43248007: Penta X syndrome (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Chromosomal disorder\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of sex chromosome\...
• \Sex chromosome abnormality - female phenotype\Female with more than three X chromosomes\Penta X syndrome
• \Anomaly of chromosome X\Penta X syndrome
• \Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of sex chromosome\...
• \Sex chromosome abnormality - female phenotype\Female with more than three X chromosomes\Penta X syndrome
• \Anomaly of chromosome X\Penta X syndrome

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
72156019	Penta X syndrome	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
72157011	XXXXX syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
72158018	Five X syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
780237011	Penta X syndrome (disorder)	en	Fully specified name	Active	Initial character 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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