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Terminology chevron_right Concepts chevron_right 699267007

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Component

699267007

The component that hold information about this concept.

Fully Specified Name (FSN)

Myosin storage myopathy (disorder)

Shortest Term

Hyaline body myopathy

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

Myosin storage myopathy (disorder)

SCTID: 699267007, Primitive, Active

699267007|Myosin storage myopathy (disorder)|

en Hyaline body myopathy
en Myosin storage myopathy
en Myosin storage myopathy (disorder)

Expression

699267007 |Myosin storage myopathy (disorder)|
 <<< 75047002 |Disorder of skeletal muscle (disorder)| + 
1899006 |Autosomal hereditary disorder (disorder)| + 
26544005 |Muscle weakness (finding)| + 
363212003 |Hereditary disorder of musculoskeletal system (disorder)| : 
        { 363698007 |Finding site (attribute)| = 127954009 |Skeletal muscle structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
2983413018 - Autosomal dominant hyaline body myopathy (en) View
2983413018	en	Synonym (core metadata concept)	Autosomal dominant hyaline body myopathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	False
5170018018 - Hyaline body myopathy (en) View
5170018018	en	Synonym (core metadata concept)	Hyaline body myopathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
2983446012 - Myosin storage myopathy (en) View
2983446012	en	Synonym (core metadata concept)	Myosin storage myopathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2983424016 - Myosin storage myopathy (disorder) (en) View
2983424016	en	Fully specified name (core metadata concept)	Myosin storage myopathy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15500175028) - 699267007 -> 1899006 (116680003) View
116680003 \|Is a (attribute)\|	1899006 \|Autosomal hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15500176027) - 699267007 -> 26544005 (116680003) View
116680003 \|Is a (attribute)\|	26544005 \|Muscle weakness (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15500177020) - 699267007 -> 363212003 (116680003) View
116680003 \|Is a (attribute)\|	363212003 \|Hereditary disorder of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4775496022) - 699267007 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4775495021) - 699267007 -> 75047002 (116680003) View
116680003 \|Is a (attribute)\|	75047002 \|Disorder of skeletal muscle (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1899006 View
1899006	Autosomal hereditary disorder (disorder)	Autosomal hereditary disorder	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
26544005 View
26544005	Muscle weakness (finding)	Yếu cơ	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
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

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 (0e218b50-fc82-5a23-b685-4e63b8cca5ff) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G71.2	TRUE	ALWAYS G71.2	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 (51bb44d2-8b59-5317-a317-adf6951f3beb) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G71.8	TRUE	ALWAYS G71.8	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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