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Terminology chevron_right Concepts chevron_right 726399005

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The component that hold information about this concept.
Deletion of part of chromosome 22 (disorder)
Deletion of part of chromosome 22
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Deletion of part of chromosome 22 (disorder)

SCTID: 726399005, Defined, Active


726399005|Deletion of part of chromosome 22 (disorder)|
  • en Deletion of part of chromosome 22
  • en Deletion of part of chromosome 22 (disorder)

726399005 |Deletion of part of chromosome 22 (disorder)|

=== 70452003 |Anomaly of chromosome pair 22 (disorder)| +
    254274004 |Deletion of part of autosome (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 371169004 |Partial monosomy (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 79229009 |Chromosome pair 22 (cell structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
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