128098009: Scott syndrome (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

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

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

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

\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)\Scott syndrome
\Disease\Disorder of cellular component of blood (disorder)\Hereditary disorder of cellular element of blood (disorder)\Inherited platelet disorder\Hereditary platelet function disorder (disorder)\Scott syndrome
\Disease\Disorder of cellular component of blood (disorder)\Platelet disorder\Qualitative platelet disorder (disorder)\Hereditary platelet function disorder (disorder)\Scott syndrome
\Disease\Disorder of cellular component of blood (disorder)\Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder (disorder)\Scott syndrome
\Disease\Disorder of hemostatic system\Platelet disorder\Qualitative platelet disorder (disorder)\Hereditary platelet function disorder (disorder)\Scott syndrome
\Disease\Disorder of hemostatic system\Platelet disorder\Inherited platelet disorder\Hereditary platelet function disorder (disorder)\Scott syndrome
\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)\Scott syndrome

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

194692010 Scott syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
732057011 Scott syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
833191000052114 Scotts syndrom sv Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets