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Terminology chevron_right Concepts chevron_right 109471001

Production
The component that hold information about this concept.
Amelogenesis imperfecta, hypocalcification type (disorder)
Amelogenesis imperfecta - hypocalcified
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Amelogenesis imperfecta, hypocalcification type (disorder)

SCTID: 109471001, Defined, Active


109471001|Amelogenesis imperfecta, hypocalcification type (disorder)|
  • en Amelogenesis imperfecta, hypocalcification type
  • en Amelogenesis imperfecta, hypocalcification type (disorder)
  • en Amelogenesis imperfecta - hypocalcified
  • en Amelogenesis imperfecta - hypomineralisation
  • en Amelogenesis imperfecta - hypomineralization

109471001 |Amelogenesis imperfecta, hypocalcification type (disorder)|

=== 78494001 |Amelogenesis imperfecta (disorder)| +
    1258915002 |Hypomineralization of enamel of teeth (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 128416000 |Impaired mineralization (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 76993005 |Enamel structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 245543004 |Dentition (body structure)| }
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