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763309005: Acute myeloid leukemia with nucleophosmin 1 somatic mutation (disorder)


Status: current, Defined. 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 Case insensitive SNOMED CT core
3638492011 Acute myeloid leukaemia with NPM1 somatic mutation en Synonym Active Initial character case insensitive SNOMED CT core
3638493018 Acute myeloid leukemia with NPM1 somatic mutation en Synonym Active Initial character case insensitive SNOMED CT core
3638494012 Acute myeloid leukemia with nucleophosmin 1 somatic mutation en Synonym Active Case insensitive SNOMED CT core
3638495013 Acute myeloid leukaemia with nucleophosmin 1 somatic mutation en Synonym Active Case insensitive 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 Case sensitive 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 Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acute myeloid leukaemia with NPM1 somatic mutation Is a Acute myeloid leukaemia due to recurrent genetic abnormality true Inferred relationship Some
Acute myeloid leukaemia with NPM1 somatic mutation Associated morphology Acute myeloid leukaemia with mutated NPM1 true Inferred relationship Some 1
Acute myeloid leukaemia with NPM1 somatic mutation Finding site Bone marrow structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Neoplasm and/or hamartoma reference set

Problem/Diagnosis reference set

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