Aliases: CPAMD4, C5a, C5b.
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 |
|---|---|---|
| Late Complement Component Deficiency | causative |
mechanism: Impaired Membrane Attack Complex Assembly; Terminal Complement Component Loss of Function
subtype: C5 Deficiency
scoped to subtype: C5 Deficiency
|
| Multisystem Inflammatory Syndrome in Children (MIS-C) | no genetic record |
mechanism: Endothelial Injury and Complement Activation
|
| Neuromyelitis Optica Spectrum Disorder with Anti-AQP4 Antibodies | no genetic record |
mechanism: Classical Complement Activation on Astrocytes
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.