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Terminology chevron_right Concepts chevron_right 230779009

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Language with ID “0b8a9d3d-bf80-5f95-936f-e431c0537844” doesn’t exist. Perhaps it was deleted?

Component

230779009

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital spastic foot (disorder)

Shortest Term

Congenital spastic foot

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Congenital spastic foot (disorder)

SCTID: 230779009, Defined, Active

230779009|Congenital spastic foot (disorder)|

en Congenital spastic foot
en Congenital spastic foot (disorder)

Expression

230779009 |Congenital spastic foot (disorder)|
 === 23853001 |Disorder of the central nervous system (disorder)| + 
66091009 |Congenital disease (disorder)| + 
75047002 |Disorder of skeletal muscle (disorder)| + 
280136002 |Disorder of soft tissue of lower limb (disorder)| + 
118932009 |Disorder of foot (disorder)| + 
5294002 |Developmental disorder (disorder)| + 
307324001 |Spastic foot (finding)| : 
        { 363698007 |Finding site (attribute)| = 21483005 |Structure of central nervous system (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 67240005 |Muscle structure of foot (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
345779013 - Congenital spastic foot (en) View
345779013	en	Synonym (core metadata concept)	Congenital spastic foot	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
618632019 - Congenital spastic foot (disorder) (en) View
618632019	en	Fully specified name (core metadata concept)	Congenital spastic foot (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (338455021) - 230779009 -> 230764002 (116680003) View
116680003 \|Is a (attribute)\|	230764002 \|Congenital and developmental anomalies of the nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2616825021) - 230779009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3337149025) - 230779009 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11301231020) - 230779009 -> 75047002 (116680003) View
116680003 \|Is a (attribute)\|	75047002 \|Disorder of skeletal muscle (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11301232029) - 230779009 -> 280136002 (116680003) View
116680003 \|Is a (attribute)\|	280136002 \|Disorder of soft tissue of lower limb (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11301234028) - 230779009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11301235027) - 230779009 -> 118932009 (116680003) View
116680003 \|Is a (attribute)\|	118932009 \|Disorder of foot (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11301236026) - 230779009 -> 5294002 (116680003) View
116680003 \|Is a (attribute)\|	5294002 \|Developmental disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11301237024) - 230779009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11301239022) - 230779009 -> 307324001 (116680003) View
116680003 \|Is a (attribute)\|	307324001 \|Spastic foot (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11573638028) - 230779009 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11573639020) - 230779009 -> 67240005 (363698007) View
363698007 \|Finding site (attribute)\|	67240005 \|Muscle structure of foot (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (994522025) - 230779009 -> 21483005 (363698007) View
363698007 \|Finding site (attribute)\|	21483005 \|Structure of central nervous system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2744275020) - 230779009 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3337150025) - 230779009 -> 21483005 (363698007) View
363698007 \|Finding site (attribute)\|	21483005 \|Structure of central nervous system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2792362021) - 230779009 -> 25087005 (363698007) View
363698007 \|Finding site (attribute)\|	25087005 \|Structure of nervous system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2774410027) - 230779009 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (338456022) - 230779009 -> 23853001 (116680003) View
116680003 \|Is a (attribute)\|	23853001 \|Disorder of the central nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
5294002 View
5294002	Developmental disorder (disorder)	Rối loạn phát triển	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
280136002 View
280136002	Disorder of soft tissue of lower limb (disorder)	Disorder of soft tissue of lower limb	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
23853001 View
23853001	Disorder of the central nervous system (disorder)	Encephalomyeloneuropathy	900000000000073002 \|Sufficiently defined by necessary conditions 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
118932009 View
118932009	Disorder of foot (disorder)	Disease of foot	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
307324001 View
307324001	Spastic foot (finding)	Spastic foot	900000000000074008 \|Necessary but not sufficient concept 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 (2e87ccc7-cb2a-53fa-a3b8-39207c8cba80) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q07.8	TRUE	ALWAYS Q07.8	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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