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726381002: Deletion of part of chromosome 11 (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
3448831016 Deletion of part of chromosome 11 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3448832011 Deletion of part of chromosome 11 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


9 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deletion of part of chromosome 11 (disorder) Is a Anomaly of chromosome pair 11 (disorder) true Inferred relationship Some
Deletion of part of chromosome 11 (disorder) Is a Deletion of part of autosome true Inferred relationship Some
Deletion of part of chromosome 11 (disorder) Associated morphology Partial monosomy (morphologic abnormality) true Inferred relationship Some 1
Deletion of part of chromosome 11 (disorder) Occurrence Congenital true Inferred relationship Some 1
Deletion of part of chromosome 11 (disorder) Finding site Chromosome pair 11 true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
11q partial monosomy syndrome Is a True Deletion of part of chromosome 11 (disorder) Inferred relationship Some
Distal partial deletion of long arm of chromosome 11 (disorder) Is a True Deletion of part of chromosome 11 (disorder) Inferred relationship Some
Oculootodental syndrome Is a True Deletion of part of chromosome 11 (disorder) Inferred relationship Some
11p partial monosomy syndrome Is a True Deletion of part of chromosome 11 (disorder) Inferred relationship Some

Reference Sets

GB English

US English

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