CD40 - dismech genes

In the knowledge base · 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.

Disorder	Relationship	Where the gene appears
Graves' Disease	untyped Risk Factor
Kawasaki Disease	untyped Promotes B/T cell and endothelial activation via CD40-CD40L co-stimulation	mechanism: Immune Response Dysregulation
Multiple Sclerosis	untyped Risk Factor	mechanism: Th1/Th17-Mediated Neuroinflammation

ClinGen gene–disease validity · snapshot 2026-10-03 · matched to entries by MONDO

An entry matches when ClinGen's MONDO disease is the entry's own disease term, a subtype term, or an exact-match mapping. An amber status marks an entry ClinGen supports the gene for (Definitive, Strong or Moderate) whose own record does not type it. A Limited, Disputed or Refuted tier on such an entry is not a gap.

ClinGen disease	MOI	Classification	dismech entry
hyper-IgM syndrome type 3 MONDO:0011735	AR	Definitive 2022-10-18	no dismech entry

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