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773346008: 20p13 microdeletion syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3723250014 20p13 microdeletion syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
3723251013 20p subtelomeric deletion syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
3723252018 Monosomy 20p13 en Synonym Active Only initial character case insensitive SNOMED CT core module
3723253011 20p13 microdeletion syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
20p13 microdeletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 2
20p13 microdeletion syndrome Associated morphology Deletion of short arm false Inferred relationship Existential restriction modifier 1
20p13 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
20p13 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
20p13 microdeletion syndrome Is a Deletion of part of short arm of chromosome 20 true Inferred relationship Existential restriction modifier
20p13 microdeletion syndrome Finding site Chromosome pair 20 true Inferred relationship Existential restriction modifier 1
20p13 microdeletion syndrome Finding site Chromosome pair 20 false Inferred relationship Existential restriction modifier 2
20p13 microdeletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
20p13 microdeletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
20p13 microdeletion syndrome Finding site Short arm of chromosome true Inferred relationship Existential restriction modifier 2
20p13 microdeletion syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
20p13 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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