738527001: Myeloid and/or lymphoid neoplasm associated with platelet derived growth factor receptor alpha rearrangement (disorder)

• SNOMED CT Concept\Clinical finding\Disease\Neoplasm and/or hamartoma\Neoplastic disease\...
• \Neoplasm of haematopoietic cell type\Malignant tumour of lymphoid haemopoietic and related tissue\Myeloid and/or lymphoid neoplasm associated with platelet derived growth factor receptor alpha rearrangement
• \Malignant neoplastic disease\Malignant tumour of lymphoid haemopoietic and related tissue\Myeloid and/or lymphoid neoplasm associated with platelet derived growth factor receptor alpha rearrangement

Status: current, Defined. Date: 31-Jan 2018. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3532634012	Myeloid/lymphoid neoplasm associated with PDGFRA rearrangement	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3532635013	Myeloid and/or lymphoid neoplasm associated with platelet derived growth factor receptor alpha rearrangement (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3532636014	Myeloid and/or lymphoid neoplasm associated with platelet derived growth factor receptor alpha rearrangement	en	Synonym	Active	Case insensitive	SNOMED CT core
3532637017	A rare malignant neoplastic disease characterised by clonal proliferation of myeloid and/or lymphoid precursors harbouring rearrangements in the PDGFRA gene, in the blood, bone marrow and often other tissues as well (spleen, lymph nodes, skin). It usually presents as chronic eosinophilic leukaemia or, less commonly, as acute myeloid leukaemia or T-lymphoblastic leukaemia with eosinophilia. Patients usually present with eosinophilia, anaemia, thrombocytopenia, neutrophilia, splenomegaly, lymphadenopathy, fever, sweating and/or weight loss. Tissue infiltration by eosinophils can manifest with skin rash, erythema, cough, neurological alterations, gastrointestinal symptoms or, rarely, endomyocardial fibrosis and restrictive cardiomyopathy.	en	Definition	Active	Case sensitive	SNOMED CT core
3532638010	A rare malignant neoplastic disease characterized by clonal proliferation of myeloid and/or lymphoid precursors harboring rearrangements in the PDGFRA gene, in the blood, bone marrow and often other tissues as well (spleen, lymph nodes, skin). It usually presents as chronic eosinophilic leukemia or, less commonly, as acute myeloid leukemia or T-lymphoblastic leukemia with eosinophilia. Patients usually present with eosinophilia, anemia, thrombocytopenia, neutrophilia, splenomegaly, lymphadenopathy, fever, sweating and/or weight loss. Tissue infiltration by eosinophils can manifest with skin rash, erythema, cough, neurological alterations, gastrointestinal symptoms or, rarely, endomyocardial fibrosis and restrictive cardiomyopathy.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Neoplasm and/or hamartoma reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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