285769009: Acute promyelocytic leukemia - hypogranular variant (disorder)

SNOMED CT Concept\Clinical finding\...

\Mass of body structure\Mass of lymphoreticular structure\Neoplasm of bone marrow\Myeloid leukaemia\Acute myeloid leukemia, disease\Acute myeloid leukaemia due to recurrent genetic abnormality\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukaemia - hypogranular variant
\Mass of body structure\Mass of lymphoreticular structure\Neoplasm of bone marrow\Acute leukaemia\Acute myeloid leukemia, disease\Acute myeloid leukaemia due to recurrent genetic abnormality\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukaemia - hypogranular variant
\Mass of body structure\Haematologic neoplasm\Neoplasm affecting haematopoietic structure\Leukaemia\Myeloid leukaemia\Acute myeloid leukemia, disease\Acute myeloid leukaemia due to recurrent genetic abnormality\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukaemia - hypogranular variant
\Mass of body structure\Haematologic neoplasm\Neoplasm affecting haematopoietic structure\Leukaemia\Acute leukaemia\Acute myeloid leukemia, disease\Acute myeloid leukaemia due to recurrent genetic abnormality\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukaemia - hypogranular variant

\Disease\Disorder of haematopoietic morphology\Myeloproliferative disorder\Myeloid leukaemia\Acute myeloid leukemia, disease\Acute myeloid leukaemia due to recurrent genetic abnormality\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukaemia - hypogranular variant
\Disease\Neoplasm and/or hamartoma\Neoplastic disease\Neoplasm of haematopoietic cell type\Malignant tumour of lymphoid haemopoietic and related tissue\Leukaemia\Myeloid leukaemia\Acute myeloid leukemia, disease\Acute myeloid leukaemia due to recurrent genetic abnormality\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukaemia - hypogranular variant
\Disease\Neoplasm and/or hamartoma\Neoplastic disease\Neoplasm of haematopoietic cell type\Malignant tumour of lymphoid haemopoietic and related tissue\Leukaemia\Acute leukaemia\Acute myeloid leukemia, disease\Acute myeloid leukaemia due to recurrent genetic abnormality\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukaemia - hypogranular variant
\Disease\Neoplasm and/or hamartoma\Neoplastic disease\Malignant neoplastic disease\Malignant tumour of lymphoid haemopoietic and related tissue\Leukaemia\Myeloid leukaemia\Acute myeloid leukemia, disease\Acute myeloid leukaemia due to recurrent genetic abnormality\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukaemia - hypogranular variant
\Disease\Neoplasm and/or hamartoma\Neoplastic disease\Malignant neoplastic disease\Malignant tumour of lymphoid haemopoietic and related tissue\Leukaemia\Acute leukaemia\Acute myeloid leukemia, disease\Acute myeloid leukaemia due to recurrent genetic abnormality\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukaemia - hypogranular variant
\Disease\Neoplasm and/or hamartoma\Neoplastic disease\Haematologic neoplasm\Neoplasm affecting haematopoietic structure\Leukaemia\Myeloid leukaemia\Acute myeloid leukemia, disease\Acute myeloid leukaemia due to recurrent genetic abnormality\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukaemia - hypogranular variant
\Disease\Neoplasm and/or hamartoma\Neoplastic disease\Haematologic neoplasm\Neoplasm affecting haematopoietic structure\Leukaemia\Acute leukaemia\Acute myeloid leukemia, disease\Acute myeloid leukaemia due to recurrent genetic abnormality\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukaemia - hypogranular variant
\Disease\Disorder of body system\Disorder of haematopoietic structure\Neoplasm affecting haematopoietic structure\Leukaemia\Myeloid leukaemia\Acute myeloid leukemia, disease\Acute myeloid leukaemia due to recurrent genetic abnormality\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukaemia - hypogranular variant
\Disease\Disorder of body system\Disorder of haematopoietic structure\Neoplasm affecting haematopoietic structure\Leukaemia\Acute leukaemia\Acute myeloid leukemia, disease\Acute myeloid leukaemia due to recurrent genetic abnormality\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukaemia - hypogranular variant
\Disease\Disorder of body system\Disorder of haematopoietic structure\Bone marrow disorder\Myeloproliferative disorder\Myeloid leukaemia\Acute myeloid leukemia, disease\Acute myeloid leukaemia due to recurrent genetic abnormality\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukaemia - hypogranular variant
\Disease\Disorder of body system\Disorder of haematopoietic structure\Bone marrow disorder\Neoplasm of bone marrow\Myeloid leukaemia\Acute myeloid leukemia, disease\Acute myeloid leukaemia due to recurrent genetic abnormality\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukaemia - hypogranular variant
\Disease\Disorder of body system\Disorder of haematopoietic structure\Bone marrow disorder\Neoplasm of bone marrow\Acute leukaemia\Acute myeloid leukemia, disease\Acute myeloid leukaemia due to recurrent genetic abnormality\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukaemia - hypogranular variant
\Disease\Disorder of body system\Haematologic neoplasm\Neoplasm affecting haematopoietic structure\Leukaemia\Myeloid leukaemia\Acute myeloid leukemia, disease\Acute myeloid leukaemia due to recurrent genetic abnormality\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukaemia - hypogranular variant
\Disease\Disorder of body system\Haematologic neoplasm\Neoplasm affecting haematopoietic structure\Leukaemia\Acute leukaemia\Acute myeloid leukemia, disease\Acute myeloid leukaemia due to recurrent genetic abnormality\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukaemia - hypogranular variant

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

424895019 Acute promyelocytic leukaemia - hypogranular variant en Synonym Active Case insensitive SNOMED CT core

424896018 Acute promyelocytic leukemia - hypogranular variant en Synonym Active Case insensitive SNOMED CT core

424897010 M3V - Acute promyelocytic leukemia - hypogranular variant en Synonym Active Case sensitive SNOMED CT core

424898017 M3V - Acute promyelocytic leukaemia - hypogranular variant en Synonym Active Case sensitive SNOMED CT core

679816011 Acute promyelocytic leukemia - hypogranular variant (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Acute promyelocytic leukaemia - hypogranular variant	Is a	Acute promyelocytic leukaemia, FAB M3	true	Inferred relationship	Some
Acute promyelocytic leukaemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Some	2
Acute promyelocytic leukaemia - hypogranular variant	Finding site	Entire haematological system	false	Inferred relationship	Some	4
Acute promyelocytic leukaemia - hypogranular variant	Finding site	Haematopoietic system structure	false	Inferred relationship	Some	5
Acute promyelocytic leukaemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Some	2
Acute promyelocytic leukaemia - hypogranular variant	Finding site	Entire haematological system	false	Inferred relationship	Some	4
Acute promyelocytic leukaemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Some	2
Acute promyelocytic leukaemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Some	1
Acute promyelocytic leukaemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Some	2
Acute promyelocytic leukaemia - hypogranular variant	Finding site	Haematopoietic system structure	false	Inferred relationship	Some	3
Acute promyelocytic leukaemia - hypogranular variant	Associated morphology	Malignant Neoplasm (Morphology)	false	Inferred relationship	Some	3
Acute promyelocytic leukaemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Some	1
Acute promyelocytic leukaemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Some	2
Acute promyelocytic leukaemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Some	1
Acute promyelocytic leukaemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Some	2
Acute promyelocytic leukaemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Some	1
Acute promyelocytic leukaemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Some	2
Acute promyelocytic leukaemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Some	1
Acute promyelocytic leukaemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Some	2
Acute promyelocytic leukaemia - hypogranular variant	Finding site	Bone marrow structure	true	Inferred relationship	Some	1
Acute promyelocytic leukaemia - hypogranular variant	Associated morphology	Acute promyelocytic leukaemia	true	Inferred relationship	Some	1
Acute promyelocytic leukaemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Some	1
Acute promyelocytic leukaemia - hypogranular variant	Course	Acute	false	Inferred relationship	Some
Acute promyelocytic leukaemia - hypogranular variant	Pathological process	Malignant neoplastic process	false	Inferred relationship	Some	1
Acute promyelocytic leukaemia - hypogranular variant	Associated morphology	Acute myeloid leukaemia, no ICD-O subtype	false	Inferred relationship	Some	1
Acute promyelocytic leukaemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Some	4
Acute promyelocytic leukaemia - hypogranular variant	Finding site	Entire haematological system	false	Inferred relationship	Some	2
Acute promyelocytic leukaemia - hypogranular variant	Associated morphology	Myeloid leukaemia (category)	false	Inferred relationship	Some	4
Acute promyelocytic leukaemia - hypogranular variant	Associated morphology	Malignant Neoplasm (Morphology)	false	Inferred relationship	Some	5
Acute promyelocytic leukaemia - hypogranular variant	Finding site	Lymphoid system structure	false	Inferred relationship	Some	3
Acute promyelocytic leukaemia - hypogranular variant	Associated morphology	Acute leukaemia	false	Inferred relationship	Some	2
Acute promyelocytic leukaemia - hypogranular variant	Associated morphology	Acute promyelocytic leukaemia	false	Inferred relationship	Some	1
Acute promyelocytic leukaemia - hypogranular variant	Associated morphology	Acute promyelocytic leukaemia	false	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

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
424895019	Acute promyelocytic leukaemia - hypogranular variant	en	Synonym	Active	Case insensitive	SNOMED CT core
424896018	Acute promyelocytic leukemia - hypogranular variant	en	Synonym	Active	Case insensitive	SNOMED CT core
424897010	M3V - Acute promyelocytic leukemia - hypogranular variant	en	Synonym	Active	Case sensitive	SNOMED CT core
424898017	M3V - Acute promyelocytic leukaemia - hypogranular variant	en	Synonym	Active	Case sensitive	SNOMED CT core
679816011	Acute promyelocytic leukemia - hypogranular variant (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core