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

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

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


Citations in the biomedical literature:


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



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

Synonym(s):
(no synonyms)

Synonym(s):
- Hereditary thrombophilia due to congenital HRG deficiency
Classification (Orphanet):
- Rare genetic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare bone disease
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
(no data available)
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:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.