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778043005: Ring chromosome 17 syndrome (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3737482017 Ring chromosome 17 syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3737483010 Ring chromosome 17 syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3737484016 Ring chromosome 17 en Synonym Active Entire term case insensitive SNOMED CT core module
3737485015 Ring 17 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 17 syndrome Is a Anomaly of chromosome pair 17 true Inferred relationship Existential restriction modifier
Ring chromosome 17 syndrome Associated morphology Ring chromosome true Inferred relationship Existential restriction modifier 1
Ring chromosome 17 syndrome Finding site Chromosome pair 17 true Inferred relationship Existential restriction modifier 1
Ring chromosome 17 syndrome Is a Chromosome replaced with ring or dicentric false Inferred relationship Existential restriction modifier
Ring chromosome 17 syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Ring chromosome 17 syndrome Is a Ring chromosome true Inferred relationship Existential restriction modifier
Ring chromosome 17 syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Ring chromosome 17 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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