0.040
248
CRC006 Carcinoid Syndrome 52 0.040
249
FCL044 Fecal Incontinence 35 0.039
250
c PNC108 Pancreatitis, Hereditary 58 0.039
251
c PRM023 Pre-Malignant Neoplasm 41 0.039
252
P PRM006 Primary Biliary Cirrhosis 51 0.039
253
P PRS040 Prostate Cancer 90 0.039
254
EXF001 Exfoliation Syndrome 57 0.039
255
P TRC086 Trichohepatoenteric Syndrome 1 48 0.039
256
SLV003 Salivary Gland Disease 47 0.039
257
P DDN001 Duodenal Ulcer 50 0.039
258
P PLN008 Peeling Skin Syndrome 45 0.039
259
CRV038 Cervical Squamous Cell Carcinoma 60 0.039
260
P SPS003 Spastic Diplegia 52 0.039
261
PRT035 Peritoneum Cancer 35 0.039
262
MLN008 Melanoma 62 0.039
263
P CLL015 Collagen Disease 50 0.039
264
ANL022 Anal Fistula 43 0.038
265
c INF067 Inflammatory Bowel Disease 10 49 0.038
266
c PRK030 Parkinson Disease 4 38 0.038
267
SRC014 Sarcoma 66 0.038
268
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.038
269
BLD044 Bladder Disease 51 0.038
270
P MSC003 Muscular Atrophy 50 0.038
271
SLP005 Sleep Disorder 53 0.038
272
c CHL120 Cholestasis, Benign Recurrent Intrahepatic 46 0.038
273
TNG004 Tongue Disease 39 0.038
274
GLB003 Globe Disease 32 0.038
275
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 33 0.038
276
P PSD087 Pseudoxanthoma Elasticum 66 0.038
277
SML014 Small Intestine Leiomyosarcoma 34 0.038
278
MDY003 Mody, Type Ii 36 0.038
279
P EXP004 Exophthalmos 53 0.038
280
c AST039 Asthma 2 28 0.038
281
c AST037 Asthma 1 28 0.037
282
JJN004 Jejunal Atresia 29 0.037
283
MLR004 Malaria 83 0.037
284
c CLR081 Colorectal Cancer 6 22 0.037
285
MTC016 Mitochondrial Neurogastrointestinal Encephalopathy Disease 27 0.037
286
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.037
287
PNC014 Pancreatic Serous Cystadenocarcinoma 22 0.037
288
SPC010 Speech and Communication Disorders 41 0.037
289
CNG034 Congestive Heart Failure 72 0.037
290
c CHL119 Cholangitis, Primary Sclerosing 44 0.037
291
SCR011 Scrapie 38 0.037
292
OST141 Osteoclastic Giant Cell Tumor of Pancreas 11 0.037
293
P KDN017 Kidney Cancer 65 0.037
294
P CHL066 Cholangitis 42 0.037
295
P ATR005 Atrophic Gastritis 45 0.037
296
APL002 Aplasia of Lacrimal and Salivary Glands 42 0.037
297
STT004 Steatorrhea 40 0.037
298
ACN026 Acinar Cell Carcinoma of Pancreas 22 0.037
299
MCN020 Mucinous Cystadenocarcinoma of Pancreas 18 0.037
300
SQM019 Squamous Cell Carcinoma of the Small Intestine 13 0.037
301
SLD011 Solid Pseudopapillary Carcinoma of Pancreas 11 0.037
302
GST039 Gastroduodenitis 31 0.037
303
VSC011 Vasculitis 62 0.036
304
BLC008 Bile Acid Synthesis Defect, Congenital, 2 38 0.036
305
TRP004 Tropical Sprue 35 0.036
306
PLC008 Placenta Disease 33 0.036
307
SQM016 Squamous Cell Carcinoma of Gallbladder and Extrahepatic Biliary Tract 12 0.036
308
P LYM033 Lymphoproliferative Syndrome 56 0.036
309
BLC007 Bile Acid Synthesis Defect, Congenital, 1 30 0.036
310
HYP266 Hypoxia 56 0.036
311
P TRM003 Tremor 54 0.036
312
MCN017 Meconium Ileus 54 0.036
313
CLN015 Colon Adenocarcinoma 50 0.036
314
DDN010 Duodenum Cancer 43 0.036
315
c CHL080 Cholestasis, Progressive Familial Intrahepatic 1 46 0.036
316
LYM024 Lymphatic System Disease 52 0.036
317
LCT019 Lactase Persistence/nonpersistence 20 0.036
318
HNS001 Hansen's Disease 30 0.036
319
c PRM126 Primary Peritoneal Carcinoma 54 0.036
320
DRM006 Dermatitis 66 0.036
321
c PRK045 Parkinson Disease 5 40 0.036
322
ADN021 Adenomatous Polyposis Coli 70 0.036
323
KPS004 Kaposi Sarcoma 67 0.036
324
GST040 Gastric Adenocarcinoma 52 0.036
325
BLR007 Biliary Tract Neoplasm 49 0.036
326
c PNC103 Pancreatic Cancer 4 29 0.036
327
UPP004 Upper Respiratory Tract Disease 46 0.036
328
UMB002 Umbilical Hernia 44 0.036
329
SCR037 Sucrase-Isomaltase Deficiency, Congenital 26 0.036
330
GNG011 Gingival Disease 46 0.036
331
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.035
332
ABL002 Ablepharon-Macrostomia Syndrome 57 0.035
333
OCL009 Ocular Cancer 59 0.035
334
ANG011 Angiodysplasia 44 0.035
335
ACH005 Achalasia 52 0.035
336
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.035
337
P DRM007 Dermatitis Herpetiformis 51 0.035
338
ALC007 Alcohol Dependence 63 0.035
339
P CWD001 Cowden Disease 64 0.035
340
CHL068 Cholestasis 59 0.035
341
ADJ001 Adjustment Disorder 38 0.034
342
c RNL016 Renal Infectious Disease 20 0.034
343
TNG002 Tangier Disease 62 0.034
344
ESP025 Esophagus Adenocarcinoma 41 0.034
345
DRR004 Diarrhea 3, Secretory Sodium, Congenital, Syndromic 23 0.034
346
P LYM026 Lymphoblastic Leukemia 62 0.034
347
SXL003 Sexual Disorder 42 0.034
348
P GLM007 Glomerulonephritis 59 0.034
349
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.034
350
CHR515 Chronic Atrial and Intestinal Dysrhythmia 18 0.034
351
HPY002 H. Pylori Infection 61 0.034
352
ADL002 Adult Syndrome 52 0.034
353
c HYP595 Hypertension, Essential 69 0.034
354
CYS039 Cystic Kidney Disease 52 0.034
355
DRR005 Diarrhea 4, Malabsorptive, Congenital 33 0.034
356
P ART023 Arthropathy 64 0.034
357
DNT012 Dental Caries 46 0.034
358
CHR028 Chronic Wasting Disease 34 0.034
359
c ALZ012 Alzheimer Disease 12 32 0.034
360
PNC028 Pancreatic Steatorrhea 34 0.034
361
BRN038 Bronchial Disease 51 0.034
362
ERY003 Erythema Multiforme 55 0.034
363
THY030 Thyroid Gland Disease 48 0.034
364
P INT070 Intestinal Obstruction 57 0.034
365
ANG054 Angina Pectoris 50 0.034
366
LKC003 Leukocyte Disease 43 0.033
367
c HPT073 Hepatitis C Virus 73 0.033
368
SPN369 Spinal Disease 39 0.033
369
BRN106 Burns 52 0.033
370
JJN003 Jejunal Cancer 29 0.033
371
c INT072 Intestinal Pseudo-Obstruction 46 0.033
372
BHC003 Behcet Syndrome 60 0.033
373
c INF074 Inflammatory Bowel Disease 15 19 0.033
374
AMN002 Amino Acid Metabolic Disorder 47 0.033
375
CNG298 Congenital Pancreatic Cyst 21 0.033
376
DMY004 Demyelinating Disease 53 0.033
377
c HMG001 Hemoglobin C Disease 47 0.033
378
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.033
379
ATM053 Autoimmune Disease 2 16 0.033
380
ZLL002 Zollinger-Ellison Syndrome 53 0.033
381
INT071 Intestinal Perforation 42 0.033
382
P THL005 Thalassemia 64 0.033
383
CRH005 Crohn's Colitis 52 0.033
384
HPT046 Hepatic Veno-Occlusive Disease 50 0.033
385
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 46 0.033
386
DGS006 Digestive Duplication Cyst of the Tongue 7 0.033
387
PRN019 Perinatal Necrotizing Enterocolitis 42 0.033
388
THY028 Thyroid Cancer 69 0.033
389
P INT001 Intrahepatic Cholestasis 59 0.033
390
ADN071 Adenocarcinoma of Gallbladder and Extrahepatic Biliary Tract 13 0.033
391
PRN015 Perinatal Intestinal Perforation 5 0.033
392
VSC044 Visceral Myopathy 51 0.033
393
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.033
394
P MCP010 Mucopolysaccharidosis 60 0.033
395
AND005 Androgen Insensitivity Syndrome, Mild 16 0.033
396
P SKN013 Skin Benign Neoplasm 43 0.033
397
c CLR083 Colorectal Cancer 8 24 0.032
398
ORL014 Oral Pharyngeal Disorders 11 0.032
399
APH002 Aphasia 54 0.032
400
c CLR087 Colorectal Cancer 12 30 0.032
401
PRS042 Prostate Disease 52 0.032
402
ISL029 Isolated Anorectal Malformation 7 0.032
403
STM007 Stomatitis 50 0.032
404
JNT002 Joint Disorders 55 0.032
405
WLL006 Wells Syndrome 59 0.032
406
P MSC005 Muscular Dystrophy 65 0.032
407
TST021 Testicular Germ Cell Tumor 69 0.032
408
P SHR029 Short Syndrome 58 0.032
409
c ATM024 Autoimmune Pancreatitis 47 0.032
410
PRP021 Peripheral Nervous System Neoplasm 46 0.032
411
BLD034 Bile Duct Carcinoma 56 0.032
412
c ACT134 Acute Liver Failure 50 0.032
413
GDS001 Good Syndrome 44 0.032
414
GNR004 Generalized Anxiety Disorder 51 0.032
415
MGC001 Megacolon 45 0.032
416
ATM015 Autoimmune Disease of Gastrointestinal Tract 34 0.032
417
ORL004 Oral Submucous Fibrosis 51 0.032
418
TBR008 Tuberculous Peritonitis 41 0.032
419
c INF073 Inflammatory Bowel Disease 12 21 0.032
420
EMB004 Embryonal Carcinoma 57 0.032
421
ISL001 Islet Cell Tumor 50 0.032
422
TTH001 Tooth Ankylosis 40 0.032
423
LYM023 Lymphatic System Cancer 33 0.032
424
ADN018 Adenoma 58 0.032
425
FNC002 Functional Diarrhea 37 0.031
426
P MDL005 Medulloblastoma 77 0.031
427
c INF068 Inflammatory Bowel Disease 13 25 0.031
428
WST001 West Syndrome 57 0.031
429
APR001 Apraxia 51 0.031
430
P AGN002 Agnosia 57 0.031
431
RDT013 Radiation Proctitis 42 0.031
432
MLK004 Malakoplakia 28 0.031
433
PRD011 Proud Syndrome 42 0.031
434
OVR063 Overnutrition 50 0.031
435
ATM054 Autoimmune Disease 3 15 0.031
436
P RNL014 Renal Cell Carcinoma 82 0.031
437
VND002 Van Der Woude Syndrome 50 0.031
438
MND006 Mondor Disease 21 0.031
439
ATP002 Atopy 66 0.031
440
c VRL010 Viral Hepatitis 60 0.031
441
c SCN046 Secondary Short Bowel Syndrome 12 0.031
442
ART016 Aortic Aneurysm 69 0.031
443
c MYC058 Myocardial Infarction 2 28 0.031
444
P ATM020 Autoimmune Enteropathy 39 0.031
445
P SJG001 Sjogren's Syndrome 50 0.031
446
BRR002 Barrett's Adenocarcinoma 44 0.031
447
HYP082 Hypopharynx Cancer 43 0.031
448
LRY017 Laryngeal Disease 34 0.031
449
ATR076 Atrophic Muscular Disease 15 0.031
450
P DBT005 Diabetes Insipidus 53 0.031
451
RHM001 Rheumatic Fever 54 0.031
452
APP010 Appendix Cancer 39 0.031
453
GLC022 Glucose/galactose Malabsorption 38 0.031
454
c HRD101 Hereditary Mixed Polyposis Syndrome 1 37 0.031
455
EWN003 Ewing Sarcoma 66 0.030
456
P CHR345 Chronic Pain 50 0.030
457
RPR002 Reproductive System Disease 41 0.030
458
TXC005 Toxic Shock Syndrome 60 0.030
459
c CNT068 Central Pain Syndrome 29 0.030
460
c CLC045 Celiac Disease 2 17 0.030
461
P DBT083 Diabetes Mellitus, Permanent Neonatal 55 0.030
462
RFR013 Refractory Celiac Disease 33 0.030
463
c DLT002 Dilated Cardiomyopathy 76 0.030
464
P HYP076 Hyperthyroidism 55 0.030
465
P ORL007 Oral Cavity Cancer 59 0.030
466
ADR012 Adrenal Gland Disease 48 0.030
467
P GST047 Gastrointestinal Neuroendocrine Tumor 36 0.030
468
MCR191 Microscopic Colitis 47 0.030
469
PRC002 Paracoccidioidomycosis 55 0.030
470
MCK002 Meckel's Diverticulum 35 0.030
471
FXF002 Fox-Fordyce Disease 36 0.030
472
ILM001 Ileum Cancer 25 0.030
473
DWN001 Down Syndrome 66 0.030
474
c CHR086 Chronic Conjunctivitis 45 0.030
475
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 0.030
476
P MTC003 Metachromatic Leukodystrophy 70 0.030
477
INT002 Intermittent Claudication 56 0.030
478
SLD003 Sialadenitis 49 0.030
479
FNC012 Functioning Pancreatic Endocrine Tumor 31 0.030
480
MSC072 Muscle Cancer 49 0.029
481
P SCL009 Sclerosing Cholangitis 48 0.029
482
DMP001 Dumping Syndrome 40 0.029
483
TRH001 Trehalase Deficiency 18 0.029
484
PYL003 Pyloric Antrum Cancer 12 0.029
485
VSC047 Vascular Malformation 45 0.029
486
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.029
487
P RTT002 Rett Syndrome 77 0.029
488
HRT007 Heart Cancer 46 0.029
489
ORL015 Oral Squamous Cell Carcinoma 57 0.029
490
P AML002 Amelogenesis Imperfecta 45 0.029
491
GRM001 Germ Cell and Embryonal Cancer 36 0.029
492
GLC006 Galactosemia 64 0.029
493
PLS009 Plasma Cell Neoplasm 48 0.029
494
P OST012 Osteoarthritis 83 0.029
495
c DRR009 Diarrhea 6 29 0.029
496
VSC009 Vascular Skin Disease 19 0.029
497
LYS003 Lysinuric Protein Intolerance 52 0.029
498
VNT001 Ventilation Pneumonitis 35 0.029
499
WLM001 Wolman Disease 57 0.029
500
BRC012 Brucellosis 66 0.029
501
P ASP006 Aspergillosis 61 0.029
502
PRD004 Prediabetes Syndrome 43 0.029
503
INT007 Intermediate Coronary Syndrome 50 0.029
504
P LKD001 Leukodystrophy 59 0.029
505
P HRT017 Heart Tumor 32 0.029
506
c ADL079 Adult Heart Tumor 16 0.029
507
P HRD018 Hair Disease 51 0.029
508
ADT003 Auditory System Disease 40 0.029
509
INT051 Intussusception 50 0.029
510
PRN011 Pernicious Anemia 44 0.029
511
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 43 0.029
512
P INT143 Interstitial Cystitis 57 0.028
513
SNS023 Sensory System Cancer 43 0.028
514
LPD027 Lip Disease 28 0.028
515
c NMN013 Niemann-Pick Disease, Type a 56 0.028
516
DYS015 Dysentery 40 0.028
517
SLM003 Salmonellosis 52 0.028
518
ESN005 Eosinophilic Gastroenteritis 50 0.028
519
HPT014 Hepatorenal Syndrome 46 0.028
520
DRR008 Diarrhea 1, Secretory Chloride, Congenital 42 0.028
521
c DLT001 Delta Chain Disease 13 0.028
522
CHR008 Choroiditis 44 0.028
523
SLC005 Selective Iga Deficiency Disease 34 0.028
524
P LRY019 Laryngitis 54 0.028
525
IRN001 Iron Deficiency Anemia 52 0.028
526
ALC009 Alcoholic Liver Cirrhosis 49 0.028
527
P TCL004 T-Cell Leukemia 47 0.028
528
c CLL013 Cell Type Cancer 46 0.028
529
P MLT074 Multiple Endocrine Neoplasia 56 0.028
530
PRT030 Parathyroid Gland Disease 47 0.028
531
c DRR007 Diarrhea 7 31 0.028
532
CMM004 Common Variable Immunodeficiency 68 0.028
533
KRT001 Keratoconjunctivitis Sicca 59 0.028
534
P HYP060 Hyperinsulinism 58 0.028
535
GST063 Gastric Cancer Risk After H. Pylori Infection 52 0.028
536
MLT001 Multiple Chemical Sensitivity 43 0.028
537
THR035 Thrombasthenia 39 0.028
538
P PRP029 Porphyria 59 0.028
539
PRD003 Periodontosis 41 0.028
540
c PRK037 Parkinson Disease 13 27 0.028
541
c INF090 Inflammatory Bowel Disease 7 26 0.028
542
P CRV031 Cervical Adenocarcinoma 53 0.027
543
CLR109 Colorectal Adenocarcinoma 51 0.027
544
c DYS166 Dysautonomia, Familial 49 0.027
545
c CLR082 Colorectal Cancer 7 20 0.027
546
PSD007 Pseudomyxoma Peritonei 48 0.027
547
GLS007 Glossitis 44 0.027
548
ENT001 Enterocele 40 0.027
549
HTS001 Hiatus Hernia 40 0.027
550
PLS002 Peliosis Hepatis 31 0.027
551
P MYL005 Myelofibrosis 67 0.027
552
c ACT068 Acute Cystitis 50 0.027
553
CHL052 Choledochal Cyst 41 0.027
554
GST095 Gastritis, Familial Giant Hypertrophic 27 0.027
555
P FML035 Familial Hyperlipidemia 48 0.027
556
GGR001 Geographic Tongue 46 0.027
557
c AML020 Amelogenesis Imperfecta, Type Iv 33 0.027
558
c THR092 Thrombophilia Due to Thrombin Defect 54 0.027
559
c RTN162 Retinitis Pigmentosa 2 48 0.027
560
PLP001 Pulpitis 47 0.027
561
ANS011 Anus Cancer 42 0.027
562
SCH014 Schistosomiasis 58 0.027
563
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.027
564
LYM116 Lymph Node Disease 47 0.027
565
AYM001 Ayme-Gripp Syndrome 41 0.027
566
GLT030 Gluten Allergy 19 0.027
567
BLC009 Bile Acid Synthesis Defect, Congenital, 4 27 0.027
568
c GLL027 Gallbladder Disease 4 22 0.027
569
P STR035 Streptococcal Group a Invasive Disease 17 0.027
570
MNT001 Mantle Cell Lymphoma 72 0.027
571
P SLV002 Salivary Gland Cancer 61 0.027
572
c AML044 Amelogenesis Imperfecta, Type Ig 33 0.027
573
c ADL017 Adult T-Cell Leukemia 60 0.027
574
P MTC069 Mitochondrial Disorders 53 0.027
575
P HYP014 Hyperuricemia 50 0.027
576
MYL020 Myelomeningocele 51 0.026
577
UND004 Undetermined Colitis 10 0.026
578
GNG012 Gingival Overgrowth 52 0.026
579
SML036 Small Intestinal Adenocarcinoma 46 0.026
580
P DNT011 Dentinogenesis Imperfecta 44 0.026
581
BLC011 Bile Acid Synthesis Defect, Congenital, 3 27 0.026
582
TTH005 Teeth Hard Tissue Disease 26 0.026
583
c SLV006 Salivary Gland Cancer, Adult 14 0.026
584
DRY001 Dry Eye Syndrome 50 0.026
585
MXD023 Mixed Cell Type Cancer 44 0.026
586
P PLR004 Pleuropulmonary Blastoma 65 0.026
587
MNR003 Mineral Metabolism Disease 38 0.026
588
P TRM004 Trimethylaminuria 40 0.026
589
GNG003 Gingival Recession 38 0.026
590
ANS003 Anisakiasis 33 0.026
591
MYC015 Mycobacterium Fortuitum 28 0.026
592
P OST005 Osteogenesis Imperfecta 69 0.026
593
c CHL082 Cholestasis, Progressive Familial Intrahepatic 3 45 0.026
594
P HYP009 Hypertrophic Pyloric Stenosis 42 0.026
595
PNC008 Pancreatic Endocrine Carcinoma 38 0.026
596
AMP003 Ampulla of Vater Neoplasm 35 0.026
597
HPT081 Hepatic Infarction 34 0.026
598
PNC013 Pancreatic Ductal Carcinoma 46 0.026
599
P PNC045 Pancreatic Agenesis 42 0.026
600
P DNT009 Dentin Dysplasia 38 0.026
601
HYP021 Hypercementosis 32 0.026
602
c CHR013 Chronic Apical Periodontitis 30 0.026
603
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.026
604
TTH002 Tooth Agenesis 54 0.026
605
ESP020 Esophageal Atresia 50 0.026
606
RCT011 Rectal Prolapse 43 0.026
607
PRL008 Paralytic Ileus 37 0.026
608
NTM001 Nutmeg Liver 31 0.026
609
INT111 Intestinal Pseudoobstruction, Neuronal 28 0.026
610
c NRP031 Neuropathy, Hereditary Sensory and Autonomic, Type Vii 22 0.026
611
MYX011 Myxozoa 17 0.026
612
LCR008 Lacrimal Apparatus Disease 37 0.026
613
c INF083 Inflammatory Bowel Disease 24 19 0.026
614
TRN003 Transverse Colon Cancer 44 0.026
615
ATR073 Atrophic Glossitis 30 0.026
616
SLL001 Sialolithiasis 29 0.026
617
DCH001 Duchenne Muscular Dystrophy 79 0.026
618
P END044 Endometriosis 66 0.026
619
PRS036 Parasitic Protozoa Infectious Disease 41 0.026
620
MCR037 Macroglossia 45 0.025
621
AND001 Anodontia 43 0.025
622
ANR003 Anorectal Stricture 13 0.025
623
PRP016 Paraplegia 49 0.025
624
P MSC007 Muscle Hypertrophy 58 0.025
625
P NPH009 Nephrolithiasis 60 0.025
626
GST009 Gastroschisis 47 0.025
627
FSS001 Fissured Tongue 35 0.025
628
ORL019 Oral Hairy Leukoplakia 34 0.025
629
PRM205 Primary Hepatic Neuroendocrine Carcinoma 27 0.025
630
DNT041 Dentin Dysplasia, Type I, with Microdontia and Misshapen Teeth 26 0.025
631
OTD001 Otodental Dysplasia 24 0.025
632
FLR007 Failure of Tooth Eruption, Primary 23 0.025
633
MCC003 Mucocele of Salivary Gland 20 0.025
634
MYC033 Myoclonus 42 0.025
635
P MYT002 Myotonic Dystrophy 48 0.025
636
ATN011 Autoinflammation with Infantile Enterocolitis 39 0.025
637
c SRC025 Sarcoidosis 1 61 0.025
638
CRR007 Cirrhosis, Cryptogenic 43 0.025
639
c OPT053 Optic Atrophy 1 43 0.025
640
NSY001 N Syndrome 36 0.025
641
EXC003 Excessive Tearing 36 0.025
642
SPP003 Suppurative Periapical Periodontitis 34 0.025
643
CSC001 Cascade Stomach 17 0.025
644
ULC002 Ulcer of Anus and Rectum 10 0.025
645
c CWD006 Cowden Syndrome 1 57 0.025
646
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.025
647
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.025
648
c PLN018 Peeling Skin Syndrome 2 40 0.025
649
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.025
650
P HYP117 Hypertriglyceridemia 61 0.025
651
ORL011 Oral Cancer 56 0.025
652
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 42 0.025
653
DNT001 Dental Fluorosis 41 0.025
654
INT052 Intestinal Volvulus 36 0.025
655
NNF001 Non-Functioning Pancreatic Endocrine Tumor 35 0.025
656
MDN001 Median Rhomboid Glossitis 29 0.025
657
NRG001 Neurogenic Bowel 28 0.025
658
PLY114 Polyglucosan Body Myopathy 2 16 0.025
659
HYD004 Hydrops of Gallbladder 12 0.025
660
c CHR465 Chronic Diarrhea Due to Guanylate Cyclase 2c Overactivity 9 0.025
661
HYP056 Hypoglycemia 61 0.025
662
RTR011 Retroperitoneal Fibrosis 39 0.025
663
GLC003 Glucose Intolerance 55 0.025
664
P BRN120 Bronchus Cancer 44 0.025
665
CLN044 Colon Adenoma 44 0.025
666
BLR028 Biliary Atresia, Extrahepatic 27 0.025
667
DNT006 Dental Pulp Necrosis 26 0.025
668
P ACT046 Acute Apical Periodontitis 17 0.025
669
PLP002 Pulp Degeneration 12 0.025
670
HYP049 Hypertrophy of Tongue Papillae 10 0.025
671
PRT011 Protein C Deficiency 52 0.025
672
SPL018 Splenomegaly 44 0.025
673
VGN023 Vaginitis 42 0.025
674
BLR004 Biliary Dyskinesia 31 0.025
675
FSH003 Fish Allergy 29 0.025
676
GST038 Gastrointestinal Adenoma 27 0.025
677
RCT023 Rectum Squamous Cell Carcinoma 20 0.025
678
GST026 Gastric Fundus Cancer 19 0.025
679
GST025 Gastric Body Carcinoma 17 0.025
680
GST087 Gastric Linitis Plastica 16 0.025
681
VSC014 Vascular Hyalinosis 14 0.025
682
ALC012 Alcoholic Gastritis 14 0.025
683
PNC040 Pancreatic Delta Cell Neoplasm 13 0.025
684
PRF001 Perforation of Bile Duct 12 0.025
685
CHL004 Cholelithiasis 48 0.025
686
P CNN004 Connective Tissue Cancer 40 0.025
687
GNR003 Generalized Atherosclerosis 37 0.025
688
c BRN108 Branchiootic Syndrome 1 34 0.025
689
SHG001 Shigellosis 54 0.024
690
DSC005 Descending Colon Cancer 32 0.024
691
P EPD025 Epidermolysis Bullosa with Pyloric Atresia 29 0.024
692
ANL005 Anal Spasm 18 0.024
693
OCC004 Occlusion of Gallbladder 13 0.024
694
STR003 Strawberry Gallbladder 9 0.024
695
IDP068 Idiopathic Malabsorption Due to Bile Acid Synthesis Defects 5 0.024
696
ATN004 Autonomic Neuropathy 45 0.024
697
c CNG031 Congenital Nervous System Abnormality 37 0.024
698
ALC006 Alcoholic Hepatitis 59 0.024
699
ASC004 Ascending Colon Cancer 31 0.024
700
SPL003 Splenic Flexure Cancer 20 0.024
701
ACC005 Accessory Pancreas 18 0.024
702
HPT005 Hepatic Flexure Cancer 17 0.024
703
LVR003 Liver Carcinoma in Situ 13 0.024
704
CNG479 Congenital Secretory Sodium Diarrhea 8 12 0.024
705
ATM077 Autoimmune Gastrointestinal Dysmotility 12 0.024
706
P CSH001 Cushing's Syndrome 65 0.024
707
c OPT055 Optic Atrophy Plus Syndrome 52 0.024
708
CRD119 Cardiac Arrest 61 0.024
709
PLS011 Plasmacytoma 56 0.024
710
OLV001 Olivopontocerebellar Atrophy 53 0.024
711
HST011 Histoplasmosis 52 0.024
712
c PLN021 Peeling Skin Syndrome 3 29 0.024
713
c SML023 Small Cell Lung Cancer, Adult 15 0.024
714
P ABD016 Abdominal Obesity-Metabolic Syndrome 41 0.024
715
CHL050 Cholesterol Ester Storage Disease 38 0.024
716
PLM012 Pulmonary Sarcoidosis 54 0.024
717
P SHR001 Short Bowel Syndrome 49 0.024
718
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 21 0.024
719
CLN004 Colon Carcinoma in Situ 33 0.024
720
CCL003 Cecal Benign Neoplasm 25 0.024
721
RCT008 Rectosigmoid Junction Neoplasm 23 0.024
722
NRN031 Neuroendocrine Tumor of the Appendix 15 0.024
723
AMB001 Amebiasis 43 0.024
724
P GLM045 Glioma 60 0.024
725
P HMN010 Hemangioma 59 0.024
726
MRB003 Morbid Obesity 58 0.024
727
PRR002 Pure Red-Cell Aplasia 47 0.024
728
ANK008 Ankyloglossia 29 0.024
729
HGH026 High Anorectal Malformation 14 0.024
730
RCT010 Rectum Carcinoma in Situ 13 0.024
731
CNG363 Congenital Enterocyte Heparan Sulfate Deficiency 4 0.024
732
EPT026 Epithelio-Exfoliative Colitis-Deafness Syndrome 4 0.024
733
c HYP615 Hyperparathyroidism, Familial Primary 56 0.024
734
P CYS018 Cystitis 52 0.024
735
NDL013 Nodular Regenerative Hyperplasia 50 0.024
736
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.024
737
P PRM016 Primary Optic Atrophy 29 0.024
738
P FRC002 Fructose Intolerance 52 0.024
739
ILT001 Ileitis 49 0.024
740
BRN056 Bronchopulmonary Dysplasia 48 0.024
741
MYC017 Mycobacterium Kansasii 40 0.024
742
P FML011 Familial Adenomatous Polyposis 68 0.023
743
WRN001 Werner Syndrome 67 0.023
744
P LYM007 Lymphangioleiomyomatosis 66 0.023
745
HPT019 Hepatic Encephalopathy 56 0.023
746
PLM010 Pulmonary Edema 54 0.023
747
BCT015 Bacteremia 48 0.023
748
c INV001 Invasive Aspergillosis 47 0.023
749
NSL022 Nasal Cavity Disease 38 0.023
750
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 15 0.023
751
LWN002 Low Anorectal Malformation 10 0.023
752
INT254 Intermediate Anorectal Malformation 9 0.023
753
DSP001 Displacement of Cardia Through Esophageal Hiatus 7 0.023
754
CNG480 Congenital Diarrhea 7 with Exudative Enteropathy 6 0.023
755
P PRT010 Parathyroid Carcinoma 63 0.023
756
CHC001 Chickenpox 51 0.023
757
MTB004 Metabolic Acidosis 48 0.023
758
EPD045 Epidermolysis Bullosa, Junctional, with Pyloric Stenosis 46 0.023
759
CCC002 Coccidiosis 51 0.023
760
PLY056 Polyposis, Juvenile Intestinal 54 0.023
761
SWN001 Swine Influenza 44 0.023
762
MYC013 Mycobacterium Abscessus 41 0.023
763
P ARC016 Auriculocondylar Syndrome 1 40 0.023
764
c CLC048 Celiac Disease 3 21 0.023
765
DSS009 Disseminated Intravascular Coagulation 51 0.023
766
GRD001 Giardiasis 40 0.023
767
P HML001 Hemolytic-Uremic Syndrome 51 0.023
768
STR008 Strongyloidiasis 51 0.023
769
PTT037 Pituitary Tumors 45 0.023
770
HRN022 Hearing Loss/deafness 26 0.023
771
P FCS002 Fucosidosis 57 0.023
772
RSC001 Rosacea 52 0.023
773
DVR002 Diverticulitis 45 0.023
774
IMM107 Immunodeficiency 31c, Autosomal Dominant 27 0.023
775
NRL016 Neural Tube Defects 76 0.023
776
c CHL081 Cholestasis, Progressive Familial Intrahepatic 2 45 0.023
777
CCT002 Cicatricial Pemphigoid 50 0.023
778
HPT020 Hepatic Vascular Disease 42 0.023
779
c INF095 Inflammatory Bowel Disease 25, Early Onset, Autosomal Recessive 35 0.023
780
MKL001 Mikulicz Disease 28 0.023
781
ABT001 Abetalipoproteinemia 60 0.023
782
P AGG001 Aggressive Periodontitis 50 0.023
783
TRC003 Trichomoniasis 41 0.023
784
P FRG001 Fragile X Syndrome 69 0.022
785
PRC003 Proctitis 41 0.022
786
c ADL096 Adult Hepatocellular Carcinoma 24 0.022
787
IMG001 Image Syndrome 50 0.022
788
c OPT059 Optic Atrophy 4 17 0.022
789
VTM002 Vitamin B12 Deficiency 44 0.022
790
BTN003 Biotinidase Deficiency 57 0.022
791
LYM020 Lymph Node Cancer 39 0.022
792
BRD001 Brody Myopathy 47 0.022
793
ESN017 Eosinophilic Granuloma 30 0.022
794
HPT077 Hepatic Venoocclusive Disease with Immunodeficiency 27 0.022
795
PPL022 Papilloma 55 0.022
796
PRM236 Primary Biliary Cholangitis 47 0.022
797
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 46 0.022
798
c OPT023 Optic Atrophy 2 25 0.022
799
c CLC037 Celiac Disease 4 20 0.022
800
BLR001 Biliary Atresia 52 0.022
801
P HMR005 Hemorrhoid 47 0.022
802
CHL056 Cheilitis 46 0.022
803
c VRL005 Viral Pneumonia 42 0.022
804
P DGR001 Digeorge Syndrome 53 0.022
805
P MWT001 Mowat-Wilson Syndrome 46 0.022
806
GST090 Gastroduodenal Crohn's Disease 25 0.022
807
SCB001 Scabies 47 0.022
808
BHR001 Behr Syndrome 42 0.022
809
c CNN010 Connective Tissue Benign Neoplasm 32 0.022
810
c MLT094 Multiple Sclerosis 3 24 0.022
811
P GNR027 Generalized Peeling Skin Syndrome 19 0.022
812
c CLC040 Celiac Disease 6 17 0.022
813
NRG002 Neurogenic Bladder 50 0.022
814
PRS034 Parasitic Helminthiasis Infectious Disease 38 0.022
815
c OPT025 Optic Atrophy 6 20 0.022
816
IMP005 Impotence 51 0.022
817
c PRS116 Prostate Cancer 1 37 0.022
818
c AML050 Amelogenesis Imperfecta, Type if 18 0.022
819
ANG020 Angiosarcoma 53 0.021
820
CRD003 Cardiac Sarcoidosis 42 0.021
821
ACL001 Acalculous Cholecystitis 35 0.021
822
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 33 0.021
823
c OPT057 Optic Atrophy 7 28 0.021
824
P BRN009 Burning Mouth Syndrome 54 0.021
825
c FML053 Familial Colorectal Cancer 51 0.021
826
CHR003 Cherubism 50 0.021
827
ANT024 Anthrax Disease 47 0.021
828
PRN039 Paraneoplastic Syndromes 32 0.021
829
c OPT024 Optic Atrophy 5 17 0.021
830
CNG368 Congenital Adrenal Hyperplasia 62 0.021
831
PRT038 Protein-Energy Malnutrition 49 0.021
832
EPD015 Epidemic Typhus 43 0.021
833
FSC002 Fascioliasis 42 0.021
834
GRN009 Granulomatous Hepatitis 39 0.021
835
OST115 Osteonecrosis of the Jaw 38 0.021
836
PRM026 Primary Systemic Mycosis 36 0.021
837
MCN001 Mucinous Adenocarcinoma 50 0.021
838
DBT010 Diabetic Neuropathy 55 0.021
839
ACH037 Achalasia-Addisonianism-Alacrimia Syndrome 45 0.021
840
HTR003 Heterotaxy 44 0.021
841
LRY004 Laryngotracheitis 30 0.021
842
c AML048 Amelogenesis Imperfecta, Type Ih 18 0.021
843
INT079 Intrahepatic Cholangiocarcinoma 56 0.021
844
JJN008 Jejunoileitis 38 0.021
845
TXC001 Toxic Megacolon 28 0.021
846
HYP160 Hyperkeratosis Lenticularis Perstans 23 0.021
847
CMM005 Common Cold 59 0.021
848
PNC033 Pancreas Adenocarcinoma 57 0.021
849
IMP002 Imperforate Anus 52 0.021
850
MLK006 Milk Allergy 47 0.021
851
FBR019 Fibromatosis 43 0.021
852
ILC002 Ileocolitis 39 0.021
853
HYP189 Hypoadrenalism 37 0.021
854
c AML047 Amelogenesis Imperfecta, Type Ia 19 0.021
855
c ATM064 Autoimmune Pancreatitis Type 1 18 0.021
856
BLM002 Bulimia Nervosa 52 0.021
857
PYL006 Pyloric Stenosis 46 0.021
858
P NRP042 Neuropathy, Hereditary Sensory and Autonomic, Type Ii 44 0.021
859
TRC023 Trichinosis 42 0.021
860
HPT067 Hepatocellular Adenoma 42 0.021
861
ELS002 Elastosis Perforans Serpiginosa 30 0.021
862
c CLC046 Celiac Disease 5 16 0.021
863
c ATM063 Autoimmune Pancreatitis Type 2 13 0.021
864
URN008 Urinary Bladder Cancer 66 0.021
865
HPT022 Hepatoblastoma 55 0.021
866
P HYP027 Hypobetalipoproteinemia 53 0.021
867
HNC001 Henoch-Schoenlein Purpura 45 0.021
868
c OST147 Osteoarthritis 1 30 0.021
869
c CHL118 Cholestasis, Benign Recurrent Intrahepatic, 2 28 0.021
870
c CLR078 Colorectal Cancer 11 17 0.021
871
c CLR084 Colorectal Cancer 9 17 0.021
872
P ATS007 Autism Spectrum Disorder 65 0.021
873
TNG003 Tongue Cancer 58 0.021
874
PYC001 Pycnodysostosis 48 0.021
875
PRT026 Parotitis 42 0.021
876
SPR007 Superior Mesenteric Artery Syndrome 41 0.021
877
c CLL012 Cell Type Benign Neoplasm 39 0.021
878
HYL004 Hyaline Fibromatosis Syndrome 38 0.021
879
c CLR077 Colorectal Cancer 10 29 0.021
880
c CLC041 Celiac Disease 7 16 0.021
881
DCB001 Decubitus Ulcer 41 0.020
882
GST093 Gastrointestinal Defects and Immunodeficiency Syndrome 39 0.020
883
CNG035 Congenital Bilateral Absence of Vas Deferens 36 0.020
884
PND004 Pandas 29 0.020
885
ADR005 Adrenal Carcinoma 57 0.020
886
LYM022 Lymphangioma 54 0.020
887
CMP002 Campylobacteriosis 47 0.020
888
HYP081 Hypolipoproteinemia 42 0.020
889
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 37 0.020
890
PRP056 Porphyria, Acute Hepatic 37 0.020
891
c AML017 Amelogenesis Imperfecta, Type Ib 34 0.020
892
c AML016 Amelogenesis Imperfecta, Type 1e 30 0.020
893
c ALG016 Alagille Syndrome 2 30 0.020
894
c AML019 Amelogenesis Imperfecta, Type Iii 29 0.020
895
c CWD005 Cowden Syndrome 4 23 0.020
896
P CLR108 Colorectal Adenoma 60 0.020
897
NRM004 Neuroma 48 0.020
898
ANG002 Angiostrongyliasis 39 0.020
899
P ENC011 Encephalomyopathy 37 0.020
900
c AML018 Amelogenesis Imperfecta, Type Ic 20 0.020
901
INF047 Infantile Free Sialic Acid Storage Disease 12 0.020
902
RYN003 Reynolds Syndrome 49 0.020
903
P ESP035 Esophagitis, Eosinophilic, 1 40 0.020
904
HPT004 Hepatic Coma 39 0.020
905
c GST048 Gastrointestinal System Benign Neoplasm 38 0.020
906
CCL002 Cecal Disease 29 0.020
907
CLN022 Colonic Atresia 24 0.020
908
c CLC039 Celiac Disease 13 18 0.020
909
c GLL025 Gallbladder Disease 2 16 0.020
910
c GLL026 Gallbladder Disease 3 16 0.020
911
P GNG025 Gingival Fibromatosis 50 0.020
912
P ACT150 Acute Adrenal Insufficiency 45 0.020
913
RCH001 Richter's Syndrome 45 0.020
914
URT031 Ureteral Disease 44 0.020
915
GRN011 Granulomatous Gastritis 28 0.020
916
c PRM158 Primary Intestinal Lymphangiectasia 23 0.020
917
EXT011 Extrapyramidal and Movement Disease 13 0.020
918
ORP003 Oropharynx Cancer 45 0.020
919
PRS115 Prosthetic Joint Infection 44 0.020
920
LVR002 Liver Angiosarcoma 43 0.020
921
GST030 Gastrinoma 42 0.020
922
c HRD012 Hereditary Elliptocytosis 42 0.020
923
MLL001 Molluscum Contagiosum 42 0.020
924
ISC015 Ischemic Colitis 39 0.020
925
FTT003 Fatty Acid Oxidation Disorders 39 0.020
926
MCR020 Microsporidiosis 39 0.020
927
P WHT013 White Sponge Nevus 1 39 0.020
928
ADR010 Adrenal Cortical Hypofunction 36 0.020
929
DDN009 Duodenal Obstruction 32 0.020
930
XNT002 Xanthogranulomatous Cholecystitis 31 0.020
931
CMM007 Common Bile Duct Disease 23 0.020
932
HRS037 Hirschsprung Disease with Type D Brachydactyly 15 0.020
933
P SLV001 Silver-Russell Syndrome 54 0.020
934
ULC007 Ulcerative Stomatitis 44 0.020
935
DRM013 Dermoid Cyst 44 0.020
936
CWM001 Cow Milk Allergy 40 0.020
937
LCH001 Leech Infestation 40 0.020
938
BLD019 Bile Duct Cystadenocarcinoma 33 0.020
939
c LVR028 Liver Failure, Transient Infantile 25 0.020
940
VGS001 Vagus Nerve Disease 18 0.020
941
HRS003 Hirschsprung Disease Ganglioneuroblastoma 15 0.020
942
SNG010 Single Median Maxillary Central Incisor 52 0.020
943
c ATM002 Autoimmune Polyendocrine Syndrome Type 1 48 0.020
944
MYL013 Myeloperoxidase Deficiency 46 0.020
945
BLD032 Bile Duct Adenocarcinoma 39 0.020
946
MRS001 Marasmus 36 0.020
947
INT050 Intestinal Impaction 31 0.020
948
ANL014 Anal Canal Adenocarcinoma 28 0.020
949
ULC008 Ulcerative Proctitis 22 0.020
950
EXT010 Extramedullary Plasmacytoma 49 0.019
951
SPP004 Suppurative Cholangitis 33 0.019
952
LNT001 Linitis Plastica 32 0.019
953
c INF145 Infantile Liver Failure Syndrome 1 25 0.019
954
c MWT002 Mowat-Wilson Syndrome Due to Monosomy 2q22 9 0.019
955
P LRY044 Larynx Cancer 57 0.019
956
PRV006 Pervasive Developmental Disorder 53 0.019
957
MTY001 Mutyh-Associated Polyposis 49 0.019
958
MYC005 Myocardial Stunning 44 0.019
959
RTC003 Root Caries 37 0.019
960
c CNG413 Congenital Short Bowel Syndrome 36 0.019
961
PNC019 Pancreatoblastoma 32 0.019
962
DNT046 Dental Abscess 28 0.019
963
STR032 Steroid Dehydrogenase Deficiency Dental Anomalies 11 0.019
964
PRT022 Protozoal Dysentery 11 0.019
965
IPX001 Ipex Syndrome 45 0.019
966
TRP008 Tropical Calcific Pancreatitis 42 0.019
967
THR009 Thrombocytopenia-Absent Radius Syndrome 41 0.019
968
GNT001 Giant Cell Reparative Granuloma 41 0.019
969
GBL002 Goblet Cell Carcinoid 34 0.019
970
BRW006 Brown Syndrome 29 0.019
971
P PLM064 Pulmonary Sequestration 27 0.019
972
P LYM124 Lymphangiectasia, Intestinal 21 0.019
973
c SCN059 Secondary Sclerosing Cholangitis 18 0.019
974
P FML321 Familial Stomach Cancer 13 0.019
975
HRS039 Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 13 0.019
976
c ATM071 Autoimmune Enteropathy Type 2 9 0.019
977
c MWT004 Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation 7 0.019
978
P MTH008 Methylmalonic Acidemia 49 0.019
979
INT017 Intestinal Schistosomiasis 45 0.019
980
SGN002 Signet Ring Cell Adenocarcinoma 45 0.019
981
FBR086 Fibrolamellar Carcinoma 45 0.019
982
TRC040 Tracheoesophageal Fistula 45 0.019
983
AZS001 Azoospermia 44 0.019
984
DFF019 Diffuse Gastric Cancer 40 0.019
985
PRV003 Perivascular Epithelioid Cell Tumor 39 0.019
986
APP009 Appendix Adenocarcinoma 38 0.019
987
NCR003 Necrotizing Sialometaplasia 34 0.019
988
c DNT027 Dentin Dysplasia, Type Ii 33 0.019
989
TTH007 Tooth Erosion 33 0.019
990
JJN007 Jejunal Adenocarcinoma 30 0.019
991
LYM035 Lymphangiectasis 28 0.019
992
LCT013 Lactase Deficiency, Congenital 22 0.019
993
SLT007 Solitary Rectal Ulcer Syndrome 19 0.019
994
IGG016 Igg4-Related Dacryoadenitis and Sialadenitis 16 0.019
995
c MLG068 Malignant Glioma 51 0.019
996
STT041 Stuttering 48 0.019
997
CRB090 Cerebral Hypoxia 45 0.019
998
FML026 Familial Lipoprotein Lipase Deficiency 44 0.019
999
KLT001 Klatskin's Tumor 42 0.019
1000
SKN022 Skin Squamous Cell Carcinoma 41 0.019
1001
P BNG071 Benign Schwannoma 38 0.019
1002
TTH008 Tooth Resorption 38 0.019
1003
CYC008 Cyclic Vomiting Syndrome 37 0.019
1004
LKS001 Leukostasis 35 0.019
1005
ALV001 Alveolar Periostitis 34 0.019
1006
SGM002 Sigmoid Neoplasm 34 0.019
1007
VGN019 Vaginal Discharge 33 0.019
1008
DVR006 Diversion Colitis 30 0.019
1009
IGG014 Igg4-Related Sclerosing Cholangitis 26 0.019
1010
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 25 0.019
1011
CHL075 Cheilitis Glandularis 21 0.019
1012
c DNT044 Dentinogenesis Imperfecta, Shields Type Iii 18 0.019
1013
CRL006 Caroli Disease, Isolated 13 0.019
1014
CLL026 Collagenous Gastritis 12 0.019
1015
IGG012 Igg4-Related Submandibular Gland Disease 8 0.019
1016
CVR006 Cavernous Hemangioma 46 0.019
1017
INT060 Intestinal Atresia 42 0.019
1018
SQM002 Squamous Cell Papilloma 40 0.019
1019
ALC005 Alcoholic Pancreatitis 36 0.019
1020
BLR027 Blue Rubber Bleb Nevus 36 0.019
1021
RCT020 Rectum Adenocarcinoma 31 0.019
1022
OVR044 Ovarian Carcinosarcoma 31 0.019
1023
CHR557 Chronic Intestinal Pseudoobstruction 29 0.019
1024
TRD003 Taurodontism 28 0.019
1025
ACH015 Achalasia, Familial Esophageal 28 0.019
1026
LRG016 Large Intestine Adenocarcinoma 26 0.019
1027
ACK001 Ackerman Syndrome 22 0.019
1028
PCD001 Pica Disease 21 0.019
1029
HPT066 Hepatoportal Sclerosis 20 0.019
1030
PYT001 Pythiosis 15 0.019
1031
MPV001 Mpv17-Related Hepatocerebral Mitochondrial Dna Depletion Syndrome 15 0.019
1032
c DNT047 Dentinogenesis Imperfecta Type 2 14 0.019
1033
c ATM070 Autoimmune Enteropathy Type 3 8 0.019
1034
ATS001 Autistic Disorder 63 0.018
1035
FBR054 Fibroma 46 0.018
1036
SMT002 Smooth Muscle Tumor 41 0.018
1037
SKL003 Skeletal Muscle Cancer 39 0.018
1038
DNT008 Denture Stomatitis 39 0.018
1039
CND006 Candida Glabrata 34 0.018
1040
ANL011 Anal Canal Carcinoma 31 0.018
1041
P HYP658 Hypoplastic Amelogenesis Imperfecta 26 0.018
1042
RSP004 Respiratory System Benign Neoplasm 25 0.018
1043
CNG002 Congenital Bile Acid Synthesis Defect 25 0.018
1044
ADN072 Adenoma of Pancreas 20 0.018
1045
FLM003 Fulminant Viral Hepatitis 19 0.018
1046
GLS013 Glossodynia 19 0.018
1047
OST007 Ostertagiasis 19 0.018
1048
HYP481 Hyperbiliverdinemia 17 0.018
1049
BLD065 Blue Diaper Syndrome 16 0.018
1050
CVR008 Cavernous Lymphangioma 15 0.018
1051
NKC001 Nk-Cell Enteropathy 13 0.018
1052
c INT019 Intestine Carcinoma in Situ 12 0.018
1053
BNG007 Benign Lymphoepithelial Lesion of Salivary Gland 10 0.018
1054
HRS038 Hirschsprung Disease with Hypoplastic Nails and Dysmorphic Facial Features 10 0.018
1055
TNG009 Tongue Squamous Cell Carcinoma 59 0.018
1056
MYM001 Myoma 52 0.018
1057
ANL004 Anal Canal Squamous Cell Carcinoma 39 0.018
1058
PRP017 Periapical Periodontitis 38 0.018
1059
CLN045 Colonic Benign Neoplasm 33 0.018
1060
DNT003 Dental Pulp Calcification 32 0.018
1061
ASC003 Ascending Cholangitis 30 0.018
1062
ANG061 Angular Cheilitis 26 0.018
1063
MTG001 Metagonimiasis 25 0.018
1064
ESN022 Eosinophilic Colitis 22 0.018
1065
ORL006 Oral Mucosa Leukoplakia 22 0.018
1066
DST016 Distomatosis 20 0.018
1067
c AML005 Amelogenesis Imperfecta Hypomaturation Type 19 0.018
1068
PRG122 Prognathism, Mandibular 18 0.018
1069
CRR013 Cirrhosis, North American Indian Childhood Type 17 0.018
1070
MCP039 Mucoepithelial Dysplasia, Hereditary 17 0.018
1071
AML046 Amelogenesis Imperfecta, Type Iia5 17 0.018
1072
ORP004 Oropharyngeal Cancer, Adult 12 0.018
1073
DNT050 Dentin Dysplasia with Sclerotic Bones 11 0.018
1074
UVL006 Uvulitis 10 0.018
1075
MTN003 Motion Sickness 48 0.018
1076
NTL004 Nut Allergy 37 0.018
1077
PLM013 Pulmonary Immaturity 34 0.018
1078
SPR012 Separation Anxiety Disorder 33 0.018
1079
FRT005 Fruit Allergy 31 0.018
1080
SKN020 Skin Papilloma 30 0.018
1081
CHL128 Childhood Hepatocellular Carcinoma 30 0.018
1082
DNT010 Dentin Caries 25 0.018
1083
MCN018 Mucinous Adenocarcinoma of the Appendix 23 0.018
1084
PRT034 Peritoneal Serous Adenocarcinoma 23 0.018
1085
PYL002 Pylorospasm 23 0.018
1086
c ALC016 Alcohol Sensitivity, Acute 21 0.018
1087
ACH039 Achalasia-Microcephaly Syndrome 17 0.018
1088
LTT006 Littoral Cell Angioma of the Spleen 16 0.018
1089
AND017 Anodontia of Permanent Dentition 14 0.018
1090
SLT010 Solitary Necrotic Tumor of the Liver 11 0.018
1091
INC023 Incisors, Fused Mandibular 10 0.018
1092
HPT028 Hepatic Cystic Hamartoma 10 0.018
1093
PNC042 Pancreatic Intraductal Papillary-Colloid Carcinoma 9 0.018
1094
DRR012 Diarrhea, Chronic, with Villous Atrophy 9 0.018
1095
SCR026 Secernentea Infections 8 0.018
1096
ACQ006 Acquired Gastric Outlet Stenosis 8 0.018
1097
c HYP058 Hypervitaminosis a 39 0.018
1098
DDN011 Duodenal Atresia 37 0.018
1099
VLL006 Villous Adenoma 32 0.018
1100
CRV068 Cervical Polyp 30 0.018
1101
MCN009 Mucinous Stomach Adenocarcinoma 28 0.018
1102
CHM005 Chemical Colitis 25 0.018
1103
RGN005 Regional Odontodysplasia 22 0.018
1104
AML024 Amelogenesis Imperfecta, Type Iia1 20 0.018
1105
AML023 Amelogenesis Imperfecta, Type Iia2 19 0.018
1106
XLN218 X-Linked Amelogenesis Imperfecta Hypoplastic/hypomaturation 2 19 0.018
1107
NRN029 Neuronal Intestinal Dysplasia 18 0.018
1108
AML043 Amelogenesis Imperfecta, Type Iia3 17 0.018
1109
AML049 Amelogenesis Imperfecta, Type Iia4 17 0.018
1110
ACT062 Acute Pericementitis 17 0.018
1111
PRT107 Proton-Pump Inhibitor-Responsive Esophageal Eosinophilia 11 0.018
1112
SGM006 Segmental Odontomaxillary Dysplasia 10 0.018
1113
MYP066 Myopathic Intestinal Pseudoobstruction 5 0.018
1114
NNH007 Non-Hypoproteinemic Hypertrophic Gastropathy 5 0.018
1115
UNC010 Unclassified Intestinal Pseudoobstruction 4 0.018
1116
P DYS005 Dyslexia 37 0.018
1117
ESP027 Esophagus Squamous Cell Carcinoma