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Terminology chevron_right Concepts chevron_right 238706002

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

Laugier-hunziker syndrome (disorder)

SCTID: 238706002, Primitive, Active


238706002|Laugier-hunziker syndrome (disorder)|
  • en Laugier-hunziker syndrome (disorder)
  • en Laugier-hunziker syndrome

238706002 |Laugier-hunziker syndrome (disorder)|

<<< 249405005 |Pigmentation of oral mucosa (disorder)| +
    402633003 |Melanonychia (disorder)| +
    107650008 |Color finding (finding)| :
        { 116676008 |Associated morphology (attribute)| = 51083003 |Structure showing abnormal deposition of pigment (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 113277000 |Oral mucous membrane structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 770802007 |Nail unit structure (body structure)| }
        { 363714003 |Interprets (attribute)| = 249402008 |Color of oral mucosa (observable entity)| }
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