FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

702417004: Supernumerary der(22)t(11;22) syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2995113011 Der(22) syndrome due to 3:1 meiotic disjunction events en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995222019 Supernumerary der(22)t(11;22) syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995585015 Supernumerary derivative 22 chromosome syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995681016 Emanuel syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2995820019 Supernumerary der(22)t(11;22) syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995830011 Supernumerary der(22) syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Emanuel syndrome est un(e) (attribut) maladie chromosomique congénitale true Inferred relationship Some
Emanuel syndrome survenue (attribut) congénital true Inferred relationship Some 1
Emanuel syndrome morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 1
Emanuel syndrome localisation d'une constatation (attribut) Chromosome structure (cell structure) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start