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Terminology chevron_right Concepts chevron_right 86444004

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Component

86444004

The component that hold information about this concept.

Fully Specified Name (FSN)

Niemann-pick disease, type c, acute form (disorder)

Shortest Term

Niemann-pick disease, type c, acute form

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

Niemann-pick disease, type c, acute form (disorder)

SCTID: 86444004, Primitive, Active

86444004|Niemann-pick disease, type c, acute form (disorder)|

en Niemann-pick disease, type c, acute form (disorder)
en Niemann-pick disease, type c, acute form

Expression

86444004 |Niemann-pick disease, type c, acute form (disorder)|
 <<< 128190004 |Inherited metabolic disorder of nervous system (disorder)| + 
66751000 |Niemann-pick disease, type c (disorder)| : 
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 25087005 |Structure of nervous system (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
828709011 - Niemann-Pick disease, type C, acute form (disorder) (en) View
828709011	en	Fully specified name (core metadata concept)	Niemann-Pick disease, type C, acute form (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
143351017 - Niemann-Pick disease, type C, acute form (en) View
143351017	en	Synonym (core metadata concept)	Niemann-Pick disease, type C, acute form	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (890852023) - 86444004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (890855020) - 86444004 -> 25087005 (363698007) View
363698007 \|Finding site (attribute)\|	25087005 \|Structure of nervous system (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (890853029) - 86444004 -> 9240003 (116676008) View
116676008 \|Associated morphology (attribute)\|	9240003 \|Niemann-pick cell (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (890854024) - 86444004 -> 16980002 (116676008) View
116676008 \|Associated morphology (attribute)\|	16980002 \|Foam cell (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (289081020) - 86444004 -> 128190004 (116680003) View
116680003 \|Is a (attribute)\|	128190004 \|Inherited metabolic disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (289082029) - 86444004 -> 66751000 (116680003) View
116680003 \|Is a (attribute)\|	66751000 \|Niemann-pick disease, type c (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
128190004 View
128190004	Inherited metabolic disorder of nervous system (disorder)	Inherited metabolic disorder of nervous system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
66751000 View
66751000	Niemann-pick disease, type c (disorder)	Niemann-pick disease type c	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 (90b880f6-e02b-5376-a90b-0e5070c38212) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E75.2	TRUE	ALWAYS E75.2	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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