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Terminology chevron_right Concepts chevron_right 722292000

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Component

722292000

The component that hold information about this concept.

Fully Specified Name (FSN)

Autosomal dominant beta2-microglobulinic amyloidosis (disorder)

Shortest Term

Variant abeta2m amyloidosis

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

Autosomal dominant beta2-microglobulinic amyloidosis (disorder)

SCTID: 722292000, Primitive, Active

722292000|Autosomal dominant beta2-microglobulinic amyloidosis (disorder)|

en Autosomal dominant beta2-microglobulinic amyloidosis
en Autosomal dominant beta2-microglobulinic amyloidosis (disorder)
en Variant abeta2m amyloidosis

Expression

722292000 |Autosomal dominant beta2-microglobulinic amyloidosis (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
406123005 |Viscus structure finding (finding)| + 
367601000119103 |Hereditary amyloidosis (disorder)| + 
1821000146108 |Hereditary metabolic disease (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 68790008 |Amyloid deposition (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 362937008 |Structure of viscus (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3331472019 - Autosomal dominant beta2-microglobulinic amyloidosis (en) View
3331472019	en	Synonym (core metadata concept)	Autosomal dominant beta2-microglobulinic amyloidosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3331471014 - Autosomal dominant beta2-microglobulinic amyloidosis (disorder) (en) View
3331471014	en	Fully specified name (core metadata concept)	Autosomal dominant beta2-microglobulinic amyloidosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3331473012 - Variant ABeta2M amyloidosis (en) View
3331473012	en	Synonym (core metadata concept)	Variant ABeta2M amyloidosis	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (12210775022) - 722292000 -> 75934005 (116680003) View
116680003 \|Is a (attribute)\|	75934005 \|Metabolic disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15281263026) - 722292000 -> 1821000146108 (116680003) View
116680003 \|Is a (attribute)\|	1821000146108 \|Hereditary metabolic disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6791430025) - 722292000 -> 123946008 (116680003) View
116680003 \|Is a (attribute)\|	123946008 \|Disorder by body site (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6791429024) - 722292000 -> 17602002 (116680003) View
116680003 \|Is a (attribute)\|	17602002 \|Amyloidosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7115935024) - 722292000 -> 367601000119103 (116680003) View
116680003 \|Is a (attribute)\|	367601000119103 \|Hereditary amyloidosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6791428027) - 722292000 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6791431026) - 722292000 -> 406123005 (116680003) View
116680003 \|Is a (attribute)\|	406123005 \|Viscus structure finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6791432022) - 722292000 -> 68790008 (116676008) View
116676008 \|Associated morphology (attribute)\|	68790008 \|Amyloid deposition (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6791433028) - 722292000 -> 362937008 (363698007) View
363698007 \|Finding site (attribute)\|	362937008 \|Structure of viscus (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1821000146108 View
1821000146108	Hereditary metabolic disease (disorder)	Hereditary metabolic disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
367601000119103 View
367601000119103	Hereditary amyloidosis (disorder)	Hereditary amyloidosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
406123005 View
406123005	Viscus structure finding (finding)	Viscus structure finding	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

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 (754ff23b-648f-555f-a083-4753e85f97a2) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E85.1	TRUE	ALWAYS E85.1 \| 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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