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Terminology chevron_right Concepts chevron_right 205532005

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Component

205532005

The component that hold information about this concept.

Fully Specified Name (FSN)

Aplasia of muscle (disorder)

Shortest Term

Absent 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

Aplasia of muscle (disorder)

SCTID: 205532005, Defined, Active

205532005|Aplasia of muscle (disorder)|

en Absent muscle
en Aplasia of muscle
en Aplasia of muscle (disorder)
en Orbinsky syndrome

Expression

205532005 |Aplasia of muscle (disorder)|
 === 73573004 |Congenital anomaly of musculoskeletal system (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 45486003 |Aplasia (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 79984008 |Skeletal muscle system 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
315188019 - Absent muscle (en) View
315188019	en	Synonym (core metadata concept)	Absent muscle	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
315186015 - Aplasia of muscle (en) View
315186015	en	Synonym (core metadata concept)	Aplasia of muscle	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
590914010 - Aplasia of muscle (disorder) (en) View
590914010	en	Fully specified name (core metadata concept)	Aplasia of muscle (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
315187012 - Orbinsky syndrome (en) View
315187012	en	Synonym (core metadata concept)	Orbinsky syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (470244028) - 205532005 -> 79984008 (363698007) View
363698007 \|Finding site (attribute)\|	79984008 \|Skeletal muscle system structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3549984028) - 205532005 -> 26107004 (363698007) View
363698007 \|Finding site (attribute)\|	26107004 \|Structure of musculoskeletal system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4980387026) - 205532005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5000584022) - 205532005 -> 79191007 (116680003) View
116680003 \|Is a (attribute)\|	79191007 \|Congenital anomaly of muscle and/or tendon (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6184804029) - 205532005 -> 699997005 (363698007) View
363698007 \|Finding site (attribute)\|	699997005 \|Skeletal muscle and/or tendon structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10533898027) - 205532005 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10533901026) - 205532005 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12921163023) - 205532005 -> 73573004 (116680003) View
116680003 \|Is a (attribute)\|	73573004 \|Congenital anomaly of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4980389028) - 205532005 -> 26107004 (363698007) View
363698007 \|Finding site (attribute)\|	26107004 \|Structure of musculoskeletal system (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5000585023) - 205532005 -> 45486003 (116676008) View
116676008 \|Associated morphology (attribute)\|	45486003 \|Aplasia (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5051604025) - 205532005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5051605029) - 205532005 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5051606028) - 205532005 -> 699997005 (363698007) View
363698007 \|Finding site (attribute)\|	699997005 \|Skeletal muscle and/or tendon structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10533899024) - 205532005 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10533900025) - 205532005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10533902022) - 205532005 -> 45486003 (116676008) View
116676008 \|Associated morphology (attribute)\|	45486003 \|Aplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (23819028) - 205532005 -> 47880003 (116680003) View
116680003 \|Is a (attribute)\|	47880003 \|Congenital absence of muscle and/or tendon (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (470246026) - 205532005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3527564022) - 205532005 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3385534026) - 205532005 -> 26107004 (363698007) View
363698007 \|Finding site (attribute)\|	26107004 \|Structure of musculoskeletal system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3476326022) - 205532005 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (470243023) - 205532005 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (470245027) - 205532005 -> 13024002 (363698007) View
363698007 \|Finding site (attribute)\|	13024002 \|Tendon structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2694109024) - 205532005 -> 271018002 (116680003) View
116680003 \|Is a (attribute)\|	271018002 \|Congenital absence of tendon (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
73573004 View
73573004	Congenital anomaly of musculoskeletal system (disorder)	Congenital musculoskeletal abnormality	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
1144581007 View
1144581007	Aplasia of pectoral muscle (disorder)	Aplasia of pectoral muscle	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
702613006 View
702613006	Aplasia 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 (0c78c964-c5c8-5038-a9ab-36a64d33f21b) 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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