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Terminology chevron_right Concepts chevron_right 719990003

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719990003
The component that hold information about this concept.
Autosomal dominant limb girdle muscular dystrophy type 1g (disorder)
Autosomal dominant limb girdle muscular dystrophy type 1g
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 1g (disorder)

SCTID: 719990003, Primitive, Active


719990003|Autosomal dominant limb girdle muscular dystrophy type 1g (disorder)|
  • en Autosomal dominant limb girdle muscular dystrophy type 1g
  • en Autosomal dominant limb girdle muscular dystrophy type 1g (disorder)

719990003 |Autosomal dominant limb girdle muscular dystrophy type 1g (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

3318735014 - Autosomal dominant limb girdle muscular dystrophy type 1G (en) View

3318735014
en
Synonym (core metadata concept)
Autosomal dominant limb girdle muscular dystrophy type 1G
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

3318734013 - Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) (en) View

3318734013
en
Fully specified name (core metadata concept)
Autosomal dominant limb girdle muscular dystrophy type 1G (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

Relationship (6644778025) - 719990003 -> 127954009 (363698007) View

363698007 |Finding site (attribute)|
127954009 |Skeletal muscle structure (body structure)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (6645816020) - 719990003 -> 4720007 (116676008) View

116676008 |Associated morphology (attribute)|
4720007 |Dystrophy (morphologic abnormality)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (11283657022) - 719990003 -> 127954009 (363698007) View

363698007 |Finding site (attribute)|
127954009 |Skeletal muscle structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11283658028) - 719990003 -> 4720007 (116676008) View

116676008 |Associated morphology (attribute)|
4720007 |Dystrophy (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11283659020) - 719990003 -> 308490002 (370135005) View

370135005 |Pathological process (attribute)|
308490002 |Pathological developmental process (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11577736022) - 719990003 -> 255314001 (263502005) View

263502005 |Clinical course (attribute)|
255314001 |Progressive (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6644775027) - 719990003 -> 127954009 (363698007) View

363698007 |Finding site (attribute)|
127954009 |Skeletal muscle structure (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (6645814023) - 719990003 -> 21390004 (116676008) View

116676008 |Associated morphology (attribute)|
21390004 |Developmental anomaly (morphologic abnormality)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (6645815024) - 719990003 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (6644773023) - 719990003 -> 240067001 (116680003) View

116680003 |Is a (attribute)|
240067001 |Autosomal dominant muscular dystrophy with limb girdle distribution (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
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 (b7928de4-c9f5-5d42-9e13-49553ea89388) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
G71.0
TRUE
ALWAYS G71.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
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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