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Hyperlipoproteinemia type 4
2 OMIM references -
2 associated genes
5 connected diseases
No signs/symptoms info
Disease Type of connection
Hyperlipoproteinemia type 5
Early-onset autosomal dominant Alzheimer disease
Autoimmune lymphoproliferative syndrome
Juvenile rheumatoid factor-negative polyarthritis
Oligoarticular juvenile arthritis
Synonym(s):
- Familial hypertriglyceridemia
Classification (Orphanet):
- Inborn errors of metabolism
- Rare endocrine disease
- Rare genetic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: -
Average age onset: adulthood
Average age of death: no data available
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
1 MeSH reference: D006953
Gene symbol UniProt reference OMIM reference
APOA5 Q6Q788606368
LIPI Q6XZB0609252
No signs/symptoms info available.