725287006: Embryopathy caused by retinoid (disorder)

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

Status: current, Defined. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3440735015	Embryopathy caused by retinoid (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3440736019	Retinoid embryopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
3440737011	Embryopathy caused by retinoid	en	Synonym	Active	Case insensitive	SNOMED CT core
3440738018	A teratogenic disorder caused by exposure to retinoid 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

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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