717158001: Partial chromosome Y deletion (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Fetal and/or neonatal disorder\Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of sex chromosome\Anomaly of chromosome Y\A genetic male infertility characterized by azoospermia or oligozoospermia due to chromosome Y microdeletion.

\Chromosomal disorder (disorder)\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of sex chromosome\Anomaly of chromosome Y\A genetic male infertility characterized by azoospermia or oligozoospermia due to chromosome Y microdeletion.

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

5401491016 A genetic male infertility characterized by azoospermia or oligozoospermia due to chromosome Y microdeletion. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

5401492011 A genetic male infertility characterised by azoospermia or oligozoospermia due to chromosome Y microdeletion. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

3308547014 Partial chromosome Y deletion (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

3308548016 Partial chromosome Y deletion en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

880441000172116 stérilité masculine par délétion de l'Y fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

925521000172116 délétion partielle du chromosome Y fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

3420081001000114 Chromosom Y-Deletion, partielle de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
A genetic male infertility characterized by azoospermia or oligozoospermia due to chromosome Y microdeletion.	Is a	Anomaly of chromosome Y	true	Inferred relationship	Some
A genetic male infertility characterized by azoospermia or oligozoospermia due to chromosome Y microdeletion.	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Some	1
A genetic male infertility characterized by azoospermia or oligozoospermia due to chromosome Y microdeletion.	Occurrence	Congenital	true	Inferred relationship	Some	1
A genetic male infertility characterized by azoospermia or oligozoospermia due to chromosome Y microdeletion.	Finding site	Sex chromosome Y	true	Inferred relationship	Some	1
A genetic male infertility characterized by azoospermia or oligozoospermia due to chromosome Y microdeletion.	Associated morphology	Partial monosomy (morphologic abnormality)	true	Inferred relationship	Some	1

Inbound Relationships

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Active

Source

Characteristic

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Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Description inactivation indicator reference set