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764855007: Acute myeloid leukemia with CCAAT/enhancer binding protein alpha somatic mutation (disorder)


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
3655314019 Acute myeloid leukaemia with CEBPA somatic mutations en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3655316017 Acute myeloid leukemia with CEBPA somatic mutations en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3655317014 Acute myeloid leukemia with CCAAT/enhancer binding protein alpha somatic mutation (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3655318016 Acute myeloid leukemia with CCAAT/enhancer binding protein alpha somatic mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3655319012 Acute myeloid leukaemia with CCAAT/enhancer binding protein alpha somatic mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5404390015 A subtype of acute myeloid leukemia with recurrent genetic abnormalities, characterized by clonal proliferation of myeloid blasts harboring somatic mutations of the CEBPA gene in the bone marrow, blood and, rarely, other tissues. It can present with anemia, thrombocytopenia, and other nonspecific symptoms related to ineffective hematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404391016 A subtype of acute myeloid leukaemia with recurrent genetic abnormalities, characterised by clonal proliferation of myeloid blasts harbouring somatic mutations of the CEBPA gene in the bone marrow, blood and, rarely, other tissues. It can present with anaemia, thrombocytopenia, and other nonspecific symptoms related to ineffective haematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3655314019 Acute myeloid leukaemia with CEBPA somatic mutations en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3655316017 Acute myeloid leukemia with CEBPA somatic mutations en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3655317014 Acute myeloid leukemia with CCAAT/enhancer binding protein alpha somatic mutation (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3655318016 Acute myeloid leukemia with CCAAT/enhancer binding protein alpha somatic mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3655319012 Acute myeloid leukaemia with CCAAT/enhancer binding protein alpha somatic mutation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3655320018 A subtype of acute myeloid leukaemia with recurrent genetic abnormalities, characterised by clonal proliferation of myeloid blasts harbouring somatic mutations of the CEBPA gene in the bone marrow, blood and rarely other tissues. It can present with anaemia, thrombocytopenia, and other nonspecific symptoms related to ineffective haematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3655321019 A subtype of acute myeloid leukemia with recurrent genetic abnormalities, characterized by clonal proliferation of myeloid blasts harboring somatic mutations of the CEBPA gene in the bone marrow, blood and rarely other tissues. It can present with anemia, thrombocytopenia, and other nonspecific symptoms related to ineffective hematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404390015 A subtype of acute myeloid leukemia with recurrent genetic abnormalities, characterized by clonal proliferation of myeloid blasts harboring somatic mutations of the CEBPA gene in the bone marrow, blood and, rarely, other tissues. It can present with anemia, thrombocytopenia, and other nonspecific symptoms related to ineffective hematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404391016 A subtype of acute myeloid leukaemia with recurrent genetic abnormalities, characterised by clonal proliferation of myeloid blasts harbouring somatic mutations of the CEBPA gene in the bone marrow, blood and, rarely, other tissues. It can present with anaemia, thrombocytopenia, and other nonspecific symptoms related to ineffective haematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3395361001000112 Akute myeloische Leukämie mit somatischen CEBPA-Genmutationen de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5946921000241112 LMA (leucémie myéloïde aigüe) avec mutation somatique de la protéine CEBPA/CCAAT (enhancer-binding protein alpha) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5946931000241114 leucémie myéloïde aigüe avec mutation somatique de la protéine 'enhancer-binding protein alpha' fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5946921000241112 LMA (leucémie myéloïde aigüe) avec mutation somatique de la protéine CEBPA/CCAAT (enhancer-binding protein alpha) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5946931000241114 leucémie myéloïde aigüe avec mutation somatique de la protéine 'enhancer-binding protein alpha' fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3395361001000112 Akute myeloische Leukämie mit somatischen CEBPA-Genmutationen de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acute myeloid leukemia with CCAAT/enhancer binding protein alpha 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 CCAAT/enhancer binding protein alpha somatic mutation (disorder) Associated morphology Acute myeloid leukemia with CEBPA mutation true Inferred relationship Existential restriction modifier (core metadata concept) 1
Acute myeloid leukemia with CCAAT/enhancer binding protein alpha somatic mutation (disorder) Finding site Bone marrow structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Acute myeloid leukemia with CCAAT/enhancer binding protein alpha 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)

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