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 |
|---|---|---|
| Cone-rod dystrophy 10 | causative germline loss of function |
mechanism: Biallelic SEMA4A Semaphorin-Domain Missense Variants
|
| Psoriasis | no genetic record |
mechanism: Keratinocyte SEMA4A Downregulation
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.