Search results for thrombophilia due to protein c deficiency

401 hits were found for thrombophilia due to protein c deficiency

# Family MCID Name MIFTS Score
1
THR068 Thrombophilia Due to Protein C Deficiency, Autosomal Recessive 27 8.074
2
PRT011 Protein C Deficiency 49 7.570
3
c THR082 Thrombophilia Due to Activated Protein C Resistance 51 7.166
4
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 20 5.185
5
P HPT021 Hepatitis 68 0.639
6
P THR015 Thrombophilia 58 0.517
7
THR024 Thrombosis 43 0.452
8
END072 Endotheliitis 41 0.433
9
P LKM002 Leukemia 72 0.410
10
P PNC044 Pancreatitis 60 0.313
11
CRB009 Cerebritis 39 0.312
12
P LVR013 Liver Disease 72 0.310
13
RTN023 Retinitis 49 0.299
14
P OBS005 Obesity 91 0.295
15
P THY032 Thyroiditis 53 0.295
16
P LNG032 Lung Cancer 94 0.293
17
P MYC007 Myocardial Infarction 77 0.257
18
PRT014 Protein S Deficiency 51 0.254
19
ISC004 Ischemia 59 0.246
20
P HRT032 Heart Disease 75 0.225
21
P NRP001 Neuropathy 57 0.224
22
P AST005 Asthma 81 0.221
23
ATH003 Atherosclerosis 65 0.217
24
c HPT003 Hepatitis a 56 0.217
25
P PNM007 Pneumonia 66 0.214
26
ART111 Artery Disease 55 0.213
27
P MYL006 Myeloid Leukemia 64 0.205
28
PRP030 Purpura 57 0.204
29
TBR010 Tuberculosis 69 0.201
30
INS024 Insulin-Like Growth Factor I 75 0.188
31
ANR040 Aneurysm 57 0.188
32
ADN018 Adenoma 58 0.188
33
P INF032 Infertility 57 0.188
34
P RTN024 Retinoblastoma 75 0.186
35
P MNN013 Meningitis 65 0.184
36
VSC007 Vascular Disease 65 0.183
37
CYS001 Cystic Fibrosis 86 0.182
38
GRW007 Growth Hormone Deficiency 48 0.180
39
P ENC018 Encephalopathy 52 0.173
40
c ACT075 Acute Myocardial Infarction 59 0.172
41
IMM136 Immune System Disease 53 0.167
42
BNS002 Bone Structure Disease 36 0.165
43
P INF037 Inflammatory Bowel Disease 62 0.163
44
P MLT019 Multiple Myeloma 82 0.163
45
BLD054 Blood Protein Disease 39 0.163
46
BRT030 Birth Defects 44 0.160
47
CLT003 Colitis 58 0.159
48
P PSR002 Psoriasis 64 0.157
49
PLM033 Pulmonary Embolism 59 0.156
50
PRT036 Peritonitis 60 0.154
51
P THL005 Thalassemia 61 0.151
52
P THR014 Thrombocytopenia 63 0.149
53
P LYM026 Lymphoblastic Leukemia 60 0.147
54
c CNT035 Central Nervous System Disease 60 0.145
55
P HMP007 Hemophilia 55 0.141
56
VSC011 Vasculitis 62 0.141
57
P PRP034 Purpura Fulminans 40 0.137
58
P RTN022 Retinal Vein Occlusion 37 0.135
59
PRP019 Peripheral Nervous System Disease 53 0.133
60
THR013 Thoracic Outlet Syndrome 49 0.131
61
ART021 Arteriosclerosis 57 0.131
62
MCS002 Mucositis 54 0.129
63
P CLL015 Collagen Disease 50 0.129
64
PRT037 Pertussis 63 0.128
65
VND001 Vein Disease 49 0.127
66
P ECL001 Eclampsia 51 0.127
67
P HMR003 Hemorrhagic Disease 55 0.126
68
c PRC016 Pre-Eclampsia 56 0.126
69
ALR002 Al-Raqad Syndrome 29 0.125
70
c HMP029 Hemophilia a 64 0.124
71
ULC004 Ulcerative Colitis 72 0.122
72
P NPH012 Nephrotic Syndrome 59 0.122
73
P HMC002 Homocystinuria 49 0.122
74
CRB039 Cerebrovascular Disease 63 0.120
75
P PLY011 Polycystic Ovary Syndrome 63 0.119
76
P ANT006 Antiphospholipid Syndrome 54 0.117
77
VSC008 Vascular Hemostatic Disease 32 0.116
78
AND005 Androgen Insensitivity Syndrome, Mild 16 0.116
79
HYP037 Hyperhomocysteinemia 49 0.116
80
CHL123 Chlamydia 58 0.113
81
P HYP060 Hyperinsulinism 57 0.112
82
P END033 Endocarditis 53 0.111
83
FTT001 Fatty Liver Disease 59 0.110
84
NRM005 Neuromuscular Disease 55 0.110
85
BCT015 Bacteremia 47 0.109
86
c CNT016 Central Retinal Vein Occlusion 35 0.108
87
PRT018 Portal Vein Thrombosis 47 0.107
88
FCT007 Factor Vii Deficiency 59 0.106
89
NTR005 Nutritional Deficiency Disease 47 0.106
90
DWR001 Dwarfism 45 0.104
91
P PLY019 Polyneuropathy 54 0.104
92
ISL003 Isolated Growth Hormone Deficiency 52 0.104
93
P MSC003 Muscular Atrophy 49 0.104
94
HDC001 Headache 53 0.103
95
TTH006 Tooth Disease 51 0.103
96
P BLD051 Blood Coagulation Disease 43 0.102
97
P HYP083 Hypopituitarism 54 0.102
98
FCT003 Factor X Deficiency 59 0.101
99
LSH001 Leishmaniasis 66 0.100
100
NRN004 Neuroendocrine Tumor 55 0.099
101
PTT006 Pituitary Adenoma 56 0.099
102
OST003 Osteonecrosis 43 0.099
103
FCT006 Factor V Deficiency 59 0.099
104
HPT074 Hepatic Adenoma, Somatic 44 0.098
105
BLD053 Blood Platelet Disease 46 0.097
106
FCT005 Factor Xiii Deficiency 46 0.097
107
PNC034 Pancreas Disease 55 0.096
108
ADJ001 Adjustment Disorder 38 0.096
109
SCK005 Sickle Cell Disease 51 0.095
110
GTR002 Goiter 52 0.095
111
c THR092 Thrombophilia Due to Thrombin Defect 50 0.095
112
THR089 Thrombophilia Due to Protein S Deficiency, Autosomal Dominant 21 0.094
113
FCT013 Factor V Leiden Thrombophilia 22 0.094
114
P CHR071 Charcot-Marie-Tooth Disease 67 0.093
115
P HML001 Hemolytic-Uremic Syndrome 49 0.093
116
ANG054 Angina Pectoris 49 0.093
117
NRL016 Neural Tube Defects 76 0.092
118
P THR005 Thrombotic Thrombocytopenic Purpura 57 0.092
119
DSS009 Disseminated Intravascular Coagulation 50 0.091
120
GLC003 Glucose Intolerance 54 0.091
121
PRP080 Peripheral Artery Disease 36 0.091
122
c HMP004 Hemophilia B 62 0.091
123
BNF002 Bone Fracture 51 0.091
124
PLM001 Pulmonary Tuberculosis 63 0.090
125
P SPN046 Spinal Muscular Atrophy 63 0.090
126
KRT004 Keratitis 70 0.090
127
ACR007 Acromegaly 66 0.090
128
P BDD001 Budd-Chiari Syndrome 56 0.090
129
P HYP076 Hyperthyroidism 53 0.089
130
MRF001 Marfan Syndrome 74 0.088
131
OTT002 Otitis Media 65 0.088
132
THR004 Thrombocytosis 52 0.087
133
CRN017 Coronary Thrombosis 47 0.087
134
CTN007 Cutaneous Leishmaniasis 61 0.087
135
PRP027 Peripheral Vascular Disease 65 0.087
136
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 48 0.087
137
HNM002 Hinman Syndrome 27 0.085
138
P PLY018 Polycythemia 56 0.083
139
P ESS003 Essential Thrombocythemia 70 0.083
140
c ACT134 Acute Liver Failure 48 0.083
141
FCT004 Factor Xii Deficiency 50 0.083
142
PTT009 Pituitary Gland Disease 46 0.083
143
P DBT005 Diabetes Insipidus 52 0.082
144
ATM055 Autoimmune Disease 4 18 0.082
145
P OVR049 Ovarian Disease 54 0.082
146
P TXP001 Toxoplasmosis 60 0.081
147
P PYL005 Pyelonephritis 52 0.081
148
MYL031 Myeloproliferative Neoplasm 57 0.080
149
P HMR012 Hemorrhagic Fever 52 0.080
150
INF034 Infective Endocarditis 50 0.080
151
P ASP006 Aspergillosis 60 0.080
152
VTM003 Vitamin Metabolic Disorder 31 0.080
153
OVR029 Ovarian Hyperstimulation Syndrome 61 0.080
154
c BCT007 Bacterial Meningitis 53 0.079
155
TTR016 Tetra-Amelia Syndrome 38 0.079
156
P RTN014 Retinal Artery Occlusion 42 0.078
157
IRR002 Irritable Bowel Syndrome 57 0.078
158
CGL001 Coagulation Protein Disease 16 0.077
159
HYP085 Hypothalamic Disease 42 0.077
160
HLL004 Hellp Syndrome 48 0.076
161
INT075 Intracranial Hypertension 48 0.076
162
GND003 Gonadal Disease 40 0.076
163
MLD001 Melioidosis 65 0.076
164
MGL001 Megaloblastic Anemia 49 0.076
165
ATM012 Autoimmune Disease of Blood 37 0.075
166
PLC007 Placental Abruption 46 0.075
167
SPT004 Septic Arthritis 55 0.075
168
PTN001 Patent Foramen Ovale 54 0.075
169
HYP064 Hypogonadotropism 35 0.075
170
P ART084 Arteriovenous Fistula 43 0.075
171
P PRD006 Prader-Willi Syndrome 65 0.074
172
THY030 Thyroid Gland Disease 49 0.074
173
TXC005 Toxic Shock Syndrome 55 0.074
174
PTT037 Pituitary Tumors 43 0.074
175
P TRN020 Turner Syndrome 65 0.074
176
THR016 Thrombophlebitis 52 0.073
177
BRN022 Bronchiectasis 49 0.073
178
LYM017 Lyme Disease 62 0.073
179
PSR001 Psoriatic Arthritis 63 0.073
180
INS001 Insulinoma 60 0.073
181
ISC002 Ischemic Optic Neuropathy 44 0.073
182
P DRM010 Dermatomyositis 59 0.072
183
MRB003 Morbid Obesity 58 0.072
184
c BLD124 Bleeding Disorder, Platelet-Type, 11 36 0.072
185
P ALP004 Alport Syndrome 70 0.071
186
VSC003 Visceral Leishmaniasis 55 0.071
187
MNN021 Meningococcemia 38 0.071
188
LMB062 Limb Ischemia 47 0.070
189
CHR005 Chorioamnionitis 47 0.070
190
HYP043 Hyperandrogenism 46 0.070
191
THR035 Thrombasthenia 41 0.070
192
P PRC031 Preeclampsia/eclampsia 1 55 0.070
193
RTN021 Retinal Vascular Occlusion 45 0.068
194
P PRC019 Precocious Puberty 50 0.068
195
ARM001 Aromatase Deficiency 57 0.068
196
VNW001 Von Willebrand's Disease 60 0.068
197
ACT087 Acth Deficiency 42 0.068
198
P ANR007 Anorexia Nervosa 60 0.068
199
FCT022 Factor Xi Deficiency, Autosomal Recessive 44 0.067
200
CRD001 Cardiac Tamponade 43 0.067
201
HPR003 Heparin-Induced Thrombocytopenia 44 0.067
202
BNM008 Bone Mineral Density, Low 17 0.067
203
FLR002 Filariasis 54 0.067
204
ATM014 Autoimmune Disease of Endocrine System 35 0.067
205
CHG001 Chagas Disease 66 0.067
206
STR067 Stroke, Ischemic 72 0.067
207
PYR037 Pyruvate Carboxylase Deficiency 39 0.067
208
CRT015 Carotid Artery Occlusion 41 0.067
209
LYM021 Lymphadenitis 57 0.067
210
c INH004 Inherited Blood Coagulation Disease 39 0.066
211
P PLZ001 Pelizaeus-Merzbacher Disease 67 0.066
212
P GCH001 Gaucher's Disease 63 0.065
213
c SVR056 Severe Hemophilia a 43 0.065
214
P PRM002 Primary Hyperoxaluria 50 0.064
215
UTR039 Uterine Fibroid 56 0.064
216
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.062
217
ADP007 Adie Pupil 35 0.062
218
c EHL032 Ehlers-Danlos Syndrome, Type Viib 50 0.062
219
AMN001 Amenorrhea 49 0.062
220
QFV001 Q Fever 55 0.061
221
c HRD088 Hereditary Neuropathies 39 0.061
222
CRN036 Craniopharyngioma 59 0.061
223
P BRC006 Brachydactyly 55 0.061
224
P VNS003 Venous Insufficiency 52 0.060
225
HYP020 Hyperprolactinemia 59 0.060
226
LPT001 Leptospirosis 57 0.060
227
SGT001 Sagittal Sinus Thrombosis 33 0.060
228
PST095 Post-Thrombotic Syndrome 48 0.060
229
INT002 Intermittent Claudication 55 0.060
230
SPL006 Splenic Infarction 33 0.060
231
P AGG001 Aggressive Periodontitis 49 0.060
232
SCT005 Scott Syndrome 51 0.059
233
P AXN001 Axonal Neuropathy 36 0.059
234
PRC002 Paracoccidioidomycosis 52 0.059
235
P DYS026 Dysfibrinogenemia 47 0.059
236
NSS002 Neisseria Meningitidis Infection 43 0.058
237
FBR009 Fibrous Dysplasia 44 0.058
238
P KLL001 Kallmann Syndrome 62 0.058
239
SPT005 Spotted Fever 49 0.058
240
THR020 Thrombophilia Due to Heparin Cofactor Ii Deficiency 20 0.058
241
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.058
242
P MYM002 Moyamoya Disease 60 0.058
243
RHM001 Rheumatic Fever 54 0.057
244
CHR001 Churg-Strauss Syndrome 47 0.057
245
AMR003 Amaurosis Fugax 37 0.057
246
c INV001 Invasive Aspergillosis 46 0.057
247
HMC014 Homocysteinemia 34 0.056
248
P AFB001 Afibrinogenemia 46 0.056
249
PLV003 Pelvic Inflammatory Disease 51 0.056
250
c ANT034 Anterior Uveitis 47 0.056
251
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 34 0.055
252
SCR008 Scrub Typhus 59 0.055
253
GLN010 Glanzmann Thrombasthenia 64 0.055
254
CRT008 Carotid Artery Dissection 39 0.055
255
LGG001 Legg-Calve-Perthes Disease 56 0.055
256
CRB132 Cerebral Sinovenous Thrombosis 29 0.055
257
P ATX010 Ataxia Neuropathy Spectrum 27 0.054
258
P HYP620 Hypoprothrombinemia 56 0.054
259
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.054
260
STC016 Sticky Platelet Syndrome 30 0.054
261
MNN017 Mononeuropathy 39 0.053
262
SLM003 Salmonellosis 51 0.052
263
c CNT028 Central Retinal Artery Occlusion 37 0.052
264
c CNT075 Central Precocious Puberty 50 0.052
265
ADR009 Adrenal Cortex Disease 39 0.052
266
P WLF004 Wolfram Syndrome 63 0.052
267
BRN026 Branch Retinal Artery Occlusion 34 0.052
268
MYL020 Myelomeningocele 50 0.051
269
RHM028 Rheumatic Heart Disease 48 0.051
270
PPL021 Papilledema 47 0.051
271
P CHR084 Chromosomal Disease 37 0.051
272
DBT087 Diabetes Insipidus, Neurohypophyseal 59 0.051
273
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 45 0.050
274
GRW024 Growth Hormone Deficiency, Isolated, Type Ii 44 0.050
275
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 52 0.050
276
PRS115 Prosthetic Joint Infection 41 0.050
277
CYS005 Cysticercosis 52 0.050
278
SRT004 Serotonin Syndrome 47 0.050
279
CCC001 Coccidioidomycosis 53 0.049
280
P SLV001 Silver-Russell Syndrome 56 0.049
281
c PRM225 Primary Thrombocytopenia 42 0.049
282
FTD001 Foot Drop 32 0.049
283
c HMG003 Hemoglobin E Disease 43 0.048
284
LVD002 Livedoid Vasculopathy 32 0.048
285
TLR001 Tularemia 41 0.048
286
INT007 Intermediate Coronary Syndrome 50 0.048
287
ISL001 Islet Cell Tumor 48 0.048
288
c CNG415 Congenital Disorder of Glycosylation, Type Ia 48 0.048
289
ADR012 Adrenal Gland Disease 48 0.048
290
SPN185 Spinal Cord Infarction 33 0.047
291
P CHR102 Charcot-Marie-Tooth Neuropathy 37 0.047
292
HMR002 Hemarthrosis 47 0.047
293
BRS090 Breast Reconstruction 38 0.047
294
c BRC081 Brachydactyly, Type C 37 0.046
295
PLC005 Placental Insufficiency 53 0.046
296
GGN002 Gigantism 32 0.046
297
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 43 0.046
298
HPT020 Hepatic Vascular Disease 42 0.046
299
RTN001 Retinal Vasculitis 43 0.046
300
QBC001 Quebec Platelet Disorder 52 0.046
301
BRN082 Bernard-Soulier Syndrome, Type C 52 0.046
302
CRR007 Cirrhosis, Cryptogenic 43 0.045
303
c SVR057 Severe Hemophilia B 31 0.045
304
ANT013 Anterior Spinal Artery Syndrome 33 0.045
305
c ACQ014 Acquired Hemophilia 40 0.045
306
CTS005 Catastrophic Antiphospholipid Syndrome 41 0.044
307
WBR001 Weber Syndrome 36 0.044
308
FCT016 Factor V and Factor Viii, Combined Deficiency of 33 0.044
309
c SVR005 Severe Pre-Eclampsia 48 0.044
310
P ACT080 Acute Pulmonary Heart Disease 31 0.044
311
DRM014 Dermatofibrosarcoma Protuberans 57 0.044
312
LRN004 Laron Dwarfism 59 0.044
313
P SCH018 Schizencephaly 52 0.044
314
VTM001 Vitamin K Deficiency Hemorrhagic Disease 31 0.044
315
P PRN026 Porencephaly 48 0.044
316
DMP001 Dumping Syndrome 40 0.044
317
SLP010 Slipped Capital Femoral Epiphysis 33 0.043
318
c AFB002 Afibrinogenemia, Congenital 52 0.043
319
P PTT050 Pituitary Adenoma, Growth Hormone-Secreting 48 0.043
320
NNT024 Neonatal Stroke 35 0.043
321
VNW005 Von Willebrand Disease, Type 1 47 0.043
322
c CHR536 Charcot-Marie-Tooth Disease, Type 1a 58 0.043
323
APP015 Apparent Mineralocorticoid Excess 52 0.043
324
NNF007 Non-Functioning Pituitary Adenoma 42 0.043
325
c ACQ042 Acquired Hemophilia a 39 0.043
326
ALV002 Alveolar Echinococcosis 44 0.042
327
FMR003 Femoral Neuropathy 37 0.042
328
LMR001 Lemierre's Syndrome 43 0.042
329
LCH001 Leech Infestation 39 0.042
330
PRG092 Pregnancy Loss, Recurrent 1 31 0.042
331
GLC036 Glucagonoma 48 0.042
332
c CHR532 Charcot-Marie-Tooth Disease, Type 2e 53 0.042
333
MTH044 Mthfr Gene Mutation 23 0.042
334
P CNG411 Congenital Disorder of Glycosylation, Type in 48 0.042
335
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 39 0.041
336
ART110 Arteritic Anterior Ischemic Optic Neuropathy 30 0.041
337
c CHR527 Charcot-Marie-Tooth Disease, Type 1b 47 0.041
338
ESN011 Eisenmenger Syndrome 46 0.041
339
GST030 Gastrinoma 41 0.041
340
MLL012 Miller Syndrome 50 0.040
341
HPT046 Hepatic Veno-Occlusive Disease 50 0.040
342
ACQ017 Acquired Von Willebrand Syndrome 36 0.040
343
RSS002 Roussy-Levy Syndrome 53 0.040
344
FRN014 Fournier Gangrene 34 0.040
345
PRM087 Premature Chromatid Separation Trait 19 0.040
346
VND002 Van Der Woude Syndrome 50 0.039
347
HYP026 Hypoglycemic Coma 37 0.039
348
ACT056 Acute Cor Pulmonale 32 0.039
349
FNC007 Functioning Pituitary Adenoma 40 0.039
350
ISC015 Ischemic Colitis 38 0.039
351
HNT002 Hantavirus Pulmonary Syndrome 47 0.039
352
CLD011 Cold Urticaria 30 0.038
353
PRP028 Peripheral Vertigo 38 0.038
354
P MRC003 Mercury Poisoning 46 0.038
355
BSL004 Basilar Artery Occlusion 34 0.038
356
CRT004 Carotid Artery Thrombosis 40 0.038
357
DJR004 Dejerine-Sottas Disease 47 0.037
358
SND002 Sneddon Syndrome 48 0.037
359
ACD009 Acid-Labile Subunit, Deficiency of 37 0.037
360
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 39 0.037
361
c MLT136 Multiple Endocrine Neoplasia 1 68 0.036
362
VLP001 Valproate Embryopathy, Susceptibility to 37 0.036
363
LGN005 Ligneous Conjunctivitis 38 0.036
364
PTT049 Pituitary Adenoma, Acth-Secreting 54 0.036
365
FNC006 Functional Gastric Disease 35 0.036
366
ACT040 Acute Poststreptococcal Glomerulonephritis 34 0.036
367
CHR034 Chromophobe Adenoma 39 0.035
368
GNT005 Giant Hemangioma 34 0.035
369
P MLD013 Mild Hemophilia a 29 0.035
370
MSN003 Mesenteric Vascular Occlusion 31 0.034
371
c CHR350 Charcot-Marie-Tooth Disease, Axonal, Type 2k 38 0.034
372
INT078 Intracranial Thrombosis 37 0.034
373
c CHR516 Charcot-Marie-Tooth Disease, Type 4c 41 0.034
374
SHW001 Shwartzman Phenomenon 37 0.033
375
P AND016 Andersen Syndrome 59 0.033
376
BLT003 Blue Toe Syndrome 35 0.033
377
LTR003 Lateral Medullary Syndrome 37 0.033
378
BRG013 Buerger Disease 54 0.032
379
ORG010 Organ System Benign Neoplasm 31 0.032
380
c BRC079 Brachydactyly, Type A2 44 0.032
381
PRC051 Paracetamol Poisoning 28 0.032
382
KRN001 Korean Hemorrhagic Fever 34 0.032
383
ESP002 Esophageal Varix 41 0.031
384
c CHR529 Charcot-Marie-Tooth Disease, Type 2i 30 0.031
385
TYP015 Type 2b Von Willebrand Disease 30 0.031
386
EPL116 Epileptic Encephalopathy, Childhood-Onset 40 0.031
387
MRN001 Marantic Endocarditis 33 0.031
388
ALC001 Alcohol-Related Birth Defect 30 0.031
389
HPT081 Hepatic Infarction 35 0.031
390
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 39 0.031
391
TBR009 Tuberculous Empyema 35 0.030
392
INT050 Intestinal Impaction 30 0.030
393
INT076 Intracranial Sinus Thrombosis 24 0.030
394
SBN001 Subendocardial Myocardial Infarction 32 0.030
395
c CHR528 Charcot-Marie-Tooth Disease, Type 2j 33 0.030
396
INT010 Intracranial Embolism 35 0.030
397
NLS001 Nelson Syndrome 48 0.030
398
CNJ001 Conjugate Gaze Palsy 28 0.029
399
ANT022 Anterior Cranial Fossa Meningioma 28 0.029
400
DYS013 Dysbaric Osteonecrosis 31 0.029
401
CRB017 Cerebral Falx Meningioma 21 0.028
Content
Loading form....