FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

726380001: Deletion of part of chromosome 10 (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3448829013 Deletion of part of chromosome 10 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3448830015 Deletion of part of chromosome 10 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3448829013 Deletion of part of chromosome 10 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3448830015 Deletion of part of chromosome 10 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5876101000241114 délétion d'une partie du chromosome 10 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5876111000241111 délétion partielle du chromosome 10 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5876101000241114 délétion d'une partie du chromosome 10 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5876111000241111 délétion partielle du chromosome 10 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

9 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deletion of part of chromosome 10 (disorder) Is a Anomaly of chromosome pair 10 (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Deletion of part of chromosome 10 (disorder) Is a Deletion of part of autosome true Inferred relationship Existential restriction modifier (core metadata concept)
Deletion of part of chromosome 10 (disorder) Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Deletion of part of chromosome 10 (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Deletion of part of chromosome 10 (disorder) Finding site Chromosome pair 10 true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
10p partial monosomy syndrome (disorder) Is a True Deletion of part of chromosome 10 (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
10q partial monosomy (disorder) Is a True Deletion of part of chromosome 10 (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start