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230786001: Congenital dysphasia (disorder)


Status: current, Defined. Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
345787014 Congenital dysphasia en Synonym Active Case insensitive SNOMED CT core
618640013 Congenital dysphasia (disorder) en Fully specified name Active Case insensitive SNOMED CT core


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital dysphasia Is a Congenital disease true Inferred relationship Some
Congenital dysphasia Is a Encephalopathy true Inferred relationship Some
Congenital dysphasia Is a Congenital anomaly of head false Inferred relationship Some
Congenital dysphasia Finding site Structure of cerebrum false Inferred relationship Some
Congenital dysphasia Occurrence Congenital false Inferred relationship Some
Congenital dysphasia Is a Dysphasia true Inferred relationship Some
Congenital dysphasia Finding site Structure of cerebrum true Inferred relationship Some 1
Congenital dysphasia Occurrence Congenital true Inferred relationship Some 1
Congenital dysphasia Interprets Speech observable true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital expressive dysphasia Is a True Congenital dysphasia Inferred relationship Some
Congenital receptive dysphasia Is a True Congenital dysphasia Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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