2893009: Anomaly of chromosome pair 10 (disorder)

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

\Disorder of foetus and/or newborn\Congenital disease\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 10 (disorder)

\Chromosomal disorder (disorder)\Congenital chromosomal disease\Anomaly of chromosome pair\Anomaly of chromosome pair 10 (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

5897015 Anomaly of chromosome pair 10 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

759666019 Anomaly of chromosome pair 10 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

5897015 Anomaly of chromosome pair 10 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

5897015 Anomaly of chromosome pair 10 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

759666019 Anomaly of chromosome pair 10 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

759666019 Anomaly of chromosome pair 10 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

965891000172114 anomalie du chromosome 10 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

965891000172114 anomalie du chromosome 10 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Anomaly of chromosome pair 10 (disorder)	Is a	Anomaly of sex chromosome	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Anomaly of chromosome pair 10 (disorder)	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Anomaly of chromosome pair 10 (disorder)	Finding site	Sex chromosome	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Anomaly of chromosome pair 10 (disorder)	Finding site	Chromosome pair 10	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Anomaly of chromosome pair 10 (disorder)	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Anomaly of chromosome pair 10 (disorder)	Is a	Anomaly of chromosome pair	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Anomaly of chromosome pair 10 (disorder)	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Anomaly of chromosome pair 10 (disorder)	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Anomaly of chromosome pair 10 (disorder)	Finding site	Chromosome pair 10	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Anomaly of chromosome pair 10 (disorder)	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Anomaly of chromosome pair 10 (disorder)	Finding site	Chromosome pair 10	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Anomaly of chromosome pair 10 (disorder)	Associated morphology	Cellular AND/OR subcellular abnormality	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
10q partial monosomy (disorder)	Is a	False	Anomaly of chromosome pair 10 (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
10p partial trisomy syndrome	Is a	False	Anomaly of chromosome pair 10 (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
10p partial monosomy syndrome (disorder)	Is a	False	Anomaly of chromosome pair 10 (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
10q partial trisomy syndrome	Is a	False	Anomaly of chromosome pair 10 (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Complete trisomy 10 syndrome	Is a	False	Anomaly of chromosome pair 10 (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Ring chromosome 10 syndrome	Is a	True	Anomaly of chromosome pair 10 (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Trisomy 10p (disorder)	Is a	False	Anomaly of chromosome pair 10 (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Deletion of part of chromosome 10 (disorder)	Is a	True	Anomaly of chromosome pair 10 (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Partial trisomy of chromosome 10 (disorder)	Is a	False	Anomaly of chromosome pair 10 (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Trisomy 10 (disorder)	Is a	True	Anomaly of chromosome pair 10 (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets