Cytoscape Web
Click node...

Hereditary thrombophilia due to congenital antithrombin deficiency
1 OMIM reference -
1 associated gene
4 connected diseases
No signs/symptoms info
Disease Type of connection
Cerebral sinovenous thrombosis
Congenital factor II deficiency
Hypoplasminogenemia
Ligneous conjunctivitis
Synonym(s):
- Hereditary thrombophilia due to congenital antithrombin 3 deficiency
Classification (Orphanet):
- Rare bone disease
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
SERPINC1 P01008107300
No signs/symptoms info available.