1237226008: Embryopathy caused by isotretinoin (disorder)

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

Status: current, Defined. Date: 31-Aug 2022. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5091249015	Embryopathy caused by isotretinoin	en	Synonym	Active	Case insensitive	SNOMED CT core
5091250015	Embryopathy caused by isotretinoin (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
5091251016	Isotretinoin syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
5091254012	A rare teratogenic embryofetopathy due to exposure to isotretinoin, an oral synthetic vitamin A derivative, which is used to treat severe recalcitrant cystic acne. Exposure to isotretinoin during the first trimester of pregnancy has been associated with an increased risk of spontaneous abortions and severe birth defects including serious craniofacial (microcephaly, asymmetric crying facies, microphthalmia, developmental abnormalities of the external ear, ocular hypertelorism), cardiovascular (conotruncal heart defects, aortic arch abnormalities), and central nervous system (hydrocephalus, microcephaly, lissencephaly, Dandy-Walker malformation, cognitive deficit) anomalies and thymic aplasia.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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