SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Chromosomal disorder  409709004

Congenital chromosomal disease  74345006

Anomaly of chromosome pair  362984008

Anomaly of chromosome pair 11  60891003

Deletion of part of chromosome 11  726381002

11p partial monosomy syndrome  4135001

WAGR syndrome   715215007

SNOMED CT code


SNOMED code715215007
nameWAGR syndrome
statusactive
date introduced2016-07-31
fully specified name(s)Chromosome 11p13 deletion syndrome (disorder)
synonyms
  • Chromosome 11p13 deletion syndrome
  • Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome
  • WAGR (Wilms tumor, aniridia, genitourinary anomalies and mental retardation) syndrome
  • WAGR syndrome
  • WAGR (Wilms tumour, aniridia, genitourinary anomalies and mental retardation) syndrome
  • Wilms tumour, aniridia, genitourinary anomalies and mental retardation syndrome
attributes - group1
OccurrenceCongenital   255399007
Associated morphologyPartial monosomy   371169004
Finding siteChromosome pair 11   16312006
attributes - group2
Finding siteChromosome pair 11   16312006
Associated morphologyDeletion of short arm   67285006
OccurrenceCongenital   255399007
parents11p partial monosomy syndrome   4135001
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Chromosomal disorder   409709004
        Congenital chromosomal disease   74345006
          Anomaly of chromosome pair   362984008
            Anomaly of chromosome pair 11   60891003
              Deletion of part of chromosome 11   726381002
                11p partial monosomy syndrome   4135001
                  WAGR syndrome   715215007

ancestors
sorted most to least specific
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