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Terminology chevron_right Concepts chevron_right 11603001

Production

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Component

11603001

The component that hold information about this concept.

Fully Specified Name (FSN)

Sickle cell retinopathy (disorder)

Shortest Term

Sickle cell retinopathy

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Sickle cell retinopathy (disorder)

SCTID: 11603001, Defined, Active

11603001|Sickle cell retinopathy (disorder)|

en Sickle cell retinopathy
en Sickle cell retinopathy (disorder)

Expression

11603001 |Sickle cell retinopathy (disorder)|
 === 29555009 |Retinal disorder (disorder)| : 
        { 363698007 |Finding site (attribute)| = 5665001 |Retinal structure (body structure)| }
        { 42752001 |Due to (attribute)| = 416417002 |Hereditary hemoglobin s (disorder)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
20053019 - Sickle cell retinopathy (en) View
20053019	en	Synonym (core metadata concept)	Sickle cell retinopathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
674285012 - Sickle cell retinopathy (disorder) (en) View
674285012	en	Fully specified name (core metadata concept)	Sickle cell retinopathy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (2781130028) - 11603001 -> 127040003 (42752001) View
42752001 \|Due to (attribute)\|	127040003 \|Hereditary hemoglobinopathy disorder homozygous for hemoglobin s (disorder)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15282727025) - 11603001 -> 416417002 (42752001) View
42752001 \|Due to (attribute)\|	416417002 \|Hereditary hemoglobin s (disorder)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (609320023) - 11603001 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (99958021) - 11603001 -> 29555009 (116680003) View
116680003 \|Is a (attribute)\|	29555009 \|Retinal disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2994623022) - 11603001 -> 399625000 (116680003) View
116680003 \|Is a (attribute)\|	399625000 \|Retinopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (99959029) - 11603001 -> 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 (609322026) - 11603001 -> 50095005 (246075003) View
246075003 \|Causative agent (attribute)\|	50095005 \|Hemoglobin s (substance)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2258072024) - 11603001 -> 62574001 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	62574001 \|Erythropenia (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2258073025) - 11603001 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2650086026) - 11603001 -> 414027002 (116680003) View
116680003 \|Is a (attribute)\|	414027002 \|Disorder of hematopoietic structure (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2680569023) - 11603001 -> 49938009 (116676008) View
116676008 \|Associated morphology (attribute)\|	49938009 \|Drepanocyte (cell)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2680570024) - 11603001 -> 49938009 (116676008) View
116676008 \|Associated morphology (attribute)\|	49938009 \|Drepanocyte (cell)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2717103020) - 11603001 -> 414128005 (363698007) View
363698007 \|Finding site (attribute)\|	414128005 \|Erythroid cell (cell)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (609318020) - 11603001 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (609321022) - 11603001 -> 49938009 (116676008) View
116676008 \|Associated morphology (attribute)\|	49938009 \|Drepanocyte (cell)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (609319028) - 11603001 -> 281833003 (363698007) View
363698007 \|Finding site (attribute)\|	281833003 \|Entire hematological system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (609323020) - 11603001 -> 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
29555009 View
29555009	Retinal disorder (disorder)	Retinopathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1285514002 View
1285514002	Nonproliferative retinopathy due to sickle cell disease (disorder)	Nonproliferative sickle cell retinopathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1231702003 View
1231702003	Disorder of retina due to sickle cell trait (disorder)	Retinopathy due to sickle cell trait	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
193370005 View
193370005	Proliferative retinopathy due to sickle cell disease (disorder)	Proliferative retinopathy due to sickle cell disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
232033003 View
232033003	Sickle cell-hemoglobin c retinopathy (disorder)	Sickle cell-hemoglobin c retinopathy	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 (45cea0be-c523-55a3-aa6f-d0b3db39922c) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D57.1	TRUE	ALWAYS D57.1	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 (c7e4215d-2a2e-57e0-840d-5979dbf6d6bf) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H36.8	TRUE	ALWAYS H36.8 \| THIS CODE MAY BE USED IN THE PRIMARY POSITION WHEN THE MANIFESTATION IS THE PRIMARY FOCUS OF CARE	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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