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Factor XIII Deficiency
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Disease • C0015530
Definition
A deficiency of blood coagulation FACTOR XIII or fibrin stabilizing factor (FSF) that prevents blood clot formation and results in a clinical hemorrhagic diathesis.
Synonyms
Factor XIII Deficiency • Deficiency, factor XIII • Deficiencies, Factor XIII • Factor XIII Deficiencies • Deficiency of factor XIII • FIBRIN STABILIZING FACTOR DEFICIENCY, CONGENITAL • LAKI-LORAND FACTOR DEFICIENCY, CONGENITAL • FACTOR XIII DEFICIENCY, CONGENITAL • FIBRINASE DEFICIENCY, CONGENITAL • Deficiency, Laki-Lorand factor • DEFIC FACTOR XIII • FACTOR XIII DEFIC • Factor XIII Deficiency [Disease/Finding]
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F13A1 gene
Hemorrhagic Disorders
Blood Coagulation Disorders, Inherited
Coagulation Protein Disorders
F13B gene
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Related concepts
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#
|
Concept name
|
Type
|
Relation
|
Support
|
Score
|
|
1
|
F13B gene
|
Gene
|
Known
|
Explain
|
95.36274
|
|
2
|
Coagulation Protein Disorders
|
Disease
|
Known
|
Explain
|
80.13237
|
|
3
|
Blood Coagulation Disorders, Inherited
|
Disease
|
Known
|
Explain
|
60.02542
|
|
4
|
Hemorrhagic Disorders
|
Disease
|
Known
|
Explain
|
54.41915
|
|
5
|
F13A1 gene
|
Gene
|
Known
|
Explain
|
45.61894
|
|
6
|
Hypoprothrombinemias
|
Disease
|
Inferred
|
Explain
|
2.43543
|
|
7
|
Factor VII Deficiency
|
Disease
|
Inferred
|
Explain
|
2.43255
|
|
8
|
Factor V Deficiency
|
Disease
|
Inferred
|
Explain
|
2.42362
|
|
9
|
Factor X Deficiency
|
Disease
|
Inferred
|
Explain
|
2.40462
|
|
10
|
Factor XI Deficiency
|
Disease
|
Inferred
|
Explain
|
2.39455
|
|
11
|
Factor XII Deficiency
|
Disease
|
Inferred
|
Explain
|
2.35862
|
|
12
|
Afibrinogenemia
|
Disease
|
Inferred
|
Explain
|
2.16322
|
|
13
|
Hemophilia B
|
Disease
|
Inferred
|
Explain
|
2.15888
|
|
14
|
Hemophilia A
|
Disease
|
Inferred
|
Explain
|
1.89782
|
|
15
|
von Willebrand Disease
|
Disease
|
Inferred
|
Explain
|
1.66926
|
|
16
|
Activated Protein C Resistance
|
Disease
|
Inferred
|
Explain
|
1.51993
|
|
17
|
Blood Coagulation Disorders
|
Disease
|
Inferred
|
Explain
|
0.91947
|
|
18
|
Thrombasthenia
|
Disease
|
Inferred
|
Explain
|
0.70740
|
|
19
|
Wiskott-Aldrich Syndrome
|
Disease
|
Inferred
|
Explain
|
0.64541
|
|
20
|
Hermanski-Pudlak Syndrome
|
Disease
|
Inferred
|
Explain
|
0.60400
|
|
21
|
Bernard-Soulier Syndrome
|
Disease
|
Inferred
|
Explain
|
0.56137
|
|
22
|
Blood Platelet Disorders
|
Disease
|
Inferred
|
Explain
|
0.46673
|
|
23
|
Platelet Storage Pool Deficiency
|
Disease
|
Inferred
|
Explain
|
0.35247
|
|
24
|
Gray Platelet Syndrome
|
Disease
|
Inferred
|
Explain
|
0.29918
|
|
25
|
Disseminated Intravascular Coagulation
|
Disease
|
Inferred
|
Explain
|
0.27954
|
|
26
|
Thrombophilia
|
Disease
|
Inferred
|
Explain
|
0.24739
|
|
27
|
Antithrombin III Deficiency
|
Disease
|
Inferred
|
Explain
|
0.24386
|
|
28
|
Thrombocythemia, Essential
|
Disease
|
Inferred
|
Explain
|
0.23980
|
|
29
|
Protein C Deficiency
|
Disease
|
Inferred
|
Explain
|
0.22966
|
|
30
|
Vitamin K Deficiency
|
Disease
|
Inferred
|
Explain
|
0.22734
|
|
31
|
F7 gene
|
Gene
|
Inferred
|
Explain
|
0.18051
|
|
32
|
Waterhouse-Friderichsen Syndrome
|
Disease
|
Inferred
|
Explain
|
0.17514
|
|
33
|
FGG gene
|
Gene
|
Inferred
|
Explain
|
0.16193
|
|
34
|
Purpura, Thrombocytopenic, Idiopathic
|
Disease
|
Inferred
|
Explain
|
0.15274
|
|
35
|
F9 gene
|
Gene
|
Inferred
|
Explain
|
0.13216
|
|
36
|
FGA gene
|
Gene
|
Inferred
|
Explain
|
0.12958
|
|
37
|
Hereditary factor I deficiency disease
|
Disease
|
Inferred
|
Explain
|
0.12928
|
|
38
|
F11 gene
|
Gene
|
Inferred
|
Explain
|
0.12741
|
|
39
|
Complement and coagulation cascades - Homo sapiens (human)
|
Pathway
|
Inferred
|
Explain
|
0.11949
|
|
40
|
Hematological Disease
|
Disease
|
Inferred
|
Explain
|
0.11399
|
|
41
|
F5 gene
|
Gene
|
Inferred
|
Explain
|
0.09592
|
|
42
|
Genetic Diseases, X-Linked
|
Disease
|
Inferred
|
Explain
|
0.09125
|
|
43
|
Sushi/SCR/CCP
|
Domain
|
Inferred
|
Explain
|
0.09006
|
|
44
|
Complement control module
|
Domain
|
Inferred
|
Explain
|
0.08443
|
|
45
|
Vascular Hemostatic Disorders
|
Disease
|
Inferred
|
Explain
|
0.08234
|
|
46
|
F12 gene
|
Gene
|
Inferred
|
Explain
|
0.07541
|
|
47
|
F2 gene
|
Gene
|
Inferred
|
Explain
|
0.07396
|
|
48
|
FGB gene
|
Gene
|
Inferred
|
Explain
|
0.07126
|
|
49
|
F10 gene
|
Gene
|
Inferred
|
Explain
|
0.06707
|
|
50
|
CFI gene
|
Gene
|
Inferred
|
Explain
|
0.05887
|
|
51
|
Alkylamine
|
Compound
|
Inferred
|
Explain
|
0.04391
|
|
52
|
Protein glutamine
|
Compound
|
Inferred
|
Explain
|
0.04391
|
|
53
|
Protein N5-alkylglutamine
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Compound
|
Inferred
|
Explain
|
0.04391
|
|
54
|
P2RX1 gene
|
Gene
|
Inferred
|
Explain
|
0.04336
|
|
55
|
Iodoacetamide
|
Compound
|
Inferred
|
Explain
|
0.04179
|
|
56
|
Lymphopenia
|
Disease
|
Inferred
|
Explain
|
0.04126
|
|
57
|
Blood Protein Disorders
|
Disease
|
Inferred
|
Explain
|
0.04111
|
|
58
|
protein-glutamine gamma-glutamyltransferase activity
|
Function
|
Inferred
|
Explain
|
0.03581
|
|
59
|
Genetic Diseases, Inborn
|
Disease
|
Inferred
|
Explain
|
0.03183
|
|
60
|
PROC gene
|
Gene
|
Inferred
|
Explain
|
0.03178
|
|
61
|
Malnutrition
|
Disease
|
Inferred
|
Explain
|
0.03156
|
|
62
|
Blood coagulation
|
Function
|
Inferred
|
Explain
|
0.02914
|
|
63
|
MTHFR gene
|
Gene
|
Inferred
|
Explain
|
0.02886
|
|
64
|
GIANT PLATELET SYNDROME WITH THROMBOCYTOPENIA
|
Disease
|
Inferred
|
Explain
|
0.02865
|
|
65
|
Protein S Deficiency
|
Disease
|
Inferred
|
Explain
|
0.02781
|
|
66
|
VWF gene
|
Gene
|
Inferred
|
Explain
|
0.02687
|
|
67
|
HEMOPHILIA A WITH VASCULAR ABNORMALITY
|
Disease
|
Inferred
|
Explain
|
0.02671
|
|
68
|
Thrombocytosis
|
Disease
|
Inferred
|
Explain
|
0.02540
|
|
69
|
Purpura
|
Disease
|
Inferred
|
Explain
|
0.02214
|
|
70
|
SERPINF2 gene
|
Gene
|
Inferred
|
Explain
|
0.02138
|
|
71
|
Blood Platelets
|
Other
|
Inferred
|
Explain
|
0.02131
|
|
72
|
von Willebrand Disease, Type 3
|
Disease
|
Inferred
|
Explain
|
0.02106
|
|
73
|
VON WILLEBRAND DISEASE, X-LINKED FORM
|
Disease
|
Inferred
|
Explain
|
0.02106
|
|
74
|
Von Willebrand disease, platelet type
|
Disease
|
Inferred
|
Explain
|
0.02062
|
|
75
|
von Willebrand Disease, Recessive Form
|
Disease
|
Inferred
|
Explain
|
0.02022
|
|
76
|
GP1BA gene
|
Gene
|
Inferred
|
Explain
|
0.01994
|
|
77
|
GP9 gene
|
Gene
|
Inferred
|
Explain
|
0.01901
|
|
78
|
platelet alpha granule lumen
|
Component
|
Inferred
|
Explain
|
0.01855
|
|
79
|
Immunologic Deficiency Syndromes
|
Disease
|
Inferred
|
Explain
|
0.01825
|
|
80
|
GP1BB gene
|
Gene
|
Inferred
|
Explain
|
0.01509
|
|
81
|
F8 gene
|
Gene
|
Inferred
|
Explain
|
0.01496
|
|
82
|
Arbutin
|
Compound
|
Inferred
|
Explain
|
0.01414
|
|
83
|
ITGA2B gene
|
Gene
|
Inferred
|
Explain
|
0.01362
|
|
84
|
Vitamin D
|
Compound
|
Inferred
|
Explain
|
0.01361
|
|
85
|
platelet degranulation
|
Function
|
Inferred
|
Explain
|
0.01326
|
|
86
|
propylene dichloride
|
Compound
|
Inferred
|
Explain
|
0.01195
|
|
87
|
Warfarin
|
Compound
|
Inferred
|
Explain
|
0.01086
|
|
88
|
Thrombocytopenia
|
Disease
|
Inferred
|
Explain
|
0.01046
|
|
89
|
Ammonia
|
Compound
|
Inferred
|
Explain
|
0.01019
|
|
90
|
Ethionine
|
Compound
|
Inferred
|
Explain
|
0.00929
|
|
91
|
PLEK gene
|
Gene
|
Inferred
|
Explain
|
0.00884
|
|
92
|
Estradiol
|
Compound
|
Inferred
|
Explain
|
0.00798
|
|
93
|
Ecchymosis
|
Disease
|
Inferred
|
Explain
|
0.00796
|
|
94
|
Avitaminosis
|
Disease
|
Inferred
|
Explain
|
0.00762
|
|
95
|
extracellular region
|
Component
|
Inferred
|
Explain
|
0.00745
|
|
96
|
Platelet Activation
|
Function
|
Inferred
|
Explain
|
0.00743
|
|
97
|
Benzbromarone
|
Compound
|
Inferred
|
Explain
|
0.00734
|
|
98
|
WAS gene
|
Gene
|
Inferred
|
Explain
|
0.00731
|
|
99
|
Thrombocytopenic purpura
|
Disease
|
Inferred
|
Explain
|
0.00716
|
|
100
|
Propylthiouracil
|
Compound
|
Inferred
|
Explain
|
0.00707
|
|