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Terminology chevron_right Concepts chevron_right 123773003

Production

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Component

123773003

The component that hold information about this concept.

Fully Specified Name (FSN)

Heterozygous hemoglobinopathy (disorder)

Shortest Term

Trait hemoglobinopathy

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

Heterozygous hemoglobinopathy (disorder)

SCTID: 123773003, Primitive, Active

123773003|Heterozygous hemoglobinopathy (disorder)|

en Heterozygous haemoglobinopathy
en Heterozygous hemoglobinopathy
en Heterozygous hemoglobinopathy (disorder)
en Trait haemoglobinopathy
en Trait hemoglobinopathy

Expression

123773003 |Heterozygous hemoglobinopathy (disorder)|
 <<< 427306008 |Hereditary 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
203430018 - Heterozygous haemoglobinopathy (en) View
203430018	en	Synonym (core metadata concept)	Heterozygous haemoglobinopathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
192262014 - Heterozygous hemoglobinopathy (en) View
192262014	en	Synonym (core metadata concept)	Heterozygous hemoglobinopathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
726899017 - Heterozygous hemoglobinopathy (disorder) (en) View
726899017	en	Fully specified name (core metadata concept)	Heterozygous hemoglobinopathy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
203429011 - Trait haemoglobinopathy (en) View
203429011	en	Synonym (core metadata concept)	Trait haemoglobinopathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
203428015 - Trait hemoglobinopathy (en) View
203428015	en	Synonym (core metadata concept)	Trait hemoglobinopathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (689252023) - 123773003 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7006921024) - 123773003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7006922028) - 123773003 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3190971023) - 123773003 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2727437023) - 123773003 -> 250228007 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	250228007 \|Red blood cell finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (155989020) - 123773003 -> 80141007 (116680003) View
116680003 \|Is a (attribute)\|	80141007 \|Hemoglobinopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3171669021) - 123773003 -> 427306008 (116680003) View
116680003 \|Is a (attribute)\|	427306008 \|Hereditary hemoglobinopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2263721020) - 123773003 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (689253029) - 123773003 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
427306008 View
427306008	Hereditary hemoglobinopathy (disorder)	Hereditary hemoglobinopathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
445542007 View
445542007	Hemoglobin o-arab trait (disorder)	Hemoglobin o-arab trait	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
7391009 View
7391009	Hemoglobin d trait (disorder)	Hemoglobin d trait	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
16402000 View
16402000	Sickle cell trait (disorder)	Drepanocytosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
46248003 View
46248003	Hemoglobin e trait (disorder)	Hemoglobin e trait	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
76050008 View
76050008	Hemoglobin c trait (disorder)	Hemoglobin c trait	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 (84f31828-d24f-560a-a5fa-c4c2a25a2f81) 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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