Search results for digestive diseases

984 hits were found for digestive diseases

# Family MCID Name MIFTS Score
1
GST050 Gastrointestinal System Disease 66 3.685
2
CHG001 Chagas Disease 72 2.554
3
P LVR013 Liver Disease 76 0.149
4
P INT068 Intestinal Disease 65 0.145
5
P PNC044 Pancreatitis 64 0.130
6
P KDN018 Kidney Disease 69 0.129
7
CRH001 Crohn's Disease 80 0.129
8
P HRT032 Heart Disease 80 0.120
9
P INF037 Inflammatory Bowel Disease 52 0.117
10
LNG099 Lung Disease 67 0.110
11
P CLC063 Celiac Disease 1 65 0.102
12
c BLD140 Blood Group, I System 37 0.102
13
P HPT021 Hepatitis 75 0.099
14
P CRN018 Coronary Artery Anomaly 69 0.098
15
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.096
16
P ADN016 Adenocarcinoma 71 0.095
17
PNC034 Pancreas Disease 59 0.089
18
VSC007 Vascular Disease 71 0.089
19
CLN019 Colonic Disease 55 0.088
20
GST045 Gastroenteritis 65 0.088
21
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.085
22
P CLR023 Colorectal Cancer 98 0.084
23
GST053 Gastric Cancer 84 0.084
24
NRN002 Neuronitis 43 0.083
25
P DRR001 Diarrhea 60 0.083
26
AGN016 Aging 65 0.082
27
c CHR089 Chronic Kidney Failure 72 0.082
28
P GST049 Gastrointestinal System Cancer 60 0.082
29
P ESP024 Esophagitis 64 0.081
30
CLT003 Colitis 63 0.081
31
ESP023 Esophageal Disease 58 0.080
32
P PNM007 Pneumonia 70 0.079
33
P ART022 Arthritis 77 0.078
34
ATM095 Autoimmune Disease 66 0.078
35
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.077
36
CYS001 Cystic Fibrosis 85 0.076
37
GST092 Gastroesophageal Reflux 64 0.075
38
RSP006 Respiratory System Disease 63 0.075
39
P PNC035 Pancreatic Cancer 89 0.074
40
P PRK057 Parkinson Disease, Late-Onset 78 0.073
41
FTT001 Fatty Liver Disease 62 0.073
42
ESP021 Esophageal Cancer 79 0.072
43
ULC004 Ulcerative Colitis 80 0.072
44
P DBT009 Diabetes Mellitus 72 0.072
45
P ENC018 Encephalopathy 58 0.072
46
DYS073 Dysphagia 47 0.072
47
P INF038 Influenza 77 0.071
48
AST005 Asthma 83 0.071
49
IRR002 Irritable Bowel Syndrome 63 0.071
50
CNS004 Constipation 57 0.070
51
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.070
52
P LKM002 Leukemia 75 0.070
53
END072 Endotheliitis 46 0.068
54
P GLL020 Gallbladder Disease 64 0.068
55
STM006 Stomach Disease 52 0.068
56
SQM006 Squamous Cell Carcinoma 74 0.067
57
P HPT023 Hepatocellular Carcinoma 94 0.067
58
MCS002 Mucositis 61 0.067
59
BLR006 Biliary Tract Disease 55 0.066
60
P LCT002 Lactose Intolerance 48 0.066
61
ISC004 Ischemia 66 0.066
62
RHM027 Rheumatic Disease 62 0.066
63
CNN005 Connective Tissue Disease 65 0.065
64
PPT005 Peptic Ulcer Disease 60 0.065
65
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.065
66
EXC002 Exocrine Pancreatic Insufficiency 45 0.064
67
P LYM118 Lymphoma 71 0.064
68
RCT017 Rectal Disease 38 0.064
69
P HYP086 Hypothyroidism 62 0.064
70
MTH009 Mouth Disease 64 0.063
71
GST023 Gastric Ulcer 57 0.063
72
DDN006 Duodenitis 46 0.063
73
BSL008 Basal Ganglia Disease 44 0.062
74
MVM001 Movement Disease 40 0.062
75
WLS001 Wilson Disease 72 0.061
76
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.060
77
P PRD008 Periodontitis 67 0.060
78
c GLL024 Gallbladder Disease 1 39 0.060
79
KWS002 Kawasaki Disease 72 0.059
80
ANR040 Aneurysm 61 0.059
81
ILT001 Ileitis 52 0.059
82
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.059
83
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.059
84
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.059
85
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.059
86
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.059
87
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.059
88
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.059
89
P ART021 Arteriosclerosis 62 0.059
90
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.059
91
LVR012 Liver Cirrhosis 73 0.059
92
PRD007 Periodontal Disease 64 0.058
93
P NRV007 Nervous System Disease 75 0.058
94
FBR012 Fabry Disease 72 0.058
95
ANX010 Anxiety 72 0.057
96
CHL067 Cholecystitis 58 0.057
97
P RHM011 Rheumatoid Arthritis 91 0.057
98
P GLY013 Glycogen Storage Disease 61 0.057
99
GST013 Gastrojejunal Ulcer 27 0.057
100
TTH006 Tooth Disease 54 0.056
101
DYS014 Dyspepsia 54 0.056
102
GST019 Gastrointestinal Stromal Tumor 74 0.056
103
CHL065 Cholangiocarcinoma 70 0.056
104
NRN004 Neuroendocrine Tumor 58 0.056
105
CRB009 Cerebritis 41 0.055
106
P BRS047 Breast Cancer 100 0.055
107
BRR014 Barrett Esophagus 64 0.055
108
RTN023 Retinitis 52 0.054
109
VRL011 Viral Infectious Disease 64 0.054
110
P NRP001 Neuropathy 63 0.053
111
CLN009 Colon Squamous Cell Carcinoma 20 0.053
112
c HPT001 Hepatitis C 73 0.053
113
c FML311 Familial Colorectal Cancer Type X 32 0.053
114
SWL001 Swallowing Disorders 36 0.052
115
PRT036 Peritonitis 67 0.052
116
GNG013 Gingivitis 64 0.052
117
ING001 Inguinal Hernia 59 0.052
118
THR024 Thrombosis 61 0.051
119
CRB025 Carbohydrate Metabolic Disorder 38 0.051
120
P AMY004 Amyloidosis 69 0.051
121
LPD008 Lipid Metabolism Disorder 59 0.051
122
c INF071 Inflammatory Bowel Disease 1 54 0.051
123
P PRT013 Portal Hypertension 59 0.051
124
P LPS004 Lupus Erythematosus 69 0.051
125
P CLL015 Collagen Disease 53 0.051
126
CRC038 Carcinoma of Stomach, Salivary Gland Type 8 0.050
127
HYP066 Hyperglycemia 64 0.050
128
UND009 Undifferentiated Carcinoma of Stomach 16 0.050
129
P HRS035 Hirschsprung Disease 1 64 0.050
130
SCR037 Sucrase-Isomaltase Deficiency, Congenital 33 0.050
131
IMM136 Immune System Disease 57 0.050
132
APP008 Appendicitis 64 0.050
133
P MYC007 Myocardial Infarction 81 0.049
134
GLC008 Glucose Metabolism Disease 38 0.049
135
ABD010 Abdominal Wall Defect 37 0.049
136
BRC012 Brucellosis 71 0.049
137
c SYS001 Systemic Lupus Erythematosus 86 0.049
138
c CHL119 Cholangitis, Primary Sclerosing 60 0.049
139
CRY003 Cryptosporidiosis 51 0.049
140
P INF032 Infertility 59 0.048
141
GST028 Gastric Squamous Cell Carcinoma 37 0.048
142
c RCR022 Recurrent Acute Pancreatitis 43 0.048
143
MLN008 Melanoma 72 0.048
144
P HST010 Histiocytosis 60 0.048
145
P LNG032 Lung Cancer 99 0.048
146
c HPT003 Hepatitis a 63 0.048
147
SLV003 Salivary Gland Disease 47 0.047
148
BRS051 Breast Disease 67 0.047
149
MNT002 Mental Depression 60 0.047
150
PLV003 Pelvic Inflammatory Disease 56 0.047
151
DGS008 Digestive System Melanoma 12 0.047
152
RSD004 Rosai-Dorfman Disease 48 0.047
153
P RNG031 Ring Chromosome Y Syndrome 29 0.047
154
CRC037 Carcinoma of Esophagus, Salivary Gland Type 8 0.047
155
c ACT027 Acute Pancreatitis 61 0.047
156
DRR016 Diarrhea 2, with Microvillus Atrophy 48 0.047
157
UND008 Undifferentiated Carcinoma of Esophagus 12 0.047
158
P ART023 Arthropathy 68 0.046
159
DGS007 Digestive Duplication 4 0.046
160
ALP046 Alport Syndrome, X-Linked 74 0.046
161
ANS012 Anus Disease 37 0.046
162
P MLT020 Multiple Sclerosis 85 0.046
163
NNL002 Nonalcoholic Steatohepatitis 56 0.046
164
ENT004 Enthesopathy 38 0.045
165
BLN006 Blind Loop Syndrome 30 0.045
166
JNT002 Joint Disorders 60 0.045
167
GST037 Gastroparesis 56 0.045
168
ACT058 Active Peptic Ulcer Disease 43 0.045
169
P ANR048 Aniridia 1 68 0.045
170
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.044
171
SPS003 Spastic Diplegia 55 0.044
172
ENT006 Enterokinase Deficiency 24 0.044
173
LYS002 Lysosomal Storage Disease 56 0.044
174
c HPT016 Hepatitis B 68 0.044
175
FCL044 Fecal Incontinence 38 0.044
176
ANR038 Anorexia Nervosa 1 21 0.043
177
BLD137 Blood Group--Ahonen 17 0.043
178
FDL002 Food Allergy 55 0.043
179
P GST044 Gastritis 61 0.043
180
P STR035 Streptococcal Group a Invasive Disease 28 0.043
181
c ACT004 Acute Diarrhea 41 0.043
182
FNC005 Functional Colonic Disease 24 0.043
183
ANG011 Angiodysplasia 48 0.043
184
THY030 Thyroid Gland Disease 51 0.043
185
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 54 0.043
186
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 35 0.042
187
SRC014 Sarcoma 68 0.042
188
c INT072 Intestinal Pseudo-Obstruction 57 0.042
189
MLR004 Malaria 86 0.042
190
P ATR005 Atrophic Gastritis 51 0.042
191
PNC118 Pancreas, Annular 37 0.041
192
VSC011 Vasculitis 66 0.041
193
SML014 Small Intestine Leiomyosarcoma 38 0.041
194
EXP004 Exophthalmos 50 0.041
195
GST039 Gastroduodenitis 33 0.041
196
P MSC003 Muscular Atrophy 55 0.041
197
BLC007 Bile Acid Synthesis Defect, Congenital, 1 34 0.041
198
CHY002 Chylomicron Retention Disease 54 0.041
199
c DPH024 Diaphragmatic Hernia, Congenital 63 0.041
200
STT004 Steatorrhea 41 0.041
201
JJN004 Jejunal Atresia 33 0.041
202
CNG034 Congestive Heart Failure 74 0.041
203
PNC014 Pancreatic Serous Cystadenocarcinoma 19 0.040
204
BLC008 Bile Acid Synthesis Defect, Congenital, 2 30 0.040
205
ALR002 Al-Raqad Syndrome 30 0.040
206
GLL018 Gallbladder Cancer 67 0.040
207
HYP266 Hypoxia 61 0.040
208
SCR011 Scrapie 40 0.040
209
OST141 Osteoclastic Giant Cell Tumor of Pancreas 13 0.040
210
P TRM003 Tremor 54 0.040
211
PRC002 Paracoccidioidomycosis 59 0.040
212
VSC044 Visceral Myopathy 52 0.040
213
MTC016 Mitochondrial Neurogastrointestinal Encephalopathy Disease 28 0.040
214
ACN026 Acinar Cell Carcinoma of Pancreas 25 0.040
215
MCN022 Mucinous Cystadenocarcinoma of the Pancreas 22 0.040
216
SQM020 Squamous Cell Carcinoma of the Pancreas 14 0.040
217
SLD012 Solid Pseudopapillary Carcinoma of the Pancreas 13 0.040
218
SQM019 Squamous Cell Carcinoma of the Small Intestine 7 0.040
219
LYM024 Lymphatic System Disease 45 0.040
220
SQM016 Squamous Cell Carcinoma of Gallbladder and Extrahepatic Biliary Tract 7 0.040
221
DRM006 Dermatitis 67 0.040
222
KPS004 Kaposi Sarcoma 73 0.040
223
ACQ007 Acquired Immunodeficiency Syndrome 65 0.040
224
PRN019 Perinatal Necrotizing Enterocolitis 56 0.039
225
P MYP004 Myopathy 69 0.039
226
P DRM007 Dermatitis Herpetiformis 56 0.039
227
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.039
228
c PNC108 Pancreatitis, Hereditary 60 0.039
229
HNS001 Hansen's Disease 31 0.039
230
ENT011 Enterocolitis 52 0.039
231
UMB002 Umbilical Hernia 43 0.039
232
P PLY023 Polycystic Liver Disease 53 0.039
233
c ATM011 Autoimmune Hepatitis 63 0.038
234
ERY003 Erythema Multiforme 60 0.038
235
P GLM007 Glomerulonephritis 61 0.038
236
DMY004 Demyelinating Disease 58 0.038
237
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 36 0.038
238
GLC022 Glucose/galactose Malabsorption 40 0.038
239
BRN106 Burns 57 0.038
240
P CWD001 Cowden Disease 67 0.038
241
HPT046 Hepatic Veno-Occlusive Disease 56 0.038
242
DRR013 Diarrhea 8, Secretory Sodium, Congenital 28 0.038
243
P PSD087 Pseudoxanthoma Elasticum 67 0.038
244
HLC007 Helicobacter Pylori Infection 64 0.037
245
LNG108 Langerhans Cell Histiocytosis 63 0.037
246
P PRM006 Primary Biliary Cirrhosis 55 0.037
247
DRR005 Diarrhea 4, Malabsorptive, Congenital 37 0.037
248
CHR515 Chronic Atrial and Intestinal Dysrhythmia 26 0.037
249
P LYM026 Lymphoblastic Leukemia 66 0.037
250
TNG002 Tangier Disease 65 0.037
251
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.037
252
EWN002 Ewing's Family of Tumors 49 0.037
253
ANL022 Anal Fistula 45 0.037
254
ANG054 Angina Pectoris 53 0.037
255
LYS003 Lysinuric Protein Intolerance 53 0.037
256
BHC003 Behcet Syndrome 68 0.037
257
c THR092 Thrombophilia Due to Thrombin Defect 61 0.037
258
P THL005 Thalassemia 65 0.037
259
c CHL134 Cholestasis, Benign Recurrent Intrahepatic, 1 45 0.037
260
CHR028 Chronic Wasting Disease 32 0.037
261
c HPT073 Hepatitis C Virus 73 0.036
262
APH002 Aphasia 58 0.036
263
ZLL002 Zollinger-Ellison Syndrome 57 0.036
264
TBR008 Tuberculous Peritonitis 46 0.036
265
P ALG028 Alagille Syndrome 1 68 0.036
266
CNG298 Congenital Pancreatic Cyst 20 0.036
267
DGS006 Digestive Duplication Cyst of the Tongue 7 0.036
268
OVR063 Overnutrition 53 0.036
269
c LCT011 Lactose Intolerance, Adult Type 24 0.036
270
ADN082 Adenocarcinoma of the Gallbladder and Extrahepatic Biliary Tract 7 0.036
271
AMY087 Amyloidosis, Hereditary, Transthyretin-Related 57 0.036
272
P CHL066 Cholangitis 52 0.035
273
P TRC086 Trichohepatoenteric Syndrome 1 54 0.035
274
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 52 0.035
275
ALP072 Alpha-Fetoprotein Deficiency 32 0.035
276
CYS039 Cystic Kidney Disease 49 0.035
277
ISL029 Isolated Anorectal Malformation 6 0.035
278
SLP005 Sleep Disorder 59 0.035
279
STM007 Stomatitis 52 0.035
280
P HYP818 Hypobetalipoproteinemia, Familial, 1 54 0.035
281
ADN018 Adenoma 63 0.035
282
c ATM024 Autoimmune Pancreatitis 49 0.035
283
P DBT005 Diabetes Insipidus 54 0.035
284
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.035
285
P INT001 Intrahepatic Cholestasis 62 0.035
286
c GLY060 Glycogen Storage Disease Ia 57 0.035
287
P ESP035 Esophagitis, Eosinophilic, 1 55 0.035
288
P AGN002 Agnosia 61 0.035
289
HYP056 Hypoglycemia 62 0.035
290
PRS042 Prostate Disease 56 0.035
291
APR001 Apraxia 52 0.035
292
BLD044 Bladder Disease 55 0.035
293
P HYP607 Hypercholesterolemia, Familial 81 0.034
294
DYS011 Dyskinesia of Esophagus 39 0.034
295
P FML018 Familial Mediterranean Fever 73 0.034
296
ESP020 Esophageal Atresia 54 0.034
297
MCR191 Microscopic Colitis 50 0.034
298
MCN017 Meconium Ileus 52 0.034
299
RDT013 Radiation Proctitis 51 0.034
300
P SJG008 Sjogren Syndrome 58 0.034
301
ESP025 Esophagus Adenocarcinoma 42 0.034
302
PLC008 Placenta Disease 48 0.034
303
P MSC005 Muscular Dystrophy 66 0.034
304
MLK004 Malakoplakia 34 0.034
305
BLD036 Bile Duct Disease 52 0.034
306
P PLM036 Pulmonary Fibrosis 68 0.034
307
RFR013 Refractory Celiac Disease 34 0.034
308
P HYP076 Hyperthyroidism 56 0.034
309
ATN004 Autonomic Neuropathy 46 0.034
310
OST012 Osteoarthritis 88 0.034
311
VND007 Van Der Woude Syndrome 1 57 0.034
312
IMM154 Immunoglobulin a Deficiency 1 45 0.034
313
PST035 Postgastrectomy Syndrome 36 0.033
314
LRY017 Laryngeal Disease 38 0.033
315
INT002 Intermittent Claudication 61 0.033
316
P SCL009 Sclerosing Cholangitis 53 0.033
317
PST030 Postcholecystectomy Syndrome 35 0.033
318
ACH005 Achalasia 52 0.033
319
ART016 Aortic Aneurysm 70 0.033
320
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.033
321
c SCN046 Secondary Short Bowel Syndrome 5 0.033
322
PRD004 Prediabetes Syndrome 46 0.033
323
PLY112 Polyarteritis Nodosa, Childhood-Onset 39 0.033
324
c CHL132 Cholestasis, Progressive Familial Intrahepatic, 1 52 0.033
325
HYP082 Hypopharynx Cancer 47 0.033
326
DMP001 Dumping Syndrome 45 0.033
327
P MCP040 Mucopolysaccharidosis-Plus Syndrome 61 0.033
328
IRN002 Iron Metabolism Disease 45 0.033
329
KRT001 Keratoconjunctivitis Sicca 63 0.033
330
BLR007 Biliary Tract Neoplasm 53 0.033
331
c CHR086 Chronic Conjunctivitis 44 0.033
332
P DLT002 Dilated Cardiomyopathy 76 0.033
333
c PLY146 Polycystic Liver Disease 1 45 0.033
334
P ASP006 Aspergillosis 65 0.033
335
TRH001 Trehalase Deficiency 21 0.032
336
c SML038 Small Cell Cancer of the Lung 67 0.032
337
P INT143 Interstitial Cystitis 63 0.032
338
P LRY019 Laryngitis 57 0.032
339
DNT012 Dental Caries 50 0.032
340
CYS013 Cystinuria 64 0.032
341
P MTC003 Metachromatic Leukodystrophy 72 0.032
342
ESN005 Eosinophilic Gastroenteritis 56 0.032
343
FXF002 Fox-Fordyce Disease 40 0.032
344
SWN001 Swine Influenza 46 0.032
345
DWN001 Down Syndrome 70 0.032
346
SLM003 Salmonellosis 56 0.032
347
PRN011 Pernicious Anemia 50 0.032
348
ATN011 Autoinflammation with Infantile Enterocolitis 39 0.032
349
LYS012 Lysosomal Acid Lipase Deficiency 60 0.032
350
CHR008 Choroiditis 47 0.032
351
DRR008 Diarrhea 1, Secretory Chloride, Congenital 47 0.032
352
GLC006 Galactosemia 64 0.032
353
CRC006 Carcinoid Syndrome 59 0.032
354
DYS015 Dysentery 43 0.032
355
CMM004 Common Variable Immunodeficiency 71 0.032
356
LKD001 Leukodystrophy 57 0.031
357
P INT070 Intestinal Obstruction 55 0.031
358
P NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 57 0.031
359
P HYP265 Hypotonia 40 0.031
360
HYP190 Hypoalphalipoproteinemia, Primary 61 0.031
361
P AML002 Amelogenesis Imperfecta 46 0.031
362
THR035 Thrombasthenia 46 0.031
363
SCH014 Schistosomiasis 62 0.031
364
CHL068 Cholestasis 60 0.031
365
IRN001 Iron Deficiency Anemia 55 0.031
366
NRL016 Neural Tube Defects 79 0.031
367
RLP002 Relapsing-Remitting Multiple Sclerosis 59 0.031
368
P PRD006 Prader-Willi Syndrome 66 0.031
369
INT071 Intestinal Perforation 44 0.031
370
DFC004 Deficiency Anemia 62 0.031
371
c NMN013 Niemann-Pick Disease, Type a 59 0.031
372
c VRL010 Viral Hepatitis 59 0.031
373
LCR008 Lacrimal Apparatus Disease 43 0.031
374
P DDN001 Duodenal Ulcer 53 0.030
375
c HRD039 Hereditary Amyloidosis 47 0.030
376
HRN026 Hernia, Hiatus 42 0.030
377
P MYL005 Myelofibrosis 75 0.030
378
ETN001 Eating Disorder 61 0.030
379
HYP060 Hyperinsulinism 56 0.030
380
GST009 Gastroschisis 55 0.030
381
GST095 Gastritis, Familial Giant Hypertrophic 28 0.030
382
P PRP029 Porphyria 62 0.030
383
c DRM040 Dermatitis Herpetiformis, Familial 32 0.030
384
ISL001 Islet Cell Tumor 54 0.030
385
DRY001 Dry Eye Syndrome 51 0.030
386
PRT037 Pertussis 70 0.030
387
TRP004 Tropical Sprue 38 0.030
388
ORL004 Oral Submucous Fibrosis 56 0.030
389
PSD007 Pseudomyxoma Peritonei 54 0.030
390
c AML020 Amelogenesis Imperfecta, Type Iv 37 0.030
391
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 21 0.030
392
P HYP014 Hyperuricemia 54 0.029
393
c CWD006 Cowden Syndrome 1 54 0.029
394
PNC033 Pancreas Adenocarcinoma 63 0.029
395
ANS003 Anisakiasis 36 0.029
396
P SRC025 Sarcoidosis 1 63 0.029
397
P RBL001 Rubella 61 0.029
398
MYC015 Mycobacterium Fortuitum 30 0.029
399
BLC009 Bile Acid Synthesis Defect, Congenital, 4 28 0.029
400
ANT009 Antithrombin Iii Deficiency 58 0.029
401
P MYP006 Myopia 56 0.029
402
P DNT011 Dentinogenesis Imperfecta 47 0.029
403
UND004 Undetermined Colitis 8 0.029
404
c CTR119 Cataract 32, Multiple Types 32 0.029
405
TNG004 Tongue Disease 37 0.029
406
c AML044 Amelogenesis Imperfecta, Type Ig 37 0.029
407
MSL001 Measles 64 0.029
408
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.029
409
MNT001 Mantle Cell Lymphoma 76 0.029
410
GST040 Gastric Adenocarcinoma 60 0.029
411
P DNT009 Dentin Dysplasia 39 0.029
412
c NRP031 Neuropathy, Hereditary Sensory and Autonomic, Type Vii 26 0.029
413
HRT031 Hartnup Disorder 48 0.029
414
HMN044 Human Immunodeficiency Virus Type 1 71 0.029
415
CLN015 Colon Adenocarcinoma 53 0.029
416
P TRM004 Trimethylaminuria 43 0.029
417
APL002 Aplasia of Lacrimal and Salivary Glands 41 0.029
418
BLC011 Bile Acid Synthesis Defect, Congenital, 3 23 0.029
419
PRM288 Permanent Molars, Secondary Retention of 23 0.029
420
TTN003 Tetanus 65 0.029
421
PHR003 Pharyngitis 59 0.028
422
PNC028 Pancreatic Steatorrhea 31 0.028
423
DRR017 Diarrhea 3, Secretory Sodium, Congenital, with or Without Other Congenital Anomalies 29 0.028
424
MYL020 Myelomeningocele 54 0.028
425
ANS011 Anus Cancer 46 0.028
426
P PNC045 Pancreatic Agenesis 40 0.028
427
PRK066 Parkinsonism with Spasticity, X-Linked 31 0.028
428
MYX011 Myxozoa 19 0.028
429
TXC005 Toxic Shock Syndrome 61 0.028
430
P MYT002 Myotonic Dystrophy 50 0.028
431
P MMB011 Membranous Nephropathy 55 0.028
432
MGC001 Megacolon 50 0.028
433
P END044 Endometriosis 71 0.028
434
MYC033 Myoclonus 40 0.028
435
TTH002 Tooth Agenesis 54 0.028
436
MCR037 Macroglossia 44 0.028
437
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 42 0.028
438
INT319 Intestinal Pseudoobstruction, Neuronal, Chronic Idiopathic, X-Linked 32 0.028
439
c DRR009 Diarrhea 6 21 0.028
440
VGN023 Vaginitis 59 0.028
441
PRP016 Paraplegia 53 0.028
442
c ACT134 Acute Liver Failure 52 0.028
443
P SML016 Small Intestine Cancer 52 0.028
444
SML036 Small Intestinal Adenocarcinoma 51 0.028
445
NRG001 Neurogenic Bowel 29 0.028
446
P CYS018 Cystitis 57 0.028
447
c PNC106 Pancreatic Agenesis 1 36 0.028
448
DBT083 Diabetes Mellitus, Permanent Neonatal 62 0.028
449
GLC003 Glucose Intolerance 58 0.028
450
P TCL004 T-Cell Leukemia 50 0.028
451
P RTT002 Rett Syndrome 82 0.028
452
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.028
453
AMP003 Ampulla of Vater Neoplasm 39 0.028
454
SPL011 Spleen Cancer 30 0.028
455
c DRR007 Diarrhea 7 19 0.028
456
HYP780 Hypoadrenocorticism, Familial 59 0.028
457
c INF145 Infantile Liver Failure Syndrome 1 33 0.028
458
CNN003 Conn's Syndrome 70 0.027
459
ALC006 Alcoholic Hepatitis 62 0.027
460
SPL018 Splenomegaly 45 0.027
461
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.027
462
RCT018 Rectal Neoplasm 53 0.027
463
SKN023 Skin Tag 41 0.027
464
BLR004 Biliary Dyskinesia 32 0.027
465
SPP003 Suppurative Periapical Periodontitis 29 0.027
466
PNC048 Pancreatic Lipase Deficiency 26 0.027
467
FLR007 Failure of Tooth Eruption, Primary 23 0.027
468
AMB001 Amebiasis 48 0.027
469
c PRM005 Primary Hyperparathyroidism 59 0.027
470
CCC002 Coccidiosis 52 0.027
471
c INV001 Invasive Aspergillosis 51 0.027
472
GST071 Gastrointestinal Carcinoma 40 0.027
473
ENT001 Enterocele 36 0.027
474
PLY114 Polyglucosan Body Myopathy 2 19 0.027
475
c CHR465 Chronic Diarrhea Due to Guanylate Cyclase 2c Overactivity 11 0.027
476
CHL004 Cholelithiasis 51 0.027
477
P AGG001 Aggressive Periodontitis 55 0.027
478
CRH005 Crohn's Colitis 53 0.027
479
MSC157 Muscular Dystrophy, Duchenne Type 74 0.027
480
P MMP001 Mumps 61 0.027
481
RSC001 Rosacea 58 0.027
482
PLM010 Pulmonary Edema 57 0.027
483
SPC010 Speech and Communication Disorders 40 0.027
484
P DBT085 Diabetes Mellitus, Insulin-Dependent 69 0.027
485
DBT087 Diabetes Insipidus, Neurohypophyseal 62 0.027
486
P GST047 Gastrointestinal Neuroendocrine Tumor 36 0.027
487
VSC014 Vascular Hyalinosis 18 0.027
488
ACC005 Accessory Pancreas 15 0.027
489
GST087 Gastric Linitis Plastica 15 0.027
490
GRD001 Giardiasis 45 0.027
491
RTR011 Retroperitoneal Fibrosis 43 0.027
492
IMM003 Immunoglobulin Alpha Deficiency 37 0.027
493
BRN056 Bronchopulmonary Dysplasia 61 0.027
494
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.027
495
CRD119 Cardiac Arrest 63 0.027
496
PLS011 Plasmacytoma 60 0.027
497
P BRN009 Burning Mouth Syndrome 56 0.027
498
P FML011 Familial Adenomatous Polyposis 71 0.027
499
BRT054 Brittle Bone Disorder 67 0.027
500
c PRD040 Periodontitis, Chronic 49 0.027
501
EPD025 Epidermolysis Bullosa with Pyloric Atresia 29 0.027
502
IDP068 Idiopathic Malabsorption Due to Bile Acid Synthesis Defects 7 0.027
503
c INF063 Inflammatory Bowel Disease 25, Autosomal Recessive 37 0.027
504
SHG001 Shigellosis 57 0.027
505
PRR002 Pure Red-Cell Aplasia 52 0.027
506
P GLM045 Glioma 61 0.026
507
HST011 Histoplasmosis 56 0.026
508
STR008 Strongyloidiasis 54 0.026
509
INT051 Intussusception 51 0.026
510
PRP007 Priapism 49 0.026
511
MTB004 Metabolic Acidosis 49 0.026
512
DPH001 Diphtheria 63 0.026
513
CHC001 Chickenpox 48 0.026
514
JJN008 Jejunoileitis 41 0.026
515
MRB003 Morbid Obesity 61 0.026
516
NRN031 Neuroendocrine Tumor of the Appendix 21 0.026
517
P HMN010 Hemangioma 61 0.026
518
NDL013 Nodular Regenerative Hyperplasia 53 0.026
519
PRS034 Parasitic Helminthiasis Infectious Disease 45 0.026
520
c CHL137 Cholestasis, Progressive Familial Intrahepatic, 3 47 0.026
521
MYC017 Mycobacterium Kansasii 42 0.026
522
CHL050 Cholesterol Ester Storage Disease 38 0.026
523
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 36 0.026
524
P ATS364 Autism 70 0.026
525
DSS009 Disseminated Intravascular Coagulation 56 0.026
526
MTC069 Mitochondrial Disorders 49 0.026
527
MYC013 Mycobacterium Abscessus 45 0.026
528
ESP027 Esophagus Squamous Cell Carcinoma 45 0.026
529
CNG363 Congenital Enterocyte Heparan Sulfate Deficiency 11 0.026
530
PRN015 Perinatal Intestinal Perforation 5 0.026
531
EPT026 Epithelio-Exfoliative Colitis-Deafness Syndrome 4 0.026
532
LYM007 Lymphangioleiomyomatosis 68 0.026
533
P SHR001 Short Bowel Syndrome 52 0.026
534
PTT037 Pituitary Tumors 49 0.026
535
P BRN019 Bernard-Soulier Syndrome 60 0.026
536
PRC003 Proctitis 44 0.026
537
c ADL017 Adult T-Cell Leukemia 63 0.026
538
ABT001 Abetalipoproteinemia 64 0.026
539
ADR012 Adrenal Gland Disease 51 0.026
540
FSC002 Fascioliasis 45 0.026
541
HGH026 High Anorectal Malformation 12 0.025
542
LWN002 Low Anorectal Malformation 10 0.025
543
INT254 Intermediate Anorectal Malformation 8 0.025
544
CNG480 Congenital Diarrhea 7 with Exudative Enteropathy 7 0.025
545
P HML001 Hemolytic-Uremic Syndrome 50 0.025
546
WRN001 Werner Syndrome 70 0.025
547
HPT019 Hepatic Encephalopathy 59 0.025
548
SLD003 Sialadenitis 49 0.025
549
GRN009 Granulomatous Hepatitis 38 0.025
550
P HYP750 Hypertriglyceridemia, Familial 55 0.025
551
PRT038 Protein-Energy Malnutrition 52 0.025
552
TRC003 Trichomoniasis 44 0.025
553
PLP001 Pulpitis 50 0.025
554
INF159 Infantile Sialic Acid Storage Disease 33 0.025
555
CCT002 Cicatricial Pemphigoid 54 0.025
556
SCB001 Scabies 50 0.025
557
c RTN162 Retinitis Pigmentosa 2 50 0.025
558
HPT014 Hepatorenal Syndrome 49 0.025
559
DDN007 Duodenal Disease 38 0.025
560
HYP081 Hypolipoproteinemia 49 0.025
561
HNC001 Henoch-Schoenlein Purpura 48 0.025
562
P FCS002 Fucosidosis 59 0.025
563
BLR001 Biliary Atresia 56 0.025
564
FNC009 Fanconi-Bickel Syndrome 53 0.025
565
VTM002 Vitamin B12 Deficiency 46 0.025
566
LPD012 Lipoid Congenital Adrenal Hyperplasia 66 0.025
567
NPH091 Nephrolithiasis, Calcium Oxalate 51 0.025
568
ACL001 Acalculous Cholecystitis 39 0.025
569
MCL006 Macular Retinal Edema 51 0.024
570
HPT077 Hepatic Venoocclusive Disease with Immunodeficiency 26 0.024
571
P FRG001 Fragile X Syndrome 69 0.024
572
PPL022 Papilloma 58 0.024
573
P HMR005 Hemorrhoid 51 0.024
574
ESP002 Esophageal Varix 46 0.024
575
PRD003 Periodontosis 45 0.024
576
CRL006 Caroli Disease, Isolated 21 0.024
577
c ALZ012 Alzheimer Disease 12 20 0.024
578
MLK006 Milk Allergy 46 0.024
579
ANG002 Angiostrongyliasis 44 0.024
580
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 40 0.024
581
ESN017 Eosinophilic Granuloma 37 0.024
582
P XRD010 Xeroderma Pigmentosum, Variant Type 62 0.024
583
DBT010 Diabetic Neuropathy 60 0.024
584
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 56 0.024
585
CHL056 Cheilitis 47 0.024
586
c HYP555 Hypertriglyceridemia, Transient Infantile 34 0.024
587
SKN019 Skin Melanoma 63 0.024
588
ORL015 Oral Squamous Cell Carcinoma 59 0.024
589
GST090 Gastroduodenal Crohn's Disease 28 0.024
590
CMM005 Common Cold 62 0.024
591
c ACT068 Acute Cystitis 50 0.024
592
P THM010 Thiamine Metabolism Dysfunction Syndrome 2 45 0.024
593
TRC023 Trichinosis 45 0.024
594
TXC001 Toxic Megacolon 34 0.024
595
c FML346 Familial Adenomatous Polyposis 1 63 0.024
596
P MWT001 Mowat-Wilson Syndrome 47 0.024
597
P PRT026 Parotitis 45 0.024
598
HYP189 Hypoadrenalism 43 0.024
599
PRN039 Paraneoplastic Syndromes 35 0.024
600
MKL001 Mikulicz Disease 28 0.024
601
LYM004 Lymphoid Interstitial Pneumonia 47 0.024
602
EPD015 Epidemic Typhus 45 0.024
603
DGR001 Digeorge Syndrome 55 0.024
604
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 43 0.024
605
OST115 Osteonecrosis of the Jaw 41 0.024
606
c ATS007 Autism Spectrum Disorder 68 0.023
607
c FRC011 Fructose Intolerance, Hereditary 56 0.023
608
IMP005 Impotence 54 0.023
609
EPD077 Epidermolysis Bullosa Junctionalis with Pyloric Atresia 51 0.023
610
GLS007 Glossitis 46 0.023
611
P ENC011 Encephalomyopathy 40 0.023
612
ISC015 Ischemic Colitis 39 0.023
613
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 38 0.023
614
c AML063 Amelogenesis Imperfecta Type 2a1 12 0.023
615
ANG020 Angiosarcoma 57 0.023
616
CHR003 Cherubism 57 0.023
617
PRM236 Primary Biliary Cholangitis 56 0.023
618
HPT022 Hepatoblastoma 55 0.023
619
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 43 0.023
620
BTN003 Biotinidase Deficiency 56 0.023
621
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 45 0.023
622
JVN014 Juvenile Polyposis Syndrome 60 0.023
623
GGR001 Geographic Tongue 52 0.023
624
DSS008 Disease of Mental Health 51 0.023
625
FBR019 Fibromatosis 47 0.023
626
ILC002 Ileocolitis 43 0.023
627
ADR010 Adrenal Cortical Hypofunction 41 0.023
628
LRY004 Laryngotracheitis 35 0.023
629
IMM179 Immunodeficiency 31c 29 0.023
630
HPT067 Hepatocellular Adenoma 43 0.023
631
SPR007 Superior Mesenteric Artery Syndrome 42 0.023
632
CMP002 Campylobacteriosis 51 0.023
633
ANT024 Anthrax Disease 47 0.023
634
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 38 0.023
635
P MTC133 Mitochondrial Myopathy 53 0.023
636
ALC009 Alcoholic Liver Cirrhosis 53 0.023
637
RYS001 Reye Syndrome 50 0.023
638
BLD063 Bile Duct Cysts 44 0.023
639
PND004 Pandas 34 0.023
640
ELS002 Elastosis Perforans Serpiginosa 34 0.023
641
HYP160 Hyperkeratosis Lenticularis Perstans 28 0.023
642
PYL006 Pyloric Stenosis 47 0.023
643
HTR003 Heterotaxy 46 0.023
644
GRN011 Granulomatous Gastritis 28 0.023
645
SQM013 Squamous Cell Carcinoma, Head and Neck 79 0.023
646
ULC007 Ulcerative Stomatitis 46 0.023
647
HPT004 Hepatic Coma 40 0.023
648
GST093 Gastrointestinal Defects and Immunodeficiency Syndrome 40 0.023
649
MRS001 Marasmus 39 0.023
650
RTC003 Root Caries 38 0.023
651
PLS002 Peliosis Hepatis 36 0.023
652
ORL005 Oral Candidiasis 51 0.022
653
URT031 Ureteral Disease 50 0.022
654
P GNG025 Gingival Fibromatosis 50 0.022
655
PRS115 Prosthetic Joint Infection 46 0.022
656
GST030 Gastrinoma 44 0.022
657
P ATM020 Autoimmune Enteropathy 39 0.022
658
c AML047 Amelogenesis Imperfecta, Type Ia 21 0.022
659
c AML050 Amelogenesis Imperfecta, Type if 20 0.022
660
INT079 Intrahepatic Cholangiocarcinoma 60 0.022
661
c CHL118 Cholestasis, Benign Recurrent Intrahepatic, 2 27 0.022
662
LYM022 Lymphangioma 53 0.022
663
P BLM007 Bulimia Nervosa 1 53 0.022
664
PYC001 Pycnodysostosis 51 0.022
665
ANS023 Anus, Imperforate 50 0.022
666
WRN003 Wernicke Encephalopathy 47 0.022
667
LCH001 Leech Infestation 43 0.022
668
PNG002 Pain Agnosia 41 0.022
669
HYL004 Hyaline Fibromatosis Syndrome 40 0.022
670
GST078 Gastrointestinal Allergy 35 0.022
671
VSD002 Vas Deferens, Congenital Bilateral Aplasia of 34 0.022
672
HPT081 Hepatic Infarction 30 0.022
673
INT050 Intestinal Impaction 27 0.022
674
HRS037 Hirschsprung Disease with Type D Brachydactyly 18 0.022
675
BLD034 Bile Duct Carcinoma 60 0.022
676
c GST103 Gastric Cancer, Hereditary Diffuse 54 0.022
677
IMM102 Immunodeficiency 14 49 0.022
678
P WHT013 White Sponge Nevus 1 46 0.022
679
ACT167 Acute Generalized Exanthematous Pustulosis 42 0.022
680
PRP017 Periapical Periodontitis 42 0.022
681
ACH015 Achalasia, Familial Esophageal 39 0.022
682
c AML017 Amelogenesis Imperfecta, Type Ib 36 0.022
683
c AML061 Amelogenesis Imperfecta, Type Ie 36 0.022
684
FLT009 Folate Malabsorption, Hereditary 36 0.022
685
c AML057 Amelogenesis Imperfecta, Type Iiia 32 0.022
686
c AML048 Amelogenesis Imperfecta, Type Ih 20 0.022
687
GNG012 Gingival Overgrowth 52 0.022
688
c PRM158 Primary Intestinal Lymphangiectasia 32 0.022
689
IGG016 Igg4-Related Dacryoadenitis and Sialadenitis 18 0.022
690
c ATM064 Autoimmune Pancreatitis Type 1 14 0.022
691
c LKM060 Leukemia, Acute Lymphoblastic 3 49 0.022
692
RYN003 Reynolds Syndrome 47 0.022
693
PRL008 Paralytic Ileus 38 0.022
694
CLN022 Colonic Atresia 27 0.022
695
HPT066 Hepatoportal Sclerosis 20 0.022
696
c AML018 Amelogenesis Imperfecta, Type Ic 19 0.022
697
INF047 Infantile Free Sialic Acid Storage Disease 12 0.022
698
c ATM063 Autoimmune Pancreatitis Type 2 12 0.022
699
P PLV020 Pelvic Organ Prolapse 63 0.022
700
RCH001 Richter's Syndrome 49 0.022
701
GNG003 Gingival Recession 45 0.022
702
MCR020 Microsporidiosis 42 0.022
703
GLS018 Glass Syndrome 38 0.022
704
P LYM124 Lymphangiectasia, Intestinal 35 0.022
705
DDN009 Duodenal Obstruction 34 0.022
706
CLR109 Colorectal Adenocarcinoma 54 0.022
707
EXT010 Extramedullary Plasmacytoma 52 0.022
708
NRM004 Neuroma 51 0.022
709
ESP018 Esophageal Candidiasis 44 0.022
710
MLL001 Molluscum Contagiosum 43 0.022
711
DNT008 Denture Stomatitis 41 0.022
712
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 31 0.022
713
c CHR013 Chronic Apical Periodontitis 31 0.022
714
P HYP009 Hypertrophic Pyloric Stenosis 45 0.021
715
DNT001 Dental Fluorosis 44 0.021
716
MYL013 Myeloperoxidase Deficiency 42 0.021
717
TTH008 Tooth Resorption 38 0.021
718
LNT001 Linitis Plastica 36 0.021
719
HYP021 Hypercementosis 35 0.021
720
ASC003 Ascending Cholangitis 33 0.021
721
DVR006 Diversion Colitis 31 0.021
722
PYL002 Pylorospasm 25 0.021
723
OST007 Ostertagiasis 20 0.021
724
HRS003 Hirschsprung Disease Ganglioneuroblastoma 17 0.021
725
c GLL027 Gallbladder Disease 4 12 0.021
726
MYC005 Myocardial Stunning 47 0.021
727
c ATM002 Autoimmune Polyendocrine Syndrome Type 1 46 0.021
728
TRN012 Transient Global Amnesia 40 0.021
729
ALC005 Alcoholic Pancreatitis 39 0.021
730
AMN002 Amino Acid Metabolic Disorder 38 0.021
731
c LVR030 Liver Failure, Infantile, Transient 27 0.021
732
c ALG016 Alagille Syndrome 2 26 0.021
733
HSH001 Hashimoto-Pritzker Syndrome 24 0.021
734
ULC008 Ulcerative Proctitis 24 0.021
735
c SCN059 Secondary Sclerosing Cholangitis 20 0.021
736
THR009 Thrombocytopenia-Absent Radius Syndrome 58 0.021
737
P SLV001 Silver-Russell Syndrome 57 0.021
738
MYM001 Myoma 56 0.021
739
AZS001 Azoospermia 47 0.021
740
TRP008 Tropical Calcific Pancreatitis 45 0.021
741
DCB001 Decubitus Ulcer 44 0.021
742
PRG017 Paraganglioma and Gastric Stromal Sarcoma 40 0.021
743
c DNT027 Dentin Dysplasia, Type Ii 38 0.021
744
SLT005 Solitary Median Maxillary Central Incisor 36 0.021
745
SPP004 Suppurative Cholangitis 32 0.021
746
STY001 Satoyoshi Syndrome 32 0.021
747
DNT046 Dental Abscess 28 0.021
748
TTH005 Teeth Hard Tissue Disease 21 0.021
749
EMB004 Embryonal Carcinoma 59 0.021
750
DRM013 Dermoid Cyst 43 0.021
751
P HRD012 Hereditary Elliptocytosis 41 0.021
752
SLL001 Sialolithiasis 41 0.021
753
PNC019 Pancreatoblastoma 33 0.021
754
BRW001 Brown-Vialetto-Van Laere Syndrome 27 0.021
755
IGG012 Igg4-Related Submandibular Gland Disease 12 0.021
756
c MWT002 Mowat-Wilson Syndrome Due to Monosomy 2q22 9 0.021
757
TRC040 Tracheoesophageal Fistula 47 0.021
758
AND001 Anodontia 46 0.021
759
P DFF019 Diffuse Gastric Cancer 43 0.021
760
IMN001 Iminoglycinuria 41 0.021
761
LKS001 Leukostasis 39 0.021
762
FNC002 Functional Diarrhea 36 0.021
763
TTH007 Tooth Erosion 36 0.021
764
GNT001 Giant Cell Reparative Granuloma 34 0.021
765
c DNT051 Dentin Dysplasia, Type I 34 0.021
766
VGN019 Vaginal Discharge 34 0.021
767
CRR017 Curry-Jones Syndrome 33 0.021
768
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 31 0.021
769
HRS039 Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 18 0.021
770
CLL026 Collagenous Gastritis 14 0.021
771
c MLG068 Malignant Glioma 66 0.021
772
P SLV002 Salivary Gland Cancer 62 0.021
773
CLR108 Colorectal Adenoma 60 0.021
774
SRC027 Sarcoma, Synovial 58 0.021
775
CVR006 Cavernous Hemangioma 48 0.021
776
c ADL096 Adult Hepatocellular Carcinoma 47 0.021
777
KLT001 Klatskin's Tumor 47 0.021
778
c CNG413 Congenital Short Bowel Syndrome 39 0.021
779
CND006 Candida Glabrata 38 0.021
780
TTH001 Tooth Ankylosis 32 0.021
781
OTD001 Otodental Dysplasia 31 0.021
782
LYM035 Lymphangiectasis 31 0.021
783
MCP039 Mucoepithelial Dysplasia, Hereditary 30 0.021
784
DNT003 Dental Pulp Calcification 28 0.021
785
LCT013 Lactase Deficiency, Congenital 26 0.021
786
P PLM064 Pulmonary Sequestration 25 0.021
787
c DNT047 Dentinogenesis Imperfecta Type 2 17 0.021
788
STR032 Steroid Dehydrogenase Deficiency Dental Anomalies 14 0.021
789
c MWT004 Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation 7 0.021
790
CYC008 Cyclic Vomiting Syndrome 50 0.020
791
MTY001 Mutyh-Associated Polyposis 42 0.020
792
PRV003 Perivascular Epithelioid Cell Tumor 42 0.020
793
DCR008 Dicarboxylic Aminoaciduria 38 0.020
794
TRD003 Taurodontism 32 0.020
795
BLD019 Bile Duct Cystadenocarcinoma 31 0.020
796
JJN007 Jejunal Adenocarcinoma 29 0.020
797
P HYP658 Hypoplastic Amelogenesis Imperfecta 27 0.020
798
PCD001 Pica Disease 26 0.020
799
CHL075 Cheilitis Glandularis 26 0.020
800
SLT007 Solitary Rectal Ulcer Syndrome 16 0.020
801
MSC007 Muscle Hypertrophy 57 0.020
802
PRV006 Pervasive Developmental Disorder 56 0.020
803
STT041 Stuttering 52 0.020
804
TRN022 Transcobalamin Ii Deficiency 47 0.020
805
PNC013 Pancreatic Ductal Carcinoma 47 0.020
806
INT060 Intestinal Atresia 42 0.020
807
APP010 Appendix Cancer 40 0.020
808
BLR027 Blue Rubber Bleb Nevus 39 0.020
809
DDN011 Duodenal Atresia 39 0.020
810
NCR003 Necrotizing Sialometaplasia 36 0.020
811
TRN003 Transverse Colon Cancer 35 0.020
812
CHR557 Chronic Intestinal Pseudoobstruction 32 0.020
813
BLR028 Biliary Atresia, Extrahepatic 32 0.020
814
ATR073 Atrophic Glossitis 30 0.020
815
IGG014 Igg4-Related Sclerosing Cholangitis 29 0.020
816
MDN001 Median Rhomboid Glossitis 28 0.020
817
GLS013 Glossodynia 21 0.020
818
MTG001 Metagonimiasis 21 0.020
819
PYT001 Pythiosis 17 0.020
820
VGS001 Vagus Nerve Disease 16 0.020
821
HRS038 Hirschsprung Disease with Hypoplastic Nails and Dysmorphic Facial Features 15 0.020
822
ANR003 Anorectal Stricture 13 0.020
823
MTN003 Motion Sickness 52 0.020
824
FBR086 Fibrolamellar Carcinoma 50 0.020
825
PNC008 Pancreatic Endocrine Carcinoma 40 0.020
826
GBL002 Goblet Cell Carcinoid 37 0.020
827
ALV001 Alveolar Periostitis 37 0.020
828
LRG016 Large Intestine Adenocarcinoma 37 0.020
829
ORL019 Oral Hairy Leukoplakia 37 0.020
830
PRM205 Primary Hepatic Neuroendocrine Carcinoma 35 0.020
831
ANL014 Anal Canal Adenocarcinoma 33 0.020
832
ANG061 Angular Cheilitis 32 0.020
833
PLT004 Platelet Glycoprotein Iv Deficiency 29 0.020
834
ADN088 Adenoma of the Pancreas 27 0.020
835
CNG002 Congenital Bile Acid Synthesis Defect 27 0.020
836
AND017 Anodontia of Permanent Dentition 25 0.020
837
ACT062 Acute Pericementitis 25 0.020
838
MCC003 Mucocele of Salivary Gland 25 0.020
839
ESN022 Eosinophilic Colitis 25 0.020
840
DST016 Distomatosis 23 0.020
841
ACK001 Ackerman Syndrome 22 0.020
842
HYP481 Hyperbiliverdinemia 22 0.020
843
ACH039 Achalasia-Microcephaly Syndrome 21 0.020
844
BLD065 Blue Diaper Syndrome 20 0.020
845
CVR008 Cavernous Lymphangioma 17 0.020
846
NKC001 Nk-Cell Enteropathy 16 0.020
847
MPV001 Mpv17-Related Hepatocerebral Mitochondrial Dna Depletion Syndrome 15 0.020
848
c SLV006 Salivary Gland Cancer, Adult 6 0.020
849
PRR016 Pierre Robin Syndrome 57 0.020
850
P HYP058 Hypervitaminosis a 48 0.020
851
FML026 Familial Lipoprotein Lipase Deficiency 46 0.020
852
ANL004 Anal Canal Squamous Cell Carcinoma 40 0.020
853
INT052 Intestinal Volvulus 38 0.020
854
FSS001 Fissured Tongue 32 0.020
855
DNT006 Dental Pulp Necrosis 29 0.020
856
NTM001 Nutmeg Liver 28 0.020
857
PRG122 Prognathism, Mandibular 23 0.020
858
AML005 Amelogenesis Imperfecta Hypomaturation Type 20 0.020
859
DNT044 Dentinogenesis Imperfecta, Shields Type Iii 19 0.020
860
FLM003 Fulminant Viral Hepatitis 18 0.020
861
DNT050 Dentin Dysplasia with Sclerotic Bones 14 0.020
862
CSC001 Cascade Stomach 12 0.020
863
UVL006 Uvulitis 12 0.020
864
BNG007 Benign Lymphoepithelial Lesion of Salivary Gland 8 0.020
865
CHL128 Childhood Hepatocellular Carcinoma 47 0.020
866
SGN002 Signet Ring Cell Adenocarcinoma 47 0.020
867
CRB090 Cerebral Hypoxia 47 0.020
868
c CNG004 Congenital Epulis 37 0.020
869
OVR044 Ovarian Carcinosarcoma 36 0.020
870
ANL011 Anal Canal Carcinoma 36 0.020
871
DSC005 Descending Colon Cancer 31 0.020
872
AML011 Amelogenesis Imperfecta, Hypoplastic/hypomaturation, X-Linked 2 25 0.020
873
P NRN029 Neuronal Intestinal Dysplasia 19 0.020
874
RCT023 Rectum Squamous Cell Carcinoma 19 0.020
875
LTT006 Littoral Cell Angioma of the Spleen 18 0.020
876
AML062 Amelogenesis Imperfecta, Hypomaturation Type, Iia5 18 0.020
877
THR030 Thoraco Abdominal Enteric Duplication 16 0.020
878
INC023 Incisors, Fused Mandibular 15 0.020
879
HPT028 Hepatic Cystic Hamartoma 14 0.020
880
ACQ006 Acquired Gastric Outlet Stenosis 13 0.020
881
HYD004 Hydrops of Gallbladder 12 0.020
882
SCR026 Secernentea Infections 12 0.020
883
PNC042 Pancreatic Intraductal Papillary-Colloid Carcinoma 10 0.020
884
c INT019 Intestine Carcinoma in Situ 6 0.020
885
c ATM070 Autoimmune Enteropathy Type 3 5 0.020
886
c ATM071 Autoimmune Enteropathy Type 2 5 0.020
887
LVR002 Liver Angiosarcoma 45 0.019
888
P DYS005 Dyslexia 39 0.019
889
HYP348 Hyperglycinuria 34 0.019
890
XNT002 Xanthogranulomatous Cholecystitis 33 0.019
891
SPL005 Splenic Artery Aneurysm 32 0.019
892
JJN003 Jejunal Cancer 30 0.019
893
DNT010 Dentin Caries 27 0.019
894
RGN005 Regional Odontodysplasia 24 0.019
895
HYP644 Hypocalcified Amelogenesis Imperfecta 24 0.019
896
NRT006 North American Indian Childhood Cirrhosis 23 0.019
897
CCL003 Cecal Benign Neoplasm 22 0.019
898
MCN018 Mucinous Adenocarcinoma of the Appendix 17 0.019
899
ORL006 Oral Mucosa Leukoplakia 16 0.019
900
P ACT046 Acute Apical Periodontitis 14 0.019
901
ALC012 Alcoholic Gastritis 14 0.019
902
GST026 Gastric Fundus Cancer 14 0.019
903
ANL005 Anal Spasm 14 0.019
904
PRT107 Proton-Pump Inhibitor-Responsive Esophageal Eosinophilia 12 0.019
905
SGM006 Segmental Odontomaxillary Dysplasia 12 0.019
906
GST025 Gastric Body Carcinoma 11 0.019
907
PYL007 Pylorus Cancer 11 0.019
908
PLP002 Pulp Degeneration 10 0.019
909
DRR012 Diarrhea, Chronic, with Villous Atrophy 8 0.019
910
PYL003 Pyloric Antrum Cancer 8 0.019
911
PRF001 Perforation of Bile Duct 8 0.019
912
HYP049 Hypertrophy of Tongue Papillae 7 0.019
913
ULC002 Ulcer of Anus and Rectum 6 0.019
914
MYP066 Myopathic Intestinal Pseudoobstruction 5 0.019
915
NNH007 Non-Hypoproteinemic Hypertrophic Gastropathy 5 0.019
916
UNC010 Unclassified Intestinal Pseudoobstruction 4 0.019
917
CLN044 Colon Adenoma 45 0.019
918
ANK008 Ankyloglossia 36 0.019
919
CLN004 Colon Carcinoma in Situ 35 0.019
920
SGM002 Sigmoid Neoplasm 33 0.019
921
ASC004 Ascending Colon Cancer 29 0.019
922
FSH003 Fish Allergy 28 0.019
923
EXR007 Exercise-Induced Anaphylaxis 27 0.019
924
VLV047 Volvulus of Midgut 24 0.019
925
TTH030 Teeth, Supernumerary 24 0.019
926
ACT016 Actinobacillosis 19 0.019
927
AML014 Amelogenesis Imperfecta, Hypomaturation Type, Iia2 19 0.019
928
AML039 Amelogenesis Imperfecta, Hypomaturation Type, Iia4 17 0.019
929
DNT004 Dientamoebiasis 17 0.019
930
SPL003 Splenic Flexure Cancer 17 0.019
931
ESP040 Esophageal Duplication Cyst 16 0.019
932
AML015 Amelogenesis Imperfecta, Hypomaturation Type, Iia3 16 0.019
933
HPT005 Hepatic Flexure Cancer 15 0.019
934
GLL034 Gallbladder Neuroendocrine Tumor 15 0.019
935
IGG008 Igg4-Related Mesenteritis 15 0.019
936
HMR013 Hemorrhagic Proctocolitis 13 0.019
937
ATM077 Autoimmune Gastrointestinal Dysmotility 11 0.019
938
AML052 Amelogenesis Imperfecta-Gingival Hyperplasia Syndrome 11 0.019
939
CHR009 Chronic Duodenal Ileus 10 0.019
940
STR003 Strawberry Gallbladder 9 0.019
941
LVR003 Liver Carcinoma in Situ 8 0.019
942
MLC005 Malocclusion Due to Protuberant Upper Front Teeth 8 0.019
943
BTH003 Bothriocephalosis 8 0.019
944
ODN001 Odontoclasia 8 0.019
945
OCC004 Occlusion of Gallbladder 7 0.019
946
CLS051 Classic Neuroendocrine Tumor of Appendix 7 0.019
947
OMP003 Omphalomesenteric Cyst 7 0.019
948
NNC014 Non-Central Nervous System-Localized Embryonal Carcinoma 6 0.019
949
c EXT020 External Pathological Resorption 6 0.019
950
IDP071 Idiopathic Copper-Associated Cirrhosis 5 0.019
951
DDN010 Duodenum Cancer 46 0.019
952
SMT002 Smooth Muscle Tumor 39 0.019
953
RCT008 Rectosigmoid Junction Neoplasm 30 0.019
954
ILM001 Ileum Cancer 27 0.019
955
KLB004 Klebsiella Infection 25 0.019
956
MYL044 Myelocystocele 25 0.019
957
BLC002 Black Piedra 15 0.019
958
RCT033 Rectal Duplication 13 0.019
959
GST055 Gastric Duplication Cysts 13 0.019
960
SLT015 Solitary Necrotic Nodule of the Liver 11 0.019
961
ISL118 Isolated Tracheoesophageal Fistula 10 0.019
962
GLS016 Glossopalatine Ankylosis 10 0.019
963
RCT010 Rectum Carcinoma in Situ 9 0.019
964
FNC012 Functioning Pancreatic Endocrine Tumor 9 0.019
965
CNG255 Congenital Temporomandibular Joint Ankylosis 7 0.019
966
MCK001 Meckel's Diverticulum Cancer 7 0.019
967
RHB006 Rhabditida Infections 7 0.019
968
BLR023 Biliary Atresia with Splenic Malformation Syndrome 7 0.019
969
LWR011 Lower Lip Fistula 6 0.019
970
CMM016 Commissural Lip Fistula 5 0.019
971
MCR334 Microcolon 33 0.018
972
CHM005 Chemical Colitis 26 0.018
973
GST038 Gastrointestinal Adenoma 19 0.018
974
LRG015 Large Intestine Adenoma 16 0.018
975
HYP727 Hypoglossia with Situs Inversus 16 0.018
976
CNG235 Congenital Microgastria 13 0.018
977
DSP001 Displacement of Cardia Through Esophageal Hiatus 8 0.018
978
CMM018 Common Mesentery 7 0.018
979
CNG334 Congenital Esophageal Diverticulum 6 0.018
980
ISL105 Isolated Agenesis of Gallbladder 5 0.018
981
TBL020 Tubular Duplication of the Esophagus 3 0.018
982
MCK029 Meckel Diverticulum 32 0.018
983
EPG004 Epignathus 18 0.018
984
CYS047 Cystic Fibrosis, Modifier of, 1 15 0.018
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