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698849002: Tetrasomy 18p (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2981459011 Tetrasomy 18p en Synonym Active Entire term case insensitive SNOMED CT core module
2981462014 18p tetrasomy en Synonym Active Entire term case insensitive SNOMED CT core module
2981466012 Tetrasomy 18p (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2981491012 18p isochromosome en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Tetrasomy 18p Is a Anomaly of chromosome pair 18 true Inferred relationship Existential restriction modifier
Tetrasomy 18p Occurrence Congenital false Inferred relationship Existential restriction modifier
Tetrasomy 18p Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Tetrasomy 18p Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Tetrasomy 18p Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 1
Tetrasomy 18p Finding site Chromosome pair 18 true Inferred relationship Existential restriction modifier 1
Tetrasomy 18p Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Tetrasomy 18p Finding site Short arm of chromosome true Inferred relationship Existential restriction modifier 2
Tetrasomy 18p Associated morphology Tetrasomy true Inferred relationship Existential restriction modifier 1
Tetrasomy 18p Associated morphology Tetrasomy true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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