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Terminology chevron_right Concepts chevron_right 770414008

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Language with ID “eb8c3f42-e1e8-5bbf-abc8-4bae7ed84e70” doesn’t exist. Perhaps it was deleted?

Component

770414008

The component that hold information about this concept.

Fully Specified Name (FSN)

Alport syndrome (disorder)

Shortest Term

Alport 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

Alport syndrome (disorder)

SCTID: 770414008, Primitive, Active

770414008|Alport syndrome (disorder)|

vi Hội chứng alport
en Alport syndrome
en Alport syndrome (disorder)

Expression

770414008 |Alport syndrome (disorder)|
 <<< 1367808005 |Collagen iv nephropathy (disorder)| + 
60700002 |Sensorineural hearing loss (disorder)| + 
788953003 |Hereditary hearing loss (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 409777003 |Chronic inflammatory morphology (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 68288006 |Glomerulus structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 91159003 |Structure of auditory system (body structure)| }
        { 363714003 |Interprets (attribute)| = 47078008 |Hearing, function (observable entity)| }
        { 42752001 |Due to (attribute)| = 32895009 |Hereditary disease (disorder)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
4811000269113 - hội chứng Alport (vi) View
4811000269113	vi	Synonym (core metadata concept)	hội chứng Alport	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
3700752011 - Alport syndrome (en) View
3700752011	en	Synonym (core metadata concept)	Alport syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
3700751016 - Alport syndrome (disorder) (en) View
3700751016	en	Fully specified name (core metadata concept)	Alport syndrome (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9617692027) - 770414008 -> 399340005 (116680003) View
116680003 \|Is a (attribute)\|	399340005 \|Hereditary nephritis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9617696029) - 770414008 -> 362991006 (116680003) View
116680003 \|Is a (attribute)\|	362991006 \|Auditory system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16374377028) - 770414008 -> 788953003 (116680003) View
116680003 \|Is a (attribute)\|	788953003 \|Hereditary hearing loss (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16376451021) - 770414008 -> 1367808005 (116680003) View
116680003 \|Is a (attribute)\|	1367808005 \|Collagen iv nephropathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16376452025) - 770414008 -> 32895009 (42752001) View
42752001 \|Due to (attribute)\|	32895009 \|Hereditary disease (disorder)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9617690024) - 770414008 -> 84499006 (116676008) View
116676008 \|Associated morphology (attribute)\|	84499006 \|Chronic inflammation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15816834022) - 770414008 -> 409777003 (116676008) View
116676008 \|Associated morphology (attribute)\|	409777003 \|Chronic inflammatory morphology (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9617691023) - 770414008 -> 47078008 (363714003) View
363714003 \|Interprets (attribute)\|	47078008 \|Hearing, function (observable entity)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9617693021) - 770414008 -> 91159003 (363698007) View
363698007 \|Finding site (attribute)\|	91159003 \|Structure of auditory system (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9617694026) - 770414008 -> 68288006 (363698007) View
363698007 \|Finding site (attribute)\|	68288006 \|Glomerulus structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9617695025) - 770414008 -> 60700002 (116680003) View
116680003 \|Is a (attribute)\|	60700002 \|Sensorineural hearing loss (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
788953003 View
788953003	Hereditary hearing loss (disorder)	Hereditary hearing loss	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1367808005 View
1367808005	Collagen iv nephropathy (disorder)	Collagen iv nephropathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
60700002 View
60700002	Sensorineural hearing loss (disorder)	Mất thính giác	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
717766000 View
717766000	Alport syndrome autosomal dominant (disorder)	Alport syndrome autosomal dominant	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
717767009 View
717767009	Alport syndrome autosomal recessive (disorder)	Alport syndrome autosomal recessive	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
717768004 View
717768004	Alport syndrome x-linked (disorder)	Alport syndrome x-linked	900000000000074008 \|Necessary but not sufficient concept 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 (e5f321e2-cf22-506a-89ca-ae4134fa9134) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q87.8	TRUE	ALWAYS Q87.8 \| 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)\|

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