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Terminology chevron_right Concepts chevron_right 41590007

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The component that hold information about this concept.
Familial amyloid polyneuropathy, jewish type (disorder)
Jewish type amyloid polyneuropathy
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Familial amyloid polyneuropathy, jewish type (disorder)

SCTID: 41590007, Primitive, Active


41590007|Familial amyloid polyneuropathy, jewish type (disorder)|
  • en Jewish type amyloid polyneuropathy
  • en Familial amyloid polyneuropathy, 33 ile-for-phe
  • en Familial amyloid polyneuropathy, jewish type
  • en Familial amyloid polyneuropathy, jewish type (disorder)

41590007 |Familial amyloid polyneuropathy, jewish type (disorder)|

<<< 42295001 |Familial amyloid polyneuropathy (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 68790008 |Amyloid deposition (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 84782009 |Peripheral nerve structure (body structure)| }
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