FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.24  |  FHIR Version n/a  User: [n/a]

880079009: 11p15 duplication syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3994439013 11p15 duplication syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3994440010 11p15 duplication 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
11p15 duplication syndrome (disorder) est un(e) (attribut) 11p partial trisomy syndrome true Inferred relationship Some
11p15 duplication syndrome (disorder) localisation d'une constatation (attribut) Chromosome pair 11 (cell structure) true Inferred relationship Some 1
11p15 duplication syndrome (disorder) survenue (attribut) congénital true Inferred relationship Some 1
11p15 duplication syndrome (disorder) morphologie associée (attribut) Partial trisomy true Inferred relationship Some 1
11p15 duplication syndrome (disorder) est un(e) (attribut) Congenital malformation true Inferred relationship Some
11p15 duplication syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start