Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 207410018 | FAB M2, t(8;21)(q22;q22) | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 207411019 | FAB M2, AML1(CBF-alpha)/ETO | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 207412014 | Acute myeloid leukemia, AML1(CBF-alpha)/ETO | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 207413016 | Acute myeloid leukemia, t(8;21) (q22;q22) | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 474609018 | Acute myeloid leukaemia, t(8;21) (q22;q22) | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 474610011 | Acute myeloid leukaemia, AML1(CBF-alpha)/ETO | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 732872011 | Acute myeloid leukemia, t(8;21) (q22;q22) (morphologic abnormality) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3009321014 | Acute myeloid leukaemia with t(8;21)(q22;q22); RUNX1-RUNX1T1 | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3009634015 | Acute myeloid leukemia with t(8;21)(q22;q22); RUNX1-RUNX1T1 | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Acute myeloid leukemia, t(8;21) (q22;q22) | Is a | Malignant neoplasm, primary | false | Inferred relationship | Existential restriction modifier | ||
| Acute myeloid leukemia, t(8;21) (q22;q22) | Is a | Acute leukemia - category | false | Inferred relationship | Existential restriction modifier | ||
| Acute myeloid leukemia, t(8;21) (q22;q22) | Is a | Myeloid leukemia - category | false | Inferred relationship | Existential restriction modifier | ||
| Acute myeloid leukemia, t(8;21) (q22;q22) | Is a | Acute myeloid leukemia with recurrent genetic abnormality | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Acute myeloid leukemia with t(8;21)(q22;q22) RUNX1-RUNX1T1 | Associated morphology | True | Acute myeloid leukemia, t(8;21) (q22;q22) | Inferred relationship | Existential restriction modifier | 1 |
This concept is not in any reference sets
FHIR