fetal aminopterin syndrome

Preferred Label : fetal aminopterin syndrome;

Origin ID

D4-01801;

UMLS CUI

C0432367;

Currated CISMeF NLP mapping
- Aminopterin embryofetopathy [ICD-11 More detail]
- Aminopterin/methotrexate embryofetopathy [ORDO Disease]
- Fetal Methotrexate Syndrome [NCIt concept]
- Fetal aminopterin syndrome (disorder) [SNOMED CT concept]
ICD-10 exact mapping(s)
- Other congenital malformation syndromes due to known exogenous causes [ICD-10 Sub-category (who)]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
- toxicology [CISMeF Metaterm]
Référence SNOMED
- aminopterin [SNOMED Notion]
SNOMED CT concept
- Fetal aminopterin syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Aminopterin embryofetopathy [ICD-11 More detail]
- Aminopterin/methotrexate embryofetopathy [ORDO Disease]
- Fetal Methotrexate Syndrome [NCIt concept]
- Fetal aminopterin syndrome (disorder) [SNOMED CT concept]
- Fetal methotrexate syndrome [MedDRA LLT]
- Foetal methotrexate syndrome [MedDRA Preferred Term]