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718615003: 8q21.11 microdeletion syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3312948011 8q21.11 microdeletion syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3312949015 8q21.11 microdeletion syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3312950015 Monosomy 8q21.11 en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
8q21.11 microdeletion syndrome Is a 8q partial monosomy syndrome true Inferred relationship Existential restriction modifier
8q21.11 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
8q21.11 microdeletion syndrome Finding site Chromosome pair 8 true Inferred relationship Existential restriction modifier 2
8q21.11 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
8q21.11 microdeletion syndrome Finding site Chromosome pair 8 true Inferred relationship Existential restriction modifier 3
8q21.11 microdeletion syndrome Associated morphology Deletion of long arm true Inferred relationship Existential restriction modifier 2
8q21.11 microdeletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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