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Terminology chevron_right Concepts chevron_right 59531002

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Component

59531002

The component that hold information about this concept.

Fully Specified Name (FSN)

Tryptophan malabsorption syndrome (disorder)

Shortest Term

Blue diaper 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

Tryptophan malabsorption syndrome (disorder)

SCTID: 59531002, Primitive, Active

59531002|Tryptophan malabsorption syndrome (disorder)|

en Blue diaper syndrome
en Tryptophan malabsorption syndrome
en Tryptophan malabsorption syndrome (disorder)

Expression

59531002 |Tryptophan malabsorption syndrome (disorder)|
 <<< 5181007 |Disorder of tryptophan metabolism (disorder)| + 
236444003 |Microscopic nephrocalcinosis (disorder)| + 
32230006 |Malabsorption syndrome (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 18115005 |Pathologic calcification, calcified structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 29704000 |Structure of parenchyma of kidney (body structure)| }
        { 363698007 |Finding site (attribute)| = 122865005 |Gastrointestinal tract structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
98879018 - Blue diaper syndrome (en) View
98879018	en	Synonym (core metadata concept)	Blue diaper syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
98878014 - Tryptophan malabsorption syndrome (en) View
98878014	en	Synonym (core metadata concept)	Tryptophan malabsorption syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
798384012 - Tryptophan malabsorption syndrome (disorder) (en) View
798384012	en	Fully specified name (core metadata concept)	Tryptophan malabsorption syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (3309632026) - 59531002 -> 64033007 (363698007) View
363698007 \|Finding site (attribute)\|	64033007 \|Kidney structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15627040024) - 59531002 -> 29704000 (363698007) View
363698007 \|Finding site (attribute)\|	29704000 \|Structure of parenchyma of kidney (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15671687023) - 59531002 -> 32230006 (116680003) View
116680003 \|Is a (attribute)\|	32230006 \|Malabsorption syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15671688029) - 59531002 -> 122865005 (363698007) View
363698007 \|Finding site (attribute)\|	122865005 \|Gastrointestinal tract structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (822070022) - 59531002 -> 64033007 (363698007) View
363698007 \|Finding site (attribute)\|	64033007 \|Kidney structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2734923024) - 59531002 -> 18115005 (116676008) View
116676008 \|Associated morphology (attribute)\|	18115005 \|Pathologic calcification, calcified structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3309631022) - 59531002 -> 18115005 (116676008) View
116676008 \|Associated morphology (attribute)\|	18115005 \|Pathologic calcification, calcified structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (244928027) - 59531002 -> 363338001 (116680003) View
116680003 \|Is a (attribute)\|	363338001 \|Hereditary disorder of the urinary system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (822069021) - 59531002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (244926028) - 59531002 -> 78626001 (116680003) View
116680003 \|Is a (attribute)\|	78626001 \|Congenital anomaly of trunk (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (244925029) - 59531002 -> 5181007 (116680003) View
116680003 \|Is a (attribute)\|	5181007 \|Disorder of tryptophan metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (244927021) - 59531002 -> 236444003 (116680003) View
116680003 \|Is a (attribute)\|	236444003 \|Microscopic nephrocalcinosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
5181007 View
5181007	Disorder of tryptophan metabolism (disorder)	Disorder of tryptophan metabolism	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
32230006 View
32230006	Malabsorption syndrome (disorder)	Malabsorption	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
236444003 View
236444003	Microscopic nephrocalcinosis (disorder)	Microscopic nephrocalcinosis	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 (1dd01614-b839-5d90-ac09-ef8cc2a4c177) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E70.8	TRUE	ALWAYS E70.8	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)\|
ExtendedMap object (b04d1c63-c0b3-5338-a090-0cd2c1a74e02) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	N29.8	TRUE	ALWAYS N29.8 \| THIS CODE MAY BE USED IN THE PRIMARY POSITION WHEN THE MANIFESTATION IS THE PRIMARY FOCUS OF CARE	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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