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Hyperlipoproteinemia type 1
3 OMIM references -
2 associated genes
3 connected diseases
No signs/symptoms info
Disease Type of connection
Hyperlipoproteinemia type 5
Familial lipoprotein lipase deficiency
Hyperlipidemia due to hepatic triglyceride lipase deficiency
Synonym(s):
- Familial hyperchylomicronemia
Classification (Orphanet):
- Rare endocrine disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal recessive
External references:
3 OMIM references -
1 MeSH reference: D008072
Gene symbol UniProt reference OMIM reference
GPIHBP1 Q8IV16612757
LMF1 Q96S06611761
No signs/symptoms info available.