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Terminology chevron_right Concepts chevron_right 240053005

Production
The component that hold information about this concept.
Hereditary myopathy limited to females (disorder)
Hereditary myopathy limited to females
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Hereditary myopathy limited to females (disorder)

SCTID: 240053005, Primitive, Active


240053005|Hereditary myopathy limited to females (disorder)|
  • en Hereditary myopathy limited to females
  • en Hereditary myopathy limited to females (disorder)

240053005 |Hereditary myopathy limited to females (disorder)|

<<< 240051007 |X-linked limb girdle muscular dystrophy with normal dystrophin (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 127954009 |Skeletal muscle structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 263502005 |Clinical course (attribute)| = 255314001 |Progressive (qualifier value)| }
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