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17760001: Anomaly of chromosome pair 13 (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
30013010 Anomaly of chromosome pair 13 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
745100012 Anomaly of chromosome pair 13 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
931371000172112 anomalie du chromosome 13 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


25 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Anomaly of chromosome pair 13 Is a Anomaly of sex chromosome false Inferred relationship Some
Anomaly of chromosome pair 13 Finding site Sex chromosome false Inferred relationship Some
Anomaly of chromosome pair 13 Occurrence Congenital false Inferred relationship Some
Anomaly of chromosome pair 13 Finding site Chromosome pair 13 false Inferred relationship Some 1
Anomaly of chromosome pair 13 Associated morphology Alteration of chromosome structure false Inferred relationship Some
Anomaly of chromosome pair 13 Is a Anomaly of chromosome pair true Inferred relationship Some
Anomaly of chromosome pair 13 Associated morphology anomalie congénitale false Inferred relationship Some 1
Anomaly of chromosome pair 13 Finding site Chromosome pair 13 false Inferred relationship Some 1
Anomaly of chromosome pair 13 Associated morphology anomalie congénitale false Inferred relationship Some
Anomaly of chromosome pair 13 Occurrence Congenital true Inferred relationship Some 1
Anomaly of chromosome pair 13 Finding site Chromosome pair 13 true Inferred relationship Some 1
Anomaly of chromosome pair 13 Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
13q partial trisomy syndrome Is a False Anomaly of chromosome pair 13 Inferred relationship Some
Partial trisomy 13 in Patau's syndrome Is a True Anomaly of chromosome pair 13 Inferred relationship Some
Complete trisomy 13 syndrome Is a False Anomaly of chromosome pair 13 Inferred relationship Some
13q partial monosomy syndrome (disorder) Is a False Anomaly of chromosome pair 13 Inferred relationship Some
13p partial trisomy syndrome Is a False Anomaly of chromosome pair 13 Inferred relationship Some
Complete trisomy 13 syndrome Is a True Anomaly of chromosome pair 13 Inferred relationship Some
Ring chromosome 13 syndrome (disorder) Is a True Anomaly of chromosome pair 13 Inferred relationship Some
Deletion of part of chromosome 13 (disorder) Is a True Anomaly of chromosome pair 13 Inferred relationship Some
Partial trisomy of chromosome 13 Is a True Anomaly of chromosome pair 13 Inferred relationship Some
Paternal uniparental disomy of chromosome 13 Is a True Anomaly of chromosome pair 13 Inferred relationship Some
Maternal uniparental disomy of chromosome 13 Is a True Anomaly of chromosome pair 13 Inferred relationship Some

Reference Sets

Description inactivation indicator reference set

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