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 |
|---|---|---|
| Heavy Chain Disease | cooperating somatic |
mechanism: Clonal Lymphoplasmacytic B-Cell Expansion
scoped to subtype: Mu-HCD
|
| MyD88 Deficiency | causative germline loss of function |
mechanism: MYD88 Loss of Function
|
| Primary Central Nervous System Lymphoma | causative somatic | |
| Diffuse Large B-Cell Lymphoma |
untyped
ABC Subtype Marker
|
|
| Schnitzler Syndrome | untyped somatic | |
| Systemic Lupus Erythematosus |
untyped
Associated
|
mechanism: TLR7/TLR9-Mediated Nucleic Acid Sensing
|
| Waldenstrom Macroglobulinemia |
untyped
Somatic Mutation
|
mechanism: MYD88 L265P Founder Mutation
subtype: MYD88-mutant Waldenstrom Macroglobulinemia
|
| Primary_Tonsillar_Lymphoma | no genetic record |
mechanism: Malignant B-cell Proliferation (Activated B-cell Type)
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.