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Terminology chevron_right Concepts chevron_right 764962002

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Component

764962002

The component that hold information about this concept.

Fully Specified Name (FSN)

Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (disorder)

Shortest Term

Bệnh não gan do khiếm khuyết kết hợp phosphoryl hóa oxy hóa typ 1

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

Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (disorder)

SCTID: 764962002, Primitive, Active

764962002|Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (disorder)|

vi Bệnh não gan do khiếm khuyết kết hợp phosphoryl hóa oxy hóa typ 1
en Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1
en Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (disorder)
en Hepatoencephalopathy due to coxpd1 (combined oxidative phosphorylation defect type 1)

Expression

764962002 |Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (disorder)|
 <<< 13920009 |Hepatic encephalopathy (disorder)| + 
66091009 |Congenital disease (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
235903001 |Metabolic and genetic disorder affecting the liver (disorder)| + 
363080007 |Digestive system hereditary disorder (disorder)| + 
363235000 |Hereditary disorder of nervous system (disorder)| + 
42357009 |Disorder of digestive system specific to fetus or newborn (disorder)| : 
        { 363698007 |Finding site (attribute)| = 10200004 |Liver structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 12738006 |Brain structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 42752001 |Due to (attribute)| = 235856003 |Disorder of liver (disorder)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
453881000003110 - bệnh não gan do khiếm khuyết kết hợp phosphoryl hóa oxy hóa typ 1 (vi) View
453881000003110	vi	Synonym (core metadata concept)	bệnh não gan do khiếm khuyết kết hợp phosphoryl hóa oxy hóa typ 1	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
3655794018 - Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (en) View
3655794018	en	Synonym (core metadata concept)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3655792019 - Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (disorder) (en) View
3655792019	en	Fully specified name (core metadata concept)	Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3655793012 - Hepatoencephalopathy due to COXPD1 (combined oxidative phosphorylation defect type 1) (en) View
3655793012	en	Synonym (core metadata concept)	Hepatoencephalopathy due to COXPD1 (combined oxidative phosphorylation defect type 1)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15880893029) - 764962002 -> 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 (13881056028) - 764962002 -> 235856003 (42752001) View
42752001 \|Due to (attribute)\|	235856003 \|Disorder of liver (disorder)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9204071021) - 764962002 -> 13920009 (116680003) View
116680003 \|Is a (attribute)\|	13920009 \|Hepatic encephalopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9204072025) - 764962002 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9204073024) - 764962002 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9204074029) - 764962002 -> 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 (9204075028) - 764962002 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9204076027) - 764962002 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9204077020) - 764962002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9211412024) - 764962002 -> 12738006 (363698007) View
363698007 \|Finding site (attribute)\|	12738006 \|Brain structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9223862026) - 764962002 -> 10200004 (363698007) View
363698007 \|Finding site (attribute)\|	10200004 \|Liver structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9223863020) - 764962002 -> 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
13920009 View
13920009	Hepatic encephalopathy (disorder)	Bệnh não gan	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
66091009 View
66091009	Congenital disease (disorder)	Congenital disease	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
363080007 View
363080007	Digestive system hereditary disorder (disorder)	Digestive system hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363235000 View
363235000	Hereditary disorder of nervous system (disorder)	Hereditary disorder of nervous system	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 (6c7f96c5-6e61-5384-bc9f-44c145cda969) 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)\|

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