Aliases: FLJ43808.
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 |
|---|---|---|
| Primary_Ciliary_Dyskinesia |
untyped
Limited evidence for PCD association
|
|
| Spermatogenic Failure 56 |
untyped
Causal
CLINGEN: moderate
|
mechanism: Loss of the DNAH10 Inner-Arm Dynein Heavy Chain
|
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 |
|---|---|---|---|
| primary ciliary dyskinesia MONDO:0016575 | AR | Limited 2026-05-07 |
Primary_Ciliary_Dyskinesia
untyped
|
| spermatogenic failure 56 MONDO:0030430 | AR | Moderate 2026-05-07 |
Spermatogenic Failure 56
untyped
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.