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57361003: Anomaly of chromosome pair 5 (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
95401013 Anomaly of chromosome pair 5 en Synonym Active Entire term case insensitive SNOMED CT core module
795975015 Anomaly of chromosome pair 5 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

24 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Anomaly of chromosome pair 5 Is a Anomaly of sex chromosome false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 5 Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 5 Occurrence Congenital false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 5 Finding site Sex chromosome false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 5 Finding site Chromosome pair 5 false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 5 Is a Anomaly of chromosome pair true Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 5 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 5 Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Anomaly of chromosome pair 5 Finding site Chromosome pair 5 false Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 5 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 5 Associated morphology Cellular AND/OR subcellular abnormality true Inferred relationship Existential restriction modifier 1
Anomaly of chromosome pair 5 Finding site Chromosome pair 5 true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
5p partial monosomy syndrome Is a False Anomaly of chromosome pair 5 Inferred relationship Existential restriction modifier
Partial trisomy of short arm of chromosome 5 Is a False Anomaly of chromosome pair 5 Inferred relationship Existential restriction modifier
5q14.3 microdeletion syndrome Is a False Anomaly of chromosome pair 5 Inferred relationship Existential restriction modifier
5q35 microduplication syndrome Is a False Anomaly of chromosome pair 5 Inferred relationship Existential restriction modifier
Deletion 5q35 Is a False Anomaly of chromosome pair 5 Inferred relationship Existential restriction modifier
Deletion of part of chromosome 5 Is a True Anomaly of chromosome pair 5 Inferred relationship Existential restriction modifier
Partial trisomy of chromosome 5 Is a True Anomaly of chromosome pair 5 Inferred relationship Existential restriction modifier
Mosaic trisomy 5 syndrome Is a True Anomaly of chromosome pair 5 Inferred relationship Existential restriction modifier
Ring chromosome 5 syndrome Is a True Anomaly of chromosome pair 5 Inferred relationship Existential restriction modifier
Tetrasomy 5p syndrome Is a True Anomaly of chromosome pair 5 Inferred relationship Existential restriction modifier
Paternal uniparental disomy of chromosome 5 Is a True Anomaly of chromosome pair 5 Inferred relationship Existential restriction modifier
Tetrasomy 5p mosaicism Is a True Anomaly of chromosome pair 5 Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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