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Terminology chevron_right Concepts chevron_right 127048005

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Component

127048005

The component that hold information about this concept.

Fully Specified Name (FSN)

Sickle cell-hemoglobin o arab disease (disorder)

Shortest Term

Sickle cell-hemoglobin o arab disease

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

Sickle cell-hemoglobin o arab disease (disorder)

SCTID: 127048005, Primitive, Active

127048005|Sickle cell-hemoglobin o arab disease (disorder)|

en Sickle cell-haemoglobin o arab disease
en Sickle cell-hemoglobin o arab disease
en Sickle cell-hemoglobin o arab disease (disorder)

Expression

127048005 |Sickle cell-hemoglobin o arab disease (disorder)|
 <<< 23269001 |Double heterozygous sickling disorder (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
474041013 - Sickle cell-Haemoglobin O Arab disease (en) View
474041013	en	Synonym (core metadata concept)	Sickle cell-Haemoglobin O Arab disease	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
336017 - Sickle cell-Hemoglobin O Arab disease (en) View
336017	en	Synonym (core metadata concept)	Sickle cell-Hemoglobin O Arab disease	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
731087015 - Sickle cell-Hemoglobin O Arab disease (disorder) (en) View
731087015	en	Fully specified name (core metadata concept)	Sickle cell-Hemoglobin O Arab disease (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (694789020) - 127048005 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7006941025) - 127048005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7006942021) - 127048005 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2785780023) - 127048005 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2785779020) - 127048005 -> 250228007 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	250228007 \|Red blood cell finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (161650023) - 127048005 -> 127040003 (116680003) View
116680003 \|Is a (attribute)\|	127040003 \|Hereditary hemoglobinopathy disorder homozygous for hemoglobin s (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (694787022) - 127048005 -> 50095005 (246075003) View
246075003 \|Causative agent (attribute)\|	50095005 \|Hemoglobin s (substance)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2264037029) - 127048005 -> 62574001 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	62574001 \|Erythropenia (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2264038023) - 127048005 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2680838025) - 127048005 -> 49938009 (116676008) View
116676008 \|Associated morphology (attribute)\|	49938009 \|Drepanocyte (cell)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2680839022) - 127048005 -> 49938009 (116676008) View
116676008 \|Associated morphology (attribute)\|	49938009 \|Drepanocyte (cell)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2687888024) - 127048005 -> 414027002 (116680003) View
116680003 \|Is a (attribute)\|	414027002 \|Disorder of hematopoietic structure (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2728270025) - 127048005 -> 414128005 (363698007) View
363698007 \|Finding site (attribute)\|	414128005 \|Erythroid cell (cell)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2769417025) - 127048005 -> 23269001 (116680003) View
116680003 \|Is a (attribute)\|	23269001 \|Double heterozygous sickling disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (694788028) - 127048005 -> 49938009 (116676008) View
116676008 \|Associated morphology (attribute)\|	49938009 \|Drepanocyte (cell)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (694790027) - 127048005 -> 281833003 (363698007) View
363698007 \|Finding site (attribute)\|	281833003 \|Entire hematological system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (694786029) - 127048005 -> 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
23269001 View
23269001	Double heterozygous sickling disorder (disorder)	Double heterozygous sickling disorder	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 (5628ca49-948f-5f51-b0c3-ffa8c765576c) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D57.8	TRUE	ALWAYS D57.8	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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