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Terminology chevron_right Concepts chevron_right 91871006

Production
The component that hold information about this concept.
Congenital absence of basisphenoid bone (disorder)
Agenesis of basisphenoid bone
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Congenital absence of basisphenoid bone (disorder)

SCTID: 91871006, Defined, Active


91871006|Congenital absence of basisphenoid bone (disorder)|
  • en Agenesis of basisphenoid bone
  • en Congenital absence of basisphenoid bone
  • en Congenital absence of basisphenoid bone (disorder)

91871006 |Congenital absence of basisphenoid bone (disorder)|

=== 92996006 |Congenital anomaly of basisphenoid bone (disorder)| +
    1145449007 |Aplasia of bone of cranium (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 782173000 |Agenesis (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 95945003 |Entire basisphenoid bone (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
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