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 |
|---|---|---|
| Split Hand-Foot Malformation | causative germline |
mechanism: Apical Ectodermal Ridge Maintenance Failure; Impaired DLX5-DLX6 Limb Regulation After Enhancer Deletion
subtype: SHFM1
scoped to subtype: SHFM1
|
| Auriculocondylar Syndrome | no genetic record |
mechanism: Reduced DLX5 and DLX6 Expression
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.