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733520002: 20q13.33 microdeletion syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3499598013 20q13.33 microdeletion syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3499599017 Monosomy 20q13.33 en Synonym Active Only initial character case insensitive SNOMED CT core module
3499600019 20q13.33 microdeletion syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
20q13.33 microdeletion syndrome Is a Deletion of part of long arm of chromosome 20 true Inferred relationship Existential restriction modifier
20q13.33 microdeletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 2
20q13.33 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
20q13.33 microdeletion syndrome Finding site Chromosome pair 20 false Inferred relationship Existential restriction modifier 2
20q13.33 microdeletion syndrome Associated morphology Deletion of long arm false Inferred relationship Existential restriction modifier 3
20q13.33 microdeletion syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
20q13.33 microdeletion syndrome Finding site Chromosome pair 20 false Inferred relationship Existential restriction modifier 3
20q13.33 microdeletion syndrome Finding site Chromosome pair 20 true Inferred relationship Existential restriction modifier 1
20q13.33 microdeletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
20q13.33 microdeletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
20q13.33 microdeletion syndrome Finding site Long arm of chromosome true Inferred relationship Existential restriction modifier 2
20q13.33 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
20q13.33 microdeletion syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
20q13.33 microdeletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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