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230786001: Congenital dysphasia (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module

Descriptions:

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

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital dysphasia Is a Disorder of brain true Inferred relationship Existential restriction modifier
Congenital dysphasia Is a Congenital anomaly of head false Inferred relationship Existential restriction modifier
Congenital dysphasia Finding site Structure of cerebrum false Inferred relationship Existential restriction modifier
Congenital dysphasia Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenital dysphasia Is a Congenital disease true Inferred relationship Existential restriction modifier
Congenital dysphasia Is a Dysphasia true Inferred relationship Existential restriction modifier
Congenital dysphasia Finding site Structure of cerebrum true Inferred relationship Existential restriction modifier 1
Congenital dysphasia Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital dysphasia Interprets Speech observable true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital expressive dysphasia Is a True Congenital dysphasia Inferred relationship Existential restriction modifier
Congenital receptive dysphasia Is a True Congenital dysphasia Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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