Halothane hepatitis

Preferred Label : Halothane hepatitis;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : ?Autosomal recessive;

Prefixed ID : 234350;

Détails

Origin ID

234350;

UMLS CUI

C0241913;

Currated CISMeF NLP mapping
- Halothane hepatitis (disorder) [SNOMED CT concept]
- halothane hepatitis [MeSH concept]
- halothane hepatitis [MeSH Supplementary Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Eosinophilia [HPO term]
- Fever [HPO term]
- Hepatitis [HPO term]
- Jaundice [HPO term]
- Multifactorial inheritance [HPO term]
- Obesity [HPO term]
- Viral hepatitis [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Halothane hepatitis (disorder) [SNOMED CT concept]
- halothane hepatitis [MeSH Supplementary Concept]
- halothane hepatitis [MeSH concept]

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

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