Familial Hyperalphalipoproteinemia
ORPHA:181428Biological anomalyAutosomal dominant
Ассоциированные гены3
| Ген | Полное название | Тип связи | Тип гена | OMIM |
|---|---|---|---|---|
| CETP | cholesteryl ester transfer protein | Disease-causing germline mutation(s) (loss of function) in | gene with protein product | 118470 |
| APOC3 | apolipoprotein C3 | Disease-causing germline mutation(s) (loss of function) in | gene with protein product | 107720 |
| SCARB1 | scavenger receptor class B member 1 | Disease-causing germline mutation(s) in | gene with protein product | 601040 |
Лекарства и терапия
Источник: Open Targets Platform (в реальном времени)
Клинические исследования
Источник: ClinicalTrials.gov (в реальном времени)