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Terminology chevron_right Concepts chevron_right 733093004

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Component

733093004

The component that hold information about this concept.

Fully Specified Name (FSN)

Banki syndrome (disorder)

Shortest Term

Banki 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

Banki syndrome (disorder)

SCTID: 733093004, Primitive, Active

733093004|Banki syndrome (disorder)|

en Banki syndrome
en Banki syndrome (disorder)

Expression

733093004 |Banki syndrome (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
41443008 |Multiple malformation syndrome with limb defect as major feature (disorder)| + 
95463009 |Congenital anomaly of joint (disorder)| + 
298149009 |Lesion of joint (disorder)| + 
363039000 |Congenital connective tissue disorder (disorder)| + 
363045008 |Connective tissue hereditary disorder (disorder)| + 
363212003 |Hereditary disorder of musculoskeletal system (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| + 
1335755001 |Disorder of ligament of joint of hand (disorder)| + 
239972001 |Soft tissue lesion of wrist and hand (disorder)| + 
174131000112101 |Disorder of ligament of wrist joint (disorder)| + 
34111000 |Congenital anomaly of hand (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 1297033003 |Abnormally fused structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 182412004 |Lunotriquetral ligament (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
3498737013 - Banki syndrome (en) View
3498737013	en	Synonym (core metadata concept)	Banki syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
3498736016 - Banki syndrome (disorder) (en) View
3498736016	en	Fully specified name (core metadata concept)	Banki syndrome (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6994297025) - 733093004 -> 428107009 (116680003) View
116680003 \|Is a (attribute)\|	428107009 \|Disorder of wrist joint (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16326651028) - 733093004 -> 174131000112101 (116680003) View
116680003 \|Is a (attribute)\|	174131000112101 \|Disorder of ligament of wrist joint (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6994292020) - 733093004 -> 239953001 (116680003) View
116680003 \|Is a (attribute)\|	239953001 \|Lesion of soft tissue (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16238844023) - 733093004 -> 239972001 (116680003) View
116680003 \|Is a (attribute)\|	239972001 \|Soft tissue lesion of wrist and hand (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6994289021) - 733093004 -> 60492000 (116680003) View
116680003 \|Is a (attribute)\|	60492000 \|Disorder of ligament (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7195847021) - 733093004 -> 280135003 (116680003) View
116680003 \|Is a (attribute)\|	280135003 \|Disorder of soft tissue of upper limb (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11176799026) - 733093004 -> 428360003 (116680003) View
116680003 \|Is a (attribute)\|	428360003 \|Arthropathy of joint of hand (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16013967026) - 733093004 -> 1335755001 (116680003) View
116680003 \|Is a (attribute)\|	1335755001 \|Disorder of ligament of joint of hand (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6994298024) - 733093004 -> 37764001 (116676008) View
116676008 \|Associated morphology (attribute)\|	37764001 \|Congenital abnormal fusion (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15840392026) - 733093004 -> 1297033003 (116676008) View
116676008 \|Associated morphology (attribute)\|	1297033003 \|Abnormally fused structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13069557027) - 733093004 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6994290028) - 733093004 -> 66510004 (116680003) View
116680003 \|Is a (attribute)\|	66510004 \|Congenital anomaly of upper limb (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10530592022) - 733093004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11176800027) - 733093004 -> 34111000 (116680003) View
116680003 \|Is a (attribute)\|	34111000 \|Congenital anomaly of hand (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6994287023) - 733093004 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6994288029) - 733093004 -> 41443008 (116680003) View
116680003 \|Is a (attribute)\|	41443008 \|Multiple malformation syndrome with limb defect as major feature (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6994291029) - 733093004 -> 95463009 (116680003) View
116680003 \|Is a (attribute)\|	95463009 \|Congenital anomaly of joint (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6994293026) - 733093004 -> 298149009 (116680003) View
116680003 \|Is a (attribute)\|	298149009 \|Lesion of joint (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6994294021) - 733093004 -> 363039000 (116680003) View
116680003 \|Is a (attribute)\|	363039000 \|Congenital connective tissue disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6994295022) - 733093004 -> 363045008 (116680003) View
116680003 \|Is a (attribute)\|	363045008 \|Connective tissue hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6994296023) - 733093004 -> 363212003 (116680003) View
116680003 \|Is a (attribute)\|	363212003 \|Hereditary disorder of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6994299027) - 733093004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6994300024) - 733093004 -> 182412004 (363698007) View
363698007 \|Finding site (attribute)\|	182412004 \|Lunotriquetral ligament (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
174131000112101 View
174131000112101	Disorder of ligament of wrist joint (disorder)	Disorder of ligament of wrist joint	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1335755001 View
1335755001	Disorder of ligament of joint of hand (disorder)	Disorder of ligament of hand	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
239972001 View
239972001	Soft tissue lesion of wrist and hand (disorder)	Soft tissue lesion of wrist and hand	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363070008 View
363070008	Developmental hereditary disorder (disorder)	Developmental hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
298149009 View
298149009	Lesion of joint (disorder)	Lesion of joint	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363039000 View
363039000	Congenital connective tissue disorder (disorder)	Congenital connective tissue disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363045008 View
363045008	Connective tissue hereditary disorder (disorder)	Connective tissue hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
11164009 View
11164009	Autosomal dominant hereditary disorder (disorder)	Ad - autosomal dominant	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
34111000 View
34111000	Congenital anomaly of hand (disorder)	Congenital anomaly of hand	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
41443008 View
41443008	Multiple malformation syndrome with limb defect as major feature (disorder)	Multiple malformation syndrome with limb defect as major feature	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
95463009 View
95463009	Congenital anomaly of joint (disorder)	Congenital anomaly of joint	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 (2baa50c4-f0df-5fc4-af04-57311fde9929) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q68.1	TRUE	ALWAYS Q68.1 \| 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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