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Terminology chevron_right Concepts chevron_right 1269318001

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The component that hold information about this concept.
Family history of congenital long qt syndrome (situation)
Family history of congenital long qt syndrome
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Family history of congenital long qt syndrome (situation)

SCTID: 1269318001, Defined, Active


1269318001|Family history of congenital long qt syndrome (situation)|
  • en Family history of congenital long qt syndrome
  • en Family history of congenital long qt syndrome (situation)

1269318001 |Family history of congenital long qt syndrome (situation)|

=== 429962007 |Family history of hereditary disease (situation)| +
    700192006 |Family history of long qt syndrome (situation)| :
        { 246090004 |Associated finding (attribute)| = 442917000 |Congenital long qt syndrome (disorder)|,
          408729009 |Finding context (attribute)| = 410515003 |Known present (qualifier value)|,
          408732007 |Subject relationship context (attribute)| = 303071001 |Person in the family (person)|,
          408731000 |Temporal context (attribute)| = 410511007 |Current or past (actual) (qualifier value)| }
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