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778000002: 3q26q27 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
3736353011 Monosomy 3q26q27 en Synonym Active Only initial character case insensitive SNOMED CT core module
3736354017 3q26q27 microdeletion syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
3736355016 3q26q27 microdeletion syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3736356015 Monosomy 3q26-q27 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
3q26q27 microdeletion syndrome Associated morphology Deletion of long arm false Inferred relationship Existential restriction modifier 1
3q26q27 microdeletion syndrome Is a Deletion of part of long arm of chromosome 3 true Inferred relationship Existential restriction modifier
3q26q27 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
3q26q27 microdeletion syndrome Finding site Chromosome pair 3 false Inferred relationship Existential restriction modifier 2
3q26q27 microdeletion syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
3q26q27 microdeletion syndrome Finding site Chromosome pair 3 true Inferred relationship Existential restriction modifier 1
3q26q27 microdeletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 2
3q26q27 microdeletion syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
3q26q27 microdeletion syndrome Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 1
3q26q27 microdeletion syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
3q26q27 microdeletion syndrome Finding site Long arm of chromosome true Inferred relationship Existential restriction modifier 2
3q26q27 microdeletion syndrome Pathological process Pathological developmental process 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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