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Terminology chevron_right Concepts chevron_right 732930007

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

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

SCTID: 732930007, Primitive, Active


732930007|Autosomal recessive limb girdle muscular dystrophy type 2t (disorder)|
  • en Autosomal recessive limb girdle muscular dystrophy type 2t
  • en Autosomal recessive limb girdle muscular dystrophy type 2t (disorder)

732930007 |Autosomal recessive limb girdle muscular dystrophy type 2t (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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