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53346000: Complete trisomy 20 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
88705015 Complete trisomy 20 syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
791455010 Complete trisomy 20 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 20 syndrome Is a Trisomy and partial trisomy of autosome true Inferred relationship Existential restriction modifier
Complete trisomy 20 syndrome Is a Anomaly of chromosome pair 20 true Inferred relationship Existential restriction modifier
Complete trisomy 20 syndrome Finding site Sex chromosome false Inferred relationship Existential restriction modifier
Complete trisomy 20 syndrome Associated morphology Alteration of chromosome structure false Inferred relationship Existential restriction modifier
Complete trisomy 20 syndrome Finding site Chromosome pair 20 false Inferred relationship Existential restriction modifier 1
Complete trisomy 20 syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Complete trisomy 20 syndrome Associated morphology Trisomy false Inferred relationship Existential restriction modifier 2
Complete trisomy 20 syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Complete trisomy 20 syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Complete trisomy 20 syndrome Finding site Chromosome pair 20 false Inferred relationship Existential restriction modifier 1
Complete trisomy 20 syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Complete trisomy 20 syndrome Finding site Chromosome pair 20 true Inferred relationship Existential restriction modifier 1
Complete trisomy 20 syndrome Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 1
Complete trisomy 20 syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Complete trisomy 20 syndrome Associated morphology Trisomy true Inferred relationship Existential restriction modifier 1
Complete trisomy 20 syndrome Is a Congenital malformation true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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