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78740005: Complete monosomy 21 (disorder)

Status: current, Defined. Date: 31-Jan 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

4555287013 Complete monosomy 21 (disorder) en Fully specified name Active Case insensitive SNOMED CT core

4555288015 Complete monosomy 21 en Synonym Active Case insensitive SNOMED CT core

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Complete monosomy 21	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	1
Complete monosomy 21	Is a	Monosomy and deletion from autosome	false	Inferred relationship	Some
Complete monosomy 21	Is a	Anomaly of chromosome pair 21	true	Inferred relationship	Some
Complete monosomy 21	Associated morphology	Congenital anomaly	false	Inferred relationship	Some
Complete monosomy 21	Finding site	Chromosome pair 21	false	Inferred relationship	Some	1
Complete monosomy 21	Occurrence	Congenital	true	Inferred relationship	Some	1
Complete monosomy 21	Finding site	Chromosome pair 21	true	Inferred relationship	Some	1
Complete monosomy 21	Associated morphology	Monosomy	true	Inferred relationship	Some	1
Complete monosomy 21	Is a	Complete monosomy of autosome	true	Inferred relationship	Some
Complete monosomy 21	Finding site	Chromosome pair 21	false	Inferred relationship	Some	1
Complete monosomy 21	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Some
Complete monosomy 21	Associated morphology	Monosomy	false	Inferred relationship	Some
Complete monosomy 21	Occurrence	Congenital	false	Inferred relationship	Some
Complete monosomy 21	Finding site	Sex chromosome	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set