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Terminology chevron_right Concepts chevron_right 61808009

Production
The component that hold information about this concept.
Multiple endocrine neoplasia, type 2 (disorder)
Mea, type 2
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Multiple endocrine neoplasia, type 2 (disorder)

SCTID: 61808009, Primitive, Active


61808009|Multiple endocrine neoplasia, type 2 (disorder)|
  • en Familial chromaffinomatosis
  • en Multiple endocrine adenomatosis, type 2
  • en Multiple endocrine neoplasia, type 2
  • en Multiple endocrine neoplasia, type 2 (disorder)
  • en Mea, type 2
  • en Men, type 2
  • en Ptc syndrome
  • en Sipple's syndrome
  • en Sipple syndrome

61808009 |Multiple endocrine neoplasia, type 2 (disorder)|

<<< 46724008 |Polyglandular activity in multiple endocrine adenomatosis (disorder)| +
    363104002 |Hereditary disorder of endocrine system (disorder)| +
    699346009 |Hereditary cancer-predisposing syndrome (disorder)| +
    11164009 |Autosomal dominant hereditary disorder (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 60549007 |Multiple endocrine adenomas (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 77637002 |Structure of multiple endocrine glands (body structure)| }
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