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722938007: Congenital central hypothyroidism (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3333987011 Congenital central hypothyroidism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3333988018 Congenital central hypothyroidism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency (disorder) Is a True Congenital central hypothyroidism (disorder) Inferred relationship Some

Reference Sets

GB English

US English

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