766708008: Isochromosomy Yp (disorder)

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

\Chromosomal disorder\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\Anomaly of sex chromosome\Anomaly of chromosome Y\Isochromosomy Yp

\Congenital disease\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\Anomaly of sex chromosome\Anomaly of chromosome Y\Isochromosomy Yp

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3662335013 Isochromosomy Yp en Synonym Active Only initial character case insensitive SNOMED CT core module
3662336014 Isochromosome Yp en Synonym Active Only initial character case insensitive SNOMED CT core module
3662337017 Isochromosomy Yp (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Isochromosomy Yp	Is a	Anomaly of chromosome Y	true	Inferred relationship	Existential restriction modifier
Isochromosomy Yp	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Isochromosomy Yp	Associated morphology	Abnormal cell structure	true	Inferred relationship	Existential restriction modifier	1
Isochromosomy Yp	Finding site	Sex chromosome Y	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets