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Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial hypodysfibrinogenemia
1 OMIM reference -
3 associated genes
No signs/symptoms info
Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
Familial hypodysfibrinogenemia

HRG
(UniProt - OMIM)
 FGA
(UniProt - OMIM)
FGB
(UniProt - OMIM)
FGG
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
HRG
(0.75)
FGA


Citations in the biomedical literature:


Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
HRG
Familial hypodysfibrinogenemia
FGA FGB FGG



Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
Familial hypodysfibrinogenemia

Synonym(s):
- Hereditary thrombophilia due to congenital HRG deficiency
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare bone disease
- Rare genetic disease
- Rare hematologic disease
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 -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.