Search results for "digestive diseases"

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

1143 hits were found for 'digestive diseases'

# Family MCID Name MIFTS Score
1
GST050 Gastrointestinal System Disease 58 3.670
2
CHG001 Chagas Disease 62 2.509
3
P LVR013 Liver Disease 76 0.134
4
P PNC044 Pancreatitis 62 0.119
5
P INT068 Intestinal Disease 60 0.118
6
CRH001 Crohn's Disease 76 0.115
7
P KDN018 Kidney Disease 64 0.109
8
P GST049 Gastrointestinal System Cancer 59 0.106
9
STM006 Stomach Disease 48 0.103
10
P CLC005 Celiac Disease 67 0.098
11
CLN019 Colonic Disease 50 0.095
12
P HPT021 Hepatitis 74 0.091
13
P CRN211 Coronary Artery Disease 74 0.091
14
LNG099 Lung Disease 63 0.090
15
P ADN016 Adenocarcinoma 69 0.090
16
P OBS005 Obesity 91 0.089
17
P CLR023 Colorectal Cancer 96 0.087
18
VSC007 Vascular Disease 51 0.087
19
HPT023 Hepatocellular Carcinoma 90 0.085
20
PNC034 Pancreas Disease 56 0.085
21
P STM004 Stomach Cancer 73 0.083
22
NTR005 Nutritional Deficiency Disease 51 0.081
23
CYS001 Cystic Fibrosis 87 0.081
24
P ENC018 Encephalopathy 59 0.079
25
P DRR001 Diarrhea 60 0.079
26
P PNC035 Pancreatic Cancer 86 0.079
27
ESP023 Esophageal Disease 52 0.078
28
GST053 Gastric Cancer 52 0.078
29
NRN002 Neuronitis 40 0.077
30
GST045 Gastroenteritis 59 0.077
31
INT253 Intestinal Benign Neoplasm 48 0.074
32
ESP021 Esophageal Cancer 75 0.074
33
c CNG401 Congenital Heart Disease 67 0.074
34
MTH009 Mouth Disease 63 0.074
35
c CNT035 Central Nervous System Disease 60 0.074
36
c PNC106 Pancreatic Agenesis 1 31 0.073
37
P ESP024 Esophagitis 62 0.072
38
RSP006 Respiratory System Disease 61 0.071
39
FTT001 Fatty Liver Disease 60 0.070
40
P NRV007 Nervous System Disease 71 0.070
41
CLT003 Colitis 56 0.069
42
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 59 0.069
43
GST092 Gastroesophageal Reflux 62 0.068
44
P PNM007 Pneumonia 67 0.068
45
IRR002 Irritable Bowel Syndrome 58 0.066
46
CHY002 Chylomicron Retention Disease 54 0.066
47
DYS073 Dysphagia 51 0.066
48
ULC004 Ulcerative Colitis 74 0.065
49
PCK002 Pick Disease 66 0.065
50
CNS004 Constipation 57 0.065
51
LPD008 Lipid Metabolism Disorder 42 0.064
52
GST023 Gastric Ulcer 56 0.064
53
c INF067 Inflammatory Bowel Disease 10 31 0.064
54
P LKM002 Leukemia 70 0.064
55
PHY002 Physical Disorder 43 0.064
56
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.064
57
ALR002 Al-Raqad Syndrome 36 0.064
58
PRP027 Peripheral Vascular Disease 69 0.063
59
END072 Endotheliitis 41 0.063
60
P MYP004 Myopathy 67 0.063
61
P INF038 Influenza 71 0.063
62
RCT017 Rectal Disease 35 0.062
63
MVM001 Movement Disease 45 0.062
64
DDN006 Duodenitis 44 0.061
65
SWL001 Swallowing Disorders 33 0.061
66
WLS001 Wilson Disease 72 0.061
67
TTH006 Tooth Disease 52 0.060
68
PLM129 Pulmonary Disease, Chronic Obstructive 61 0.060
69
P PRD008 Periodontitis 46 0.060
70
P GLL020 Gallbladder Disease 59 0.060
71
P BRS047 Breast Cancer 100 0.060
72
P LYM118 Lymphoma 68 0.059
73
c PND001 Pain Disorder 53 0.059
74
LCT002 Lactose Intolerance 45 0.059
75
EXC002 Exocrine Pancreatic Insufficiency 41 0.059
76
CNN005 Connective Tissue Disease 60 0.059
77
GST078 Gastrointestinal Allergy 41 0.059
78
P ART022 Arthritis 73 0.058
79
PRD007 Periodontal Disease 42 0.058
80
c INF071 Inflammatory Bowel Disease 1 51 0.058
81
FDL002 Food Allergy 56 0.058
82
MSC004 Muscle Tissue Disease 35 0.057
83
CHL067 Cholecystitis 57 0.057
84
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.056
85
PRP019 Peripheral Nervous System Disease 52 0.056
86
CRB025 Carbohydrate Metabolic Disorder 46 0.056
87
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 35 0.056
88
P PRK057 Parkinson Disease, Late-Onset 72 0.056
89
PPT005 Peptic Ulcer Disease 58 0.056
90
GST013 Gastrojejunal Ulcer 23 0.055
91
LRN003 Learning Disability 49 0.055
92
BSL008 Basal Ganglia Disease 40 0.054
93
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 57 0.054
94
SKN016 Skin Disease 69 0.054
95
c INH020 Inherited Metabolic Disorder 49 0.054
96
P RSP003 Respiratory Failure 68 0.054
97
P MSC033 Muscle Disorders 52 0.054
98
LVR012 Liver Cirrhosis 71 0.054
99
KWS002 Kawasaki Disease 70 0.054
100
NRM005 Neuromuscular Disease 56 0.053
101
ANR040 Aneurysm 56 0.053
102
P AST005 Asthma 80 0.053
103
RHM027 Rheumatic Disease 55 0.053
104
ART021 Arteriosclerosis 59 0.053
105
GST019 Gastrointestinal Stromal Tumor 73 0.053
106
C3D001 C3 Deficiency 50 0.053
107
PLY023 Polycystic Liver Disease 57 0.053
108
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 55 0.053
109
P RHM011 Rheumatoid Arthritis 87 0.052
110
P GLY013 Glycogen Storage Disease 58 0.052
111
RCT018 Rectal Neoplasm 53 0.052
112
GNG013 Gingivitis 61 0.052
113
PRM025 Primary Bacterial Infectious Disease 42 0.052
114
DYS014 Dyspepsia 50 0.052
115
CRB009 Cerebritis 36 0.051
116
ING001 Inguinal Hernia 57 0.051
117
BLR006 Biliary Tract Disease 50 0.051
118
c CLR079 Colorectal Cancer 2 29 0.051
119
ATH003 Atherosclerosis 63 0.051
120
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.050
121
FNC005 Functional Colonic Disease 32 0.050
122
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.050
123
c CHR089 Chronic Kidney Failure 67 0.050
124
RTN023 Retinitis 49 0.050
125
ACD009 Acid-Labile Subunit, Deficiency of 37 0.050
126
CNJ003 Conjunctiva Squamous Cell Carcinoma 19 0.049
127
ISC004 Ischemia 56 0.049
128
PRT036 Peritonitis 65 0.049
129
c HPT001 Hepatitis C 68 0.049
130
APP008 Appendicitis 61 0.049
131
FCL044 Fecal Incontinence 34 0.049
132
P PLM036 Pulmonary Fibrosis 69 0.049
133
GST028 Gastric Squamous Cell Carcinoma 39 0.049
134
P GST044 Gastritis 64 0.049
135
NRN004 Neuroendocrine Tumor 54 0.048
136
FNC006 Functional Gastric Disease 33 0.048
137
VND001 Vein Disease 51 0.048
138
P NRV006 Nervous System Cancer 62 0.048
139
BLN006 Blind Loop Syndrome 29 0.048
140
c CLR085 Colorectal Cancer 1 39 0.048
141
c ACT027 Acute Pancreatitis 59 0.048
142
P PRT013 Portal Hypertension 61 0.048
143
END035 Endocrine Gland Cancer 50 0.048
144
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.047
145
DSS008 Disease of Mental Health 48 0.047
146
c INF086 Inflammatory Bowel Disease 3 20 0.047
147
GST071 Gastrointestinal Carcinoma 37 0.047
148
P LPS004 Lupus Erythematosus 63 0.047
149
END038 Endocrine Pancreas Disease 42 0.047
150
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.047
151
P TRC086 Trichohepatoenteric Syndrome 1 46 0.047
152
CSY001 C Syndrome 49 0.047
153
BLD054 Blood Protein Disease 38 0.047
154
P SML016 Small Intestine Cancer 54 0.046
155
ETN001 Eating Disorder 59 0.046
156
UND009 Undifferentiated Carcinoma of Stomach 17 0.046
157
CRC038 Carcinoma of Stomach, Salivary Gland Type 14 0.046
158
c GLL024 Gallbladder Disease 1 34 0.046
159
ALL026 Allergic Hypersensitivity Disease 53 0.046
160
c INF078 Inflammatory Bowel Disease 2 23 0.046
161
ANS012 Anus Disease 32 0.046
162
VSC006 Vascular Cancer 51 0.046
163
DGS007 Digestive Duplication 7 0.046
164
c SYS001 Systemic Lupus Erythematosus 87 0.046
165
GLC008 Glucose Metabolism Disease 44 0.046
166
P ALG002 Alagille Syndrome 70 0.046
167
INC022 Inclusion-Cell Disease 46 0.046
168
IMM127 Immune System Cancer 41 0.045
169
NWC001 Newcastle Disease 51 0.045
170
ABD010 Abdominal Wall Defect 37 0.045
171
CHL127 Cholangiocarcinoma, Susceptibility to 55 0.045
172
CRY003 Cryptosporidiosis 47 0.045
173
P MYC007 Myocardial Infarction 80 0.045
174
ATN002 Autonomic Nervous System Disease 46 0.045
175
P CNG015 Congenital Diaphragmatic Hernia 58 0.045
176
P HYP607 Hypercholesterolemia, Familial 77 0.045
177
P NRP001 Neuropathy 57 0.045
178
P HST010 Histiocytosis 56 0.045
179
MLN008 Melanoma 61 0.045
180
c BLD124 Bleeding Disorder, Platelet-Type, 11 37 0.044
181
HDN004 Head and Neck Carcinoma 54 0.044
182
c RCR022 Recurrent Acute Pancreatitis 36 0.044
183
P PRM006 Primary Biliary Cirrhosis 55 0.044
184
P SPS003 Spastic Diplegia 49 0.044
185
DGS008 Digestive System Melanoma 18 0.044
186
CTS003 Coats Disease 57 0.044
187
DFC004 Deficiency Anemia 64 0.044
188
P ADD001 Addison's Disease 60 0.044
189
c HPT003 Hepatitis a 55 0.044
190
P LNG032 Lung Cancer 92 0.044
191
P HRS035 Hirschsprung Disease 1 58 0.044
192
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 34 0.043
193
c PNC094 Pancreatic Cancer 1 27 0.043
194
BRS051 Breast Disease 57 0.043
195
PLV003 Pelvic Inflammatory Disease 52 0.043
196
DDN007 Duodenal Disease 34 0.043
197
HYP066 Hyperglycemia 61 0.043
198
UND008 Undifferentiated Carcinoma of Esophagus 15 0.043
199
CRC037 Carcinoma of Esophagus, Salivary Gland Type 14 0.043
200
ACT058 Active Peptic Ulcer Disease 44 0.043
201
P CRD011 Cardiomyopathy 66 0.043
202
c PNC095 Pancreatic Cancer 3 31 0.043
203
c PRK031 Parkinson Disease 1 54 0.043
204
TNG009 Tongue Squamous Cell Carcinoma 73 0.043
205
P ALP004 Alport Syndrome 68 0.043
206
c ATM011 Autoimmune Hepatitis 62 0.043
207
RSD004 Rosai-Dorfman Disease 40 0.043
208
DYS011 Dyskinesia of Esophagus 31 0.042
209
BRT030 Birth Defects 44 0.042
210
ACR041 Acromelic Frontonasal Dysostosis 45 0.042
211
GLL018 Gallbladder Cancer 63 0.042
212
PST035 Postgastrectomy Syndrome 33 0.042
213
PYL007 Pylorus Cancer 19 0.042
214
NSD001 Nose Disease 51 0.042
215
PNC048 Pancreatic Lipase Deficiency 25 0.042
216
CND002 Conduct Disorder 54 0.042
217
PLV005 Pelviureteric Junction Obstruction 43 0.042
218
c INF088 Inflammatory Bowel Disease 5 20 0.041
219
SQM013 Squamous Cell Carcinoma, Head and Neck 70 0.041
220
PST030 Postcholecystectomy Syndrome 31 0.041
221
c CHR096 Chronic Pulmonary Heart Disease 40 0.041
222
P HYP086 Hypothyroidism 63 0.041
223
c CRN175 Coronary Heart Disease 4 19 0.041
224
c CLR080 Colorectal Cancer 5 32 0.041
225
c HPT016 Hepatitis B 61 0.041
226
c MTB001 Metabolic Syndrome X 61 0.041
227
ENT006 Enterokinase Deficiency 23 0.041
228
c CLR075 Colorectal Cancer 3 37 0.041
229
BLD036 Bile Duct Disease 47 0.041
230
P AMY004 Amyloidosis 63 0.041
231
SPL011 Spleen Cancer 38 0.040
232
c ACT004 Acute Diarrhea 38 0.040
233
MLT021 Multiple System Atrophy 71 0.040
234
c INF087 Inflammatory Bowel Disease 4 26 0.040
235
INT051 Intussusception 50 0.040
236
c PRM023 Pre-Malignant Neoplasm 42 0.040
237
LYS002 Lysosomal Storage Disease 51 0.040
238
SQM014 Squamous Cell Carcinoma of Pancreas 18 0.040
239
c PNC108 Pancreatitis, Hereditary 59 0.040
240
CRC006 Carcinoid Syndrome 51 0.040
241
c PNC111 Pancreatic Cancer 2 33 0.040
242
JJN004 Jejunal Atresia 31 0.040
243
CRV038 Cervical Squamous Cell Carcinoma 58 0.040
244
P DDN001 Duodenal Ulcer 51 0.040
245
PRT035 Peritoneum Cancer 34 0.039
246
P PRS040 Prostate Cancer 89 0.039
247
ATM052 Autoimmune Disease 1 26 0.039
248
P CLL015 Collagen Disease 49 0.039
249
P ATR005 Atrophic Gastritis 47 0.039
250
ANL022 Anal Fistula 43 0.039
251
SRC014 Sarcoma 66 0.039
252
PHR003 Pharyngitis 58 0.039
253
P MSC003 Muscular Atrophy 51 0.039
254
EXF001 Exfoliation Syndrome 56 0.039
255
c INF089 Inflammatory Bowel Disease 6 19 0.038
256
c CHL120 Cholestasis, Benign Recurrent Intrahepatic 38 0.038
257
MLR004 Malaria 80 0.038
258
P CHL066 Cholangitis 48 0.038
259
P PSD087 Pseudoxanthoma Elasticum 65 0.038
260
BLD044 Bladder Disease 50 0.038
261
SML014 Small Intestine Leiomyosarcoma 36 0.038
262
TNG004 Tongue Disease 40 0.038
263
P PLN008 Peeling Skin Syndrome 45 0.038
264
GST039 Gastroduodenitis 32 0.038
265
MTC016 Mitochondrial Neurogastrointestinal Encephalopathy Disease 24 0.038
266
c PRM126 Primary Peritoneal Carcinoma 54 0.038
267
P SKN013 Skin Benign Neoplasm 38 0.038
268
P EXP004 Exophthalmos 56 0.038
269
GST088 Gastric Endocrine Tumor 16 0.038
270
VSC011 Vasculitis 62 0.038
271
GST037 Gastroparesis 54 0.038
272
CLN015 Colon Adenocarcinoma 55 0.038
273
c CLR081 Colorectal Cancer 6 23 0.038
274
SCR011 Scrapie 34 0.037
275
STT004 Steatorrhea 41 0.037
276
GST040 Gastric Adenocarcinoma 57 0.037
277
c PRK030 Parkinson Disease 4 38 0.037
278
ADM013 Adamantinoma of Long Bones 57 0.037
279
SLP005 Sleep Disorder 52 0.037
280
ANX002 Anxiety Disorder 67 0.037
281
PNC014 Pancreatic Serous Cystadenocarcinoma 21 0.037
282
CNG034 Congestive Heart Failure 72 0.037
283
CHL071 Child Syndrome 58 0.037
284
HYP266 Hypoxia 55 0.037
285
OST141 Osteoclastic Giant Cell Tumor of Pancreas 12 0.037
286
KDS001 Kid Syndrome 53 0.037
287
c AST037 Asthma 1 35 0.037
288
P TRM003 Tremor 54 0.037
289
ADR007 Adrenoleukodystrophy 74 0.037
290
TRP004 Tropical Sprue 36 0.037
291
ACN026 Acinar Cell Carcinoma of Pancreas 22 0.037
292
MCN020 Mucinous Cystadenocarcinoma of Pancreas 17 0.037
293
SLD011 Solid Pseudopapillary Carcinoma of Pancreas 10 0.037
294
SQM015 Squamous Cell Carcinoma of Small Intestine 14 0.037
295
c AST039 Asthma 2 28 0.037
296
ADL002 Adult Syndrome 53 0.037
297
UPP004 Upper Respiratory Tract Disease 48 0.037
298
c CHL080 Cholestasis, Progressive Familial Intrahepatic 1 45 0.037
299
SCR037 Sucrase-Isomaltase Deficiency, Congenital 26 0.037
300
P KDN017 Kidney Cancer 67 0.037
301
KPS004 Kaposi Sarcoma 69 0.037
302
SPC010 Speech and Communication Disorders 42 0.037
303
MCN017 Meconium Ileus 53 0.036
304
ESP025 Esophagus Adenocarcinoma 42 0.036
305
ADN021 Adenomatous Polyposis Coli 71 0.036
306
PLC008 Placenta Disease 33 0.036
307
LYM024 Lymphatic System Disease 49 0.036
308
P ESN007 Eosinophilia 61 0.036
309
P DRM007 Dermatitis Herpetiformis 48 0.036
310
BLR007 Biliary Tract Neoplasm 49 0.036
311
UMB002 Umbilical Hernia 40 0.036
312
HNS001 Hansen's Disease 30 0.036
313
c PNC103 Pancreatic Cancer 4 30 0.036
314
ACH005 Achalasia 55 0.036
315
DDN010 Duodenum Cancer 41 0.036
316
DRM006 Dermatitis 58 0.036
317
LNG024 Langerhans-Cell Histiocytosis 64 0.036
318
ANG011 Angiodysplasia 44 0.036
319
CHL068 Cholestasis 57 0.036
320
P GLM007 Glomerulonephritis 56 0.036
321
ERY003 Erythema Multiforme 57 0.036
322
PRN019 Perinatal Necrotizing Enterocolitis 47 0.036
323
GLC022 Glucose/galactose Malabsorption 38 0.035
324
SLV003 Salivary Gland Disease 47 0.035
325
P ART023 Arthropathy 63 0.035
326
GNG011 Gingival Disease 50 0.035
327
TNG002 Tangier Disease 61 0.035
328
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.035
329
ALC007 Alcohol Dependence 66 0.035
330
P CWD001 Cowden Disease 63 0.035
331
BRN106 Burns 52 0.035
332
c HYP595 Hypertension, Essential 69 0.035
333
P INF032 Infertility 61 0.035
334
SPC003 Specific Developmental Disorder 39 0.035
335
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 36 0.035
336
c PRK045 Parkinson Disease 5 43 0.035
337
OCL009 Ocular Cancer 61 0.035
338
P LYM026 Lymphoblastic Leukemia 60 0.035
339
CHR515 Chronic Atrial and Intestinal Dysrhythmia 19 0.035
340
MCR094 Microvillus Inclusion Disease 49 0.035
341
P INT070 Intestinal Obstruction 55 0.035
342
PNC028 Pancreatic Steatorrhea 34 0.035
343
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.034
344
JJN003 Jejunal Cancer 29 0.034
345
HPY002 H. Pylori Infection 58 0.034
346
BRN038 Bronchial Disease 54 0.034
347
CLC007 Calcium Metabolism Disease 39 0.034
348
DNT012 Dental Caries 45 0.034
349
c RNL016 Renal Infectious Disease 22 0.034
350
CYS039 Cystic Kidney Disease 49 0.034
351
c CLL013 Cell Type Cancer 46 0.034
352
THY030 Thyroid Gland Disease 52 0.034
353
SKN023 Skin Tag 48 0.034
354
NNL002 Nonalcoholic Steatohepatitis 49 0.034
355
ANG054 Angina Pectoris 48 0.034
356
c INT072 Intestinal Pseudo-Obstruction 45 0.034
357
SXL003 Sexual Disorder 45 0.034
358
CHR028 Chronic Wasting Disease 33 0.034
359
BHC003 Behcet Syndrome 60 0.034
360
c HPT073 Hepatitis C Virus 72 0.034
361
P THL005 Thalassemia 61 0.034
362
CRH005 Crohn's Colitis 50 0.034
363
P INT001 Intrahepatic Cholestasis 58 0.034
364
LKC003 Leukocyte Disease 45 0.034
365
INT071 Intestinal Perforation 40 0.034
366
THY028 Thyroid Cancer 71 0.034
367
ZLL002 Zollinger-Ellison Syndrome 49 0.034
368
BLD034 Bile Duct Carcinoma 56 0.034
369
PNC118 Pancreas, Annular 26 0.034
370
ADJ001 Adjustment Disorder 38 0.033
371
CNG298 Congenital Pancreatic Cyst 20 0.033
372
HPT046 Hepatic Veno-Occlusive Disease 46 0.033
373
RPR002 Reproductive System Disease 45 0.033
374
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 46 0.033
375
DGS006 Digestive Duplication Cyst of the Tongue 7 0.033
376
STM007 Stomatitis 50 0.033
377
P MCP010 Mucopolysaccharidosis 58 0.033
378
c ALZ012 Alzheimer Disease 12 19 0.033
379
DMY004 Demyelinating Disease 52 0.033
380
P MSC005 Muscular Dystrophy 64 0.033
381
PRN015 Perinatal Intestinal Perforation 5 0.033
382
PRC002 Paracoccidioidomycosis 57 0.033
383
MGC001 Megacolon 50 0.033
384
c CHL119 Cholangitis, Primary Sclerosing 31 0.033
385
TTH001 Tooth Ankylosis 38 0.033
386
TBR008 Tuberculous Peritonitis 37 0.033
387
c HMG001 Hemoglobin C Disease 46 0.033
388
PRP021 Peripheral Nervous System Neoplasm 49 0.033
389
c ACT134 Acute Liver Failure 46 0.033
390
c ATM024 Autoimmune Pancreatitis 46 0.033
391
LCT019 Lactase Persistence/nonpersistence 19 0.033
392
ISL029 Isolated Anorectal Malformation 5 0.033
393
MDD011 Mood Disorder 60 0.032
394
PRS042 Prostate Disease 50 0.032
395
ATM053 Autoimmune Disease 2 16 0.032
396
ORL004 Oral Submucous Fibrosis 52 0.032
397
c CLR083 Colorectal Cancer 8 26 0.032
398
TST021 Testicular Germ Cell Tumor 67 0.032
399
c INF074 Inflammatory Bowel Disease 15 18 0.032
400
WLL006 Wells Syndrome 57 0.032
401
ADN018 Adenoma 59 0.032
402
GNR004 Generalized Anxiety Disorder 49 0.032
403
LYM023 Lymphatic System Cancer 35 0.032
404
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.032
405
ORL011 Oral Cancer 53 0.032
406
c CLR087 Colorectal Cancer 12 32 0.032
407
VND002 Van Der Woude Syndrome 50 0.032
408
MCR191 Microscopic Colitis 46 0.032
409
BLC007 Bile Acid Synthesis Defect, Congenital, 1 28 0.032
410
FNC002 Functional Diarrhea 39 0.032
411
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.032
412
P MDL005 Medulloblastoma 76 0.032
413
c VRL010 Viral Hepatitis 60 0.032
414
RDT013 Radiation Proctitis 43 0.032
415
BLC008 Bile Acid Synthesis Defect, Congenital, 2 27 0.032
416
c DLT002 Dilated Cardiomyopathy 75 0.032
417
P DBT005 Diabetes Insipidus 53 0.032
418
OVR063 Overnutrition 49 0.032
419
MLK004 Malakoplakia 28 0.032
420
BRR002 Barrett's Adenocarcinoma 45 0.032
421
ART016 Aortic Aneurysm 67 0.031
422
MVD001 Moved to 60 0.031
423
GDS001 Good Syndrome 46 0.031
424
MDY003 Mody, Type Ii 36 0.031
425
ISL001 Islet Cell Tumor 51 0.031
426
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 77 0.031
427
GRD001 Giardiasis 40 0.031
428
P RNL014 Renal Cell Carcinoma 80 0.031
429
EWN003 Ewing Sarcoma 63 0.031
430
P HYP076 Hyperthyroidism 59 0.031
431
ILM001 Ileum Cancer 35 0.031
432
ALC009 Alcoholic Liver Cirrhosis 53 0.031
433
c CHR086 Chronic Conjunctivitis 46 0.031
434
P ATM020 Autoimmune Enteropathy 37 0.031
435
ATP002 Atopy 62 0.031
436
c SCN046 Secondary Short Bowel Syndrome 13 0.031
437
c INF073 Inflammatory Bowel Disease 12 20 0.031
438
INT002 Intermittent Claudication 56 0.031
439
LRY017 Laryngeal Disease 33 0.031
440
P LFR001 Li-Fraumeni Syndrome 79 0.031
441
MCC003 Mucocele of Salivary Gland 22 0.031
442
SLD003 Sialadenitis 45 0.031
443
ABL002 Ablepharon-Macrostomia Syndrome 51 0.031
444
ADR012 Adrenal Gland Disease 49 0.031
445
MND006 Mondor Disease 20 0.031
446
P ASP006 Aspergillosis 61 0.031
447
PRD011 Proud Syndrome 42 0.031
448
c INF068 Inflammatory Bowel Disease 13 23 0.031
449
P DBT083 Diabetes Mellitus, Permanent Neonatal 51 0.031
450
HYP080 Hypogonadism 54 0.030
451
APP010 Appendix Cancer 38 0.030
452
P MTC003 Metachromatic Leukodystrophy 71 0.030
453
RFR013 Refractory Celiac Disease 32 0.030
454
c CLC045 Celiac Disease 2 17 0.030
455
ORL015 Oral Squamous Cell Carcinoma 55 0.030
456
HPT014 Hepatorenal Syndrome 47 0.030
457
HYP082 Hypopharynx Cancer 40 0.030
458
c HRD101 Hereditary Mixed Polyposis Syndrome 1 24 0.030
459
c MYC058 Myocardial Infarction 2 28 0.030
460
DYS015 Dysentery 42 0.030
461
ATM054 Autoimmune Disease 3 16 0.030
462
MCK002 Meckel's Diverticulum 36 0.030
463
P GST047 Gastrointestinal Neuroendocrine Tumor 39 0.030
464
END077 Endocrine Tumor of Colon 13 0.030
465
P CHR345 Chronic Pain 45 0.030
466
MSC072 Muscle Cancer 47 0.030
467
PLS009 Plasma Cell Neoplasm 47 0.030
468
P SCL009 Sclerosing Cholangitis 47 0.030
469
P AML002 Amelogenesis Imperfecta 43 0.030
470
DWN001 Down Syndrome 65 0.030
471
CHR008 Choroiditis 43 0.030
472
P CHR084 Chromosomal Disease 37 0.030
473
INT007 Intermediate Coronary Syndrome 52 0.030
474
P RTT002 Rett Syndrome 77 0.030
475
P LRY019 Laryngitis 55 0.030
476
THR035 Thrombasthenia 41 0.030
477
P LKD001 Leukodystrophy 58 0.030
478
CHR103 Charge Syndrome 64 0.030
479
WLM001 Wolman Disease 55 0.030
480
GLS007 Glossitis 46 0.030
481
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.029
482
TRH001 Trehalase Deficiency 19 0.029
483
PYL003 Pyloric Antrum Cancer 12 0.029
484
LYS003 Lysinuric Protein Intolerance 51 0.029
485
GLC006 Galactosemia 64 0.029
486
SCH014 Schistosomiasis 59 0.029
487
P OST012 Osteoarthritis 81 0.029
488
CNG368 Congenital Adrenal Hyperplasia 60 0.029
489
GND003 Gonadal Disease 41 0.029
490
PLP001 Pulpitis 45 0.029
491
GRM001 Germ Cell and Embryonal Cancer 38 0.029
492
SNS023 Sensory System Cancer 45 0.029
493
DMP001 Dumping Syndrome 39 0.029
494
P INT143 Interstitial Cystitis 57 0.029
495
PRN011 Pernicious Anemia 41 0.029
496
P CRV031 Cervical Adenocarcinoma 52 0.029
497
ESN005 Eosinophilic Gastroenteritis 46 0.029
498
FNC012 Functioning Pancreatic Endocrine Tumor 14 0.029
499
VSC009 Vascular Skin Disease 21 0.029
500
c DRR009 Diarrhea 6 30 0.029
501
AYM001 Ayme-Gripp Syndrome 40 0.029
502
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.029
503
VSC047 Vascular Malformation 45 0.029
504
PRD003 Periodontosis 40 0.029
505
c THR092 Thrombophilia Due to Thrombin Defect 56 0.029
506
c ACT068 Acute Cystitis 50 0.029
507
IRN001 Iron Deficiency Anemia 51 0.029
508
HRT007 Heart Cancer 51 0.029
509
P HRD018 Hair Disease 48 0.029
510
GST063 Gastric Cancer Risk After H. Pylori Infection 52 0.029
511
c DLT001 Delta Chain Disease 14 0.029
512
ANS003 Anisakiasis 46 0.029
513
LPD027 Lip Disease 35 0.029
514
CLR109 Colorectal Adenocarcinoma 50 0.029
515
CMM004 Common Variable Immunodeficiency 68 0.028
516
AMN002 Amino Acid Metabolic Disorder 48 0.028
517
ADT003 Auditory System Disease 49 0.028
518
P HRT017 Heart Tumor 34 0.028
519
P PRC019 Precocious Puberty 53 0.028
520
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 40 0.028
521
c ADL079 Adult Heart Tumor 17 0.028
522
PLS002 Peliosis Hepatis 32 0.028
523
P PRP029 Porphyria 56 0.028
524
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.028
525
LDD001 Ladd Syndrome 60 0.028
526
c DYS166 Dysautonomia, Familial 54 0.028
527
P TCL004 T-Cell Leukemia 44 0.028
528
c NMN013 Niemann-Pick Disease, Type a 55 0.028
529
P HYP060 Hyperinsulinism 58 0.028
530
PRT030 Parathyroid Gland Disease 49 0.028
531
P FML035 Familial Hyperlipidemia 49 0.028
532
DRR008 Diarrhea 1, Secretory Chloride, Congenital 42 0.028
533
CHL052 Choledochal Cyst 40 0.028
534
P MLT074 Multiple Endocrine Neoplasia 55 0.028
535
P HYP014 Hyperuricemia 49 0.028
536
c DRR007 Diarrhea 7 32 0.028
537
GGR001 Geographic Tongue 45 0.028
538
PSD007 Pseudomyxoma Peritonei 51 0.028
539
P MYL005 Myelofibrosis 67 0.028
540
MNT001 Mantle Cell Lymphoma 72 0.028
541
APL002 Aplasia of Lacrimal and Salivary Glands 32 0.027
542
HTS001 Hiatus Hernia 40 0.027
543
MLT001 Multiple Chemical Sensitivity 43 0.027
544
MYC015 Mycobacterium Fortuitum 29 0.027
545
PRS036 Parasitic Protozoa Infectious Disease 45 0.027
546
GNG012 Gingival Overgrowth 52 0.027
547
PNC013 Pancreatic Ductal Carcinoma 45 0.027
548
ORL014 Oral Pharyngeal Disorders 13 0.027
549
P KLL001 Kallmann Syndrome 61 0.027
550
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 42 0.027
551
LYM116 Lymph Node Disease 42 0.027
552
P AGN002 Agnosia 56 0.027
553
P SLV002 Salivary Gland Cancer 60 0.027
554
ENT001 Enterocele 39 0.027
555
P STR035 Streptococcal Group a Invasive Disease 15 0.027
556
c CLR082 Colorectal Cancer 7 22 0.027
557
TXC005 Toxic Shock Syndrome 61 0.027
558
EMB004 Embryonal Carcinoma 55 0.027
559
c GLL027 Gallbladder Disease 4 25 0.027
560
SML036 Small Intestinal Adenocarcinoma 46 0.027
561
P PLR004 Pleuropulmonary Blastoma 63 0.027
562
TYP011 Typhus 57 0.027
563
TTH002 Tooth Agenesis 54 0.027
564
GNG003 Gingival Recession 37 0.027
565
c CHR013 Chronic Apical Periodontitis 26 0.027
566
c ADL017 Adult T-Cell Leukemia 59 0.027
567
P OST005 Osteogenesis Imperfecta 68 0.027
568
P MTC069 Mitochondrial Disorders 51 0.027
569
DPB001 Deep Brain Stimulation for Parkinson's Disease 23 0.027
570
SLC005 Selective Iga Deficiency Disease 23 0.027
571
P DNT011 Dentinogenesis Imperfecta 42 0.027
572
HYP021 Hypercementosis 31 0.027
573
c PRK037 Parkinson Disease 13 27 0.027
574
ALC006 Alcoholic Hepatitis 60 0.027
575
c INF090 Inflammatory Bowel Disease 7 18 0.027
576
ANS011 Anus Cancer 44 0.027
577
HYP064 Hypogonadotropism 38 0.027
578
P HYP009 Hypertrophic Pyloric Stenosis 40 0.027
579
c PRM005 Primary Hyperparathyroidism 56 0.027
580
PRP016 Paraplegia 49 0.027
581
APH002 Aphasia 52 0.027
582
INT111 Intestinal Pseudoobstruction, Neuronal 31 0.026
583
P TRM004 Trimethylaminuria 41 0.026
584
DNT001 Dental Fluorosis 42 0.026
585
c CNT075 Central Precocious Puberty 49 0.026
586
AMP003 Ampulla of Vater Neoplasm 35 0.026
587
ESP020 Esophageal Atresia 48 0.026
588
PRL008 Paralytic Ileus 37 0.026
589
P PNC045 Pancreatic Agenesis 44 0.026
590
GLT030 Gluten Allergy 19 0.026
591
MNR003 Mineral Metabolism Disease 39 0.026
592
PRT011 Protein C Deficiency 52 0.026
593
ATM015 Autoimmune Disease of Gastrointestinal Tract 33 0.026
594
MYL020 Myelomeningocele 50 0.026
595
SLL001 Sialolithiasis 39 0.026
596
MYX011 Myxozoa 18 0.026
597
TTH005 Teeth Hard Tissue Disease 27 0.026
598
c SLV006 Salivary Gland Cancer, Adult 14 0.026
599
c CHL082 Cholestasis, Progressive Familial Intrahepatic 3 33 0.026
600
c SRC025 Sarcoidosis 1 58 0.026
601
MXD023 Mixed Cell Type Cancer 45 0.026
602
DCH001 Duchenne Muscular Dystrophy 81 0.026
603
P HYP117 Hypertriglyceridemia 65 0.026
604
PLM010 Pulmonary Edema 56 0.026
605
PLM012 Pulmonary Sarcoidosis 54 0.026
606
DNT041 Dentin Dysplasia, Type I, with Microdontia and Misshapen Teeth 27 0.026
607
AND001 Anodontia 40 0.026
608
RCT011 Rectal Prolapse 41 0.026
609
SPP003 Suppurative Periapical Periodontitis 33 0.026
610
RCT008 Rectosigmoid Junction Neoplasm 38 0.026
611
NNF001 Non-Functioning Pancreatic Endocrine Tumor 38 0.026
612
TRN003 Transverse Colon Cancer 38 0.026
613
P END044 Endometriosis 53 0.026
614
P NPH009 Nephrolithiasis 59 0.026
615
P MYT002 Myotonic Dystrophy 46 0.026
616
BRN056 Bronchopulmonary Dysplasia 56 0.026
617
MCR037 Macroglossia 45 0.026
618
PNC008 Pancreatic Endocrine Carcinoma 39 0.026
619
P DNT009 Dentin Dysplasia 37 0.026
620
ANR003 Anorectal Stricture 13 0.026
621
NTM001 Nutmeg Liver 30 0.026
622
SPL018 Splenomegaly 45 0.026
623
MYC033 Myoclonus 41 0.026
624
P SJG001 Sjogren's Syndrome 55 0.026
625
HYP056 Hypoglycemia 60 0.026
626
P SHR029 Short Syndrome 60 0.026
627
CHL004 Cholelithiasis 48 0.026
628
ATR073 Atrophic Glossitis 30 0.026
629
MDN001 Median Rhomboid Glossitis 29 0.026
630
AMB001 Amebiasis 43 0.026
631
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.026
632
PLS011 Plasmacytoma 57 0.026
633
P CSH001 Cushing's Syndrome 65 0.026
634
NSY001 N Syndrome 42 0.026
635
FLR007 Failure of Tooth Eruption, Primary 22 0.025
636
DRR004 Diarrhea 3, Secretory Sodium, Congenital, Syndromic 22 0.025
637
ORL019 Oral Hairy Leukoplakia 33 0.025
638
APR001 Apraxia 50 0.025
639
P HMN010 Hemangioma 62 0.025
640
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 40 0.025
641
P CYS018 Cystitis 54 0.025
642
RTR011 Retroperitoneal Fibrosis 40 0.025
643
FSS001 Fissured Tongue 34 0.025
644
OTD001 Otodental Dysplasia 26 0.025
645
DNT006 Dental Pulp Necrosis 25 0.025
646
ULC002 Ulcer of Anus and Rectum 9 0.025
647
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.025
648
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.025
649
ATN011 Autoinflammation with Infantile Enterocolitis 36 0.025
650
VGN023 Vaginitis 41 0.025
651
WST001 West Syndrome 61 0.025
652
c RTN162 Retinitis Pigmentosa 2 50 0.025
653
c OPT053 Optic Atrophy 1 43 0.025
654
INT052 Intestinal Volvulus 32 0.025
655
P EPD025 Epidermolysis Bullosa with Pyloric Atresia 33 0.025
656
CSC001 Cascade Stomach 16 0.025
657
HPT081 Hepatic Infarction 20 0.025
658
HYD004 Hydrops of Gallbladder 13 0.025
659
CLN044 Colon Adenoma 43 0.025
660
FML011 Familial Adenomatous Polyposis 68 0.025
661
CHC001 Chickenpox 50 0.025
662
ATN004 Autonomic Neuropathy 44 0.025
663
PRR002 Pure Red-Cell Aplasia 47 0.025
664
c CWD006 Cowden Syndrome 1 43 0.025
665
DRR005 Diarrhea 4, Malabsorptive, Congenital 20 0.025
666
BLR028 Biliary Atresia, Extrahepatic 25 0.025
667
DSC005 Descending Colon Cancer 31 0.025
668
P ACT046 Acute Apical Periodontitis 15 0.025
669
HYP049 Hypertrophy of Tongue Papillae 7 0.025
670
PLP002 Pulp Degeneration 9 0.025
671
NRG001 Neurogenic Bowel 25 0.025
672
GST087 Gastric Linitis Plastica 16 0.025
673
c BRN108 Branchiootic Syndrome 1 36 0.025
674
GNR003 Generalized Atherosclerosis 35 0.025
675
CRD119 Cardiac Arrest 63 0.025
676
HPT019 Hepatic Encephalopathy 58 0.025
677
DSS009 Disseminated Intravascular Coagulation 52 0.025
678
BCT015 Bacteremia 50 0.025
679
NSL022 Nasal Cavity Disease 41 0.025
680
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 24 0.025
681
VSC014 Vascular Hyalinosis 16 0.025
682
PLY114 Polyglucosan Body Myopathy 2 15 0.025
683
GST026 Gastric Fundus Cancer 20 0.025
684
ALC012 Alcoholic Gastritis 14 0.025
685
c INT019 Intestine Carcinoma in Situ 14 0.025
686
ISL004 Isolated Gonadotropin-Releasing Hormone Deficiency 17 0.025
687
PRF001 Perforation of Bile Duct 10 0.025
688
PNC040 Pancreatic Delta Cell Neoplasm 15 0.025
689
FSH003 Fish Allergy 29 0.025
690
PRS034 Parasitic Helminthiasis Infectious Disease 47 0.025
691
P FRC002 Fructose Intolerance 54 0.025
692
CHL050 Cholesterol Ester Storage Disease 39 0.025
693
HPT020 Hepatic Vascular Disease 43 0.025
694
ABT001 Abetalipoproteinemia 60 0.025
695
P ORG009 Organ System Cancer 45 0.025
696
SHG001 Shigellosis 52 0.025
697
c PLN018 Peeling Skin Syndrome 2 36 0.025
698
P AGG001 Aggressive Periodontitis 49 0.025
699
MMB002 Membranous Glomerulonephritis 47 0.025
700
c INF083 Inflammatory Bowel Disease 24 18 0.025
701
ANL005 Anal Spasm 15 0.025
702
CLN004 Colon Carcinoma in Situ 35 0.025
703
STR003 Strawberry Gallbladder 8 0.025
704
GST025 Gastric Body Carcinoma 19 0.025
705
BLR004 Biliary Dyskinesia 29 0.025
706
OCC004 Occlusion of Gallbladder 15 0.025
707
NRM018 Normosmic Congenital Hypogonadotropic Hypogonadism 36 0.025
708
IDP068 Idiopathic Malabsorption Due to Bile Acid Synthesis Defects 5 0.025
709
IDP034 Idiopathic Central Precocious Puberty 27 0.025
710
OLV001 Olivopontocerebellar Atrophy 53 0.024
711
NDL013 Nodular Regenerative Hyperplasia 46 0.024
712
ILT001 Ileitis 48 0.024
713
BRN039 Bronchial Neoplasm 35 0.024
714
RSC001 Rosacea 54 0.024
715
P CNN004 Connective Tissue Cancer 44 0.024
716
LVR003 Liver Carcinoma in Situ 13 0.024
717
ACC005 Accessory Pancreas 18 0.024
718
ATM077 Autoimmune Gastrointestinal Dysmotility 11 0.024
719
GST038 Gastrointestinal Adenoma 28 0.024
720
c OPT055 Optic Atrophy Plus Syndrome 55 0.024
721
MRB003 Morbid Obesity 59 0.024
722
WRN001 Werner Syndrome 69 0.024
723
P ORL007 Oral Cavity Cancer 58 0.024
724
P SHR001 Short Bowel Syndrome 51 0.024
725
c INV001 Invasive Aspergillosis 44 0.024
726
P GLM045 Glioma 53 0.024
727
c SML023 Small Cell Lung Cancer, Adult 17 0.024
728
CCL003 Cecal Benign Neoplasm 27 0.024
729
HYP231 Hypothalamic Hamartomas 35 0.024
730
RCT023 Rectum Squamous Cell Carcinoma 22 0.024
731
HPT005 Hepatic Flexure Cancer 16 0.024
732
ASC004 Ascending Colon Cancer 31 0.024
733
SPL003 Splenic Flexure Cancer 16 0.024
734
END073 Endocrine Tumor of the Appendix 13 0.024
735
P LYM007 Lymphangioleiomyomatosis 65 0.024
736
PRD004 Prediabetes Syndrome 40 0.024
737
MYC017 Mycobacterium Kansasii 40 0.024
738
c CNG031 Congenital Nervous System Abnormality 39 0.024
739
BLR001 Biliary Atresia 52 0.024
740
STR008 Strongyloidiasis 51 0.024
741
MTB004 Metabolic Acidosis 49 0.024
742
RCT010 Rectum Carcinoma in Situ 13 0.024
743
HGH026 High Anorectal Malformation 12 0.024
744
GLL031 Gallbladder Endocrine Tumor 12 0.024
745
CNG363 Congenital Enterocyte Heparan Sulfate Deficiency 4 0.024
746
EPT026 Epithelio-Exfoliative Colitis-Deafness Syndrome 4 0.024
747
DVR002 Diverticulitis 47 0.024
748
P HML001 Hemolytic-Uremic Syndrome 50 0.024
749
VTM002 Vitamin B12 Deficiency 45 0.024
750
GRN009 Granulomatous Hepatitis 37 0.024
751
PLY056 Polyposis, Juvenile Intestinal 54 0.023
752
MYC013 Mycobacterium Abscessus 41 0.023
753
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 13 0.023
754
DSP001 Displacement of Cardia Through Esophageal Hiatus 6 0.023
755
LWN002 Low Anorectal Malformation 9 0.023
756
INT254 Intermediate Anorectal Malformation 7 0.023
757
GST055 Gastric Duplication Cysts 12 0.023
758
P FCS002 Fucosidosis 57 0.023
759
MLK006 Milk Allergy 50 0.023
760
P PRM016 Primary Optic Atrophy 29 0.023
761
P FRG001 Fragile X Syndrome 68 0.023
762
c PLN021 Peeling Skin Syndrome 3 30 0.023
763
TRC003 Trichomoniasis 41 0.023
764
PPL022 Papilloma 54 0.023
765
PRN039 Paraneoplastic Syndromes 42 0.023
766
PRC003 Proctitis 42 0.023
767
P PRT010 Parathyroid Carcinoma 61 0.023
768
SWN001 Swine Influenza 42 0.023
769
PTT037 Pituitary Tumors 45 0.023
770
BTN003 Biotinidase Deficiency 56 0.023
771
c VRL005 Viral Pneumonia 44 0.023
772
NRL016 Neural Tube Defects 76 0.023
773
HNC001 Henoch-Schoenlein Purpura 45 0.023
774
EPD045 Epidermolysis Bullosa, Junctional, with Pyloric Stenosis 37 0.023
775
OBS015 Obesity, Hyperphagia, and Developmental Delay 35 0.023
776
JJN008 Jejunoileitis 38 0.023
777
CCT002 Cicatricial Pemphigoid 50 0.023
778
IMM107 Immunodeficiency 31c, Autosomal Dominant 27 0.023
779
CHL056 Cheilitis 48 0.023
780
HRN022 Hearing Loss/deafness 23 0.023
781
c CHL081 Cholestasis, Progressive Familial Intrahepatic 2 30 0.023
782
PRT038 Protein-Energy Malnutrition 48 0.023
783
NRG002 Neurogenic Bladder 47 0.023
784
c CLC048 Celiac Disease 3 21 0.023
785
MKL001 Mikulicz Disease 28 0.023
786
PRM026 Primary Systemic Mycosis 40 0.023
787
TRC023 Trichinosis 44 0.023
788
VNT001 Ventilation Pneumonitis 35 0.023
789
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 45 0.022
790
CRR007 Cirrhosis, Cryptogenic 38 0.022
791
P DGR001 Digeorge Syndrome 52 0.022
792
SCB001 Scabies 45 0.022
793
ANG020 Angiosarcoma 53 0.022
794
HPT077 Hepatic Venoocclusive Disease with Immunodeficiency 27 0.022
795
CMP002 Campylobacteriosis 47 0.022
796
FSC002 Fascioliasis 39 0.022
797
HYP081 Hypolipoproteinemia 42 0.022
798
CNG035 Congenital Bilateral Absence of Vas Deferens 40 0.022
799
BRD001 Brody Myopathy 49 0.022
800
c FML053 Familial Colorectal Cancer 50 0.022
801
P MWT001 Mowat-Wilson Syndrome 50 0.022
802
CMM005 Common Cold 58 0.022
803
P HMR005 Hemorrhoid 45 0.022
804
BLM002 Bulimia Nervosa 54 0.022
805
ACL001 Acalculous Cholecystitis 35 0.022
806
c OPT059 Optic Atrophy 4 18 0.022
807
ANT024 Anthrax Disease 50 0.022
808
TNG003 Tongue Cancer 59 0.022
809
c OPT023 Optic Atrophy 2 25 0.022
810
LYM020 Lymph Node Cancer 41 0.022
811
LYM022 Lymphangioma 55 0.022
812
OST115 Osteonecrosis of the Jaw 37 0.022
813
P HYP027 Hypobetalipoproteinemia 52 0.022
814
URN008 Urinary Bladder Cancer 64 0.022
815
BHR001 Behr Syndrome 43 0.022
816
INT079 Intrahepatic Cholangiocarcinoma 55 0.022
817
c CLC037 Celiac Disease 4 20 0.022
818
HYP189 Hypoadrenalism 39 0.022
819
MCN001 Mucinous Adenocarcinoma 48 0.022
820
HPT004 Hepatic Coma 39 0.022
821
HPT022 Hepatoblastoma 57 0.022
822
c CNN010 Connective Tissue Benign Neoplasm 31 0.022
823
c GST048 Gastrointestinal System Benign Neoplasm 40 0.022
824
VSC044 Visceral Myopathy 44 0.022
825
c INF095 Inflammatory Bowel Disease 25, Early Onset, Autosomal Recessive 35 0.022
826
GST090 Gastroduodenal Crohn's Disease 26 0.022
827
LCH001 Leech Infestation 35 0.022
828
NRM004 Neuroma 47 0.022
829
c CLL012 Cell Type Benign Neoplasm 41 0.022
830
ADR005 Adrenal Carcinoma 57 0.022
831
IMP002 Imperforate Anus 54 0.022
832
IMP005 Impotence 49 0.022
833
c PRS116 Prostate Cancer 1 39 0.022
834
DBT010 Diabetic Neuropathy 55 0.022
835
c OPT025 Optic Atrophy 6 23 0.022
836
ILC002 Ileocolitis 38 0.022
837
ANG002 Angiostrongyliasis 40 0.022
838
c OPT024 Optic Atrophy 5 18 0.022
839
PYC001 Pycnodysostosis 51 0.021
840
CHR003 Cherubism 50 0.021
841
HYP160 Hyperkeratosis Lenticularis Perstans 25 0.021
842
c MLT094 Multiple Sclerosis 3 26 0.021
843
CWM001 Cow Milk Allergy 39 0.021
844
c NRP042 Neuropathy, Hereditary Sensory and Autonomic, Type Ii 42 0.021
845
ISC015 Ischemic Colitis 38 0.021
846
TXC001 Toxic Megacolon 26 0.021
847
PNM003 Pneumatosis Cystoides Intestinalis 32 0.021
848
ELS002 Elastosis Perforans Serpiginosa 30 0.021
849
PYL006 Pyloric Stenosis 46 0.021
850
P CLR108 Colorectal Adenoma 60 0.021
851
P GNR027 Generalized Peeling Skin Syndrome 21 0.021
852
c CLC040 Celiac Disease 6 17 0.021
853
PRT026 Parotitis 42 0.021
854
GST002 Gastric Mucosal Hypertrophy 35 0.021
855
SPR007 Superior Mesenteric Artery Syndrome 37 0.021
856
MRS001 Marasmus 39 0.021
857
CRD003 Cardiac Sarcoidosis 39 0.021
858
FBR019 Fibromatosis 40 0.021
859
c CHL118 Cholestasis, Benign Recurrent Intrahepatic, 2 26 0.021
860
DCB001 Decubitus Ulcer 44 0.021
861
P LRY016 Laryngeal Carcinoma 60 0.021
862
PND004 Pandas 30 0.021
863
LRY004 Laryngotracheitis 29 0.021
864
ADR010 Adrenal Cortical Hypofunction 38 0.021
865
HPT067 Hepatocellular Adenoma 41 0.021
866
HYL004 Hyaline Fibromatosis Syndrome 38 0.021
867
ACH037 Achalasia-Addisonianism-Alacrimia Syndrome 45 0.021
868
c ATM002 Autoimmune Polyendocrine Syndrome Type 1 47 0.021
869
c OPT057 Optic Atrophy 7 27 0.021
870
ORP003 Oropharynx Cancer 48 0.021
871
P ESP035 Esophagitis, Eosinophilic, 1 40 0.021
872
PNC033 Pancreas Adenocarcinoma 54 0.021
873
MYC005 Myocardial Stunning 44 0.021
874
URT031 Ureteral Disease 45 0.021
875
PLY073 Polyposis, Gastric 32 0.021
876
BLD032 Bile Duct Adenocarcinoma 39 0.021
877
INT050 Intestinal Impaction 28 0.021
878
P WHT013 White Sponge Nevus 1 40 0.021
879
INT017 Intestinal Schistosomiasis 45 0.021
880
P ENC011 Encephalomyopathy 35 0.021
881
c ATM064 Autoimmune Pancreatitis Type 1 17 0.021
882
P SLV001 Silver-Russell Syndrome 54 0.021
883
P ATS007 Autism Spectrum Disorder 64 0.021
884
ULC007 Ulcerative Stomatitis 44 0.021
885
LVR002 Liver Angiosarcoma 44 0.021
886
DRM013 Dermoid Cyst 39 0.021
887
EXT010 Extramedullary Plasmacytoma 49 0.021
888
SPP004 Suppurative Cholangitis 35 0.021
889
SNG010 Single Median Maxillary Central Incisor 52 0.021
890
CCL002 Cecal Disease 31 0.021
891
PRV003 Perivascular Epithelioid Cell Tumor 38 0.021
892
c ATM063 Autoimmune Pancreatitis Type 2 12 0.021
893
DDN009 Duodenal Obstruction 35 0.021
894
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 36 0.021
895
GST093 Gastrointestinal Defects and Immunodeficiency Syndrome 37 0.021
896
MCR020 Microsporidiosis 38 0.021
897
c OST147 Osteoarthritis 1 31 0.021
898
INF047 Infantile Free Sialic Acid Storage Disease 14 0.021
899
RCH001 Richter's Syndrome 45 0.021
900
BLD019 Bile Duct Cystadenocarcinoma 32 0.021
901
c CLC046 Celiac Disease 5 17 0.021
902
TTH008 Tooth Resorption 38 0.021
903
c CLR078 Colorectal Cancer 11 19 0.021
904
PRP056 Porphyria, Acute Hepatic 36 0.020
905
P ACT150 Acute Adrenal Insufficiency 36 0.020
906
c PRM158 Primary Intestinal Lymphangiectasia 19 0.020
907
DVR006 Diversion Colitis 32 0.020
908
RYN003 Reynolds Syndrome 49 0.020
909
c ALG016 Alagille Syndrome 2 28 0.020
910
RTC003 Root Caries 36 0.020
911
c CLR084 Colorectal Cancer 9 19 0.020
912
c GLL025 Gallbladder Disease 2 18 0.020
913
c GLL026 Gallbladder Disease 3 18 0.020
914
BLC009 Bile Acid Synthesis Defect, Congenital, 4 24 0.020
915
c AML020 Amelogenesis Imperfecta, Type Iv 26 0.020
916
STT041 Stuttering 48 0.020
917
c CLR077 Colorectal Cancer 10 33 0.020
918
c CWD005 Cowden Syndrome 4 23 0.020
919
EPD015 Epidemic Typhus 37 0.020
920
MLL001 Molluscum Contagiosum 44 0.020
921
c CLC039 Celiac Disease 13 19 0.020
922
SGN002 Signet Ring Cell Adenocarcinoma 45 0.020
923
c CLC041 Celiac Disease 7 15 0.020
924
NCR003 Necrotizing Sialometaplasia 35 0.020
925
c MLG068 Malignant Glioma 49 0.020
926
OVR044 Ovarian Carcinosarcoma 42 0.020
927
CLN022 Colonic Atresia 23 0.020
928
HPT066 Hepatoportal Sclerosis 21 0.020
929
FTT003 Fatty Acid Oxidation Disorders 38 0.020
930
MTY001 Mutyh-Associated Polyposis 48 0.020
931
MYL013 Myeloperoxidase Deficiency 46 0.020
932
c HRD012 Hereditary Elliptocytosis 42 0.020
933
HRS037 Hirschsprung Disease with Type D Brachydactyly 16 0.020
934
APP009 Appendix Adenocarcinoma 40 0.020
935
ADR022 Adrenomyeloneuropathy 37 0.020
936
CRV068 Cervical Polyp 40 0.020
937
EXT011 Extrapyramidal and Movement Disease 13 0.020
938
ANL014 Anal Canal Adenocarcinoma 30 0.020
939
LNT001 Linitis Plastica 32 0.020
940
JJN007 Jejunal Adenocarcinoma 29 0.020
941
PRM205 Primary Hepatic Neuroendocrine Carcinoma 26 0.020
942
UND004 Undetermined Colitis 5 0.020
943
c AML044 Amelogenesis Imperfecta, Type Ig 27 0.020
944
c DNT027 Dentin Dysplasia, Type Ii 34 0.020
945
AZS001 Azoospermia 43 0.020
946
GBL002 Goblet Cell Carcinoid 29 0.020
947
HRS003 Hirschsprung Disease Ganglioneuroblastoma 14 0.020
948
GNT001 Giant Cell Reparative Granuloma 41 0.020
949
CMM007 Common Bile Duct Disease 25 0.020
950
ASC003 Ascending Cholangitis 28 0.020
951
ACH015 Achalasia, Familial Esophageal 29 0.020
952
c LVR028 Liver Failure, Transient Infantile 22 0.020
953
P GNG025 Gingival Fibromatosis 49 0.020
954
TRC040 Tracheoesophageal Fistula 41 0.020
955
VGS001 Vagus Nerve Disease 17 0.020
956
GST030 Gastrinoma 39 0.020
957
PNC019 Pancreatoblastoma 31 0.020
958
LKS001 Leukostasis 39 0.020
959
PRP017 Periapical Periodontitis 35 0.020
960
GRN011 Granulomatous Gastritis 28 0.020
961
NRN029 Neuronal Intestinal Dysplasia 31 0.020
962
THR009 Thrombocytopenia-Absent Radius Syndrome 52 0.020
963
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 26 0.020
964
TRP008 Tropical Calcific Pancreatitis 42 0.020
965
IPX001 Ipex Syndrome 35 0.020
966
PRV006 Pervasive Developmental Disorder 49 0.020
967
MPV001 Mpv17-Related Hepatocerebral Mitochondrial Dna Depletion Syndrome 16 0.020
968
P BNG071 Benign Schwannoma 38 0.020
969
STR032 Steroid Dehydrogenase Deficiency Dental Anomalies 12 0.020
970
DFF019 Diffuse Gastric Cancer 41 0.020
971
ULC008 Ulcerative Proctitis 22 0.020
972
LYM035 Lymphangiectasis 28 0.020
973
c SCN059 Secondary Sclerosing Cholangitis 17 0.020
974
ATS001 Autistic Disorder 60 0.019
975
c INF145 Infantile Liver Failure Syndrome 1 21 0.019
976
BRW006 Brown Syndrome 31 0.019
977
TTH007 Tooth Erosion 33 0.019
978
SGM002 Sigmoid Neoplasm 34 0.019
979
PRT022 Protozoal Dysentery 10 0.019
980
c FML321 Familial Stomach Cancer 17 0.019
981
c MWT002 Mowat-Wilson Syndrome Due to Monosomy 2q22 9 0.019
982
CND006 Candida Glabrata 35 0.019
983
VGN019 Vaginal Discharge 32 0.019
984
P PLM064 Pulmonary Sequestration 26 0.019
985
BLC011 Bile Acid Synthesis Defect, Congenital, 3 23 0.019
986
CHL128 Childhood Hepatocellular Carcinoma 30 0.019
987
c CNG413 Congenital Short Bowel Syndrome 34 0.019
988
ANG061 Angular Cheilitis 32 0.019
989
CYC008 Cyclic Vomiting Syndrome 39 0.019
990
BLR027 Blue Rubber Bleb Nevus 33 0.019
991
MYM001 Myoma 51 0.019
992
KLT001 Klatskin's Tumor 42 0.019
993
c DNT047 Dentinogenesis Imperfecta Type 2 11 0.019
994
HRS039 Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 14 0.019
995
P LRY044 Larynx Cancer 48 0.019
996
CRB090 Cerebral Hypoxia 45 0.019
997
NTL004 Nut Allergy 38 0.019
998
RCT020 Rectum Adenocarcinoma 30 0.019
999
SMT002 Smooth Muscle Tumor 41 0.019
1000
VLL006 Villous Adenoma 32 0.019
1001
P MTH008 Methylmalonic Acidemia 51 0.019
1002
CLN045 Colonic Benign Neoplasm 38 0.019
1003
IGG016 Igg4-Related Dacryoadenitis and Sialadenitis 14 0.019
1004
ALC005 Alcoholic Pancreatitis 35 0.019
1005
IGG012 Igg4-Related Submandibular Gland Disease 8 0.019
1006
c MWT004 Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation 7 0.019
1007
c ATM071 Autoimmune Enteropathy Type 2 7 0.019
1008
IGG014 Igg4-Related Sclerosing Cholangitis 24 0.019
1009
CVR008 Cavernous Lymphangioma 15 0.019
1010
LCT013 Lactase Deficiency, Congenital 24 0.019
1011
c DNT044 Dentinogenesis Imperfecta, Shields Type Iii 19 0.019
1012
P LYM124 Lymphangiectasia, Intestinal 23 0.019
1013
CRR013 Cirrhosis, North American Indian Childhood Type 19 0.019
1014
ACK001 Ackerman Syndrome 21 0.019
1015
TRD003 Taurodontism 28 0.019
1016
CHR557 Chronic Intestinal Pseudoobstruction 25 0.019
1017
ALV001 Alveolar Periostitis 34 0.019
1018
CRL006 Caroli Disease, Isolated 13 0.019
1019
PYT001 Pythiosis 16 0.019
1020
SKL003 Skeletal Muscle Cancer 41 0.019
1021
LRG016 Large Intestine Adenocarcinoma 28 0.019
1022
ESN022 Eosinophilic Colitis 19 0.019
1023
SLT007 Solitary Rectal Ulcer Syndrome 19 0.019
1024
GST095 Gastritis, Familial Giant Hypertrophic 19 0.019
1025
CHL075 Cheilitis Glandularis 21 0.019
1026
GST009 Gastroschisis 31 0.019
1027
P EPL003 Epulis 34 0.019
1028
PYL002 Pylorospasm 23 0.019
1029
CNG002 Congenital Bile Acid Synthesis Defect 23 0.019
1030
SKN022 Skin Squamous Cell Carcinoma 41 0.019
1031
FBR054 Fibroma 44 0.019
1032
CLL026 Collagenous Gastritis 12 0.019
1033
MTN003 Motion Sickness 48 0.019
1034
CVR006 Cavernous Hemangioma 46 0.019
1035
PRG122 Prognathism, Mandibular 18 0.019
1036
MCP039 Mucoepithelial Dysplasia, Hereditary 18 0.019
1037
HPT012 Hepatocellular Fibrolamellar Carcinoma 26 0.019
1038
HRS038 Hirschsprung Disease with Hypoplastic Nails and Dysmorphic Facial Features 12 0.019
1039
SQM002 Squamous Cell Papilloma 40 0.019
1040
UVL006 Uvulitis 13 0.019
1041
XNT002 Xanthogranulomatous Cholecystitis 30 0.019
1042
INT060 Intestinal Atresia 37 0.019
1043
DNT046 Dental Abscess 26 0.019
1044
BNG007 Benign Lymphoepithelial Lesion of Salivary Gland 8 0.019
1045
PRT034 Peritoneal Serous Adenocarcinoma 27 0.019
1046
P HYP658 Hypoplastic Amelogenesis Imperfecta 24 0.019
1047
RSP004 Respiratory System Benign Neoplasm 24 0.019
1048
c ATM070 Autoimmune Enteropathy Type 3 7 0.019
1049
FLM003 Fulminant Viral Hepatitis 18 0.019
1050</