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721220004: Familial developmental dysphasia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3324652014 Familial developmental dysphasia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3324653016 Familial developmental dysphasia en Synonym Active Entire term case insensitive SNOMED CT core module
3324654010 Billard Toutain Maheut syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial developmental dysphasia Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Familial developmental dysphasia Is a Familial disease true Inferred relationship Existential restriction modifier
Familial developmental dysphasia Is a Developmental dysphasia true Inferred relationship Existential restriction modifier
Familial developmental dysphasia Interprets Speech observable true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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