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

1148906001: Acute myeloid leukemia with t(8;21)(q22;q22) RUNX1-RUNX1T1 (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4552771015 Acute myeloid leukemia with t(8;21)(q22;q22) RUNX1-RUNX1T1 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4552772010 Acute myeloid leukemia with t(8;21)(q22;q22) RUNX1-RUNX1T1 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4552773017 Acute myeloid leukaemia with t(8;21)(q22;q22) RUNX1-RUNX1T1 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acute myeloid leukemia with t(8;21)(q22;q22) RUNX1-RUNX1T1 (disorder) Finding site Bone marrow structure true Inferred relationship Some 1
Acute myeloid leukemia with t(8;21)(q22;q22) RUNX1-RUNX1T1 (disorder) Is a Acute myeloid leukemia due to recurrent genetic abnormality false Inferred relationship Some
Acute myeloid leukemia with t(8;21)(q22;q22) RUNX1-RUNX1T1 (disorder) Associated morphology Acute myeloid leukemia with RUNX1::RUNX1T1 fusion true Inferred relationship Some 1
Acute myeloid leukemia with t(8;21)(q22;q22) RUNX1-RUNX1T1 (disorder) Is a Acute myeloid leukemia, disease true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start