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725390002: Acute myeloid leukemia with t(8;16)(p11;p13) translocation (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
3441957011 Acute myeloid leukemia with t(8;16)(p11;p13) translocation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3441958018 Acute myeloid leukemia with t(8;16)(p11;p13) translocation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3441959014 Acute myeloid leukaemia with t(8;16)(p11;p13) translocation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5403450011 A distinct form of acute myeloid leukemia (AML) in which this chromosomal anomaly is found de novo or in therapy-related AML cases, and is characterized by frequent extramedullary involvement (mainly hepatomegaly, splenomegaly, lymphadenopathies, cutaneous infiltration, but also gum, bone, central nervous system, testicles involvement), severe coagulation disorder (disseminated intravascular coagulopathy or primary fibrinolysis) and poor prognosis. Morphologically, a blast population with a myelomonocytic stage of differentiation is observed. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403451010 A distinct form of acute myeloid leukaemia (AML) in which this chromosomal anomaly is found de novo or in therapy-related AML cases, and is characterised by frequent extramedullary involvement (mainly hepatomegaly, splenomegaly, lymphadenopathies, cutaneous infiltration, but also gum, bone, central nervous system, testicles involvement), severe coagulation disorder (disseminated intravascular coagulopathy or primary fibrinolysis) and poor prognosis. Morphologically, a blast population with a myelomonocytic stage of differentiation is observed. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3441957011 Acute myeloid leukemia with t(8;16)(p11;p13) translocation (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3441957011 Acute myeloid leukemia with t(8;16)(p11;p13) translocation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3441958018 Acute myeloid leukemia with t(8;16)(p11;p13) translocation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3441958018 Acute myeloid leukemia with t(8;16)(p11;p13) translocation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3441959014 Acute myeloid leukaemia with t(8;16)(p11;p13) translocation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3441959014 Acute myeloid leukaemia with t(8;16)(p11;p13) translocation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3441960016 A distinct form of acute myeloid leukemia in which this chromosomal anomaly is found de novo or in therapy-related cases. The disease is characterized by frequent extramedullary involvement (mainly hepatomegaly, splenomegaly, lymphadenopathies, cutaneous infiltration, but also gum, bone, central nervous system, testicles involvement), severe coagulation disorder (disseminated intravascular coagulopathy or primary fibrinolysis) and poor prognosis. Morphologically, a blast population with a myelomonocytic stage of differentiation is observed. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3441961017 A distinct form of acute myeloid leukaemia in which this chromosomal anomaly is found de novo or in therapy-related cases. The disease is characterised by frequent extramedullary involvement (mainly hepatomegaly, splenomegaly, lymphadenopathies, cutaneous infiltration, but also gum, bone, central nervous system, testicles involvement), severe coagulation disorder (disseminated intravascular coagulopathy or primary fibrinolysis) and poor prognosis. Morphologically, a blast population with a myelomonocytic stage of differentiation is observed. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403450011 A distinct form of acute myeloid leukemia (AML) in which this chromosomal anomaly is found de novo or in therapy-related AML cases, and is characterized by frequent extramedullary involvement (mainly hepatomegaly, splenomegaly, lymphadenopathies, cutaneous infiltration, but also gum, bone, central nervous system, testicles involvement), severe coagulation disorder (disseminated intravascular coagulopathy or primary fibrinolysis) and poor prognosis. Morphologically, a blast population with a myelomonocytic stage of differentiation is observed. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403451010 A distinct form of acute myeloid leukaemia (AML) in which this chromosomal anomaly is found de novo or in therapy-related AML cases, and is characterised by frequent extramedullary involvement (mainly hepatomegaly, splenomegaly, lymphadenopathies, cutaneous infiltration, but also gum, bone, central nervous system, testicles involvement), severe coagulation disorder (disseminated intravascular coagulopathy or primary fibrinolysis) and poor prognosis. Morphologically, a blast population with a myelomonocytic stage of differentiation is observed. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3425241001000117 Akute myeloische Leukämie mit Translokation t(8;16)(p11;p13) de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
989541000172117 leucémie myéloblastique aigüe associée à une translocation t(8;16)(p11;p13) fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
989541000172117 leucémie myéloblastique aigüe associée à une translocation t(8;16)(p11;p13) fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3425241001000117 Akute myeloische Leukämie mit Translokation t(8;16)(p11;p13) 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 leukaemia with t(8;16)(p11;p13) translocation Is a Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie false Inferred relationship Existential restriction modifier (core metadata concept)
Acute myeloid leukaemia with t(8;16)(p11;p13) translocation Associated morphology Acute myeloid leukemia with t(8;16)(p11;p13) translocation true Inferred relationship Existential restriction modifier (core metadata concept) 1
Acute myeloid leukaemia with t(8;16)(p11;p13) translocation Finding site Bone marrow structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Acute myeloid leukaemia with t(8;16)(p11;p13) translocation 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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