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Terminology chevron_right Concepts chevron_right 73856006

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Component

73856006

The component that hold information about this concept.

Fully Specified Name (FSN)

Cutis laxa with osteodystrophy (disorder)

Shortest Term

Cutis laxa with bone dystrophy

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

Cutis laxa with osteodystrophy (disorder)

SCTID: 73856006, Primitive, Active

73856006|Cutis laxa with osteodystrophy (disorder)|

en Cutis laxa with bone dystrophy
en Cutis laxa with osteodystrophy
en Cutis laxa with osteodystrophy (disorder)
en Cutis laxa with joint laxity and retarded development

Expression

73856006 |Cutis laxa with osteodystrophy (disorder)|
 <<< 58588007 |Cutis laxa (disorder)| + 
12010005 |Osteodystrophy (disorder)| + 
50279003 |Metabolic bone disease (disorder)| + 
312225001 |Musculoskeletal and connective tissue disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 272673000 |Bone structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 21793004 |Connective tissue structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 39937001 |Skin structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
122650011 - Cutis laxa with bone dystrophy (en) View
122650011	en	Synonym (core metadata concept)	Cutis laxa with bone dystrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
122648015 - Cutis laxa with osteodystrophy (en) View
122648015	en	Synonym (core metadata concept)	Cutis laxa with osteodystrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
814290010 - Cutis laxa with osteodystrophy (disorder) (en) View
814290010	en	Fully specified name (core metadata concept)	Cutis laxa with osteodystrophy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
122649011 - Cutis laxa with joint laxity and retarded development (en) View
122649011	en	Synonym (core metadata concept)	Cutis laxa with joint laxity and retarded development	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
122651010 - Cutis laxa with joint laxity AND retarded development (en) View
122651010	en	Synonym (core metadata concept)	Cutis laxa with joint laxity AND retarded development	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (858131024) - 73856006 -> 21793004 (363698007) View
363698007 \|Finding site (attribute)\|	21793004 \|Connective tissue structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4971509029) - 73856006 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11174608023) - 73856006 -> 312225001 (116680003) View
116680003 \|Is a (attribute)\|	312225001 \|Musculoskeletal and connective tissue disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (858132028) - 73856006 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3003812024) - 73856006 -> 362975008 (116680003) View
116680003 \|Is a (attribute)\|	362975008 \|Degenerative disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3566994027) - 73856006 -> 95324001 (116680003) View
116680003 \|Is a (attribute)\|	95324001 \|Skin lesion (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3654689027) - 73856006 -> 43451003 (116676008) View
116676008 \|Associated morphology (attribute)\|	43451003 \|Congenital deficiency (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (858128023) - 73856006 -> 272673000 (363698007) View
363698007 \|Finding site (attribute)\|	272673000 \|Bone structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (858130020) - 73856006 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3354910027) - 73856006 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3354911028) - 73856006 -> 272673000 (363698007) View
363698007 \|Finding site (attribute)\|	272673000 \|Bone structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3617067021) - 73856006 -> 43451003 (116676008) View
116676008 \|Associated morphology (attribute)\|	43451003 \|Congenital deficiency (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3617068027) - 73856006 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (858126022) - 73856006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1681683023) - 73856006 -> 363212003 (116680003) View
116680003 \|Is a (attribute)\|	363212003 \|Hereditary disorder of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (858127029) - 73856006 -> 113192009 (363698007) View
363698007 \|Finding site (attribute)\|	113192009 \|Skeletal system structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2041569020) - 73856006 -> 50279003 (116680003) View
116680003 \|Is a (attribute)\|	50279003 \|Metabolic bone disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (268163020) - 73856006 -> 8447006 (116680003) View
116680003 \|Is a (attribute)\|	8447006 \|Congenital anomaly of skeletal bone (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (858129026) - 73856006 -> 181769001 (363698007) View
363698007 \|Finding site (attribute)\|	181769001 \|Connective tissue (substance)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (268161022) - 73856006 -> 58588007 (116680003) View
116680003 \|Is a (attribute)\|	58588007 \|Cutis laxa (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (268162026) - 73856006 -> 12010005 (116680003) View
116680003 \|Is a (attribute)\|	12010005 \|Osteodystrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
12010005 View
12010005	Osteodystrophy (disorder)	Osteodystrophy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
312225001 View
312225001	Musculoskeletal and connective tissue disorder (disorder)	Musculoskeletal and connective tissue disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
50279003 View
50279003	Metabolic bone disease (disorder)	Metabolic bone disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
58588007 View
58588007	Cutis laxa (disorder)	Cutis laxa	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 (00fa8cd0-8f0a-54bb-919b-ddfc8f296970) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q82.8	TRUE	ALWAYS Q82.8	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)\|
ExtendedMap object (33063e6a-f9bd-5792-b93e-77acefeb327a) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q78.9	TRUE	ALWAYS Q78.9	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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