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Terminology chevron_right Concepts chevron_right 771447009

Production

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Component

771447009

The component that hold information about this concept.

Fully Specified Name (FSN)

Laminin subunit beta 2 related infantile-onset nephrotic syndrome (disorder)

Shortest Term

Lamb2-related infantile-onset nephrotic 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

Laminin subunit beta 2 related infantile-onset nephrotic syndrome (disorder)

SCTID: 771447009, Primitive, Active

771447009|Laminin subunit beta 2 related infantile-onset nephrotic syndrome (disorder)|

vi Hội chứng thận hư khởi phát ở trẻ sơ sinh liên quan đến lamb2
en Lamb2 (laminin subunit beta 2) related infantile-onset nephrotic syndrome
en Lamb2-related infantile-onset nephrotic syndrome
en Laminin subunit beta 2 related infantile-onset nephrotic syndrome
en Laminin subunit beta 2 related infantile-onset nephrotic syndrome (disorder)

Expression

771447009 |Laminin subunit beta 2 related infantile-onset nephrotic syndrome (disorder)|
 <<< 236381000 |Steroid-resistant nephrotic syndrome (disorder)| + 
367591000119105 |Hereditary nephropathy (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
1367653005 |Genetic disease of glomerulus (disorder)| : 
        { 363698007 |Finding site (attribute)| = 68288006 |Glomerulus structure (body structure)|,
246454002 |Occurrence (attribute)| = 3658006 |Infancy (qualifier value)| }
        { 363713009 |Has interpretation (attribute)| = 281302008 |Above reference range (qualifier value)|,
363714003 |Interprets (attribute)| = 57378007 |Measurement of protein in urine (procedure)| }
        { 363713009 |Has interpretation (attribute)| = 281300000 |Below reference range (qualifier value)|,
363714003 |Interprets (attribute)| = 26758005 |Albumin measurement (procedure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
4651000269113 - hội chứng thận hư khởi phát ở trẻ sơ sinh liên quan đến LAMB2 (vi) View
4651000269113	vi	Synonym (core metadata concept)	hội chứng thận hư khởi phát ở trẻ sơ sinh liên quan đến LAMB2	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
3706241010 - LAMB2 (laminin subunit beta 2) related infantile-onset nephrotic syndrome (en) View
3706241010	en	Synonym (core metadata concept)	LAMB2 (laminin subunit beta 2) related infantile-onset nephrotic syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
3706240011 - LAMB2-related infantile-onset nephrotic syndrome (en) View
3706240011	en	Synonym (core metadata concept)	LAMB2-related infantile-onset nephrotic syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
3706239014 - Laminin subunit beta 2 related infantile-onset nephrotic syndrome (en) View
3706239014	en	Synonym (core metadata concept)	Laminin subunit beta 2 related infantile-onset nephrotic syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3706242015 - Laminin subunit beta 2 related infantile-onset nephrotic syndrome (disorder) (en) View
3706242015	en	Fully specified name (core metadata concept)	Laminin subunit beta 2 related infantile-onset nephrotic syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16374924029) - 771447009 -> 1367653005 (116680003) View
116680003 \|Is a (attribute)\|	1367653005 \|Genetic disease of glomerulus (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10500433028) - 771447009 -> 236381000 (116680003) View
116680003 \|Is a (attribute)\|	236381000 \|Steroid-resistant nephrotic syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10500434023) - 771447009 -> 367591000119105 (116680003) View
116680003 \|Is a (attribute)\|	367591000119105 \|Hereditary nephropathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10500435024) - 771447009 -> 68288006 (363698007) View
363698007 \|Finding site (attribute)\|	68288006 \|Glomerulus structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10500436020) - 771447009 -> 3658006 (246454002) View
246454002 \|Occurrence (attribute)\|	3658006 \|Infancy (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10500437027) - 771447009 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11102258029) - 771447009 -> 26758005 (363714003) View
363714003 \|Interprets (attribute)\|	26758005 \|Albumin measurement (procedure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11102259021) - 771447009 -> 57378007 (363714003) View
363714003 \|Interprets (attribute)\|	57378007 \|Measurement of protein in urine (procedure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11102260027) - 771447009 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11102261028) - 771447009 -> 281302008 (363713009) View
363713009 \|Has interpretation (attribute)\|	281302008 \|Above reference range (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1367653005 View
1367653005	Genetic disease of glomerulus (disorder)	Genetic disease of glomerulus	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
367591000119105 View
367591000119105	Hereditary nephropathy (disorder)	Hereditary nephropathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
85995004 View
85995004	Autosomal recessive hereditary disorder (disorder)	Hereditary disorder trait, nos	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
236381000 View
236381000	Steroid-resistant nephrotic syndrome (disorder)	Steroid-resistant nephrotic syndrome	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 (5aca09a2-9be3-595d-8dab-5d80497eca78) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	N04.8	TRUE	ALWAYS N04.8 \| 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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