dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 399187006

Production

add

Component

399187006

The component that hold information about this concept.

Fully Specified Name (FSN)

Hemochromatosis (disorder)

Shortest Term

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

Hemochromatosis (disorder)

SCTID: 399187006, Primitive, Active

399187006|Hemochromatosis (disorder)|

vi Bệnh nhiễm sắc tố sắt mô
en Haemochromatosis
en Hemochromatosis
en Hemochromatosis (disorder)
en Iron storage disease

Expression

399187006 |Hemochromatosis (disorder)|
 <<< 60737008 |Iron overload (disorder)| : 
        { 246075003 |Causative agent (attribute)| = 767270007 |Iron and iron compound (substance)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
519901000003113 - bệnh nhiễm sắc tố sắt mô (vi) View
519901000003113	vi	Synonym (core metadata concept)	bệnh nhiễm sắc tố sắt mô	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3013368016 - Haemochromatosis (en) View
3013368016	en	Synonym (core metadata concept)	Haemochromatosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
1778642010 - Hemochromatosis (en) View
1778642010	en	Synonym (core metadata concept)	Hemochromatosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
1767107013 - Hemochromatosis (disorder) (en) View
1767107013	en	Fully specified name (core metadata concept)	Hemochromatosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
1786734019 - Iron storage disease (en) View
1786734019	en	Synonym (core metadata concept)	Iron storage disease	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9327840029) - 399187006 -> 767270007 (246075003) View
246075003 \|Causative agent (attribute)\|	767270007 \|Iron and iron compound (substance)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2889173022) - 399187006 -> 105840005 (246075003) View
246075003 \|Causative agent (attribute)\|	105840005 \|Iron and/or iron compound (substance)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2283354026) - 399187006 -> 3829006 (246075003) View
246075003 \|Causative agent (attribute)\|	3829006 \|Iron (substance)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2283353021) - 399187006 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2244695027) - 399187006 -> 60737008 (116680003) View
116680003 \|Is a (attribute)\|	60737008 \|Iron overload (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
60737008 View
60737008	Iron overload (disorder)	Iron excess	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
399053004 View
399053004	Idiopathic hemochromatosis (disorder)	Idiopathic hemochromatosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
35400008 View
35400008	Hereditary hemochromatosis (disorder)	Primary hemochromatosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
6160004 View
6160004	Neonatal hemochromatosis (disorder)	Neonatal hemochromatosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
399144008 View
399144008	Bronze diabetes (disorder)	Bronze diabetes	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
399170009 View
399170009	Primary hemochromatosis (disorder)	Primary hemochromatosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
53836006 View
53836006	Secondary hemochromatosis (disorder)	Secondary hemochromatosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (0240e751-f138-5907-8de9-20925438664f) 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)\|

Terminology chevron_right Concepts chevron_right 399187006

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches