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 |
|---|---|---|
| Autosomal dominant striatal neurodegeneration | causative germline |
mechanism: PDE8B Cyclic Nucleotide Phosphodiesterase Loss
|
| Primary Pigmented Nodular Adrenocortical Disease | causative germline |
mechanism: Phosphodiesterase Loss and Impaired cAMP Degradation
subtype: PPNAD3
scoped to subtype: PPNAD3
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.