Fetal isotretinoin syndrome

Preferred Label : Fetal isotretinoin syndrome;

ICD-11 definition : Isotretinoin embryopathy is an association of malformations caused by the teratogenic effect of isotretinoin, a drug marketed for the treatment of cystic acne. The risk of malformations after exposure to oral isotretinoin has been evaluated to be around 20%. The affected infants may present hydrocephalus, microcephaly, ear malformations, conotruncal heart defects and limb abnormalities. There is also increased risk of spontaneous abortion and premature delivery. Isotretinoin may also have effects on child behavior.;

Obsolete resource : false;

Details

Origin ID

409507920;

UMLS CUI

C2930972;

CISMeF manual mappings
- Accutane embryopathy [MeSH concept]
- Isotretinoin syndrome [ORDO Disease]
- accutane embryopathy [MeSH Supplementary Concept]
Manual NTBT mappings (CISMeF)
- Fetal Retinoid Syndrome [NCIt concept]
- Fetal retinoid syndrome [MedDRA LLT]
- Foetal retinoid syndrome [MedDRA Preferred Term]
See also inter- (CISMeF)
- retinoic acid embryopathy [SNOMED Notion]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Accutane embryopathy [MeSH concept]
- Embryopathy caused by isotretinoin (disorder) [SNOMED CT concept]
- Isotretinoin syndrome [ORDO Disease]
- accutane embryopathy [MeSH Supplementary Concept]
Validated automatic mappings to NTBT
- Retinoic acid embryopathy (disorder) [Inactive SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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