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"

310 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 30 8.168
2
PRT011 Protein C Deficiency 52 7.700
3
c THR082 Thrombophilia Due to Activated Protein C Resistance 57 6.698
4
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 22 4.667
5
P HPT021 Hepatitis 74 0.699
6
P THR015 Thrombophilia 59 0.604
7
END072 Endotheliitis 41 0.483
8
P LKM002 Leukemia 70 0.450
9
CRB009 Cerebritis 36 0.350
10
P PNC044 Pancreatitis 62 0.346
11
RTN023 Retinitis 49 0.332
12
P THY032 Thyroiditis 57 0.331
13
P OBS005 Obesity 91 0.323
14
P LNG032 Lung Cancer 92 0.317
15
P LVR013 Liver Disease 76 0.300
16
PRT014 Protein S Deficiency 54 0.298
17
P MYC007 Myocardial Infarction 80 0.287
18
THR013 Thoracic Outlet Syndrome 48 0.260
19
ISC004 Ischemia 56 0.256
20
P NRP001 Neuropathy 57 0.253
21
PRP030 Purpura 60 0.252
22
P ENC018 Encephalopathy 59 0.245
23
ATH003 Atherosclerosis 63 0.242
24
P AST005 Asthma 80 0.237
25
P HRT032 Heart Disease 64 0.233
26
ART111 Artery Disease 56 0.229
27
P MYL006 Myeloid Leukemia 67 0.227
28
ALR002 Al-Raqad Syndrome 36 0.221
29
P RTN024 Retinoblastoma 75 0.213
30
ANR040 Aneurysm 56 0.205
31
CYS001 Cystic Fibrosis 87 0.202
32
c ACT075 Acute Myocardial Infarction 61 0.202
33
BLD054 Blood Protein Disease 38 0.201
34
P INF032 Infertility 61 0.199
35
P MYL007 Myeloma 52 0.196
36
PLM033 Pulmonary Embolism 59 0.188
37
P PSR002 Psoriasis 63 0.184
38
VSC008 Vascular Hemostatic Disease 30 0.182
39
LVR012 Liver Cirrhosis 71 0.179
40
CLT003 Colitis 56 0.179
41
c THR092 Thrombophilia Due to Thrombin Defect 56 0.176
42
c MLT019 Multiple Myeloma 77 0.176
43
P PRP034 Purpura Fulminans 41 0.173
44
P HMP007 Hemophilia 55 0.169
45
P THR014 Thrombocytopenia 63 0.168
46
P THL005 Thalassemia 61 0.166
47
VSC007 Vascular Disease 51 0.163
48
P LYM026 Lymphoblastic Leukemia 60 0.163
49
PRP027 Peripheral Vascular Disease 69 0.160
50
VND001 Vein Disease 51 0.159
51
P HYP086 Hypothyroidism 63 0.158
52
VSC011 Vasculitis 62 0.154
53
P RTN022 Retinal Vein Occlusion 36 0.153
54
P ECL001 Eclampsia 55 0.153
55
P BLD051 Blood Coagulation Disease 44 0.151
56
HYP037 Hyperhomocysteinemia 49 0.149
57
c HMP029 Hemophilia a 61 0.149
58
TNP003 Tn Polyagglutination Syndrome, Somatic 30 0.148
59
ART021 Arteriosclerosis 59 0.147
60
P ANT006 Antiphospholipid Syndrome 60 0.146
61
FCT003 Factor X Deficiency 62 0.146
62
ULC004 Ulcerative Colitis 74 0.146
63
BRT030 Birth Defects 44 0.145
64
P HMC002 Homocystinuria 52 0.145
65
P NPH012 Nephrotic Syndrome 55 0.140
66
c PRC016 Pre-Eclampsia 57 0.140
67
P PLM037 Pulmonary Hypertension 78 0.138
68
STR067 Stroke, Ischemic 74 0.138
69
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 35 0.137
70
P PLY011 Polycystic Ovary Syndrome 64 0.137
71
PRT018 Portal Vein Thrombosis 48 0.137
72
FCT006 Factor V Deficiency 62 0.136
73
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.136
74
NRM005 Neuromuscular Disease 56 0.135
75
P END033 Endocarditis 52 0.135
76
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.134
77
TTH006 Tooth Disease 52 0.132
78
FCT001 Factor Viii Deficiency 41 0.131
79
SCK005 Sickle Cell Disease 51 0.129
80
DSS009 Disseminated Intravascular Coagulation 52 0.129
81
ACR041 Acromelic Frontonasal Dysostosis 45 0.128
82
FTT001 Fatty Liver Disease 60 0.128
83
NRL016 Neural Tube Defects 76 0.128
84
c CNT035 Central Nervous System Disease 60 0.127
85
c PRT045 Prothrombin-Related Thrombophilia 25 0.127
86
GLB003 Globe Disease 34 0.126
87
c CNT016 Central Retinal Vein Occlusion 34 0.125
88
P PLY019 Polyneuropathy 53 0.125
89
BLD053 Blood Platelet Disease 44 0.125
90
HPT074 Hepatic Adenoma, Somatic 35 0.124
91
P MSC003 Muscular Atrophy 51 0.124
92
FCT007 Factor Vii Deficiency 60 0.123
93
c INH004 Inherited Blood Coagulation Disease 38 0.123
94
P BDD001 Budd-Chiari Syndrome 52 0.122
95
THR004 Thrombocytosis 55 0.121
96
CRB039 Cerebrovascular Disease 49 0.120
97
ANG054 Angina Pectoris 48 0.118
98
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 50 0.118
99
c HMP004 Hemophilia B 61 0.117
100
PRP080 Peripheral Artery Disease 35 0.117
101
FCT013 Factor V Leiden Thrombophilia 20 0.116
102
P HML001 Hemolytic-Uremic Syndrome 50 0.115
103
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.114
104
OST003 Osteonecrosis 45 0.114
105
GST019 Gastrointestinal Stromal Tumor 73 0.112
106
P ESN007 Eosinophilia 61 0.112
107
THR089 Thrombophilia Due to Protein S Deficiency, Autosomal Dominant 21 0.111
108
FCT005 Factor Xiii Deficiency 42 0.111
109
CRN017 Coronary Thrombosis 46 0.109
110
P CHR071 Charcot-Marie-Tooth Disease 66 0.109
111
FCT004 Factor Xii Deficiency 51 0.109
112
INF034 Infective Endocarditis 50 0.109
113
INT075 Intracranial Hypertension 52 0.109
114
HDC001 Headache 52 0.108
115
PLC008 Placenta Disease 33 0.108
116
P ESS003 Essential Thrombocythemia 66 0.108
117
THR035 Thrombasthenia 41 0.107
118
ISC002 Ischemic Optic Neuropathy 45 0.106
119
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.106
120
PLC007 Placental Abruption 46 0.105
121
HPR003 Heparin-Induced Thrombocytopenia 45 0.105
122
THR016 Thrombophlebitis 55 0.105
123
P SPN046 Spinal Muscular Atrophy 62 0.104
124
CRT015 Carotid Artery Occlusion 43 0.103
125
PTN001 Patent Foramen Ovale 55 0.102
126
HLL004 Hellp Syndrome 48 0.102
127
c INF067 Inflammatory Bowel Disease 10 31 0.101
128
MRF001 Marfan Syndrome 73 0.099
129
PRT012 Prothrombin Deficiency 43 0.099
130
INT002 Intermittent Claudication 56 0.099
131
P PLY018 Polycythemia 58 0.098
132
SGT001 Sagittal Sinus Thrombosis 32 0.097
133
P PRC031 Preeclampsia/eclampsia 1 53 0.097
134
HMC014 Homocysteinemia 32 0.096
135
THR088 Thrombophilia Due to Protein S Deficiency, Autosomal Recessive 18 0.096
136
FCT022 Factor Xi Deficiency, Autosomal Recessive 55 0.095
137
BNF002 Bone Fracture 46 0.095
138
c ACT210 Acute Respiratory Distress Syndrome 55 0.095
139
SCT005 Scott Syndrome 51 0.095
140
LMB062 Limb Ischemia 48 0.093
141
IRR002 Irritable Bowel Syndrome 58 0.092
142
ATM012 Autoimmune Disease of Blood 36 0.091
143
c INF071 Inflammatory Bowel Disease 1 51 0.091
144
KWS001 Kwashiorkor 45 0.091
145
GLN010 Glanzmann Thrombasthenia 64 0.091
146
MGL001 Megaloblastic Anemia 51 0.090
147
EXF001 Exfoliation Syndrome 56 0.090
148
ATM055 Autoimmune Disease 4 16 0.089
149
c SVR056 Severe Hemophilia a 44 0.089
150
VNW007 Von Willebrand Disease 57 0.088
151
MRB003 Morbid Obesity 59 0.088
152
CRB132 Cerebral Sinovenous Thrombosis 30 0.088
153
c HMG003 Hemoglobin E Disease 44 0.088
154
OVR029 Ovarian Hyperstimulation Syndrome 59 0.088
155
P UTR038 Uterine Disease 38 0.087
156
CRV045 Cervical Intraepithelial Neoplasia 41 0.087
157
PST095 Post-Thrombotic Syndrome 48 0.087
158
P VNS003 Venous Insufficiency 53 0.087
159
SPN185 Spinal Cord Infarction 36 0.087
160
P HYP620 Hypoprothrombinemia 50 0.087
161
PRG092 Pregnancy Loss, Recurrent 1 33 0.086
162
BRN026 Branch Retinal Artery Occlusion 37 0.086
163
P DRM010 Dermatomyositis 59 0.086
164
CGL001 Coagulation Protein Disease 14 0.086
165
P ART084 Arteriovenous Fistula 40 0.085
166
P RTN014 Retinal Artery Occlusion 32 0.084
167
CRD001 Cardiac Tamponade 43 0.084
168
PPL021 Papilledema 47 0.084
169
HYP063 Hypersplenism 49 0.084
170
P PLZ001 Pelizaeus-Merzbacher Disease 63 0.083
171
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 0.082
172
INT051 Intussusception 50 0.082
173
PRP028 Peripheral Vertigo 42 0.082
174
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 30 0.081
175
LVD002 Livedoid Vasculopathy 33 0.081
176
P SZR006 Seizure Disorder 56 0.081
177
ACT058 Active Peptic Ulcer Disease 44 0.081
178
SND002 Sneddon Syndrome 45 0.081
179
RTN021 Retinal Vascular Occlusion 33 0.080
180
ART110 Arteritic Anterior Ischemic Optic Neuropathy 32 0.080
181
CTS005 Catastrophic Antiphospholipid Syndrome 39 0.079
182
ISC015 Ischemic Colitis 38 0.079
183
AMR003 Amaurosis Fugax 38 0.079
184
BNM008 Bone Mineral Density, Low 28 0.078
185
HPT020 Hepatic Vascular Disease 43 0.078
186
P AXN001 Axonal Neuropathy 37 0.077
187
PYR037 Pyruvate Carboxylase Deficiency 37 0.077
188
LCH001 Leech Infestation 35 0.076
189
ACN019 Acanthamoeba Keratitis 28 0.076
190
P PRN026 Porencephaly 47 0.076
191
ATM014 Autoimmune Disease of Endocrine System 37 0.076
192
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 45 0.076
193
THR020 Thrombophilia Due to Heparin Cofactor Ii Deficiency 21 0.075
194
MCL006 Macular Retinal Edema 42 0.075
195
THY030 Thyroid Gland Disease 52 0.075
196
P PRM002 Primary Hyperoxaluria 54 0.075
197
FRN014 Fournier Gangrene 33 0.074
198
ANT013 Anterior Spinal Artery Syndrome 27 0.074
199
QBC001 Quebec Platelet Disorder 51 0.074
200
BLT003 Blue Toe Syndrome 33 0.074
201
INT007 Intermediate Coronary Syndrome 52 0.074
202
P DYS026 Dysfibrinogenemia 36 0.074
203
SPT005 Spotted Fever 56 0.074
204
ALC009 Alcoholic Liver Cirrhosis 53 0.073
205
c ACQ014 Acquired Hemophilia 42 0.073
206
KRN001 Korean Hemorrhagic Fever 39 0.073
207
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.073
208
P GNT005 Giant Hemangioma 34 0.073
209
c HRD088 Hereditary Neuropathies 35 0.072
210
P KLL001 Kallmann Syndrome 61 0.072
211
HPT002 Hepatic Vein Thrombosis 38 0.071
212
MTR003 Mitral Valve Stenosis 40 0.071
213
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.071
214
BRG013 Buerger Disease 54 0.071
215
P GCH001 Gaucher's Disease 63 0.071
216
c CHR431 Chronic Venous Insufficiency 43 0.071
217
MRN001 Marantic Endocarditis 34 0.071
218
VSC047 Vascular Malformation 45 0.070
219
OCY001 Oocyte Maturation Defect 31 0.070
220
INT050 Intestinal Impaction 28 0.070
221
MYT019 May-Thurner Syndrome 21 0.070
222
DBT006 Diabetic Macular Edema 46 0.070
223
MGR028 Migraine with or Without Aura 1 49 0.070
224
VTM001 Vitamin K Deficiency Hemorrhagic Disease 37 0.069
225
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 42 0.069
226
SNS003 Sensory Peripheral Neuropathy 44 0.069
227
MNN017 Mononeuropathy 37 0.069
228
CHR001 Churg-Strauss Syndrome 48 0.069
229
P ACT080 Acute Pulmonary Heart Disease 31 0.068
230
VNW005 Von Willebrand Disease, Type 1 48 0.068
231
P MYM002 Moyamoya Disease 60 0.067
232
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 32 0.067
233
P TRN034 Transverse Myelitis 43 0.067
234
CCN007 Cocoon Syndrome 32 0.067
235
INT010 Intracranial Embolism 32 0.066
236
LGG001 Legg-Calve-Perthes Disease 58 0.066
237
CRT049 Critical Limb Ischemia 51 0.066
238
NNT024 Neonatal Stroke 34 0.065
239
MYL020 Myelomeningocele 50 0.065
240
BRN082 Bernard-Soulier Syndrome, Type C 51 0.065
241
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 43 0.064
242
P SCH018 Schizencephaly 51 0.063
243
MTH044 Mthfr Gene Mutation 21 0.063
244
BRS090 Breast Reconstruction 38 0.063
245
c ART101 Aortic Valve Disease 2 56 0.063
246
MSN003 Mesenteric Vascular Occlusion 34 0.063
247
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.062
248
P CHR102 Charcot-Marie-Tooth Neuropathy 43 0.062
249
FNT004 Fainting 33 0.062
250
LMR001 Lemierre's Syndrome 43 0.062
251
P WLF004 Wolfram Syndrome 62 0.062
252
c AFB002 Afibrinogenemia, Congenital 51 0.062
253
SBN001 Subendocardial Myocardial Infarction 33 0.062
254
HMR002 Hemarthrosis 47 0.062
255
P CHR084 Chromosomal Disease 37 0.061
256
c SVR057 Severe Hemophilia B 30 0.061
257
c ACQ042 Acquired Hemophilia a 39 0.061
258
ANN002 Anencephaly 50 0.061
259
SPN035 Spindle Cell Sarcoma 48 0.059
260
ACQ017 Acquired Von Willebrand Syndrome 35 0.059
261
CRN020 Coronary Restenosis 34 0.059
262
RTN001 Retinal Vasculitis 43 0.059
263
FMR003 Femoral Neuropathy 34 0.059
264
P FBR031 Febrile Seizures 53 0.058
265
c CNG415 Congenital Disorder of Glycosylation, Type Ia 46 0.058
266
ESN011 Eisenmenger Syndrome 45 0.058
267
c PRM225 Primary Thrombocytopenia 42 0.057
268
OCL022 Ocular Melanoma 53 0.057
269
SPL011 Spleen Cancer 38 0.057
270
QLT001 Qualitative Platelet Defect 30 0.057
271
WBR001 Weber Syndrome 36 0.056
272
HNT002 Hantavirus Pulmonary Syndrome 51 0.056
273
CNT060 Central Serous Chorioretinopathy 42 0.055
274
CLD011 Cold Urticaria 36 0.055
275
CRT004 Carotid Artery Thrombosis 38 0.055
276
PRM087 Premature Chromatid Separation Trait 19 0.054
277
LYM022 Lymphangioma 55 0.054
278
c CHR536 Charcot-Marie-Tooth Disease, Type 1a 55 0.054
279
INF133 Inferior Vena Cava Interruption 28 0.053
280
P MLD013 Mild Hemophilia a 28 0.053
281
CPL005 Capillary Disease 39 0.053
282
HPT046 Hepatic Veno-Occlusive Disease 46 0.052
283
c CHR527 Charcot-Marie-Tooth Disease, Type 1b 48 0.052
284
SRC011 Sarcocystosis 35 0.052
285
LGN005 Ligneous Conjunctivitis 28 0.051
286
VND002 Van Der Woude Syndrome 50 0.051
287
TYP015 Type 2b Von Willebrand Disease 29 0.051
288
c ACQ005 Acquired Thrombocytopenia 35 0.050
289
c ART106 Arterial Calcification, Generalized, of Infancy, 1 32 0.049
290
c ACT072 Acute Laryngitis 37 0.049
291
P AND016 Andersen Syndrome 57 0.049
292
CRB017 Cerebral Falx Meningioma 18 0.049
293
BNP002 Bone Epithelioid Hemangioma 18 0.049
294
ANT022 Anterior Cranial Fossa Meningioma 26 0.049
295
c PST001 Posterior Myocardial Infarction 32 0.049
296
ARG001 Argentine Hemorrhagic Fever 35 0.048
297
RYN001 Raynaud Disease 41 0.048
298
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 46 0.048
299
ALP044 Alpha-1-Antichymotrypsin Deficiency 24 0.048
300
c CHR532 Charcot-Marie-Tooth Disease, Type 2e 45 0.048
301
TYP017 Type 2n Von Willebrand Disease 19 0.048
302
DJR004 Dejerine-Sottas Disease 48 0.048
303
RSS002 Roussy-Levy Syndrome 51 0.047
304
INT076 Intracranial Sinus Thrombosis 22 0.047
305
TYP016 Type 2m Von Willebrand Disease 18 0.046
306
MTR007 Motor Peripheral Neuropathy 44 0.046
307
c PLM127 Pulmonary Hypertension, Primary, 3 31 0.046
308
LKS001 Leukostasis 39 0.044
309
DYS013 Dysbaric Osteonecrosis 33 0.042
310
c CHR549 Charcot-Marie-Tooth Disease Type 2l 19 0.040