Loading...
dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 448054001

Production
add
448054001
The component that hold information about this concept.
Adult onset autosomal dominant leukodystrophy (disorder)
Adult onset autosomal dominant leucodystrophy
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Adult onset autosomal dominant leukodystrophy (disorder)

SCTID: 448054001, Defined, Active


448054001|Adult onset autosomal dominant leukodystrophy (disorder)|
  • en Adult onset autosomal dominant leucodystrophy
  • en Adult onset autosomal dominant leukodystrophy
  • en Adult onset autosomal dominant leukodystrophy (disorder)

448054001 |Adult onset autosomal dominant leukodystrophy (disorder)|

=== 11164009 |Autosomal dominant hereditary disorder (disorder)| +
    192781003 |Leukodystrophy (disorder)| +
    106018006 |Hereditary degenerative disease of central nervous system (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 125495003 |Myelin sheath alteration (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 54115001 |Myelinated nerve fiber structure (body structure)|,
          246454002 |Occurrence (attribute)| = 41847000 |Adulthood (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 389080008 |White matter structure of brain and spinal cord (body structure)|,
          246454002 |Occurrence (attribute)| = 41847000 |Adulthood (qualifier value)| }
Active

2899695010 - Adult onset autosomal dominant leucodystrophy (en) View

2899695010
en
Synonym (core metadata concept)
Adult onset autosomal dominant leucodystrophy
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

2899696011 - Adult onset autosomal dominant leukodystrophy (en) View

2899696011
en
Synonym (core metadata concept)
Adult onset autosomal dominant leukodystrophy
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

2898387014 - Adult onset autosomal dominant leukodystrophy (disorder) (en) View

2898387014
en
Fully specified name (core metadata concept)
Adult onset autosomal dominant leukodystrophy (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (3819222028) - 448054001 -> 41847000 (246454002) View

246454002 |Occurrence (attribute)|
41847000 |Adulthood (qualifier value)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (9464606021) - 448054001 -> 363235000 (116680003) View

116680003 |Is a (attribute)|
363235000 |Hereditary disorder of nervous system (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (12089410020) - 448054001 -> 41847000 (246454002) View

246454002 |Occurrence (attribute)|
41847000 |Adulthood (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (12089411024) - 448054001 -> 41847000 (246454002) View

246454002 |Occurrence (attribute)|
41847000 |Adulthood (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (12089412028) - 448054001 -> 106018006 (116680003) View

116680003 |Is a (attribute)|
106018006 |Hereditary degenerative disease of central nervous system (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (3819223022) - 448054001 -> 4720007 (116676008) View

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

Relationship (3824084022) - 448054001 -> 25087005 (363698007) View

363698007 |Finding site (attribute)|
25087005 |Structure of nervous system (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (6164780024) - 448054001 -> 4720007 (116676008) View

116676008 |Associated morphology (attribute)|
4720007 |Dystrophy (morphologic abnormality)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9464607028) - 448054001 -> 54115001 (363698007) View

363698007 |Finding site (attribute)|
54115001 |Myelinated nerve fiber structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9464608022) - 448054001 -> 389080008 (363698007) View

363698007 |Finding site (attribute)|
389080008 |White matter structure of brain and spinal cord (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (3812911021) - 448054001 -> 11164009 (116680003) View

116680003 |Is a (attribute)|
11164009 |Autosomal dominant hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (3812912025) - 448054001 -> 192781003 (116680003) View

116680003 |Is a (attribute)|
192781003 |Leukodystrophy (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (3824083027) - 448054001 -> 125495003 (116676008) View

116676008 |Associated morphology (attribute)|
125495003 |Myelin sheath alteration (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

106018006 View

106018006
Hereditary degenerative disease of central nervous system (disorder)
Hereditary degenerative disease of central nervous system
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

11164009 View

11164009
Autosomal dominant hereditary disorder (disorder)
Ad - autosomal dominant
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

192781003 View

192781003
Leukodystrophy (disorder)
Leucodystrophy
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (86c31929-647d-5a5f-9d2a-b507d75bb841) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
E75.2
TRUE
ALWAYS E75.2
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)|
esc