Wilms tumor 2 - CISMeF

Preferred Label : Wilms tumor 2;

Symbol : WT2;

CISMeF acronym : WT2;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant; Somatic mutation;

Molecular basis : Caused by mutation in the H19 gene (H19, 103290.0002);

Neoplasia : Nephroblastoma (Wilms tumor);

Prefixed ID : #194071;

Details

Origin ID

194071;

UMLS CUI

C3887743;

Broader ORDO disease(s)
- Nephroblastoma [ORDO Disease]
Currated CISMeF NLP mapping
- Familial Wilms tumor 2 [MeSH concept]
- familial wilms tumor 2 [MeSH Supplementary Concept]
Genes related to phenotype
- H19/igf2-imprinting control region [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Nephroblastoma [HPO term]
- Somatic mutation [HPO term]
NCIt concept(s)
- WT2 Gene [NCIt concept]
- WT2 Protein [NCIt concept]
- WT2 wt Allele [NCIt concept]
ORDO concept(s)
- Nephroblastoma [ORDO Disease]
See also inter- (CISMeF)
- H19 wt Allele [NCIt concept]
- WT2 Gene [NCIt concept]
- WT2 Protein [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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