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Terminology chevron_right Concepts chevron_right 25765006

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Language with ID “edb06b02-cf19-5fdd-bf79-e1ce3a4384f3” doesn’t exist. Perhaps it was deleted?

Component

25765006

The component that hold information about this concept.

Fully Specified Name (FSN)

Neonatal iminoglycinuria (disorder)

Shortest Term

Neonatal iminoglycinuria

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

Neonatal iminoglycinuria (disorder)

SCTID: 25765006, Defined, Active

25765006|Neonatal iminoglycinuria (disorder)|

en Neonatal iminoglycinuria
en Neonatal iminoglycinuria (disorder)

Expression

25765006 |Neonatal iminoglycinuria (disorder)|
 === 84121007 |Iminoglycinuria (disorder)| + 
363224005 |Neonatal renal disorder (disorder)| + 
736652002 |Neonatal metabolic disorder (disorder)| : 
        { 246454002 |Occurrence (attribute)| = 255407002 |Neonatal (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 64033007 |Kidney structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
43175012 - Neonatal iminoglycinuria (en) View
43175012	en	Synonym (core metadata concept)	Neonatal iminoglycinuria	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
756120012 - Neonatal iminoglycinuria (disorder) (en) View
756120012	en	Fully specified name (core metadata concept)	Neonatal iminoglycinuria (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (736732022) - 25765006 -> 64033007 (363698007) View
363698007 \|Finding site (attribute)\|	64033007 \|Kidney structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (736734023) - 25765006 -> 255407002 (246454002) View
246454002 \|Occurrence (attribute)\|	255407002 \|Neonatal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7239296027) - 25765006 -> 736652002 (116680003) View
116680003 \|Is a (attribute)\|	736652002 \|Neonatal metabolic disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (189906027) - 25765006 -> 22561006 (116680003) View
116680003 \|Is a (attribute)\|	22561006 \|Endocrine and/or metabolic disorder specific to the fetus or newborn (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (736735024) - 25765006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2689960021) - 25765006 -> 363224005 (116680003) View
116680003 \|Is a (attribute)\|	363224005 \|Neonatal renal disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (189907020) - 25765006 -> 363104002 (116680003) View
116680003 \|Is a (attribute)\|	363104002 \|Hereditary disorder of endocrine system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (189908026) - 25765006 -> 4184009 (116680003) View
116680003 \|Is a (attribute)\|	4184009 \|Congenital anomaly of endocrine gland (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (189909023) - 25765006 -> 363290007 (116680003) View
116680003 \|Is a (attribute)\|	363290007 \|Reproductive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (736733028) - 25765006 -> 127944005 (363698007) View
363698007 \|Finding site (attribute)\|	127944005 \|Entire endocrine gonad (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (189905028) - 25765006 -> 84121007 (116680003) View
116680003 \|Is a (attribute)\|	84121007 \|Iminoglycinuria (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
736652002 View
736652002	Neonatal metabolic disorder (disorder)	Neonatal metabolic disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363224005 View
363224005	Neonatal renal disorder (disorder)	Neonatal renal disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
84121007 View
84121007	Iminoglycinuria (disorder)	Iminoglycinuria	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 (66eeb126-e677-5cd3-875f-1d921f907579) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E72.0	TRUE	ALWAYS E72.0	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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