Search results for thrombophilia due to protein c deficiency

344 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 26 8.109
2
PRT011 Protein C Deficiency 52 7.596
3
c THR082 Thrombophilia Due to Activated Protein C Resistance 54 7.204
4
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 19 5.204
5
P HPT021 Hepatitis 69 0.630
6
P THR015 Thrombophilia 59 0.547
7
THR024 Thrombosis 57 0.461
8
END072 Endotheliitis 42 0.431
9
P LKM002 Leukemia 71 0.403
10
CRB009 Cerebritis 39 0.312
11
P PNC044 Pancreatitis 61 0.308
12
RTN023 Retinitis 50 0.299
13
P THY032 Thyroiditis 54 0.293
14
P LNG032 Lung Cancer 95 0.289
15
P LVR013 Liver Disease 75 0.286
16
P OBS005 Obesity 92 0.279
17
P MYC007 Myocardial Infarction 79 0.259
18
PRT014 Protein S Deficiency 53 0.255
19
ISC004 Ischemia 61 0.235
20
P HRT032 Heart Disease 75 0.229
21
P NRP001 Neuropathy 59 0.225
22
P AST005 Asthma 82 0.217
23
ATH003 Atherosclerosis 65 0.215
24
c HPT003 Hepatitis a 59 0.215
25
P ENC018 Encephalopathy 59 0.207
26
ART111 Artery Disease 55 0.206
27
PRP030 Purpura 58 0.205
28
P MYL006 Myeloid Leukemia 66 0.203
29
ADN018 Adenoma 58 0.187
30
P INF032 Infertility 59 0.187
31
INS024 Insulin-Like Growth Factor I 75 0.186
32
ANR040 Aneurysm 57 0.186
33
P RTN024 Retinoblastoma 74 0.183
34
CYS001 Cystic Fibrosis 83 0.181
35
GRW007 Growth Hormone Deficiency 50 0.179
36
THR013 Thoracic Outlet Syndrome 50 0.176
37
c ACT075 Acute Myocardial Infarction 60 0.172
38
P INF037 Inflammatory Bowel Disease 63 0.168
39
BLD054 Blood Protein Disease 37 0.165
40
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.164
41
P MLT019 Multiple Myeloma 83 0.162
42
ALR002 Al-Raqad Syndrome 36 0.160
43
PLM033 Pulmonary Embolism 60 0.160
44
CLT003 Colitis 60 0.160
45
P PSR002 Psoriasis 61 0.154
46
P THR014 Thrombocytopenia 64 0.153
47
VSC007 Vascular Disease 67 0.153
48
P THL005 Thalassemia 64 0.152
49
VSC008 Vascular Hemostatic Disease 30 0.151
50
P LYM026 Lymphoblastic Leukemia 62 0.145
51
c THR092 Thrombophilia Due to Thrombin Defect 54 0.145
52
P HYP086 Hypothyroidism 64 0.143
53
P HMP007 Hemophilia 57 0.140
54
PRP027 Peripheral Vascular Disease 68 0.139
55
P RTN022 Retinal Vein Occlusion 38 0.138
56
P PRP034 Purpura Fulminans 41 0.137
57
VSC011 Vasculitis 62 0.136
58
VND001 Vein Disease 47 0.135
59
HYP056 Hypoglycemia 61 0.135
60
C3D001 C3 Deficiency 53 0.134
61
P BLD051 Blood Coagulation Disease 42 0.133
62
P PLM037 Pulmonary Hypertension 79 0.133
63
CRH001 Crohn's Disease 75 0.131
64
c PRC016 Pre-Eclampsia 56 0.130
65
ART021 Arteriosclerosis 58 0.130
66
MCS002 Mucositis 55 0.129
67
IMM136 Immune System Disease 51 0.129
68
P ECL001 Eclampsia 54 0.129
69
ACD009 Acid-Labile Subunit, Deficiency of 45 0.127
70
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.127
71
P HMR003 Hemorrhagic Disease 57 0.126
72
ULC004 Ulcerative Colitis 76 0.126
73
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.125
74
P NPH012 Nephrotic Syndrome 59 0.124
75
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.124
76
c HMP029 Hemophilia a 63 0.122
77
ACR041 Acromelic Frontonasal Dysostosis 45 0.122
78
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.121
79
BRT030 Birth Defects 43 0.121
80
P HMC002 Homocystinuria 50 0.119
81
P ANT006 Antiphospholipid Syndrome 56 0.118
82
P PLY011 Polycystic Ovary Syndrome 65 0.118
83
FCT003 Factor X Deficiency 61 0.117
84
FTT001 Fatty Liver Disease 59 0.117
85
NRM005 Neuromuscular Disease 56 0.117
86
HYP037 Hyperhomocysteinemia 50 0.116
87
TTH006 Tooth Disease 52 0.115
88
CRB039 Cerebrovascular Disease 63 0.115
89
STR067 Stroke, Ischemic 75 0.114
90
AND005 Androgen Insensitivity Syndrome, Mild 16 0.111
91
P HYP060 Hyperinsulinism 58 0.111
92
HYP066 Hyperglycemia 61 0.110
93
c CNT016 Central Retinal Vein Occlusion 36 0.110
94
FCT007 Factor Vii Deficiency 61 0.109
95
P END033 Endocarditis 54 0.109
96
PRT018 Portal Vein Thrombosis 49 0.108
97
P MSC003 Muscular Atrophy 50 0.107
98
c CNT035 Central Nervous System Disease 60 0.107
99
PRP019 Peripheral Nervous System Disease 55 0.107
100
P ATX030 Ataxia-Telangiectasia 77 0.105
101
PLC008 Placenta Disease 33 0.104
102
FCT006 Factor V Deficiency 57 0.103
103
PRP080 Peripheral Artery Disease 37 0.103
104
DWR001 Dwarfism 47 0.103
105
HDC001 Headache 54 0.102
106
GST019 Gastrointestinal Stromal Tumor 73 0.102
107
OST003 Osteonecrosis 45 0.102
108
c PRT045 Prothrombin-Related Thrombophilia 24 0.101
109
ISL003 Isolated Growth Hormone Deficiency 52 0.101
110
P HYP083 Hypopituitarism 54 0.101
111
PTT006 Pituitary Adenoma 56 0.101
112
FCT013 Factor V Leiden Thrombophilia 22 0.100
113
HPT074 Hepatic Adenoma, Somatic 50 0.100
114
PNC034 Pancreas Disease 58 0.099
115
THR089 Thrombophilia Due to Protein S Deficiency, Autosomal Dominant 20 0.098
116
NRN004 Neuroendocrine Tumor 56 0.098
117
SCK005 Sickle Cell Disease 51 0.097
118
HNM002 Hinman Syndrome 25 0.096
119
P HML001 Hemolytic-Uremic Syndrome 51 0.095
120
FCT005 Factor Xiii Deficiency 43 0.094
121
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 49 0.094
122
P CHR071 Charcot-Marie-Tooth Disease 67 0.093
123
THR004 Thrombocytosis 55 0.092
124
P OVR049 Ovarian Disease 56 0.092
125
DSS009 Disseminated Intravascular Coagulation 51 0.092
126
P BDD001 Budd-Chiari Syndrome 56 0.092
127
P SPN046 Spinal Muscular Atrophy 65 0.091
128
SPC003 Specific Developmental Disorder 38 0.091
129
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.091
130
c HMP004 Hemophilia B 62 0.091
131
BNF002 Bone Fracture 50 0.091
132
GLC003 Glucose Intolerance 55 0.091
133
ACR007 Acromegaly 66 0.090
134
NRL016 Neural Tube Defects 76 0.090
135
P HYP076 Hyperthyroidism 55 0.089
136
MRF001 Marfan Syndrome 73 0.089
137
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.089
138
c INH004 Inherited Blood Coagulation Disease 36 0.088
139
CRC006 Carcinoid Syndrome 52 0.088
140
ATM055 Autoimmune Disease 4 15 0.087
141
CRN017 Coronary Thrombosis 48 0.086
142
P PLY018 Polycythemia 58 0.085
143
MYL031 Myeloproliferative Neoplasm 58 0.084
144
P UTR038 Uterine Disease 37 0.084
145
P SZR006 Seizure Disorder 56 0.084
146
HYP085 Hypothalamic Disease 44 0.084
147
TTR016 Tetra-Amelia Syndrome 36 0.083
148
SXD001 Sex Differentiation Disease 38 0.083
149
ATM012 Autoimmune Disease of Blood 35 0.082
150
CGL001 Coagulation Protein Disease 14 0.082
151
P ESS003 Essential Thrombocythemia 70 0.081
152
OVR029 Ovarian Hyperstimulation Syndrome 61 0.081
153
P HMR012 Hemorrhagic Fever 56 0.080
154
P DBT005 Diabetes Insipidus 53 0.080
155
PTT009 Pituitary Gland Disease 47 0.080
156
CRB037 Cerebral Palsy 66 0.080
157
P RTN014 Retinal Artery Occlusion 44 0.079
158
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 33 0.079
159
FCT004 Factor Xii Deficiency 50 0.079
160
INT075 Intracranial Hypertension 50 0.079
161
PLC007 Placental Abruption 47 0.078
162
IRR002 Irritable Bowel Syndrome 58 0.078
163
GND003 Gonadal Disease 39 0.078
164
HLL004 Hellp Syndrome 50 0.077
165
INF034 Infective Endocarditis 51 0.076
166
P ART084 Arteriovenous Fistula 44 0.076
167
c ATM010 Autoimmune Hemolytic Anemia 60 0.076
168
PTN001 Patent Foramen Ovale 55 0.076
169
PTT037 Pituitary Tumors 45 0.075
170
THR016 Thrombophlebitis 53 0.074
171
LMB062 Limb Ischemia 48 0.074
172
INS001 Insulinoma 61 0.073
173
BNM008 Bone Mineral Density, Low 16 0.073
174
P TRN020 Turner Syndrome 65 0.073
175
RTN021 Retinal Vascular Occlusion 32 0.073
176
MRB003 Morbid Obesity 58 0.073
177
P DRM010 Dermatomyositis 62 0.072
178
P ALP004 Alport Syndrome 69 0.071
179
VNW001 Von Willebrand's Disease 61 0.071
180
THY030 Thyroid Gland Disease 48 0.071
181
VSC047 Vascular Malformation 45 0.071
182
ISC002 Ischemic Optic Neuropathy 37 0.071
183
ACT087 Acth Deficiency 43 0.071
184
P PRC031 Preeclampsia/eclampsia 1 51 0.071
185
ATM014 Autoimmune Disease of Endocrine System 36 0.069
186
HPR003 Heparin-Induced Thrombocytopenia 45 0.069
187
P PRC019 Precocious Puberty 51 0.068
188
P OCY001 Oocyte Maturation Defect 38 0.068
189
ADP007 Adie Pupil 34 0.068
190
HYP043 Hyperandrogenism 47 0.067
191
CCN007 Cocoon Syndrome 45 0.067
192
P ANR007 Anorexia Nervosa 61 0.067
193
P GCH001 Gaucher's Disease 62 0.066
194
FCT022 Factor Xi Deficiency, Autosomal Recessive 53 0.066
195
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.066
196
P PRM002 Primary Hyperoxaluria 51 0.065
197
c SVR056 Severe Hemophilia a 43 0.065
198
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.065
199
THR020 Thrombophilia Due to Heparin Cofactor Ii Deficiency 19 0.064
200
P VNS003 Venous Insufficiency 54 0.064
201
INT002 Intermittent Claudication 56 0.063
202
UTR039 Uterine Fibroid 57 0.063
203
MGR028 Migraine with or Without Aura 1 47 0.063
204
c HRD088 Hereditary Neuropathies 40 0.062
205
AMN001 Amenorrhea 50 0.061
206
P AXN001 Axonal Neuropathy 38 0.061
207
CHR001 Churg-Strauss Syndrome 49 0.061
208
SPL006 Splenic Infarction 35 0.061
209
CRN036 Craniopharyngioma 59 0.061
210
PYR037 Pyruvate Carboxylase Deficiency 37 0.060
211
SGT001 Sagittal Sinus Thrombosis 35 0.060
212
HYP020 Hyperprolactinemia 60 0.060
213
c HMG003 Hemoglobin E Disease 44 0.060
214
P KLL001 Kallmann Syndrome 61 0.060
215
P CHR084 Chromosomal Disease 32 0.060
216
AMR003 Amaurosis Fugax 38 0.059
217
SNS003 Sensory Peripheral Neuropathy 45 0.059
218
GRW004 Growth Retardation with Deafness and Mental Retardation Due to Igf1 Deficiency 39 0.059
219
PST095 Post-Thrombotic Syndrome 47 0.059
220
ADR009 Adrenal Cortex Disease 39 0.058
221
P MYM002 Moyamoya Disease 61 0.058
222
FBR009 Fibrous Dysplasia 45 0.058
223
P DYS026 Dysfibrinogenemia 45 0.057
224
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.057
225
FST010 Fasting Hypoglycemia 39 0.056
226
CRB132 Cerebral Sinovenous Thrombosis 31 0.056
227
SRT004 Serotonin Syndrome 49 0.056
228
c EHL032 Ehlers-Danlos Syndrome, Type Viib 49 0.056
229
P AFB001 Afibrinogenemia 48 0.056
230
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.055
231
P ATX010 Ataxia Neuropathy Spectrum 30 0.055
232
LGG001 Legg-Calve-Perthes Disease 57 0.055
233
PRG092 Pregnancy Loss, Recurrent 1 31 0.055
234
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 33 0.055
235
P FBR031 Febrile Seizures 53 0.055
236
OST115 Osteonecrosis of the Jaw 38 0.055
237
P HYP050 Hyperinsulinemic Hypoglycemia 56 0.055
238
BRN026 Branch Retinal Artery Occlusion 38 0.054
239
FTD001 Foot Drop 33 0.054
240
c SYS004 Systemic Mastocytosis 60 0.054
241
P WLF004 Wolfram Syndrome 61 0.053
242
HMC014 Homocysteinemia 35 0.053
243
PPL021 Papilledema 47 0.053
244
ISL001 Islet Cell Tumor 50 0.052
245
P HYP620 Hypoprothrombinemia 54 0.052
246
c CNT075 Central Precocious Puberty 49 0.052
247
STC016 Sticky Platelet Syndrome 29 0.052
248
ADR012 Adrenal Gland Disease 48 0.051
249
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 0.051
250
c PRM225 Primary Thrombocytopenia 39 0.051
251
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 55 0.051
252
HPT020 Hepatic Vascular Disease 42 0.051
253
P PND002 Pendred Syndrome 55 0.051
254
LVD002 Livedoid Vasculopathy 32 0.051
255
HMC020 Homocystinuria, B6-Responsive and Nonresponsive Types 43 0.050
256
c ART106 Arterial Calcification, Generalized, of Infancy, 1 39 0.050
257
P CHR102 Charcot-Marie-Tooth Neuropathy 41 0.050
258
c MLT136 Multiple Endocrine Neoplasia 1 69 0.049
259
c CHR431 Chronic Venous Insufficiency 44 0.049
260
GRW024 Growth Hormone Deficiency, Isolated, Type Ii 45 0.049
261
WBR001 Weber Syndrome 41 0.048
262
VNW005 Von Willebrand Disease, Type 1 49 0.048
263
ADR005 Adrenal Carcinoma 57 0.048
264
P SLV001 Silver-Russell Syndrome 54 0.048
265
c PLM127 Pulmonary Hypertension, Primary, 3 28 0.048
266
SPN185 Spinal Cord Infarction 34 0.048
267
c SVR005 Severe Pre-Eclampsia 49 0.047
268
P MDL022 Medullary Thyroid Carcinoma, Familial 63 0.047
269
P PRN026 Porencephaly 48 0.047
270
c ACQ014 Acquired Hemophilia 42 0.047
271
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.047
272
RTN001 Retinal Vasculitis 44 0.046
273
ART110 Arteritic Anterior Ischemic Optic Neuropathy 31 0.046
274
P FNC043 Fanconi Anemia, Complementation Group E 55 0.046
275
CVR006 Cavernous Hemangioma 46 0.045
276
GGN002 Gigantism 32 0.045
277
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.045
278
c ACQ042 Acquired Hemophilia a 40 0.045
279
c CNG411 Congenital Disorder of Glycosylation, Type in 49 0.044
280
DMP001 Dumping Syndrome 40 0.044
281
SLP010 Slipped Capital Femoral Epiphysis 34 0.044
282
P MGR003 Migraine with Aura 52 0.043
283
c CHR536 Charcot-Marie-Tooth Disease, Type 1a 58 0.043
284
END021 Endomyocardial Fibrosis 49 0.043
285
GLC036 Glucagonoma 46 0.043
286
CTN014 Cutaneous Mastocytosis 49 0.043
287
MTH044 Mthfr Gene Mutation 21 0.043
288
c CHR532 Charcot-Marie-Tooth Disease, Type 2e 49 0.043
289
c CHR527 Charcot-Marie-Tooth Disease, Type 1b 49 0.043
290
NNF007 Non-Functioning Pituitary Adenoma 41 0.043
291
LRN004 Laron Dwarfism 58 0.043
292
CRR007 Cirrhosis, Cryptogenic 43 0.042
293
PNC053 Pancreatic Islet Cell Tumors 35 0.042
294
LCH001 Leech Infestation 40 0.042
295
c AFB002 Afibrinogenemia, Congenital 54 0.042
296
GST030 Gastrinoma 42 0.042
297
INT060 Intestinal Atresia 42 0.041
298
PLY125 Polycythemia Vera, Somatic 63 0.041
299
HYP026 Hypoglycemic Coma 39 0.040
300
RSS002 Roussy-Levy Syndrome 50 0.040
301
PRP028 Peripheral Vertigo 38 0.040
302
NLS001 Nelson Syndrome 47 0.039
303
FRN014 Fournier Gangrene 35 0.039
304
FNC007 Functioning Pituitary Adenoma 41 0.039
305
ACN019 Acanthamoeba Keratitis 32 0.039
306
DJR004 Dejerine-Sottas Disease 46 0.039
307
P PTT050 Pituitary Adenoma, Growth Hormone-Secreting 48 0.039
308
MTR007 Motor Peripheral Neuropathy 37 0.038
309
VST004 Vestibular Disease 44 0.038
310
VND002 Van Der Woude Syndrome 50 0.038
311
ISC015 Ischemic Colitis 39 0.038
312
QLT001 Qualitative Platelet Defect 32 0.037
313
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 49 0.037
314
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 33 0.037
315
MSN003 Mesenteric Vascular Occlusion 34 0.037
316
NNT024 Neonatal Stroke 36 0.037
317
SND002 Sneddon Syndrome 44 0.037
318
GNT005 Giant Hemangioma 35 0.035
319
P AND016 Andersen Syndrome 58 0.035
320
PRM087 Premature Chromatid Separation Trait 18 0.035
321
INT078 Intracranial Thrombosis 36 0.035
322
BRG013 Buerger Disease 53 0.034
323
PRC051 Paracetamol Poisoning 27 0.034
324
MST001 Mast-Cell Sarcoma 40 0.034
325
c PRM149 Primary Hypereosinophilic Syndrome 38 0.034
326
CHR034 Chromophobe Adenoma 40 0.033
327
KRN001 Korean Hemorrhagic Fever 39 0.033
328
MYT019 May-Thurner Syndrome 23 0.032
329
c MYT012 Myotonia Congenita, Recessive 32 0.032
330
INT050 Intestinal Impaction 31 0.032
331
BLT003 Blue Toe Syndrome 35 0.032
332
HPT081 Hepatic Infarction 34 0.032
333
SHH001 Sheehan Syndrome 44 0.031
334
INT010 Intracranial Embolism 32 0.031
335
SMH001 Sm-Ahnmd 26 0.031
336
INT076 Intracranial Sinus Thrombosis 24 0.030
337
LFF001 Loeffler Endocarditis 25 0.030
338
MRN001 Marantic Endocarditis 32 0.030
339
c CHR529 Charcot-Marie-Tooth Disease, Type 2i 30 0.030
340
CRB017 Cerebral Falx Meningioma 21 0.030
341
c CHR528 Charcot-Marie-Tooth Disease, Type 2j 32 0.029
342
MYL059 Myeloid and Lymphoid Neoplasms with Eosinophilia and Abnormalities of Pdgfra, Pdgfrb, and Fgfr1 29 0.029
343
ANT022 Anterior Cranial Fossa Meningioma 28 0.028
344
MYL045 Myelofibrosis with Myeloid Metaplasia, Somatic 36 0.027
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