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880086001: 12q24.31-q24.32 deletion syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4009247014 12q24.31-q24.32 deletion syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
4009248016 12q24.31-q24.32 deletion syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
12q24.31-q24.32 deletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
12q24.31-q24.32 deletion syndrome Is a Deletion of part of long arm of chromosome 12 true Inferred relationship Existential restriction modifier
12q24.31-q24.32 deletion syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
12q24.31-q24.32 deletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 1
12q24.31-q24.32 deletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
12q24.31-q24.32 deletion syndrome Finding site Chromosome pair 12 true Inferred relationship Existential restriction modifier 1
12q24.31-q24.32 deletion syndrome Associated morphology Deletion of long arm false Inferred relationship Existential restriction modifier 2
12q24.31-q24.32 deletion syndrome Finding site Chromosome pair 12 false Inferred relationship Existential restriction modifier 2
12q24.31-q24.32 deletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
12q24.31-q24.32 deletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
12q24.31-q24.32 deletion syndrome Finding site Long arm of chromosome true Inferred relationship Existential restriction modifier 2
12q24.31-q24.32 deletion syndrome Associated morphology Partial monosomy 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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