Previous symbols: IFNABR.
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 |
|---|---|---|
| Down_syndrome |
untyped
Risk Factor
|
|
| IFNAR2 Deficiency |
untyped
Causal
|
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 |
|---|---|---|---|
| immunodeficiency 45 MONDO:0014727 | AR | Definitive 2026-03-19 |
IFNAR2 Deficiency
untyped
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.