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Hyperlipoproteinemia type 5
1 OMIM reference -
4 associated genes
27 connected diseases
No signs/symptoms info
Disease Type of connection
Hyperlipoproteinemia type 1
Familial lipoprotein lipase deficiency
Hyperlipoproteinemia type 4
Early-onset autosomal dominant Alzheimer disease
Donnai-Barrow syndrome
Myxofibrosarcoma
Osteogenesis imperfecta type 3
Dysequilibrium syndrome
Essential thrombocythemia
Myelofibrosis with myeloid metaplasia
Autoimmune lymphoproliferative syndrome
B-cell chronic lymphocytic leukemia
Juvenile rheumatoid factor-negative polyarthritis
Mantle cell lymphoma
Monomelic amyotrophy
Multiple myeloma
Oligoarticular juvenile arthritis
Pseudohypoaldosteronism type 2E
X-linked Emery-Dreifuss muscular dystrophy
Familial apolipoprotein C-II deficiency
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Cholesterol-ester transfer protein deficiency
Synonym(s):
- Major hyperlipidemia
Classification (Orphanet):
- Inborn errors of metabolism
- Rare endocrine disease
- Rare genetic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: D006954
Gene symbol UniProt reference OMIM reference
APOA5 Q6Q788606368
CREB3L3 Q68CJ9611998
GPIHBP1 Q8IV16612757
LPL P06858609708
No signs/symptoms info available.