Fetal Methotrexate Syndrome

Preferred Label : Fetal Methotrexate Syndrome;

Alternative definition : NICHD: A teratogenic disorder observed in a newborn or child of a mother who was exposed to methotrexate during pregnancy. Manifestations of the syndrome include craniofacial, digital, and skeletal malformations.;

NCI Metathesaurus CUI : CL428818;

Détails

Origin ID

C98928;

UMLS CUI

C0432367;

Currated CISMeF NLP mapping
- Fetal aminopterin syndrome (disorder) [SNOMED CT concept]
- Fetal methotrexate syndrome [MedDRA LLT]
- Foetal methotrexate syndrome [MedDRA Preferred Term]
- fetal aminopterin syndrome [SNOMED Notion]
See also inter- (CISMeF)
- Aminopterin embryofetopathy [ICD-11 More detail]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Aminopterin embryofetopathy [ICD-11 More detail]
- Aminopterin/methotrexate embryofetopathy [ORDO Disease]
- Fetal aminopterin syndrome (disorder) [SNOMED CT concept]
- Fetal methotrexate syndrome [MedDRA LLT]
- Foetal methotrexate syndrome [MedDRA Preferred Term]
- fetal aminopterin syndrome [SNOMED Notion]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Neonatal Research Network Terminology [NCIt concept]
- Perinatal Terminology [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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