Cytoscape Web
Click node...

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

HRG
(UniProt - OMIM)
 MEFV
(UniProt - OMIM)
TNFRSF1A
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
HRG
(0.63)
TNFRSF1A


Citations in the biomedical literature:


Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
HRG
Intermittent hydrarthrosis
MEFV TNFRSF1A



Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
Intermittent hydrarthrosis

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 systemic or rheumatologic 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 -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.