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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 renal amyloidosis due to fibrinogen A alpha-chain variant
1 associated gene
No signs/symptoms info
Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
Familial renal amyloidosis due to fibrinogen A alpha-chain variant

HRG
(UniProt - OMIM)
 FGA
(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 renal amyloidosis due to fibrinogen A alpha-chain variant
FGA



Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
Familial renal amyloidosis due to fibrinogen A alpha-chain variant

Synonym(s):
- Hereditary thrombophilia due to congenital HRG deficiency
Synonym(s):
- Familial amyloid nephropathy due to fibrinogen A alpha-chain variant
- Fibrinogen A alpha-chain amyloidosis
- Hereditary amyloid nephropathy due to fibrinogen A alpha-chain variant
- Hereditary renal amyloidosis due to fibrinogen A alpha-chain variant
Classification (Orphanet):
- Rare bone disease
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.