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1142106007: Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4536636017 Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4536637014 Transient congenital hypothyroidism due to dual oxidase 2 mutation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) Is a Congenital hypothyroidism true Inferred relationship Some
Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) Is a Transient hypothyroidism true Inferred relationship Some
Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) Finding site Thyroid structure true Inferred relationship Some 1
Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) Occurrence Congenital true Inferred relationship Some 1
Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) Due to Chromosomal disorder (disorder) true Inferred relationship Some 2
Transient congenital hypothyroidism due to dual oxidase 2 mutation (disorder) Clinical course Transitory true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Description inactivation indicator reference set

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