Wagro syndrome

Preferred Label : Wagro syndrome;

Symbol : WAGRO;

CISMeF acronym : WAGRO;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Wagr syndrome with obesity; Chromosome 11p13-p12 deletion syndrome; Wilms tumor, aniridia, genitourinary anomalies, mental retardation, and obesity syndrome;

Description : For a detailed discussion of the WAGR syndrome, see 194072. In a subgroup of individuals with the WAGR syndrome, obesity develops. The phenotype in this subset is associated with haploinsufficiency for the;

Prefixed ID : #612469;

Details

Origin ID

612469;

UMLS CUI

C2675904;

Currated CISMeF NLP mapping
- WAGRO Syndrome [NCIt concept]
- wilms tumor, aniridia, genitourinary anomalies, mental retardation, and obesity syndrome [MeSH concept]
- wilms tumor, aniridia, genitourinary anomalies, mental retardation, and obesity syndrome [MeSH Supplementary Concept]
ORDO concept(s)
- WAGR syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- WAGRO Syndrome [NCIt concept]
- wilms tumor, aniridia, genitourinary anomalies, mental retardation, and obesity syndrome [MeSH Supplementary Concept]
- wilms tumor, aniridia, genitourinary anomalies, mental retardation, and obesity syndrome [MeSH concept]

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