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Terminology chevron_right Concepts chevron_right 770939009

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770939009
The component that hold information about this concept.
Huntington disease-like 3 (disorder)
Huntington disease-like 3
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

Huntington disease-like 3 (disorder)

SCTID: 770939009, Primitive, Active


770939009|Huntington disease-like 3 (disorder)|
  • en Huntington disease-like 3
  • en Huntington disease-like 3 (disorder)

770939009 |Huntington disease-like 3 (disorder)|

<<< 78689005 |Chronic brain syndrome (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| +
    363235000 |Hereditary disorder of nervous system (disorder)| +
    702376003 |Huntington disease-like syndrome (disorder)| :
        { 263502005 |Clinical course (attribute)| = 255314001 |Progressive (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 32610002 |Basal ganglion structure (body structure)| }
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
          363714003 |Interprets (attribute)| = 363847004 |Movement observable (observable entity)| }
Active

3703531018 - Huntington disease-like 3 (en) View

3703531018
en
Synonym (core metadata concept)
Huntington disease-like 3
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
True

3703532013 - Huntington disease-like 3 (disorder) (en) View

3703532013
en
Fully specified name (core metadata concept)
Huntington disease-like 3 (disorder)
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
True

Relationship (15512971022) - 770939009 -> 255324009 (363714003) View

363714003 |Interprets (attribute)|
255324009 |Movement (observable entity)|
4
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (13882848029) - 770939009 -> 255324009 (363714003) View

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

Relationship (15502043024) - 770939009 -> 263654008 (363713009) View

363713009 |Has interpretation (attribute)|
263654008 |Abnormal (qualifier value)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15512972026) - 770939009 -> 363847004 (363714003) View

363714003 |Interprets (attribute)|
363847004 |Movement observable (observable entity)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9643752029) - 770939009 -> 255314001 (263502005) View

263502005 |Clinical course (attribute)|
255314001 |Progressive (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9643757024) - 770939009 -> 32610002 (363698007) View

363698007 |Finding site (attribute)|
32610002 |Basal ganglion structure (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9643753023) - 770939009 -> 85995004 (116680003) View

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

Relationship (9643754028) - 770939009 -> 363235000 (116680003) View

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

Relationship (9643755027) - 770939009 -> 702376003 (116680003) View

116680003 |Is a (attribute)|
702376003 |Huntington disease-like syndrome (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9643756026) - 770939009 -> 78689005 (116680003) View

116680003 |Is a (attribute)|
78689005 |Chronic brain syndrome (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

702376003 View

702376003
Huntington disease-like syndrome (disorder)
Huntington disease-like syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

78689005 View

78689005
Chronic brain syndrome (disorder)
Chronic brain syndrome
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

363235000 View

363235000
Hereditary disorder of nervous system (disorder)
Hereditary disorder of nervous system
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (e04d266a-462e-5606-91d3-71f07a535930) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
G10
TRUE
ALWAYS G10 | 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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