familial hypobetalipoproteinemia 2 (Q32146679)
Jump to navigation
Jump to search
hypobetalipoproteinemia that has material basis in homozygous or compound heterozygous mutation in the ANGPTL3 gene on chromosome 1p31
- FHBL2
- combined familial hypolipidemia
- HYPOBETALIPOPROTEINEMIA, FAMILIAL, 2; FHBL2
- familial hypobetalipoproteinemia type 2
- HYPOBETALIPOPROTEINEMIA, FAMILIAL, 2
- Hypobetalipoproteinemia, Familial, type 2
- Hypolipidemia, Familial, Combined
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | familial hypobetalipoproteinemia 2 |
hypobetalipoproteinemia that has material basis in homozygous or compound heterozygous mutation in the ANGPTL3 gene on chromosome 1p31 |
|
Statements
1 reference
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference