783251006: Hereditary thrombocytopenia with normal platelets (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Abnormal blood cell count\Platelet count abnormal\Platelet count below reference range\Thrombocytopenia\Hereditary thrombocytopenic disorder\Hereditary thrombocytopenia with normal platelets
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Abnormal blood cell count\Cytopenia\Platelet count below reference range\Thrombocytopenia\Hereditary thrombocytopenic disorder\Hereditary thrombocytopenia with normal platelets
• \Evaluation finding\Measurement finding\Measurement finding outside reference range\Measurement finding below reference range\Cytopenia\Platelet count below reference range\Thrombocytopenia\Hereditary thrombocytopenic disorder\Hereditary thrombocytopenia with normal platelets
• \Evaluation finding\Measurement finding\Platelet count - finding\Platelet count abnormal\Platelet count below reference range\Thrombocytopenia\Hereditary thrombocytopenic disorder\Hereditary thrombocytopenia with normal platelets
• \Evaluation finding\Haematopoietic system finding\Haemostatic system finding\Platelet count - finding\Platelet count abnormal\Platelet count below reference range\Thrombocytopenia\Hereditary thrombocytopenic disorder\Hereditary thrombocytopenia with normal platelets
• \Finding of blood, lymphatics and immune system\Blood disease\...
• \Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary thrombocytopenic disorder\Hereditary thrombocytopenia with normal platelets
• \Platelet disorder\Thrombocytopenia\Hereditary thrombocytopenic disorder\Hereditary thrombocytopenia with normal platelets
• \Platelet disorder\Inherited platelet disorder\Hereditary thrombocytopenic disorder\Hereditary thrombocytopenia with normal platelets
• \Functional finding\Disorder of haemostatic system\Platelet disorder\...
• \Thrombocytopenia\Hereditary thrombocytopenic disorder\Hereditary thrombocytopenia with normal platelets
• \Inherited platelet disorder\Hereditary thrombocytopenic disorder\Hereditary thrombocytopenia with normal platelets
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary thrombocytopenic disorder\Hereditary thrombocytopenia with normal platelets
• \Disease\Blood disease\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary thrombocytopenic disorder\Hereditary thrombocytopenia with normal platelets
• \Disease\Blood disease\Platelet disorder\Thrombocytopenia\Hereditary thrombocytopenic disorder\Hereditary thrombocytopenia with normal platelets
• \Disease\Blood disease\Platelet disorder\Inherited platelet disorder\Hereditary thrombocytopenic disorder\Hereditary thrombocytopenia with normal platelets
• \Disease\Disorder of haemostatic system\Platelet disorder\Thrombocytopenia\Hereditary thrombocytopenic disorder\Hereditary thrombocytopenia with normal platelets
• \Disease\Disorder of haemostatic system\Platelet disorder\Inherited platelet disorder\Hereditary thrombocytopenic disorder\Hereditary thrombocytopenia with normal platelets
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary thrombocytopenic disorder\Hereditary thrombocytopenia with normal platelets

Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3758280016	Hereditary thrombocytopenia with normal platelets	en	Synonym	Active	Case insensitive	SNOMED CT core
3758282012	Hereditary thrombocytopenia with normal platelets (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3758283019	A rare genetic isolated constitutional thrombocytopenia disease with characteristics of decreased platelet counts not associated with platelet morphology or function impairment, in multiple members of a family. Manifestations are variable, typically ranging from asymptomatic to mild bleeding diathesis (e.g. easy bruising, epistaxis, petechiae). Occasionally, a more severe bleeding tendency has been associated and a mild predisposition to infection and eczema has been reported.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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