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717334008: Idiopathic congenital hypothyroidism (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3309081018 Idiopathic congenital hypothyroidism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3309082013 Idiopathic congenital hypothyroidism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401564016 Idiopathic congenital hypothyroidism is a type of primary congenital hypothyroidism whose cause and prevalence are unknown. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Idiopathic congenital hypothyroidism (disorder) Is a Idiopathic disease true Inferred relationship Some
Idiopathic congenital hypothyroidism (disorder) Is a Congenital hypothyroidism true Inferred relationship Some
Idiopathic congenital hypothyroidism (disorder) Occurrence Congenital true Inferred relationship Some 1
Idiopathic congenital hypothyroidism (disorder) Finding site Thyroid structure false Inferred relationship Some 2
Idiopathic congenital hypothyroidism (disorder) Is a Primary hypothyroidism true Inferred relationship Some
Idiopathic congenital hypothyroidism (disorder) Finding site Thyroid structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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