Loading...
dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 718849008

Production
add
718849008
The component that hold information about this concept.
X-linked neurodegenerative syndrome bertini type (disorder)
X-linked neurodegenerative syndrome bertini type
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

X-linked neurodegenerative syndrome bertini type (disorder)

SCTID: 718849008, Primitive, Active


718849008|X-linked neurodegenerative syndrome bertini type (disorder)|
  • en X-linked neurodegenerative syndrome bertini type
  • en X-linked neurodegenerative syndrome bertini type (disorder)

718849008 |X-linked neurodegenerative syndrome bertini type (disorder)|

<<< 1162976004 |X-linked recessive hereditary disease (disorder)| +
    362975008 |Degenerative disorder (disorder)| +
    66091009 |Congenital disease (disorder)| +
    763597000 |Hereditary ataxia (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 107669003 |Degenerative abnormality (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 25087005 |Structure of nervous system (body structure)| }
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
Active

3314127014 - X-linked neurodegenerative syndrome Bertini type (en) View

3314127014
en
Synonym (core metadata concept)
X-linked neurodegenerative syndrome Bertini type
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
True

3314126017 - X-linked neurodegenerative syndrome Bertini type (disorder) (en) View

3314126017
en
Fully specified name (core metadata concept)
X-linked neurodegenerative syndrome Bertini type (disorder)
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
True

Relationship (6619036021) - 718849008 -> 128430005 (116680003) View

116680003 |Is a (attribute)|
128430005 |X-linked hereditary disease (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (6619038022) - 718849008 -> 363235000 (116680003) View

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

Relationship (14023192027) - 718849008 -> 1162976004 (116680003) View

116680003 |Is a (attribute)|
1162976004 |X-linked recessive hereditary disease (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (14023193021) - 718849008 -> 66091009 (116680003) View

116680003 |Is a (attribute)|
66091009 |Congenital disease (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (14023194026) - 718849008 -> 763597000 (116680003) View

116680003 |Is a (attribute)|
763597000 |Hereditary ataxia (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (14023195025) - 718849008 -> 255399007 (246454002) View

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

Relationship (6619039025) - 718849008 -> 33359002 (116676008) View

116676008 |Associated morphology (attribute)|
33359002 |Degeneration (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (12090936025) - 718849008 -> 107669003 (116676008) View

116676008 |Associated morphology (attribute)|
107669003 |Degenerative abnormality (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6619037028) - 718849008 -> 362975008 (116680003) View

116680003 |Is a (attribute)|
362975008 |Degenerative disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6619040028) - 718849008 -> 25087005 (363698007) View

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

1162976004 View

1162976004
X-linked recessive hereditary disease (disorder)
X-linked recessive hereditary disease
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

763597000 View

763597000
Hereditary ataxia (disorder)
Hereditary ataxia
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

66091009 View

66091009
Congenital disease (disorder)
Congenital disease
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

362975008 View

362975008
Degenerative disorder (disorder)
Degenerative disorder
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (33ac348c-b13d-5ab1-9b9c-8a867075ba79) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
G31.8
TRUE
ALWAYS G31.8 | 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