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Terminology chevron_right Concepts chevron_right 66729008

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Component

66729008

The component that hold information about this concept.

Fully Specified Name (FSN)

Hemoglobin d disease (disorder)

Shortest Term

Homozygous for hb d

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 d disease (disorder)

SCTID: 66729008, Primitive, Active

66729008|Hemoglobin d disease (disorder)|

en Haemoglobin d-d disease
en Hemoglobin d disease (disorder)
en Haemoglobin d disease
en Hemoglobin d-d disease
en Hemoglobin d disease

Expression

66729008 |Hemoglobin d 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
500508012 - Homozygous for Hb D (en) View
500508012	en	Synonym (core metadata concept)	Homozygous for Hb D	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
500510014 - Haemoglobin D-D disease (en) View
500510014	en	Synonym (core metadata concept)	Haemoglobin D-D disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
806374019 - Hemoglobin D disease (disorder) (en) View
806374019	en	Fully specified name (core metadata concept)	Hemoglobin D disease (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
500509016 - Haemoglobin D disease (en) View
500509016	en	Synonym (core metadata concept)	Haemoglobin D disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
110849018 - Hemoglobin D-D disease (en) View
110849018	en	Synonym (core metadata concept)	Hemoglobin D-D disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
110848014 - Hemoglobin D disease (en) View
110848014	en	Synonym (core metadata concept)	Hemoglobin D disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (840587029) - 66729008 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7006772024) - 66729008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7006773025) - 66729008 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2735932028) - 66729008 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2735933022) - 66729008 -> 250228007 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	250228007 \|Red blood cell finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2269084027) - 66729008 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (840586022) - 66729008 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (256646027) - 66729008 -> 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
685081000119104 View
685081000119104	Hemoglobin d beta plus thalassemia (disorder)	Hemoglobin d beta plus thalassemia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
685091000119101 View
685091000119101	Hemoglobin d beta zero thalassemia (disorder)	Hemoglobin d beta zero thalassemia	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 (201e2f7e-ce33-56c7-8154-2a74d0f290c9) 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 (290c5619-3994-5d89-9932-552ebc825c19) 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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