Previous symbols: RH. Aliases: Rh30a, Rh4, RhPI, RhII, DIIIc, CD240D, SLC42A5.
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 |
|---|---|---|
| Hemolytic Disease of the Fetus and Newborn | susceptibility |
mechanism: Fetomaternal Hemorrhage and Exposure to Paternally Inherited Red Cell Antigens; Maternal Alloimmunization and IgG Alloantibody Production
|
| Rh Deficiency Syndrome | causative |
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.