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Terminology chevron_right Concepts chevron_right 254131007

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

Worth disease (disorder)

SCTID: 254131007, Primitive, Active


254131007|Worth disease (disorder)|
  • en Autosomal dominant osteosclerosis
  • en Worth disease
  • en Worth disease (disorder)

254131007 |Worth disease (disorder)|

<<< 254130008 |Endosteal hyperostoses (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 25723000 |Dysplasia (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 272673000 |Bone structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 363713009 |Has interpretation (attribute)| = 281302008 |Above reference range (qualifier value)|,
          363714003 |Interprets (attribute)| = 312681000 |Bone density scan (procedure)| }
        { 363713009 |Has interpretation (attribute)| = 281300000 |Below reference range (qualifier value)|,
          363714003 |Interprets (attribute)| = 43857005 |Osteoclast turnover rate (observable entity)| }
        { 263502005 |Clinical course (attribute)| = 255314001 |Progressive (qualifier value)| }
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