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726723004: Ring chromosome 13 syndrome (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3452190018 Ring chromosome 13 syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3452191019 Ring chromosome 13 syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3452192014 Ring chromosome 13 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 13 syndrome Is a Anomaly of chromosome pair 13 true Inferred relationship Existential restriction modifier
Ring chromosome 13 syndrome Is a Chromosome replaced with ring or dicentric false Inferred relationship Existential restriction modifier
Ring chromosome 13 syndrome Associated morphology Ring chromosome true Inferred relationship Existential restriction modifier 1
Ring chromosome 13 syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Ring chromosome 13 syndrome Finding site Chromosome pair 13 true Inferred relationship Existential restriction modifier 1
Ring chromosome 13 syndrome Is a Ring chromosome true Inferred relationship Existential restriction modifier
Ring chromosome 13 syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Ring chromosome 13 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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