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"

343 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 8.103
2
PRT011 Protein C Deficiency 52 7.597
3
c THR082 Thrombophilia Due to Activated Protein C Resistance 54 7.198
4
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 19 5.200
5
P HPT021 Hepatitis 69 0.648
6
P THR015 Thrombophilia 59 0.548
7
THR024 Thrombosis 57 0.465
8
END072 Endotheliitis 42 0.438
9
P LKM002 Leukemia 71 0.408
10
CRB009 Cerebritis 39 0.315
11
P PNC044 Pancreatitis 61 0.312
12
RTN023 Retinitis 50 0.301
13
P THY032 Thyroiditis 54 0.297
14
P LVR013 Liver Disease 75 0.293
15
P LNG032 Lung Cancer 95 0.292
16
P OBS005 Obesity 92 0.282
17
P MYC007 Myocardial Infarction 79 0.262
18
PRT014 Protein S Deficiency 53 0.256
19
ISC004 Ischemia 61 0.237
20
P HRT032 Heart Disease 75 0.232
21
P NRP001 Neuropathy 59 0.226
22
c HPT003 Hepatitis a 59 0.222
23
P AST005 Asthma 82 0.219
24
ATH003 Atherosclerosis 65 0.218
25
ART111 Artery Disease 55 0.209
26
P ENC018 Encephalopathy 59 0.208
27
PRP030 Purpura 58 0.207
28
P MYL006 Myeloid Leukemia 66 0.206
29
ADN018 Adenoma 58 0.189
30
P INF032 Infertility 59 0.188
31
INS024 Insulin-Like Growth Factor I 75 0.188
32
ANR040 Aneurysm 57 0.187
33
P RTN024 Retinoblastoma 74 0.185
34
CYS001 Cystic Fibrosis 83 0.182
35
GRW007 Growth Hormone Deficiency 50 0.180
36
THR013 Thoracic Outlet Syndrome 50 0.176
37
c ACT075 Acute Myocardial Infarction 60 0.174
38
P INF037 Inflammatory Bowel Disease 63 0.170
39
BLD054 Blood Protein Disease 37 0.167
40
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.165
41
P MLT019 Multiple Myeloma 83 0.164
42
ALR002 Al-Raqad Syndrome 36 0.162
43
CLT003 Colitis 60 0.161
44
PLM033 Pulmonary Embolism 60 0.161
45
P PSR002 Psoriasis 61 0.156
46
P THR014 Thrombocytopenia 64 0.155
47
VSC007 Vascular Disease 67 0.154
48
P THL005 Thalassemia 64 0.154
49
VSC008 Vascular Hemostatic Disease 30 0.152
50
P LYM026 Lymphoblastic Leukemia 62 0.147
51
c THR092 Thrombophilia Due to Thrombin Defect 54 0.145
52
P HYP086 Hypothyroidism 64 0.144
53
P HMP007 Hemophilia 57 0.141
54
PRP027 Peripheral Vascular Disease 69 0.141
55
P PRP034 Purpura Fulminans 41 0.139
56
P RTN022 Retinal Vein Occlusion 38 0.139
57
VSC011 Vasculitis 62 0.138
58
VND001 Vein Disease 47 0.136
59
HYP056 Hypoglycemia 61 0.135
60
C3D001 C3 Deficiency 53 0.135
61
P PLM037 Pulmonary Hypertension 79 0.135
62
P BLD051 Blood Coagulation Disease 42 0.135
63
CRH001 Crohn's Disease 75 0.133
64
c PRC016 Pre-Eclampsia 56 0.131
65
ART021 Arteriosclerosis 58 0.131
66
MCS002 Mucositis 55 0.130
67
IMM136 Immune System Disease 51 0.130
68
P ECL001 Eclampsia 54 0.130
69
ACD009 Acid-Labile Subunit, Deficiency of 45 0.128
70
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.128
71
ULC004 Ulcerative Colitis 76 0.127
72
P HMR003 Hemorrhagic Disease 57 0.127
73
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.126
74
P NPH012 Nephrotic Syndrome 59 0.125
75
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.124
76
c HMP029 Hemophilia a 63 0.123
77
ACR041 Acromelic Frontonasal Dysostosis 45 0.123
78
BRT030 Birth Defects 43 0.122
79
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.122
80
P HMC002 Homocystinuria 50 0.120
81
P PLY011 Polycystic Ovary Syndrome 65 0.119
82
P ANT006 Antiphospholipid Syndrome 56 0.119
83
FTT001 Fatty Liver Disease 59 0.118
84
FCT003 Factor X Deficiency 61 0.118
85
NRM005 Neuromuscular Disease 56 0.117
86
HYP037 Hyperhomocysteinemia 50 0.117
87
CRB039 Cerebrovascular Disease 63 0.116
88
TTH006 Tooth Disease 52 0.116
89
STR067 Stroke, Ischemic 75 0.114
90
AND005 Androgen Insensitivity Syndrome, Mild 16 0.112
91
P HYP060 Hyperinsulinism 58 0.112
92
HYP066 Hyperglycemia 61 0.111
93
c CNT016 Central Retinal Vein Occlusion 36 0.111
94
FCT007 Factor Vii Deficiency 61 0.110
95
P END033 Endocarditis 54 0.110
96
PRT018 Portal Vein Thrombosis 49 0.109
97
P MSC003 Muscular Atrophy 50 0.108
98
c CNT035 Central Nervous System Disease 60 0.108
99
PRP019 Peripheral Nervous System Disease 55 0.107
100
P ATX030 Ataxia-Telangiectasia 77 0.106
101
GST019 Gastrointestinal Stromal Tumor 73 0.104
102
FCT006 Factor V Deficiency 57 0.104
103
PLC008 Placenta Disease 33 0.104
104
PRP080 Peripheral Artery Disease 37 0.104
105
DWR001 Dwarfism 47 0.103
106
HDC001 Headache 54 0.103
107
OST003 Osteonecrosis 45 0.103
108
ISL003 Isolated Growth Hormone Deficiency 52 0.102
109
c PRT045 Prothrombin-Related Thrombophilia 24 0.102
110
PTT006 Pituitary Adenoma 56 0.101
111
P HYP083 Hypopituitarism 54 0.101
112
HPT074 Hepatic Adenoma, Somatic 50 0.101
113
FCT013 Factor V Leiden Thrombophilia 22 0.101
114
PNC034 Pancreas Disease 58 0.100
115
NRN004 Neuroendocrine Tumor 56 0.099
116
THR089 Thrombophilia Due to Protein S Deficiency, Autosomal Dominant 20 0.098
117
SCK005 Sickle Cell Disease 51 0.098
118
HNM002 Hinman Syndrome 25 0.097
119
P HML001 Hemolytic-Uremic Syndrome 51 0.095
120
FCT005 Factor Xiii Deficiency 43 0.095
121
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 49 0.094
122
P CHR071 Charcot-Marie-Tooth Disease 67 0.094
123
THR004 Thrombocytosis 55 0.093
124
P OVR049 Ovarian Disease 56 0.093
125
DSS009 Disseminated Intravascular Coagulation 51 0.093
126
P BDD001 Budd-Chiari Syndrome 56 0.092
127
SPC003 Specific Developmental Disorder 38 0.092
128
BNF002 Bone Fracture 50 0.092
129
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.091
130
GLC003 Glucose Intolerance 55 0.091
131
c HMP004 Hemophilia B 62 0.091
132
ACR007 Acromegaly 66 0.090
133
NRL016 Neural Tube Defects 76 0.090
134
MRF001 Marfan Syndrome 73 0.090
135
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.090
136
P HYP076 Hyperthyroidism 55 0.090
137
P SPN046 Spinal Muscular Atrophy 65 0.089
138
c INH004 Inherited Blood Coagulation Disease 36 0.089
139
CRC006 Carcinoid Syndrome 52 0.088
140
ATM055 Autoimmune Disease 4 15 0.088
141
P PLY018 Polycythemia 58 0.086
142
CRN017 Coronary Thrombosis 48 0.086
143
MYL031 Myeloproliferative Neoplasm 58 0.085
144
P UTR038 Uterine Disease 37 0.085
145
HYP085 Hypothalamic Disease 44 0.084
146
TTR016 Tetra-Amelia Syndrome 36 0.084
147
SXD001 Sex Differentiation Disease 38 0.084
148
ATM012 Autoimmune Disease of Blood 35 0.083
149
CGL001 Coagulation Protein Disease 14 0.083
150
P ESS003 Essential Thrombocythemia 70 0.082
151
OVR029 Ovarian Hyperstimulation Syndrome 61 0.081
152
P HMR012 Hemorrhagic Fever 56 0.081
153
P DBT005 Diabetes Insipidus 53 0.081
154
P SZR006 Seizure Disorder 56 0.080
155
PTT009 Pituitary Gland Disease 47 0.080
156
CRB037 Cerebral Palsy 66 0.080
157
IRR002 Irritable Bowel Syndrome 58 0.080
158
P RTN014 Retinal Artery Occlusion 44 0.080
159
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 33 0.079
160
PLC007 Placental Abruption 47 0.079
161
INT075 Intracranial Hypertension 50 0.079
162
FCT004 Factor Xii Deficiency 50 0.079
163
GND003 Gonadal Disease 39 0.078
164
HLL004 Hellp Syndrome 50 0.077
165
c ATM010 Autoimmune Hemolytic Anemia 61 0.077
166
INF034 Infective Endocarditis 51 0.077
167
P ART084 Arteriovenous Fistula 44 0.076
168
PTN001 Patent Foramen Ovale 55 0.076
169
PTT037 Pituitary Tumors 45 0.075
170
LMB062 Limb Ischemia 48 0.075
171
THR016 Thrombophlebitis 53 0.075
172
INS001 Insulinoma 61 0.074
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 59 0.073
177
P ALP004 Alport Syndrome 69 0.073
178
P DRM010 Dermatomyositis 62 0.073
179
VNW001 Von Willebrand's Disease 61 0.072
180
THY030 Thyroid Gland Disease 48 0.072
181
VSC047 Vascular Malformation 45 0.071
182
ISC002 Ischemic Optic Neuropathy 37 0.071
183
P PRC031 Preeclampsia/eclampsia 1 51 0.071
184
ACT087 Acth Deficiency 43 0.071
185
ATM014 Autoimmune Disease of Endocrine System 36 0.070
186
HPR003 Heparin-Induced Thrombocytopenia 45 0.069
187
P OCY001 Oocyte Maturation Defect 38 0.069
188
P PRC019 Precocious Puberty 51 0.069
189
ADP007 Adie Pupil 34 0.069
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 0.067
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
P VNS003 Venous Insufficiency 54 0.064
200
THR020 Thrombophilia Due to Heparin Cofactor Ii Deficiency 19 0.064
201
INT002 Intermittent Claudication 56 0.064
202
UTR039 Uterine Fibroid 57 0.064
203
MGR028 Migraine with or Without Aura 1 47 0.063
204
c HRD088 Hereditary Neuropathies 40 0.062
205
P AXN001 Axonal Neuropathy 38 0.062
206
AMN001 Amenorrhea 50 0.061
207
SPL006 Splenic Infarction 35 0.061
208
CHR001 Churg-Strauss Syndrome 49 0.061
209
CRN036 Craniopharyngioma 59 0.061
210
PYR037 Pyruvate Carboxylase Deficiency 37 0.061
211
SGT001 Sagittal Sinus Thrombosis 35 0.060
212
P CHR084 Chromosomal Disease 32 0.060
213
c HMG003 Hemoglobin E Disease 44 0.060
214
HYP020 Hyperprolactinemia 60 0.060
215
P KLL001 Kallmann Syndrome 61 0.060
216
AMR003 Amaurosis Fugax 38 0.060
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 0.059
221
P MYM002 Moyamoya Disease 61 0.058
222
FBR009 Fibrous Dysplasia 45 0.058
223
P DYS026 Dysfibrinogenemia 45 0.058
224
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.058
225
FST010 Fasting Hypoglycemia 39 0.057
226
CRB132 Cerebral Sinovenous Thrombosis 31 0.057
227
SRT004 Serotonin Syndrome 49 0.056
228
P AFB001 Afibrinogenemia 48 0.056
229
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.056
230
LGG001 Legg-Calve-Perthes Disease 57 0.056
231
P ATX010 Ataxia Neuropathy Spectrum 30 0.055
232
PRG092 Pregnancy Loss, Recurrent 1 31 0.055
233
OST115 Osteonecrosis of the Jaw 38 0.055
234
P FBR031 Febrile Seizures 53 0.055
235
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 33 0.055
236
BRN026 Branch Retinal Artery Occlusion 38 0.055
237
c SYS004 Systemic Mastocytosis 60 0.055
238
c EHL032 Ehlers-Danlos Syndrome, Type Viib 49 0.055
239
FTD001 Foot Drop 33 0.054
240
HMC014 Homocysteinemia 35 0.054
241
P WLF004 Wolfram Syndrome 61 0.054
242
ISL001 Islet Cell Tumor 50 0.053
243
PPL021 Papilledema 47 0.053
244
P HYP620 Hypoprothrombinemia 54 0.053
245
c CNT075 Central Precocious Puberty 49 0.052
246
STC016 Sticky Platelet Syndrome 29 0.052
247
c PRM225 Primary Thrombocytopenia 39 0.052
248
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 55 0.052
249
HPT020 Hepatic Vascular Disease 42 0.052
250
ADR012 Adrenal Gland Disease 48 0.052
251
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 0.052
252
P PND002 Pendred Syndrome 55 0.052
253
HMC020 Homocystinuria, B6-Responsive and Nonresponsive Types 43 0.051
254
LVD002 Livedoid Vasculopathy 32 0.051
255
c ART106 Arterial Calcification, Generalized, of Infancy, 1 39 0.051
256
P CHR102 Charcot-Marie-Tooth Neuropathy 41 0.050
257
c MLT136 Multiple Endocrine Neoplasia 1 69 0.050
258
c CHR431 Chronic Venous Insufficiency 44 0.050
259
GRW024 Growth Hormone Deficiency, Isolated, Type Ii 45 0.049
260
WBR001 Weber Syndrome 41 0.049
261
VNW005 Von Willebrand Disease, Type 1 49 0.049
262
P SLV001 Silver-Russell Syndrome 54 0.048
263
ADR005 Adrenal Carcinoma 57 0.048
264
c PLM127 Pulmonary Hypertension, Primary, 3 28 0.048
265
P MDL022 Medullary Thyroid Carcinoma, Familial 63 0.048
266
SPN185 Spinal Cord Infarction 34 0.048
267
c SVR005 Severe Pre-Eclampsia 49 0.048
268
P PRN026 Porencephaly 48 0.047
269
c ACQ014 Acquired Hemophilia 42 0.047
270
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.047
271
RTN001 Retinal Vasculitis 44 0.047
272
P FNC043 Fanconi Anemia, Complementation Group E 55 0.047
273
ART110 Arteritic Anterior Ischemic Optic Neuropathy 31 0.047
274
CVR006 Cavernous Hemangioma 46 0.045
275
GGN002 Gigantism 32 0.045
276
c ACQ042 Acquired Hemophilia a 40 0.045
277
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.045
278
c CNG411 Congenital Disorder of Glycosylation, Type in 49 0.044
279
DMP001 Dumping Syndrome 40 0.044
280
SLP010 Slipped Capital Femoral Epiphysis 34 0.044
281
CTN014 Cutaneous Mastocytosis 49 0.043
282
c CHR527 Charcot-Marie-Tooth Disease, Type 1b 49 0.043
283
c CHR536 Charcot-Marie-Tooth Disease, Type 1a 58 0.043
284
P MGR003 Migraine with Aura 52 0.043
285
END021 Endomyocardial Fibrosis 49 0.043
286
GLC036 Glucagonoma 46 0.043
287
MTH044 Mthfr Gene Mutation 21 0.043
288
LRN004 Laron Dwarfism 58 0.043
289
NNF007 Non-Functioning Pituitary Adenoma 41 0.043
290
PNC053 Pancreatic Islet Cell Tumors 35 0.042
291
LCH001 Leech Infestation 40 0.042
292
c AFB002 Afibrinogenemia, Congenital 54 0.042
293
CRR007 Cirrhosis, Cryptogenic 43 0.042
294
GST030 Gastrinoma 42 0.042
295
c CHR532 Charcot-Marie-Tooth Disease, Type 2e 49 0.042
296
INT060 Intestinal Atresia 42 0.041
297
PLY125 Polycythemia Vera, Somatic 63 0.041
298
RSS002 Roussy-Levy Syndrome 50 0.041
299
HYP026 Hypoglycemic Coma 39 0.041
300
PRP028 Peripheral Vertigo 38 0.040
301
NLS001 Nelson Syndrome 47 0.040
302
FRN014 Fournier Gangrene 35 0.040
303
FNC007 Functioning Pituitary Adenoma 41 0.039
304
ACN019 Acanthamoeba Keratitis 32 0.039
305
P PTT050 Pituitary Adenoma, Growth Hormone-Secreting 48 0.039
306
DJR004 Dejerine-Sottas Disease 46 0.039
307
MTR007 Motor Peripheral Neuropathy 37 0.039
308
VST004 Vestibular Disease 44 0.039
309
ISC015 Ischemic Colitis 39 0.038
310
QLT001 Qualitative Platelet Defect 32 0.038
311
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 49 0.038
312
VND002 Van Der Woude Syndrome 50 0.038
313
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 33 0.037
314
MSN003 Mesenteric Vascular Occlusion 34 0.037
315
NNT024 Neonatal Stroke 36 0.037
316
SND002 Sneddon Syndrome 44 0.037
317
P AND016 Andersen Syndrome 58 0.036
318
GNT005 Giant Hemangioma 35 0.036
319
PRM087 Premature Chromatid Separation Trait 18 0.035
320
INT078 Intracranial Thrombosis 36 0.035
321
BRG013 Buerger Disease 53 0.035
322
PRC051 Paracetamol Poisoning 27 0.035
323
MST001 Mast-Cell Sarcoma 40 0.034
324
c PRM149 Primary Hypereosinophilic Syndrome 38 0.034
325
CHR034 Chromophobe Adenoma 40 0.034
326
KRN001 Korean Hemorrhagic Fever 39 0.033
327
MYT019 May-Thurner Syndrome 23 0.032
328
c MYT012 Myotonia Congenita, Recessive 32 0.032
329
INT050 Intestinal Impaction 31 0.032
330
BLT003 Blue Toe Syndrome 35 0.032
331
HPT081 Hepatic Infarction 34 0.032
332
SHH001 Sheehan Syndrome 44 0.031
333
INT010 Intracranial Embolism 32 0.031
334
SMH001 Sm-Ahnmd 26 0.031
335
INT076 Intracranial Sinus Thrombosis 24 0.031
336
LFF001 Loeffler Endocarditis 25 0.030
337
MRN001 Marantic Endocarditis 32 0.030
338
c CHR529 Charcot-Marie-Tooth Disease, Type 2i 30 0.030
339
CRB017 Cerebral Falx Meningioma 21 0.030
340
c CHR528 Charcot-Marie-Tooth Disease, Type 2j 32 0.029
341
MYL059 Myeloid and Lymphoid Neoplasms with Eosinophilia and Abnormalities of Pdgfra, Pdgfrb, and Fgfr1 29 0.029
342
ANT022 Anterior Cranial Fossa Meningioma 28 0.028
343
MYL045 Myelofibrosis with Myeloid Metaplasia, Somatic 36 0.027