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77269002: Complete trisomy 16 syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
128252015 Complete trisomy 16 syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
818080019 Complete trisomy 16 syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Complete trisomy 16 syndrome Is a Anomaly of chromosome pair 16 true Inferred relationship Existential restriction modifier
Complete trisomy 16 syndrome Is a Trisomy and partial trisomy of autosome true Inferred relationship Existential restriction modifier
Complete trisomy 16 syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Complete trisomy 16 syndrome Finding site Chromosome pair 16 false Inferred relationship Existential restriction modifier 1
Complete trisomy 16 syndrome Finding site Sex chromosome false Inferred relationship Existential restriction modifier
Complete trisomy 16 syndrome Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Complete trisomy 16 syndrome Associated morphology Trisomy false Inferred relationship Existential restriction modifier 2
Complete trisomy 16 syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Complete trisomy 16 syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Complete trisomy 16 syndrome Finding site Chromosome pair 16 false Inferred relationship Existential restriction modifier 1
Complete trisomy 16 syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Complete trisomy 16 syndrome Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 1
Complete trisomy 16 syndrome Finding site Chromosome pair 16 true Inferred relationship Existential restriction modifier 1
Complete trisomy 16 syndrome Is a Congenital malformation true Inferred relationship Existential restriction modifier
Complete trisomy 16 syndrome Associated morphology Trisomy true Inferred relationship Existential restriction modifier 1
Complete trisomy 16 syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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