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Familial apolipoprotein C-II deficiency
1 OMIM reference -
1 associated gene
13 connected diseases
No signs/symptoms info
Disease Type of connection
Congenital analbuminemia
Familial lipoprotein lipase deficiency
Hyperlipoproteinemia type 5
Alpha-crystallinopathy
Familial isolated dilated cardiomyopathy
Fatal infantile hypertonic myofibrillar myopathy
Posterior polar cataract
Zonular cataract
Familial renal amyloidosis due to Apolipoprotein AII variant
Homozygous familial hypercholesterolemia
Hyperlipidemia type 3
Lipoprotein glomerulopathy
Sea-blue histiocytosis
Synonym(s):
- Familial apoC-II deficiency
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
APOC2 P02655608083
No signs/symptoms info available.