Wilms tumor 4 - CISMeF

Preferred Label : Wilms tumor 4;

Symbol : WT4;

CISMeF acronym : FWT1; WT4;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : FWT1; Familial wilms tumor 1;

Description : For a general phenotypic description and discussion of genetic heterogeneity of Wilms tumor, see WT1 (194070).;

Inheritance : Autosomal dominant;

Molecular basis : Linked to locus at 17q12-q21.;

Neoplasia : Nephroblastoma (Wilms tumor);

Prefixed ID : %601363;

Details

Origin ID

601363;

UMLS CUI

C1832426;

Currated CISMeF NLP mapping
- wilms tumor 4 [MeSH concept]
- wilms tumor 4 [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Nephroblastoma [HPO term]
ORDO concept(s)
- Nephroblastoma [ORDO Disease]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- wilms tumor 4 [MeSH Supplementary Concept]
- wilms tumor 4 [MeSH concept]

Keyword's position in hierarchy(ies) :

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