Aliases: CPX-I.
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 |
|---|---|---|
| CPLX1-Related Developmental and Epileptic Encephalopathy | causative germline |
mechanism: Complexin-1 Loss of Function
diagnosis: CPLX1 Molecular Diagnosis
discussion: (unnamed)
|
| Essential Tremor | susceptibility | |
| Wolf-Hirschhorn_Syndrome | susceptibility |
mechanism: Candidate Multigene Neuronal-Communication Dysfunction
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.