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Familial thrombomodulin anomalies
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Cerebral sinovenous thrombosis
3 associated genes
No signs/symptoms info
Familial thrombomodulin anomalies
Cerebral sinovenous thrombosis

THBD
(UniProt - OMIM)
 F2
(UniProt - OMIM)
F5
(UniProt - OMIM)
PROZ
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
THBD
(0.9)
F2


Citations in the biomedical literature:


Familial thrombomodulin anomalies
THBD
Cerebral sinovenous thrombosis
F2 F5 PROZ



Familial thrombomodulin anomalies
Cerebral sinovenous thrombosis

Synonym(s):
(no synonyms)

Synonym(s):
- CSVT
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare neurologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: C536900
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.