Wilms tumor 5 - CISMeF

Preferred Label : Wilms tumor 5;

Symbol : WT5;

CISMeF acronym : WTSL; WT5;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : WTSL; Wilms tumor, susceptibility to;

Inheritance : Autosomal dominant; Somatic mutation;

Molecular basis : Linked to a locus at 7p15-p11.2.;

Neoplasia : Nephroblastoma (Wilms tumor);

Prefixed ID : #601583;

Details

Origin ID

601583;

UMLS CUI

C1832099;

Currated CISMeF NLP mapping
- Wilms tumor and radial bilateral aplasia [MeSH concept]
- wilms tumor and radial bilateral aplasia [MeSH Supplementary Concept]
Genes related to phenotype
- Pou domain, class 6, transcription factor 2 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Nephroblastoma [HPO term]
- Somatic mutation [HPO term]
ORDO concept(s)
- Nephroblastoma [ORDO Disease]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Wilms tumor and radial bilateral aplasia [MeSH concept]
- wilms tumor and radial bilateral aplasia [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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