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Familial lipoprotein lipase deficiency
1 OMIM reference -
1 associated gene
21 connected diseases
No signs/symptoms info
Disease Type of connection
Hyperlipoproteinemia type 5
Hyperlipoproteinemia type 1
Donnai-Barrow syndrome
Dysequilibrium syndrome
Essential thrombocythemia
Myelofibrosis with myeloid metaplasia
B-cell chronic lymphocytic leukemia
Mantle cell lymphoma
Monomelic amyotrophy
Multiple myeloma
Pseudohypoaldosteronism type 2E
X-linked Emery-Dreifuss muscular dystrophy
Familial apolipoprotein C-II deficiency
Early-onset autosomal dominant Alzheimer disease
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):
- LPL 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
LPL P06858609708
No signs/symptoms info available.