Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Mar 2015. Module: SNOMED CT Netherlands NRC maintained module (core metadata concept)
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 28581000146111 | Acute myeloid leukemia with FLT3 mutation (morphologic abnormality) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 28591000146113 | Acute myeloid leukemia with FLT3 mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 4184871000146111 | acute myeloïde leukemie met FLT3-mutatie | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 4184881000146113 | acute myeloïde leukemie met FLT3-mutatie (afwijkende morfologie) | nl | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Acute myeloid leukemia with FLT3 mutation (morphologic abnormality) | Is a | acute myeloïde leukemie - categorie (afwijkende morfologie) | false | Inferred relationship | Some | ||
| Acute myeloid leukemia with FLT3 mutation (morphologic abnormality) | Is a | Acute myeloid leukemia (morphologic abnormality) | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Acute myeloid leukemia with FLT3 mutation (disorder) | Associated morphology | True | Acute myeloid leukemia with FLT3 mutation (morphologic abnormality) | Inferred relationship | Some | 1 |
This concept is not in any reference sets
FHIR