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Terminology chevron_right Concepts chevron_right 38776003

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Component

38776003

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital absence of skeletal muscle (disorder)

Shortest Term

Congenital absence of skeletal muscle

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 absence of skeletal muscle (disorder)

SCTID: 38776003, Defined, Active

38776003|Congenital absence of skeletal muscle (disorder)|

en Congenital absence of skeletal muscle
en Congenital absence of skeletal muscle (disorder)

Expression

38776003 |Congenital absence of skeletal muscle (disorder)|
 === 89886004 |Congenital anomaly of skeletal muscle (disorder)| + 
47880003 |Congenital absence of muscle and/or tendon (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 418560003 |Absence (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 127954009 |Skeletal muscle structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
64536012 - Congenital absence of skeletal muscle (en) View
64536012	en	Synonym (core metadata concept)	Congenital absence of skeletal muscle	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
775102011 - Congenital absence of skeletal muscle (disorder) (en) View
775102011	en	Fully specified name (core metadata concept)	Congenital absence of skeletal muscle (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
64537015 - Congenital absence of skeletal muscle, NOS (en) View
64537015	en	Synonym (core metadata concept)	Congenital absence of skeletal muscle, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (5925352026) - 38776003 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13186728020) - 38776003 -> 418560003 (116676008) View
116676008 \|Associated morphology (attribute)\|	418560003 \|Absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4982116027) - 38776003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4991563022) - 38776003 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5000956021) - 38776003 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5925353020) - 38776003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5925354025) - 38776003 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10516466026) - 38776003 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (768750025) - 38776003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2227609025) - 38776003 -> 276654001 (116680003) View
116680003 \|Is a (attribute)\|	276654001 \|Congenital malformation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3404386027) - 38776003 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3451430022) - 38776003 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5051617027) - 38776003 -> 47880003 (116680003) View
116680003 \|Is a (attribute)\|	47880003 \|Congenital absence of muscle and/or tendon (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (768749025) - 38776003 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2595248022) - 38776003 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (768748022) - 38776003 -> 79984008 (363698007) View
363698007 \|Finding site (attribute)\|	79984008 \|Skeletal muscle system structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2595247028) - 38776003 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (768751026) - 38776003 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (211016028) - 38776003 -> 89886004 (116680003) View
116680003 \|Is a (attribute)\|	89886004 \|Congenital anomaly of skeletal muscle (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
47880003 View
47880003	Congenital absence of muscle and/or tendon (disorder)	Congenital absence of muscle and tendon	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
89886004 View
89886004	Congenital anomaly of skeletal muscle (disorder)	Congenital anomaly of skeletal muscle	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1144579005 View
1144579005	Aplasia of muscle of abdominal wall (disorder)	Aplasia of muscle of abdominal wall	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1144580008 View
1144580008	Aplasia of muscle of pelvis (disorder)	Aplasia of muscle of pelvis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1145378009 View
1145378009	Aplasia of muscle of limb (disorder)	Aplasia of muscle of limb	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
771261002 View
771261002	Digital extensor muscle aplasia with polyneuropathy (disorder)	Hamanishi ueba tsuji syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
432993002 View
432993002	Congenital absence of quadriceps muscle (disorder)	Congenital absence of quadriceps muscle	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
42190000 View
42190000	Congenital absence of abdominal muscle (disorder)	Congenital absence of abdominal muscle	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
27262009 View
27262009	Congenital absence of pectoral muscle (disorder)	Congenital absence of pectoral muscle	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
72424001 View
72424001	Congenital absence of diaphragm (disorder)	Aplasia of diaphragm	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (f54fcdde-b8b2-536b-9be6-f48143ed95bd) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q79.8	TRUE	ALWAYS Q79.8	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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