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Terminology chevron_right Concepts chevron_right 771334000

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771334000
The component that hold information about this concept.
Autosomal dominant limb-girdle muscular dystrophy type 1h (disorder)
Autosomal dominant limb-girdle muscular dystrophy type 1h
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Autosomal dominant limb-girdle muscular dystrophy type 1h (disorder)

SCTID: 771334000, Primitive, Active


771334000|Autosomal dominant limb-girdle muscular dystrophy type 1h (disorder)|
  • en Autosomal dominant limb-girdle muscular dystrophy type 1h
  • en Autosomal dominant limb-girdle muscular dystrophy type 1h (disorder)

771334000 |Autosomal dominant limb-girdle muscular dystrophy type 1h (disorder)|

<<< 240067001 |Autosomal dominant 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)| }
Active

3705802011 - Autosomal dominant limb-girdle muscular dystrophy type 1H (en) View

3705802011
en
Synonym (core metadata concept)
Autosomal dominant limb-girdle muscular dystrophy type 1H
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

3705803018 - Autosomal dominant limb-girdle muscular dystrophy type 1H (disorder) (en) View

3705803018
en
Fully specified name (core metadata concept)
Autosomal dominant limb-girdle muscular dystrophy type 1H (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

240067001 View

240067001
Autosomal dominant muscular dystrophy with limb girdle distribution (disorder)
Autosomal dominant muscular dystrophy with limb girdle distribution
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (c560d40f-0540-53dc-9f64-ea58de88704e) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
G71.0
TRUE
ALWAYS G71.0
447561005 |Snomed ct source code to target map code correlation not specified (foundation metadata concept)|
447637006 |Map source concept is properly classified (foundation metadata concept)|
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