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721305008: Acute myeloid leukemia due to recurrent genetic abnormality (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3324918013 Acute myeloid leukemia due to recurrent genetic abnormality (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3324919017 Acute myeloid leukemia due to recurrent genetic abnormality en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3324920011 Acute myeloid leukaemia due to recurrent genetic abnormality en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


17 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acute myeloid leukemia due to recurrent genetic abnormality (disorder) est un(e) (attribut) Acute myeloid leukaemia, disease true Inferred relationship Some
Acute myeloid leukemia due to recurrent genetic abnormality (disorder) morphologie associée (attribut) Acute myeloid leukemia with recurrent genetic abnormality (morphologic abnormality) true Inferred relationship Some 1
Acute myeloid leukemia due to recurrent genetic abnormality (disorder) localisation d'une constatation (attribut) Bone marrow structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2); RPN1-EVI1 est un(e) (attribut) True Acute myeloid leukemia due to recurrent genetic abnormality (disorder) Inferred relationship Some
Acute myeloid leukemia with t(8;21)(q22;q22) RUNX1-RUNX1T1 (disorder) est un(e) (attribut) True Acute myeloid leukemia due to recurrent genetic abnormality (disorder) Inferred relationship Some
Acute myeloid leukemia with 11q23 abnormality (disorder) est un(e) (attribut) True Acute myeloid leukemia due to recurrent genetic abnormality (disorder) Inferred relationship Some
Acute promyelocytic leukemia, FAB M3 est un(e) (attribut) True Acute myeloid leukemia due to recurrent genetic abnormality (disorder) Inferred relationship Some
Acute myelomonocytic leukaemia - eosinophilic variant est un(e) (attribut) True Acute myeloid leukemia due to recurrent genetic abnormality (disorder) Inferred relationship Some
Acute myeloid leukemia with t(9:11)(p22;q23); MLLT3-MLL (disorder) est un(e) (attribut) False Acute myeloid leukemia due to recurrent genetic abnormality (disorder) Inferred relationship Some
Acute myeloid leukemia with t(8;16)(p11;p13) translocation (disorder) est un(e) (attribut) True Acute myeloid leukemia due to recurrent genetic abnormality (disorder) Inferred relationship Some
Acute myeloid leukemia with t(6;9)(p23;q34) translocation (disorder) est un(e) (attribut) True Acute myeloid leukemia due to recurrent genetic abnormality (disorder) Inferred relationship Some
Acute myeloid leukemia with FMS-like tyrosine kinase-3 mutation (disorder) est un(e) (attribut) True Acute myeloid leukemia due to recurrent genetic abnormality (disorder) Inferred relationship Some
Acute myeloid leukemia with nucleophosmin 1 somatic mutation (disorder) est un(e) (attribut) True Acute myeloid leukemia due to recurrent genetic abnormality (disorder) Inferred relationship Some
Megakaryoblastic acute myeloid leukaemia with t(1;22)(p13;q13) est un(e) (attribut) True Acute myeloid leukemia due to recurrent genetic abnormality (disorder) Inferred relationship Some
Acute myeloid leukaemia with CEBPA somatic mutations est un(e) (attribut) True Acute myeloid leukemia due to recurrent genetic abnormality (disorder) Inferred relationship Some

Reference Sets

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