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838355002: Acute myeloid leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22) CBFB-MYH11 (disorder)


Status: current, Primitive. Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3896560019 Acute myeloid leukaemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22) CBFB-MYH11 en Synonym Active Initial character case insensitive SNOMED CT core
3896561015 Acute myeloid leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22) CBFB-MYH11 (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3896562010 Acute myeloid leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22) CBFB-MYH11 en Synonym Active Initial character case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acute myeloid leukaemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22) CBFB-MYH11 Is a Acute myelomonocytic leukaemia - eosinophilic variant true Inferred relationship Some
Acute myeloid leukaemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22) CBFB-MYH11 Finding site Bone marrow structure true Inferred relationship Some 1
Acute myeloid leukaemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22) CBFB-MYH11 Associated morphology Acute myeloid leukaemia with abnormal marrow eosinophils true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Neoplasm and/or hamartoma reference set

Problem/Diagnosis reference set

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