205657006: Whole chromosome trisomy, mosaicism (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Chromosomal disorder\Autosomal chromosomal disorder\Autosomal duplication\Trisomy and partial trisomy of autosome\Whole chromosome trisomy, mosaicism
• \Chromosomal disorder\Duplication of chromosome\Autosomal duplication\Trisomy and partial trisomy of autosome\Whole chromosome trisomy, mosaicism
• \Chromosomal disorder\Congenital chromosomal disease\Trisomy and partial trisomy of autosome\Whole chromosome trisomy, mosaicism
• \Congenital disease\Congenital chromosomal disease\Trisomy and partial trisomy of autosome\Whole chromosome trisomy, mosaicism

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
315399011	Whole chromosome trisomy, mosaicism	en	Synonym	Active	Case insensitive	SNOMED CT core
315400016	Whole chromosome trisomy, mitotic nondisjunction	en	Synonym	Active	Case insensitive	SNOMED CT core
591055019	Whole chromosome trisomy, mosaicism (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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