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Terminology chevron_right Concepts chevron_right 784346006

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Component

784346006

The component that hold information about this concept.

Fully Specified Name (FSN)

Navajo neurohepatopathy (disorder)

Shortest Term

Navajo neuropathy

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

Navajo neurohepatopathy (disorder)

SCTID: 784346006, Primitive, Active

784346006|Navajo neurohepatopathy (disorder)|

vi Bệnh thần kinh - gan navajo
en Navajo neurohepatopathy
en Navajo neurohepatopathy (disorder)
en Navajo neuropathy

Expression

784346006 |Navajo neurohepatopathy (disorder)|
 <<< 363080007 |Digestive system hereditary disorder (disorder)| + 
237995002 |Depletion of mitochondrial deoxyribonucleic acid (disorder)| + 
128190004 |Inherited metabolic disorder of nervous system (disorder)| + 
235903001 |Metabolic and genetic disorder affecting the liver (disorder)| + 
42357009 |Disorder of digestive system specific to fetus or newborn (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| : 
        { 363698007 |Finding site (attribute)| = 10200004 |Liver structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 25087005 |Structure of nervous system (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
453151000003111 - bệnh thần kinh - gan Navajo (vi) View
453151000003111	vi	Synonym (core metadata concept)	bệnh thần kinh - gan Navajo	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
3763712017 - Navajo neurohepatopathy (en) View
3763712017	en	Synonym (core metadata concept)	Navajo neurohepatopathy	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
3763713010 - Navajo neurohepatopathy (disorder) (en) View
3763713010	en	Fully specified name (core metadata concept)	Navajo neurohepatopathy (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
3763711012 - Navajo neuropathy (en) View
3763711012	en	Synonym (core metadata concept)	Navajo neuropathy	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15880945023) - 784346006 -> 42357009 (116680003) View
116680003 \|Is a (attribute)\|	42357009 \|Disorder of digestive system specific to fetus or newborn (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11372587020) - 784346006 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11372588026) - 784346006 -> 25087005 (363698007) View
363698007 \|Finding site (attribute)\|	25087005 \|Structure of nervous system (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11372589023) - 784346006 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11372590025) - 784346006 -> 237995002 (116680003) View
116680003 \|Is a (attribute)\|	237995002 \|Depletion of mitochondrial deoxyribonucleic acid (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11372591026) - 784346006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11372592022) - 784346006 -> 10200004 (363698007) View
363698007 \|Finding site (attribute)\|	10200004 \|Liver structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11372593028) - 784346006 -> 128190004 (116680003) View
116680003 \|Is a (attribute)\|	128190004 \|Inherited metabolic disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11372594023) - 784346006 -> 235903001 (116680003) View
116680003 \|Is a (attribute)\|	235903001 \|Metabolic and genetic disorder affecting the liver (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11372595024) - 784346006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	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
42357009 View
42357009	Disorder of digestive system specific to fetus or newborn (disorder)	Perinatal digestive system disorders	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
235903001 View
235903001	Metabolic and genetic disorder affecting the liver (disorder)	Rối loạn chuyển hóa và di truyền ảnh hưởng đến gan	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
237995002 View
237995002	Depletion of mitochondrial deoxyribonucleic acid (disorder)	Depletion of mitochondrial dna	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363080007 View
363080007	Digestive system hereditary disorder (disorder)	Digestive system hereditary disorder	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 (cb6796c5-ba3a-55d8-a41d-ab0ae20bc342) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E88.8	TRUE	ALWAYS E88.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	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 (de513a26-4e32-5738-87c5-5f7c33d8827f) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E74.4	TRUE	ALWAYS E74.4 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	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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