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Terminology chevron_right Concepts chevron_right 726614009

Production
The component that hold information about this concept.
Autosomal recessive limb girdle muscular dystrophy type 2p (disorder)
Autosomal recessive limb girdle muscular dystrophy type 2p
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Autosomal recessive limb girdle muscular dystrophy type 2p (disorder)

SCTID: 726614009, Primitive, Active


726614009|Autosomal recessive limb girdle muscular dystrophy type 2p (disorder)|
  • en Autosomal recessive limb girdle muscular dystrophy type 2p
  • en Autosomal recessive limb girdle muscular dystrophy type 2p (disorder)

726614009 |Autosomal recessive limb girdle muscular dystrophy type 2p (disorder)|

<<< 240054004 |Autosomal recessive muscular dystrophy with limb girdle distribution (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 127954009 |Skeletal muscle structure (body structure)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 263502005 |Clinical course (attribute)| = 255314001 |Progressive (qualifier value)| }
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