familial partial lipodystrophy type 4
GPTKB entity
Statements (18)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
genetic disorder
lipodystrophy |
| gptkbp:affects |
adipose tissue
|
| gptkbp:hasGeneticCause |
PLIN1 gene mutation
|
| https://www.w3.org/2000/01/rdf-schema#label |
familial partial lipodystrophy type 4
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:OMIM |
613877
|
| gptkbp:onset |
childhood
|
| gptkbp:symptom |
gptkb:diabetes_mellitus
insulin resistance hypertriglyceridemia muscular appearance loss of subcutaneous fat |
| gptkbp:treatment |
dietary management
insulin sensitizers lipid-lowering agents |
| gptkbp:bfsParent |
gptkb:PLIN1
|
| gptkbp:bfsLayer |
8
|