Search results for coil

392 hits were found for coil

# Family MCID Name MIFTS Score
1
P SPN046 Spinal Muscular Atrophy 63 4.480
2
c SPH013 Spherocytosis, Type 1 53 2.608
3
ISC001 Ischemic Neuropathy 26 2.559
4
ANR040 Aneurysm 61 0.621
5
CRB009 Cerebritis 41 0.423
6
CRB086 Cerebral Aneurysms 42 0.421
7
P INT030 Intracranial Aneurysm 58 0.346
8
ART005 Arteriovenous Malformation 64 0.182
9
CRB039 Cerebrovascular Disease 68 0.173
10
ART140 Arteries, Anomalies of 51 0.170
11
PLM151 Pulmonary Arteriovenous Fistulas 33 0.160
12
PLM052 Pulmonary Arteriovenous Malformation 35 0.156
13
P NRB001 Neuroblastoma 73 0.133
14
LNG099 Lung Disease 67 0.133
15
P PLM034 Pulmonary Emphysema 59 0.133
16
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.129
17
RSP006 Respiratory System Disease 63 0.129
18
P LKM002 Leukemia 75 0.120
19
MNT002 Mental Depression 60 0.120
20
P BRS047 Breast Cancer 100 0.115
21
P PTN014 Patent Ductus Arteriosus 1 45 0.115
22
MDD011 Mood Disorder 64 0.110
23
END072 Endotheliitis 46 0.110
24
SPL005 Splenic Artery Aneurysm 32 0.110
25
PSY004 Psychotic Disorder 72 0.105
26
VSC007 Vascular Disease 71 0.105
27
P MJR001 Major Depressive Disorder 70 0.105
28
c BLD140 Blood Group, I System 37 0.105
29
P HYD006 Hydrocephalus 68 0.100
30
P PLY014 Polycystic Kidney Disease 60 0.100
31
RTN023 Retinitis 52 0.100
32
P LNG032 Lung Cancer 99 0.088
33
ISC004 Ischemia 66 0.088
34
PRS047 Prostatitis 59 0.088
35
EPD016 Epidermolysis Bullosa 57 0.088
36
P CRN074 Coronary Artery Aneurysm 47 0.088
37
DDN006 Duodenitis 46 0.088
38
P PRS040 Prostate Cancer 88 0.082
39
c SML038 Small Cell Cancer of the Lung 67 0.082
40
P PNC044 Pancreatitis 64 0.082
41
P DDN001 Duodenal Ulcer 53 0.082
42
P MYT002 Myotonic Dystrophy 50 0.082
43
P PLM064 Pulmonary Sequestration 25 0.082
44
P CLR023 Colorectal Cancer 98 0.074
45
P HPT021 Hepatitis 75 0.074
46
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.074
47
P KDN018 Kidney Disease 69 0.074
48
THR024 Thrombosis 61 0.074
49
P EPD003 Epidermolysis Bullosa Simplex 53 0.074
50
P PLY017 Polyarteritis Nodosa 51 0.074
51
c MTR002 Mitral Valve Insufficiency 46 0.074
52
PLY112 Polyarteritis Nodosa, Childhood-Onset 39 0.074
53
P RTT002 Rett Syndrome 82 0.067
54
P RTN008 Retinitis Pigmentosa 81 0.067
55
P HRT032 Heart Disease 80 0.067
56
NRL016 Neural Tube Defects 79 0.067
57
P LVR013 Liver Disease 76 0.067
58
ANX010 Anxiety 72 0.067
59
ART016 Aortic Aneurysm 70 0.067
60
P MYL006 Myeloid Leukemia 69 0.067
61
PNC041 Pancreatic Ductal Adenocarcinoma 67 0.067
62
VRC005 Varicose Veins 64 0.067
63
P ENC018 Encephalopathy 58 0.067
64
P TCL004 T-Cell Leukemia 50 0.067
65
HYP063 Hypersplenism 49 0.067
66
c LBR014 Leber Congenital Amaurosis 4 48 0.067
67
P ART084 Arteriovenous Fistula 46 0.067
68
MLB001 Mulibrey Nanism 46 0.067
69
P RTN014 Retinal Artery Occlusion 45 0.067
70
CRT008 Carotid Artery Dissection 42 0.067
71
CRT015 Carotid Artery Occlusion 42 0.067
72
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.067
73
CRN006 Coronary Aneurysm 32 0.067
74
PTN004 Patent Ductus Venosus 26 0.067
75
P HPT023 Hepatocellular Carcinoma 94 0.058
76
MLR004 Malaria 86 0.058
77
STR067 Stroke, Ischemic 84 0.058
78
P NRV007 Nervous System Disease 75 0.058
79
CNG034 Congestive Heart Failure 74 0.058
80
THY028 Thyroid Cancer 72 0.058
81
NRF026 Neurofibromatosis, Type Iv, of Riccardi 72 0.058
82
P MNN013 Meningitis 71 0.058
83
P ADN016 Adenocarcinoma 71 0.058
84
SRC014 Sarcoma 68 0.058
85
GST050 Gastrointestinal System Disease 66 0.058
86
P PRS038 Personality Disorder 65 0.058
87
TRG002 Trigeminal Neuralgia 60 0.058
88
SFT003 Soft Tissue Sarcoma 58 0.058
89
URN009 Urinary System Disease 58 0.058
90
P MSC003 Muscular Atrophy 55 0.058
91
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.058
92
PRP016 Paraplegia 53 0.058
93
CRB004 Cerebral Artery Occlusion 46 0.058
94
MDS022 Mediastinitis 44 0.058
95
NRN002 Neuronitis 43 0.058
96
P CRN035 Cranial Nerve Palsy 42 0.058
97
TTL012 Total Anomalous Pulmonary Venous Return 1 42 0.058
98
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.058
99
GST039 Gastroduodenitis 33 0.058
100
PLV004 Pelvic Varices 24 0.058
101
SBC002 Subclavian Artery Aneurysm 23 0.058
102
CRN197 Coronary Arterial Fistulas 19 0.058
103
c SPR115 Spermatogenic Failure 19 15 0.058
104
c SPR114 Spermatogenic Failure 20 15 0.058
105
P RHM011 Rheumatoid Arthritis 91 0.047
106
MYL069 Myeloma, Multiple 86 0.047
107
GST053 Gastric Cancer 84 0.047
108
c LKM063 Leukemia, Chronic Myeloid 80 0.047
109
P PLM037 Pulmonary Hypertension 79 0.047
110
P DLT002 Dilated Cardiomyopathy 76 0.047
111
MLD001 Melioidosis 73 0.047
112
LVR012 Liver Cirrhosis 73 0.047
113
BRN028 Brain Cancer 72 0.047
114
HMN044 Human Immunodeficiency Virus Type 1 71 0.047
115
P LYM118 Lymphoma 71 0.047
116
P SCH015 Schizophrenia 71 0.047
117
WRN001 Werner Syndrome 70 0.047
118
P TTR001 Tetralogy of Fallot 70 0.047
119
P EPL164 Epilepsy 70 0.047
120
c MNN043 Meningioma, Familial 69 0.047
121
P ATR011 Atrial Fibrillation 68 0.047
122
OBS002 Obsessive-Compulsive Disorder 68 0.047
123
LYM017 Lyme Disease 68 0.047
124
DMN002 Dementia 68 0.047
125
c HRD010 Hereditary Spastic Paraplegia 68 0.047
126
DRM006 Dermatitis 67 0.047
127
PRT036 Peritonitis 67 0.047
128
P AST007 Astrocytoma 66 0.047
129
INS001 Insulinoma 66 0.047
130
c CNT035 Central Nervous System Disease 65 0.047
131
MSL001 Measles 64 0.047
132
BLL006 Bullous Pemphigoid 64 0.047
133
P LNG064 Lung Cancer Susceptibility 3 64 0.047
134
P NRP001 Neuropathy 63 0.047
135
P HYP055 Hypoplastic Left Heart Syndrome 63 0.047
136
PLM033 Pulmonary Embolism 62 0.047
137
P SLV002 Salivary Gland Cancer 62 0.047
138
HYP266 Hypoxia 61 0.047
139
P EHL001 Ehlers-Danlos Syndrome 61 0.047
140
P ACT074 Acute Lymphocytic Leukemia 61 0.047
141
P DYS154 Dystonia 61 0.047
142
c AFB002 Afibrinogenemia, Congenital 61 0.047
143
P BPL003 Bipolar Disorder 61 0.047
144
NRM005 Neuromuscular Disease 60 0.047
145
CLR108 Colorectal Adenoma 60 0.047
146
CHR177 Chromophobe Renal Cell Carcinoma 59 0.047
147
PNC034 Pancreas Disease 59 0.047
148
ESP023 Esophageal Disease 58 0.047
149
P PRG013 Paraganglioma 57 0.047
150
GST023 Gastric Ulcer 57 0.047
151
P PRM011 Primary Ciliary Dyskinesia 57 0.047
152
PLM010 Pulmonary Edema 57 0.047
153
P THY032 Thyroiditis 56 0.047
154
BLD131 Bladder Urothelial Carcinoma 55 0.047
155
HDC001 Headache 55 0.047
156
ASP003 Aseptic Meningitis 54 0.047
157
HPT009 Hepatopulmonary Syndrome 53 0.047
158
FBR032 Fibromuscular Dysplasia 53 0.047
159
CRT013 Carotid Stenosis 52 0.047
160
c HMN021 Human T-Cell Leukemia Virus Type 1 52 0.047
161
P CHL066 Cholangitis 52 0.047
162
VRC001 Varicocele 52 0.047
163
c CRD233 Cardiomyopathy, Dilated, 1b 51 0.047
164
P CRV039 Cervicitis 49 0.047
165
HYD002 Hydronephrosis 49 0.047
166
P AFB001 Afibrinogenemia 49 0.047
167
PRP007 Priapism 49 0.047
168
P RNL017 Renal Oncocytoma 49 0.047
169
P LSS002 Lissencephaly 49 0.047
170
STS002 Situs Inversus 48 0.047
171
ANG011 Angiodysplasia 48 0.047
172
PLM102 Palmoplantar Keratoderma, Epidermolytic 47 0.047
173
P JNC001 Junctional Epidermolysis Bullosa 47 0.047
174
LCK001 Locked-in Syndrome 47 0.047
175
c MSC050 Muscular Dystrophy, Congenital, 1b 45 0.047
176
c CHR020 Chronic Interstitial Cystitis 44 0.047
177
P OPT048 Opitz-Gbbb Syndrome 41 0.047
178
SPS057 Spasticity 41 0.047
179
P HMF004 Hemifacial Spasm 41 0.047
180
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.047
181
c HYP543 Hypoplastic Left Heart Syndrome 1 38 0.047
182
c DYS165 Dysfibrinogenemia, Congenital 37 0.047
183
OBS004 Obstructive Hydrocephalus 37 0.047
184
BSL004 Basilar Artery Occlusion 35 0.047
185
CRT012 Cortical Blindness 34 0.047
186
MTL005 Metal Allergy 32 0.047
187
APC009 Apocrine Gland Secretion, Variation in 29 0.047
188
PLM058 Pulmonary Atresia with Intact Ventricular Septum 29 0.047
189
P RNG031 Ring Chromosome Y Syndrome 29 0.047
190
c SMT018 Smith-Mccort Dysplasia 2 24 0.047
191
PRX034 Peroxisome Disorders 20 0.047
192
MND005 Mondini Dysplasia 17 0.047
193
c ALZ002 Alzheimer Disease Type 1 15 0.047
194
c SPR113 Spermatogenic Failure 18 14 0.047
195
ORB016 Orbital Varix 14 0.047
196
P PNC035 Pancreatic Cancer 89 0.033
197
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.033
198
CYS001 Cystic Fibrosis 85 0.033
199
P OVR042 Ovarian Cancer 82 0.033
200
P MYC007 Myocardial Infarction 81 0.033
201
ESP021 Esophageal Cancer 79 0.033
202
LYM133 Lymphoma, Hodgkin, Classic 78 0.033
203
P ART022 Arthritis 77 0.033
204
P INF038 Influenza 77 0.033
205
P WSK001 Wiskott-Aldrich Syndrome 76 0.033
206
SQM006 Squamous Cell Carcinoma 74 0.033
207
GST019 Gastrointestinal Stromal Tumor 74 0.033
208
MSC157 Muscular Dystrophy, Duchenne Type 74 0.033
209
KPS004 Kaposi Sarcoma 73 0.033
210
c CHR089 Chronic Kidney Failure 72 0.033
211
PRP027 Peripheral Vascular Disease 71 0.033
212
P RSP003 Respiratory Failure 71 0.033
213
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.033
214
P PNM007 Pneumonia 70 0.033
215
P TBR001 Tuberous Sclerosis 69 0.033
216
P MYP004 Myopathy 69 0.033
217
P CRN018 Coronary Artery Anomaly 69 0.033
218
P PLZ001 Pelizaeus-Merzbacher Disease 68 0.033
219
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.033
220
OTT002 Otitis Media 67 0.033
221
P ATT013 Attention Deficit-Hyperactivity Disorder 67 0.033
222
SPN186 Spinal Cord Injury 67 0.033
223
P MSC005 Muscular Dystrophy 66 0.033
224
P KDN017 Kidney Cancer 66 0.033
225
TKY002 Takayasu Arteritis 66 0.033
226
VSC011 Vasculitis 66 0.033
227
AGN016 Aging 65 0.033
228
P ART067 Aortic Aneurysm, Familial Thoracic 1 65 0.033
229
GLL008 Gilles De La Tourette Syndrome 64 0.033
230
NRL005 Neurilemmoma 64 0.033
231
c LPM012 Lipomatosis, Multiple 64 0.033
232
GST092 Gastroesophageal Reflux 64 0.033
233
MSC152 Muscular Dystrophy, Becker Type 64 0.033
234
P ESP024 Esophagitis 64 0.033
235
ADN018 Adenoma 63 0.033
236
c TBR025 Tuberous Sclerosis 1 63 0.033
237
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.033
238
CRD119 Cardiac Arrest 63 0.033
239
P HYP086 Hypothyroidism 62 0.033
240
P AGN002 Agnosia 61 0.033
241
NRV006 Nervous System Cancer 61 0.033
242
ETN001 Eating Disorder 61 0.033
243
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.033
244
P HMN010 Hemangioma 61 0.033
245
LMY014 Leiomyoma, Uterine 61 0.033
246
BRN056 Bronchopulmonary Dysplasia 61 0.033
247
P GLM045 Glioma 61 0.033
248
AVN001 Avian Influenza 60 0.033
249
ALP103 Alpha-1-Antitrypsin Deficiency 60 0.033
250
P BRN019 Bernard-Soulier Syndrome 60 0.033
251
P INF032 Infertility 59 0.033
252
MLG077 Malignant Peripheral Nerve Sheath Tumor 59 0.033
253
P VNT002 Ventricular Septal Defect 59 0.033
254
HPT019 Hepatic Encephalopathy 59 0.033
255
END030 End Stage Renal Failure 59 0.033
256
P LMY004 Leiomyosarcoma 59 0.033
257
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.033
258
P PLY019 Polyneuropathy 58 0.033
259
APH002 Aphasia 58 0.033
260
LMY002 Leiomyoma 58 0.033
261
PPL022 Papilloma 58 0.033
262
P LTR001 Lateral Sclerosis 58 0.033
263
P END033 Endocarditis 58 0.033
264
LYM019 Lymphosarcoma 58 0.033
265
PTT046 Pituitary Hormone Deficiency, Combined, 2 57 0.033
266
ART017 Aortic Disease 57 0.033
267
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.033
268
P LRY044 Larynx Cancer 57 0.033
269
c CRP023 Carpenter Syndrome 1 57 0.033
270
URN010 Urinary Tract Obstruction 57 0.033
271
c PRG042 Progressive Familial Heart Block, Type Ia 57 0.033
272
P RNL100 Renal Hypodysplasia/aplasia 1 57 0.033
273
c PRG018 Paragangliomas 1 57 0.033
274
NPH009 Nephrolithiasis 57 0.033
275
P LRY019 Laryngitis 57 0.033
276
INF034 Infective Endocarditis 56 0.033
277
BNF002 Bone Fracture 56 0.033
278
PRS042 Prostate Disease 56 0.033
279
P MYP006 Myopia 56 0.033
280
PLV003 Pelvic Inflammatory Disease 56 0.033
281
NRT004 Neuritis 55 0.033
282
BRN022 Bronchiectasis 55 0.033
283
SPS003 Spastic Diplegia 55 0.033
284
MGR028 Migraine with or Without Aura 1 55 0.033
285
BRN071 Brain Injury 54 0.033
286
P TRC086 Trichohepatoenteric Syndrome 1 54 0.033
287
c OVR114 Ovarian Cancer 1 54 0.033
288
TCD001 Tic Disorder 54 0.033
289
QDR001 Quadriplegia 54 0.033
290
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.033
291
P VNS003 Venous Insufficiency 53 0.033
292
PRP019 Peripheral Nervous System Disease 53 0.033
293
MSC033 Muscle Disorders 53 0.033
294
P OBS001 Obstructive Jaundice 53 0.033
295
P CRD132 Cardiac Conduction Defect 53 0.033
296
c BLM008 Bulimia Nervosa 2 53 0.033
297
c PNS012 Paine Syndrome 52 0.033
298
ACT049 Acute Disseminated Encephalomyelitis 52 0.033
299
NNT012 Neonatal Jaundice 51 0.033
300
THY030 Thyroid Gland Disease 51 0.033
301
c MLG074 Malignant Mesenchymoma 51 0.033
302
PRS045 Prostatic Hypertrophy 51 0.033
303
PRT029 Parathyroid Adenoma 50 0.033
304
CHL061 Childhood Leukemia 50 0.033
305
HMN032 Human Herpesvirus 8 50 0.033
306
RTN003 Retinal Ischemia 50 0.033
307
P HML001 Hemolytic-Uremic Syndrome 50 0.033
308
BRD004 Borderline Personality Disorder 50 0.033
309
P EPT020 Epithelioid Hemangioendothelioma 50 0.033
310
P MYM013 Moyamoya Disease 1 50 0.033
311
URT031 Ureteral Disease 50 0.033
312
TRN044 Transposition of the Great Arteries 49 0.033
313
MNN009 Meningoencephalitis 49 0.033
314
URT010 Ureteral Obstruction 49 0.033
315
FSC004 Fasciitis 48 0.033
316
DFN245 Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct 48 0.033
317
CHR008 Choroiditis 47 0.033
318
DYS073 Dysphagia 47 0.033
319
TRC062 Tricuspid Atresia 47 0.033
320
MNL001 Monilethrix 47 0.033
321
c CRD187 Cardiomyopathy, Dilated, 3b 46 0.033
322
ESP002 Esophageal Varix 46 0.033
323
P EPN001 Ependymoblastoma 46 0.033
324
EPD070 Epidermoid Cysts 46 0.033
325
ANG046 Angioimmunoblastic T-Cell Lymphoma 46 0.033
326
HRT012 Heart Valve Disease 45 0.033
327
ANH002 Anhidrosis 45 0.033
328
P HRN001 Horner's Syndrome 45 0.033
329
LYM024 Lymphatic System Disease 45 0.033
330
BRN080 Brain Ischemia 45 0.033
331
BSL008 Basal Ganglia Disease 44 0.033
332
HRT011 Heart Septal Defect 44 0.033
333
RGH001 Right Bundle Branch Block 44 0.033
334
EST005 Esotropia 43 0.033
335
HMN016 Hemangioendothelioma 43 0.033
336
MYF001 Myofibroma 42 0.033
337
PRG008 Paragonimiasis 42 0.033
338
SPR007 Superior Mesenteric Artery Syndrome 42 0.033
339
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 42 0.033
340
EXT022 Exotropia 41 0.033
341
PNG002 Pain Agnosia 41 0.033
342
RTR001 Retrograde Amnesia 40 0.033
343
CRD003 Cardiac Sarcoidosis 40 0.033
344
c PRG043 Progressive Familial Heart Block, Type Ib 40 0.033
345
MVM001 Movement Disease 40 0.033
346
c CNT028 Central Retinal Artery Occlusion 40 0.033
347
PRT019 Protein-Losing Enteropathy 40 0.033
348
P SPR013 Spiradenoma 39 0.033
349
MSC004 Muscle Tissue Disease 39 0.033
350
RMN001 Rumination Disorder 39 0.033
351
BLT003 Blue Toe Syndrome 38 0.033
352
c PLM022 Pulmonary Valve Insufficiency 38 0.033
353
LRY017 Laryngeal Disease 38 0.033
354
PTL009 Patella, Chondromalacia of 37 0.033
355
CHN011 Chondromalacia 36 0.033
356
c TRC022 Tricuspid Valve Insufficiency 36 0.033
357
P CNN004 Connective Tissue Cancer 35 0.033
358
BRN026 Branch Retinal Artery Occlusion 35 0.033
359
INT016 Intraductal Papilloma 35 0.033
360
P CMM008 Communicating Hydrocephalus 35 0.033
361
MSC012 Muscular Dystrophy, Duchenne and Becker Type 35 0.033
362
HRS011 Horseshoe Kidney 35 0.033
363
c HYP581 Hypotrichosis 6 35 0.033
364
MSN004 Mesenchymal Cell Neoplasm 35 0.033
365
c TRC078 Trichohepatoenteric Syndrome 2 34 0.033
366
TYL001 Taylor's Syndrome 33 0.033
367
FRN013 Frontotemporal Dementia, Chromosome 3-Linked 33 0.033
368
ASC003 Ascending Cholangitis 33 0.033
369
CRB147 Cerebellofaciodental Syndrome 32 0.033
370
c MYT029 Myotonia Congenita, Autosomal Recessive 32 0.033
371
HDR001 Hidrocystoma 31 0.033
372
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.033
373
VND005 Van Den Ende-Gupta Syndrome 29 0.033
374
ARL004 Aural Atresia, Congenital 27 0.033
375
EXT009 Extratemporal Epilepsy 27 0.033
376
c SPR086 Spermatogenic Failure 3 25 0.033
377
ADH006 Adhesive Otitis Media 25 0.033
378
LCR011 Lacrimal Gland Carcinoma 25 0.033
379
RGH006 Right Aortic Arch 25 0.033
380
c CNT068 Central Pain Syndrome 25 0.033
381
CHR189 Chromosome 12p Deletion 23 0.033
382
CRP004 Corpus Luteum Cyst 23 0.033
383
ADT001 Auditory Agnosia 22 0.033
384
THN005 Thunderclap Headache 17 0.033
385
PLM051 Pulmonary Arterio-Veinous Fistula 17 0.033
386
CHM002 Chmp2b-Related Frontotemporal Dementia 17 0.033
387
c PST018 Posterior Cerebral Artery Infarction 15 0.033
388
EXT062 Extracranial Carotid Artery Aneurysm 15 0.033
389
MND008 Mandibular Arteriovenous Malformation 12 0.033
390
CNG519 Congenital Gerbode Defect 10 0.033
391
PRT027 Partial Arterial Retinal Occlusion 10 0.033
392
ATR076 Atrophic Muscular Disease 6 0.033
Content
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