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715215007: Chromosome 11p13 deletion syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3301886014 Chromosome 11p13 deletion syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3301887017 Chromosome 11p13 deletion syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3301888010 Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3301889019 WAGR (Wilms tumor, aniridia, genitourinary anomalies and mental retardation) syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3301890011 WAGR syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3301891010 WAGR (Wilms tumour, aniridia, genitourinary anomalies and mental retardation) syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3301892015 Wilms tumour, aniridia, genitourinary anomalies and mental retardation syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chromosome 11p13 deletion syndrome Associated morphology Monosomy false Inferred relationship Existential restriction modifier 4
Chromosome 11p13 deletion syndrome Is a 11p partial monosomy syndrome true Inferred relationship Existential restriction modifier
Chromosome 11p13 deletion syndrome Associated morphology Nephroblastoma false Inferred relationship Existential restriction modifier 3
Chromosome 11p13 deletion syndrome Finding site Structure of parenchyma of kidney false Inferred relationship Existential restriction modifier 3
Chromosome 11p13 deletion syndrome Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 5
Chromosome 11p13 deletion syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 5
Chromosome 11p13 deletion syndrome Finding site Iris structure false Inferred relationship Existential restriction modifier 5
Chromosome 11p13 deletion syndrome Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 2
Chromosome 11p13 deletion syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Chromosome 11p13 deletion syndrome Finding site Chromosome pair 11 false Inferred relationship Existential restriction modifier 2
Chromosome 11p13 deletion syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
Chromosome 11p13 deletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Chromosome 11p13 deletion syndrome Finding site Iris structure false Inferred relationship Existential restriction modifier 1
Chromosome 11p13 deletion syndrome Associated morphology Absence false Inferred relationship Existential restriction modifier 1
Chromosome 11p13 deletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 1
Chromosome 11p13 deletion syndrome Finding site Chromosome pair 11 true Inferred relationship Existential restriction modifier 1
Chromosome 11p13 deletion syndrome Finding site Chromosome pair 11 true Inferred relationship Existential restriction modifier 2
Chromosome 11p13 deletion syndrome Associated morphology Deletion of short arm true Inferred relationship Existential restriction modifier 2
Chromosome 11p13 deletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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