Search results for "digestive diseases"

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

1160 hits were found for 'digestive diseases'

# Family MCID Name MIFTS Score
1
GST050 Gastrointestinal System Disease 54 3.644
2
CHG001 Chagas Disease 62 2.486
3
P LVR013 Liver Disease 72 0.133
4
P INT068 Intestinal Disease 61 0.125
5
P PNC044 Pancreatitis 60 0.117
6
CRH001 Crohn's Disease 76 0.115
7
P GST049 Gastrointestinal System Cancer 60 0.114
8
P HRT032 Heart Disease 76 0.109
9
STM006 Stomach Disease 50 0.105
10
P CLC005 Celiac Disease 67 0.098
11
LNG099 Lung Disease 62 0.095
12
P OBS005 Obesity 93 0.095
13
CLN019 Colonic Disease 50 0.095
14
P CLR023 Colorectal Cancer 97 0.093
15
P CRN211 Coronary Artery Disease 75 0.091
16
PNC034 Pancreas Disease 57 0.091
17
P HPT021 Hepatitis 70 0.090
18
GST053 Gastric Cancer 77 0.087
19
CYS001 Cystic Fibrosis 86 0.087
20
HPT023 Hepatocellular Carcinoma 91 0.087
21
P ADN016 Adenocarcinoma 69 0.086
22
NTR005 Nutritional Deficiency Disease 39 0.083
23
P PNC035 Pancreatic Cancer 85 0.078
24
NRN002 Neuronitis 42 0.076
25
GST045 Gastroenteritis 60 0.076
26
PHY002 Physical Disorder 44 0.076
27
INT253 Intestinal Benign Neoplasm 50 0.076
28
MTH009 Mouth Disease 63 0.076
29
VSC007 Vascular Disease 67 0.076
30
ESP023 Esophageal Disease 53 0.075
31
ESP021 Esophageal Cancer 75 0.074
32
P DRR001 Diarrhea 51 0.073
33
c PNC106 Pancreatic Agenesis 1 40 0.073
34
P ESP024 Esophagitis 62 0.071
35
CLT003 Colitis 59 0.069
36
P PNM007 Pneumonia 66 0.069
37
PCK002 Pick Disease 67 0.069
38
GST092 Gastroesophageal Reflux 61 0.068
39
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.067
40
CHY002 Chylomicron Retention Disease 59 0.066
41
DYS073 Dysphagia 49 0.065
42
FTT001 Fatty Liver Disease 60 0.065
43
ULC004 Ulcerative Colitis 75 0.065
44
LPD008 Lipid Metabolism Disorder 58 0.065
45
RCT017 Rectal Disease 39 0.064
46
c INF067 Inflammatory Bowel Disease 10 51 0.064
47
P ART022 Arthritis 75 0.064
48
PRP027 Peripheral Vascular Disease 69 0.064
49
CNS004 Constipation 57 0.063
50
RSP006 Respiratory System Disease 62 0.063
51
GST023 Gastric Ulcer 55 0.063
52
P LKM002 Leukemia 70 0.063
53
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.063
54
MVM001 Movement Disease 54 0.062
55
P INF038 Influenza 74 0.062
56
P MYP004 Myopathy 67 0.062
57
END072 Endotheliitis 42 0.062
58
P ENC018 Encephalopathy 59 0.062
59
SWL001 Swallowing Disorders 34 0.061
60
P BRS047 Breast Cancer 100 0.061
61
PLM129 Pulmonary Disease, Chronic Obstructive 62 0.060
62
ISB001 Isobutyryl-Coa Dehydrogenase Deficiency 60 0.060
63
DDN006 Duodenitis 44 0.060
64
P GLL020 Gallbladder Disease 59 0.059
65
CNN005 Connective Tissue Disease 61 0.059
66
WLS001 Wilson Disease 72 0.059
67
TTH006 Tooth Disease 52 0.059
68
CRB025 Carbohydrate Metabolic Disorder 47 0.058
69
PRD007 Periodontal Disease 43 0.058
70
EXC002 Exocrine Pancreatic Insufficiency 43 0.058
71
GLC008 Glucose Metabolism Disease 47 0.058
72
c INF071 Inflammatory Bowel Disease 1 51 0.058
73
GST078 Gastrointestinal Allergy 41 0.058
74
MSC004 Muscle Tissue Disease 36 0.058
75
P LYM118 Lymphoma 70 0.058
76
P NRV007 Nervous System Disease 71 0.057
77
c PND001 Pain Disorder 55 0.057
78
LCT002 Lactose Intolerance 45 0.056
79
P PRK057 Parkinson Disease, Late-Onset 72 0.056
80
FDL002 Food Allergy 54 0.056
81
BSL008 Basal Ganglia Disease 43 0.055
82
P HYP607 Hypercholesterolemia, Familial 77 0.055
83
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.055
84
PPT005 Peptic Ulcer Disease 56 0.055
85
GST013 Gastrojejunal Ulcer 25 0.055
86
P AST005 Asthma 82 0.054
87
LRN003 Learning Disability 51 0.054
88
P MSC033 Muscle Disorders 52 0.054
89
P PRD008 Periodontitis 46 0.054
90
KWS002 Kawasaki Disease 70 0.054
91
RCT018 Rectal Neoplasm 55 0.054
92
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 55 0.053
93
c INH020 Inherited Metabolic Disorder 49 0.053
94
NRM005 Neuromuscular Disease 57 0.053
95
P RSP003 Respiratory Failure 70 0.053
96
c CLR079 Colorectal Cancer 2 31 0.053
97
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 57 0.053
98
RHM027 Rheumatic Disease 57 0.053
99
LVR012 Liver Cirrhosis 67 0.053
100
GST019 Gastrointestinal Stromal Tumor 72 0.053
101
SKN016 Skin Disease 68 0.052
102
ART021 Arteriosclerosis 59 0.052
103
ANR040 Aneurysm 57 0.052
104
P GLY013 Glycogen Storage Disease 59 0.052
105
P RHM011 Rheumatoid Arthritis 88 0.052
106
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.052
107
CLN009 Colon Squamous Cell Carcinoma 25 0.051
108
IMM127 Immune System Cancer 42 0.051
109
DYS014 Dyspepsia 50 0.051
110
PRM025 Primary Bacterial Infectious Disease 43 0.051
111
BLR006 Biliary Tract Disease 51 0.051
112
GNG013 Gingivitis 60 0.050
113
CSY001 C Syndrome 49 0.050
114
c CHR089 Chronic Kidney Failure 66 0.050
115
CRB009 Cerebritis 38 0.050
116
ATH003 Atherosclerosis 62 0.050
117
FNC005 Functional Colonic Disease 30 0.050
118
ING001 Inguinal Hernia 57 0.050
119
P PRP019 Peripheral Nervous System Disease 54 0.050
120
ISC004 Ischemia 59 0.050
121
GST071 Gastrointestinal Carcinoma 41 0.049
122
P ALP004 Alport Syndrome 68 0.049
123
ETN001 Eating Disorder 60 0.049
124
RTN023 Retinitis 49 0.049
125
c HPT001 Hepatitis C 68 0.049
126
P PLM036 Pulmonary Fibrosis 68 0.049
127
P ALG002 Alagille Syndrome 72 0.048
128
c FML311 Familial Colorectal Cancer Type X 36 0.048
129
PLY023 Polycystic Liver Disease 57 0.048
130
c GLL024 Gallbladder Disease 1 38 0.048
131
FCL044 Fecal Incontinence 35 0.048
132
FNC006 Functional Gastric Disease 34 0.048
133
NRN004 Neuroendocrine Tumor 54 0.048
134
BLN006 Blind Loop Syndrome 30 0.048
135
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.048
136
GST028 Gastric Squamous Cell Carcinoma 39 0.047
137
c INF086 Inflammatory Bowel Disease 3 21 0.047
138
P NRV006 Nervous System Cancer 62 0.047
139
P GST044 Gastritis 58 0.047
140
END035 Endocrine Gland Cancer 52 0.047
141
PRT036 Peritonitis 62 0.047
142
ALR002 Al-Raqad Syndrome 36 0.047
143
APP008 Appendicitis 60 0.047
144
END038 Endocrine Pancreas Disease 43 0.046
145
NNL002 Nonalcoholic Steatohepatitis 53 0.046
146
CHL067 Cholecystitis 56 0.046
147
P LPS004 Lupus Erythematosus 63 0.046
148
P PRT013 Portal Hypertension 59 0.046
149
ACD009 Acid-Labile Subunit, Deficiency of 48 0.046
150
c INF078 Inflammatory Bowel Disease 2 24 0.046
151
BLD054 Blood Protein Disease 40 0.046
152
BNS002 Bone Structure Disease 36 0.046
153
ALL026 Allergic Hypersensitivity Disease 53 0.046
154
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.046
155
UND009 Undifferentiated Carcinoma of Stomach 18 0.046
156
CRC038 Carcinoma of Stomach, Salivary Gland Type 15 0.046
157
NWC001 Newcastle Disease 54 0.046
158
VSC006 Vascular Cancer 54 0.046
159
c ACT027 Acute Pancreatitis 56 0.046
160
c CLR085 Colorectal Cancer 1 42 0.045
161
ANS012 Anus Disease 32 0.045
162
P SML016 Small Intestine Cancer 54 0.045
163
c SYS001 Systemic Lupus Erythematosus 87 0.045
164
ABD010 Abdominal Wall Defect 38 0.045
165
P HRS035 Hirschsprung Disease 1 59 0.045
166
ATN002 Autonomic Nervous System Disease 47 0.045
167
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.045
168
MCR094 Microvillus Inclusion Disease 51 0.045
169
c BLD124 Bleeding Disorder, Platelet-Type, 11 42 0.045
170
c RCR022 Recurrent Acute Pancreatitis 41 0.045
171
P MYC007 Myocardial Infarction 79 0.044
172
IMM136 Immune System Disease 50 0.044
173
P CNG015 Congenital Diaphragmatic Hernia 58 0.044
174
P LNG032 Lung Cancer 94 0.044
175
CTS003 Coats Disease 57 0.044
176
P SPS003 Spastic Diplegia 53 0.044
177
GLT021 Glutaricaciduria, Type I 48 0.044
178
c PNC108 Pancreatitis, Hereditary 67 0.044
179
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 34 0.044
180
c CLR075 Colorectal Cancer 3 30 0.044
181
DFC004 Deficiency Anemia 65 0.044
182
C3D001 C3 Deficiency 53 0.044
183
CHL071 Child Syndrome 58 0.044
184
P HST010 Histiocytosis 55 0.044
185
ACR041 Acromelic Frontonasal Dysostosis 46 0.044
186
BRT030 Birth Defects 43 0.044
187
P ADD001 Addison's Disease 62 0.044
188
P PRS040 Prostate Cancer 89 0.044
189
c PRK031 Parkinson Disease 1 55 0.044
190
KDS001 Kid Syndrome 53 0.044
191
CRY003 Cryptosporidiosis 46 0.043
192
c PNC094 Pancreatic Cancer 1 29 0.043
193
CND002 Conduct Disorder 56 0.043
194
CHL127 Cholangiocarcinoma, Susceptibility to 55 0.043
195
PLV003 Pelvic Inflammatory Disease 53 0.043
196
HDN004 Head and Neck Carcinoma 55 0.043
197
CRD118 Cardiovascular Cancer 47 0.043
198
c HPT003 Hepatitis a 59 0.043
199
c CRN174 Coronary Heart Disease 2 22 0.043
200
P PSD087 Pseudoxanthoma Elasticum 67 0.043
201
P CRD011 Cardiomyopathy 67 0.043
202
DDN007 Duodenal Disease 34 0.043
203
UND008 Undifferentiated Carcinoma of Esophagus 16 0.043
204
CRC037 Carcinoma of Esophagus, Salivary Gland Type 15 0.043
205
c PNC095 Pancreatic Cancer 3 32 0.043
206
VND001 Vein Disease 52 0.043
207
ACT058 Active Peptic Ulcer Disease 46 0.043
208
RSD004 Rosai-Dorfman Disease 39 0.043
209
DGS007 Digestive Duplication 8 0.043
210
DYS011 Dyskinesia of Esophagus 33 0.043
211
PHR003 Pharyngitis 58 0.042
212
TNG009 Tongue Squamous Cell Carcinoma 74 0.042
213
P NRP001 Neuropathy 60 0.042
214
PYL007 Pylorus Cancer 20 0.042
215
HYP066 Hyperglycemia 60 0.042
216
PNC048 Pancreatic Lipase Deficiency 26 0.041
217
c INF088 Inflammatory Bowel Disease 5 21 0.041
218
SQM013 Squamous Cell Carcinoma, Head and Neck 70 0.041
219
DSS008 Disease of Mental Health 55 0.041
220
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 56 0.041
221
NSD001 Nose Disease 52 0.041
222
ADM013 Adamantinoma of Long Bones 59 0.041
223
PST035 Postgastrectomy Syndrome 34 0.041
224
PLV005 Pelviureteric Junction Obstruction 45 0.041
225
c CHR096 Chronic Pulmonary Heart Disease 40 0.041
226
GLL018 Gallbladder Cancer 63 0.041
227
c CRN175 Coronary Heart Disease 4 21 0.041
228
c CLR080 Colorectal Cancer 5 35 0.041
229
c HPT016 Hepatitis B 64 0.041
230
PST030 Postcholecystectomy Syndrome 34 0.041
231
MLT021 Multiple System Atrophy 71 0.041
232
ENT006 Enterokinase Deficiency 23 0.041
233
c INF087 Inflammatory Bowel Disease 4 27 0.040
234
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 24 0.040
235
P HYP086 Hypothyroidism 65 0.040
236
c ATM011 Autoimmune Hepatitis 58 0.040
237
SPC003 Specific Developmental Disorder 40 0.040
238
P AMY004 Amyloidosis 64 0.040
239
c ACT004 Acute Diarrhea 38 0.040
240
LYS002 Lysosomal Storage Disease 52 0.040
241
ANX002 Anxiety Disorder 69 0.040
242
SQM014 Squamous Cell Carcinoma of Pancreas 19 0.040
243
c PNC111 Pancreatic Cancer 2 30 0.040
244
BLD036 Bile Duct Disease 48 0.040
245
SPL011 Spleen Cancer 37 0.040
246
P PRM006 Primary Biliary Cirrhosis 52 0.039
247
c PRM023 Pre-Malignant Neoplasm 43 0.039
248
ATM052 Autoimmune Disease 1 28 0.039
249
CRC006 Carcinoid Syndrome 51 0.039
250
c CHL120 Cholestasis, Benign Recurrent Intrahepatic 45 0.039
251
P INF032 Infertility 61 0.039
252
SKN023 Skin Tag 46 0.039
253
CRV038 Cervical Squamous Cell Carcinoma 59 0.039
254
P DDN001 Duodenal Ulcer 51 0.039
255
PRT035 Peritoneum Cancer 39 0.039
256
MDY003 Mody, Type Ii 38 0.039
257
ADN021 Adenomatous Polyposis Coli 76 0.039
258
c INF089 Inflammatory Bowel Disease 6 20 0.039
259
EXF001 Exfoliation Syndrome 57 0.039
260
P CLL015 Collagen Disease 49 0.039
261
P PLN008 Peeling Skin Syndrome 47 0.038
262
SRC014 Sarcoma 66 0.038
263
P ALX003 Alexander Disease 64 0.038
264
BLD044 Bladder Disease 51 0.038
265
P MSC003 Muscular Atrophy 51 0.038
266
TNG004 Tongue Disease 41 0.038
267
c CHL080 Cholestasis, Progressive Familial Intrahepatic 1 46 0.038
268
c PRK030 Parkinson Disease 4 39 0.038
269
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 30 0.038
270
SML014 Small Intestine Leiomyosarcoma 36 0.038
271
MLR004 Malaria 79 0.037
272
GST088 Gastric Endocrine Tumor 17 0.037
273
c CLR081 Colorectal Cancer 6 24 0.037
274
P EXP004 Exophthalmos 54 0.037
275
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.037
276
JJN004 Jejunal Atresia 28 0.037
277
SLP005 Sleep Disorder 53 0.037
278
P CHL066 Cholangitis 49 0.037
279
c AST037 Asthma 1 31 0.037
280
SCR011 Scrapie 39 0.037
281
GST037 Gastroparesis 53 0.037
282
PNC014 Pancreatic Serous Cystadenocarcinoma 22 0.037
283
c AST039 Asthma 2 31 0.037
284
OST141 Osteoclastic Giant Cell Tumor of Pancreas 11 0.037
285
APL002 Aplasia of Lacrimal and Salivary Glands 44 0.037
286
SCR037 Sucrase-Isomaltase Deficiency, Congenital 27 0.037
287
STT004 Steatorrhea 40 0.037
288
c CHL119 Cholangitis, Primary Sclerosing 33 0.037
289
GST039 Gastroduodenitis 31 0.037
290
SPC010 Speech and Communication Disorders 46 0.037
291
P ATR005 Atrophic Gastritis 45 0.037
292
ACN026 Acinar Cell Carcinoma of Pancreas 23 0.037
293
MCN020 Mucinous Cystadenocarcinoma of Pancreas 18 0.037
294
SQM015 Squamous Cell Carcinoma of Small Intestine 15 0.037
295
SLD011 Solid Pseudopapillary Carcinoma of Pancreas 11 0.037
296
P KDN017 Kidney Cancer 67 0.036
297
BLC008 Bile Acid Synthesis Defect, Congenital, 2 37 0.036
298
CNG034 Congestive Heart Failure 71 0.036
299
TRP004 Tropical Sprue 36 0.036
300
SQM016 Squamous Cell Carcinoma of Gallbladder and Extrahepatic Biliary Tract 13 0.036
301
c PRM126 Primary Peritoneal Carcinoma 54 0.036
302
P DBT083 Diabetes Mellitus, Permanent Neonatal 53 0.036
303
VSC011 Vasculitis 62 0.036
304
P LYM033 Lymphoproliferative Syndrome 53 0.036
305
MCN017 Meconium Ileus 54 0.036
306
GST040 Gastric Adenocarcinoma 52 0.036
307
PLC008 Placenta Disease 36 0.036
308
CLN015 Colon Adenocarcinoma 49 0.036
309
LCT019 Lactase Persistence/nonpersistence 18 0.036
310
LYM024 Lymphatic System Disease 50 0.036
311
KPS004 Kaposi Sarcoma 66 0.036
312
UPP004 Upper Respiratory Tract Disease 48 0.036
313
P TRM003 Tremor 54 0.036
314
HYP266 Hypoxia 55 0.036
315
BLR007 Biliary Tract Neoplasm 52 0.036
316
c PNC103 Pancreatic Cancer 4 31 0.036
317
HNS001 Hansen's Disease 29 0.036
318
DDN010 Duodenum Cancer 44 0.035
319
DRM006 Dermatitis 61 0.035
320
TNG002 Tangier Disease 61 0.035
321
UMB002 Umbilical Hernia 43 0.035
322
GNG011 Gingival Disease 51 0.035
323
c PRK045 Parkinson Disease 5 44 0.035
324
ACH005 Achalasia 54 0.035
325
P ESN007 Eosinophilia 61 0.035
326
OCL009 Ocular Cancer 62 0.035
327
ALC007 Alcohol Dependence 65 0.035
328
ESP025 Esophagus Adenocarcinoma 40 0.035
329
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 26 0.035
330
CHL068 Cholestasis 58 0.035
331
DRR004 Diarrhea 3, Secretory Sodium, Congenital, Syndromic 23 0.034
332
SLV003 Salivary Gland Disease 49 0.034
333
DRR005 Diarrhea 4, Malabsorptive, Congenital 21 0.034
334
CHR515 Chronic Atrial and Intestinal Dysrhythmia 19 0.034
335
P ART023 Arthropathy 63 0.034
336
c HYP595 Hypertension, Essential 69 0.034
337
c RNL016 Renal Infectious Disease 24 0.034
338
P LYM026 Lymphoblastic Leukemia 60 0.034
339
P GLM007 Glomerulonephritis 56 0.034
340
ANL022 Anal Fistula 42 0.034
341
ERY003 Erythema Multiforme 57 0.034
342
PNC028 Pancreatic Steatorrhea 35 0.034
343
SXL003 Sexual Disorder 47 0.034
344
GLC006 Galactosemia 67 0.034
345
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.034
346
HPY002 H. Pylori Infection 58 0.034
347
CYS039 Cystic Kidney Disease 52 0.034
348
CHR028 Chronic Wasting Disease 34 0.034
349
c CLL013 Cell Type Cancer 48 0.034
350
ADJ001 Adjustment Disorder 38 0.034
351
DNT012 Dental Caries 46 0.034
352
VSC044 Visceral Myopathy 51 0.034
353
ANG054 Angina Pectoris 51 0.034
354
c ALZ012 Alzheimer Disease 12 25 0.034
355
P INT070 Intestinal Obstruction 56 0.034
356
BRN038 Bronchial Disease 54 0.033
357
c HPT073 Hepatitis C Virus 72 0.033
358
P RTT002 Rett Syndrome 78 0.033
359
BRN106 Burns 52 0.033
360
JJN003 Jejunal Cancer 30 0.033
361
PNC118 Pancreas, Annular 27 0.033
362
THY030 Thyroid Gland Disease 51 0.033
363
LKC003 Leukocyte Disease 47 0.033
364
BHC003 Behcet Syndrome 61 0.033
365
PRN019 Perinatal Necrotizing Enterocolitis 44 0.033
366
CNG298 Congenital Pancreatic Cyst 21 0.033
367
DGS008 Digestive System Melanoma 16 0.033
368
DMY004 Demyelinating Disease 55 0.033
369
P MTC003 Metachromatic Leukodystrophy 71 0.033
370
SPN369 Spinal Disease 41 0.033
371
AMN002 Amino Acid Metabolic Disorder 48 0.033
372
INT071 Intestinal Perforation 41 0.033
373
P THL005 Thalassemia 61 0.033
374
TST021 Testicular Germ Cell Tumor 70 0.033
375
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 38 0.033
376
DGS006 Digestive Duplication Cyst of the Tongue 7 0.033
377
JNT002 Joint Disorders 56 0.033
378
CRH005 Crohn's Colitis 52 0.033
379
ZLL002 Zollinger-Ellison Syndrome 47 0.033
380
P SKN013 Skin Benign Neoplasm 46 0.033
381
P TRC086 Trichohepatoenteric Syndrome 1 46 0.033
382
P MCP010 Mucopolysaccharidosis 58 0.033
383
c HMG001 Hemoglobin C Disease 47 0.033
384
VND002 Van Der Woude Syndrome 51 0.033
385
ADN071 Adenocarcinoma of Gallbladder and Extrahepatic Biliary Tract 15 0.033
386
PRN015 Perinatal Intestinal Perforation 5 0.033
387
ATM053 Autoimmune Disease 2 19 0.033
388
HPT046 Hepatic Veno-Occlusive Disease 45 0.033
389
TBR008 Tuberculous Peritonitis 41 0.033
390
c CLR087 Colorectal Cancer 12 33 0.033
391
PRP021 Peripheral Nervous System Neoplasm 50 0.032
392
c INF074 Inflammatory Bowel Disease 15 19 0.032
393
c CLR083 Colorectal Cancer 8 27 0.032
394
ORL014 Oral Pharyngeal Disorders 14 0.032
395
THY028 Thyroid Cancer 68 0.032
396
ISL029 Isolated Anorectal Malformation 7 0.032
397
STM007 Stomatitis 50 0.032
398
PRS042 Prostate Disease 52 0.032
399
c ACT134 Acute Liver Failure 50 0.032
400
c ATM024 Autoimmune Pancreatitis 46 0.032
401
BLD034 Bile Duct Carcinoma 55 0.032
402
P MDL005 Medulloblastoma 77 0.032
403
SCR035 Sacral Agenesis with Vertebral Anomalies 33 0.032
404
P MSC005 Muscular Dystrophy 64 0.032
405
ORL004 Oral Submucous Fibrosis 51 0.032
406
WLL006 Wells Syndrome 56 0.032
407
P SHR029 Short Syndrome 60 0.032
408
MGC001 Megacolon 50 0.032
409
TTH001 Tooth Ankylosis 39 0.032
410
EMB004 Embryonal Carcinoma 56 0.032
411
GNR004 Generalized Anxiety Disorder 51 0.032
412
LYM023 Lymphatic System Cancer 35 0.032
413
BLC007 Bile Acid Synthesis Defect, Congenital, 1 30 0.032
414
ADN018 Adenoma 59 0.031
415
GDS001 Good Syndrome 45 0.031
416
FNC002 Functional Diarrhea 38 0.031
417
GLC022 Glucose/galactose Malabsorption 38 0.031
418
P RNL014 Renal Cell Carcinoma 81 0.031
419
c VRL010 Viral Hepatitis 61 0.031
420
c INF073 Inflammatory Bowel Disease 12 21 0.031
421
WST001 West Syndrome 61 0.031
422
ISL001 Islet Cell Tumor 50 0.031
423
TXC005 Toxic Shock Syndrome 61 0.031
424
OVR063 Overnutrition 49 0.031
425
RDT013 Radiation Proctitis 43 0.031
426
c SCN046 Secondary Short Bowel Syndrome 15 0.031
427
PRD011 Proud Syndrome 42 0.031
428
BRR002 Barrett's Adenocarcinoma 45 0.031
429
EWN003 Ewing Sarcoma 64 0.031
430
P DBT005 Diabetes Insipidus 53 0.031
431
P ATM020 Autoimmune Enteropathy 38 0.031
432
c HRD101 Hereditary Mixed Polyposis Syndrome 1 37 0.031
433
ART016 Aortic Aneurysm 67 0.031
434
ATM054 Autoimmune Disease 3 18 0.031
435
LRY017 Laryngeal Disease 37 0.030
436
c INF068 Inflammatory Bowel Disease 13 24 0.030
437
ATR076 Atrophic Muscular Disease 18 0.030
438
ATP002 Atopy 63 0.030
439
c NMN013 Niemann-Pick Disease, Type a 57 0.030
440
HYP082 Hypopharynx Cancer 45 0.030
441
P ORL007 Oral Cavity Cancer 58 0.030
442
PRC002 Paracoccidioidomycosis 55 0.030
443
LYS003 Lysinuric Protein Intolerance 50 0.030
444
c DLT002 Dilated Cardiomyopathy 75 0.030
445
RPR002 Reproductive System Disease 46 0.030
446
DRR008 Diarrhea 1, Secretory Chloride, Congenital 43 0.030
447
MND006 Mondor Disease 21 0.030
448
c CLC045 Celiac Disease 2 18 0.030
449
c MYC058 Myocardial Infarction 2 29 0.030
450
ADR012 Adrenal Gland Disease 49 0.030
451
MCC003 Mucocele of Salivary Gland 21 0.030
452
P HYP076 Hyperthyroidism 56 0.030
453
MCR191 Microscopic Colitis 47 0.030
454
RFR013 Refractory Celiac Disease 33 0.030
455
ABL002 Ablepharon-Macrostomia Syndrome 57 0.030
456
c CHR086 Chronic Conjunctivitis 46 0.030
457
INT002 Intermittent Claudication 56 0.030
458
P CHR345 Chronic Pain 49 0.030
459
APP010 Appendix Cancer 40 0.030
460
P GST047 Gastrointestinal Neuroendocrine Tumor 39 0.030
461
MCK002 Meckel's Diverticulum 36 0.030
462
END077 Endocrine Tumor of Colon 14 0.030
463
WLM001 Wolman Disease 56 0.030
464
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 46 0.030
465
ANG011 Angiodysplasia 44 0.030
466
c CHL082 Cholestasis, Progressive Familial Intrahepatic 3 46 0.030
467
ILM001 Ileum Cancer 27 0.030
468
SLD003 Sialadenitis 48 0.030
469
FXF002 Fox-Fordyce Disease 39 0.030
470
OBS015 Obesity, Hyperphagia, and Developmental Delay 46 0.030
471
P ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 60 0.029
472
PLS009 Plasma Cell Neoplasm 48 0.029
473
MSC072 Muscle Cancer 51 0.029
474
TRH001 Trehalase Deficiency 17 0.029
475
PYL003 Pyloric Antrum Cancer 13 0.029
476
P SCL009 Sclerosing Cholangitis 47 0.029
477
ORL015 Oral Squamous Cell Carcinoma 56 0.029
478
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 76 0.029
479
P ASP006 Aspergillosis 60 0.029
480
BRC012 Brucellosis 65 0.029
481
INT051 Intussusception 50 0.029
482
P AML002 Amelogenesis Imperfecta 43 0.029
483
GRM001 Germ Cell and Embryonal Cancer 39 0.029
484
VNT001 Ventilation Pneumonitis 37 0.029
485
P OST012 Osteoarthritis 82 0.029
486
FNC012 Functioning Pancreatic Endocrine Tumor 16 0.029
487
PRD004 Prediabetes Syndrome 43 0.029
488
c DRR009 Diarrhea 6 31 0.029
489
VSC047 Vascular Malformation 45 0.029
490
VSC009 Vascular Skin Disease 22 0.029
491
INT007 Intermediate Coronary Syndrome 52 0.029
492
HPT014 Hepatorenal Syndrome 46 0.029
493
SNS023 Sensory System Cancer 46 0.029
494
GST063 Gastric Cancer Risk After H. Pylori Infection 53 0.029
495
DMP001 Dumping Syndrome 42 0.029
496
HRT007 Heart Cancer 50 0.029
497
ALC009 Alcoholic Liver Cirrhosis 48 0.029
498
LPD027 Lip Disease 36 0.029
499
P HRD018 Hair Disease 50 0.029
500
PRN011 Pernicious Anemia 46 0.029
501
P CWD006 Cowden Syndrome 1 68 0.029
502
P LKD001 Leukodystrophy 58 0.029
503
c DLT001 Delta Chain Disease 16 0.028
504
P HRT017 Heart Tumor 35 0.028
505
c ADL079 Adult Heart Tumor 19 0.028
506
P INT143 Interstitial Cystitis 57 0.028
507
ESN005 Eosinophilic Gastroenteritis 49 0.028
508
P DRM007 Dermatitis Herpetiformis 46 0.028
509
c ACT068 Acute Cystitis 50 0.028
510
THR035 Thrombasthenia 42 0.028
511
DYS015 Dysentery 41 0.028
512
P LRY019 Laryngitis 55 0.028
513
ADT003 Auditory System Disease 51 0.028
514
CHR008 Choroiditis 43 0.028
515
c INT072 Intestinal Pseudo-Obstruction 46 0.028
516
SLC005 Selective Iga Deficiency Disease 39 0.028
517
P CRV031 Cervical Adenocarcinoma 52 0.028
518
IRN001 Iron Deficiency Anemia 51 0.028
519
P TCL004 T-Cell Leukemia 46 0.028
520
AYM001 Ayme-Gripp Syndrome 45 0.028
521
c DRR007 Diarrhea 7 33 0.028
522
P MLT074 Multiple Endocrine Neoplasia 55 0.028
523
ADL002 Adult Syndrome 53 0.028
524
PRT030 Parathyroid Gland Disease 49 0.028
525
P HYP060 Hyperinsulinism 59 0.028
526
c OPT053 Optic Atrophy 1 46 0.028
527
c DYS166 Dysautonomia, Familial 50 0.028
528
MLT001 Multiple Chemical Sensitivity 43 0.028
529
P PRP029 Porphyria 58 0.027
530
PRD003 Periodontosis 41 0.027
531
PLS002 Peliosis Hepatis 31 0.027
532
PLP001 Pulpitis 47 0.027
533
c RTN162 Retinitis Pigmentosa 2 51 0.027
534
P HYP027 Hypobetalipoproteinemia 52 0.027
535
CLR109 Colorectal Adenocarcinoma 50 0.027
536
c AML016 Amelogenesis Imperfecta, Type 1e 24 0.027
537
c CLR082 Colorectal Cancer 7 23 0.027
538
P MYL005 Myelofibrosis 67 0.027
539
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.027
540
P FML035 Familial Hyperlipidemia 50 0.027
541
ENT001 Enterocele 41 0.027
542
P TRM004 Trimethylaminuria 40 0.027
543
GLS007 Glossitis 44 0.027
544
HTS001 Hiatus Hernia 38 0.027
545
GST095 Gastritis, Familial Giant Hypertrophic 27 0.027
546
c PRK037 Parkinson Disease 13 28 0.027
547
c THR092 Thrombophilia Due to Thrombin Defect 56 0.027
548
P SLV002 Salivary Gland Cancer 61 0.027
549
PSD007 Pseudomyxoma Peritonei 47 0.027
550
c AML044 Amelogenesis Imperfecta, Type Ig 27 0.027
551
c AML020 Amelogenesis Imperfecta, Type Iv 27 0.027
552
SCH014 Schistosomiasis 58 0.027
553
GGR001 Geographic Tongue 44 0.027
554
CHL052 Choledochal Cyst 40 0.027
555
c GLL027 Gallbladder Disease 4 25 0.027
556
LYM116 Lymph Node Disease 44 0.027
557
P STR035 Streptococcal Group a Invasive Disease 18 0.027
558
MNT001 Mantle Cell Lymphoma 70 0.027
559
P PLR004 Pleuropulmonary Blastoma 64 0.027
560
P SPN301 Spinocerebellar Ataxia 2 63 0.027
561
c INF090 Inflammatory Bowel Disease 7 19 0.027
562
ANS011 Anus Cancer 44 0.027
563
P HYP014 Hyperuricemia 50 0.026
564
P AGN002 Agnosia 56 0.026
565
ATM033 Autoimmune Polyendocrinopathy Syndrome , Type I, with or Without Reversible Metaphyseal Dysplasia 51 0.026
566
c ADL017 Adult T-Cell Leukemia 58 0.026
567
P MTC069 Mitochondrial Disorders 52 0.026
568
GNG012 Gingival Overgrowth 52 0.026
569
GNG003 Gingival Recession 38 0.026
570
ANS003 Anisakiasis 37 0.026
571
c NRP031 Neuropathy, Hereditary Sensory and Autonomic, Type Vii 22 0.026
572
P INT001 Intrahepatic Cholestasis 57 0.026
573
P DNT011 Dentinogenesis Imperfecta 42 0.026
574
HYP021 Hypercementosis 31 0.026
575
GLT030 Gluten Allergy 20 0.026
576
CRR007 Cirrhosis, Cryptogenic 44 0.026
577
DCH001 Duchenne Muscular Dystrophy 80 0.026
578
MXD023 Mixed Cell Type Cancer 47 0.026
579
APH002 Aphasia 53 0.026
580
TTH002 Tooth Agenesis 55 0.026
581
c CHR013 Chronic Apical Periodontitis 29 0.026
582
TTH005 Teeth Hard Tissue Disease 28 0.026
583
MLK004 Malakoplakia 27 0.026
584
MNR003 Mineral Metabolism Disease 41 0.026
585
ESP020 Esophageal Atresia 49 0.026
586
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 43 0.026
587
P DNT009 Dentin Dysplasia 37 0.026
588
MYC015 Mycobacterium Fortuitum 27 0.026
589
P OST005 Osteogenesis Imperfecta 67 0.026
590
MYL020 Myelomeningocele 50 0.026
591
PNC013 Pancreatic Ductal Carcinoma 47 0.026
592
P PNC045 Pancreatic Agenesis 44 0.026
593
RCT011 Rectal Prolapse 43 0.026
594
INT111 Intestinal Pseudoobstruction, Neuronal 28 0.026
595
PRS036 Parasitic Protozoa Infectious Disease 45 0.026
596
P FRC002 Fructose Intolerance 53 0.026
597
AND001 Anodontia 41 0.026
598
PRL008 Paralytic Ileus 39 0.026
599
MYX011 Myxozoa 16 0.026
600
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 44 0.026
601
EPD045 Epidermolysis Bullosa, Junctional, with Pyloric Stenosis 37 0.026
602
DNT001 Dental Fluorosis 43 0.025
603
P HYP009 Hypertrophic Pyloric Stenosis 41 0.025
604
PNC008 Pancreatic Endocrine Carcinoma 39 0.025
605
NTM001 Nutmeg Liver 31 0.025
606
SLL001 Sialolithiasis 30 0.025
607
PRM205 Primary Hepatic Neuroendocrine Carcinoma 28 0.025
608
ANR003 Anorectal Stricture 13 0.025
609
P NPH009 Nephrolithiasis 60 0.025
610
P MSC007 Muscle Hypertrophy 59 0.025
611
TRN003 Transverse Colon Cancer 43 0.025
612
AMP003 Ampulla of Vater Neoplasm 36 0.025
613
SPP003 Suppurative Periapical Periodontitis 33 0.025
614
ORL019 Oral Hairy Leukoplakia 33 0.025
615
ATR073 Atrophic Glossitis 31 0.025
616
OTD001 Otodental Dysplasia 25 0.025
617
DNT041 Dentin Dysplasia, Type I, with Microdontia and Misshapen Teeth 25 0.025
618
FLR007 Failure of Tooth Eruption, Primary 23 0.025
619
PLY114 Polyglucosan Body Myopathy 2 16 0.025
620
c SRC025 Sarcoidosis 1 58 0.025
621
ATM015 Autoimmune Disease of Gastrointestinal Tract 34 0.025
622
IMM107 Immunodeficiency 31c, Autosomal Dominant 27 0.025
623
PRP016 Paraplegia 49 0.025
624
MCR037 Macroglossia 45 0.025
625
FSS001 Fissured Tongue 34 0.025
626
MDN001 Median Rhomboid Glossitis 28 0.025
627
HPT081 Hepatic Infarction 24 0.025
628
ULC002 Ulcer of Anus and Rectum 11 0.025
629
P HYP117 Hypertriglyceridemia 65 0.025
630
ORL011 Oral Cancer 55 0.025
631
PLY056 Polyposis, Juvenile Intestinal 55 0.025
632
P END044 Endometriosis 53 0.025
633
ATN011 Autoinflammation with Infantile Enterocolitis 41 0.025
634
c HYP615 Hyperparathyroidism, Familial Primary 55 0.025
635
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.025
636
P MYT002 Myotonic Dystrophy 47 0.025
637
INT052 Intestinal Volvulus 36 0.025
638
DNT006 Dental Pulp Necrosis 26 0.025
639
CSC001 Cascade Stomach 18 0.025
640
c CHR465 Chronic Diarrhea Due to Guanylate Cyclase 2c Overactivity 9 0.025
641
MYC033 Myoclonus 41 0.025
642
CHR103 Charge Syndrome 64 0.025
643
NSY001 N Syndrome 39 0.025
644
P HRD008 Hereditary Hemorrhagic Telangiectasia 71 0.025
645
ALC006 Alcoholic Hepatitis 59 0.025
646
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.025
647
c PLN018 Peeling Skin Syndrome 2 35 0.025
648
CLN044 Colon Adenoma 45 0.025
649
FSH003 Fish Allergy 30 0.025
650
NRG001 Neurogenic Bowel 30 0.025
651
BLR028 Biliary Atresia, Extrahepatic 26 0.025
652
P ACT046 Acute Apical Periodontitis 16 0.025
653
PLP002 Pulp Degeneration 13 0.025
654
HYD004 Hydrops of Gallbladder 12 0.025
655
CNG479 Congenital Secretory Sodium Diarrhea 8 11 0.025
656
HYP049 Hypertrophy of Tongue Papillae 10 0.025
657
PRT011 Protein C Deficiency 51 0.025
658
SPL018 Splenomegaly 44 0.025
659
GLC003 Glucose Intolerance 55 0.025
660
PLM012 Pulmonary Sarcoidosis 54 0.025
661
GNR003 Generalized Atherosclerosis 38 0.025
662
c INF083 Inflammatory Bowel Disease 24 19 0.025
663
HYP056 Hypoglycemia 61 0.025
664
c OPT055 Optic Atrophy Plus Syndrome 54 0.025
665
APR001 Apraxia 48 0.025
666
P BRN120 Bronchus Cancer 46 0.025
667
VGN023 Vaginitis 42 0.025
668
RTR011 Retroperitoneal Fibrosis 38 0.025
669
GST026 Gastric Fundus Cancer 20 0.025
670
PNC040 Pancreatic Delta Cell Neoplasm 16 0.025
671
VSC014 Vascular Hyalinosis 16 0.025
672
GST087 Gastric Linitis Plastica 15 0.025
673
ALC012 Alcoholic Gastritis 14 0.025
674
PRF001 Perforation of Bile Duct 13 0.025
675
CHL004 Cholelithiasis 48 0.025
676
SHG001 Shigellosis 53 0.025
677
c BRN108 Branchiootic Syndrome 1 36 0.025
678
c CHL081 Cholestasis, Progressive Familial Intrahepatic 2 43 0.024
679
DSC005 Descending Colon Cancer 32 0.024
680
BLR004 Biliary Dyskinesia 30 0.024
681
GST025 Gastric Body Carcinoma 19 0.024
682
OCC004 Occlusion of Gallbladder 16 0.024
683
ANL005 Anal Spasm 16 0.024
684
STR003 Strawberry Gallbladder 9 0.024
685
IDP068 Idiopathic Malabsorption Due to Bile Acid Synthesis Defects 5 0.024
686
P CSH001 Cushing's Syndrome 64 0.024
687
PLS011 Plasmacytoma 56 0.024
688
NRL016 Neural Tube Defects 76 0.024
689
ATN004 Autonomic Neuropathy 44 0.024
690
c CNG031 Congenital Nervous System Abnormality 39 0.024
691
AMB001 Amebiasis 42 0.024
692
CLN004 Colon Carcinoma in Situ 35 0.024
693
GST038 Gastrointestinal Adenoma 29 0.024
694
RCT008 Rectosigmoid Junction Neoplasm 23 0.024
695
ACC005 Accessory Pancreas 19 0.024
696
LVR003 Liver Carcinoma in Situ 14 0.024
697
HST011 Histoplasmosis 54 0.024
698
P CNN004 Connective Tissue Cancer 45 0.024
699
CRD119 Cardiac Arrest 63 0.024
700
P SJG001 Sjogren's Syndrome 53 0.024
701
CHL050 Cholesterol Ester Storage Disease 37 0.024
702
BRN056 Bronchopulmonary Dysplasia 49 0.024
703
c SML023 Small Cell Lung Cancer, Adult 17 0.024
704
ASC004 Ascending Colon Cancer 32 0.024
705
P EPD025 Epidermolysis Bullosa with Pyloric Atresia 32 0.024
706
CCL003 Cecal Benign Neoplasm 25 0.024
707
RCT023 Rectum Squamous Cell Carcinoma 23 0.024
708
SPL003 Splenic Flexure Cancer 19 0.024
709
HPT005 Hepatic Flexure Cancer 16 0.024
710
END073 Endocrine Tumor of the Appendix 14 0.024
711
P ABD016 Abdominal Obesity-Metabolic Syndrome 26 0.024
712
P SHR001 Short Bowel Syndrome 48 0.024
713
PRR002 Pure Red-Cell Aplasia 46 0.024
714
c PLN021 Peeling Skin Syndrome 3 31 0.024
715
P HMN010 Hemangioma 60 0.024
716
MRB003 Morbid Obesity 58 0.024
717
BTN003 Biotinidase Deficiency 56 0.024
718
PLM010 Pulmonary Edema 56 0.024
719
IMG001 Image Syndrome 55 0.024
720
P CYS018 Cystitis 53 0.024
721
CHC001 Chickenpox 52 0.024
722
P PRM016 Primary Optic Atrophy 32 0.024
723
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 23 0.024
724
ANK008 Ankyloglossia 29 0.024
725
RCT010 Rectum Carcinoma in Situ 14 0.024
726
GLL031 Gallbladder Endocrine Tumor 14 0.024
727
HGH026 High Anorectal Malformation 13 0.024
728
EPT026 Epithelio-Exfoliative Colitis-Deafness Syndrome 4 0.024
729
CNG363 Congenital Enterocyte Heparan Sulfate Deficiency 4 0.024
730
P GLM045 Glioma 58 0.024
731
HPT019 Hepatic Encephalopathy 56 0.024
732
c INV001 Invasive Aspergillosis 47 0.024
733
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 32 0.024
734
WRN001 Werner Syndrome 67 0.023
735
P LYM007 Lymphangioleiomyomatosis 65 0.023
736
NDL013 Nodular Regenerative Hyperplasia 49 0.023
737
MYC017 Mycobacterium Kansasii 40 0.023
738
ABT001 Abetalipoproteinemia 60 0.023
739
P MTH033 Methylmalonic Aciduria, Vitamin B12-Responsive 53 0.023
740
DSS009 Disseminated Intravascular Coagulation 51 0.023
741
NSL022 Nasal Cavity Disease 42 0.023
742
ILT001 Ileitis 49 0.023
743
P CHR084 Chromosomal Disease 37 0.023
744
HPT020 Hepatic Vascular Disease 44 0.023
745
GRD001 Giardiasis 40 0.023
746
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 15 0.023
747
LWN002 Low Anorectal Malformation 10 0.023
748
INT254 Intermediate Anorectal Malformation 8 0.023
749
DSP001 Displacement of Cardia Through Esophageal Hiatus 7 0.023
750
CNG480 Congenital Diarrhea 7 with Exudative Enteropathy 6 0.023
751
HYP080 Hypogonadism 54 0.023
752
MTB004 Metabolic Acidosis 48 0.023
753
BCT015 Bacteremia 48 0.023
754
P FCS002 Fucosidosis 57 0.023
755
RSC001 Rosacea 53 0.023
756
CCC002 Coccidiosis 49 0.023
757
STR008 Strongyloidiasis 50 0.023
758
MYC013 Mycobacterium Abscessus 40 0.023
759
P FRG001 Fragile X Syndrome 68 0.023
760
P PRT010 Parathyroid Carcinoma 62 0.023
761
DVR002 Diverticulitis 47 0.023
762
HRN022 Hearing Loss/deafness 25 0.023
763
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 45 0.023
764
c CLC048 Celiac Disease 3 22 0.023
765
GND003 Gonadal Disease 43 0.023
766
TRC003 Trichomoniasis 41 0.023
767
BLD087 Bladder Cancer, Somatic 67 0.023
768
PRS034 Parasitic Helminthiasis Infectious Disease 42 0.022
769
c OPT059 Optic Atrophy 4 19 0.022
770
CCT002 Cicatricial Pemphigoid 51 0.022
771
PTT037 Pituitary Tumors 45 0.022
772
MKL001 Mikulicz Disease 28 0.022
773
VTM002 Vitamin B12 Deficiency 44 0.022
774
PPL022 Papilloma 55 0.022
775
BRD001 Brody Myopathy 49 0.022
776
CHL056 Cheilitis 45 0.022
777
LYM020 Lymph Node Cancer 41 0.022
778
PRC003 Proctitis 43 0.022
779
ESN017 Eosinophilic Granuloma 34 0.022
780
HPT077 Hepatic Venoocclusive Disease with Immunodeficiency 27 0.022
781
BLR001 Biliary Atresia 51 0.022
782
CHR003 Cherubism 50 0.022
783
P MWT001 Mowat-Wilson Syndrome 46 0.022
784
BHR001 Behr Syndrome 44 0.022
785
c VRL005 Viral Pneumonia 42 0.022
786
c OPT023 Optic Atrophy 2 27 0.022
787
P HMR005 Hemorrhoid 48 0.022
788
SCB001 Scabies 45 0.022
789
CNG035 Congenital Bilateral Absence of Vas Deferens 36 0.022
790
PRT038 Protein-Energy Malnutrition 49 0.022
791
c CLC037 Celiac Disease 4 22 0.022
792
NRG002 Neurogenic Bladder 50 0.022
793
MTC016 Mitochondrial Neurogastrointestinal Encephalopathy Disease 23 0.022
794
P HLP001 Holoprosencephaly 62 0.022
795
P BRN009 Burning Mouth Syndrome 57 0.022
796
P DGR001 Digeorge Syndrome 52 0.022
797
SWN001 Swine Influenza 37 0.022
798
c OPT025 Optic Atrophy 6 22 0.022
799
c FML053 Familial Colorectal Cancer 50 0.022
800
CRD003 Cardiac Sarcoidosis 43 0.022
801
c PRS116 Prostate Cancer 1 41 0.022
802
GST090 Gastroduodenal Crohn's Disease 25 0.022
803
ANT024 Anthrax Disease 48 0.021
804
ACH037 Achalasia-Addisonianism-Alacrimia Syndrome 45 0.021
805
EPD015 Epidemic Typhus 44 0.021
806
PRM236 Primary Biliary Cholangitis 43 0.021
807
c CNN010 Connective Tissue Benign Neoplasm 35 0.021
808
c OPT057 Optic Atrophy 7 29 0.021
809
c CHL118 Cholestasis, Benign Recurrent Intrahepatic, 2 28 0.021
810
c MLT094 Multiple Sclerosis 3 26 0.021
811
c OPT024 Optic Atrophy 5 20 0.021
812
c ATM064 Autoimmune Pancreatitis Type 1 19 0.021
813
c AML050 Amelogenesis Imperfecta, Type if 18 0.021
814
ANG020 Angiosarcoma 52 0.021
815
PYC001 Pycnodysostosis 49 0.021
816
TRC023 Trichinosis 43 0.021
817
GST093 Gastrointestinal Defects and Immunodeficiency Syndrome 42 0.021
818
PRP056 Porphyria, Acute Hepatic 37 0.021
819
c INF095 Inflammatory Bowel Disease 25, Early Onset, Autosomal Recessive 33 0.021
820
P GNR027 Generalized Peeling Skin Syndrome 22 0.021
821
c CLC040 Celiac Disease 6 18 0.021
822
c AML048 Amelogenesis Imperfecta, Type Ih 18 0.021
823
c ATM063 Autoimmune Pancreatitis Type 2 14 0.021
824
GRN009 Granulomatous Hepatitis 38 0.021
825
FSC002 Fascioliasis 38 0.021
826
OST115 Osteonecrosis of the Jaw 37 0.021
827
ACL001 Acalculous Cholecystitis 36 0.021
828
MCN001 Mucinous Adenocarcinoma 50 0.021
829
IMP005 Impotence 50 0.021
830
PRN039 Paraneoplastic Syndromes 33 0.021
831
CMM005 Common Cold 58 0.021
832
KLN001 Klinefelter's Syndrome 55 0.021
833
CMP002 Campylobacteriosis 47 0.021
834
HYL004 Hyaline Fibromatosis Syndrome 39 0.021
835
JJN008 Jejunoileitis 37 0.021
836
LRY004 Laryngotracheitis 28 0.021
837
INT079 Intrahepatic Cholangiocarcinoma 55 0.021
838
DBT010 Diabetic Neuropathy 55 0.021
839
P PRC019 Precocious Puberty 51 0.021
840
c NRP042 Neuropathy, Hereditary Sensory and Autonomic, Type Ii 43 0.021
841
PRM026 Primary Systemic Mycosis 41 0.021
842
HYP189 Hypoadrenalism 40 0.021
843
TXC001 Toxic Megacolon 28 0.021
844
HYP160 Hyperkeratosis Lenticularis Perstans 23 0.021
845
TNG003 Tongue Cancer 60 0.021
846
BLM002 Bulimia Nervosa 54 0.021
847
IMP002 Imperforate Anus 52 0.021
848
MLK006 Milk Allergy 44 0.021
849
HPT004 Hepatic Coma 40 0.021
850
ADR005 Adrenal Carcinoma 56 0.021
851
FBR019 Fibromatosis 42 0.021
852
HPT067 Hepatocellular Adenoma 42 0.021
853
c CLL012 Cell Type Benign Neoplasm 41 0.021
854
ILC002 Ileocolitis 38 0.021
855
c AML047 Amelogenesis Imperfecta, Type Ia 19 0.021
856
PRT026 Parotitis 42 0.021
857
ANG002 Angiostrongyliasis 39 0.021
858
PNM003 Pneumatosis Cystoides Intestinalis 31 0.021
859
ELS002 Elastosis Perforans Serpiginosa 28 0.021
860
c CLR078 Colorectal Cancer 11 20 0.021
861
c CLC046 Celiac Disease 5 18 0.021
862
P ATS007 Autism Spectrum Disorder 64 0.021
863
LYM022 Lymphangioma 54 0.021
864
HPT022 Hepatoblastoma 53 0.021
865
DCB001 Decubitus Ulcer 44 0.021
866
ISC015 Ischemic Colitis 40 0.021
867
c OST147 Osteoarthritis 1 33 0.021
868
c CLR077 Colorectal Cancer 10 31 0.021
869
PNC033 Pancreas Adenocarcinoma 55 0.020
870
P ESP035 Esophagitis, Eosinophilic, 1 42 0.020
871
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 37 0.020
872
c ALG016 Alagille Syndrome 2 29 0.020
873
PND004 Pandas 28 0.020
874
c CLR084 Colorectal Cancer 9 20 0.020
875
P CLR108 Colorectal Adenoma 60 0.020
876
RYN003 Reynolds Syndrome 49 0.020
877
NRM004 Neuroma 48 0.020
878
URT031 Ureteral Disease 47 0.020
879
c GST048 Gastrointestinal System Benign Neoplasm 41 0.020
880
CWM001 Cow Milk Allergy 40 0.020
881
c AML017 Amelogenesis Imperfecta, Type Ib 22 0.020
882
c AML019 Amelogenesis Imperfecta, Type Iii 21 0.020
883
c AML018 Amelogenesis Imperfecta, Type Ic 20 0.020
884
c CLC041 Celiac Disease 7 17 0.020
885
SNG010 Single Median Maxillary Central Incisor 53 0.020
886
PYL006 Pyloric Stenosis 46 0.020
887
P ENC011 Encephalomyopathy 34 0.020
888
CCL002 Cecal Disease 31 0.020
889
c LVR028 Liver Failure, Transient Infantile 25 0.020
890
c CLC039 Celiac Disease 13 20 0.020
891
c GLL025 Gallbladder Disease 2 19 0.020
892
c GLL026 Gallbladder Disease 3 19 0.020
893
INF047 Infantile Free Sialic Acid Storage Disease 13 0.020
894
MRS001 Marasmus 39 0.020
895
P WHT013 White Sponge Nevus 1 38 0.020
896
MCR020 Microsporidiosis 38 0.020
897
ADR010 Adrenal Cortical Hypofunction 38 0.020
898
CLN022 Colonic Atresia 24 0.020
899
c CNT075 Central Precocious Puberty 53 0.020
900
P ACT150 Acute Adrenal Insufficiency 45 0.020
901
RCH001 Richter's Syndrome 44 0.020
902
c HRD012 Hereditary Elliptocytosis 41 0.020
903
c PRD030 Periodontitis 1, Juvenile 35 0.020
904
INT050 Intestinal Impaction 31 0.020
905
BLC009 Bile Acid Synthesis Defect, Congenital, 4 26 0.020
906
c CWD005 Cowden Syndrome 4 23 0.020
907
EXT011 Extrapyramidal and Movement Disease 15 0.020
908
P SLV001 Silver-Russell Syndrome 54 0.020
909
EXT010 Extramedullary Plasmacytoma 49 0.020
910
MYL013 Myeloperoxidase Deficiency 46 0.020
911
ULC007 Ulcerative Stomatitis 44 0.020
912
LCH001 Leech Infestation 37 0.020
913
HRS037 Hirschsprung Disease with Type D Brachydactyly 16 0.020
914
UND004 Undetermined Colitis 9 0.020
915
P LRY044 Larynx Cancer 59 0.020
916
ORP003 Oropharynx Cancer 47 0.020
917
SML036 Small Intestinal Adenocarcinoma 45 0.020
918
DRM013 Dermoid Cyst 43 0.020
919
PRS115 Prosthetic Joint Infection 43 0.020
920
MLL001 Molluscum Contagiosum 41 0.020
921
BLD032 Bile Duct Adenocarcinoma 40 0.020
922
FTT003 Fatty Acid Oxidation Disorders 38 0.020
923
HYP064 Hypogonadotropism 38 0.020
924
DDN009 Duodenal Obstruction 32 0.020
925
VGS001 Vagus Nerve Disease 20 0.020
926
c SLV006 Salivary Gland Cancer, Adult 14 0.020
927
HRS003 Hirschsprung Disease Ganglioneuroblastoma 14 0.020
928
P KLL001 Kallmann Syndrome 60 0.020
929
MYC005 Myocardial Stunning 44 0.020
930
LVR002 Liver Angiosarcoma 44 0.020
931
CMM007 Common Bile Duct Disease 26 0.020
932
c INF145 Infantile Liver Failure Syndrome 1 21 0.020
933
STT041 Stuttering 48 0.019
934
INT017 Intestinal Schistosomiasis 46 0.019
935
TRP008 Tropical Calcific Pancreatitis 42 0.019
936
TTH008 Tooth Resorption 38 0.019
937
RTC003 Root Caries 37 0.019
938
c CNG413 Congenital Short Bowel Syndrome 36 0.019
939
LNT001 Linitis Plastica 32 0.019
940
BLD019 Bile Duct Cystadenocarcinoma 32 0.019
941
c SCN059 Secondary Sclerosing Cholangitis 19 0.019
942
c MWT002 Mowat-Wilson Syndrome Due to Monosomy 2q22 9 0.019
943
c MLG068 Malignant Glioma 50 0.019
944
IPX001 Ipex Syndrome 45 0.019
945
GST030 Gastrinoma 41 0.019
946
PRV003 Perivascular Epithelioid Cell Tumor 39 0.019
947
NCR003 Necrotizing Sialometaplasia 34 0.019
948
DVR006 Diversion Colitis 32 0.019
949
ULC008 Ulcerative Proctitis 23 0.019
950
LCT013 Lactase Deficiency, Congenital 22 0.019
951
STR032 Steroid Dehydrogenase Deficiency Dental Anomalies 11 0.019
952
AZS001 Azoospermia 48 0.019
953
MTY001 Mutyh-Associated Polyposis 47 0.019
954
CVR006 Cavernous Hemangioma 46 0.019
955
GNT001 Giant Cell Reparative Granuloma 42 0.019
956
SQM002 Squamous Cell Papilloma 41 0.019
957
DNT008 Denture Stomatitis 39 0.019
958
SPP004 Suppurative Cholangitis 33 0.019
959
PNC019 Pancreatoblastoma 32 0.019
960
ANL014 Anal Canal Adenocarcinoma 30 0.019
961
LYM035 Lymphangiectasis 28 0.019
962
BRW006 Brown Syndrome 26 0.019
963
P PLM064 Pulmonary Sequestration 26 0.019
964
BLC011 Bile Acid Synthesis Defect, Congenital, 3 25 0.019
965
P LYM124 Lymphangiectasia, Intestinal 25 0.019
966
HPT066 Hepatoportal Sclerosis 20 0.019
967
c DNT044 Dentinogenesis Imperfecta, Shields Type Iii 18 0.019
968
IGG016 Igg4-Related Dacryoadenitis and Sialadenitis 17 0.019
969
HRS039 Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 14 0.019
970
c ATM071 Autoimmune Enteropathy Type 2 9 0.019
971
c MWT004 Mowat-Wilson Syndrome Due to a Zeb2 Point Mutation 7 0.019
972
THR009 Thrombocytopenia-Absent Radius Syndrome 54 0.019
973
PRV006 Pervasive Developmental Disorder 50 0.019
974
KLT001 Klatskin's Tumor 42 0.019
975
P BNG071 Benign Schwannoma 37 0.019
976
TTH007 Tooth Erosion 35 0.019
977
c DNT027 Dentin Dysplasia, Type Ii 32 0.019
978
ACH015 Achalasia, Familial Esophageal 28 0.019
979
GRN011 Granulomatous Gastritis 27 0.019
980
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 25 0.019
981
CRB090 Cerebral Hypoxia 48 0.019
982
SGN002 Signet Ring Cell Adenocarcinoma 45 0.019
983
P FBR084 Fibromatosis, Gingival, 1 43 0.019
984
SMT002 Smooth Muscle Tumor 41 0.019
985
SKN022 Skin Squamous Cell Carcinoma 41 0.019
986
CRV068 Cervical Polyp 41 0.019
987
APP009 Appendix Adenocarcinoma 40 0.019
988
NNF001 Non-Functioning Pancreatic Endocrine Tumor 38 0.019
989
PRP017 Periapical Periodontitis 36 0.019
990
ALC005 Alcoholic Pancreatitis 36 0.019
991
GBL002 Goblet Cell Carcinoid 33 0.019
992
VGN019 Vaginal Discharge 33 0.019
993
JJN007 Jejunal Adenocarcinoma 29 0.019
994
ASC003 Ascending Cholangitis 29 0.019
995
IGG014 Igg4-Related Sclerosing Cholangitis 25 0.019
996
CHL075 Cheilitis Glandularis 21 0.019
997
SLT007 Solitary Rectal Ulcer Syndrome 20 0.019
998
P FML321 Familial Stomach Cancer 16 0.019
999
MPV001 Mpv17-Related Hepatocerebral Mitochondrial Dna Depletion Syndrome 16 0.019
1000
CRL006 Caroli Disease, Isolated 13 0.019
1001
IGG012 Igg4-Related Submandibular Gland Disease 8 0.019
1002
ATS001 Autistic Disorder 59 0.019
1003
GST009 Gastroschisis 43 0.019
1004
FBR054 Fibroma 43 0.019
1005
SKL003 Skeletal Muscle Cancer 41 0.019
1006
INT060 Intestinal Atresia 40 0.019
1007
DFF019 Diffuse Gastric Cancer 39 0.019
1008
CYC008 Cyclic Vomiting Syndrome 38 0.019
1009
SGM002 Sigmoid Neoplasm 35 0.019
1010
CND006 Candida Glabrata 34 0.019
1011
BLR027 Blue Rubber Bleb Nevus 33 0.019
1012
ANG061 Angular Cheilitis 31 0.019
1013
XNT002 Xanthogranulomatous Cholecystitis 30 0.019
1014
CHR557 Chronic Intestinal Pseudoobstruction 29 0.019
1015
RSP004 Respiratory System Benign Neoplasm 28 0.019
1016
TRD003 Taurodontism 27 0.019
1017
P HYP658 Hypoplastic Amelogenesis Imperfecta 27 0.019
1018
ACK001 Ackerman Syndrome 24 0.019
1019
AML046 Amelogenesis Imperfecta, Type Iia5 17 0.019
1020
PYT001 Pythiosis 15 0.019
1021
c DNT047 Dentinogenesis Imperfecta Type 2 11 0.019
1022
c ATM070 Autoimmune Enteropathy Type 3 9 0.019
1023
ALV001 Alveolar Periostitis 35 0.018
1024
ESN022 Eosinophilic Colitis 22 0.018
1025
FLM003 Fulminant Viral Hepatitis 19 0.018
1026
GLS013 Glossodynia 19 0.018
1027
HYP481 Hyperbiliverdinemia 17 0.018
1028
CVR008 Cavernous Lymphangioma 15 0.018
1029
NKC001 Nk-Cell Enteropathy 15 0.018
1030
c INT019 Intestine Carcinoma in Situ 14 0.018
1031
HRS038 Hirschsprung Disease with Hypoplastic Nails and Dysmorphic Facial Features 11 0.018
1032
PRT022 Protozoal Dysentery 11 0.018
1033
BNG007 Benign Lymphoepithelial Lesion of Salivary Gland 10 0.018
1034
MYM001 Myoma 51 0.018
1035
ANL004 Anal Canal Squamous Cell Carcinoma 41 0.018
1036
LKS001 Leukostasis 39 0.018
1037
NTL004 Nut Allergy 37 0.018
1038
RCT020 Rectum Adenocarcinoma 34 0.018
1039
P EPL003 Epulis 33 0.018
1040
LRG016 Large Intestine Adenocarcinoma 29 0.018
1041
DNT046 Dental Abscess 27 0.018
1042
HPT012 Hepatocellular Fibrolamellar Carcinoma 27 0.018
1043
MTG001 Metagonimiasis 26 0.018
1044
DST016 Distomatosis 24 0.018
1045
PYL002 Pylorospasm 23 0.018
1046
ORL006 Oral Mucosa Leukoplakia 22 0.018
1047
ADN072 Adenoma of Pancreas 22 0.018