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Familial thrombomodulin anomalies
1 OMIM reference -
1 associated gene
5 connected diseases
No signs/symptoms info
Disease Type of connection
Atypical hemolytic uremic syndrome with thrombomodulin anomaly
Cerebral sinovenous thrombosis
Congenital factor II deficiency
Hereditary thrombophilia due to congenital protein C deficiency
Congenital plasminogen activator inhibitor type 1 deficiency
Synonym(s):
(no synonyms)
Classification (Orphanet):
- 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 -
1 MeSH reference: C536900
Gene symbol UniProt reference OMIM reference
THBD P07204188040
No signs/symptoms info available.