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Terminology chevron_right Concepts chevron_right 236418003

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Component

236418003

The component that hold information about this concept.

Fully Specified Name (FSN)

Thin basement membrane disease (disorder)

Shortest Term

Benign familial hematuria

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Thin basement membrane disease (disorder)

SCTID: 236418003, Defined, Active

236418003|Thin basement membrane disease (disorder)|

en Benign familial haematuria
en Benign familial hematuria
en Thin basement membrane disease
en Thin basement membrane disease (disorder)
en Thin basement membrane nephropathy

Expression

236418003 |Thin basement membrane disease (disorder)|
 === 20917003 |Chronic glomerulonephritis (disorder)| + 
79131000119100 |Kidney lesion (disorder)| + 
11164009 |Autosomal dominant hereditary disorder (disorder)| + 
1367808005 |Collagen iv nephropathy (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 125481001 |Basement membrane alteration (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 68288006 |Glomerulus structure (body structure)| }
        { 263502005 |Clinical course (attribute)| = 90734009 |Chronic (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 409777003 |Chronic inflammatory morphology (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 68288006 |Glomerulus structure (body structure)| }
        { 42752001 |Due to (attribute)| = 32895009 |Hereditary disease (disorder)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3758367017 - Benign familial haematuria (en) View
3758367017	en	Synonym (core metadata concept)	Benign familial haematuria	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3758368010 - Benign familial hematuria (en) View
3758368010	en	Synonym (core metadata concept)	Benign familial hematuria	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
354399015 - Thin basement membrane disease (en) View
354399015	en	Synonym (core metadata concept)	Thin basement membrane disease	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
625008013 - Thin basement membrane disease (disorder) (en) View
625008013	en	Fully specified name (core metadata concept)	Thin basement membrane disease (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
354398011 - Thin basement membrane nephropathy (en) View
354398011	en	Synonym (core metadata concept)	Thin basement membrane nephropathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (51460022) - 236418003 -> 20917003 (116680003) View
116680003 \|Is a (attribute)\|	20917003 \|Chronic glomerulonephritis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11286007023) - 236418003 -> 197679002 (116680003) View
116680003 \|Is a (attribute)\|	197679002 \|Glomerular disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11286009021) - 236418003 -> 367591000119105 (116680003) View
116680003 \|Is a (attribute)\|	367591000119105 \|Hereditary nephropathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11286010027) - 236418003 -> 128290005 (116680003) View
116680003 \|Is a (attribute)\|	128290005 \|Chronic disease of genitourinary system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16376457020) - 236418003 -> 1367808005 (116680003) View
116680003 \|Is a (attribute)\|	1367808005 \|Collagen iv nephropathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16376458026) - 236418003 -> 32895009 (42752001) View
42752001 \|Due to (attribute)\|	32895009 \|Hereditary disease (disorder)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16376459023) - 236418003 -> 68288006 (363698007) View
363698007 \|Finding site (attribute)\|	68288006 \|Glomerulus structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16376460029) - 236418003 -> 409777003 (116676008) View
116676008 \|Associated morphology (attribute)\|	409777003 \|Chronic inflammatory morphology (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3024288024) - 236418003 -> 90734009 (263502005) View
263502005 \|Clinical course (attribute)\|	90734009 \|Chronic (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3462935024) - 236418003 -> 84499006 (116676008) View
116676008 \|Associated morphology (attribute)\|	84499006 \|Chronic inflammation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11286008029) - 236418003 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5983550028) - 236418003 -> 79131000119100 (116680003) View
116680003 \|Is a (attribute)\|	79131000119100 \|Kidney lesion (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3348372024) - 236418003 -> 68288006 (363698007) View
363698007 \|Finding site (attribute)\|	68288006 \|Glomerulus structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3348373025) - 236418003 -> 125481001 (116676008) View
116676008 \|Associated morphology (attribute)\|	125481001 \|Basement membrane alteration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (522479026) - 236418003 -> 125481001 (116676008) View
116676008 \|Associated morphology (attribute)\|	125481001 \|Basement membrane alteration (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (522482020) - 236418003 -> 84499006 (116676008) View
116676008 \|Associated morphology (attribute)\|	84499006 \|Chronic inflammation (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (522485022) - 236418003 -> 68288006 (363698007) View
363698007 \|Finding site (attribute)\|	68288006 \|Glomerulus structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (522480028) - 236418003 -> 90734009 (260908002) View
260908002 \|Course (attribute)\|	90734009 \|Chronic (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (522481029) - 236418003 -> 23583003 (116676008) View
116676008 \|Associated morphology (attribute)\|	23583003 \|Inflammation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (458392028) - 236418003 -> 64033007 (363698007) View
363698007 \|Finding site (attribute)\|	64033007 \|Kidney structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1367808005 View
1367808005	Collagen iv nephropathy (disorder)	Collagen iv nephropathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
79131000119100 View
79131000119100	Kidney lesion (disorder)	Kidney lesion	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
20917003 View
20917003	Chronic glomerulonephritis (disorder)	Viêm cầu thận mạn tính	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 (868a74b5-5254-5922-b1b6-142c031537c0) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	N03.8	TRUE	ALWAYS N03.8 \| 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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