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 |
|---|---|---|
| Hereditary Spherocytosis | causative |
mechanism: Red Cell Membrane Protein Deficiency
subtype: HS Type 2 (SPTB-related)
scoped to subtype: HS Type 2 (SPTB-related)
|
| Hereditary Elliptocytosis |
untyped
Causative
|
mechanism: Red Cell Cytoskeleton Protein Defects
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.