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Terminology chevron_right Concepts chevron_right 445542007

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Component

445542007

The component that hold information about this concept.

Fully Specified Name (FSN)

Hemoglobin o-arab trait (disorder)

Shortest Term

Hemoglobin o-arab trait

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

Hemoglobin o-arab trait (disorder)

SCTID: 445542007, Primitive, Active

445542007|Hemoglobin o-arab trait (disorder)|

en Haemoglobin o-arab trait
en Hemoglobin o-arab trait
en Hemoglobin o-arab trait (disorder)

Expression

445542007 |Hemoglobin o-arab trait (disorder)|
 <<< 123773003 |Heterozygous hemoglobinopathy (disorder)| + 
127038008 |Hereditary hemoglobinopathy due to globin chain mutation (disorder)| : 
        { 363698007 |Finding site (attribute)| = 41898006 |Erythrocyte (cell)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
2872030010 - Haemoglobin O-Arab trait (en) View
2872030010	en	Synonym (core metadata concept)	Haemoglobin O-Arab trait	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
2872029017 - Hemoglobin O-Arab trait (en) View
2872029017	en	Synonym (core metadata concept)	Hemoglobin O-Arab trait	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
2870553013 - Hemoglobin O-Arab trait (disorder) (en) View
2870553013	en	Fully specified name (core metadata concept)	Hemoglobin O-Arab trait (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (5977800022) - 445542007 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7007742023) - 445542007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7007743029) - 445542007 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3778890026) - 445542007 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3775268020) - 445542007 -> 123773003 (116680003) View
116680003 \|Is a (attribute)\|	123773003 \|Heterozygous hemoglobinopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3775269028) - 445542007 -> 127038008 (116680003) View
116680003 \|Is a (attribute)\|	127038008 \|Hereditary hemoglobinopathy due to globin chain mutation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
123773003 View
123773003	Heterozygous hemoglobinopathy (disorder)	Trait hemoglobinopathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
127038008 View
127038008	Hereditary hemoglobinopathy due to globin chain mutation (disorder)	Structural hemoglobinopathy	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 (ee62ec7f-3b22-52bc-8726-144371f866fa) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D58.2	TRUE	ALWAYS D58.2	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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