FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

397340004: Acute myeloid leukemia with recurrent genetic abnormality (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
1765258017 Acute myeloid leukemia with recurrent genetic abnormality (morphologic abnormality) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1773083010 Acute myeloid leukaemia with recurrent genetic abnormality en Synonym Active Entire term case insensitive SNOMED CT core module
1774369012 Acute myeloid leukemia with recurrent genetic abnormality en Synonym Active Entire term case insensitive SNOMED CT core module
1785800017 AML with recurrent genetic abnormality en Synonym Active Entire term case sensitive SNOMED CT core module

15 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acute myeloid leukemia with recurrent genetic abnormality Is a Acute myeloid leukemia, no International Classification of Diseases for Oncology subtype false Inferred relationship Existential restriction modifier
Acute myeloid leukemia with recurrent genetic abnormality Is a Acute myeloid leukemia - category false Inferred relationship Existential restriction modifier
Acute myeloid leukemia with recurrent genetic abnormality Is a Acute myeloid leukemia true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Acute myeloid leukemia, t(8;21) (q22;q22) Is a True Acute myeloid leukemia with recurrent genetic abnormality Inferred relationship Existential restriction modifier
Acute myeloid leukemia, 11q23 abnormalities Is a True Acute myeloid leukemia with recurrent genetic abnormality Inferred relationship Existential restriction modifier
Acute promyelocytic leukemia, t(15;17)(q22;q11-12) Is a True Acute myeloid leukemia with recurrent genetic abnormality Inferred relationship Existential restriction modifier
Acute myeloid leukemia with abnormal marrow eosinophils and inv(16)(p13q22) or t(16;16)(p13;q22) Is a True Acute myeloid leukemia with recurrent genetic abnormality Inferred relationship Existential restriction modifier
Acute myeloid leukemia due to recurrent genetic abnormality Associated morphology True Acute myeloid leukemia with recurrent genetic abnormality Inferred relationship Existential restriction modifier 1
Acute myeloid leukemia with t(8;16)(p11;p13) translocation Is a True Acute myeloid leukemia with recurrent genetic abnormality Inferred relationship Existential restriction modifier
Acute myeloid leukemia with t(6;9)(p23;q34); DEK-NUP214 Is a True Acute myeloid leukemia with recurrent genetic abnormality Inferred relationship Existential restriction modifier
Acute myeloid leukemia with FMS-like tyrosine kinase-3 mutation Is a True Acute myeloid leukemia with recurrent genetic abnormality Inferred relationship Existential restriction modifier
Acute myeloid leukemia with mutated NPM1 Is a True Acute myeloid leukemia with recurrent genetic abnormality Inferred relationship Existential restriction modifier
Acute myeloid leukemia (megakaryoblastic) with t(1;22)(p13;q13); RBM15-MKL1 Is a True Acute myeloid leukemia with recurrent genetic abnormality Inferred relationship Existential restriction modifier
Acute myeloid leukemia with mutation of CCAAT enhancer binding protein alpha gene Is a True Acute myeloid leukemia with 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 with recurrent genetic abnormality Inferred relationship Existential restriction modifier
Acute myeloid leukemia with BCR-ABL1 Is a True Acute myeloid leukemia with recurrent genetic abnormality Inferred relationship Existential restriction modifier
Acute myeloid leukemia with mutated RUNX1 Is a True Acute myeloid leukemia with recurrent genetic abnormality Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start