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 |
|---|---|---|
| Centronuclear Myopathy | causative |
mechanism: MAP3K20 kinase deficiency
subtype: MAP3K20-CNM
scoped to subtype: MAP3K20-CNM
|
| Split-Foot Malformation with Mesoaxial Polydactyly | causative germline |
mechanism: Biallelic MAP3K20 SAM-Domain Lesions; Constitutive ZAK-alpha Kinase Activation; Loss of Normal ZAK-alpha SAM Domain Structure
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.