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 |
|---|---|---|
| Androgenetic Alopecia | susceptibility germline |
mechanism: Polygenic Susceptibility
|
| Odonto-Onycho-Dermal Dysplasia | untyped | |
| Taurodontism |
untyped
Susceptibility
|
|
| Tooth Agenesis |
untyped
Pathogenic Variants
|
mechanism: WNT/beta-catenin Signaling Deficiency
subtype: WNT10A-related
scoped to subtype: WNT10A-related
|
An entry matches when ClinGen's MONDO disease is the entry's own disease term, a subtype term, or an exact-match mapping. An amber status marks an entry ClinGen supports the gene for (Definitive, Strong or Moderate) whose own record does not type it. A Limited, Disputed or Refuted tier on such an entry is not a gap.
| ClinGen disease | MOI | Classification | dismech entry |
|---|---|---|---|
| ectodermal dysplasia WNT10A related MONDO:0100358 | SD | Definitive 2022-05-21 |
no dismech entry |
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.