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Familial renal amyloidosis due to Apolipoprotein AII variant
1 associated gene
20 connected diseases
No signs/symptoms info
Disease Type of connection
Congenital analbuminemia
Apolipoprotein A-I deficiency
Familial renal amyloidosis due to Apolipoprotein AI variant
Primary systemic amyloidosis
Congenital bilateral absence of vas deferens
Cystic fibrosis
Hereditary chronic pancreatitis
Hereditary combined deficiency of vitamin K-dependent clotting factors
Idiopathic bronchiectasis
Male infertility with normal virilization due to meiosis defect
Behçet disease
Immunodeficiency due to an early component of complement deficiency
Congenital chronic diarrhea with protein-losing enteropathy
Familial LCAT deficiency
Familial apolipoprotein C-II deficiency
Fish-eye disease
Homozygous familial hypercholesterolemia
Hyperlipidemia type 3
Lipoprotein glomerulopathy
Sea-blue histiocytosis
Synonym(s):
- Apolipoprotein AII amyloidosis
- Familial amyloid nephropathy due to apolipoprotein AII variant
- Hereditary amyloid nephropathy due to Apolipoprotein AII variant
- Hereditary renal amyloidosis due to apolipoprotein AII 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
APOA2 P02652107670
No signs/symptoms info available.