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726381002: Deletion of part of chromosome 11 (disorder)


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

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 SNOMED CT core module
3448832011 Deletion of part of chromosome 11 en Synonym Active Entire term case insensitive SNOMED CT core module


9 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deletion of part of chromosome 11 Is a Anomaly of chromosome pair 11 true Inferred relationship Existential restriction modifier
Deletion of part of chromosome 11 Is a Deletion of part of autosome true Inferred relationship Existential restriction modifier
Deletion of part of chromosome 11 Associated morphology Partial monosomy true Inferred relationship Existential restriction modifier 1
Deletion of part of chromosome 11 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Deletion of part of chromosome 11 Finding site Chromosome pair 11 true Inferred relationship Existential restriction modifier 1

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

This concept is not in any reference sets

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