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

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

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 SNOMED CT core module
3324919017 Acute myeloid leukemia due to recurrent genetic abnormality en Synonym Active Entire term case insensitive SNOMED CT core module
3324920011 Acute myeloid leukaemia due to recurrent genetic abnormality en Synonym Active Entire term case insensitive SNOMED CT core module

18 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acute myeloid leukemia due to recurrent genetic abnormality Is a Acute myeloid leukemia, disease true Inferred relationship Existential restriction modifier
Acute myeloid leukemia due to recurrent genetic abnormality Associated morphology Acute myeloid leukemia with recurrent genetic abnormality true Inferred relationship Existential restriction modifier 1
Acute myeloid leukemia due to recurrent genetic abnormality Finding site Bone marrow structure true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Acute promyelocytic leukemia, FAB M3 Is a True Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Existential restriction modifier
Acute myelomonocytic leukemia - eosinophilic variant Is a True Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Existential restriction modifier
Acute myeloid leukemia with t(9:11)(p22;q23); MLLT3-MLL Is a False Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Existential restriction modifier
Acute myeloid leukemia with t(8;16)(p11;p13) translocation Is a True Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Existential restriction modifier
Acute myeloid leukemia with t(6;9)(p23;q34) translocation Is a True Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Existential restriction modifier
Acute myeloid leukemia with FMS-like tyrosine kinase-3 mutation Is a True Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Existential restriction modifier
Acute myeloid leukemia with nucleophosmin 1 somatic mutation Is a True Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Existential restriction modifier
Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13) Is a True Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Existential restriction modifier
Acute myeloid leukemia with CCAAT/enhancer binding protein alpha somatic mutation Is a True Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Existential restriction modifier
Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2); RPN1-EVI1 Is a True Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Existential restriction modifier
Acute myeloid leukemia with t(8;21)(q22;q22) RUNX1-RUNX1T1 Is a True Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Existential restriction modifier
Acute myeloid leukemia with 11q23 abnormality Is a True Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Existential restriction modifier
Acute myeloid leukemia with BCR-ABL1 Is a True Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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