Search results for Indomethacin

804 hits were found for Indomethacin

# Family MCID Name MIFTS Score
1
FTL018 Fetal Indomethacin Syndrome 20 6.569
2
P PTN014 Patent Ductus Arteriosus 1 60 0.513
3
GST023 Gastric Ulcer 53 0.294
4
ENT011 Enterocolitis 51 0.269
5
PRN019 Perinatal Necrotizing Enterocolitis 59 0.248
6
P PNC044 Pancreatitis 61 0.242
7
P HDC001 Headache 57 0.225
8
c ACT027 Acute Pancreatitis 60 0.219
9
OST012 Osteoarthritis 78 0.214
10
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.197
11
GT001 Gout 64 0.179
12
P RHM011 Rheumatoid Arthritis 80 0.176
13
BRN056 Bronchopulmonary Dysplasia 57 0.174
14
P ART022 Arthritis 69 0.170
15
HMC012 Hemicrania Continua 28 0.169
16
SPN051 Spondylitis 51 0.167
17
48X005 48,xyyy 39 0.167
18
PRX009 Paroxysmal Hemicrania 33 0.167
19
INF009 Inflammatory Spondylopathy 31 0.167
20
c SPN225 Spondyloarthropathy 1 73 0.165
21
P KDN018 Kidney Disease 72 0.163
22
P CLR023 Colorectal Cancer 99 0.159
23
P CTR002 Cataract 60 0.159
24
P GLM007 Glomerulonephritis 57 0.159
25
PLY012 Polyhydramnios 46 0.157
26
c ACT071 Acute Kidney Failure 60 0.154
27
c EXD008 Exudative Vitreoretinopathy 1 71 0.152
28
INT071 Intestinal Perforation 51 0.137
29
P NPH012 Nephrotic Syndrome 60 0.135
30
PPT005 Peptic Ulcer Disease 59 0.135
31
PNG002 Pain Agnosia 51 0.135
32
P DBT005 Diabetes Insipidus 55 0.132
33
OLG003 Oligohydramnios 51 0.130
34
P PLM037 Pulmonary Hypertension 67 0.125
35
BNR002 Bone Resorption Disease 48 0.125
36
c HYP595 Hypertension, Essential 84 0.123
37
MCL006 Macular Retinal Edema 55 0.123
38
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.120
39
P DRR001 Diarrhea 55 0.120
40
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.118
41
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.118
42
INT075 Intracranial Hypertension 53 0.118
43
c MGR028 Migraine with or Without Aura 1 67 0.115
44
CRB037 Cerebral Palsy 69 0.110
45
HYP056 Hypoglycemia 66 0.110
46
P GST044 Gastritis 56 0.110
47
LNG099 Lung Disease 60 0.107
48
HYP005 Hypokalemia 55 0.107
49
CNG034 Congestive Heart Failure 69 0.104
50
P ADN016 Adenocarcinoma 64 0.104
51
CYT002 Cytokine Deficiency 42 0.104
52
ISC004 Ischemia 58 0.101
53
PRV004 Periventricular Leukomalacia 52 0.101
54
c PNS012 Paine Syndrome 61 0.098
55
CHL014 Cholera 59 0.098
56
PRT058 Pure Autonomic Failure 59 0.098
57
PRC013 Pericarditis 54 0.098
58
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.098
59
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.098
60
PLM010 Pulmonary Edema 54 0.095
61
ENT004 Enthesopathy 49 0.095
62
HDN002 Head Injury 46 0.095
63
P CLS010 Cluster Headache 42 0.095
64
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.092
65
P GLM045 Glioma 63 0.092
66
BRN004 Brain Edema 56 0.092
67
FLL008 Folliculitis 46 0.092
68
GLL048 Glial Tumor 45 0.092
69
ESN016 Eosinophilic Pustular Folliculitis 25 0.092
70
P PRD008 Periodontitis 64 0.089
71
P PSR002 Psoriasis 62 0.089
72
HYP266 Hypoxia 57 0.089
73
PST011 Pustulosis of Palm and Sole 52 0.089
74
PRT036 Peritonitis 64 0.085
75
P ART023 Arthropathy 62 0.085
76
TXC005 Toxic Shock Syndrome 62 0.085
77
DRM006 Dermatitis 61 0.085
78
ADN018 Adenoma 59 0.085
79
P INF037 Inflammatory Bowel Disease 54 0.085
80
ADL002 Adult Syndrome 70 0.082
81
CLN015 Colon Adenocarcinoma 65 0.082
82
PLR008 Pleurisy 50 0.082
83
ILT001 Ileitis 50 0.082
84
BRN071 Brain Injury 49 0.082
85
c TRC022 Tricuspid Valve Insufficiency 45 0.082
86
P TRN020 Turner Syndrome 67 0.078
87
c PRC016 Pre-Eclampsia 63 0.078
88
P NTR004 Neutropenia 63 0.078
89
c BRN108 Branchiootic Syndrome 1 62 0.078
90
LVR012 Liver Cirrhosis 62 0.078
91
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.078
92
P UVT001 Uveitis 57 0.078
93
P BRT004 Bartter Disease 52 0.078
94
STM007 Stomatitis 50 0.078
95
BLR004 Biliary Dyskinesia 38 0.078
96
P ALZ034 Alzheimer Disease 88 0.074
97
P RSP003 Respiratory Failure 74 0.074
98
ALL026 Allergic Hypersensitivity Disease 62 0.074
99
NTR005 Nutritional Deficiency Disease 62 0.074
100
NWB001 Newborn Respiratory Distress Syndrome 58 0.074
101
CHL067 Cholecystitis 57 0.074
102
P FBR017 Fibrosarcoma 56 0.074
103
PRS030 Persistent Fetal Circulation Syndrome 52 0.074
104
P PRC012 Pericardial Effusion 51 0.074
105
CHR005 Chorioamnionitis 51 0.074
106
HMP001 Hemopericardium 48 0.074
107
ANR004 Anuria 46 0.074
108
P HYP120 Hypoaldosteronism 36 0.074
109
P GST053 Gastric Cancer 83 0.070
110
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.070
111
KRT019 Keratitis, Hereditary 65 0.070
112
PRT037 Pertussis 65 0.070
113
CLT003 Colitis 62 0.070
114
SPN186 Spinal Cord Injury 60 0.070
115
SQM006 Squamous Cell Carcinoma 60 0.070
116
GST050 Gastrointestinal System Disease 56 0.070
117
P DDN001 Duodenal Ulcer 52 0.070
118
NPH003 Nephrocalcinosis 51 0.070
119
P RNV001 Renovascular Hypertension 48 0.070
120
URT010 Ureteral Obstruction 45 0.070
121
BCK006 Back Pain 42 0.070
122
HYP188 Hypnic Headache 20 0.070
123
P HRT032 Heart Disease 75 0.065
124
GLB015 Glioblastoma Multiforme 75 0.065
125
CRH001 Crohn's Disease 74 0.065
126
ULC004 Ulcerative Colitis 73 0.065
127
DWN001 Down Syndrome 70 0.065
128
c RHB024 Rhabdomyosarcoma 2 67 0.065
129
P HRP006 Herpes Simplex 65 0.065
130
P BRS044 Breast Adenocarcinoma 59 0.065
131
CNT047 Contact Dermatitis 58 0.065
132
P URT039 Urticaria 58 0.065
133
LNG108 Langerhans Cell Histiocytosis 58 0.065
134
P SZR006 Seizure Disorder 56 0.065
135
ACT058 Active Peptic Ulcer Disease 55 0.065
136
NTR046 Neutrophil Migration 50 0.065
137
HST010 Histiocytosis 48 0.065
138
c HYD064 Hydrocephalus, Congenital, 1 48 0.065
139
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.065
140
P BRS047 Breast Cancer 97 0.060
141
c SYS001 Systemic Lupus Erythematosus 86 0.060
142
P BLD134 Bladder Cancer 79 0.060
143
AST005 Asthma 76 0.060
144
P APL001 Aplastic Anemia 74 0.060
145
DFC004 Deficiency Anemia 70 0.060
146
P PNM007 Pneumonia 68 0.060
147
P HYP098 Hypereosinophilic Syndrome 67 0.060
148
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.060
149
P HYD006 Hydrocephalus 66 0.060
150
P PLM036 Pulmonary Fibrosis 65 0.060
151
P ADL010 Adult Respiratory Distress Syndrome 65 0.060
152
c SVR001 Severe Acute Respiratory Syndrome 62 0.060
153
P ESP024 Esophagitis 62 0.060
154
P VSC011 Vasculitis 62 0.060
155
HYP066 Hyperglycemia 61 0.060
156
P MCR010 Microcephaly 59 0.060
157
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.060
158
CNS004 Constipation 58 0.060
159
c ACT134 Acute Liver Failure 56 0.060
160
P SLM003 Salmonellosis 55 0.060
161
SPS003 Spastic Diplegia 51 0.060
163
TRM010 Traumatic Brain Injury 51 0.060
164
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.060
165
ATX019 Ataxia with Vitamin E Deficiency 42 0.060
166
P PRS040 Prostate Cancer 97 0.055
167
P MYC007 Myocardial Infarction 70 0.055
168
c PNC108 Pancreatitis, Hereditary 70 0.055
169
P MLN008 Melanoma 69 0.055
170
P LKM002 Leukemia 68 0.055
171
P THR014 Thrombocytopenia 67 0.055
172
CRB039 Cerebrovascular Disease 67 0.055
173
P CNJ013 Conjunctivitis 65 0.055
174
SRC014 Sarcoma 65 0.055
175
PPL049 Papillon-Lefevre Syndrome 65 0.055
176
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.055
177
HYD038 Hydrops Fetalis, Nonimmune 62 0.055
178
ATM095 Autoimmune Disease 62 0.055
179
CHL068 Cholestasis 61 0.055
180
ANR040 Aneurysm 59 0.055
181
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.055
182
P PYL005 Pyelonephritis 56 0.055
183
P SPN052 Spondyloarthropathy 54 0.055
184
PRT082 Preterm Premature Rupture of the Membranes 54 0.055
185
FRZ001 Frozen Shoulder 53 0.055
186
SPN035 Spindle Cell Sarcoma 53 0.055
187
MTB004 Metabolic Acidosis 50 0.055
188
47X002 47,xyy 49 0.055
189
BRS064 Bursitis 48 0.055
190
P PSD003 Pseudohypoaldosteronism 44 0.055
191
c PRS136 Prostate Cancer, Hereditary, 6 33 0.055
192
c PRS130 Prostate Cancer, Hereditary, 8 32 0.055
193
PRR001 Periarthritis 32 0.055
194
CGH002 Cough Headache 21 0.055
195
ESP021 Esophageal Cancer 90 0.049
197
STR067 Stroke, Ischemic 81 0.049
198
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.049
199
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.049
200
END057 Endometrial Cancer 74 0.049
201
P FML011 Familial Adenomatous Polyposis 72 0.049
202
c LKM063 Leukemia, Chronic Myeloid 72 0.049
203
P SLP006 Sleep Apnea 69 0.049
204
P LPR021 Leprosy 3 69 0.049
205
P LYM118 Lymphoma 68 0.049
206
BRN024 Bronchitis 68 0.049
207
P DMN002 Dementia 66 0.049
208
P DBT009 Diabetes Mellitus 64 0.049
209
c JVN010 Juvenile Rheumatoid Arthritis 64 0.049
210
P END044 Endometriosis 63 0.049
211
PSR001 Psoriatic Arthritis 61 0.049
212
RTN017 Retinal Detachment 61 0.049
213
P LPS004 Lupus Erythematosus 61 0.049
214
P MYL006 Myeloid Leukemia 60 0.049
215
P CRB101 Cerebrooculofacioskeletal Syndrome 1 60 0.049
216
ACQ007 Acquired Immunodeficiency Syndrome 60 0.049
217
CYS010 Cystinosis 59 0.049
218
P ALC033 Alcohol Use Disorder 58 0.049
219
P INF032 Infertility 57 0.049
220
HMR039 Hemorrhage, Intracerebral 57 0.049
221
PNM008 Pneumothorax 56 0.049
222
PLS011 Plasmacytoma 56 0.049
223
ALL010 Allergic Contact Dermatitis 56 0.049
224
MCS002 Mucositis 56 0.049
225
AGN016 Aging 56 0.049
226
PRP030 Purpura 54 0.049
227
TND005 Tendinitis 54 0.049
228
P INT068 Intestinal Disease 53 0.049
229
c MCR113 Microvascular Complications of Diabetes 3 52 0.049
230
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.049
231
OCL069 Ocular Motor Apraxia 51 0.049
232
ANK001 Ankylosis 51 0.049
233
THR016 Thrombophlebitis 51 0.049
234
P RNL007 Renal Tubular Acidosis 51 0.049
235
QDR001 Quadriplegia 48 0.049
236
c MCR120 Microvascular Complications of Diabetes 7 47 0.049
237
KHN001 Kuhnt-Junius Degeneration 47 0.049
238
c CNG216 Congenital Hydrocephalus 47 0.049
239
RTR008 Root Resorption 45 0.049
240
P PRL003 Proliferative Glomerulonephritis 44 0.049
241
CVD001 Covid-19 44 0.049
242
P CRN026 Corneal Edema 43 0.049
243
EPC002 Epicondylitis 41 0.049
244
c MCR130 Microvascular Complications of Diabetes 6 41 0.049
245
c MCR133 Microvascular Complications of Diabetes 4 41 0.049
246
VLL006 Villous Adenoma 40 0.049
247
HNS001 Hansen's Disease 34 0.049
248
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.049
249
CHL079 Children's Interstitial Lung Disease 26 0.049
250
P PRM227 Primary Orthostatic Hypotension 25 0.049
251
EXR004 Exertional Headache 15 0.049
252
P OVR042 Ovarian Cancer 88 0.043
253
P LNG064 Lung Cancer Susceptibility 3 78 0.043
254
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.043
255
P CNR004 Cone-Rod Dystrophy 2 73 0.043
256
P RTN024 Retinoblastoma 73 0.043
257
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.043
258
P AMY004 Amyloidosis 70 0.043
259
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.043
260
P LKM062 Leukemia, Acute Lymphoblastic 69 0.043
261
P TMP003 Temporal Arteritis 68 0.043
262
P LVR013 Liver Disease 68 0.043
263
P INF038 Influenza 68 0.043
264
RCK004 Rickets 68 0.043
265
P CLC063 Celiac Disease 1 66 0.043
266
P SKN015 Skin Carcinoma 66 0.043
267
CHG001 Chagas Disease 66 0.043
268
P MNN013 Meningitis 66 0.043
269
KHL003 Kohlschutter-Tonz Syndrome 65 0.043
270
GTL001 Gitelman Syndrome 65 0.043
271
SKN016 Skin Disease 63 0.043
272
LPP008 Lipoprotein Quantitative Trait Locus 62 0.043
273
P PRM006 Primary Biliary Cirrhosis 62 0.043
274
OST003 Osteonecrosis 61 0.043
275
P ENC018 Encephalopathy 61 0.043
276
OSS012 Osseous Heteroplasia, Progressive 61 0.043
277
SPP011 Suppression of Tumorigenicity 12 59 0.043
278
P MYC008 Myocarditis 59 0.043
279
PRT013 Portal Hypertension 59 0.043
280
P BND020 Bone Disease 59 0.043
281
THY029 Thyroid Carcinoma 59 0.043
282
HLC007 Helicobacter Pylori Infection 59 0.043
283
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.043
284
P BCL017 B-Cell Lymphoma 58 0.043
285
FML063 Familial Glucocorticoid Deficiency 58 0.043
286
P EXN002 Exanthem 57 0.043
287
DSS009 Disseminated Intravascular Coagulation 57 0.043
288
P CRD246 Cardiovascular System Disease 57 0.043
289
SCH014 Schistosomiasis 57 0.043
290
AYM001 Ayme-Gripp Syndrome 57 0.043
291
ERY051 Erythroleukemia, Familial 56 0.043
292
P MLN007 Male Infertility 55 0.043
293
HYP060 Hyperinsulinism 54 0.043
294
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.043
295
c FML008 Familial Retinoblastoma 53 0.043
296
c GLL024 Gallbladder Disease 1 53 0.043
297
PRP016 Paraplegia 52 0.043
298
P RCT021 Rectum Cancer 52 0.043
299
ART140 Arteries, Anomalies of 52 0.043
300
P MGR003 Migraine with Aura 52 0.043
301
c PNC106 Pancreatic Agenesis 1 51 0.043
302
MYL020 Myelomeningocele 51 0.043
303
CYS014 Cystadenocarcinoma 51 0.043
304
END086 End Stage Renal Disease 51 0.043
305
P CHL066 Cholangitis 51 0.043
306
P MMB011 Membranous Nephropathy 50 0.043
307
P OVR082 Overgrowth Syndrome 50 0.043
308
P ECL001 Eclampsia 50 0.043
309
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.043
310
P OBS001 Obstructive Jaundice 50 0.043
311
MCN001 Mucinous Adenocarcinoma 49 0.043
312
PLP001 Pulpitis 49 0.043
313
CHL004 Cholelithiasis 49 0.043
314
PNC034 Pancreas Disease 48 0.043
315
P SCL015 Scleritis 48 0.043
316
SXL003 Sexual Disorder 47 0.043
317
c MLG069 Malignant Hypertension 47 0.043
318
P RNL015 Renal Hypertension 47 0.043
319
CLN045 Colonic Benign Neoplasm 46 0.043
320
CYN002 Cyanosis, Transient Neonatal 45 0.043
321
CRB004 Cerebral Artery Occlusion 45 0.043
322
P CHR345 Chronic Pain 44 0.043
323
APP009 Appendix Adenocarcinoma 44 0.043
324
ART006 Arthus Reaction 44 0.043
325
SNL007 Senile Cataract 42 0.043
326
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.043
327
ANX004 Anoxia 40 0.043
328
MCN008 Mucinous Cystadenocarcinoma 40 0.043
329
MCL003 Macular Holes 40 0.043
330
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.043
331
ALL014 Allergic Encephalomyelitis 38 0.043
332
P ANT061 Antenatal Bartter Syndrome 37 0.043
333
SCR003 Secretory Diarrhea 37 0.043
334
CRV025 Cervical Incompetence 34 0.043
335
FLL019 Follicular Mucinosis 31 0.043
336
CLN002 Colon Mucinous Adenocarcinoma 28 0.043
337
P LNG032 Lung Cancer 98 0.035
338
MYL069 Myeloma, Multiple 85 0.035
339
c LKM061 Leukemia, Acute Myeloid 84 0.035
340
MLR004 Malaria 81 0.035
341
P GLM040 Glioma Susceptibility 1 81 0.035
342
INS024 Insulin-Like Growth Factor I 79 0.035
343
IMM167 Immune Deficiency Disease 78 0.035
344
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.035
345
c ATR087 Atrial Standstill 1 75 0.035
346
SCK003 Sickle Cell Anemia 74 0.035
347
c MNN043 Meningioma, Familial 74 0.035
348
SVR004 Severe Combined Immunodeficiency 73 0.035
349
c HYP836 Hypercholesterolemia, Familial, 1 73 0.035
350
P FML018 Familial Mediterranean Fever 73 0.035
351
ANX010 Anxiety 73 0.035
352
P MLT020 Multiple Sclerosis 72 0.035
353
OTT002 Otitis Media 72 0.035
354
P SRC025 Sarcoidosis 1 70 0.035
355
PLM001 Pulmonary Tuberculosis 69 0.035
356
ART016 Aortic Aneurysm 69 0.035
357
SKN019 Skin Melanoma 68 0.035
358
CNN005 Connective Tissue Disease 68 0.035
359
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.035
360
P HPT021 Hepatitis 67 0.035
361
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.035
362
ALL003 Allergic Rhinitis 67 0.035
363
THY111 Thyroid Carcinoma, Familial Medullary 67 0.035
364
OST159 Osteogenic Sarcoma 66 0.035
365
ANG054 Angina Pectoris 66 0.035
366
c SML038 Small Cell Cancer of the Lung 65 0.035
367
TTN003 Tetanus 65 0.035
368
BRR014 Barrett Esophagus 65 0.035
369
ATH013 Atherosclerosis Susceptibility 65 0.035
370
P THY023 Thymoma 65 0.035
371
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.035
372
APN008 Apnea, Obstructive Sleep 64 0.035
373
BRC012 Brucellosis 64 0.035
374
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.035
375
DSM004 Desmoid Tumor 64 0.035
376
P VSC007 Vascular Disease 63 0.035
377
ANR007 Anorexia Nervosa 63 0.035
378
DPR016 Depression 63 0.035
379
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.035
380
P ORT004 Orthostatic Intolerance 62 0.035
381
MNN042 Meningioma, Radiation-Induced 62 0.035
382
CRC021 Carcinosarcoma 62 0.035
383
HPT019 Hepatic Encephalopathy 60 0.035
384
RHM001 Rheumatic Fever 60 0.035
385
ING001 Inguinal Hernia 60 0.035
386
INS001 Insulinoma 60 0.035
387
HYD002 Hydronephrosis 60 0.035
388
P OPT006 Optic Nerve Disease 60 0.035
389
P BRN022 Bronchiectasis 59 0.035
390
VSL002 Visual Epilepsy 59 0.035
391
P CYS018 Cystitis 59 0.035
392
P SYP003 Syphilis 58 0.035
393
EYD002 Eye Disease 58 0.035
394
CRV038 Cervical Squamous Cell Carcinoma 58 0.035
395
P RHN004 Rhinitis 57 0.035
396
THR024 Thrombosis 57 0.035
397
P FCL005 Focal Segmental Glomerulosclerosis 57 0.035
398
BLR008 Bilirubin Metabolic Disorder 57 0.035
399
P ANG015 Angioedema 57 0.035
400
LST001 Listeriosis 56 0.035
401
P NRP001 Neuropathy 56 0.035
402
BCT022 Bacterial Infectious Disease 56 0.035
403
DFF005 Diffuse Large B-Cell Lymphoma 55 0.035
404
P GRV001 Graves' Disease 55 0.035
405
P HYP076 Hyperthyroidism 55 0.035
406
P DRM007 Dermatitis Herpetiformis 55 0.035
407
URN010 Urinary Tract Obstruction 55 0.035
408
HMP005 Hemiplegia 55 0.035
409
BRN015 Bronchiolo-Alveolar Adenocarcinoma 54 0.035
410
ADN024 Adenine Phosphoribosyltransferase Deficiency 54 0.035
411
DBT010 Diabetic Neuropathy 54 0.035
412
MMM001 Mammary Paget's Disease 53 0.035
413
P INS002 in Situ Carcinoma 53 0.035
414
OCL006 Ocular Hypertension 53 0.035
415
P ORL007 Oral Cavity Cancer 53 0.035
416
GTR002 Goiter 53 0.035
417
P PTS002 Ptosis 53 0.035
418
ACR041 Acromelic Frontonasal Dysostosis 52 0.035
419
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.035
420
DYS015 Dysentery 52 0.035
421
P MSC003 Muscular Atrophy 52 0.035
422
c THY107 Thymoma, Familial 52 0.035
423
HYP014 Hyperuricemia 52 0.035
424
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.035
425
FDL002 Food Allergy 51 0.035
426
ASP003 Aseptic Meningitis 51 0.035
427
P HYP040 Hypospadias 51 0.035
428
SKN013 Skin Benign Neoplasm 51 0.035
429
P FNC004 Fanconi Syndrome 50 0.035
430
RDC002 Radiculopathy 50 0.035
431
SPN021 Spinal Meningioma 50 0.035
432
THY125 Thyroid Gland Medullary Carcinoma 50 0.035
433
LPR001 Lepromatous Leprosy 50 0.035
434
HYP017 Hypophosphatemia 50 0.035
435
P OTS001 Otosclerosis 49 0.035
436
INP001 Inappropriate Adh Syndrome 49 0.035
437
STP011 Stapes Ankylosis with Broad Thumbs and Toes 49 0.035
438
URM002 Uremia 49 0.035
439
c BCT013 Bacterial Pneumonia 48 0.035
440
INT067 Interstitial Nephritis 48 0.035
441
SPL018 Splenomegaly 48 0.035
442
PYL006 Pyloric Stenosis 48 0.035
443
PLC007 Placental Abruption 48 0.035
444
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.035
445
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.035
446
CRN027 Corneal Neovascularization 47 0.035
447
P CLL015 Collagen Disease 47 0.035
448
c INH020 Inherited Metabolic Disorder 47 0.035
449
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.035
450
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.035
451
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.035
452
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.035
453
P OVR046 Ovarian Cyst 47 0.035
454
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.035
455
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.035
456
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.035
457
c BRT042 Bartter Syndrome, Type 3 46 0.035
458
c DRR009 Diarrhea 6 46 0.035
459
c MLG068 Malignant Glioma 46 0.035
460
OLG001 Oligospermia 45 0.035
461
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.035
462
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.035
463
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.035
464
HPT004 Hepatic Coma 45 0.035
465
TWN001 Twin-to-Twin Transfusion Syndrome 45 0.035
466
SYN005 Synostosis 45 0.035
467
P RDL002 Radioulnar Synostosis 45 0.035
468
PLN005 Palindromic Rheumatism 45 0.035
469
GRN017 Granulocytopenia 44 0.035
470
PTT037 Pituitary Tumors 44 0.035
471
IRT001 Iritis 44 0.035
472
c ORT011 Orthostatic Hypotension 1 44 0.035
473
VLV044 Vulvar Intraepithelial Neoplasia 44 0.035
474
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.035
475
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.035
476
DPR002 Depersonalization Disorder 43 0.035
477
LWC001 Low Compliance Bladder 43 0.035
478
ANG011 Angiodysplasia 43 0.035
479
SCR001 Secretory Meningioma 41 0.035
480
PST053 Postherpetic Neuralgia 40 0.035
481
P FNC034 Fanconi Renotubular Syndrome 2 40 0.035
482
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 40 0.035
483
ALD013 Aldosterone-Producing Adenoma 39 0.035
484
CRV045 Cervical Intraepithelial Neoplasia 39 0.035
485
CHL039 Choledocholithiasis 38 0.035
486
HYP264 Hypertonia 38 0.035
487
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 38 0.035
488
SHW001 Shwartzman Phenomenon 37 0.035
489
P PST059 Pustular Psoriasis 37 0.035
490
PRR004 Preretinal Fibrosis 37 0.035
491
GLM044 Glomerular Disease 37 0.035
492
PNB004 Panbronchiolitis, Diffuse 37 0.035
493
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.035
494
c DRM040 Dermatitis Herpetiformis, Familial 35 0.035
495
CHR178 Chromosomal Triplication 35 0.035
496
c LKM005 Leukemia, T-Cell, Chronic 34 0.035
497
LTT002 Letterer-Siwe Disease 33 0.035
498
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.035
499
JJN008 Jejunoileitis 31 0.035
500
PNG001 Pinguecula 31 0.035
501
PRC051 Paracetamol Poisoning 30 0.035
502
RVR002 Reversible Cerebral Vasoconstriction Syndrome 28 0.035
503
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.035
504
CHR010 Chorioangioma 27 0.035
505
c ORT012 Orthostatic Hypotension 2 26 0.035
506
c PTN012 Patent Ductus Arteriosus 3 25 0.035
507
c RRH030 Rare Headache 15 0.035
508
P HPT023 Hepatocellular Carcinoma 100 0.025
509
NRL016 Neural Tube Defects 82 0.025
510
P ATX030 Ataxia-Telangiectasia 82 0.025
511
CYS001 Cystic Fibrosis 81 0.025
512
c NRF023 Neurofibromatosis, Type Ii 80 0.025
513
c DLT002 Dilated Cardiomyopathy 79 0.025
514
PFF001 Pfeiffer Syndrome 79 0.025
515
MRF001 Marfan Syndrome 77 0.025
516
CRV035 Cervical Cancer 76 0.025
517
BRN028 Brain Cancer 74 0.025
518
P SCH015 Schizophrenia 74 0.025
519
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.025
520
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.025
521
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.025
522
c HPT073 Hepatitis C Virus 72 0.025
523
P GRF003 Graft-Versus-Host Disease 72 0.025
524
P PHC003 Pheochromocytoma 71 0.025
525
ACR007 Acromegaly 71 0.025
526
HMN044 Human Immunodeficiency Virus Type 1 71 0.025
527
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.025
528
P TTR001 Tetralogy of Fallot 70 0.025
529
c CHR684 Chronic Kidney Disease 70 0.025
530
LYM133 Lymphoma, Hodgkin, Classic 69 0.025
531
P HYP086 Hypothyroidism 69 0.025
532
MST024 Mastocytosis, Cutaneous 69 0.025
533
P ANG001 Angelman Syndrome 69 0.025
534
P SYS005 Systemic Scleroderma 68 0.025
535
CMM004 Common Variable Immunodeficiency 68 0.025
536
c BSL007 Basal Cell Carcinoma 68 0.025
537
PNC129 Pancreatic Adenocarcinoma 68 0.025
538
P CRD119 Cardiac Arrest 67 0.025
539
BRK010 Burkitt Lymphoma 67 0.025
540
PSY004 Psychotic Disorder 67 0.025
541
FBR011 Fibrodysplasia Ossificans Progressiva 67 0.025
542
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.025
543
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.025
544
ALC007 Alcohol Dependence 66 0.025
545
P NSP012 Nasopharyngeal Carcinoma 66 0.025
546
ART001 Arterial Tortuosity Syndrome 66 0.025
547
ACH004 Achondroplasia 66 0.025
548
AND002 Androgen Insensitivity Syndrome 66 0.025
549
P DRM053 Dermatitis, Atopic 66 0.025
550
P ART005 Arteriovenous Malformation 65 0.025
551
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.025
552
P DYS154 Dystonia 65 0.025
553
IRR002 Irritable Bowel Syndrome 65 0.025
554
P PRS038 Personality Disorder 65 0.025
555
c DBT099 Diabetes Mellitus, Type I 65 0.025
556
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.025
557
OVR029 Ovarian Hyperstimulation Syndrome 64 0.025
558
CLF027 Cleft Palate, Isolated 64 0.025
559
P MST009 Mastocytosis 64 0.025
560
DGR001 Digeorge Syndrome 64 0.025
561
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.025
562
OST017 Osteomyelitis 64 0.025
563
LSH001 Leishmaniasis 63 0.025
564
P HML002 Hemolytic Anemia 63 0.025
565
P ANR048 Aniridia 1 63 0.025
566
P HYP055 Hypoplastic Left Heart Syndrome 63 0.025
567
c OPT053 Optic Atrophy 1 63 0.025
568
LPD008 Lipid Metabolism Disorder 62 0.025
569
c FNC043 Fanconi Anemia, Complementation Group E 62 0.025
570
P TRC086 Trichohepatoenteric Syndrome 1 62 0.025
571
c ANM038 Anemia, Autoimmune Hemolytic 62 0.025
572
CTN007 Cutaneous Leishmaniasis 62 0.025
573
MSL001 Measles 62 0.025
574
P INT143 Interstitial Cystitis 61 0.025
575
ART141 Arteriovenous Malformations of the Brain 61 0.025
576
APP008 Appendicitis 61 0.025
577
P HMN010 Hemangioma 61 0.025
578
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.025
579
LGN002 Legionellosis 60 0.025
580
P KDN017 Kidney Cancer 60 0.025
581
CHR288 Chronic Recurrent Multifocal Osteomyelitis 60 0.025
582
ACN002 Acanthosis Nigricans 60 0.025
583
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.025
584
VRC005 Varicose Veins 60 0.025
585
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.025
586
ORL011 Oral Cancer 60 0.025
587
STT001 Status Epilepticus 60 0.025
588
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.025
589
P AXN002 Axenfeld-Rieger Syndrome 59 0.025
590
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.025
591
c HPT016 Hepatitis B 59 0.025
592
P SLP005 Sleep Disorder 59 0.025
593
PLM033 Pulmonary Embolism 59 0.025
594
P MLN069 Melanoma, Uveal 59 0.025
595
GNG013 Gingivitis 59 0.025
596
P GLL022 Guillain-Barre Syndrome 59 0.025
597
GLB001 Gilbert Syndrome 58 0.025
598
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.025
599
P INT070 Intestinal Obstruction 58 0.025
600
P PGT001 Paget's Disease of Bone 58 0.025
601
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.025
602
MNT002 Mental Depression 58 0.025
603
LYM027 Lymphopenia 58 0.025
604
BRG013 Buerger Disease 58 0.025
605
P PRP019 Peripheral Nervous System Disease 58 0.025
606
MNR012 Meniere Disease 57 0.025
607
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.025
608
P PRN023 Prion Disease 57 0.025
609
c MST023 Mesothelioma, Malignant 57 0.025
610
VSC002 Vascular Dementia 57 0.025
611
INT303 Intracranial Hypertension, Idiopathic 57 0.025
612
PHR003 Pharyngitis 57 0.025
613
P BPL003 Bipolar Disorder 56 0.025
614
P MYS005 Myositis 56 0.025
615
c INT072 Intestinal Pseudo-Obstruction 56 0.025
616
SFT003 Soft Tissue Sarcoma 56 0.025
617
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 56 0.025
618
HST011 Histoplasmosis 55 0.025
619
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.025
620
LMB062 Limb Ischemia 55 0.025
621
MMB001 Membranoproliferative Glomerulonephritis 55 0.025
622
c BCT007 Bacterial Meningitis 55 0.025
623
NPH009 Nephrolithiasis 55 0.025
624
P ANT006 Antiphospholipid Syndrome 55 0.025
625
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.025
626
P ALP106 Alport Syndrome 1, X-Linked 55 0.025
627
END040 Endogenous Depression 55 0.025
628
SYN007 Synovitis 54 0.025
629
AMN003 Amnestic Disorder 54 0.025
630
GLC003 Glucose Intolerance 54 0.025
631
RLP001 Relapsing Polychondritis 54 0.025
632
THR013 Thoracic Outlet Syndrome 54 0.025
633
AMN001 Amenorrhea 54 0.025
634
LYM040 Lymphoblastic Lymphoma 54 0.025
635
PPL022 Papilloma 54 0.025
636
P TRM003 Tremor 54 0.025
637
PRC002 Paracoccidioidomycosis 54 0.025
638
CLL003 Cellulitis 54 0.025
639
PRS045 Prostatic Hypertrophy 53 0.025
640
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.025
641
TRC023 Trichinosis 53 0.025
642
KRT006 Keratoconjunctivitis 53 0.025
643
NNT012 Neonatal Jaundice 53 0.025
644
ACR058 Acrofacial Dysostosis 1, Nager Type 53 0.025
645
IRD001 Iridocyclitis 53 0.025
646
c VRL010 Viral Hepatitis 52 0.025
647
P SML001 Small Cell Carcinoma 52 0.025
648
P CHN059 Chondrocalcinosis 52 0.025
649
IMP005 Impotence 52 0.025
650
P THY032 Thyroiditis 52 0.025
651
ART074 Aortic Dissection 52 0.025
652
ONC002 Onchocerciasis 52 0.025
653
LMY002 Leiomyoma 52 0.025
654
THR004 Thrombocytosis 51 0.025
655
PRS021 Prostatic Adenoma 51 0.025
656
ILS001 Ileus 51 0.025
657
P AST007 Astrocytoma 51 0.025
658
PNN001 Panniculitis 51 0.025
659
P RNL028 Renal Tubular Dysgenesis 51 0.025
660
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.025
661
P ESN008 Eosinophilic Pneumonia 50 0.025
662
P MTR003 Mitral Valve Stenosis 50 0.025
663
PRT018 Portal Vein Thrombosis 50 0.025
664
c AMY009 Amyloidosis Aa 50 0.025
665
TRY001 Trypanosomiasis 50 0.025
666
c LRG001 Large Cell Carcinoma 50 0.025
667
c PSR021 Psoriasis 14, Pustular 50 0.025
668
P CRY007 Cryoglobulinemia, Familial Mixed 50 0.025
669
P MYT002 Myotonic Dystrophy 49 0.025
670
P IGN003 Iga Nephropathy 1 49 0.025
671
PRS129 Prostatic Hyperplasia, Benign 49 0.025
672
XNT003 Xanthomatosis 49 0.025
673
P MGR001 Migraine Without Aura 49 0.025
674
P CMP008 Compartment Syndrome 49 0.025
675
RYN001 Raynaud Disease 48 0.025
676
WTH001 Withdrawal Disorder 48 0.025
677
CRY004 Cryoglobulinemia 48 0.025
678
IGG001 Iga Glomerulonephritis 48 0.025
679
PTT004 Pituitary Apoplexy 48 0.025
680
INT010 Intracranial Embolism 48 0.025
681
RCT020 Rectum Adenocarcinoma 48 0.025
682
PRP007 Priapism 47 0.025
683
GRM005 Germ Cell Cancer 47 0.025
684
MCC002 Mucocutaneous Leishmaniasis 47 0.025
685
P PRR002 Pure Red-Cell Aplasia 47 0.025
686
VRN004 Vernal Keratoconjunctivitis 47 0.025
687
CRD001 Cardiac Tamponade 47 0.025
688
PRC003 Proctitis 47 0.025
689
GLS007 Glossitis 47 0.025
690
SRT004 Serotonin Syndrome 47 0.025
691
P KRN004 Kernicterus 47 0.025
692
ANV001 Anovulation 47 0.025
693
P CRC039 Coarctation of Aorta 47 0.025
694
RYN005 Raynaud Phenomenon 47 0.025
695
LYM019 Lymphosarcoma 46 0.025
696
ASP004 Asphyxia Neonatorum 46 0.025
697
RTN020 Retinal Vascular Disease 46 0.025
698
P BNG032 Benign Mesothelioma 46 0.025
699
ADR040 Adrenal Gland Pheochromocytoma 46 0.025
700
P HMR005 Hemorrhoid 46 0.025
701
SQM002 Squamous Cell Papilloma 46 0.025
702
P HRN001 Horner's Syndrome 45 0.025
703
SYN036 Syncope 45 0.025
704
TRT001 Teratocarcinoma 45 0.025
705
URL001 Urolithiasis 45 0.025
706
CRT015 Carotid Artery Occlusion 45 0.025
707
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.025
708
RTR001 Retrograde Amnesia 44 0.025
709
c PCH010 Pachyonychia Congenita 3 44 0.025
710
P BLP003 Blepharospasm 44 0.025
711
ACT164 Actinic Prurigo 44 0.025
712
HPT082 Hepatic Adenomas, Familial 44 0.025
713
P TST026 Testicular Germ Cell Cancer 43 0.025
714
RDC006 Red Cell Aplasia 43 0.025
715
ORL015 Oral Squamous Cell Carcinoma 43 0.025
716
P HYP265 Hypotonia 43 0.025
717
STL007 Steel Syndrome 43 0.025
718
P AVS003 Avascular Necrosis 42 0.025
719
PNM013 Pneumococcal Meningitis 42 0.025
720
c RTN047 Retinitis Pigmentosa 18 42 0.025
721
P DST107 Distal Renal Tubular Acidosis 42 0.025
722
IDP091 Idiopathic Nephrotic Syndrome 42 0.025
723
P RNG032 Ring Chromosome 42 0.025
724
TND006 Tendinosis 42 0.025
725
FBR019 Fibromatosis 41 0.025
726
P KLZ004 Kala-Azar 1 41 0.025
727
RST023 Resting Heart Rate, Variation in 41 0.025
728
MSN004 Mesenchymal Cell Neoplasm 41 0.025
729
c FML015 Familial Nephrotic Syndrome 41 0.025
730
c MJR024 Major Affective Disorder 9 41 0.025
731
ACT088 Acute Insulin Response 41 0.025
732
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.025
733
ANG049 Angioedema Induced by Ace Inhibitors 40 0.025
734
PRM024 Primary Angle-Closure Glaucoma 40 0.025
735
CRB086 Cerebral Aneurysms 40 0.025
736
OCL010 Ocular Hypotension 39 0.025
737
LNG030 Lung Adenoma 39 0.025
738
SPS004 Spastic Quadriplegia 39 0.025
739
c PRG020 Paragangliomas 3 39 0.025
740
ADP007 Adie Pupil 39 0.025
742
BLR002 Bile Reflux 39 0.025
743
SCR011 Scrapie 39 0.025
744
c MLG157 Malignant Pheochromocytoma 38 0.025
745
PRN039 Paraneoplastic Syndromes 38 0.025
746
c MJR022 Major Affective Disorder 8 38 0.025
747
c CHR098 Chronic Pyelonephritis 38 0.025
748
PRS123 Persistent Generalized Lymphadenopathy 37 0.025
749
ADR048 Adrenal Hyperplasia, Congenital, Due to 3-Beta-Hydroxysteroid Dehydrogenase 2 Deficiency 37 0.025
750
CRB009 Cerebritis 37 0.025
751
TTH008 Tooth Resorption 37 0.025
752
PNC016 Pancreatic Cholera 37 0.025
753
c BCT006 Bacterial Conjunctivitis 37 0.025
754
SYS071 Systemic Autoimmune Disease 37 0.025
755
INT011 Interstitial Emphysema 36 0.025
756
PLC002 Plica Syndrome 36 0.025
757
c ACT036 Acute Cholangitis 36 0.025
758
CHM005 Chemical Colitis 35 0.025
759
VRN001 Vernal Conjunctivitis 35 0.025
760
ATX010 Ataxia Neuropathy Spectrum 34 0.025
762
CRT008 Carotid Artery Dissection 33 0.025
763
ALR002 Al-Raqad Syndrome 33 0.025
764
ACT064 Acute Necrotizing Encephalitis 33 0.025
765
CNG064 Congenital Chloride Diarrhea 32 0.025
766
HST004 Histiocytoid Hemangioma 32 0.025
767
MYC015 Mycobacterium Fortuitum 32 0.025
768
ORB008 Orbital Plasma Cell Granuloma 31 0.025
769
c PRG019 Paragangliomas 2 31 0.025
770
SRC009 Sarcomatosis 31 0.025
771
RSP007 Respiratory Distress Syndrome, Infant 30 0.025
772
c PST008 Posterior Scleritis 30 0.025
773
ACT228 Acute Radiation Syndrome 29 0.025
774
MYC088 Mycobacterium Avium Complex Infections 29 0.025
775
PHS025 Phosphatase, Acid, of Tissues 28 0.025
776
ANS021 Anisocoria 27 0.025
777
ARG004 Argyria 27 0.025
778
HNM002 Hinman Syndrome 27 0.025
779
CYT018 Cytochrome P450 2d6 Variant 27 0.025
780
OLC001 Olecranon Bursitis 27 0.025
781
DFF015 Diffuse Glomerulonephritis 26 0.025
782
BNG077 Benign Idiopathic Neonatal Seizures 26 0.025
783
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.025
784
ACT162 Acute Sensory Ataxic Neuropathy 26 0.025
785
ACT094 Acute Articular Rheumatism 26 0.025
786
THY006 Thymus Lymphoma 26 0.025
787
ANT078 Antipyrine Metabolism 24 0.025
788
APN006 Apnea of Prematurity 24 0.025
789
MLL006 Mollaret Meningitis 23 0.025
790
RGH006 Right Aortic Arch 23 0.025
791
CHL131 Chlorpropamide-Alcohol Flushing 22 0.025
792
c HRD156 Hereditary Central Diabetes Insipidus 22 0.025
793
c RNG019 Ring Chromosome 3 22 0.025
794
THY020 Thyroid Hyalinizing Trabecular Adenoma 21 0.025
795
NWD001 New Daily-Persistent Headache 21 0.025
796
BNT001 Banti's Syndrome 21 0.025
797
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.025
798
AND005 Androgen Insensitivity Syndrome, Mild 19 0.025
799
CNG116 Congenital Nephrotic Syndrome Finnish Type 18 0.025
800
FML327 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis 17 0.025
801
BLD137 Blood Group--Ahonen 16 0.025
802
PST037 Pasteurella Multocida Infection 14 0.025
803
TRG013 Trigeminal Autonomic Cephalalgia 14 0.025
804
ERY018 Erythema Nodosum, Idiopathic 10 0.025
Content
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