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16569009: Anomaly of chromosome pair 15 (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
28033019 Anomaly of chromosome pair 15 en Synonym Active Entire term case insensitive SNOMED CT core module
743616010 Anomaly of chromosome pair 15 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


22 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Anomaly of chromosome pair 15 Is a Anomaly of sex chromosome false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 15 Occurrence Congenital false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 15 Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 15 Finding site Chromosome pair 15 false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 15 Finding site Sex chromosome false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 15 Is a Anomaly of chromosome pair true Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 15 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 15 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 15 Finding site Chromosome pair 15 false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 15 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 15 Finding site Chromosome pair 15 true Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 15 Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group
15q partial monosomy syndrome Is a False Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier
15q partial trisomy syndrome Is a False Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier
Angelman syndrome Is a False Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier
Prader-Willi syndrome Is a False Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier
Microdeletion of chromosome 15q13.3 Is a False Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier
Microdeletion of chromosome 15q24 Is a False Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier
15q14 microdeletion syndrome Is a False Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier
Isodicentric chromosome 15 syndrome Is a True Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier
Deletion of part of chromosome 15 Is a True Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier
Partial trisomy of chromosome 15 Is a True Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier
Ring chromosome 15 syndrome Is a True Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier
Mosaic trisomy 15 syndrome Is a True Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier
Maternal uniparental disomy of chromosome 15 Is a True Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier
Uniparental disomy of paternal origin of chromosome 15 Is a True Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier
Tetrasomy 15q Is a True Anomaly of chromosome pair 15 Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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