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Familial renal amyloidosis due to fibrinogen A alpha-chain variant
1 associated gene
19 connected diseases
No signs/symptoms info
Disease Type of connection
Familial afibrinogenemia
Familial dysfibrinogenemia
Familial hypodysfibrinogenemia
Familial hypofibrinogenemia
Autosomal dominant macrothrombocytopenia
Fetal and neonatal alloimmune thrombocytopenia
Glanzmann thrombasthenia
Cerebral sinovenous thrombosis
Congenital factor II deficiency
Congenital factor XIII deficiency
Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
Apolipoprotein A-I deficiency
Congenital analbuminemia
Familial renal amyloidosis due to Apolipoprotein AI variant
Primary systemic amyloidosis
Amyotrophic lateral sclerosis
B-cell chronic lymphocytic leukemia
Fibronectin glomerulopathy
Congenital alpha2 antiplasmin 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 genetic disease
- Rare renal disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
FGA P02671134820
No signs/symptoms info available.