Hepatitis, fulminant viral, susceptibility to

Preferred Label : Hepatitis, fulminant viral, susceptibility to;

Symbol : FVH;

CISMeF acronym : FVH;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal recessive;

Molecular basis : Caused by mutation in the interleukin 18-binding protein gene (IL18BP, 604113.0001);

Laboratory abnormalities : Abnormal liver enzymes;

Prefixed ID : #618549;

Details

Origin ID

618549;

UMLS CUI

C5231406;

Genes related to phenotype
- Interleukin 18-binding protein [OMIM gene]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Coma [HPO term]
- Elevated hepatic transaminase [HPO term]
- Fatigue [HPO term]
- Fulminant hepatitis [HPO term]
- Gingival bleeding [HPO term]
- Hashimoto thyroiditis [HPO term]
- Hepatic failure [HPO term]
- Hepatomegaly [HPO term]
- Jaundice [HPO term]
- Nausea [HPO term]
- Poor appetite [HPO term]
- Type I diabetes mellitus [HPO term]
Semantic type(s)
- Finding [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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