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Terminology chevron_right Concepts chevron_right 230670003

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

Familial infantile myasthenia (disorder)

SCTID: 230670003, Primitive, Active


230670003|Familial infantile myasthenia (disorder)|
  • en Familial infantile myasthenia
  • en Familial infantile myasthenia (disorder)
  • en Fim - familial infantile myasthenia

230670003 |Familial infantile myasthenia (disorder)|

<<< 230672006 |Congenital myasthenia (disorder)| +
    55051001 |Myasthenia gravis, juvenile form (disorder)| :
        { 363698007 |Finding site (attribute)| = 31627007 |Neuromuscular junction (cell structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 263680009 |Autoimmune process (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 127954009 |Skeletal muscle structure (body structure)| }
        { 370135005 |Pathological process (attribute)| = 472963003 |Hypersensitivity process (qualifier value)| }
Active
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