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Terminology chevron_right Concepts chevron_right 764627005

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The component that hold information about this concept.
Mosaic trisomy 3 syndrome (disorder)
Trisomy 3 mosaicism
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Mosaic trisomy 3 syndrome (disorder)

SCTID: 764627005, Defined, Active


764627005|Mosaic trisomy 3 syndrome (disorder)|
  • en Mosaic trisomy 3 syndrome
  • en Mosaic trisomy 3 syndrome (disorder)
  • en Mosaic trisomy chromosome 3
  • en Trisomy 3 mosaicism

764627005 |Mosaic trisomy 3 syndrome (disorder)|

=== 13674001 |Anomaly of chromosome pair 3 (disorder)| +
    270521004 |Trisomy and partial trisomy of autosome (disorder)| +
    82354003 |Multiple system malformation syndrome (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 11704001 |Chromosome mosaicism (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 113355002 |Chromosome pair 3 (cell structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 78989007 |Trisomy (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 113355002 |Chromosome pair 3 (cell structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
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