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53392002: Anomaly of chromosome pair 16 (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
88771011 Anomaly of chromosome pair 16 en Synonym Active Entire term case insensitive SNOMED CT core module
791506016 Anomaly of chromosome pair 16 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

29 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Anomaly of chromosome pair 16 Is a Anomaly of sex chromosome false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 16 Occurrence Congenital false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 16 Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 16 Finding site Sex chromosome false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 16 Finding site Chromosome pair 16 false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 16 Is a Anomaly of chromosome pair true Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 16 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 16 Finding site Chromosome pair 16 false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 16 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 16 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 16 Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 16 Finding site Chromosome pair 16 true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
16q partial monosomy syndrome Is a False Anomaly of chromosome pair 16 Inferred relationship Existential restriction modifier
16q partial trisomy syndrome Is a False Anomaly of chromosome pair 16 Inferred relationship Existential restriction modifier
Complete trisomy 16 syndrome Is a True Anomaly of chromosome pair 16 Inferred relationship Existential restriction modifier
16p partial trisomy syndrome Is a False Anomaly of chromosome pair 16 Inferred relationship Existential restriction modifier
Chromosome 16p11.2 deletion syndrome Is a False Anomaly of chromosome pair 16 Inferred relationship Existential restriction modifier
16p11.2p12.2 microdeletion syndrome Is a False Anomaly of chromosome pair 16 Inferred relationship Existential restriction modifier
16p13.11 microdeletion syndrome Is a False Anomaly of chromosome pair 16 Inferred relationship Existential restriction modifier
Deletion of part of chromosome 16 Is a True Anomaly of chromosome pair 16 Inferred relationship Existential restriction modifier
Partial trisomy of chromosome 16 Is a True Anomaly of chromosome pair 16 Inferred relationship Existential restriction modifier
Ring chromosome 16 syndrome Is a True Anomaly of chromosome pair 16 Inferred relationship Existential restriction modifier
Mosaic trisomy 16 syndrome Is a True Anomaly of chromosome pair 16 Inferred relationship Existential restriction modifier
Maternal uniparental disomy of chromosome 16 Is a True Anomaly of chromosome pair 16 Inferred relationship Existential restriction modifier
16p12.1p12.3 triplication syndrome Is a True Anomaly of chromosome pair 16 Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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