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

78740005: syndroom van volledige monosomie 21 (aandoening)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4555287013 Complete monosomy 21 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4555288015 Complete monosomy 21 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
7877761000146110 syndroom van volledige monosomie 21 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7877771000146116 volledige monosomie 21 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7877781000146119 syndroom van volledige monosomie 21 (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Complete monosomy 21 (disorder) Is a Monosomy and deletion from autosome (disorder) false Inferred relationship Some
Complete monosomy 21 (disorder) Is a Anomaly of chromosome pair 21 true Inferred relationship Some
Complete monosomy 21 (disorder) Finding site Chromosome pair 21 false Inferred relationship Some 1
Complete monosomy 21 (disorder) Associated morphology Alteration of chromosome structure false Inferred relationship Some
Complete monosomy 21 (disorder) Associated morphology Monosomy false Inferred relationship Some
Complete monosomy 21 (disorder) Occurrence Congenital false Inferred relationship Some
Complete monosomy 21 (disorder) Finding site Sex chromosome false Inferred relationship Some
Complete monosomy 21 (disorder) Associated morphology congenitale anomalie (afwijkende morfologie) false Inferred relationship Some 1
Complete monosomy 21 (disorder) Associated morphology congenitale anomalie (afwijkende morfologie) false Inferred relationship Some
Complete monosomy 21 (disorder) Finding site Chromosome pair 21 false Inferred relationship Some 1
Complete monosomy 21 (disorder) Occurrence Congenital true Inferred relationship Some 1
Complete monosomy 21 (disorder) Finding site Chromosome pair 21 true Inferred relationship Some 1
Complete monosomy 21 (disorder) Associated morphology Monosomy true Inferred relationship Some 1
Complete monosomy 21 (disorder) Is a Complete monosomy of autosome (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start