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Terminology chevron_right Concepts chevron_right 93035001

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

Congenital fenestration of basioccipital bone (disorder)

SCTID: 93035001, Defined, Active


93035001|Congenital fenestration of basioccipital bone (disorder)|
  • en Congenital basioccipital hole
  • en Congenital fenestration of basioccipital bone
  • en Congenital fenestration of basioccipital bone (disorder)

93035001 |Congenital fenestration of basioccipital bone (disorder)|

=== 92995005 |Congenital anomaly of basioccipital bone (disorder)| +
    879976004 |Lesion of bone (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 16255008 |Fenestration (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 33898000 |Structure of basilar part of occipital bone (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
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