Search results for "thrombophilia due to protein c deficiency"

The MalaCard for "thrombophilia due to protein c deficiency" has been retired.
Searching MalaCards for entries containing "thrombophilia due to protein c deficiency"

329 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 8.097
2
PRT011 Protein C Deficiency 51 7.603
3
c THR082 Thrombophilia Due to Activated Protein C Resistance 57 7.202
4
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 20 5.198
5
P HPT021 Hepatitis 70 0.651
6
P THR015 Thrombophilia 59 0.579
7
END072 Endotheliitis 42 0.445
8
P LKM002 Leukemia 70 0.415
9
CRB009 Cerebritis 38 0.326
10
P PNC044 Pancreatitis 60 0.318
11
RTN023 Retinitis 49 0.312
12
P THY032 Thyroiditis 54 0.304
13
P LVR013 Liver Disease 72 0.303
14
P LNG032 Lung Cancer 94 0.292
15
P OBS005 Obesity 93 0.288
16
PRT014 Protein S Deficiency 52 0.269
17
P MYC007 Myocardial Infarction 79 0.269
18
ISC004 Ischemia 59 0.239
19
P HRT032 Heart Disease 76 0.236
20
P NRP001 Neuropathy 60 0.235
21
c HPT003 Hepatitis a 59 0.228
22
ATH003 Atherosclerosis 62 0.224
23
P AST005 Asthma 82 0.222
24
PRP030 Purpura 59 0.215
25
P ENC018 Encephalopathy 59 0.215
26
ART111 Artery Disease 57 0.214
27
P MYL006 Myeloid Leukemia 67 0.208
28
ANR040 Aneurysm 57 0.195
29
P INF032 Infertility 61 0.194
30
P RTN024 Retinoblastoma 75 0.188
31
CYS001 Cystic Fibrosis 86 0.187
32
BLD054 Blood Protein Disease 40 0.185
33
c ACT075 Acute Myocardial Infarction 60 0.183
34
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.174
35
PLM033 Pulmonary Embolism 59 0.167
36
ALR002 Al-Raqad Syndrome 36 0.166
37
CLT003 Colitis 59 0.166
38
LVR012 Liver Cirrhosis 67 0.165
39
VSC007 Vascular Disease 67 0.165
40
THR013 Thoracic Outlet Syndrome 49 0.165
41
P MLT019 Multiple Myeloma 80 0.161
42
VSC008 Vascular Hemostatic Disease 33 0.161
43
P PSR002 Psoriasis 63 0.159
44
P THL005 Thalassemia 61 0.157
45
P THR014 Thrombocytopenia 64 0.155
46
c THR092 Thrombophilia Due to Thrombin Defect 56 0.154
47
P LYM026 Lymphoblastic Leukemia 60 0.150
48
VND001 Vein Disease 52 0.150
49
P HYP086 Hypothyroidism 65 0.150
50
PRP027 Peripheral Vascular Disease 69 0.148
51
P PRP034 Purpura Fulminans 42 0.148
52
P HMP007 Hemophilia 56 0.147
53
VSC011 Vasculitis 62 0.147
54
P RTN022 Retinal Vein Occlusion 37 0.144
55
P HMR003 Hemorrhagic Disease 57 0.141
56
C3D001 C3 Deficiency 53 0.141
57
P BLD051 Blood Coagulation Disease 45 0.137
58
P ECL001 Eclampsia 54 0.137
59
ART021 Arteriosclerosis 59 0.137
60
STR067 Stroke, Ischemic 77 0.136
61
BRT030 Birth Defects 43 0.135
62
c HMP029 Hemophilia a 64 0.133
63
FCT003 Factor X Deficiency 62 0.133
64
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.130
65
ULC004 Ulcerative Colitis 75 0.129
66
ACR041 Acromelic Frontonasal Dysostosis 46 0.129
67
HYP037 Hyperhomocysteinemia 50 0.128
68
P ANT006 Antiphospholipid Syndrome 58 0.128
69
P PLM037 Pulmonary Hypertension 79 0.128
70
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.127
71
P CLL015 Collagen Disease 49 0.125
72
IMM136 Immune System Disease 50 0.125
73
c BLD124 Bleeding Disorder, Platelet-Type, 11 42 0.125
74
NRM005 Neuromuscular Disease 57 0.123
75
P PLY011 Polycystic Ovary Syndrome 66 0.122
76
FCT006 Factor V Deficiency 60 0.120
77
P END033 Endocarditis 52 0.120
78
PRT018 Portal Vein Thrombosis 49 0.119
79
FTT001 Fatty Liver Disease 60 0.118
80
FCT007 Factor Vii Deficiency 62 0.116
81
TTH006 Tooth Disease 52 0.116
82
c CNT016 Central Retinal Vein Occlusion 35 0.115
83
BLD053 Blood Platelet Disease 46 0.115
84
GLB003 Globe Disease 35 0.113
85
AND005 Androgen Insensitivity Syndrome, Mild 16 0.111
86
P MSC003 Muscular Atrophy 51 0.111
87
c CNT035 Central Nervous System Disease 59 0.110
88
DSS009 Disseminated Intravascular Coagulation 51 0.108
89
PLC008 Placenta Disease 36 0.108
90
HDC001 Headache 54 0.108
91
P ATX030 Ataxia-Telangiectasia 76 0.107
92
OST003 Osteonecrosis 45 0.107
93
c HMP004 Hemophilia B 62 0.107
94
PRP080 Peripheral Artery Disease 36 0.107
95
SPN369 Spinal Disease 41 0.106
96
c PRT045 Prothrombin-Related Thrombophilia 23 0.105
97
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 50 0.104
98
FCT013 Factor V Leiden Thrombophilia 21 0.104
99
THR089 Thrombophilia Due to Protein S Deficiency, Autosomal Dominant 20 0.103
100
ANG054 Angina Pectoris 51 0.103
101
P BDD001 Budd-Chiari Syndrome 56 0.103
102
c INH004 Inherited Blood Coagulation Disease 39 0.102
103
THR004 Thrombocytosis 55 0.102
104
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.101
105
GST019 Gastrointestinal Stromal Tumor 72 0.101
106
FCT005 Factor Xiii Deficiency 42 0.101
107
P ESN007 Eosinophilia 61 0.101
108
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.101
109
SCK005 Sickle Cell Disease 49 0.101
110
P HML001 Hemolytic-Uremic Syndrome 50 0.100
111
NRL016 Neural Tube Defects 76 0.097
112
CRN017 Coronary Thrombosis 48 0.097
113
P HMR012 Hemorrhagic Fever 55 0.095
114
HPT074 Hepatic Adenoma, Somatic 51 0.095
115
P SPN046 Spinal Muscular Atrophy 63 0.093
116
HDN002 Head Injury 45 0.093
117
BNF002 Bone Fracture 47 0.093
118
INF034 Infective Endocarditis 50 0.093
119
P CHR071 Charcot-Marie-Tooth Disease 66 0.092
120
FCT004 Factor Xii Deficiency 51 0.092
121
SPC003 Specific Developmental Disorder 40 0.092
122
c INF067 Inflammatory Bowel Disease 10 51 0.092
123
HNM002 Hinman Syndrome 25 0.090
124
MRF001 Marfan Syndrome 73 0.090
125
P RTN014 Retinal Artery Occlusion 43 0.090
126
ATM055 Autoimmune Disease 4 18 0.090
127
INT075 Intracranial Hypertension 53 0.089
128
PLC007 Placental Abruption 47 0.089
129
HLL004 Hellp Syndrome 49 0.089
130
P PLY018 Polycythemia 57 0.089
131
ISC002 Ischemic Optic Neuropathy 46 0.088
132
P ESS003 Essential Thrombocythemia 68 0.088
133
c ACT210 Acute Respiratory Distress Syndrome 57 0.088
134
CRT015 Carotid Artery Occlusion 43 0.087
135
THR035 Thrombasthenia 42 0.087
136
VNW001 Von Willebrand's Disease 61 0.087
137
TTR016 Tetra-Amelia Syndrome 36 0.087
138
P UTR038 Uterine Disease 40 0.087
139
PTN001 Patent Foramen Ovale 54 0.086
140
EXF001 Exfoliation Syndrome 57 0.086
141
THR016 Thrombophlebitis 52 0.086
142
ATM012 Autoimmune Disease of Blood 37 0.085
143
P PRM002 Primary Hyperoxaluria 56 0.084
144
OVR029 Ovarian Hyperstimulation Syndrome 60 0.084
145
CGL001 Coagulation Protein Disease 16 0.084
146
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 30 0.083
147
P SZR006 Seizure Disorder 57 0.083
148
P PRC031 Preeclampsia/eclampsia 1 57 0.082
149
c INF071 Inflammatory Bowel Disease 1 51 0.082
150
MNN021 Meningococcemia 38 0.081
151
c ATM011 Autoimmune Hepatitis 58 0.081
152
FCT022 Factor Xi Deficiency, Autosomal Recessive 56 0.081
153
INT002 Intermittent Claudication 56 0.080
154
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 47 0.079
155
HPR003 Heparin-Induced Thrombocytopenia 46 0.079
156
P ART084 Arteriovenous Fistula 44 0.079
157
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 76 0.078
158
BNM008 Bone Mineral Density, Low 19 0.078
159
LMB062 Limb Ischemia 48 0.077
160
SGT001 Sagittal Sinus Thrombosis 33 0.077
161
MRB003 Morbid Obesity 58 0.076
162
SCT005 Scott Syndrome 50 0.076
163
SPL006 Splenic Infarction 35 0.076
164
KWS001 Kwashiorkor 44 0.076
165
P DRM010 Dermatomyositis 58 0.076
166
RTN021 Retinal Vascular Occlusion 34 0.075
167
c HMG003 Hemoglobin E Disease 44 0.075
168
RTN017 Retinal Detachment 57 0.075
169
P VNS003 Venous Insufficiency 53 0.074
170
CRD001 Cardiac Tamponade 44 0.073
171
P ALP004 Alport Syndrome 68 0.073
172
VSC047 Vascular Malformation 45 0.073
173
c SVR056 Severe Hemophilia a 46 0.073
174
HMC014 Homocysteinemia 34 0.072
175
PST095 Post-Thrombotic Syndrome 50 0.072
176
ATM014 Autoimmune Disease of Endocrine System 37 0.072
177
HMC020 Homocystinuria, B6-Responsive and Nonresponsive Types 55 0.072
178
HYP063 Hypersplenism 48 0.072
179
INT051 Intussusception 50 0.071
180
CMP005 Campomelic Dysplasia 72 0.071
181
P AFB001 Afibrinogenemia 46 0.071
182
P OCY001 Oocyte Maturation Defect 39 0.071
183
P HYP620 Hypoprothrombinemia 54 0.071
184
THY030 Thyroid Gland Disease 51 0.071
185
ACT058 Active Peptic Ulcer Disease 46 0.070
186
MYL001 Myelitis 48 0.070
187
CCN007 Cocoon Syndrome 35 0.069
188
ADP007 Adie Pupil 34 0.069
189
CRB132 Cerebral Sinovenous Thrombosis 31 0.068
190
P PLZ001 Pelizaeus-Merzbacher Disease 64 0.068
191
INT007 Intermediate Coronary Syndrome 52 0.068
192
LGG001 Legg-Calve-Perthes Disease 57 0.068
193
THR020 Thrombophilia Due to Heparin Cofactor Ii Deficiency 19 0.068
194
P DYS026 Dysfibrinogenemia 41 0.068
195
PPL021 Papilledema 48 0.067
196
CPL007 Capillary Malformation-Arteriovenous Malformation 41 0.067
197
SPN185 Spinal Cord Infarction 36 0.067
198
HPT020 Hepatic Vascular Disease 44 0.066
199
PRG092 Pregnancy Loss, Recurrent 1 34 0.066
200
RTN020 Retinal Vascular Disease 50 0.066
201
MGR028 Migraine with or Without Aura 1 50 0.066
202
P HRD008 Hereditary Hemorrhagic Telangiectasia 71 0.065
203
MCL006 Macular Retinal Edema 40 0.065
204
c SVR005 Severe Pre-Eclampsia 48 0.064
205
BRN026 Branch Retinal Artery Occlusion 39 0.064
206
AMR003 Amaurosis Fugax 38 0.064
207
PYR037 Pyruvate Carboxylase Deficiency 37 0.064
208
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 0.064
209
c HRD088 Hereditary Neuropathies 41 0.064
210
P CHR084 Chromosomal Disease 37 0.062
211
P AXN001 Axonal Neuropathy 38 0.062
212
DBT006 Diabetic Macular Edema 47 0.061
213
CTS005 Catastrophic Antiphospholipid Syndrome 41 0.061
214
SPT005 Spotted Fever 56 0.061
215
P KLL001 Kallmann Syndrome 60 0.061
216
P ACT080 Acute Pulmonary Heart Disease 32 0.061
217
SNS003 Sensory Peripheral Neuropathy 47 0.061
218
LVD002 Livedoid Vasculopathy 31 0.060
219
PRP028 Peripheral Vertigo 41 0.060
220
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 49 0.060
221
c AFB002 Afibrinogenemia, Congenital 54 0.060
222
ART110 Arteritic Anterior Ischemic Optic Neuropathy 32 0.060
223
ALC009 Alcoholic Liver Cirrhosis 48 0.060
224
QBC001 Quebec Platelet Disorder 50 0.059
225
CHR001 Churg-Strauss Syndrome 49 0.059
226
GLN010 Glanzmann Thrombasthenia 63 0.059
227
LCH001 Leech Infestation 37 0.059
228
c GCH015 Gaucher Disease, Type I 66 0.059
229
ISC015 Ischemic Colitis 40 0.059
230
P ATX010 Ataxia Neuropathy Spectrum 28 0.058
231
P MYM002 Moyamoya Disease 60 0.058
232
MNN017 Mononeuropathy 40 0.058
233
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 32 0.057
234
P PRN026 Porencephaly 47 0.057
235
CRT049 Critical Limb Ischemia 51 0.057
236
P FBR031 Febrile Seizures 52 0.057
237
FTD001 Foot Drop 32 0.057
238
ACN019 Acanthamoeba Keratitis 31 0.057
239
CPL005 Capillary Disease 40 0.057
240
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.056
241
VTM001 Vitamin K Deficiency Hemorrhagic Disease 36 0.056
242
ANT013 Anterior Spinal Artery Syndrome 29 0.056
243
c ACQ014 Acquired Hemophilia 42 0.055
244
P WLF004 Wolfram Syndrome 61 0.055
245
MYL020 Myelomeningocele 50 0.055
246
c PRM225 Primary Thrombocytopenia 42 0.054
247
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 44 0.054
248
SND002 Sneddon Syndrome 44 0.053
249
VNW005 Von Willebrand Disease, Type 1 50 0.053
250
c NPH055 Nephrotic Syndrome, Type 1 59 0.053
251
P CHR102 Charcot-Marie-Tooth Neuropathy 43 0.053
252
FRN014 Fournier Gangrene 34 0.052
253
PLC005 Placental Insufficiency 50 0.052
254
GNT005 Giant Hemangioma 33 0.052
255
BLT003 Blue Toe Syndrome 35 0.052
256
MGL016 Megaloblastic Anemia-1, Finnish Type 46 0.052
257
CHR466 Chronic Thromboembolic Pulmonary Hypertension 37 0.052
258
BRS090 Breast Reconstruction 39 0.052
259
CRM001 Crimean-Congo Hemorrhagic Fever 54 0.052
260
PRC051 Paracetamol Poisoning 27 0.052
261
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.051
262
c CHR431 Chronic Venous Insufficiency 44 0.051
263
KRN001 Korean Hemorrhagic Fever 40 0.051
264
FNT004 Fainting 33 0.051
265
HMR002 Hemarthrosis 48 0.051
266
PMS001 Poems Syndrome 55 0.051
267
MYT019 May-Thurner Syndrome 23 0.050
268
ANN002 Anencephaly 52 0.050
269
c PLM127 Pulmonary Hypertension, Primary, 3 30 0.050
270
c SVR057 Severe Hemophilia B 32 0.050
271
BRN082 Bernard-Soulier Syndrome, Type C 50 0.050
272
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 34 0.050
273
ESP002 Esophageal Varix 44 0.049
274
BRG013 Buerger Disease 53 0.049
275
c CNG415 Congenital Disorder of Glycosylation, Type Ia 45 0.049
276
P SCH018 Schizencephaly 51 0.049
277
WBR001 Weber Syndrome 37 0.049
278
MRN001 Marantic Endocarditis 32 0.049
279
RTN001 Retinal Vasculitis 44 0.049
280
NNT024 Neonatal Stroke 37 0.049
281
INT050 Intestinal Impaction 31 0.049
282
FCT016 Factor V and Factor Viii, Combined Deficiency of 32 0.048
283
MSN003 Mesenteric Vascular Occlusion 34 0.048
284
LMR001 Lemierre's Syndrome 41 0.047
285
INT010 Intracranial Embolism 35 0.047
286
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 43 0.047
287
c ACQ042 Acquired Hemophilia a 39 0.046
288
CRN020 Coronary Restenosis 40 0.046
289
FMR003 Femoral Neuropathy 34 0.046
290
MTH044 Mthfr Gene Mutation 22 0.045
291
ACQ017 Acquired Von Willebrand Syndrome 36 0.045
292
INT060 Intestinal Atresia 40 0.045
293
LYM022 Lymphangioma 54 0.045
294
ESN011 Eisenmenger Syndrome 44 0.045
295
CRR007 Cirrhosis, Cryptogenic 44 0.044
296
c CHR527 Charcot-Marie-Tooth Disease, Type 1b 51 0.043
297
SBN001 Subendocardial Myocardial Infarction 33 0.043
298
c CHR536 Charcot-Marie-Tooth Disease, Type 1a 56 0.043
299
CRT004 Carotid Artery Thrombosis 41 0.043
300
HNT002 Hantavirus Pulmonary Syndrome 51 0.043
301
PLY125 Polycythemia Vera, Somatic 63 0.043
302
MTR003 Mitral Valve Stenosis 45 0.042
303
CLD011 Cold Urticaria 33 0.041
304
QLT001 Qualitative Platelet Defect 32 0.041
305
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 46 0.040
306
HPT046 Hepatic Veno-Occlusive Disease 45 0.040
307
P MLD013 Mild Hemophilia a 30 0.039
308
VND002 Van Der Woude Syndrome 51 0.039
309
c CHR532 Charcot-Marie-Tooth Disease, Type 2e 47 0.039
310
RSS002 Roussy-Levy Syndrome 52 0.038
311
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 50 0.038
312
RYN001 Raynaud Disease 44 0.038
313
P AND016 Andersen Syndrome 58 0.038
314
TYP015 Type 2b Von Willebrand Disease 30 0.038
315
DJR004 Dejerine-Sottas Disease 47 0.037
316
INF133 Inferior Vena Cava Interruption 30 0.037
317
c PST001 Posterior Myocardial Infarction 32 0.037
318
PRM087 Premature Chromatid Separation Trait 19 0.037
319
MTR007 Motor Peripheral Neuropathy 43 0.037
320
LGN005 Ligneous Conjunctivitis 28 0.036
321
ALP044 Alpha-1-Antichymotrypsin Deficiency 24 0.036
322
TYP017 Type 2n Von Willebrand Disease 18 0.035
323
ARG001 Argentine Hemorrhagic Fever 34 0.035
324
SRC011 Sarcocystosis 29 0.035
325
ANT022 Anterior Cranial Fossa Meningioma 26 0.033
326
CRB017 Cerebral Falx Meningioma 18 0.033
327
INT076 Intracranial Sinus Thrombosis 24 0.033
328
TYP016 Type 2m Von Willebrand Disease 17 0.032
329
c CHR549 Charcot-Marie-Tooth Disease Type 2l 18 0.030