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Terminology chevron_right Concepts chevron_right 770562000

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The component that hold information about this concept.
Maternal uniparental disomy of chromosome 1 (disorder)
Maternal uniparental disomy of chromosome 1
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Maternal uniparental disomy of chromosome 1 (disorder)

SCTID: 770562000, Defined, Active


770562000|Maternal uniparental disomy of chromosome 1 (disorder)|
  • en Maternal uniparental disomy of chromosome 1
  • en Maternal uniparental disomy of chromosome 1 (disorder)

770562000 |Maternal uniparental disomy of chromosome 1 (disorder)|

=== 74769007 |Anomaly of chromosome pair 1 (disorder)| +
    726401004 |Uniparental disomy of maternal origin (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 41669009 |Alteration of chromosome structure (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 46507000 |Chromosome pair 1 (cell structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
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