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

SNOMED CT Concept\Clinical finding\...

\Finding of blood, lymphatics and immune system\Disorder of cellular component of blood\...

\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary platelet function disorder\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia

\Platelet disorder\Qualitative platelet disorder\Hereditary platelet function disorder\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia
\Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia

\Functional finding\Disorder of hemostatic system\Platelet disorder\...

\Qualitative platelet disorder\Hereditary platelet function disorder\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia

\Inherited platelet disorder\Hereditary platelet function disorder\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia

\Disease\Genetic disease\Hereditary disease\Hereditary cancer-predisposing syndrome\Familial platelet syndrome with predisposition to acute myelogenous leukemia
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary platelet function disorder\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Familial platelet syndrome with predisposition to acute myelogenous leukemia
\Disease\Disorder of cellular component of blood\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary platelet function disorder\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia
\Disease\Disorder of cellular component of blood\Platelet disorder\Qualitative platelet disorder\Hereditary platelet function disorder\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia
\Disease\Disorder of cellular component of blood\Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia
\Disease\Disorder of hemostatic system\Platelet disorder\Qualitative platelet disorder\Hereditary platelet function disorder\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia
\Disease\Disorder of hemostatic system\Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary platelet function disorder\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia
\Disease\Congenital disease\Platelet storage pool defect\Dense body defect\Familial platelet syndrome with predisposition to acute myelogenous leukemia

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

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 SNOMED CT core module

3437136012 Familial platelet syndrome with predisposition to acute myelogenous leukemia en Synonym Active Entire term case insensitive SNOMED CT core module

3437137015 Familial platelet syndrome with predisposition to acute myelogenous leukaemia en Synonym Active Entire term case insensitive SNOMED CT core module

3437138013 Familial platelet disorder with associated myeloid malignancy en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial platelet syndrome with predisposition to acute myelogenous leukemia	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier
Familial platelet syndrome with predisposition to acute myelogenous leukemia	Is a	Dense body defect	true	Inferred relationship	Existential restriction modifier
Familial platelet syndrome with predisposition to acute myelogenous leukemia	Is a	Hereditary cancer-predisposing syndrome	true	Inferred relationship	Existential restriction modifier
Familial platelet syndrome with predisposition to acute myelogenous leukemia	Finding site	Structure of hematological system	false	Inferred relationship	Existential restriction modifier	1
Familial platelet syndrome with predisposition to acute myelogenous leukemia	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	3
Familial platelet syndrome with predisposition to acute myelogenous leukemia	Has interpretation	Abnormal	false	Inferred relationship	Existential restriction modifier	2
Familial platelet syndrome with predisposition to acute myelogenous leukemia	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier	2
Familial platelet syndrome with predisposition to acute myelogenous leukemia	Finding site	Structure of hematological system	true	Inferred relationship	Existential restriction modifier	1
Familial platelet syndrome with predisposition to acute myelogenous leukemia	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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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	SNOMED CT core module
3437136012	Familial platelet syndrome with predisposition to acute myelogenous leukemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3437137015	Familial platelet syndrome with predisposition to acute myelogenous leukaemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3437138013	Familial platelet disorder with associated myeloid malignancy	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module