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47017007: Ring chromosome 1 syndrome (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
78364012 Ring chromosome 1 syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
784429013 Ring chromosome 1 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 1 syndrome Is a Anomaly of chromosome pair 1 true Inferred relationship Existential restriction modifier
Ring chromosome 1 syndrome Is a Chromosome replaced with ring or dicentric false Inferred relationship Existential restriction modifier
Ring chromosome 1 syndrome Finding site Chromosome pair 1 false Inferred relationship Existential restriction modifier 1
Ring chromosome 1 syndrome Finding site Sex chromosome false Inferred relationship Existential restriction modifier
Ring chromosome 1 syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Ring chromosome 1 syndrome Associated morphology Ring chromosome true Inferred relationship Existential restriction modifier 1
Ring chromosome 1 syndrome Finding site Chromosome pair 1 false Inferred relationship Existential restriction modifier 2
Ring chromosome 1 syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Ring chromosome 1 syndrome Finding site Chromosome pair 1 false Inferred relationship Existential restriction modifier 2
Ring chromosome 1 syndrome Finding site Chromosome pair 1 false Inferred relationship Existential restriction modifier 1
Ring chromosome 1 syndrome Finding site Chromosome pair 1 false Inferred relationship Existential restriction modifier 1
Ring chromosome 1 syndrome Finding site Chromosome pair 1 false Inferred relationship Existential restriction modifier 2
Ring chromosome 1 syndrome Finding site Chromosome pair 1 false Inferred relationship Existential restriction modifier 1
Ring chromosome 1 syndrome Finding site Chromosome pair 1 false Inferred relationship Existential restriction modifier 2
Ring chromosome 1 syndrome Finding site Chromosome pair 1 true Inferred relationship Existential restriction modifier 1
Ring chromosome 1 syndrome Finding site Chromosome pair 1 false Inferred relationship Existential restriction modifier 2
Ring chromosome 1 syndrome Finding site Chromosome pair 1 false Inferred relationship Existential restriction modifier 2
Ring chromosome 1 syndrome Finding site Chromosome pair 1 false Inferred relationship Existential restriction modifier 1
Ring chromosome 1 syndrome Associated morphology Ring chromosome false Inferred relationship Existential restriction modifier 2
Ring chromosome 1 syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Ring chromosome 1 syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Ring chromosome 1 syndrome Associated morphology Cellular AND/OR subcellular abnormality false Inferred relationship Existential restriction modifier 1
Ring chromosome 1 syndrome Finding site Chromosome pair 1 false Inferred relationship Existential restriction modifier 1
Ring chromosome 1 syndrome Is a Ring chromosome true Inferred relationship Existential restriction modifier
Ring chromosome 1 syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Ring chromosome 1 syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Ring chromosome 1 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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