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765484001: Ring chromosome 19 syndrome (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3658945012 Ring chromosome 19 syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3658946013 Ring chromosome 19 en Synonym Active Entire term case insensitive SNOMED CT core module
3658947016 Ring chromosome 19 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
Ring chromosome 19 syndrome Finding site Chromosome pair 19 true Inferred relationship Existential restriction modifier 1
Ring chromosome 19 syndrome Is a Chromosome replaced with ring or dicentric false Inferred relationship Existential restriction modifier
Ring chromosome 19 syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Ring chromosome 19 syndrome Is a Anomaly of chromosome pair 19 true Inferred relationship Existential restriction modifier
Ring chromosome 19 syndrome Associated morphology Ring chromosome true Inferred relationship Existential restriction modifier 1
Ring chromosome 19 syndrome Is a Ring chromosome true Inferred relationship Existential restriction modifier
Ring chromosome 19 syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Ring chromosome 19 syndrome Is a Multiple system malformation syndrome 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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