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FHIR Server FHIR Server 3.7.4-SNAPSHOT
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FHIR
© HL7.org
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Server Home |
FHIR Server FHIR Server 3.7.4-SNAPSHOT
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FHIR Version n/a
User: [n/a]
Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3638491016 | Acute myeloid leukemia with nucleophosmin 1 somatic mutation (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3638492011 | Acute myeloid leukaemia with NPM1 somatic mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3638493018 | Acute myeloid leukemia with NPM1 somatic mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3638494012 | Acute myeloid leukemia with nucleophosmin 1 somatic mutation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3638495013 | Acute myeloid leukaemia with nucleophosmin 1 somatic mutation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5403994011 | A subtype of acute myeloid leukemia with recurrent genetic abnormalities characterized by leukocytosis, thrombocytosis and nonspecific symptoms related to ineffective hematopoiesis (fatigue, bleeding and bruising, recurrent infections, bone pain), with frequent extramedullary involvement typically presenting as gingival hyperplasia and lymphadenopathy. The disease is characterized by clonal proliferation of myeloid blasts harboring mutations of the NPM1 gene in the bone marrow, blood and other tissues. It is associated with multilineage dysplasia, involving the myeloid, monocytic, erythroid, and megakaryocytic cell lineages. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5403995012 | A subtype of acute myeloid leukaemia with recurrent genetic abnormalities characterised by leukocytosis, thrombocytosis and nonspecific symptoms related to ineffective haematopoiesis (fatigue, bleeding and bruising, recurrent infections, bone pain), with frequent extramedullary involvement typically presenting as gingival hyperplasia and lymphadenopathy. The disease is characterised by clonal proliferation of myeloid blasts harbouring mutations of the NPM1 gene in the bone marrow, blood and other tissues. It is associated with multilineage dysplasia, involving the myeloid, monocytic, erythroid, and megakaryocytic cell lineages. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3638491016 | Acute myeloid leukemia with nucleophosmin 1 somatic mutation (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3638492011 | Acute myeloid leukaemia with NPM1 somatic mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3638493018 | Acute myeloid leukemia with NPM1 somatic mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3638494012 | Acute myeloid leukemia with nucleophosmin 1 somatic mutation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3638495013 | Acute myeloid leukaemia with nucleophosmin 1 somatic mutation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3638496014 | A subtype of acute myeloid leukemia with recurrent genetic abnormalities characterized by clonal proliferation of myeloid blasts harboring mutations of the NPM1 gene in the bone marrow, blood and other tissues. It is associated with multilineage dysplasia, involving the myeloid, monocytic, erythroid, and megakaryocytic cell lineages. Patients usually present with leukocytosis, thrombocytosis and nonspecific symptoms related to ineffective hematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain), with frequent extramedullary involvement typically presenting as gingival hyperplasia and lymphadenopathy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3638497017 | A subtype of acute myeloid leukaemia with recurrent genetic abnormalities characterised by clonal proliferation of myeloid blasts harbouring mutations of the NPM1 gene in the bone marrow, blood and other tissues. It is associated with multilineage dysplasia, involving the myeloid, monocytic, erythroid, and megakaryocytic cell lineages. Patients usually present with leukocytosis, thrombocytosis and nonspecific symptoms related to ineffective haematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain), with frequent extramedullary involvement typically presenting as gingival hyperplasia and lymphadenopathy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5403994011 | A subtype of acute myeloid leukemia with recurrent genetic abnormalities characterized by leukocytosis, thrombocytosis and nonspecific symptoms related to ineffective hematopoiesis (fatigue, bleeding and bruising, recurrent infections, bone pain), with frequent extramedullary involvement typically presenting as gingival hyperplasia and lymphadenopathy. The disease is characterized by clonal proliferation of myeloid blasts harboring mutations of the NPM1 gene in the bone marrow, blood and other tissues. It is associated with multilineage dysplasia, involving the myeloid, monocytic, erythroid, and megakaryocytic cell lineages. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5403995012 | A subtype of acute myeloid leukaemia with recurrent genetic abnormalities characterised by leukocytosis, thrombocytosis and nonspecific symptoms related to ineffective haematopoiesis (fatigue, bleeding and bruising, recurrent infections, bone pain), with frequent extramedullary involvement typically presenting as gingival hyperplasia and lymphadenopathy. The disease is characterised by clonal proliferation of myeloid blasts harbouring mutations of the NPM1 gene in the bone marrow, blood and other tissues. It is associated with multilineage dysplasia, involving the myeloid, monocytic, erythroid, and megakaryocytic cell lineages. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3446731001000110 | Akute myeloische Leukämie mit somatischen NPM1-Genmutationen | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| 6046981000241116 | leucémie myéloïde aigüe avec mutations somatiques de NPM1 (nucléophosmine 1) | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| 6046991000241119 | LMA (leucémie myéloïde aigüe) avec mutations somatiques de NPM1 (nucléophosmine 1) | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| 6046981000241116 | leucémie myéloïde aigüe avec mutations somatiques de NPM1 (nucléophosmine 1) | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| 6046991000241119 | LMA (leucémie myéloïde aigüe) avec mutations somatiques de NPM1 (nucléophosmine 1) | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| 3446731001000110 | Akute myeloische Leukämie mit somatischen NPM1-Genmutationen | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Acute myeloid leukemia with nucleophosmin 1 somatic mutation (disorder) | Is a | Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie | false | Inferred relationship | Existential restriction modifier (core metadata concept) | ||
| Acute myeloid leukemia with nucleophosmin 1 somatic mutation (disorder) | Associated morphology | Acute myeloid leukaemia with mutated NPM1 | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
| Acute myeloid leukemia with nucleophosmin 1 somatic mutation (disorder) | Finding site | Bone marrow structure | true | Inferred relationship | Existential restriction modifier (core metadata concept) | 1 | |
| Acute myeloid leukemia with nucleophosmin 1 somatic mutation (disorder) | Is a | Acute myeloid leukemia, disease | true | Inferred relationship | Existential restriction modifier (core metadata concept) |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)