205684007: Turner's phenotype, karyotype normal (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\...
• \Disorder of foetus and/or newborn\Congenital disease (disorder)\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of sex chromosome\...
• \Sex chromosome abnormality - female phenotype\Turner syndrome\Turner's phenotype, karyotype normal (disorder)
• \Anomaly of chromosome X\Turner syndrome\Turner's phenotype, karyotype normal (disorder)
• \Chromosomal disorder (disorder)\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of sex chromosome\...
• \Sex chromosome abnormality - female phenotype\Turner syndrome\Turner's phenotype, karyotype normal (disorder)
• \Anomaly of chromosome X\Turner syndrome\Turner's phenotype, karyotype normal (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
315435019	Turner's phenotype, karyotype normal	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
591086013	Turner's phenotype, karyotype normal (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2838267014	Turner phenotype, karyotype normal	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Description inactivation indicator reference set

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