In the knowledge base ยท computed from kb/ at build time

Disorders

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.

DisorderRelationshipWhere the gene appears
Cranial Neuralgia susceptibility
scoped to subtype: Trigeminal
Gonorrhea susceptibility
Late Complement Component Deficiency causative
mechanism: Impaired Membrane Attack Complex Assembly; Terminal Complement Component Loss of Function
subtype: C8 Beta Deficiency; C8 Deficiency
scoped to subtype: C8 Beta Deficiency

Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.