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Terminology chevron_right Concepts chevron_right 1299153008

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Component

1299153008

The component that hold information about this concept.

Fully Specified Name (FSN)

Digenic hemochromatosis (disorder)

Shortest Term

Digenic hemochromatosis

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

Digenic hemochromatosis (disorder)

SCTID: 1299153008, Primitive, Active

1299153008|Digenic hemochromatosis (disorder)|

en Digenic haemochromatosis
en Digenic hemochromatosis
en Digenic hemochromatosis (disorder)

Expression

1299153008 |Digenic hemochromatosis (disorder)|
 <<< 235903001 |Metabolic and genetic disorder affecting the liver (disorder)| + 
35400008 |Hereditary hemochromatosis (disorder)| + 
363080007 |Digestive system hereditary disorder (disorder)| + 
86095007 |Inborn error of metabolism (disorder)| + 
42357009 |Disorder of digestive system specific to fetus or newborn (disorder)| : 
        { 246075003 |Causative agent (attribute)| = 767270007 |Iron and iron compound (substance)| }
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 10200004 |Liver structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
5296172011 - Digenic haemochromatosis (en) View
5296172011	en	Synonym (core metadata concept)	Digenic haemochromatosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
5296175013 - Digenic hemochromatosis (en) View
5296175013	en	Synonym (core metadata concept)	Digenic hemochromatosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
5296174012 - Digenic hemochromatosis (disorder) (en) View
5296174012	en	Fully specified name (core metadata concept)	Digenic hemochromatosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15856108029) - 1299153008 -> 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 (15856109021) - 1299153008 -> 35400008 (116680003) View
116680003 \|Is a (attribute)\|	35400008 \|Hereditary hemochromatosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15856110027) - 1299153008 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15856111028) - 1299153008 -> 86095007 (116680003) View
116680003 \|Is a (attribute)\|	86095007 \|Inborn error of metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15856112024) - 1299153008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15856113025) - 1299153008 -> 10200004 (363698007) View
363698007 \|Finding site (attribute)\|	10200004 \|Liver structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15856114020) - 1299153008 -> 767270007 (246075003) View
246075003 \|Causative agent (attribute)\|	767270007 \|Iron and iron compound (substance)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15887380028) - 1299153008 -> 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

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
35400008 View
35400008	Hereditary hemochromatosis (disorder)	Primary hemochromatosis	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
86095007 View
86095007	Inborn error of metabolism (disorder)	Inborn error of metabolism	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

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 (04d9fced-21f7-5509-8ae0-402122982e47) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E83.1	TRUE	ALWAYS E83.1	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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