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Terminology chevron_right Concepts chevron_right 733452000

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733452000
The component that hold information about this concept.
Leukoencephalopathy, dystonia, motor neuropathy syndrome (disorder)
Leucoencephalopathy, dystonia, motor neuropathy syndrome
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

Leukoencephalopathy, dystonia, motor neuropathy syndrome (disorder)

SCTID: 733452000, Primitive, Active


733452000|Leukoencephalopathy, dystonia, motor neuropathy syndrome (disorder)|
  • en Leucoencephalopathy, dystonia, motor neuropathy syndrome
  • en Leukoencephalopathy, dystonia, motor neuropathy syndrome
  • en Leukoencephalopathy, dystonia, motor neuropathy syndrome (disorder)

733452000 |Leukoencephalopathy, dystonia, motor neuropathy syndrome (disorder)|

<<< 22811006 |Leukoencephalopathy (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| +
    238066006 |Loss of single peroxisomal function (disorder)| +
    128190004 |Inherited metabolic disorder of nervous system (disorder)| :
        { 363698007 |Finding site (attribute)| = 68523003 |Cerebral white matter structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
Active

3789578011 - Leucoencephalopathy, dystonia, motor neuropathy syndrome (en) View

3789578011
en
Synonym (core metadata concept)
Leucoencephalopathy, dystonia, motor neuropathy syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3499457015 - Leukoencephalopathy, dystonia, motor neuropathy syndrome (en) View

3499457015
en
Synonym (core metadata concept)
Leukoencephalopathy, dystonia, motor neuropathy syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3499458013 - Leukoencephalopathy, dystonia, motor neuropathy syndrome (disorder) (en) View

3499458013
en
Fully specified name (core metadata concept)
Leukoencephalopathy, dystonia, motor neuropathy syndrome (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (7001687022) - 733452000 -> 363235000 (116680003) View

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

Relationship (15120428024) - 733452000 -> 128190004 (116680003) View

116680003 |Is a (attribute)|
128190004 |Inherited metabolic disorder of nervous system (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (7001684026) - 733452000 -> 22811006 (116680003) View

116680003 |Is a (attribute)|
22811006 |Leukoencephalopathy (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (7001685025) - 733452000 -> 85995004 (116680003) View

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

Relationship (7001686029) - 733452000 -> 238066006 (116680003) View

116680003 |Is a (attribute)|
238066006 |Loss of single peroxisomal function (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (7001688028) - 733452000 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (7001689020) - 733452000 -> 68523003 (363698007) View

363698007 |Finding site (attribute)|
68523003 |Cerebral white matter structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

128190004 View

128190004
Inherited metabolic disorder of nervous system (disorder)
Inherited metabolic disorder of nervous system
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

22811006 View

22811006
Leukoencephalopathy (disorder)
Leucoencephalopathy
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

238066006 View

238066006
Loss of single peroxisomal function (disorder)
Loss of single peroxisomal function
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (3e400cfd-5c66-568c-902f-d12df04b2b01) View

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