285769009: Acute promyelocytic leukemia - hypogranular variant (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Mass of body structure\Mass of lymphoreticular structure\Neoplasm of bone marrow\Myeloid leukemia\Acute myeloid leukemia, disease\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Mass of body structure\Mass of lymphoreticular structure\Neoplasm of bone marrow\Acute leukemia\Acute myeloid leukemia, disease\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Mass of body structure\Hematologic neoplasm\Neoplasm affecting hematopoietic structure (disorder)\Leukemia, disease (disorder)\Myeloid leukemia\Acute myeloid leukemia, disease\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Mass of body structure\Hematologic neoplasm\Neoplasm affecting hematopoietic structure (disorder)\Leukemia, disease (disorder)\Acute leukemia\Acute myeloid leukemia, disease\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant

\Disease\Disorder of hematopoietic morphology\Myeloproliferative disorder (disorder)\Myeloid leukemia\Acute myeloid leukemia, disease\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of hematopoietic cell type (disorder)\Malignant neoplasm of lymphoid, hematopoietic and/or related tissue (disorder)\Leukemia, disease (disorder)\Myeloid leukemia\Acute myeloid leukemia, disease\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of hematopoietic cell type (disorder)\Malignant neoplasm of lymphoid, hematopoietic and/or related tissue (disorder)\Leukemia, disease (disorder)\Acute leukemia\Acute myeloid leukemia, disease\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant neoplasm of lymphoid, hematopoietic and/or related tissue (disorder)\Leukemia, disease (disorder)\Myeloid leukemia\Acute myeloid leukemia, disease\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Malignant neoplastic disease (disorder)\Malignant neoplasm of lymphoid, hematopoietic and/or related tissue (disorder)\Leukemia, disease (disorder)\Acute leukemia\Acute myeloid leukemia, disease\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Hematologic neoplasm\Neoplasm affecting hematopoietic structure (disorder)\Leukemia, disease (disorder)\Myeloid leukemia\Acute myeloid leukemia, disease\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Hematologic neoplasm\Neoplasm affecting hematopoietic structure (disorder)\Leukemia, disease (disorder)\Acute leukemia\Acute myeloid leukemia, disease\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Disorder of body system\Disorder of hematopoietic structure (disorder)\Neoplasm affecting hematopoietic structure (disorder)\Leukemia, disease (disorder)\Myeloid leukemia\Acute myeloid leukemia, disease\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Disorder of body system\Disorder of hematopoietic structure (disorder)\Neoplasm affecting hematopoietic structure (disorder)\Leukemia, disease (disorder)\Acute leukemia\Acute myeloid leukemia, disease\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Disorder of body system\Disorder of hematopoietic structure (disorder)\Bone marrow disorder\Myeloproliferative disorder (disorder)\Myeloid leukemia\Acute myeloid leukemia, disease\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Disorder of body system\Disorder of hematopoietic structure (disorder)\Bone marrow disorder\Neoplasm of bone marrow\Myeloid leukemia\Acute myeloid leukemia, disease\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Disorder of body system\Disorder of hematopoietic structure (disorder)\Bone marrow disorder\Neoplasm of bone marrow\Acute leukemia\Acute myeloid leukemia, disease\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Disorder of body system\Hematologic neoplasm\Neoplasm affecting hematopoietic structure (disorder)\Leukemia, disease (disorder)\Myeloid leukemia\Acute myeloid leukemia, disease\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Disorder of body system\Hematologic neoplasm\Neoplasm affecting hematopoietic structure (disorder)\Leukemia, disease (disorder)\Acute leukemia\Acute myeloid leukemia, disease\Acute promyelocytic leukaemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Acute promyelocytic leukemia - hypogranular variant	Is a	Acute promyelocytic leukaemia, FAB M3	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Acute promyelocytic leukemia - hypogranular variant	Course	Acute	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Acute promyelocytic leukemia - hypogranular variant	Pathological process	Malignant neoplastic process	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Acute promyelocytic leukemia - hypogranular variant	Associated morphology	Acute myeloid leukemia, no International Classification of Diseases for Oncology subtype	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Acute promyelocytic leukemia - hypogranular variant	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Acute promyelocytic leukemia - hypogranular variant	Associated morphology	Myeloid leukemia - category	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Acute promyelocytic leukemia - hypogranular variant	Associated morphology	néoplasie maligne (morphologie)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Acute promyelocytic leukemia - hypogranular variant	Finding site	Lymphoid system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Acute promyelocytic leukemia - hypogranular variant	Associated morphology	Acute leukemia (morphologic abnormality)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Acute promyelocytic leukemia - hypogranular variant	Associated morphology	Acute promyelocytic leukemia with PML::RARA fusion	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Acute promyelocytic leukemia - hypogranular variant	Associated morphology	Acute promyelocytic leukemia with PML::RARA fusion	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Acute promyelocytic leukemia - hypogranular variant	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Acute promyelocytic leukemia - hypogranular variant	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Acute promyelocytic leukemia - hypogranular variant	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Acute promyelocytic leukemia - hypogranular variant	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Acute promyelocytic leukemia - hypogranular variant	Associated morphology	néoplasie maligne (morphologie)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Acute promyelocytic leukemia - hypogranular variant	Associated morphology	Acute promyelocytic leukemia with PML::RARA fusion	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
424895019	Acute promyelocytic leukaemia - hypogranular variant	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
424896018	Acute promyelocytic leukemia - hypogranular variant	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
424897010	M3V - Acute promyelocytic leukemia - hypogranular variant	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
424898017	M3V - Acute promyelocytic leukaemia - hypogranular variant	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
679816011	Acute promyelocytic leukemia - hypogranular variant (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
424895019	Acute promyelocytic leukaemia - hypogranular variant	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
424895019	Acute promyelocytic leukaemia - hypogranular variant	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
424896018	Acute promyelocytic leukemia - hypogranular variant	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
424896018	Acute promyelocytic leukemia - hypogranular variant	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
424897010	M3V - Acute promyelocytic leukemia - hypogranular variant	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
424897010	M3V - Acute promyelocytic leukemia - hypogranular variant	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
424898017	M3V - Acute promyelocytic leukaemia - hypogranular variant	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
679816011	Acute promyelocytic leukemia - hypogranular variant (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
679816011	Acute promyelocytic leukemia - hypogranular variant (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5993431000241117	variante hypogranulaire d'une leucémie promyélocytaire aigüe	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5993441000241110	leucémie promyélocytaire aigüe de type hypogranulaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5993431000241117	variante hypogranulaire d'une leucémie promyélocytaire aigüe	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5993441000241110	leucémie promyélocytaire aigüe de type hypogranulaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module