FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  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
4837391000052111 11p15-duplikationssyndromet sv Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
11p15 duplication syndrome (disorder) Is a 11p partial trisomy syndrome true Inferred relationship Some
11p15 duplication syndrome (disorder) Finding site Chromosome pair 11 true Inferred relationship Some 1
11p15 duplication syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
11p15 duplication syndrome (disorder) Associated morphology Partial trisomy true Inferred relationship Some 1
11p15 duplication syndrome (disorder) Is a 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