Phenytoin toxicity

Preferred Label : Phenytoin toxicity;

CISMeF acronym : FHS;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Arene oxide detoxification defect; Diphenylhydantoin, defect in hydroxylation of;

Included titles and symbols : Fetal hydantoin syndrome; FHS;

Prefixed ID : %617955;

Détails

Origin ID

617955;

UMLS CUI

C0149969;

Automatic exact mappings (from CISMeF team)
- FSH [MedDRA LLT]
- Fetal Hydantoin Syndrome [NCIt concept]
- Fetal hydantoin syndrome [ORDO Disease]
- Fetal hydantoin syndrome [MeSH concept]
- Fetal hydantoin syndrome [ICD-10 Sub-category]
- Fetal hydantoin syndrome [MedDRA LLT]
- Fetal hydantoin syndrome (disorder) [SNOMED CT concept]
- Foetal hydantoin syndrome [MedDRA LLT]
- arene oxide detoxification defect [MeSH concept]
- diphenylhydantoin, defect in hydroxylation of [MeSH concept]
- diphenylhydantoin, defect in hydroxylation of [MeSH Supplementary Concept]
- fetal hydantoin syndrome [MeSH Supplementary Concept]
- fetal hydantoin syndrome [SNOMED Notion]
CISMeF manual mappings
- Phenytoin toxicity [ORDO Disease]
- arene oxide detoxification defect [MeSH Supplementary Concept]
Semantic type(s)
- Injury or Poisoning [UMLS semantic type]
UMLS correspondences (same concept)
- Phenytoin toxicity [ORDO Disease]

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