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Terminology chevron_right Concepts chevron_right 1145483000

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The component that hold information about this concept.
Congenital hypoplasia of phalanx of middle finger (disorder)
Congenital hypoplasia of phalanx of middle finger
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Congenital hypoplasia of phalanx of middle finger (disorder)

SCTID: 1145483000, Defined, Active


1145483000|Congenital hypoplasia of phalanx of middle finger (disorder)|
  • en Congenital hypoplasia of phalanx of middle finger
  • en Congenital hypoplasia of phalanx of middle finger (disorder)

1145483000 |Congenital hypoplasia of phalanx of middle finger (disorder)|

=== 1145506008 |Congenital hypoplasia of phalanx of hand (disorder)| +
    1145492002 |Congenital hypoplasia of middle finger (disorder)| +
    896863000 |Structural abnormality of phalanx of middle finger (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 55199003 |Hypoplasia (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 72228000 |Structure of phalanx of middle finger (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
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