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

\Disease\Disorder of hematopoietic cell proliferation\Myeloproliferative disorder\Myeloid leukemia\Acute myeloid leukemia, disease\Acute myeloid leukemia due to recurrent genetic abnormality\Acute promyelocytic leukemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Neoplasm and/or hamartoma\Neoplastic disease\Neoplasm of hematopoietic cell type\Malignant tumor of lymphoid, hemopoietic AND/OR related tissue\Leukemia, disease\Myeloid leukemia\Acute myeloid leukemia, disease\Acute myeloid leukemia due to recurrent genetic abnormality\Acute promyelocytic leukemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Neoplasm and/or hamartoma\Neoplastic disease\Neoplasm of hematopoietic cell type\Malignant tumor of lymphoid, hemopoietic AND/OR related tissue\Leukemia, disease\Acute leukemia, disease\Acute myeloid leukemia, disease\Acute myeloid leukemia due to recurrent genetic abnormality\Acute promyelocytic leukemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Neoplasm and/or hamartoma\Neoplastic disease\Malignant neoplastic disease\Malignant tumor of lymphoid, hemopoietic AND/OR related tissue\Leukemia, disease\Myeloid leukemia\Acute myeloid leukemia, disease\Acute myeloid leukemia due to recurrent genetic abnormality\Acute promyelocytic leukemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Neoplasm and/or hamartoma\Neoplastic disease\Malignant neoplastic disease\Malignant tumor of lymphoid, hemopoietic AND/OR related tissue\Leukemia, disease\Acute leukemia, disease\Acute myeloid leukemia, disease\Acute myeloid leukemia due to recurrent genetic abnormality\Acute promyelocytic leukemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Neoplasm and/or hamartoma\Neoplastic disease\Hematologic neoplasm\Neoplasm affecting hematopoietic structure\Leukemia, disease\Myeloid leukemia\Acute myeloid leukemia, disease\Acute myeloid leukemia due to recurrent genetic abnormality\Acute promyelocytic leukemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Neoplasm and/or hamartoma\Neoplastic disease\Hematologic neoplasm\Neoplasm affecting hematopoietic structure\Leukemia, disease\Acute leukemia, disease\Acute myeloid leukemia, disease\Acute myeloid leukemia due to recurrent genetic abnormality\Acute promyelocytic leukemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Disorder of body system\Disorder of hematopoietic structure\Neoplasm affecting hematopoietic structure\Leukemia, disease\Myeloid leukemia\Acute myeloid leukemia, disease\Acute myeloid leukemia due to recurrent genetic abnormality\Acute promyelocytic leukemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Disorder of body system\Disorder of hematopoietic structure\Neoplasm affecting hematopoietic structure\Leukemia, disease\Acute leukemia, disease\Acute myeloid leukemia, disease\Acute myeloid leukemia due to recurrent genetic abnormality\Acute promyelocytic leukemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Disorder of body system\Disorder of hematopoietic structure\Bone marrow disorder\Myeloproliferative disorder\Myeloid leukemia\Acute myeloid leukemia, disease\Acute myeloid leukemia due to recurrent genetic abnormality\Acute promyelocytic leukemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Disorder of body system\Disorder of hematopoietic structure\Bone marrow disorder\Neoplasm of bone marrow\Myeloid leukemia\Acute myeloid leukemia, disease\Acute myeloid leukemia due to recurrent genetic abnormality\Acute promyelocytic leukemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Disorder of body system\Disorder of hematopoietic structure\Bone marrow disorder\Neoplasm of bone marrow\Acute leukemia, disease\Acute myeloid leukemia, disease\Acute myeloid leukemia due to recurrent genetic abnormality\Acute promyelocytic leukemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Disorder of body system\Hematologic neoplasm\Neoplasm affecting hematopoietic structure\Leukemia, disease\Myeloid leukemia\Acute myeloid leukemia, disease\Acute myeloid leukemia due to recurrent genetic abnormality\Acute promyelocytic leukemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant
\Disease\Disorder of body system\Hematologic neoplasm\Neoplasm affecting hematopoietic structure\Leukemia, disease\Acute leukemia, disease\Acute myeloid leukemia, disease\Acute myeloid leukemia due to recurrent genetic abnormality\Acute promyelocytic leukemia, FAB M3\Acute promyelocytic leukemia - hypogranular variant

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

Descriptions:

Id Description Lang Type Status Case? Module

424895019 Acute promyelocytic leukaemia - hypogranular variant en Synonym Active Entire term case insensitive SNOMED CT core module
424896018 Acute promyelocytic leukemia - hypogranular variant en Synonym Active Entire term case insensitive SNOMED CT core module
424897010 M3V - Acute promyelocytic leukemia - hypogranular variant en Synonym Active Entire term case sensitive SNOMED CT core module
424898017 M3V - Acute promyelocytic leukaemia - hypogranular variant en Synonym Active Entire term case sensitive SNOMED CT core module
679816011 Acute promyelocytic leukemia - hypogranular variant (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Acute promyelocytic leukemia - hypogranular variant	Is a	Acute promyelocytic leukemia, FAB M3	true	Inferred relationship	Existential restriction modifier
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier	1
Acute promyelocytic leukemia - hypogranular variant	Course	Acute	false	Inferred relationship	Existential restriction modifier
Acute promyelocytic leukemia - hypogranular variant	Pathological process	Malignant neoplastic process	false	Inferred relationship	Existential restriction modifier	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	1
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier	4
Acute promyelocytic leukemia - hypogranular variant	Finding site	Entire hematological system	false	Inferred relationship	Existential restriction modifier	2
Acute promyelocytic leukemia - hypogranular variant	Associated morphology	Myeloid leukemia - category	false	Inferred relationship	Existential restriction modifier	4
Acute promyelocytic leukemia - hypogranular variant	Associated morphology	Malignant neoplasm of primary, secondary, or uncertain origin	false	Inferred relationship	Existential restriction modifier	5
Acute promyelocytic leukemia - hypogranular variant	Finding site	Lymphoid system structure	false	Inferred relationship	Existential restriction modifier	3
Acute promyelocytic leukemia - hypogranular variant	Associated morphology	Acute leukemia	false	Inferred relationship	Existential restriction modifier	2
Acute promyelocytic leukemia - hypogranular variant	Associated morphology	Acute promyelocytic leukemia, t(15;17)(q22;q11-12)	false	Inferred relationship	Existential restriction modifier	1
Acute promyelocytic leukemia - hypogranular variant	Associated morphology	Acute promyelocytic leukemia, t(15;17)(q22;q11-12)	false	Inferred relationship	Existential restriction modifier	1
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier	2
Acute promyelocytic leukemia - hypogranular variant	Finding site	Entire hematological system	false	Inferred relationship	Existential restriction modifier	4
Acute promyelocytic leukemia - hypogranular variant	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier	5
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier	2
Acute promyelocytic leukemia - hypogranular variant	Finding site	Entire hematological system	false	Inferred relationship	Existential restriction modifier	4
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier	2
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier	1
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier	2
Acute promyelocytic leukemia - hypogranular variant	Finding site	Hematopoietic system structure	false	Inferred relationship	Existential restriction modifier	3
Acute promyelocytic leukemia - hypogranular variant	Associated morphology	Malignant neoplasm of primary, secondary, or uncertain origin	false	Inferred relationship	Existential restriction modifier	3
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier	1
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier	2
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier	1
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier	2
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier	1
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier	2
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier	1
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	false	Inferred relationship	Existential restriction modifier	2
Acute promyelocytic leukemia - hypogranular variant	Finding site	Bone marrow structure	true	Inferred relationship	Existential restriction modifier	1
Acute promyelocytic leukemia - hypogranular variant	Associated morphology	Acute promyelocytic leukemia, t(15;17)(q22;q11-12)	true	Inferred relationship	Existential restriction modifier	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	Active	Entire term case insensitive	SNOMED CT core module
424896018	Acute promyelocytic leukemia - hypogranular variant	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
424897010	M3V - Acute promyelocytic leukemia - hypogranular variant	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
424898017	M3V - Acute promyelocytic leukaemia - hypogranular variant	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
679816011	Acute promyelocytic leukemia - hypogranular variant (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module