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Terminology chevron_right Concepts chevron_right 76050008

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Component

76050008

The component that hold information about this concept.

Fully Specified Name (FSN)

Hemoglobin c trait (disorder)

Shortest Term

Hemoglobin c 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 c trait (disorder)

SCTID: 76050008, Primitive, Active

76050008|Hemoglobin c trait (disorder)|

en Haemoglobin c-a disorder
en Hemoglobin c trait (disorder)
en Haemoglobin c trait
en Hemoglobin c-a disorder
en Hemoglobin c trait
en Heterozygous for hb c

Expression

76050008 |Hemoglobin c trait (disorder)|
 <<< 127038008 |Hereditary hemoglobinopathy due to globin chain mutation (disorder)| + 
123773003 |Heterozygous hemoglobinopathy (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
503179014 - Haemoglobin C-A disorder (en) View
503179014	en	Synonym (core metadata concept)	Haemoglobin C-A disorder	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
816728014 - Hemoglobin C trait (disorder) (en) View
816728014	en	Fully specified name (core metadata concept)	Hemoglobin C trait (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
503178018 - Haemoglobin C trait (en) View
503178018	en	Synonym (core metadata concept)	Haemoglobin C trait	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
126316013 - Hemoglobin C-A disorder (en) View
126316013	en	Synonym (core metadata concept)	Hemoglobin C-A disorder	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
126315012 - Hemoglobin C trait (en) View
126315012	en	Synonym (core metadata concept)	Hemoglobin C trait	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
503177011 - Heterozygous for Hb C (en) View
503177011	en	Synonym (core metadata concept)	Heterozygous for Hb C	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (863870026) - 76050008 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7006831029) - 76050008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7006832020) - 76050008 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2737226027) - 76050008 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2737227020) - 76050008 -> 250228007 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	250228007 \|Red blood cell finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2772010020) - 76050008 -> 123773003 (116680003) View
116680003 \|Is a (attribute)\|	123773003 \|Heterozygous hemoglobinopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2269885025) - 76050008 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (863869027) - 76050008 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (271653020) - 76050008 -> 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 (40a14d5c-c36e-5ee4-bd42-7cf7cf01dac1) 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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