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Terminology chevron_right Concepts chevron_right 95241002

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

Rhinocephaly (disorder)

SCTID: 95241002, Primitive, Active


95241002|Rhinocephaly (disorder)|
  • en Rhinocephaly
  • en Rhinocephaly (disorder)

95241002 |Rhinocephaly (disorder)|

<<< 54873004 |Congenital anomaly of orbit proper (disorder)| +
    205798005 |Cyclopia (disorder)| +
    128274005 |Congenital anomaly of nose (disorder)| +
    371522000 |Disorder of bony orbit (disorder)| +
    51655004 |Congenital anomaly of skull (disorder)| +
    879976004 |Lesion of bone (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 408737001 |Malposition (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 279542008 |Region of nose (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 1297033003 |Abnormally fused structure (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 110528008 |Bony orbit structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
Active
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