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Terminology chevron_right Concepts chevron_right 721069005

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Component

721069005

The component that hold information about this concept.

Fully Specified Name (FSN)

Short fifth metacarpal insulin resistance syndrome (disorder)

Shortest Term

Short fifth metacarpal insulin resistance 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

Short fifth metacarpal insulin resistance syndrome (disorder)

SCTID: 721069005, Primitive, Active

721069005|Short fifth metacarpal insulin resistance syndrome (disorder)|

en Short fifth metacarpal insulin resistance syndrome
en Short fifth metacarpal insulin resistance syndrome (disorder)

Expression

721069005 |Short fifth metacarpal insulin resistance syndrome (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
32339005 |Longitudinal deficiency of metacarpal bone (disorder)| + 
41443008 |Multiple malformation syndrome with limb defect as major feature (disorder)| + 
363212003 |Hereditary disorder of musculoskeletal system (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| + 
897274007 |Abnormally short fifth metacarpal (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 11182007 |Abnormally short growth (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 731681002 |Entire bone of fifth metacarpal (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
3323322016 - Short fifth metacarpal insulin resistance syndrome (en) View
3323322016	en	Synonym (core metadata concept)	Short fifth metacarpal insulin resistance syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3323320012 - Short fifth metacarpal insulin resistance syndrome (disorder) (en) View
3323320012	en	Fully specified name (core metadata concept)	Short fifth metacarpal insulin resistance syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16344874023) - 721069005 -> 897274007 (116680003) View
116680003 \|Is a (attribute)\|	897274007 \|Abnormally short fifth metacarpal (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6754151029) - 721069005 -> 263402008 (363698007) View
363698007 \|Finding site (attribute)\|	263402008 \|Entire fifth metacarpal (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13881767022) - 721069005 -> 731681002 (363698007) View
363698007 \|Finding site (attribute)\|	731681002 \|Entire bone of fifth metacarpal (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13069291027) - 721069005 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6754147026) - 721069005 -> 363045008 (116680003) View
116680003 \|Is a (attribute)\|	363045008 \|Connective tissue hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10518688026) - 721069005 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6754144022) - 721069005 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6754145023) - 721069005 -> 32339005 (116680003) View
116680003 \|Is a (attribute)\|	32339005 \|Longitudinal deficiency of metacarpal bone (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6754146024) - 721069005 -> 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 (6754148020) - 721069005 -> 363212003 (116680003) View
116680003 \|Is a (attribute)\|	363212003 \|Hereditary disorder of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6754149028) - 721069005 -> 11182007 (116676008) View
116676008 \|Associated morphology (attribute)\|	11182007 \|Abnormally short growth (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6754150028) - 721069005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
897274007 View
897274007	Abnormally short fifth metacarpal (disorder)	Shortened fifth metacarpal	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
32339005 View
32339005	Longitudinal deficiency of metacarpal bone (disorder)	Longitudinal deficiency of metacarpal bone	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
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
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 (7796566a-19cf-5891-855e-571aa516aea6) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E34.8	TRUE	ALWAYS E34.8 \| 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)\|
ExtendedMap object (dde7903e-5f20-5786-84a6-00fe7860550b) 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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