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128098009: Scott syndrome (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
194692010 Scott syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
732057011 Scott syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

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