Wilms tumor 3 - CISMeF

Preferred Label : Wilms tumor 3;

Symbol : WT3;

CISMeF acronym : WT3;

Type : Phenotype or locus, molecular basis unknown;

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

Inheritance : Autosomal dominant;

Molecular basis : Linked to a locus at 16q.;

Neoplasia : Nephroblastoma (Wilms tumor);

Prefixed ID : %194090;

Détails

Origin ID

194090;

UMLS CUI

C1860265;

Currated CISMeF NLP mapping
- wilms tumor 3 [MeSH concept]
- wilms tumor 3 [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Nephroblastoma [HPO term]
ORDO concept(s)
- Nephroblastoma [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- wilms tumor 3 [MeSH Supplementary Concept]
- wilms tumor 3 [MeSH concept]

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

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