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765485000: Ring chromosome 2 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
3658949018 Ring chromosome 2 syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3658950018 Ring chromosome 2 syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3658951019 Ring chromosome 2 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
Ring chromosome 2 syndrome Is a Anomaly of chromosome pair 2 true Inferred relationship Existential restriction modifier
Ring chromosome 2 syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Ring chromosome 2 syndrome Is a Chromosome replaced with ring or dicentric false Inferred relationship Existential restriction modifier
Ring chromosome 2 syndrome Associated morphology Ring chromosome true Inferred relationship Existential restriction modifier 1
Ring chromosome 2 syndrome Finding site Chromosome pair 2 true Inferred relationship Existential restriction modifier 1
Ring chromosome 2 syndrome Is a Ring chromosome true Inferred relationship Existential restriction modifier
Ring chromosome 2 syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Ring chromosome 2 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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