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Terminology chevron_right Concepts chevron_right 1186861004

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1186861004
The component that hold information about this concept.
Classical pantothenate kinase associated neurodegeneration (disorder)
Classical pantothenate kinase associated neurodegeneration
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

Classical pantothenate kinase associated neurodegeneration (disorder)

SCTID: 1186861004, Primitive, Active


1186861004|Classical pantothenate kinase associated neurodegeneration (disorder)|
  • en Classical pantothenate kinase associated neurodegeneration
  • en Classical pantothenate kinase associated neurodegeneration (disorder)

1186861004 |Classical pantothenate kinase associated neurodegeneration (disorder)|

<<< 106018006 |Hereditary degenerative disease of central nervous system (disorder)| +
    2992000 |Pigmentary pallidal degeneration (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 40299004 |Pigmentary degeneration (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 14738005 |Globus pallidus structure (body structure)| }
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
          363714003 |Interprets (attribute)| = 363847004 |Movement observable (observable entity)| }
Active

4667855017 - Classical pantothenate kinase associated neurodegeneration (en) View

4667855017
en
Synonym (core metadata concept)
Classical pantothenate kinase associated neurodegeneration
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

4667856016 - Classical pantothenate kinase associated neurodegeneration (disorder) (en) View

4667856016
en
Fully specified name (core metadata concept)
Classical pantothenate kinase associated neurodegeneration (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (15512999029) - 1186861004 -> 255324009 (363714003) View

363714003 |Interprets (attribute)|
255324009 |Movement (observable entity)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (14957549020) - 1186861004 -> 255324009 (363714003) View

363714003 |Interprets (attribute)|
255324009 |Movement (observable entity)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (15502059024) - 1186861004 -> 263654008 (363713009) View

363713009 |Has interpretation (attribute)|
263654008 |Abnormal (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15513000028) - 1186861004 -> 363847004 (363714003) View

363714003 |Interprets (attribute)|
363847004 |Movement observable (observable entity)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (14957546029) - 1186861004 -> 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 (14957547022) - 1186861004 -> 2992000 (116680003) View

116680003 |Is a (attribute)|
2992000 |Pigmentary pallidal degeneration (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (14957548028) - 1186861004 -> 85995004 (116680003) View

116680003 |Is a (attribute)|
85995004 |Autosomal recessive hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (14957550020) - 1186861004 -> 14738005 (363698007) View

363698007 |Finding site (attribute)|
14738005 |Globus pallidus structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (14957551024) - 1186861004 -> 40299004 (116676008) View

116676008 |Associated morphology (attribute)|
40299004 |Pigmentary degeneration (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

2992000 View

2992000
Pigmentary pallidal degeneration (disorder)
Hallervorden-spatz disease
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

85995004 View

85995004
Autosomal recessive hereditary disorder (disorder)
Hereditary disorder trait, nos
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (d2529d8c-3244-5ab6-9585-bd10c63f3fd8) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
G23.0
TRUE
ALWAYS G23.0
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)|
esc