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Terminology chevron_right Concepts chevron_right 28835009

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Component

28835009

The component that hold information about this concept.

Fully Specified Name (FSN)

Retinitis pigmentosa (disorder)

Shortest Term

Viêm võng mạc sắc tố

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

Retinitis pigmentosa (disorder)

SCTID: 28835009, Primitive, Active

28835009|Retinitis pigmentosa (disorder)|

vi Viêm võng mạc sắc tố
en Retinitis pigmentosa
en Retinitis pigmentosa (disorder)
en Rp - retinitis pigmentosa

Expression

28835009 |Retinitis pigmentosa (disorder)|
 <<< 41799005 |Hereditary retinal dystrophy (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 5665001 |Retinal structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
462171000003118 - viêm võng mạc sắc tố (vi) View
462171000003118	vi	Synonym (core metadata concept)	viêm võng mạc sắc tố	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
48282015 - Retinitis pigmentosa (en) View
48282015	en	Synonym (core metadata concept)	Retinitis pigmentosa	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
759560017 - Retinitis pigmentosa (disorder) (en) View
759560017	en	Fully specified name (core metadata concept)	Retinitis pigmentosa (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
1226074019 - RP - Retinitis pigmentosa (en) View
1226074019	en	Synonym (core metadata concept)	RP - Retinitis pigmentosa	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (744119023) - 28835009 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5049078021) - 28835009 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5049079029) - 28835009 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (194935024) - 28835009 -> 1899006 (116680003) View
116680003 \|Is a (attribute)\|	1899006 \|Autosomal hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (194934023) - 28835009 -> 41799005 (116680003) View
116680003 \|Is a (attribute)\|	41799005 \|Hereditary retinal dystrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
41799005 View
41799005	Hereditary retinal dystrophy (disorder)	Hereditary retinal dystrophy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1231663000 View
1231663000	Retinitis pigmentosa due to systemic disease (disorder)	Retinitis pigmentosa due to systemic disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
232054005 View
232054005	X-linked retinitis pigmentosa (disorder)	X-linked retinitis pigmentosa	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
782949007 View
782949007	Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder)	Friedman goodman syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
232053004 View
232053004	Autosomal recessive retinitis pigmentosa (disorder)	Autosomal recessive retinitis pigmentosa	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
733113002 View
733113002	Hypogonadotropic hypogonadism retinitis pigmentosa syndrome (disorder)	Chang davidson carlson syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
232052009 View
232052009	Autosomal dominant retinitis pigmentosa (disorder)	Autosomal dominant retinitis pigmentosa	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
25362006 View
25362006	Phytanic acid storage disease (disorder)	Hmsn iv	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
237984008 View
237984008	Neurogenic muscle weakness, ataxia and retinitis pigmentosa (disorder)	Narp syndrome	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 (0867fec8-b41b-573e-8ada-58f3360611ac) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G11.1	IFA 73119000 \| Retinitis pigmentosa-deafness-ataxia syndrome (disorder) \|	IF RETINITIS PIGMENTOSA-DEAFNESS-ATAXIA SYNDROME CHOOSE G11.1 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (0fc28211-0c6e-5b00-abe3-7a086a31c1be) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	OTHERWISE TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|
ExtendedMap object (3adb05f4-3ab6-5a69-853f-0e6caa556418) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H90.5	IFA 57838006 \| Retinitis pigmentosa-deafness syndrome (disorder) \|	IF RETINITIS PIGMENTOSA-DEAFNESS SYNDROME CHOOSE H90.5 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (444de7d3-cde9-58f4-ba11-45447192b0c9) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G60.1	IFA 25362006 \| Phytanic acid storage disease (disorder) \|	IF A CHOOSE G60.1 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (940f1598-a005-5917-b7cb-657d215cca33) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H35.5	OTHERWISE TRUE	ALWAYS H35.5	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 (95f863b0-44cb-5e24-91ca-a8f2b2791fd6) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H35.5	TRUE	ALWAYS H35.5	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 (bd2833ee-3810-54d1-8bf7-edad208bafbf) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	OTHERWISE TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (0867fec8-b41b-573e-8ada-58f3360611ac) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G11.1	IFA 73119000 \| Retinitis pigmentosa-deafness-ataxia syndrome (disorder) \|	IF RETINITIS PIGMENTOSA-DEAFNESS-ATAXIA SYNDROME CHOOSE G11.1 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (0fc28211-0c6e-5b00-abe3-7a086a31c1be) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	OTHERWISE TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|
ExtendedMap object (3adb05f4-3ab6-5a69-853f-0e6caa556418) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H90.5	IFA 57838006 \| Retinitis pigmentosa-deafness syndrome (disorder) \|	IF RETINITIS PIGMENTOSA-DEAFNESS SYNDROME CHOOSE H90.5 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (444de7d3-cde9-58f4-ba11-45447192b0c9) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G60.1	IFA 25362006 \| Phytanic acid storage disease (disorder) \|	IF A CHOOSE G60.1 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (940f1598-a005-5917-b7cb-657d215cca33) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H35.5	OTHERWISE TRUE	ALWAYS H35.5	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 (95f863b0-44cb-5e24-91ca-a8f2b2791fd6) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H35.5	TRUE	ALWAYS H35.5	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 (bd2833ee-3810-54d1-8bf7-edad208bafbf) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	OTHERWISE TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|

Terminology chevron_right Concepts chevron_right 28835009

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