retinoic acid embryopathy

Preferred Label : retinoic acid embryopathy;

Origin ID

D4-01824;

UMLS CUI

C0432364;

Currated CISMeF NLP mapping
- Fetal Retinoid Syndrome [NCIt concept]
- Isotretinoin syndrome [ORDO Disease]
- Retinoic acid embryopathy (disorder) [Inactive SNOMED CT concept]
ICD-10 exact mapping(s)
- Fetus and newborn affected by other maternal medication [ICD-10 Sub-category (who)]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
- toxicology [CISMeF Metaterm]
Référence SNOMED
- tretinoin [SNOMED Notion]
SNOMED CT concept
- Retinoic acid embryopathy (disorder) [Inactive SNOMED CT concept]
See also inter- (CISMeF)
- Fetal isotretinoin syndrome [ICD-11 More detail]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Fetal Retinoid Syndrome [NCIt concept]
- Fetal retinoid syndrome [MedDRA LLT]
- Foetal retinoid syndrome [MedDRA Preferred Term]
- Isotretinoin embryopathy like syndrome [MeSH concept]
- Isotretinoin embryopathy-like syndrome [OMIM Phenotype]
- Isotretinoin embryopathy-like syndrome (disorder) [SNOMED CT concept]
- Isotretinoin-like syndrome [ORDO Disease]
- Retinoic acid embryopathy (disorder) [Inactive SNOMED CT concept]
- isotretinoin embryopathy like syndrome [MeSH Supplementary Concept]