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Terminology chevron_right Concepts chevron_right 722763000

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722763000
The component that hold information about this concept.
Infantile dystonia parkinsonism (disorder)
Infantile dystonia parkinsonism
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

Infantile dystonia parkinsonism (disorder)

SCTID: 722763000, Primitive, Active


722763000|Infantile dystonia parkinsonism (disorder)|
  • en Dopamine transporter deficiency syndrome
  • en Infantile dystonia parkinsonism
  • en Infantile dystonia parkinsonism (disorder)
  • en Parkinsonism-dystonia infantile

722763000 |Infantile dystonia parkinsonism (disorder)|

<<< 15802004 |Dystonia (disorder)| +
    32798002 |Parkinsonism (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| +
    363235000 |Hereditary disorder of nervous system (disorder)| :
        { 363698007 |Finding site (attribute)| = 32610002 |Basal ganglion structure (body structure)|,
          246454002 |Occurrence (attribute)| = 3658006 |Infancy (qualifier value)| }
        { 363713009 |Has interpretation (attribute)| = 255361000 |Slow (qualifier value)|,
          363714003 |Interprets (attribute)| = 363847004 |Movement observable (observable entity)| }
Active

3333388012 - Dopamine transporter deficiency syndrome (en) View

3333388012
en
Synonym (core metadata concept)
Dopamine transporter deficiency syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3333389016 - Infantile dystonia parkinsonism (en) View

3333389016
en
Synonym (core metadata concept)
Infantile dystonia parkinsonism
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

3333387019 - Infantile dystonia parkinsonism (disorder) (en) View

3333387019
en
Fully specified name (core metadata concept)
Infantile dystonia parkinsonism (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3333390013 - Parkinsonism-dystonia infantile (en) View

3333390013
en
Synonym (core metadata concept)
Parkinsonism-dystonia infantile
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

Relationship (13882590027) - 722763000 -> 255324009 (363714003) View

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

Relationship (13882591028) - 722763000 -> 255361000 (363713009) View

363713009 |Has interpretation (attribute)|
255361000 |Slow (qualifier value)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (16350716024) - 722763000 -> 363847004 (363714003) View

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

Relationship (16350717026) - 722763000 -> 255361000 (363713009) View

363713009 |Has interpretation (attribute)|
255361000 |Slow (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6792010023) - 722763000 -> 15802004 (116680003) View

116680003 |Is a (attribute)|
15802004 |Dystonia (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6792011022) - 722763000 -> 32798002 (116680003) View

116680003 |Is a (attribute)|
32798002 |Parkinsonism (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6792012026) - 722763000 -> 85995004 (116680003) View

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

Relationship (6792013020) - 722763000 -> 363235000 (116680003) View

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

Relationship (6792014025) - 722763000 -> 3658006 (246454002) View

246454002 |Occurrence (attribute)|
3658006 |Infancy (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6792015029) - 722763000 -> 32610002 (363698007) View

363698007 |Finding site (attribute)|
32610002 |Basal ganglion structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

15802004 View

15802004
Dystonia (disorder)
Dystonia
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

32798002 View

32798002
Parkinsonism (disorder)
Parkinsonism
900000000000074008 |Necessary but not sufficient concept 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 (2479ddc1-40df-5344-9ad7-52c241a2e8be) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
G24.8
TRUE
ALWAYS G24.8 | 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