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Terminology chevron_right Concepts chevron_right 416417002

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Component

416417002

The component that hold information about this concept.

Fully Specified Name (FSN)

Hereditary hemoglobin s (disorder)

Shortest Term

Hereditary hemoglobin s

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

Hereditary hemoglobin s (disorder)

SCTID: 416417002, Primitive, Active

416417002|Hereditary hemoglobin s (disorder)|

en Hereditary haemoglobin s
en Hereditary hemoglobin s
en Hereditary hemoglobin s (disorder)

Expression

416417002 |Hereditary hemoglobin s (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
2548929015 - Hereditary haemoglobin S (en) View
2548929015	en	Synonym (core metadata concept)	Hereditary haemoglobin S	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
2548928011 - Hereditary hemoglobin S (en) View
2548928011	en	Synonym (core metadata concept)	Hereditary hemoglobin S	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
2546627012 - Hereditary hemoglobin S (disorder) (en) View
2546627012	en	Fully specified name (core metadata concept)	Hereditary hemoglobin S (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (5975345025) - 416417002 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7007666023) - 416417002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7007667025) - 416417002 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2785071027) - 416417002 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2785072023) - 416417002 -> 250228007 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	250228007 \|Red blood cell finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2768787025) - 416417002 -> 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
417357006 View
417357006	Sickling disorder due to hemoglobin s (disorder)	Sickle cell disease	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

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (1bf1494a-eb54-5c60-98bd-d0b44786a65d) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D57.3	TRUE	ALWAYS D57.3	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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