128098009: Scott syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of blood, lymphatics and immune system\Blood disease\...

\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary platelet function disorder\Scott syndrome

\Platelet disorder\Qualitative platelet disorder\Hereditary platelet function disorder\Scott syndrome
\Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder\Scott syndrome

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

\Qualitative platelet disorder\Hereditary platelet function disorder\Scott syndrome

\Inherited platelet disorder\Hereditary platelet function disorder\Scott syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary platelet function disorder\Scott syndrome
\Disease\Blood disease\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary platelet function disorder\Scott syndrome
\Disease\Blood disease\Platelet disorder\Qualitative platelet disorder\Hereditary platelet function disorder\Scott syndrome
\Disease\Blood disease\Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder\Scott syndrome
\Disease\Disorder of haemostatic system\Platelet disorder\Qualitative platelet disorder\Hereditary platelet function disorder\Scott syndrome
\Disease\Disorder of haemostatic system\Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder\Scott syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of cellular element of blood\Inherited platelet disorder\Hereditary platelet function disorder\Scott syndrome

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

194692010 Scott syndrome en Synonym Active Case sensitive SNOMED CT core

732057011 Scott syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Scott syndrome	Has interpretation	Abnormal	false	Inferred relationship	Some	2
Scott syndrome	Interprets	Haemostatic function	true	Inferred relationship	Some	2
Scott syndrome	Has interpretation	Abnormal	true	Inferred relationship	Some	2
Scott syndrome	Is a	Hereditary platelet function disorder	true	Inferred relationship	Some
Scott syndrome	Finding site	Haematopoietic system structure	false	Inferred relationship	Some
Scott syndrome	Has definitional manifestation	Platelet finding	false	Inferred relationship	Some
Scott syndrome	Has definitional manifestation	Haemostatic system finding	false	Inferred relationship	Some
Scott syndrome	Finding site	Body system structure	true	Inferred relationship	Some	1
Scott syndrome	Finding site	Platelet	false	Inferred relationship	Some
Scott syndrome	Finding site	Haematopoietic system structure	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set