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Terminology chevron_right Concepts chevron_right 770722002

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  • Language with ID “bfc1237a-04dc-5d5a-a4c2-dd209be87768” doesn’t exist. Perhaps it was deleted?
770722002
The component that hold information about this concept.
Proximal myopathy with extrapyramidal signs (disorder)
Proximal myopathy with extrapyramidal signs
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

Proximal myopathy with extrapyramidal signs (disorder)

SCTID: 770722002, Primitive, Active


770722002|Proximal myopathy with extrapyramidal signs (disorder)|
  • en Proximal myopathy with extrapyramidal signs
  • en Proximal myopathy with extrapyramidal signs (disorder)

770722002 |Proximal myopathy with extrapyramidal signs (disorder)|

<<< 363235000 |Hereditary disorder of nervous system (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| +
    76349003 |Extrapyramidal disease (disorder)| +
    193255007 |Proximal myopathy (disorder)| +
    363212003 |Hereditary disorder of musculoskeletal system (disorder)| :
        { 363698007 |Finding site (attribute)| = 127954009 |Skeletal muscle structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 76375004 |Extrapyramidal system structure (body structure)| }
        { 363714003 |Interprets (attribute)| = 363847004 |Movement observable (observable entity)| }
Active

3702245015 - Proximal myopathy with extrapyramidal signs (en) View

3702245015
en
Synonym (core metadata concept)
Proximal myopathy with extrapyramidal signs
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3702246019 - Proximal myopathy with extrapyramidal signs (disorder) (en) View

3702246019
en
Fully specified name (core metadata concept)
Proximal myopathy with extrapyramidal signs (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (13882846025) - 770722002 -> 255324009 (363714003) View

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

Relationship (16350674020) - 770722002 -> 363847004 (363714003) View

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

Relationship (9635706021) - 770722002 -> 76375004 (363698007) View

363698007 |Finding site (attribute)|
76375004 |Extrapyramidal system structure (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9635709025) - 770722002 -> 127954009 (363698007) View

363698007 |Finding site (attribute)|
127954009 |Skeletal muscle structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9635707028) - 770722002 -> 85995004 (116680003) View

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

Relationship (9635708022) - 770722002 -> 76349003 (116680003) View

116680003 |Is a (attribute)|
76349003 |Extrapyramidal disease (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9635710024) - 770722002 -> 193255007 (116680003) View

116680003 |Is a (attribute)|
193255007 |Proximal myopathy (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9635711023) - 770722002 -> 363212003 (116680003) View

116680003 |Is a (attribute)|
363212003 |Hereditary disorder of musculoskeletal system (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9635712027) - 770722002 -> 363235000 (116680003) View

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

76349003 View

76349003
Extrapyramidal disease (disorder)
Bệnh ngoại tháp
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

193255007 View

193255007
Proximal myopathy (disorder)
Proximal myopathy
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

ExtendedMap object (17169278-9fc2-516f-b7ad-b41a688ffe44) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
G71.3
TRUE
ALWAYS G71.3 | 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)|

ExtendedMap object (abefffcb-07da-5836-a3d2-4e74f9cf64ba) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
G72.8
TRUE
ALWAYS G72.8 | 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)|
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