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Terminology chevron_right Concepts chevron_right 407000

Production
The component that hold information about this concept.
Congenital hepatomegaly (disorder)
Gan to bẩm sinh
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Congenital hepatomegaly (disorder)

SCTID: 407000, Defined, Active


407000|Congenital hepatomegaly (disorder)|
  • vi Gan to bẩm sinh
  • en Congenital hepatomegaly
  • en Congenital hepatomegaly (disorder)

407000 |Congenital hepatomegaly (disorder)|

=== 89166001 |Congenital anomaly of liver (disorder)| +
    80515008 |Large liver (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 442021009 |Enlargement (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 181268008 |Entire liver (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
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