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763406004: Ring chromosome 16 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
3642123012 Ring chromosome 16 syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3642124018 Ring chromosome 16 syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3642125017 Ring chromosome 16 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 16 syndrome Is a Anomaly of chromosome pair 16 true Inferred relationship Existential restriction modifier
Ring chromosome 16 syndrome Is a Chromosome replaced with ring or dicentric false Inferred relationship Existential restriction modifier
Ring chromosome 16 syndrome Associated morphology Ring chromosome true Inferred relationship Existential restriction modifier 1
Ring chromosome 16 syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Ring chromosome 16 syndrome Finding site Chromosome pair 16 true Inferred relationship Existential restriction modifier 1
Ring chromosome 16 syndrome Is a Ring chromosome true Inferred relationship Existential restriction modifier
Ring chromosome 16 syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Ring chromosome 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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