Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3787724019 | Acute myeloid leukemia with biallelic mutation of CEBPA (CCAAT enhancer binding protein alpha) gene | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3787725018 | Acute myeloid leukaemia with biallelic mutation of CEBPA (CCAAT enhancer binding protein alpha) gene | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3787735012 | Acute myeloid leukemia with biallelic mutation of CCAAT enhancer binding protein alpha gene | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3787736013 | Acute myeloid leukaemia with biallelic mutation of CCAAT enhancer binding protein alpha gene | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5143680013 | Acute myeloid leukemia with biallelic CEBPA mutation (morphologic abnormality) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5143681012 | Acute myeloid leukemia with biallelic CEBPA mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5143682017 | Acute myeloid leukaemia with biallelic CEBPA mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Acute myeloid leukemia with biallelic CEBPA mutation (morphologic abnormality) | Is a | Acute myeloid leukemia with CEBPA mutation (morphologic abnormality) | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR