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Terminology chevron_right Concepts chevron_right 65986000

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The component that hold information about this concept.
Fetal aminopterin syndrome (disorder)
Fetal aminopterin syndrome
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Fetal aminopterin syndrome (disorder)

SCTID: 65986000, Defined, Active


65986000|Fetal aminopterin syndrome (disorder)|
  • en Aminopterin embryopathy syndrome
  • en Fetal aminopterin/methotrexate syndrome
  • en Fetal aminopterin syndrome
  • en Fetal aminopterin syndrome (disorder)
  • en Foetal aminopterin/methotrexate syndrome
  • en Foetal aminopterin syndrome

65986000 |Fetal aminopterin syndrome (disorder)|

=== 199547006 |Fetal disorder caused by drug or medicament (disorder)| +
    609520005 |Disorder of fetal structure (disorder)| +
    363127005 |Fetal disorder caused by chemicals (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
          246075003 |Causative agent (attribute)| = 6790004 |Aminopterin (substance)|,
          246454002 |Occurrence (attribute)| = 303112003 |Fetal period (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
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