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Terminology chevron_right Concepts chevron_right 193370005

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Component

193370005

The component that hold information about this concept.

Fully Specified Name (FSN)

Proliferative retinopathy due to sickle cell disease (disorder)

Shortest Term

Proliferative retinopathy due to sickle cell disease

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

Proliferative retinopathy due to sickle cell disease (disorder)

SCTID: 193370005, Defined, Active

193370005|Proliferative retinopathy due to sickle cell disease (disorder)|

en Proliferative retinopathy due to sickle cell disease
en Proliferative retinopathy due to sickle cell disease (disorder)

Expression

193370005 |Proliferative retinopathy due to sickle cell disease (disorder)|
 === 11603001 |Sickle cell retinopathy (disorder)| + 
46674002 |Nondiabetic proliferative retinopathy (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 13018008 |Neovascularization (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 5665001 |Retinal structure (body structure)| }
        { 42752001 |Due to (attribute)| = 127040003 |Hereditary hemoglobinopathy disorder homozygous for hemoglobin s (disorder)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
297780010 - Proliferative retinopathy due to sickle cell disease (en) View
297780010	en	Synonym (core metadata concept)	Proliferative retinopathy due to sickle cell disease	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
577250019 - Proliferative retinopathy due to sickle cell disease (disorder) (en) View
577250019	en	Fully specified name (core metadata concept)	Proliferative retinopathy due to sickle cell disease (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (2791764022) - 193370005 -> 127040003 (42752001) View
42752001 \|Due to (attribute)\|	127040003 \|Hereditary hemoglobinopathy disorder homozygous for hemoglobin s (disorder)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (960827026) - 193370005 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2874945028) - 193370005 -> 13018008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13018008 \|Neovascularization (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3289588027) - 193370005 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3289589024) - 193370005 -> 13018008 (116676008) View
116676008 \|Associated morphology (attribute)\|	13018008 \|Neovascularization (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2791765023) - 193370005 -> 30217000 (116676008) View
116676008 \|Associated morphology (attribute)\|	30217000 \|Proliferation (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (960828020) - 193370005 -> 50095005 (246075003) View
246075003 \|Causative agent (attribute)\|	50095005 \|Hemoglobin s (substance)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2273261021) - 193370005 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2273262025) - 193370005 -> 62574001 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	62574001 \|Erythropenia (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2682189023) - 193370005 -> 49938009 (116676008) View
116676008 \|Associated morphology (attribute)\|	49938009 \|Drepanocyte (cell)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2682190025) - 193370005 -> 49938009 (116676008) View
116676008 \|Associated morphology (attribute)\|	49938009 \|Drepanocyte (cell)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2742595028) - 193370005 -> 414128005 (363698007) View
363698007 \|Finding site (attribute)\|	414128005 \|Erythroid cell (cell)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2773812023) - 193370005 -> 46674002 (116680003) View
116680003 \|Is a (attribute)\|	46674002 \|Nondiabetic proliferative retinopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (960830022) - 193370005 -> 49938009 (116676008) View
116676008 \|Associated morphology (attribute)\|	49938009 \|Drepanocyte (cell)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (960832025) - 193370005 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (960831021) - 193370005 -> 281833003 (363698007) View
363698007 \|Finding site (attribute)\|	281833003 \|Entire hematological system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (960829028) - 193370005 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (326796020) - 193370005 -> 11603001 (116680003) View
116680003 \|Is a (attribute)\|	11603001 \|Sickle cell retinopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
11603001 View
11603001	Sickle cell retinopathy (disorder)	Sickle cell retinopathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
46674002 View
46674002	Nondiabetic proliferative retinopathy (disorder)	Nondiabetic proliferative retinopathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
685574841000119108 View
685574841000119108	Proliferative retinopathy of left eye due to sickle cell disease (disorder)	Proliferative retinopathy of left eye due to sickle cell disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
961739241000119108 View
961739241000119108	Proliferative retinopathy of right eye due to sickle cell disease (disorder)	Proliferative retinopathy of right eye due to sickle cell disease	900000000000073002 \|Sufficiently defined by necessary conditions 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 (409e2780-a04e-5923-b58e-e7d015078f6b) 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 (e2c4fc27-3367-5ef2-a892-5635bb269491) 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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