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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. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3655314019 Acute myeloid leukaemia with CEBPA somatic mutations en Synonym Active Only initial character case insensitive SNOMED CT core module
3655316017 Acute myeloid leukemia with CEBPA somatic mutations en Synonym Active Only initial character case insensitive SNOMED CT core module
3655317014 Acute myeloid leukemia with CCAAT/enhancer binding protein alpha somatic mutation (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3655318016 Acute myeloid leukemia with CCAAT/enhancer binding protein alpha somatic mutation en Synonym Active Only initial character case insensitive SNOMED CT core module
3655319012 Acute myeloid leukaemia with CCAAT/enhancer binding protein alpha somatic mutation en Synonym Active Only initial character case insensitive SNOMED CT core 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 Is a Acute myeloid leukemia due to recurrent genetic abnormality true Inferred relationship Existential restriction modifier
Acute myeloid leukemia with CCAAT/enhancer binding protein alpha somatic mutation Associated morphology Acute myeloid leukemia with mutation of CCAAT enhancer binding protein alpha gene true Inferred relationship Existential restriction modifier 1
Acute myeloid leukemia with CCAAT/enhancer binding protein alpha somatic mutation Finding site Bone marrow structure true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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