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Terminology chevron_right Concepts chevron_right 722760002

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Component

722760002

The component that hold information about this concept.

Fully Specified Name (FSN)

Dense deposit disease (disorder)

Shortest Term

Dense deposit disease

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

Dense deposit disease (disorder)

SCTID: 722760002, Primitive, Active

722760002|Dense deposit disease (disorder)|

en Mcgn (mesangiocapillary glomerulonephritis) type ii
en Membranoproliferative glomerulonephritis type 2
en Mpgnii - membranoproliferative glomerulonephritis type ii
en Mesangiocapillary glomerulonephritis type 2
en Dense deposit disease
en Dense deposit disease (disorder)

Expression

722760002 |Dense deposit disease (disorder)|
 <<< 722758004 |Complement component 3 glomerulopathy (disorder)| + 
399340005 |Hereditary nephritis (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 123749006 |Chronic proliferative inflammation (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 18602000 |Structure of glomerular mesangium (body structure)| }
        { 263502005 |Clinical course (attribute)| = 90734009 |Chronic (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 1338011001 |Complement component 3 deposit (morphologic abnormality)|,
246075003 |Causative agent (attribute)| = 10473000 |Complement component c3 (substance)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
5244191012 - MCGN (mesangiocapillary glomerulonephritis) type II (en) View
5244191012	en	Synonym (core metadata concept)	MCGN (mesangiocapillary glomerulonephritis) type II	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
4652577015 - MCGN type II - mesangiocapillary glomerulonephritis type II (en) View
4652577015	en	Synonym (core metadata concept)	MCGN type II - mesangiocapillary glomerulonephritis type II	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
4652576012 - Membranoproliferative glomerulonephritis type 2 (en) View
4652576012	en	Synonym (core metadata concept)	Membranoproliferative glomerulonephritis type 2	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
4652578013 - MPGNII - membranoproliferative glomerulonephritis type II (en) View
4652578013	en	Synonym (core metadata concept)	MPGNII - membranoproliferative glomerulonephritis type II	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
3758323019 - Mesangiocapillary glomerulonephritis type 2 (en) View
3758323019	en	Synonym (core metadata concept)	Mesangiocapillary glomerulonephritis type 2	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3333379015 - Dense deposit disease (en) View
3333379015	en	Synonym (core metadata concept)	Dense deposit disease	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3333378011 - Dense deposit disease (disorder) (en) View
3333378011	en	Fully specified name (core metadata concept)	Dense deposit disease (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (14924964023) - 722760002 -> 80321008 (116680003) View
116680003 \|Is a (attribute)\|	80321008 \|Mesangiocapillary glomerulonephritis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16046068022) - 722760002 -> 10473000 (246075003) View
246075003 \|Causative agent (attribute)\|	10473000 \|Complement component c3 (substance)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16046077026) - 722760002 -> 1338011001 (116676008) View
116676008 \|Associated morphology (attribute)\|	1338011001 \|Complement component 3 deposit (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11286024028) - 722760002 -> 68288006 (363698007) View
363698007 \|Finding site (attribute)\|	68288006 \|Glomerulus structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14924963028) - 722760002 -> 399340005 (116680003) View
116680003 \|Is a (attribute)\|	399340005 \|Hereditary nephritis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14924965024) - 722760002 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14924966020) - 722760002 -> 18602000 (363698007) View
363698007 \|Finding site (attribute)\|	18602000 \|Structure of glomerular mesangium (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6806742021) - 722760002 -> 90734009 (263502005) View
263502005 \|Clinical course (attribute)\|	90734009 \|Chronic (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6806744022) - 722760002 -> 68288006 (363698007) View
363698007 \|Finding site (attribute)\|	68288006 \|Glomerulus structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6806746024) - 722760002 -> 68288006 (363698007) View
363698007 \|Finding site (attribute)\|	68288006 \|Glomerulus structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6807396025) - 722760002 -> 84499006 (116676008) View
116676008 \|Associated morphology (attribute)\|	84499006 \|Chronic inflammation (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6807397023) - 722760002 -> 2952002 (116676008) View
116676008 \|Associated morphology (attribute)\|	2952002 \|Proliferative inflammation (morphologic abnormality)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11286023023) - 722760002 -> 123749006 (116676008) View
116676008 \|Associated morphology (attribute)\|	123749006 \|Chronic proliferative inflammation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6806741025) - 722760002 -> 722758004 (116680003) View
116680003 \|Is a (attribute)\|	722758004 \|Complement component 3 glomerulopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
722758004 View
722758004	Complement component 3 glomerulopathy (disorder)	Complement component 3 glomerulopathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
399340005 View
399340005	Hereditary nephritis (disorder)	Alport's syndrome	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

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
714813000 View
714813000	Recurrent hematuria co-occurrent and due to dense deposit disease (disorder)	Recurrent hematuria co-occurrent and due to dense deposit disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
714814006 View
714814006	Persistent hematuria co-occurrent and due to dense deposit disease (disorder)	Persistent hematuria co-occurrent and due to dense deposit disease	900000000000073002 \|Sufficiently defined by necessary conditions 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 (25165598-faee-54d0-9d99-df380f912156) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	N03.6	TRUE	ALWAYS N03.6 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION \| POSSIBLE REQUIREMENT FOR AN EXTERNAL CAUSE CODE	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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