890202007: Embryopathy caused by acitretin (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Fetal finding\Fetal disorder\...
• \Disorder of fetal structure\Retinoid embryopathy\Embryopathy due to acitretin
• \Fetus with drug damage\Retinoid embryopathy\Embryopathy due to acitretin
• \Disease\Disorder of fetus or newborn\Fetal disorder\Disorder of fetal structure\Retinoid embryopathy\Embryopathy due to acitretin
• \Disease\Disorder of fetus or newborn\Fetal disorder\Fetus with drug damage\Retinoid embryopathy\Embryopathy due to acitretin
• \Disease\Developmental disorder\Disorder of fetal structure\Retinoid embryopathy\Embryopathy due to acitretin

Status: current, Defined. Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4009842013	Foetal acitretin syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
4009844014	Acitretin embryofoetopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
4009845010	Acitretin embryopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
4009846011	Fetal acitretin syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
4009847019	Acitretin embryofetopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
4013006018	Embryopathy caused by acitretin (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
4013007010	Embryopathy caused by acitretin	en	Synonym	Active	Case insensitive	SNOMED CT core
4552911000168114	Embryopathy due to acitretin	en	Synonym	Active	Case insensitive	SNOMED Clinical Terms Australian extension
4009848012	A rare teratogenic disorder due to acitretin exposure during the first trimester of pregnancy, carrying a risk of fetal malformations of approximately 20%, including central nervous system, craniofacial, ear, thymic, cardiac and limb anomalies.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start