Aliases: RAP3, APOA-V.
Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.
| Disorder | Relationship | Where the gene appears |
|---|---|---|
| Familial Chylomicronemia Syndrome | causative |
mechanism: Defective LPL Maturation, Trafficking, and Activation
|
| Hyperlipidemia | causative |
mechanism: Impaired Lipoprotein Lipase Activity and ApoC-III Dysregulation
subtype: Hyperlipoproteinemia Type V
scoped to subtype: Hyperlipoproteinemia Type V
|
| MEND Syndrome | modifier |
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.