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
CD16 Deficiency disputed germline partial loss of function
mechanism: FCGR3A L66H Substitution
Kawasaki Disease untyped
Mediates immune-complex driven neutrophil/monocyte activation
mechanism: Immune Response Dysregulation

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