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Terminology chevron_right Concepts chevron_right 428850001

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

Li-fraumeni syndrome (disorder)

SCTID: 428850001, Primitive, Active


428850001|Li-fraumeni syndrome (disorder)|
  • en Li-fraumeni syndrome
  • en Li-fraumeni syndrome (disorder)

428850001 |Li-fraumeni syndrome (disorder)|

<<< 55352002 |Familial neoplastic disease (disorder)| +
    11164009 |Autosomal dominant hereditary disorder (disorder)| +
    699346009 |Hereditary cancer-predisposing syndrome (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 108369006 |Neoplasm (morphologic abnormality)| }
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