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Terminology chevron_right Concepts chevron_right 25065001

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Component

25065001

The component that hold information about this concept.

Fully Specified Name (FSN)

Hemoglobin e disease (disorder)

Shortest Term

Homozygous for hb e

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 e disease (disorder)

SCTID: 25065001, Primitive, Active

25065001|Hemoglobin e disease (disorder)|

en Haemoglobin e-e disease
en Hemoglobin e disease (disorder)
en Haemoglobin e disease
en Hemoglobin e disease
en Hemoglobin e-e disease
en Homozygous for hb e

Expression

25065001 |Hemoglobin e disease (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
482564013 - Haemoglobin E-E disease (en) View
482564013	en	Synonym (core metadata concept)	Haemoglobin E-E disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
755202015 - Hemoglobin E disease (disorder) (en) View
755202015	en	Fully specified name (core metadata concept)	Hemoglobin E disease (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
482565014 - Haemoglobin E disease (en) View
482565014	en	Synonym (core metadata concept)	Haemoglobin E disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
41996013 - Hemoglobin E disease (en) View
41996013	en	Synonym (core metadata concept)	Hemoglobin E disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
41997016 - Hemoglobin E-E disease (en) View
41997016	en	Synonym (core metadata concept)	Hemoglobin E-E disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
482566010 - Homozygous for Hb E (en) View
482566010	en	Synonym (core metadata concept)	Homozygous for Hb E	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (735046021) - 25065001 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7006627021) - 25065001 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7006628027) - 25065001 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2730261020) - 25065001 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2730262029) - 25065001 -> 250228007 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	250228007 \|Red blood cell finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2265383020) - 25065001 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (735045020) - 25065001 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (188835029) - 25065001 -> 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
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
234392002 View
234392002	Hemoglobin e/beta thalassemia disease (disorder)	Hemoglobin e/beta thalassemia disease	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 (13359d10-1b95-5a8b-b9d7-c5153283588a) 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)\|
ExtendedMap object (5432de70-3df0-530d-a2b3-3d00686b8eb4) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q89.9	TRUE	ALWAYS Q89.9	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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