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1153345005: Myelodysplastic syndrome with single lineage dysplasia (disorder)

SNOMED CT Concept\Clinical finding\...

\Mass of body structure\Mass of lymphoreticular structure\Neoplasm of bone marrow\Myelodysplastic syndrome\Myelodysplastic syndrome with single lineage dysplasia
\Mass of body structure\Hematologic neoplasm\Neoplasm affecting hematopoietic structure\Myelodysplastic syndrome\Myelodysplastic syndrome with single lineage dysplasia

\Disease\Disorder of hematopoietic cell proliferation\Myeloproliferative disorder\Myelodysplastic syndrome\Myelodysplastic syndrome with single lineage dysplasia
\Disease\Neoplasm and/or hamartoma\Neoplastic disease\Neoplasm of hematopoietic cell type\Malignant tumor of lymphoid, hemopoietic AND/OR related tissue\Myelodysplastic syndrome\Myelodysplastic syndrome with single lineage dysplasia
\Disease\Neoplasm and/or hamartoma\Neoplastic disease\Malignant neoplastic disease\Malignant tumor of lymphoid, hemopoietic AND/OR related tissue\Myelodysplastic syndrome\Myelodysplastic syndrome with single lineage dysplasia
\Disease\Neoplasm and/or hamartoma\Neoplastic disease\Hematologic neoplasm\Neoplasm affecting hematopoietic structure\Myelodysplastic syndrome\Myelodysplastic syndrome with single lineage dysplasia
\Disease\Disorder of body system\Disorder of hematopoietic structure\Neoplasm affecting hematopoietic structure\Myelodysplastic syndrome\Myelodysplastic syndrome with single lineage dysplasia
\Disease\Disorder of body system\Disorder of hematopoietic structure\Bone marrow disorder\Myeloproliferative disorder\Myelodysplastic syndrome\Myelodysplastic syndrome with single lineage dysplasia
\Disease\Disorder of body system\Disorder of hematopoietic structure\Bone marrow disorder\Neoplasm of bone marrow\Myelodysplastic syndrome\Myelodysplastic syndrome with single lineage dysplasia
\Disease\Disorder of body system\Hematologic neoplasm\Neoplasm affecting hematopoietic structure\Myelodysplastic syndrome\Myelodysplastic syndrome with single lineage dysplasia

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

Descriptions:

Id Description Lang Type Status Case? Module

4564081012 Refractory cytopaenia with unilineage dysplasia en Synonym Active Entire term case insensitive SNOMED CT core module

4564083010 Refractory cytopenia with unilineage dysplasia en Synonym Active Entire term case insensitive SNOMED CT core module

4953707011 Myelodysplastic syndrome with single lineage dysplasia en Synonym Active Entire term case insensitive SNOMED CT core module

4953708018 Myelodysplastic syndrome with single lineage dysplasia (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
Myelodysplastic syndrome with single lineage dysplasia	Finding site	Bone marrow structure	true	Inferred relationship	Existential restriction modifier	1
Myelodysplastic syndrome with single lineage dysplasia	Is a	Myelodysplastic syndrome	true	Inferred relationship	Existential restriction modifier
Myelodysplastic syndrome with single lineage dysplasia	Associated morphology	Refractory cytopenia with unilineage dysplasia	false	Inferred relationship	Existential restriction modifier	1
Myelodysplastic syndrome with single lineage dysplasia	Associated morphology	Myelodysplastic syndrome with single lineage dysplasia	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Myelodysplastic syndrome: Refractory anemia, without ringed sideroblasts, without excess blasts	Is a	True	Myelodysplastic syndrome with single lineage dysplasia	Inferred relationship	Existential restriction modifier
Refractory neutropenia	Is a	True	Myelodysplastic syndrome with single lineage dysplasia	Inferred relationship	Existential restriction modifier
Refractory thrombocytopenia	Is a	True	Myelodysplastic syndrome with single lineage dysplasia	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
4564081012	Refractory cytopaenia with unilineage dysplasia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
4564083010	Refractory cytopenia with unilineage dysplasia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
4953707011	Myelodysplastic syndrome with single lineage dysplasia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
4953708018	Myelodysplastic syndrome with single lineage dysplasia (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module