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Terminology chevron_right Concepts chevron_right 784352007

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Component

784352007

The component that hold information about this concept.

Fully Specified Name (FSN)

X-linked scapuloperoneal muscular dystrophy (disorder)

Shortest Term

X-linked scapuloperoneal 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 scapuloperoneal muscular dystrophy (disorder)

SCTID: 784352007, Primitive, Active

784352007|X-linked scapuloperoneal muscular dystrophy (disorder)|

en X-linked scapuloperoneal muscular dystrophy
en X-linked scapuloperoneal muscular dystrophy (disorder)
en X-linked scapuloperoneal syndrome

Expression

784352007 |X-linked scapuloperoneal muscular dystrophy (disorder)|
 <<< 193225000 |Hereditary progressive muscular dystrophy (disorder)| + 
129620000 |Scapuloperoneal muscular dystrophy (disorder)| + 
1162984000 |X-linked dominant hereditary disease (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 127954009 |Skeletal muscle structure (body structure)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 263502005 |Clinical course (attribute)| = 255314001 |Progressive (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3763743012 - X-linked scapuloperoneal muscular dystrophy (en) View
3763743012	en	Synonym (core metadata concept)	X-linked scapuloperoneal muscular dystrophy	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
3763742019 - X-linked scapuloperoneal muscular dystrophy (disorder) (en) View
3763742019	en	Fully specified name (core metadata concept)	X-linked scapuloperoneal muscular dystrophy (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
3763744018 - X-linked scapuloperoneal syndrome (en) View
3763744018	en	Synonym (core metadata concept)	X-linked scapuloperoneal syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (11373160024) - 784352007 -> 128430005 (116680003) View
116680003 \|Is a (attribute)\|	128430005 \|X-linked hereditary disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13952157026) - 784352007 -> 1162984000 (116680003) View
116680003 \|Is a (attribute)\|	1162984000 \|X-linked dominant hereditary disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11373155020) - 784352007 -> 193225000 (116680003) View
116680003 \|Is a (attribute)\|	193225000 \|Hereditary progressive muscular dystrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11373156021) - 784352007 -> 129620000 (116680003) View
116680003 \|Is a (attribute)\|	129620000 \|Scapuloperoneal muscular dystrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11373157028) - 784352007 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11373158022) - 784352007 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11373159025) - 784352007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11572669020) - 784352007 -> 255314001 (263502005) View
263502005 \|Clinical course (attribute)\|	255314001 \|Progressive (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1162984000 View
1162984000	X-linked dominant hereditary disease (disorder)	X-linked dominant hereditary disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
193225000 View
193225000	Hereditary progressive muscular dystrophy (disorder)	Hereditary progressive muscular dystrophy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
129620000 View
129620000	Scapuloperoneal muscular dystrophy (disorder)	Emery-dreifuss muscular dystrophy	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 (0e94ca3a-3300-5c39-9ffe-126e3acdb1c6) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G71.0	TRUE	ALWAYS G71.0 \| 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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