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Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
1 OMIM reference -
1 associated gene
11 connected diseases
No signs/symptoms info
Disease Type of connection
Immunodeficiency due to an early component of complement deficiency
Familial afibrinogenemia
Familial dysfibrinogenemia
Familial hypodysfibrinogenemia
Familial hypofibrinogenemia
Familial renal amyloidosis due to fibrinogen A alpha-chain variant
Fibronectin glomerulopathy
Intermittent hydrarthrosis
TRAPS syndrome
Hypoplasminogenemia
Ligneous conjunctivitis
Synonym(s):
- Hereditary thrombophilia due to congenital HRG deficiency
Classification (Orphanet):
- Rare bone disease
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
HRG P04196142640
No signs/symptoms info available.