766708008: Isochromosomy Yp (disorder)

• SNOMED CT Concept\Clinical finding\Disease\...
• \Chromosomal disorder\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of sex chromosome\Anomaly of chromosome Y\Isochromosomy Yp
• \Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of sex chromosome\Anomaly of chromosome Y\Isochromosomy Yp

Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3662335013	Isochromosomy Yp	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3662336014	Isochromosome Yp	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3662337017	Isochromosomy Yp (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3662338010	Isochromosomy Yp is a rare gonosome anomaly characterised by various clinical presentations including normal healthy fertile males, male phenotype with infertility, and males with ambiguous genitalia or incomplete masculinisation.	en	Definition	Active	Case sensitive	SNOMED CT core
3662339019	Isochromosomy Yp is a rare gonosome anomaly characterized by various clinical presentations including normal healthy fertile males, male phenotype with infertility, and males with ambiguous genitalia or incomplete masculinization.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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