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703820005: Acute myeloid leukemia with mutated NPM1 (morphologic abnormality)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3008865018 Acute myeloid leukemia with mutated NPM1 (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3009734012 Acute myeloid leukaemia with mutated NPM1 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3009834017 Acute myeloid leukemia with mutated NPM1 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acute myeloid leukemia with mutated NPM1 (morphologic abnormality) Is a Acute myeloid leukemia, no International Classification of Diseases for Oncology subtype false Inferred relationship Some
Acute myeloid leukemia with mutated NPM1 (morphologic abnormality) Is a Acute myeloid leukemia with recurrent genetic abnormality false Inferred relationship Some
Acute myeloid leukemia with mutated NPM1 (morphologic abnormality) Is a Acute myeloid leukemia (morphologic abnormality) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
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. Associated morphology True Acute myeloid leukemia with mutated NPM1 (morphologic abnormality) Inferred relationship Some 1

This concept is not in any reference sets

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