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Antithrombin deficiency
Antithrombin deficiency
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
ANTISYNTHETASE SYNDROME
C2609059
IL1B
Unknown
—
Disgenet
Antifolate resistance
MAPK signaling pathway
Cytokine-cytokine receptor interaction
NF-kappa B signaling pathway
Necroptosis
Osteoclast differentiation
Toll-like receptor signaling pathway
NOD-like receptor signaling pathway
Cytosolic DNA-sensing pathway
C-type lectin receptor signaling pathway
Hematopoietic cell lineage
IL-17 signaling pathway
Th17 cell differentiation
TNF signaling pathway
Inflammatory mediator regulation of TRP channels
Non-alcoholic fatty liver disease
AGE-RAGE signaling pathway in diabetic complications
Alcoholic liver disease
Type I diabetes mellitus
Alzheimer disease
Prion disease
Pathways of neurodegeneration - multiple diseases
Pathogenic Escherichia coli infection
Shigellosis
Salmonella infection
Pertussis
Legionellosis
Yersinia infection
Leishmaniasis
Chagas disease
African trypanosomiasis
Malaria
Amoebiasis
Tuberculosis
Measles
Human cytomegalovirus infection
Influenza A
Herpes simplex virus 1 infection
Coronavirus disease - COVID-19
Inflammatory bowel disease
Rheumatoid arthritis
Graft-versus-host disease
Lipid and atherosclerosis
Fluid shear stress and atherosclerosis
Interleukin-1 processing
CLEC7A/inflammasome pathway
Interleukin-10 signaling
Interleukin-4 and Interleukin-13 signaling
Interleukin-1 signaling
Purinergic signaling in leishmaniasis infection
+47 more
MUC5B
Unknown
—
Disgenet
IL-17 signaling pathway
Salivary secretion
Defective GALNT3 causes familial hyperphosphatemic tumoral calcinosis (HFTC)
Defective C1GALT1C1 causes Tn polyagglutination syndrome (TNPS)
Defective GALNT12 causes colorectal cancer 1 (CRCS1)
Dectin-2 family
O-linked glycosylation of mucins
Termination of O-glycan biosynthesis
+5 more
ANTITHROMBIN III DEFICIENCY
613118
C0272375
MESH:D020152
SERPINC1
Unknown
6435583
CTD
,
Disgenet
,
HPO
Complement and coagulation cascades
Intrinsic Pathway of Fibrin Clot Formation
Common Pathway of Fibrin Clot Formation
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)
Post-translational protein phosphorylation
+2 more
All
3
Causal
0
Unknown
3
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
3
CTD
1
HPO
1
GWAS catalog
0
GenCC
0
ClinGen
0
Related Diseases
Diseases that share the most curated genes with Antithrombin deficiency.
5
View disease cluster →
Craniocerebral trauma
1 shared gene
SERPINC1
Related via 1 shared gene including SERPINC1.
Hereditary antithrombin deficiency
1 shared gene
SERPINC1
Related via 1 shared gene including SERPINC1.
Pyogenic arthritis-pyoderma gangrenosum-acne syndrome
1 shared gene
IL1B
Related via 1 shared gene including IL1B.
Diffuse panbronchiolitis
1 shared gene
MUC5B
Related via 1 shared gene including MUC5B.
Myoclonic epilepsy with ragged red fibers
1 shared gene
IL1B
Related via 1 shared gene including IL1B.
1
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