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Terminology chevron_right Concepts chevron_right 770757004

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Component

770757004

The component that hold information about this concept.

Fully Specified Name (FSN)

X-linked parkinsonism with spasticity syndrome (disorder)

Shortest Term

X-linked parkinsonism with spasticity syndrome

Definition Status

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

Summary

X-linked parkinsonism with spasticity syndrome (disorder)

SCTID: 770757004, Primitive, Active

770757004|X-linked parkinsonism with spasticity syndrome (disorder)|

en X-linked parkinsonism with spasticity syndrome
en X-linked parkinsonism with spasticity syndrome (disorder)
en Xpds - x-linked parkinsonism with spasticity syndrome

Expression

770757004 |X-linked parkinsonism with spasticity syndrome (disorder)|
 <<< 363212003 |Hereditary disorder of musculoskeletal system (disorder)| + 
363235000 |Hereditary disorder of nervous system (disorder)| + 
75047002 |Disorder of skeletal muscle (disorder)| + 
32798002 |Parkinsonism (disorder)| + 
221360009 |Spasticity (finding)| + 
1162976004 |X-linked recessive hereditary disease (disorder)| : 
        { 363713009 |Has interpretation (attribute)| = 35105006 |Increased (qualifier value)|,
363714003 |Interprets (attribute)| = 6918002 |Muscle tone (observable entity)| }
        { 363698007 |Finding site (attribute)| = 127954009 |Skeletal muscle structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 32610002 |Basal ganglion structure (body structure)| }
        { 363713009 |Has interpretation (attribute)| = 255361000 |Slow (qualifier value)|,
363714003 |Interprets (attribute)| = 363847004 |Movement observable (observable entity)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3702479016 - X-linked parkinsonism with spasticity syndrome (en) View
3702479016	en	Synonym (core metadata concept)	X-linked parkinsonism with spasticity syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
3702478012 - X-linked parkinsonism with spasticity syndrome (disorder) (en) View
3702478012	en	Fully specified name (core metadata concept)	X-linked parkinsonism with spasticity syndrome (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
3702480018 - XPDS - X-linked parkinsonism with spasticity syndrome (en) View
3702480018	en	Synonym (core metadata concept)	XPDS - X-linked parkinsonism with spasticity syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13882570020) - 770757004 -> 255324009 (363714003) View
363714003 \|Interprets (attribute)\|	255324009 \|Movement (observable entity)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13882571024) - 770757004 -> 255361000 (363713009) View
363713009 \|Has interpretation (attribute)\|	255361000 \|Slow (qualifier value)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16350676022) - 770757004 -> 363847004 (363714003) View
363714003 \|Interprets (attribute)\|	363847004 \|Movement observable (observable entity)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16350677029) - 770757004 -> 255361000 (363713009) View
363713009 \|Has interpretation (attribute)\|	255361000 \|Slow (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9635573028) - 770757004 -> 128430005 (116680003) View
116680003 \|Is a (attribute)\|	128430005 \|X-linked hereditary disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13952149029) - 770757004 -> 1162976004 (116680003) View
116680003 \|Is a (attribute)\|	1162976004 \|X-linked recessive hereditary disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9635577027) - 770757004 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9635580026) - 770757004 -> 32610002 (363698007) View
363698007 \|Finding site (attribute)\|	32610002 \|Basal ganglion structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9635571026) - 770757004 -> 363212003 (116680003) View
116680003 \|Is a (attribute)\|	363212003 \|Hereditary disorder of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9635572022) - 770757004 -> 35105006 (363713009) View
363713009 \|Has interpretation (attribute)\|	35105006 \|Increased (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9635574023) - 770757004 -> 6918002 (363714003) View
363714003 \|Interprets (attribute)\|	6918002 \|Muscle tone (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9635575024) - 770757004 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9635576020) - 770757004 -> 75047002 (116680003) View
116680003 \|Is a (attribute)\|	75047002 \|Disorder of skeletal muscle (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9635578021) - 770757004 -> 32798002 (116680003) View
116680003 \|Is a (attribute)\|	32798002 \|Parkinsonism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9635579029) - 770757004 -> 221360009 (116680003) View
116680003 \|Is a (attribute)\|	221360009 \|Spasticity (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
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
32798002 View
32798002	Parkinsonism (disorder)	Parkinsonism	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
75047002 View
75047002	Disorder of skeletal muscle (disorder)	Disorder of muscle	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
221360009 View
221360009	Spasticity (finding)	Co cứng	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363212003 View
363212003	Hereditary disorder of musculoskeletal system (disorder)	Hereditary disorder of musculoskeletal system	900000000000073002 \|Sufficiently defined by necessary conditions 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

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (b2a4daf5-01d3-5cf7-9343-43fbf26af380) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G20	TRUE	ALWAYS G20 \| 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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