Search results for CAD

398 hits were found for CAD

# Family MCID Name MIFTS Score
1
c EPL183 Epileptic Encephalopathy, Early Infantile, 50 35 17.777
2
CLD007 Cold Agglutinin Disease 45 3.731
3
P HYP724 Hyperlipoproteinemia, Type Iii 73 3.716
4
FML325 Familial Cervical Artery Dissection 15 3.644
5
CRV068 Cervical Polyp 27 2.858
6
HRW001 Hair Whorl 36 0.643
7
LPP008 Lipoprotein Quantitative Trait Locus 62 0.595
8
ART140 Arteries, Anomalies of 52 0.534
9
P CRN300 Coronary Heart Disease 1 63 0.355
10
ISC004 Ischemia 58 0.338
11
ATH013 Atherosclerosis Susceptibility 65 0.210
12
ANG054 Angina Pectoris 66 0.207
13
P MYC007 Myocardial Infarction 70 0.204
14
P HRT032 Heart Disease 75 0.191
15
P CRD246 Cardiovascular System Disease 57 0.188
16
CRN030 Coronary Stenosis 50 0.159
17
INT007 Intermediate Coronary Syndrome 55 0.151
18
P VSC007 Vascular Disease 63 0.133
19
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.133
20
CNG034 Congestive Heart Failure 69 0.128
21
c HYP595 Hypertension, Essential 84 0.123
22
P SCL018 Scoliosis 60 0.123
23
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.123
24
c ACT075 Acute Myocardial Infarction 57 0.123
25
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.118
26
PRP027 Peripheral Vascular Disease 71 0.118
27
P DBT009 Diabetes Mellitus 64 0.118
28
BNR002 Bone Resorption Disease 48 0.112
29
STR067 Stroke, Ischemic 81 0.106
30
c HYP836 Hypercholesterolemia, Familial, 1 73 0.106
31
P HYP750 Hypertriglyceridemia, Familial 62 0.106
32
P BRS047 Breast Cancer 97 0.100
33
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.100
34
P TRN020 Turner Syndrome 67 0.100
35
LPD008 Lipid Metabolism Disorder 62 0.100
36
GLS018 Glass Syndrome 57 0.100
37
P ART021 Arteriosclerosis 54 0.100
38
IDP070 Idiopathic Scoliosis 42 0.100
39
RDN001 Reading Disorder 40 0.100
40
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.094
41
CRB039 Cerebrovascular Disease 67 0.094
42
DPR016 Depression 63 0.094
43
AGN016 Aging 56 0.094
44
P SCL057 Scoliosis, Isolated 1 41 0.094
45
P CLR023 Colorectal Cancer 99 0.087
46
P LNG032 Lung Cancer 98 0.087
47
P KDN018 Kidney Disease 72 0.087
48
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.087
49
c FNC043 Fanconi Anemia, Complementation Group E 62 0.087
50
MNT002 Mental Depression 58 0.087
51
CLF001 Cleft Lip 53 0.087
52
DNT012 Dental Caries 53 0.087
53
PRP080 Peripheral Artery Disease 53 0.087
54
BRX001 Bruxism 50 0.087
55
P CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.087
56
P PRD008 Periodontitis 64 0.079
57
c FML035 Familial Hyperlipidemia 55 0.079
58
CLF004 Cleft Lip/palate 54 0.079
59
47X002 47,xyy 49 0.079
60
48X005 48,xyyy 39 0.079
61
ENP001 Enophthalmos 35 0.079
62
P ALZ034 Alzheimer Disease 88 0.071
63
MYL069 Myeloma, Multiple 85 0.071
64
c CHR684 Chronic Kidney Disease 70 0.071
65
P SLP006 Sleep Apnea 69 0.071
66
P LVR013 Liver Disease 68 0.071
67
FTT001 Fatty Liver Disease 61 0.071
68
SQM006 Squamous Cell Carcinoma 60 0.071
69
PLM033 Pulmonary Embolism 59 0.071
70
CRD132 Cardiac Conduction Defect 58 0.071
71
THR024 Thrombosis 57 0.071
72
HMF006 Hemifacial Microsomia 55 0.071
73
P AML002 Amelogenesis Imperfecta 55 0.071
74
HMC014 Homocysteinemia 53 0.071
75
ASP030 Aspirin Resistance 39 0.071
76
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.071
77
PLY150 Polykaryocytosis Inducer 31 0.071
78
P BLD134 Bladder Cancer 79 0.061
79
c ATR087 Atrial Standstill 1 75 0.061
80
P OST002 Osteoporosis 74 0.061
81
SVR004 Severe Combined Immunodeficiency 73 0.061
82
c THR092 Thrombophilia Due to Thrombin Defect 73 0.061
83
DWN001 Down Syndrome 70 0.061
84
P CRN037 Craniosynostosis 68 0.061
85
P MCR115 Microvascular Complications of Diabetes 5 66 0.061
86
c ANM038 Anemia, Autoimmune Hemolytic 62 0.061
87
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.061
88
HYP066 Hyperglycemia 61 0.061
89
P MYL006 Myeloid Leukemia 60 0.061
90
DCT002 Ductal Carcinoma in Situ 59 0.061
91
ANR040 Aneurysm 59 0.061
92
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.061
93
HYP060 Hyperinsulinism 54 0.061
94
P ALP008 Alopecia 54 0.061
95
P INS002 in Situ Carcinoma 53 0.061
96
CRT016 Carotid Artery Disease 52 0.061
97
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.061
98
GNG003 Gingival Recession 44 0.061
99
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.061
100
RST023 Resting Heart Rate, Variation in 41 0.061
102
P HPT023 Hepatocellular Carcinoma 100 0.050
103
NRL016 Neural Tube Defects 82 0.050
104
c MNN043 Meningioma, Familial 74 0.050
105
DFC004 Deficiency Anemia 70 0.050
106
ADL002 Adult Syndrome 70 0.050
107
LYM133 Lymphoma, Hodgkin, Classic 69 0.050
108
P OCL013 Oculodentodigital Dysplasia 69 0.050
109
P MJR001 Major Depressive Disorder 68 0.050
110
P THR014 Thrombocytopenia 67 0.050
111
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.050
112
c FML021 Familial Hypercholesterolemia 66 0.050
113
P ATR011 Atrial Fibrillation 66 0.050
114
c SML038 Small Cell Cancer of the Lung 65 0.050
115
P PLM036 Pulmonary Fibrosis 65 0.050
116
P PRS038 Personality Disorder 65 0.050
117
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.050
118
MSC007 Muscle Hypertrophy 64 0.050
119
P HML002 Hemolytic Anemia 63 0.050
120
ANR007 Anorexia Nervosa 63 0.050
121
P ECT006 Ectodermal Dysplasia 62 0.050
122
P PSR002 Psoriasis 62 0.050
123
P VSC011 Vasculitis 62 0.050
124
ALL026 Allergic Hypersensitivity Disease 62 0.050
125
MNN042 Meningioma, Radiation-Induced 62 0.050
126
OST003 Osteonecrosis 61 0.050
127
INT002 Intermittent Claudication 61 0.050
128
P HMN010 Hemangioma 61 0.050
129
TTH002 Tooth Agenesis 60 0.050
130
LNG099 Lung Disease 60 0.050
131
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.050
132
P PRN023 Prion Disease 57 0.050
133
HYP266 Hypoxia 57 0.050
134
P MYS005 Myositis 56 0.050
135
P SZR006 Seizure Disorder 56 0.050
136
MCS002 Mucositis 56 0.050
137
GLC003 Glucose Intolerance 54 0.050
138
c PRD040 Periodontitis, Chronic 53 0.050
139
c PSR017 Psoriasis 2 53 0.050
140
EXP004 Exophthalmos 52 0.050
141
PST011 Pustulosis of Palm and Sole 52 0.050
142
c PSR023 Psoriasis 1 52 0.050
143
FML037 Female Breast Cancer 52 0.050
144
HYP014 Hyperuricemia 52 0.050
145
END086 End Stage Renal Disease 51 0.050
146
HYP081 Hypolipoproteinemia 51 0.050
147
c HNT004 Huntington Disease-Like 2 50 0.050
148
SPN021 Spinal Meningioma 50 0.050
149
CRT013 Carotid Stenosis 50 0.050
150
STM007 Stomatitis 50 0.050
151
PLP001 Pulpitis 49 0.050
152
HLX001 Helix Syndrome 47 0.050
153
c PSR032 Psoriasis 11 47 0.050
154
MYC005 Myocardial Stunning 46 0.050
155
RTR008 Root Resorption 45 0.050
156
ATN004 Autonomic Neuropathy 45 0.050
157
ASP026 Asplenia, Isolated Congenital 44 0.050
158
AND001 Anodontia 43 0.050
159
ORL015 Oral Squamous Cell Carcinoma 43 0.050
160
TRP009 Triple X Syndrome 42 0.050
161
CYT002 Cytokine Deficiency 42 0.050
162
c PSR028 Psoriasis 7 42 0.050
163
ATX019 Ataxia with Vitamin E Deficiency 42 0.050
164
MMM006 Mammographic Density 41 0.050
165
c PSR018 Psoriasis 13 41 0.050
166
SCR001 Secretory Meningioma 41 0.050
167
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.050
168
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.050
169
c HNT011 Huntington Disease-Like 3 38 0.050
170
TTH008 Tooth Resorption 37 0.050
171
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.050
172
DNT008 Denture Stomatitis 35 0.050
173
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.050
174
PLM028 Pulmonary Coin Lesion 33 0.050
175
TQP001 Taqi Polymorphism 32 0.050
176
MXL008 Maxillary Sinus Cancer 32 0.050
177
CRN051 Craniofacial Microsomia 28 0.050
178
CHL079 Children's Interstitial Lung Disease 26 0.050
179
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.050
180
AND017 Anodontia of Permanent Dentition 23 0.050
181
ART109 Arterial Thoracic Outlet Syndrome 22 0.050
182
THY020 Thyroid Hyalinizing Trabecular Adenoma 21 0.050
183
P SNS011 Sinus Cancer 21 0.050
184
P PRS040 Prostate Cancer 97 0.035
185
ESP021 Esophageal Cancer 90 0.035
186
c LKM061 Leukemia, Acute Myeloid 84 0.035
187
P RHM011 Rheumatoid Arthritis 80 0.035
188
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.035
189
c DLT002 Dilated Cardiomyopathy 79 0.035
190
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.035
191
END057 Endometrial Cancer 74 0.035
192
P SCH015 Schizophrenia 74 0.035
193
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.035
194
P CNR004 Cone-Rod Dystrophy 2 73 0.035
195
ANX010 Anxiety 73 0.035
196
P NRB001 Neuroblastoma 72 0.035
197
HMN044 Human Immunodeficiency Virus Type 1 71 0.035
198
P SRC025 Sarcoidosis 1 70 0.035
199
P ATS364 Autism 70 0.035
200
PLM001 Pulmonary Tuberculosis 69 0.035
201
P MLN008 Melanoma 69 0.035
202
P ART022 Arthritis 69 0.035
203
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.035
204
ART016 Aortic Aneurysm 69 0.035
205
P LYM118 Lymphoma 68 0.035
206
RCK004 Rickets 68 0.035
207
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 68 0.035
208
CHR103 Charge Syndrome 67 0.035
209
BRK010 Burkitt Lymphoma 67 0.035
210
PSY004 Psychotic Disorder 67 0.035
211
c ATS007 Autism Spectrum Disorder 67 0.035
212
c RHB024 Rhabdomyosarcoma 2 67 0.035
213
LPT001 Leptospirosis 66 0.035
214
OST159 Osteogenic Sarcoma 66 0.035
215
P TRC072 Treacher Collins Syndrome 1 66 0.035
216
P DMN002 Dementia 66 0.035
217
P MSC005 Muscular Dystrophy 66 0.035
218
P NSP012 Nasopharyngeal Carcinoma 66 0.035
219
HYP056 Hypoglycemia 66 0.035
220
TNG002 Tangier Disease 65 0.035
221
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.035
222
P CLD001 Cleidocranial Dysplasia 65 0.035
223
KWS002 Kawasaki Disease 65 0.035
224
c DBT099 Diabetes Mellitus, Type I 65 0.035
225
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.035
226
APN008 Apnea, Obstructive Sleep 64 0.035
227
NRM005 Neuromuscular Disease 64 0.035
228
c JVN010 Juvenile Rheumatoid Arthritis 64 0.035
229
GT001 Gout 64 0.035
230
ART002 Arts Syndrome 64 0.035
231
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.035
232
P NTR004 Neutropenia 63 0.035
233
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.035
234
PLG002 Plague 63 0.035
235
TRN015 Transient Cerebral Ischemia 63 0.035
236
P TRC086 Trichohepatoenteric Syndrome 1 62 0.035
237
P ART023 Arthropathy 62 0.035
238
LSC001 Lesch-Nyhan Syndrome 62 0.035
239
MDD011 Mood Disorder 62 0.035
240
P ENC018 Encephalopathy 61 0.035
241
P SJG008 Sjogren Syndrome 61 0.035
242
c LPM012 Lipomatosis, Multiple 60 0.035
243
TRG002 Trigeminal Neuralgia 60 0.035
244
c JVN061 Juvenile Arthritis 60 0.035
245
CRD223 Cardiac Arrhythmia 60 0.035
246
ACQ007 Acquired Immunodeficiency Syndrome 60 0.035
247
c ACT071 Acute Kidney Failure 60 0.035
248
P MYC008 Myocarditis 59 0.035
249
THY029 Thyroid Carcinoma 59 0.035
250
GNG013 Gingivitis 59 0.035
251
BRN002 Bronchiolitis 59 0.035
252
ADN018 Adenoma 59 0.035
253
BLM002 Bulimia Nervosa 57 0.035
254
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.035
255
P BPL003 Bipolar Disorder 56 0.035
256
PNM008 Pneumothorax 56 0.035
257
c LSS005 Lissencephaly 1 56 0.035
258
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.035
259
TRN018 Transitional Cell Carcinoma 56 0.035
260
LBL001 Lobular Neoplasia 56 0.035
261
P NRP001 Neuropathy 56 0.035
262
SCH003 Schizophreniform Disorder 56 0.035
263
PRS047 Prostatitis 56 0.035
264
P NRF002 Neurofibromatosis 56 0.035
265
INT030 Intracranial Aneurysm 56 0.035
266
P PNM006 Pneumoconiosis 56 0.035
267
MCL006 Macular Retinal Edema 55 0.035
268
LMB062 Limb Ischemia 55 0.035
269
P CRB154 Cerebrocostomandibular Syndrome 55 0.035
270
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.035
271
ACT058 Active Peptic Ulcer Disease 55 0.035
272
END040 Endogenous Depression 55 0.035
273
HYP732 Hyperalphalipoproteinemia 1 54 0.035
274
CRT017 Cartilage Disease 54 0.035
275
GST037 Gastroparesis 54 0.035
276
DBT010 Diabetic Neuropathy 54 0.035
277
AGN012 Agnathia-Otocephaly Complex 53 0.035
278
HRT012 Heart Valve Disease 53 0.035
279
PLS016 Plasma Cell Leukemia 53 0.035
280
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.035
281
NRT001 Neurotic Disorder 53 0.035
282
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.035
283
CLB010 Coloboma of Macula 52 0.035
284
ACR041 Acromelic Frontonasal Dysostosis 52 0.035
285
P SML001 Small Cell Carcinoma 52 0.035
286
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.035
287
P RCT021 Rectum Cancer 52 0.035
288
P DNT011 Dentinogenesis Imperfecta 52 0.035
289
P NLX004 Neu-Laxova Syndrome 1 52 0.035
290
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.035
291
LNG031 Lung Benign Neoplasm 51 0.035
292
BHR001 Behr Syndrome 51 0.035
293
SCH012 Schizoaffective Disorder 50 0.035
294
PST021 Postpartum Depression 50 0.035
295
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.035
296
HMG002 Hemoglobinuria 50 0.035
297
P MTH008 Methylmalonic Acidemia 50 0.035
298
c CHR418 Chronic Leukemia 49 0.035
299
LFT001 Left Bundle Branch Hemiblock 49 0.035
300
PCT003 Pectus Excavatum 49 0.035
301
DYS009 Dysthymic Disorder 49 0.035
302
c HYP837 Hypercholesterolemia, Familial, 2 49 0.035
303
c HPT015 Hepatitis D 49 0.035
304
VCC001 Vaccinia 49 0.035
305
c BCT013 Bacterial Pneumonia 48 0.035
306
ATS010 Autosomal Recessive Disease 48 0.035
307
ADT003 Auditory System Disease 48 0.035
308
ASP007 Aspiration Pneumonia 48 0.035
309
SCL003 Social Phobia 48 0.035
310
VTM033 Vitamin K Deficiency Bleeding 48 0.035
311
DBT006 Diabetic Macular Edema 48 0.035
312
c MTR002 Mitral Valve Insufficiency 48 0.035
313
FBR032 Fibromuscular Dysplasia 48 0.035
314
FBR009 Fibrous Dysplasia 48 0.035
315
MDD010 Middle Ear Disease 48 0.035
316
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.035
317
INT010 Intracranial Embolism 48 0.035
318
ANT018 Anthracosis 48 0.035
319
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.035
320
c INH020 Inherited Metabolic Disorder 47 0.035
321
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.035
322
AML029 Ameloblastoma 46 0.035
323
LYM019 Lymphosarcoma 46 0.035
324
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.035
325
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.035
326
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.035
327
CMP034 Complete Androgen Insensitivity Syndrome 46 0.035
328
FCL012 Facial Paralysis 46 0.035
329
CLN045 Colonic Benign Neoplasm 46 0.035
330
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.035
331
CRN019 Coronary Artery Vasospasm 46 0.035
332
HDN002 Head Injury 46 0.035
333
HMF009 Hemifacial Hyperplasia 45 0.035
334
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.035
335
TRT001 Teratocarcinoma 45 0.035
336
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.035
337
GNG011 Gingival Disease 45 0.035
338
DWR001 Dwarfism 44 0.035
339
P PLM149 Palmoplantar Keratoderma and Congenital Alopecia 2 44 0.035
340
P BCT020 Bacteremia 2 44 0.035
341
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.035
342
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.035
343
DVR002 Diverticulitis 43 0.035
344
P MJR007 Major Affective Disorder 1 43 0.035
345
PHY002 Physical Disorder 42 0.035
346
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.035
347
DNT014 Dental Pulp Disease 42 0.035
348
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.035
349
BCK006 Back Pain 42 0.035
350
c HYP841 Hypoalphalipoproteinemia, Primary, 1 41 0.035
351
P CHR342 Chiari Malformation 41 0.035
352
49X006 49, Xxxxy Syndrome 41 0.035
353
MTL005 Metal Allergy 41 0.035
354
PLG004 Plagiocephaly 41 0.035
355
c MJR024 Major Affective Disorder 9 41 0.035
356
PRS063 Paresthesia 41 0.035
357
OST115 Osteonecrosis of the Jaw 40 0.035
358
TBL003 Tubular Adenocarcinoma 40 0.035
359
PLM005 Pleomorphic Lipoma 40 0.035
360
HYP008 Hypertensive Retinopathy 39 0.035
361
CRV045 Cervical Intraepithelial Neoplasia 39 0.035
362
c ACQ005 Acquired Thrombocytopenia 39 0.035
363
CVT001 Cavitary Optic Disc Anomalies 38 0.035
364
c MJR022 Major Affective Disorder 8 38 0.035
365
c ZMM002 Zimmermann-Laband Syndrome 1 36 0.035
366
c AMY088 Amyotrophic Lateral Sclerosis 3 36 0.035
367
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.035
368
c MJR008 Major Affective Disorder 2 35 0.035
369
AMR003 Amaurosis Fugax 34 0.035
370
c MJR023 Major Affective Disorder 7 33 0.035
371
RTC003 Root Caries 33 0.035
372
c MJR003 Major Affective Disorder 6 33 0.035
373
c MJR006 Major Affective Disorder 5 33 0.035
374
c PRS136 Prostate Cancer, Hereditary, 6 33 0.035
375
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.035
376
TTH030 Teeth, Supernumerary 33 0.035
377
c PRS130 Prostate Cancer, Hereditary, 8 32 0.035
378
BLR030 Bilirubin, Serum Level of, Quantitative Trait Locus 1 32 0.035
379
ERY069 Erythrokeratoderma ''en Cocardes'' 30 0.035
380
AML065 Amelia 30 0.035
381
MXL017 Maxillary Cancer 29 0.035
382
PRX008 Paroxysmal Cold Hemoglobinuria 29 0.035
383
c MJR004 Major Affective Disorder 4 28 0.035
384
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.035
385
ATM069 Autoimmune Hemolytic Anemia, Warm Type 28 0.035
386
P SKL005 Skull Base Meningioma 27 0.035
387
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.035
388
MND001 Mandibular Cancer 24 0.035
389
PPL054 Popliteal Cyst 23 0.035
390
HDG004 Hodgkin's Granuloma 23 0.035
391
HDG006 Hodgkin's Paragranuloma 22 0.035
392
c ZMM003 Zimmermann-Laband Syndrome 2 22 0.035
393
NWN001 New-Onset Refractory Status Epilepticus 21 0.035
394
c CLD019 Cleidocranial Dysplasia Spectrum Disorder 21 0.035
395
WRM004 Warm Antibody Hemolytic Anemia 20 0.035
396
SPH003 Sphenoorbital Meningioma 17 0.035
397
CYS035 Cystic Adventitial Disease 12 0.035
398
c INF052 Infantile Scoliosis 12 0.035
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