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764940002: Inherited acute myeloid leukemia (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3655684018 Inherited acute myeloid leukemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3655685017 Inherited acute myeloid leukaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3655686016 Inherited acute myeloid leukemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3655687013 Pure familial acute myeloid leukemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3655688015 Pure familial acute myeloid leukaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5404406015 Inherited acute myeloid leukemia (AML) is a rare, malignant hematologic disease characterized by clonal proliferation of myeloid blasts, primarily involving the bone marrow, in association with congenital disorders (e.g. Fanconi anemia, dyskeratosis congenita, Bloom syndrome, Down syndrome, congenital neutropenia, neurofibromatosis, etc.) and genetic defects predisposing to AML. Patients present with signs and symptoms related to ineffective hematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly, etc.). Depending on the underlying genetic defect, there may be additional cancer risks and other health problems present. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404407012 Inherited acute myeloid leukaemia (AML) is a rare, malignant haematologic disease characterised by clonal proliferation of myeloid blasts, primarily involving the bone marrow, in association with congenital disorders (e.g. Fanconi anaemia, dyskeratosis congenita, Bloom syndrome, Down syndrome, congenital neutropenia, neurofibromatosis, etc.) and genetic defects predisposing to AML. Patients present with signs and symptoms related to ineffective haematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly, etc.). Depending on the underlying genetic defect, there may be additional cancer risks and other health problems present. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3655684018 Inherited acute myeloid leukemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3655685017 Inherited acute myeloid leukaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3655686016 Inherited acute myeloid leukemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3655687013 Pure familial acute myeloid leukemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3655688015 Pure familial acute myeloid leukaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3655689011 A rare malignant hematologic disease characterized by clonal proliferation of myeloid blasts, primarily involving the bone marrow, in association with congenital disorders (e.g. Fanconi anemia, dyskeratosis congenita, Bloom syndrome, Down syndrome, congenital neutropenia, neurofibromatosis) and genetic defects predisposing to acute myeloid leukemia. Patients present with signs and symptoms related to ineffective hematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly). Depending on the underlying genetic defect, there may be additional cancer risks and other health problems present. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3655690019 A rare malignant haematologic disease characterised by clonal proliferation of myeloid blasts, primarily involving the bone marrow, in association with congenital disorders (e.g. Fanconi anemia, dyskeratosis congenita, Bloom syndrome, Down syndrome, congenital neutropenia, neurofibromatosis) and genetic defects predisposing to acute myeloid leukaemia. Patients present with signs and symptoms related to ineffective haematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly). Depending on the underlying genetic defect, there may be additional cancer risks and other health problems present. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404406015 Inherited acute myeloid leukemia (AML) is a rare, malignant hematologic disease characterized by clonal proliferation of myeloid blasts, primarily involving the bone marrow, in association with congenital disorders (e.g. Fanconi anemia, dyskeratosis congenita, Bloom syndrome, Down syndrome, congenital neutropenia, neurofibromatosis, etc.) and genetic defects predisposing to AML. Patients present with signs and symptoms related to ineffective hematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly, etc.). Depending on the underlying genetic defect, there may be additional cancer risks and other health problems present. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404407012 Inherited acute myeloid leukaemia (AML) is a rare, malignant haematologic disease characterised by clonal proliferation of myeloid blasts, primarily involving the bone marrow, in association with congenital disorders (e.g. Fanconi anaemia, dyskeratosis congenita, Bloom syndrome, Down syndrome, congenital neutropenia, neurofibromatosis, etc.) and genetic defects predisposing to AML. Patients present with signs and symptoms related to ineffective haematopoesis (fatigue, bleeding and bruising, recurrent infections, bone pain) and/or extramedullary site involvement (gingivitis, splenomegaly, etc.). Depending on the underlying genetic defect, there may be additional cancer risks and other health problems present. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3381291001000111 Akute myeloische Leukämie, vererbte de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
886501000172119 AML (acute myeloid leukemia) familiale fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
910741000172116 leucémie aigüe myéloïde héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
886501000172119 AML (acute myeloid leukemia) familiale fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
910741000172116 leucémie aigüe myéloïde héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3381291001000111 Akute myeloische Leukämie, vererbte 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
Inherited acute myeloid leukemia (disorder) Associated with Congenital disease true Inferred relationship Existential restriction modifier (core metadata concept) 2
Inherited acute myeloid leukemia (disorder) Is a Acute myeloid leukemia, disease true Inferred relationship Existential restriction modifier (core metadata concept)
Inherited acute myeloid leukemia (disorder) Is a Hereditary disorder by system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Inherited acute myeloid leukemia (disorder) Finding site Bone marrow structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inherited acute myeloid leukemia (disorder) Associated morphology Acute myeloid leukemia - category false Inferred relationship Existential restriction modifier (core metadata concept) 1
Inherited acute myeloid leukemia (disorder) Associated morphology Acute myeloid leukaemia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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