725034002: Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Finding of blood, lymphatics and immune system\Disorder of cellular component of blood (disorder)\...
• \Hereditary disorder of cellular element of blood (disorder)\Inherited platelet disorder\Hereditary platelet function disorder (disorder)\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)
• \Platelet disorder\Qualitative platelet disorder (disorder)\Hereditary platelet function disorder (disorder)\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)
• \Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder (disorder)\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)
• \Functional finding\Disorder of hemostatic system\Platelet disorder\...
• \Qualitative platelet disorder (disorder)\Hereditary platelet function disorder (disorder)\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)
• \Inherited platelet disorder\Hereditary platelet function disorder (disorder)\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)
• \Disease\Genetic disease\Hereditary disease\Hereditary cancer-predisposing syndrome\Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Inherited platelet disorder\Hereditary platelet function disorder (disorder)\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)
• \Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)
• \Disease\Disorder of cellular component of blood (disorder)\Hereditary disorder of cellular element of blood (disorder)\Inherited platelet disorder\Hereditary platelet function disorder (disorder)\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)
• \Disease\Disorder of cellular component of blood (disorder)\Platelet disorder\Qualitative platelet disorder (disorder)\Hereditary platelet function disorder (disorder)\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)
• \Disease\Disorder of cellular component of blood (disorder)\Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder (disorder)\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)
• \Disease\Disorder of hemostatic system\Platelet disorder\Qualitative platelet disorder (disorder)\Hereditary platelet function disorder (disorder)\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)
• \Disease\Disorder of hemostatic system\Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder (disorder)\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood (disorder)\Inherited platelet disorder\Hereditary platelet function disorder (disorder)\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3437135011	Familial platelet syndrome with predisposition to acute myelogenous leukemia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3437136012	Familial platelet syndrome with predisposition to acute myelogenous leukemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3437137015	Familial platelet syndrome with predisposition to acute myelogenous leukaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3437138013	Familial platelet disorder with associated myeloid malignancy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5403362011	A rare, genetic, constitutional thrombocytopenia disease characterized by mild to moderate thrombocytopenia, abnormal platelet function and a propensity to develop hematological malignancies, mainly of myeloid origin.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5403363018	A rare, genetic, constitutional thrombocytopenia disease characterised by mild to moderate thrombocytopenia, abnormal platelet function and a propensity to develop haematological malignancies, mainly of myeloid origin.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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