Search results for digestive diseases

1088 hits were found for digestive diseases

# Family MCID Name MIFTS Score
1
GST050 Gastrointestinal System Disease 53 3.669
2
CHG001 Chagas Disease 66 2.498
3
P LVR013 Liver Disease 72 0.142
4
P INT068 Intestinal Disease 59 0.136
5
P GST049 Gastrointestinal System Cancer 59 0.126
6
P PNC044 Pancreatitis 60 0.123
7
P KDN018 Kidney Disease 65 0.121
8
CRH001 Crohn's Disease 73 0.118
9
P HRT032 Heart Disease 75 0.113
10
P OBS005 Obesity 91 0.104
11
P INF037 Inflammatory Bowel Disease 62 0.103
12
MTH009 Mouth Disease 62 0.102
13
P CLC005 Celiac Disease 69 0.101
14
STM006 Stomach Disease 47 0.100
15
PHY002 Physical Disorder 43 0.100
16
LNG099 Lung Disease 61 0.099
17
P ADN016 Adenocarcinoma 69 0.093
18
P HPT021 Hepatitis 68 0.093
19
P CRN211 Coronary Artery Disease 73 0.092
20
PNC034 Pancreas Disease 55 0.089
21
CLN019 Colonic Disease 51 0.087
22
P CLR023 Colorectal Cancer 95 0.085
23
VSC007 Vascular Disease 65 0.084
24
GST045 Gastroenteritis 57 0.079
25
P DRR001 Diarrhea 59 0.079
26
PCK002 Pick Disease 68 0.079
27
NRN002 Neuronitis 39 0.078
28
c CNT035 Central Nervous System Disease 60 0.078
29
ESP021 Esophageal Cancer 74 0.077
30
CYS001 Cystic Fibrosis 86 0.077
31
P PNC035 Pancreatic Cancer 84 0.076
32
P ESP024 Esophagitis 59 0.076
33
CLT003 Colitis 58 0.075
34
P STM004 Stomach Cancer 72 0.074
35
P PNM007 Pneumonia 66 0.074
36
P HYP729 Hypersensitivity Reaction Disease 43 0.073
37
ESP023 Esophageal Disease 50 0.073
38
FTT001 Fatty Liver Disease 59 0.073
39
P ART022 Arthritis 72 0.072
40
IMM136 Immune System Disease 53 0.071
41
GST092 Gastroesophageal Reflux 62 0.071
42
IRR002 Irritable Bowel Syndrome 57 0.070
43
GLC008 Glucose Metabolism Disease 44 0.070
44
RSP006 Respiratory System Disease 60 0.070
45
ULC004 Ulcerative Colitis 72 0.070
46
c PND001 Pain Disorder 55 0.070
47
CNS004 Constipation 56 0.069
48
BRT030 Birth Defects 44 0.068
49
P INF038 Influenza 71 0.068
50
DYS073 Dysphagia 47 0.067
51
P HPT023 Hepatocellular Carcinoma 89 0.066
52
MVM001 Movement Disease 52 0.065
53
P LKM002 Leukemia 72 0.065
54
END072 Endotheliitis 41 0.064
55
SQM006 Squamous Cell Carcinoma 69 0.064
56
P NRV007 Nervous System Disease 70 0.063
57
GST023 Gastric Ulcer 54 0.063
58
MCS002 Mucositis 54 0.063
59
PLM129 Pulmonary Disease, Chronic Obstructive 62 0.062
60
DDN006 Duodenitis 40 0.062
61
P AST005 Asthma 81 0.062
62
ISC004 Ischemia 59 0.062
63
GST078 Gastrointestinal Allergy 39 0.062
64
RCT017 Rectal Disease 38 0.062
65
RHM027 Rheumatic Disease 57 0.061
66
EXC002 Exocrine Pancreatic Insufficiency 42 0.061
67
P BRS047 Breast Cancer 100 0.061
68
P GLL020 Gallbladder Disease 58 0.061
69
MSC004 Muscle Tissue Disease 37 0.061
70
CNN005 Connective Tissue Disease 61 0.060
71
PPT005 Peptic Ulcer Disease 57 0.060
72
P LYM118 Lymphoma 69 0.060
73
PRD007 Periodontal Disease 42 0.060
74
TTH006 Tooth Disease 51 0.060
75
BLR006 Biliary Tract Disease 53 0.059
76
PRP019 Peripheral Nervous System Disease 53 0.059
77
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.059
78
LCT002 Lactose Intolerance 43 0.058
79
NLL002 Null Syndrome 26 0.058
80
BSL008 Basal Ganglia Disease 44 0.058
81
ADL002 Adult Syndrome 57 0.057
82
WLS001 Wilson Disease 73 0.057
83
LPD008 Lipid Metabolism Disorder 57 0.057
84
GST013 Gastrojejunal Ulcer 24 0.057
85
FBR012 Fabry Disease 71 0.057
86
P MSC033 Muscle Disorders 52 0.056
87
DYS014 Dyspepsia 50 0.056
88
c CLL013 Cell Type Cancer 48 0.056
89
GNG013 Gingivitis 61 0.055
90
P PRD008 Periodontitis 46 0.055
91
KWS002 Kawasaki Disease 67 0.055
92
VRL011 Viral Infectious Disease 59 0.055
93
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 53 0.055
94
LVR012 Liver Cirrhosis 66 0.055
95
CND002 Conduct Disorder 53 0.054
96
ANR040 Aneurysm 57 0.054
97
ART021 Arteriosclerosis 57 0.054
98
GST019 Gastrointestinal Stromal Tumor 74 0.054
99
EYD002 Eye Disease 57 0.054
100
CLN009 Colon Squamous Cell Carcinoma 27 0.054
101
P GLY013 Glycogen Storage Disease 59 0.053
102
P RHM011 Rheumatoid Arthritis 87 0.053
103
NRN004 Neuroendocrine Tumor 55 0.053
104
FNC005 Functional Colonic Disease 30 0.052
105
ATH003 Atherosclerosis 65 0.052
106
ING001 Inguinal Hernia 57 0.052
107
CRB009 Cerebritis 39 0.051
108
P PRT013 Portal Hypertension 58 0.051
109
c CHR089 Chronic Kidney Failure 65 0.051
110
PRM025 Primary Bacterial Infectious Disease 42 0.051
111
RTN023 Retinitis 49 0.050
112
c FML311 Familial Colorectal Cancer Type X 35 0.050
113
ANX002 Anxiety Disorder 66 0.050
114
BNS002 Bone Structure Disease 36 0.050
115
GST028 Gastric Squamous Cell Carcinoma 39 0.050
116
c HPT001 Hepatitis C 62 0.050
117
SWL001 Swallowing Disorders 32 0.050
118
P NRP001 Neuropathy 57 0.050
119
BLN006 Blind Loop Syndrome 28 0.049
120
PRT036 Peritonitis 60 0.048
121
ANS012 Anus Disease 31 0.048
122
CRC038 Carcinoma of Stomach, Salivary Gland Type 15 0.048
123
P AMY004 Amyloidosis 64 0.048
124
APP008 Appendicitis 59 0.048
125
CHL067 Cholecystitis 55 0.048
126
P CLL015 Collagen Disease 50 0.048
127
UND009 Undifferentiated Carcinoma of Stomach 16 0.048
128
THR024 Thrombosis 43 0.048
129
BLD054 Blood Protein Disease 39 0.048
130
P LPS004 Lupus Erythematosus 63 0.048
131
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 23 0.047
132
c GLL024 Gallbladder Disease 1 36 0.047
133
NNL002 Nonalcoholic Steatohepatitis 50 0.047
134
CRB025 Carbohydrate Metabolic Disorder 47 0.047
135
c ACT027 Acute Pancreatitis 56 0.047
136
END035 Endocrine Gland Cancer 50 0.047
137
NWC001 Newcastle Disease 51 0.047
138
HYP066 Hyperglycemia 59 0.047
139
ABD010 Abdominal Wall Defect 37 0.047
140
FNC006 Functional Gastric Disease 35 0.047
141
ATN002 Autonomic Nervous System Disease 48 0.046
142
SKN023 Skin Tag 46 0.046
143
c CLR079 Colorectal Cancer 2 30 0.046
144
PNC118 Pancreas, Annular 36 0.046
145
P MYC007 Myocardial Infarction 77 0.046
146
c SYS001 Systemic Lupus Erythematosus 86 0.046
147
c RCR022 Recurrent Acute Pancreatitis 40 0.046
148
CTS003 Coats Disease 58 0.046
149
P CNG015 Congenital Diaphragmatic Hernia 60 0.046
150
NTR005 Nutritional Deficiency Disease 47 0.046
151
P LNG032 Lung Cancer 94 0.046
152
KDS001 Kid Syndrome 57 0.046
153
CHL071 Child Syndrome 59 0.045
154
RCT018 Rectal Neoplasm 53 0.045
155
MDY003 Mody, Type Ii 40 0.045
156
DGS008 Digestive System Melanoma 18 0.045
157
P HST010 Histiocytosis 54 0.045
158
P INF032 Infertility 57 0.045
159
GST071 Gastrointestinal Carcinoma 40 0.045
160
P ORL007 Oral Cavity Cancer 57 0.045
161
BRS051 Breast Disease 60 0.045
162
MNT002 Mental Depression 52 0.045
163
P ADD001 Addison's Disease 62 0.045
164
CRC037 Carcinoma of Esophagus, Salivary Gland Type 15 0.045
165
P GST044 Gastritis 55 0.045
166
CRY003 Cryptosporidiosis 46 0.045
167
c PRK031 Parkinson Disease 1 51 0.045
168
c CRN174 Coronary Heart Disease 2 21 0.044
169
CHL127 Cholangiocarcinoma, Susceptibility to 47 0.044
170
UND008 Undifferentiated Carcinoma of Esophagus 15 0.044
171
DGS007 Digestive Duplication 8 0.044
172
SLV003 Salivary Gland Disease 44 0.044
173
P CRD011 Cardiomyopathy 67 0.044
174
MCR094 Microvillus Inclusion Disease 50 0.044
175
c HPT003 Hepatitis a 56 0.044
176
VND001 Vein Disease 49 0.044
177
PLV003 Pelvic Inflammatory Disease 51 0.044
178
RSD004 Rosai-Dorfman Disease 44 0.044
179
P HRS035 Hirschsprung Disease 1 58 0.044
180
P HYP607 Hypercholesterolemia, Familial 75 0.044
181
CRD118 Cardiovascular Cancer 45 0.044
182
FDL002 Food Allergy 51 0.044
183
PNC048 Pancreatic Lipase Deficiency 30 0.044
184
CSY001 C Syndrome 53 0.043
185
P ART023 Arthropathy 62 0.043
186
c CLR085 Colorectal Cancer 1 46 0.043
187
PST035 Postgastrectomy Syndrome 33 0.043
188
JNT002 Joint Disorders 55 0.043
189
NSD001 Nose Disease 49 0.043
190
GLL018 Gallbladder Cancer 59 0.042
191
PST030 Postcholecystectomy Syndrome 32 0.042
192
GST037 Gastroparesis 52 0.042
193
ENT006 Enterokinase Deficiency 23 0.042
194
END038 Endocrine Pancreas Disease 42 0.042
195
SQM020 Squamous Cell Carcinoma of the Pancreas 22 0.042
196
P ALG028 Alagille Syndrome 1 63 0.042
197
SQM013 Squamous Cell Carcinoma, Head and Neck 69 0.041
198
P SPS003 Spastic Diplegia 52 0.041
199
c ATM011 Autoimmune Hepatitis 57 0.041
200
c ACT004 Acute Diarrhea 37 0.041
201
FCL044 Fecal Incontinence 34 0.041
202
c HPT016 Hepatitis B 62 0.041
203
LYS002 Lysosomal Storage Disease 52 0.041
204
ORL011 Oral Cancer 56 0.041
205
P TRC086 Trichohepatoenteric Syndrome 1 51 0.041
206
VSC006 Vascular Cancer 52 0.041
207
c PNC111 Pancreatic Cancer 2 29 0.041
208
SPL011 Spleen Cancer 37 0.041
209
END030 End Stage Renal Failure 51 0.041
210
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 31 0.041
211
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 26 0.040
212
CRV038 Cervical Squamous Cell Carcinoma 57 0.040
213
P PRM006 Primary Biliary Cirrhosis 50 0.040
214
MLN008 Melanoma 70 0.040
215
SRC014 Sarcoma 66 0.040
216
ATM052 Autoimmune Disease 1 27 0.040
217
c PRM023 Pre-Malignant Neoplasm 43 0.039
218
DRG001 Drug Psychosis 41 0.039
219
TNG004 Tongue Disease 41 0.039
220
BLC007 Bile Acid Synthesis Defect, Congenital, 1 34 0.039
221
SML014 Small Intestine Leiomyosarcoma 35 0.039
222
c PRK030 Parkinson Disease 4 41 0.039
223
P ALP004 Alport Syndrome 70 0.039
224
DYS011 Dyskinesia of Esophagus 32 0.039
225
P PSD087 Pseudoxanthoma Elasticum 67 0.039
226
JJN004 Jejunal Atresia 29 0.039
227
P CHL066 Cholangitis 48 0.039
228
EXP004 Exophthalmos 50 0.039
229
BLC008 Bile Acid Synthesis Defect, Congenital, 2 29 0.039
230
PNC014 Pancreatic Serous Cystadenocarcinoma 22 0.039
231
MTC016 Mitochondrial Neurogastrointestinal Encephalopathy Disease 27 0.039
232
MLR004 Malaria 82 0.038
233
P MSC003 Muscular Atrophy 49 0.038
234
DSS008 Disease of Mental Health 53 0.038
235
CHY002 Chylomicron Retention Disease 52 0.038
236
c CHL119 Cholangitis, Primary Sclerosing 47 0.038
237
c CHL120 Cholestasis, Benign Recurrent Intrahepatic 38 0.038
238
OST141 Osteoclastic Giant Cell Tumor of Pancreas 11 0.038
239
c CLR080 Colorectal Cancer 5 34 0.038
240
SCR011 Scrapie 36 0.038
241
P ATR005 Atrophic Gastritis 47 0.038
242
ACN026 Acinar Cell Carcinoma of Pancreas 23 0.038
243
MCN020 Mucinous Cystadenocarcinoma of Pancreas 17 0.038
244
SLD012 Solid Pseudopapillary Carcinoma of the Pancreas 15 0.038
245
SQM019 Squamous Cell Carcinoma of the Small Intestine 14 0.038
246
STT004 Steatorrhea 40 0.038
247
c CLR075 Colorectal Cancer 3 29 0.038
248
CNG034 Congestive Heart Failure 70 0.038
249
SQM016 Squamous Cell Carcinoma of Gallbladder and Extrahepatic Biliary Tract 11 0.038
250
TRP004 Tropical Sprue 35 0.038
251
GST039 Gastroduodenitis 30 0.038
252
VSC011 Vasculitis 62 0.038
253
ALR002 Al-Raqad Syndrome 29 0.038
254
HYP266 Hypoxia 55 0.037
255
LCT019 Lactase Persistence/nonpersistence 21 0.037
256
c CRN175 Coronary Heart Disease 4 20 0.037
257
P SML016 Small Intestine Cancer 51 0.037
258
P TRM003 Tremor 53 0.037
259
KPS004 Kaposi Sarcoma 67 0.037
260
ACH005 Achalasia 47 0.037
261
c PNC094 Pancreatic Cancer 1 27 0.037
262
BLR007 Biliary Tract Neoplasm 50 0.037
263
SCR037 Sucrase-Isomaltase Deficiency, Congenital 28 0.037
264
LYM024 Lymphatic System Disease 49 0.037
265
UMB002 Umbilical Hernia 43 0.037
266
DDN007 Duodenal Disease 34 0.037
267
P ENC018 Encephalopathy 52 0.037
268
c PNC095 Pancreatic Cancer 3 31 0.037
269
P MYP004 Myopathy 68 0.037
270
UPP004 Upper Respiratory Tract Disease 46 0.036
271
DRM006 Dermatitis 63 0.036
272
HNS001 Hansen's Disease 29 0.036
273
PRC002 Paracoccidioidomycosis 52 0.036
274
c CHL080 Cholestasis, Progressive Familial Intrahepatic 1 46 0.036
275
ANG011 Angiodysplasia 43 0.036
276
P PLY023 Polycystic Liver Disease 49 0.036
277
ACQ007 Acquired Immunodeficiency Syndrome 60 0.036
278
ESP025 Esophagus Adenocarcinoma 46 0.036
279
c PRK045 Parkinson Disease 5 37 0.036
280
P DRM007 Dermatitis Herpetiformis 52 0.036
281
DRR004 Diarrhea 3, Secretory Sodium, Congenital, Syndromic 26 0.036
282
PYL007 Pylorus Cancer 20 0.036
283
CHL068 Cholestasis 58 0.036
284
DRR005 Diarrhea 4, Malabsorptive, Congenital 33 0.036
285
P CWD001 Cowden Disease 65 0.036
286
ADJ001 Adjustment Disorder 38 0.036
287
CHR515 Chronic Atrial and Intestinal Dysrhythmia 22 0.036
288
HPY002 H. Pylori Infection 60 0.035
289
MCK002 Meckel's Diverticulum 35 0.035
290
PNC028 Pancreatic Steatorrhea 34 0.035
291
DNT012 Dental Caries 46 0.035
292
P GLM007 Glomerulonephritis 55 0.035
293
c PNC108 Pancreatitis, Hereditary 57 0.035
294
SLP005 Sleep Disorder 54 0.035
295
TNG002 Tangier Disease 62 0.035
296
ANL022 Anal Fistula 40 0.035
297
P LYM026 Lymphoblastic Leukemia 60 0.035
298
CHR028 Chronic Wasting Disease 32 0.035
299
ERY003 Erythema Multiforme 53 0.035
300
CYS039 Cystic Kidney Disease 50 0.035
301
JJN003 Jejunal Cancer 30 0.035
302
THY030 Thyroid Gland Disease 49 0.035
303
HPT046 Hepatic Veno-Occlusive Disease 50 0.035
304
DMY004 Demyelinating Disease 53 0.035
305
c INT072 Intestinal Pseudo-Obstruction 41 0.035
306
c INF087 Inflammatory Bowel Disease 4 41 0.035
307
CNG298 Congenital Pancreatic Cyst 23 0.035
308
BHC003 Behcet Syndrome 62 0.034
309
RPR002 Reproductive System Disease 43 0.034
310
AND005 Androgen Insensitivity Syndrome, Mild 16 0.034
311
P DDN001 Duodenal Ulcer 48 0.034
312
LKC003 Leukocyte Disease 46 0.034
313
c ALZ012 Alzheimer Disease 12 24 0.034
314
ANG054 Angina Pectoris 49 0.034
315
DGS006 Digestive Duplication Cyst of the Tongue 7 0.034
316
ZLL002 Zollinger-Ellison Syndrome 53 0.034
317
AMN002 Amino Acid Metabolic Disorder 48 0.034
318
INT071 Intestinal Perforation 40 0.034
319
c HPT073 Hepatitis C Virus 70 0.034
320
PRN019 Perinatal Necrotizing Enterocolitis 45 0.034
321
BRN106 Burns 52 0.034
322
ADN082 Adenocarcinoma of the Gallbladder and Extrahepatic Biliary Tract 12 0.034
323
PRN015 Perinatal Intestinal Perforation 5 0.034
324
ATM053 Autoimmune Disease 2 18 0.034
325
P THL005 Thalassemia 61 0.034
326
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 47 0.034
327
APH002 Aphasia 55 0.034
328
P PLN008 Peeling Skin Syndrome 49 0.034
329
ISL029 Isolated Anorectal Malformation 7 0.034
330
CRH005 Crohn's Colitis 50 0.034
331
ETN001 Eating Disorder 56 0.034
332
TTH001 Tooth Ankylosis 37 0.034
333
ORL004 Oral Submucous Fibrosis 51 0.033
334
OCL009 Ocular Cancer 58 0.033
335
STM007 Stomatitis 49 0.033
336
P PLM036 Pulmonary Fibrosis 68 0.033
337
P INT001 Intrahepatic Cholestasis 56 0.033
338
c ATM024 Autoimmune Pancreatitis 46 0.033
339
MGC001 Megacolon 46 0.033
340
MCN017 Meconium Ileus 49 0.033
341
DDN010 Duodenum Cancer 43 0.033
342
P AGN002 Agnosia 59 0.033
343
P MSC005 Muscular Dystrophy 65 0.033
344
ADN018 Adenoma 58 0.033
345
PRS042 Prostate Disease 51 0.033
346
GST040 Gastric Adenocarcinoma 51 0.033
347
ISL001 Islet Cell Tumor 48 0.033
348
BLD044 Bladder Disease 50 0.032
349
ESP020 Esophageal Atresia 50 0.032
350
APR001 Apraxia 49 0.032
351
P RNL014 Renal Cell Carcinoma 80 0.032
352
HYP056 Hypoglycemia 60 0.032
353
OVR063 Overnutrition 48 0.032
354
BRR002 Barrett's Adenocarcinoma 43 0.032
355
MLK004 Malakoplakia 31 0.032
356
BRN038 Bronchial Disease 53 0.032
357
P DBT005 Diabetes Insipidus 52 0.032
358
HYP082 Hypopharynx Cancer 44 0.032
359
c CHR096 Chronic Pulmonary Heart Disease 40 0.032
360
BLD036 Bile Duct Disease 48 0.032
361
RDT013 Radiation Proctitis 46 0.032
362
c SCN046 Secondary Short Bowel Syndrome 12 0.032
363
VND002 Van Der Woude Syndrome 50 0.032
364
PRP021 Peripheral Nervous System Neoplasm 48 0.032
365
GLC022 Glucose/galactose Malabsorption 39 0.032
366
ART016 Aortic Aneurysm 67 0.032
367
ATM054 Autoimmune Disease 3 18 0.032
368
RFR013 Refractory Celiac Disease 33 0.032
369
PRT035 Peritoneum Cancer 37 0.032
370
WLL006 Wells Syndrome 58 0.032
371
P SJG001 Sjogren's Syndrome 49 0.032
372
GDS001 Good Syndrome 46 0.032
373
P NPH012 Nephrotic Syndrome 59 0.031
374
ATN004 Autonomic Neuropathy 42 0.031
375
LRY017 Laryngeal Disease 36 0.031
376
P GRM010 Germ Cells Tumors 34 0.031
377
c CLC045 Celiac Disease 2 18 0.031
378
ADR012 Adrenal Gland Disease 48 0.031
379
P GST047 Gastrointestinal Neuroendocrine Tumor 34 0.031
380
P HYP076 Hyperthyroidism 53 0.031
381
ADN021 Adenomatous Polyposis Coli 71 0.031
382
c DLT002 Dilated Cardiomyopathy 74 0.031
383
c VRL010 Viral Hepatitis 58 0.031
384
BCT015 Bacteremia 47 0.031
385
ILM001 Ileum Cancer 26 0.031
386
c CHR086 Chronic Conjunctivitis 45 0.031
387
c INF088 Inflammatory Bowel Disease 5 32 0.031
388
c INF067 Inflammatory Bowel Disease 10 23 0.031
389
MCR191 Microscopic Colitis 46 0.031
390
TRH001 Trehalase Deficiency 18 0.030
391
PRD004 Prediabetes Syndrome 43 0.030
392
INT002 Intermittent Claudication 55 0.030
393
SXL003 Sexual Disorder 42 0.030
394
FXF002 Fox-Fordyce Disease 37 0.030
395
P MTC003 Metachromatic Leukodystrophy 70 0.030
396
c MYC058 Myocardial Infarction 2 28 0.030
397
DWN001 Down Syndrome 69 0.030
398
SLD003 Sialadenitis 46 0.030
399
PYL003 Pyloric Antrum Cancer 13 0.030
400
P SCL009 Sclerosing Cholangitis 47 0.030
401
P OST012 Osteoarthritis 79 0.030
402
P AML002 Amelogenesis Imperfecta 44 0.030
403
LYS003 Lysinuric Protein Intolerance 53 0.030
404
CRC006 Carcinoid Syndrome 48 0.030
405
DMP001 Dumping Syndrome 40 0.030
406
P RTT002 Rett Syndrome 82 0.030
407
c DRR009 Diarrhea 6 33 0.030
408
P ASP006 Aspergillosis 60 0.030
409
SPC003 Specific Developmental Disorder 38 0.030
410
INT051 Intussusception 48 0.030
411
GRM001 Germ Cell and Embryonal Cancer 38 0.030
412
GLC006 Galactosemia 66 0.030
413
P LKD001 Leukodystrophy 56 0.030
414
WLM001 Wolman Disease 58 0.030
415
BRC012 Brucellosis 61 0.030
416
P HRD018 Hair Disease 50 0.030
417
c PLY146 Polycystic Liver Disease 1 42 0.030
418
LPD027 Lip Disease 29 0.030
419
ESN005 Eosinophilic Gastroenteritis 51 0.029
420
SLM003 Salmonellosis 51 0.029
421
PRN011 Pernicious Anemia 43 0.029
422
SLC005 Selective Iga Deficiency Disease 34 0.029
423
WST001 West Syndrome 58 0.029
424
HPT014 Hepatorenal Syndrome 45 0.029
425
THR035 Thrombasthenia 41 0.029
426
DYS015 Dysentery 39 0.029
427
CHR008 Choroiditis 43 0.029
428
SWN001 Swine Influenza 35 0.029
429
c CLR081 Colorectal Cancer 6 31 0.029
430
P INT070 Intestinal Obstruction 55 0.029
431
c NMN013 Niemann-Pick Disease, Type a 58 0.029
432
c VRL005 Viral Pneumonia 42 0.029
433
DRR008 Diarrhea 1, Secretory Chloride, Congenital 37 0.029
434
P LRY019 Laryngitis 53 0.029
435
P INT143 Interstitial Cystitis 54 0.029
436
VNT001 Ventilation Pneumonitis 34 0.029
437
IRN001 Iron Deficiency Anemia 51 0.029
438
PSD007 Pseudomyxoma Peritonei 49 0.029
439
ALC009 Alcoholic Liver Cirrhosis 48 0.029
440
SNS023 Sensory System Cancer 44 0.029
441
DFC004 Deficiency Anemia 60 0.029
442
P HYP060 Hyperinsulinism 57 0.029
443
KRT001 Keratoconjunctivitis Sicca 59 0.029
444
CMM004 Common Variable Immunodeficiency 68 0.029
445
PRD003 Periodontosis 41 0.029
446
c CLR083 Colorectal Cancer 8 26 0.029
447
P DBT083 Diabetes Mellitus, Permanent Neonatal 56 0.028
448
MSC072 Muscle Cancer 50 0.028
449
c DRR007 Diarrhea 7 30 0.028
450
PRT030 Parathyroid Gland Disease 47 0.028
451
VSC044 Visceral Myopathy 48 0.028
452
PLS002 Peliosis Hepatis 31 0.028
453
P PRP029 Porphyria 59 0.028
454
GST063 Gastric Cancer Risk After H. Pylori Infection 53 0.028
455
GGR001 Geographic Tongue 47 0.028
456
GLS007 Glossitis 43 0.028
457
HTS001 Hiatus Hernia 39 0.028
458
TBR008 Tuberculous Peritonitis 39 0.028
459
c CLR087 Colorectal Cancer 12 33 0.028
460
ORL014 Oral Pharyngeal Disorders 14 0.028
461
BLD034 Bile Duct Carcinoma 55 0.028
462
CHL052 Choledochal Cyst 39 0.028
463
c AML020 Amelogenesis Imperfecta, Type Iv 34 0.028
464
PLP001 Pulpitis 44 0.028
465
HPT081 Hepatic Infarction 35 0.028
466
GST095 Gastritis, Familial Giant Hypertrophic 24 0.028
467
c PRK037 Parkinson Disease 13 28 0.028
468
c DYS166 Dysautonomia, Familial 49 0.028
469
BLC009 Bile Acid Synthesis Defect, Congenital, 4 29 0.028
470
RLP002 Relapsing-Remitting Multiple Sclerosis 54 0.028
471
c GLL027 Gallbladder Disease 4 23 0.028
472
P HYP014 Hyperuricemia 50 0.028
473
c AML044 Amelogenesis Imperfecta, Type Ig 33 0.028
474
c RTN162 Retinitis Pigmentosa 2 51 0.028
475
MYL020 Myelomeningocele 50 0.027
476
CLN015 Colon Adenocarcinoma 49 0.027
477
P DNT011 Dentinogenesis Imperfecta 43 0.027
478
GNG003 Gingival Recession 41 0.027
479
ANS003 Anisakiasis 30 0.027
480
BLC011 Bile Acid Synthesis Defect, Congenital, 3 28 0.027
481
SCH014 Schistosomiasis 56 0.027
482
DRY001 Dry Eye Syndrome 48 0.027
483
ANS011 Anus Cancer 39 0.027
484
HYP021 Hypercementosis 31 0.027
485
P MTC069 Mitochondrial Disorders 55 0.027
486
MNT001 Mantle Cell Lymphoma 72 0.027
487
P FCL005 Focal Segmental Glomerulosclerosis 60 0.027
488
SML036 Small Intestinal Adenocarcinoma 47 0.027
489
P TRM004 Trimethylaminuria 41 0.027
490
MYC015 Mycobacterium Fortuitum 28 0.027
491
P STR035 Streptococcal Group a Invasive Disease 17 0.027
492
MCR037 Macroglossia 45 0.027
493
P PNC045 Pancreatic Agenesis 43 0.027
494
P HYP009 Hypertrophic Pyloric Stenosis 41 0.027
495
AMP003 Ampulla of Vater Neoplasm 36 0.027
496
PRL008 Paralytic Ileus 35 0.027
497
P DNT009 Dentin Dysplasia 34 0.027
498
c CHR013 Chronic Apical Periodontitis 28 0.027
499
TTH005 Teeth Hard Tissue Disease 26 0.027
500
GLT030 Gluten Allergy 19 0.027
501
P TCL004 T-Cell Leukemia 46 0.027
502
GNG012 Gingival Overgrowth 51 0.027
503
PNC013 Pancreatic Ductal Carcinoma 45 0.027
504
FNC002 Functional Diarrhea 39 0.027
505
BLR028 Biliary Atresia, Extrahepatic 31 0.027
506
MYX011 Myxozoa 17 0.027
507
P OST005 Osteogenesis Imperfecta 68 0.027
508
MNR003 Mineral Metabolism Disease 40 0.027
509
RCT011 Rectal Prolapse 41 0.027
510
SLL001 Sialolithiasis 37 0.027
511
APP010 Appendix Cancer 36 0.027
512
INT111 Intestinal Pseudoobstruction, Neuronal 31 0.027
513
c PNC103 Pancreatic Cancer 4 31 0.027
514
c NRP031 Neuropathy, Hereditary Sensory and Autonomic, Type Vii 23 0.027
515
PRT037 Pertussis 63 0.027
516
LCR008 Lacrimal Apparatus Disease 40 0.027
517
TTH002 Tooth Agenesis 52 0.027
518
AND001 Anodontia 42 0.027
519
DNT001 Dental Fluorosis 40 0.027
520
NTM001 Nutmeg Liver 31 0.027
521
DNT041 Dentin Dysplasia, Type I, with Microdontia and Misshapen Teeth 28 0.027
522
OTD001 Otodental Dysplasia 28 0.027
523
MSL001 Measles 58 0.027
524
TRN003 Transverse Colon Cancer 43 0.026
525
GST009 Gastroschisis 40 0.026
526
ANR003 Anorectal Stricture 13 0.026
527
EXF001 Exfoliation Syndrome 57 0.026
528
ALL026 Allergic Hypersensitivity Disease 52 0.026
529
PRP016 Paraplegia 48 0.026
530
P MYT002 Myotonic Dystrophy 48 0.026
531
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 43 0.026
532
FSS001 Fissured Tongue 35 0.026
533
ORL019 Oral Hairy Leukoplakia 34 0.026
534
ATR073 Atrophic Glossitis 27 0.026
535
FLR007 Failure of Tooth Eruption, Primary 24 0.026
536
CSC001 Cascade Stomach 18 0.026
537
P RBL001 Rubella 53 0.026
538
MYC033 Myoclonus 41 0.026
539
CLN045 Colonic Benign Neoplasm 45 0.026
540
APL002 Aplasia of Lacrimal and Salivary Glands 38 0.026
541
ENT001 Enterocele 31 0.026
542
MCC003 Mucocele of Salivary Gland 19 0.026
543
c ACT134 Acute Liver Failure 48 0.026
544
DCH001 Duchenne Muscular Dystrophy 79 0.026
545
INT052 Intestinal Volvulus 35 0.026
546
MDN001 Median Rhomboid Glossitis 26 0.026
547
SPP003 Suppurative Periapical Periodontitis 24 0.026
548
PLY114 Polyglucosan Body Myopathy 2 17 0.026
549
c CHR465 Chronic Diarrhea Due to Guanylate Cyclase 2c Overactivity 9 0.026
550
P DBT085 Diabetes Mellitus, Insulin-Dependent 79 0.026
551
P END044 Endometriosis 53 0.026
552
DNT006 Dental Pulp Necrosis 27 0.026
553
NRG001 Neurogenic Bowel 27 0.026
554
ACC005 Accessory Pancreas 21 0.026
555
P ACT046 Acute Apical Periodontitis 16 0.026
556
DRR013 Diarrhea 8, Secretory Sodium, Congenital 16 0.026
557
PLP002 Pulp Degeneration 13 0.026
558
HYD004 Hydrops of Gallbladder 12 0.026
559
HYP049 Hypertrophy of Tongue Papillae 9 0.026
560
ULC002 Ulcer of Anus and Rectum 9 0.026
561
c CWD006 Cowden Syndrome 1 51 0.026
562
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.026
563
P HYP117 Hypertriglyceridemia 61 0.026
564
GST026 Gastric Fundus Cancer 19 0.026
565
VSC014 Vascular Hyalinosis 17 0.026
566
GST087 Gastric Linitis Plastica 16 0.026
567
ALC012 Alcoholic Gastritis 13 0.026
568
PRF001 Perforation of Bile Duct 12 0.026
569
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.026
570
GLC003 Glucose Intolerance 54 0.026
571
P MMP001 Mumps 54 0.026
572
SPL018 Splenomegaly 45 0.026
573
RTR011 Retroperitoneal Fibrosis 38 0.026
574
TTN003 Tetanus 60 0.025
575
P SML001 Small Cell Carcinoma 55 0.025
576
CHL004 Cholelithiasis 47 0.025
577
VGN023 Vaginitis 41 0.025
578
DSC005 Descending Colon Cancer 31 0.025
579
BLR004 Biliary Dyskinesia 30 0.025
580
P EPD025 Epidermolysis Bullosa with Pyloric Atresia 28 0.025
581
ANL005 Anal Spasm 18 0.025
582
OCC004 Occlusion of Gallbladder 15 0.025
583
STR003 Strawberry Gallbladder 8 0.025
584
IDP068 Idiopathic Malabsorption Due to Bile Acid Synthesis Defects 5 0.025
585
CRR007 Cirrhosis, Cryptogenic 43 0.025
586
CRD119 Cardiac Arrest 59 0.025
587
SHG001 Shigellosis 52 0.025
588
NSY001 N Syndrome 44 0.025
589
MND006 Mondor Disease 22 0.025
590
NLP001 Nail-Patella Syndrome 55 0.025
591
CLN044 Colon Adenoma 43 0.025
592
CLN004 Colon Carcinoma in Situ 34 0.025
593
GST038 Gastrointestinal Adenoma 30 0.025
594
ASC004 Ascending Colon Cancer 29 0.025
595
RCT023 Rectum Squamous Cell Carcinoma 22 0.025
596
RCT008 Rectosigmoid Junction Neoplasm 22 0.025
597
SPL003 Splenic Flexure Cancer 20 0.025
598
HPT005 Hepatic Flexure Cancer 17 0.025
599
PNC040 Pancreatic Delta Cell Neoplasm 15 0.025
600
LVR003 Liver Carcinoma in Situ 14 0.025
601
ILT001 Ileitis 46 0.025
602
PRP007 Priapism 45 0.025
603
AMB001 Amebiasis 43 0.025
604
P CSH001 Cushing's Syndrome 65 0.025
605
ESP027 Esophagus Squamous Cell Carcinoma 38 0.025
606
CCL003 Cecal Benign Neoplasm 24 0.025
607
NRN031 Neuroendocrine Tumor of the Appendix 16 0.025
608
ATM015 Autoimmune Disease of Gastrointestinal Tract 31 0.025
609
P NRV006 Nervous System Cancer 59 0.025
610
DPH001 Diphtheria 57 0.025
611
HST011 Histoplasmosis 51 0.025
612
BRN056 Bronchopulmonary Dysplasia 48 0.025
613
c PLN018 Peeling Skin Syndrome 2 43 0.025
614
CHL050 Cholesterol Ester Storage Disease 37 0.025
615
ANK008 Ankyloglossia 35 0.025
616
RCT010 Rectum Carcinoma in Situ 14 0.025
617
CNG363 Congenital Enterocyte Heparan Sulfate Deficiency 4 0.025
618
EPT026 Epithelio-Exfoliative Colitis-Deafness Syndrome 4 0.025
619
P GLM045 Glioma 59 0.025
620
ALC006 Alcoholic Hepatitis 58 0.025
621
PLS011 Plasmacytoma 56 0.025
622
TXC005 Toxic Shock Syndrome 55 0.025
623
P CYS018 Cystitis 52 0.025
624
NDL013 Nodular Regenerative Hyperplasia 47 0.025
625
PLM012 Pulmonary Sarcoidosis 53 0.025
626
P HMN010 Hemangioma 59 0.024
627
PRR002 Pure Red-Cell Aplasia 46 0.024
628
PRS036 Parasitic Protozoa Infectious Disease 42 0.024
629
P ABD016 Abdominal Obesity-Metabolic Syndrome 41 0.024
630
P FML011 Familial Adenomatous Polyposis 69 0.024
631
MRB003 Morbid Obesity 58 0.024
632
MTB004 Metabolic Acidosis 47 0.024
633
c CHL082 Cholestasis, Progressive Familial Intrahepatic 3 44 0.024
634
MYC017 Mycobacterium Kansasii 38 0.024
635
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 15 0.024
636
HGH026 High Anorectal Malformation 15 0.024
637
LWN002 Low Anorectal Malformation 10 0.024
638
INT254 Intermediate Anorectal Malformation 10 0.024
639
DSP001 Displacement of Cardia Through Esophageal Hiatus 7 0.024
640
CNG480 Congenital Diarrhea 7 with Exudative Enteropathy 6 0.024
641
P LYM007 Lymphangioleiomyomatosis 66 0.024
642
PRT011 Protein C Deficiency 49 0.024
643
CHC001 Chickenpox 43 0.024
644
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 25 0.024
645
P SHR001 Short Bowel Syndrome 47 0.024
646
c INV001 Invasive Aspergillosis 46 0.024
647
WRN001 Werner Syndrome 68 0.024
648
PLM010 Pulmonary Edema 52 0.024
649
VSC047 Vascular Malformation 43 0.024
650
GNR003 Generalized Atherosclerosis 37 0.024
651
c FML015 Familial Nephrotic Syndrome 36 0.024
652
c ADL017 Adult T-Cell Leukemia 58 0.024
653
DSS009 Disseminated Intravascular Coagulation 50 0.024
654
DNY001 Denys-Drash Syndrome 54 0.024
655
GRD001 Giardiasis 40 0.024
656
WLM007 Wilms Tumor Susceptibility-5 55 0.024
657
DVR002 Diverticulitis 42 0.024
658
c CLC048 Celiac Disease 3 24 0.024
659
RSC001 Rosacea 53 0.024
660
STR008 Strongyloidiasis 50 0.024
661
P HML001 Hemolytic-Uremic Syndrome 49 0.024
662
MYC013 Mycobacterium Abscessus 41 0.024
663
PRC003 Proctitis 40 0.024
664
c CNG031 Congenital Nervous System Abnormality 39 0.024
665
c PLN024 Peeling Skin Syndrome 4 32 0.024
666
P FCS002 Fucosidosis 59 0.023
667
CCC002 Coccidiosis 49 0.023
668
IGG001 Iga Glomerulonephritis 48 0.023
669
PTT037 Pituitary Tumors 43 0.023
670
P ATM020 Autoimmune Enteropathy 38 0.023
671
NRL016 Neural Tube Defects 76 0.023
672
ABT001 Abetalipoproteinemia 59 0.023
673
CCT002 Cicatricial Pemphigoid 47 0.023
674
ORL015 Oral Squamous Cell Carcinoma 55 0.023
675
LPD004 Lipoid Nephrosis 43 0.023
676
c INF095 Inflammatory Bowel Disease 25, Early Onset, Autosomal Recessive 37 0.023
677
MKL001 Mikulicz Disease 27 0.023
678
PPL022 Papilloma 54 0.023
679
TRC003 Trichomoniasis 40 0.023
680
HPT077 Hepatic Venoocclusive Disease with Immunodeficiency 29 0.023
681
P AGG001 Aggressive Periodontitis 49 0.023
682
P FRG001 Fragile X Syndrome 67 0.023
683
HPT019 Hepatic Encephalopathy 54 0.023
684
BLR001 Biliary Atresia 51 0.023
685
GNR004 Generalized Anxiety Disorder 49 0.023
686
EPD045 Epidermolysis Bullosa, Junctional, with Pyloric Stenosis 47 0.023
687
P HMR005 Hemorrhoid 46 0.023
688
c CLC037 Celiac Disease 4 21 0.023
689
PLY056 Polyposis, Juvenile Intestinal 53 0.023
690
CRS001 Crescentic Glomerulonephritis 41 0.023
691
PRS034 Parasitic Helminthiasis Infectious Disease 40 0.023
692
ESN017 Eosinophilic Granuloma 29 0.023
693
SCB001 Scabies 46 0.023
694
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 46 0.023
695
CHL056 Cheilitis 45 0.023
696
P DGR001 Digeorge Syndrome 54 0.023
697
VTM002 Vitamin B12 Deficiency 45 0.023
698
GRN009 Granulomatous Hepatitis 37 0.023
699
IMG001 Image Syndrome 58 0.022
700
ANG020 Angiosarcoma 52 0.022
701
c GLM029 Glomerulosclerosis, Focal Segmental, 1 48 0.022
702
P MWT001 Mowat-Wilson Syndrome 48 0.022
703
NPH010 Nephrosclerosis 42 0.022
704
FSC002 Fascioliasis 39 0.022
705
ACL001 Acalculous Cholecystitis 35 0.022
706
c CLC040 Celiac Disease 6 18 0.022
707
c DLT001 Delta Chain Disease 14 0.022
708
c HYP615 Hyperparathyroidism, Familial Primary 53 0.022
709
CHR003 Cherubism 51 0.022
710
c ADL096 Adult Hepatocellular Carcinoma 44 0.022
711
P CRV031 Cervical Adenocarcinoma 52 0.022
712
HNC001 Henoch-Schoenlein Purpura 44 0.022
713
KDN013 Kidney Hypertrophy 31 0.022
714
PRN039 Paraneoplastic Syndromes 31 0.022
715
c OPT025 Optic Atrophy 6 23 0.022
716
c AML050 Amelogenesis Imperfecta, Type if 19 0.022
717
BTN003 Biotinidase Deficiency 57 0.022
718
c FRC011 Fructose Intolerance, Hereditary 46 0.022
719
c CHL081 Cholestasis, Progressive Familial Intrahepatic 2 45 0.022
720
OST115 Osteonecrosis of the Jaw 38 0.022
721
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 34 0.022
722
GST090 Gastroduodenal Crohn's Disease 21 0.022
723
PRM236 Primary Biliary Cholangitis 49 0.022
724
FBR019 Fibromatosis 43 0.022
725
ANT024 Anthrax Disease 41 0.022
726
EPD015 Epidemic Typhus 40 0.022
727
c OPT024 Optic Atrophy 5 21 0.022
728
DBT010 Diabetic Neuropathy 54 0.022
729
CLR109 Colorectal Adenocarcinoma 49 0.022
730
IMP005 Impotence 49 0.022
731
IMM107 Immunodeficiency 31c, Autosomal Dominant 29 0.022
732
P BRN009 Burning Mouth Syndrome 52 0.022
733
c MCR113 Microvascular Complications of Diabetes 3 44 0.022
734
LYM020 Lymph Node Cancer 42 0.022
735
P ENC011 Encephalomyopathy 37 0.022
736
HYP189 Hypoadrenalism 36 0.022
737
LRY004 Laryngotracheitis 35 0.022
738
c MLT094 Multiple Sclerosis 3 26 0.022
739
CNG368 Congenital Adrenal Hyperplasia 63 0.022
740
INT079 Intrahepatic Cholangiocarcinoma 55 0.022
741
HPT022 Hepatoblastoma 54 0.022
742
PRT038 Protein-Energy Malnutrition 48 0.022
743
HTR003 Heterotaxy 44 0.022
744
TRC023 Trichinosis 41 0.022
745
c OST147 Osteoarthritis 1 35 0.022
746
JJN008 Jejunoileitis 34 0.022
747
ILC002 Ileocolitis 34 0.022
748
TXC001 Toxic Megacolon 28 0.022
749
P GNR027 Generalized Peeling Skin Syndrome 22 0.022
750
HRN022 Hearing Loss/deafness 16 0.022
751
HYP160 Hyperkeratosis Lenticularis Perstans 24 0.022
752
CMM005 Common Cold 57 0.022
753
PNG002 Pain Agnosia 39 0.022
754
IMP002 Imperforate Anus 52 0.021
755
PYC001 Pycnodysostosis 50 0.021
756
PYL006 Pyloric Stenosis 45 0.021
757
PRT026 Parotitis 42 0.021
758
HPT067 Hepatocellular Adenoma 41 0.021
759
ANG002 Angiostrongyliasis 39 0.021
760
ELS002 Elastosis Perforans Serpiginosa 30 0.021
761
c CHL118 Cholestasis, Benign Recurrent Intrahepatic, 2 29 0.021
762
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 29 0.021
763
c AML047 Amelogenesis Imperfecta, Type Ia 21 0.021
764
c ATM064 Autoimmune Pancreatitis Type 1 18 0.021
765
c CLC046 Celiac Disease 5 18 0.021
766
LYM022 Lymphangioma 51 0.021
767
P NRP042 Neuropathy, Hereditary Sensory and Autonomic, Type Ii 45 0.021
768
GST093 Gastrointestinal Defects and Immunodeficiency Syndrome 40 0.021
769
SPR007 Superior Mesenteric Artery Syndrome 40 0.021
770
c CLR082 Colorectal Cancer 7 23 0.021
771
c CLC041 Celiac Disease 7 16 0.021
772
c ATM063 Autoimmune Pancreatitis Type 2 15 0.021
773
P ATS007 Autism Spectrum Disorder 65 0.021
774
URN008 Urinary Bladder Cancer 63 0.021
775
P HYP027 Hypobetalipoproteinemia 54 0.021
776
FRS002 Frasier Syndrome 49 0.021
777
ISC015 Ischemic Colitis 38 0.021
778
PND004 Pandas 29 0.021
779
c CLR078 Colorectal Cancer 11 20 0.021
780
ORL005 Oral Candidiasis 46 0.021
781
CMP002 Campylobacteriosis 45 0.021
782
c CLL012 Cell Type Benign Neoplasm 40 0.021
783
P ESP035 Esophagitis, Eosinophilic, 1 39 0.021
784
HYL004 Hyaline Fibromatosis Syndrome 39 0.021
785
CNG035 Congenital Bilateral Absence of Vas Deferens 37 0.021
786
c ALG016 Alagille Syndrome 2 32 0.021
787
c AML048 Amelogenesis Imperfecta, Type Ih 20 0.021
788
P CLR108 Colorectal Adenoma 59 0.021
789
c PRM126 Primary Peritoneal Carcinoma 55 0.021
790
RYN003 Reynolds Syndrome 51 0.021
791
PRS055 Pierson Syndrome 50 0.021
792
DRM013 Dermoid Cyst 44 0.021
793
HYP081 Hypolipoproteinemia 42 0.021
794
c AML017 Amelogenesis Imperfecta, Type Ib 34 0.021
795
c AML016 Amelogenesis Imperfecta, Type 1e 31 0.021
796
c CWD005 Cowden Syndrome 4 23 0.021
797
c CLR084 Colorectal Cancer 9 20 0.021
798
HRS037 Hirschsprung Disease with Type D Brachydactyly 16 0.021
799
P MSC007 Muscle Hypertrophy 56 0.021
800
P GNG025 Gingival Fibromatosis 51 0.021
801
HYP291 Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia 46 0.021
802
P WHT013 White Sponge Nevus 1 40 0.021
803
ADR010 Adrenal Cortical Hypofunction 37 0.021
804
NCR003 Necrotizing Sialometaplasia 33 0.021
805
c CLR077 Colorectal Cancer 10 33 0.021
806
c AML057 Amelogenesis Imperfecta, Type Iiia 29 0.021
807
c AML018 Amelogenesis Imperfecta, Type Ic 21 0.021
808
INF047 Infantile Free Sialic Acid Storage Disease 12 0.021
809
BLM002 Bulimia Nervosa 51 0.021
810
NRM004 Neuroma 46 0.021
811
URT031 Ureteral Disease 43 0.021
812
ACT058 Active Peptic Ulcer Disease 40 0.021
813
HPT004 Hepatic Coma 39 0.021
814
PRV003 Perivascular Epithelioid Cell Tumor 39 0.021
815
MCR020 Microsporidiosis 38 0.021
816
CCL002 Cecal Disease 30 0.021
817
c PRM158 Primary Intestinal Lymphangiectasia 28 0.021
818
CLN022 Colonic Atresia 25 0.021
819
c CLC039 Celiac Disease 13 19 0.021
820
c GLL025 Gallbladder Disease 2 18 0.021
821
PNC033 Pancreas Adenocarcinoma 56 0.021
822
PRS115 Prosthetic Joint Infection 41 0.021
823
c GST048 Gastrointestinal System Benign Neoplasm 37 0.021
824
MRS001 Marasmus 36 0.021
825
RTC003 Root Caries 36 0.021
826
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 32 0.021
827
c GLL026 Gallbladder Disease 3 18 0.021
828
UND004 Undetermined Colitis 9 0.021
829
c ACT068 Acute Cystitis 45 0.021
830
RCH001 Richter's Syndrome 45 0.021
831
MYC005 Myocardial Stunning 44 0.021
832
GST030 Gastrinoma 41 0.021
833
c HRD012 Hereditary Elliptocytosis 41 0.021
834
MLL001 Molluscum Contagiosum 31 0.021
835
EXT011 Extrapyramidal and Movement Disease 14 0.021
836
P MTH008 Methylmalonic Acidemia 56 0.020
837
MYL013 Myeloperoxidase Deficiency 46 0.020
838
SNG010 Single Median Maxillary Central Incisor 45 0.020
839
DDN009 Duodenal Obstruction 31 0.020
840
c LVR028 Liver Failure, Transient Infantile 28 0.020
841
VGS001 Vagus Nerve Disease 18 0.020
842
HRS003 Hirschsprung Disease Ganglioneuroblastoma 17 0.020
843
P SLV001 Silver-Russell Syndrome 56 0.020
844
c ATM002 Autoimmune Polyendocrine Syndrome Type 1 48 0.020
845
EXT010 Extramedullary Plasmacytoma 48 0.020
846
CVR006 Cavernous Hemangioma 45 0.020
847
INT253 Intestinal Benign Neoplasm 43 0.020
848
P PRG017 Paraganglioma and Gastric Stromal Sarcoma 42 0.020
849
ULC007 Ulcerative Stomatitis 42 0.020
850
LCH001 Leech Infestation 39 0.020
851
GBL002 Goblet Cell Carcinoid 34 0.020
852
PNC019 Pancreatoblastoma 30 0.020
853
PRM205 Primary Hepatic Neuroendocrine Carcinoma 26 0.020
854
ULC008 Ulcerative Proctitis 22 0.020
855
THR009 Thrombocytopenia-Absent Radius Syndrome 58 0.020
856
EMB004 Embryonal Carcinoma 55 0.020
857
LVR002 Liver Angiosarcoma 39 0.020
858
c DNT027 Dentin Dysplasia, Type Ii 35 0.020
859
GST016 Gastric Signet Ring Cell Adenocarcinoma 33 0.020
860
BLD019 Bile Duct Cystadenocarcinoma 33 0.020
861
INT050 Intestinal Impaction 30 0.020
862
c INF145 Infantile Liver Failure Syndrome 1 24 0.020
863
c SCN059 Secondary Sclerosing Cholangitis 19 0.020
864
c MWT002 Mowat-Wilson Syndrome Due to Monosomy 2q22 8 0.020
865
c MLG068 Malignant Glioma 59 0.020
866
TRC040 Tracheoesophageal Fistula 46 0.020
867
P ACT150 Acute Adrenal Insufficiency 46 0.020
868
SGN002 Signet Ring Cell Adenocarcinoma 43 0.020
869
FBR054 Fibroma 41 0.020
870
TRN012 Transient Global Amnesia 39 0.020
871
BLD032 Bile Duct Adenocarcinoma 38 0.020
872
TTH008 Tooth Resorption 38 0.020
873
DVR006 Diversion Colitis 30 0.020
874
STY001 Satoyoshi Syndrome 28 0.020
875
ANL014 Anal Canal Adenocarcinoma 28 0.020
876
LYM035 Lymphangiectasis 27 0.020
877
GRN011 Granulomatous Gastritis 26 0.020
878
c FML268 Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Minimal Changes 22 0.020
879
P SLV002 Salivary Gland Cancer 60 0.020
880
MYR002 Mayer-Rokitansky-Kuster-Hauser Syndrome 57 0.020
881
STT041 Stuttering 49 0.020
882
KLT001 Klatskin's Tumor 43 0.020
883
CWM001 Cow Milk Allergy 39 0.020
884
TTH007 Tooth Erosion 33 0.020
885
c PNC106 Pancreatic Agenesis 1 33 0.020
886
LNT001 Linitis Plastica 32 0.020
887
BRW006 Brown Syndrome 31 0.020
888
CRR015 Curry-Jones Syndrome, Somatic Mosaic 28 0.020
889
RSP004 Respiratory System Benign Neoplasm 27 0.020
890
GLB003 Globe Disease 26 0.020
891
P LYM124 Lymphangiectasia, Intestinal 26 0.020
892
c FML339 Familial Adenomatous Polyposis 4 23 0.020
893
HPT066 Hepatoportal Sclerosis 19 0.020
894
IGG016 Igg4-Related Dacryoadenitis and Sialadenitis 15 0.020
895
HRS039 Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 15 0.020
896
c MWT004 Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation 7 0.020
897
P LRY044 Larynx Cancer 57 0.020
898
FBR086 Fibrolamellar Carcinoma 45 0.020
899
AZS001 Azoospermia 45 0.020
900
TRP008 Tropical Calcific Pancreatitis 44 0.020
901
c CNG413 Congenital Short Bowel Syndrome 37 0.020
902
SMT002 Smooth Muscle Tumor 37 0.020
903
SPP004 Suppurative Cholangitis 31 0.020
904
JJN007 Jejunal Adenocarcinoma 28 0.020
905
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 27 0.020
906
P PLM064 Pulmonary Sequestration 26 0.020
907
LCT013 Lactase Deficiency, Congenital 24 0.020
908
SLT007 Solitary Rectal Ulcer Syndrome 19 0.020
909
c FML321 Familial Stomach Cancer 17 0.020
910
CRL006 Caroli Disease, Isolated 15 0.020
911
STR032 Steroid Dehydrogenase Deficiency Dental Anomalies 12 0.020
912
c ATM071 Autoimmune Enteropathy Type 2 8 0.020
913
NPH091 Nephrolithiasis, Calcium Oxalate 44 0.019
914
CYC008 Cyclic Vomiting Syndrome 39 0.019
915
DFF021 Diffuse Mesangial Sclerosis 37 0.019
916
ALC005 Alcoholic Pancreatitis 36 0.019
917
SGM002 Sigmoid Neoplasm 34 0.019
918
VGN019 Vaginal Discharge 32 0.019
919
GNT001 Giant Cell Reparative Granuloma 31 0.019
920
XNT002 Xanthogranulomatous Cholecystitis 30 0.019
921
DNT046 Dental Abscess 27 0.019
922
PYL002 Pylorospasm 22 0.019
923
CHL075 Cheilitis Glandularis 22 0.019
924
c DNT044 Dentinogenesis Imperfecta, Shields Type Iii 21 0.019
925
OST007 Ostertagiasis 18 0.019
926
MPV001 Mpv17-Related Hepatocerebral Mitochondrial Dna Depletion Syndrome 15 0.019
927
c SLV006 Salivary Gland Cancer, Adult 15 0.019
928
CLL026 Collagenous Gastritis 12 0.019
929
IGG012 Igg4-Related Submandibular Gland Disease 8 0.019
930
TNG009 Tongue Squamous Cell Carcinoma 54 0.019
931
FML026 Familial Lipoprotein Lipase Deficiency 48 0.019
932
DCB001 Decubitus Ulcer 42 0.019
933
PRP017 Periapical Periodontitis 37 0.019
934
BLR027 Blue Rubber Bleb Nevus 37 0.019
935
CHR557 Chronic Intestinal Pseudoobstruction 30 0.019
936
TRD003 Taurodontism 29 0.019
937
IGG014 Igg4-Related Sclerosing Cholangitis 26 0.019
938
ACK001 Ackerman Syndrome 24 0.019
939
PCD001 Pica Disease 23 0.019
940
PYT001 Pythiosis 15 0.019
941
c DNT047 Dentinogenesis Imperfecta Type 2 14 0.019
942
HRS038 Hirschsprung Disease with Hypoplastic Nails and Dysmorphic Facial Features 14 0.019
943
c INT019 Intestine Carcinoma in Situ 14 0.019
944
c ATM070 Autoimmune Enteropathy Type 3 8 0.019
945
PRV006 Pervasive Developmental Disorder 50 0.019
946
INT060 Intestinal Atresia 41 0.019
947
SKN022 Skin Squamous Cell Carcinoma 40 0.019
948
ESP018 Esophageal Candidiasis 39 0.019
949
DFF019 Diffuse Gastric Cancer 39 0.019
950
DNT008 Denture Stomatitis 38 0.019
951
CND006 Candida Glabrata 34 0.019
952
ANL011 Anal Canal Carcinoma 33 0.019
953
ALV001 Alveolar Periostitis 32 0.019
954
OVR044 Ovarian Carcinosarcoma 31 0.019
955
LRG016 Large Intestine Adenocarcinoma 28 0.019
956
P HYP658 Hypoplastic Amelogenesis Imperfecta 26 0.019
957
ACT062 Acute Pericementitis 23 0.019
958
MCP039 Mucoepithelial Dysplasia, Hereditary 22 0.019
959
FML307 Familial Calcium Pyrophosphate Deposition 20 0.019
960
ACH039 Achalasia-Microcephaly Syndrome 19 0.019
961
GLS013 Glossodynia 19 0.019
962
HYP481 Hyperbiliverdinemia 19 0.019
963
BLD065 Blue Diaper Syndrome 17 0.019
964
NKC001 Nk-Cell Enteropathy 15 0.019
965
CVR008 Cavernous Lymphangioma 15 0.019
966
BNG007 Benign Lymphoepithelial Lesion of Salivary Gland 10 0.019
967
ATS001 Autistic Disorder 63 0.019
968
MYM001 Myoma 51 0.019
969
SQM002 Squamous Cell Papilloma 40 0.019
970
PNC008 Pancreatic Endocrine Carcinoma 36 0.019
971
ANL004 Anal Canal Squamous Cell Carcinoma 33 0.019
972
DNT003 Dental Pulp Calcification 32 0.019
973
ANG061 Angular Cheilitis 29 0.019
974
ACH015 Achalasia, Familial Esophageal 29 0.019
975
CNG002 Congenital Bile Acid Synthesis Defect 25 0.019
976
ESN022 Eosinophilic Colitis 23 0.019
977
ADN072 Adenoma of Pancreas 22 0.019
978
DST016 Distomatosis 21 0.019
979
PRG122 Prognathism, Mandibular 20 0.019
980
FLM003 Fulminant Viral Hepatitis 19 0.019
981
AML046 Amelogenesis Imperfecta, Type Iia5 18 0.019
982
DNT050 Dentin Dysplasia with Sclerotic Bones 12 0.019
983
UVL006 Uvulitis 10 0.019
984
PRT022 Protozoal Dysentery 10 0.019
985
MTN003 Motion Sickness 47 0.019
986
CRB090 Cerebral Hypoxia 44 0.019
987
CHL128 Childhood Hepatocellular Carcinoma 41 0.019
988
DDN011 Duodenal Atresia 37 0.019
989
LKS001 Leukostasis 35 0.019
990
c ATR022 Atrial Septal Defect 3 35 0.019
991
SQM018 Squamous Cell Carcinoma of the Oral Tongue 34 0.019
992
RNL013 Renal Adenoma 32 0.019
993
CRV068 Cervical Polyp 32 0.019
994
FRT005 Fruit Allergy 31 0.019
995
ASC003 Ascending Cholangitis 30 0.019
996
RCT020 Rectum Adenocarcinoma 30 0.019
997
FSH003 Fish Allergy 29 0.019
998
CNG116 Congenital Nephrotic Syndrome Finnish Type 27 0.019
999
MCN018 Mucinous Adenocarcinoma of the Appendix 24 0.019
1000
NRT006 North American Indian Childhood Cirrhosis 23 0.019
1001
ORL006 Oral Mucosa Leukoplakia 20 0.019
1002
AML005 Amelogenesis Imperfecta Hypomaturation Type 18 0.019
1003
NRN029 Neuronal Intestinal Dysplasia 18 0.019
1004
AND017 Anodontia of Permanent Dentition 16 0.019
1005
c FML267 Familial Idiopathic Steroid-Resistant Nephrotic Syndrome with Diffuse Mesangial Sclerosis 15 0.019
1006
LTT006 Littoral Cell Angioma of the Spleen 15 0.019
1007
THR030 Thoraco Abdominal Enteric Duplication 14 0.019
1008
P SPR075 Sporadic Idiopathic Steroid-Resistant Nephrotic Syndrome with Diffuse Mesangial Sclerosis 12 0.019
1009
INC023 Incisors, Fused Mandibular 11 0.019
1010
HPT028 Hepatic Cystic Hamartoma 10 0.019
1011
SCR026 Secernentea Infections 10 0.019
1012
DRR012 Diarrhea, Chronic, with Villous Atrophy 9 0.019
1013
PNC042 Pancreatic Intraductal Papillary-Colloid Carcinoma 9 0.019
1014
ACQ006 Acquired Gastric Outlet Stenosis 8 0.019
1015
SKL003 Skeletal Muscle Cancer 41 0.018
1016
c HYP058 Hypervitaminosis a 37 0.018
1017
DNT010 Dentin Caries 25 0.018
1018
CHM005 Chemical Colitis 25 0.018
1019
MVD008 Moved to 155310 25 0.018
1020
RGN005 Regional Odontodysplasia 22 0.018
1021
HYP644 Hypocalcified Amelogenesis Imperfecta 22 0.018
1022
AML024 Amelogenesis Imperfecta, Type Iia1 21 0.018
1023
AML023 Amelogenesis Imperfecta, Type Iia2 20 0.018
1024
GST025 Gastric Body Carcinoma 19 0.018
1025
XLN218 X-Linked Amelogenesis Imperfecta Hypoplastic/hypomaturation 2 19 0.018
1026
AML043 Amelogenesis Imperfecta, Type Iia3 18 0.018
1027
AML049 Amelogenesis Imperfecta, Type Iia4 18 0.018
1028
ATM077 Autoimmune Gastrointestinal Dysmotility 14 0.018
1029
PRT107 Proton-Pump Inhibitor-Responsive Esophageal Eosinophilia 11 0.018
1030
SGM006 Segmental Odontomaxillary Dysplasia 10 0.018
1031
NNH007 Non-Hypoproteinemic Hypertrophic Gastropathy 4 0.018
1032
MYP066 Myopathic Intestinal Pseudoobstruction 4 0.018
1033
UNC010 Unclassified Intestinal Pseudoobstruction 4 0.018
1034
P DYS005 Dyslexia 36 0.018
1035
SKN020 Skin Papilloma 31 0.018
1036
SPL005 Splenic Artery Aneurysm 29 0.018
1037
MCN009 Mucinous Stomach Adenocarcinoma 29 0.018
1038
VLV047 Volvulus of Midgut 21 0.018
1039
ACT016 Actinobacillosis 18 0.018
1040
DNT004 Dientamoebiasis 15 0.018
1041
BLC002 Black Piedra 15 0.018
1042
ESP040 Esophageal Duplication Cyst 15 0.018
1043
CMM001 Common Bile Duct Neoplasm 15 0.018
1044
FNC012 Functioning Pancreatic Endocrine Tumor 15 0.018
1045
MVD002 Moved to 204690 12 0.018
1046
GLL034 Gallbladder Neuroendocrine Tumor 12 0.018
1047
IGG008 Igg4-Related Mesenteritis 12 0.018
1048
CRV034 Cervical Benign Neoplasm 12 0.018
1049
CLS051 Classic Neuroendocrine Tumor of Appendix 11 0.018
1050
GST022 Gastric Pylorus Carcinoma 10 0.018
1051
CHR009 Chronic Duodenal Ileus 10 0.018
1052
HMR013 Hemorrhagic Proctocolitis 9 0.018
1053
HGH022 High-Grade Dysplasia in Patients with Barrett Esophagus 9 0.018
1054
OMP003 Omphalomesenteric Cyst 7 0.018
1055
ODN001 Odontoclasia 7 0.018
1056
MCK001 Meckel's Diverticulum Cancer 7 0.018
1057
BTH003 Bothriocephalosis 6 0.018
1058
NNC014 Non-Central Nervous System-Localized Embryonal Carcinoma 6 0.018
1059
c EXT020 External Pathological Resorption 5 0.018
1060
PLM013 Pulmonary Immaturity 37 0.018
1061
VLL001 Villous Adenocarcinoma 34 0.018
1062
SPR012 Separation Anxiety Disorder 34 0.018
1063
PRS011 Persian Gulf Syndrome 23 0.018
1064
KLB004 Klebsiella Infection 22 0.018
1065
MYL044 Myelocystocele 22 0.018
1066
LRG015 Large Intestine Adenoma 14 0.018
1067
LRY006 Larynx Squamous Papilloma 14 0.018
1068
RCT033 Rectal Duplication 12 0.018
1069
GST055 Gastric Duplication Cysts 12 0.018
1070
SLT015 Solitary Necrotic Nodule of the Liver 12 0.018
1071
GLS016 Glossopalatine Ankylosis 9 0.018
1072
CNG255 Congenital Temporomandibular Joint Ankylosis 6 0.018
1073
BLR023 Biliary Atresia with Splenic Malformation Syndrome 6 0.018
1074
RHB006 Rhabditida Infections 6 0.018
1075
LWR011 Lower Lip Fistula 5 0.018
1076
CMM016 Commissural Lip Fistula 4 0.018
1077
CRC008 Carcinoma of the Vocal Tract 4 0.018
1078
ISL102 Isolated Tracheo-Esophageal Fistula 4 0.018
1079
EXR007 Exercise-Induced Anaphylaxis 24 0.018
1080
CMM018 Common Mesentery 14 0.018
1081
HYP727 Hypoglossia with Situs Inversus 14 0.018
1082
PRT024 Partial Optic Atrophy 14 0.018
1083
SQM001 Squamous Cell Papilloma of Skin 12 0.018
1084
CNG235 Congenital Microgastria 12 0.018
1085
CNG334 Congenital Esophageal Diverticulum 6 0.018
1086
ISL105 Isolated Agenesis of Gallbladder 4 0.018
1087
TBL020 Tubular Duplication of the Esophagus 3 0.018
1088
EPG004 Epignathus 16 0.017
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