FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

702345009: Ring chromosome 14 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
2995389010 Ring chromosome 14 syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2995489011 Ring chromosome 14 en Synonym Active Entire term case insensitive SNOMED CT core module
2995651012 Ring chromosome 14 syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
2995728019 Ring 14 syndrome 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 14 syndrome Is a Chromosome replaced with ring or dicentric false Inferred relationship Existential restriction modifier
Ring chromosome 14 syndrome Associated morphology Ring chromosome true Inferred relationship Existential restriction modifier 1
Ring chromosome 14 syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Ring chromosome 14 syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 2
Ring chromosome 14 syndrome Finding site Chromosome structure false Inferred relationship Existential restriction modifier 2
Ring chromosome 14 syndrome Is a Anomaly of chromosome pair 14 true Inferred relationship Existential restriction modifier
Ring chromosome 14 syndrome Is a Ring chromosome true Inferred relationship Existential restriction modifier
Ring chromosome 14 syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Ring chromosome 14 syndrome Finding site Chromosome pair 14 true Inferred relationship Existential restriction modifier 1
Ring chromosome 14 syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Ring chromosome 14 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

Back to Start