dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 232054005

Production

add

Component

232054005

The component that hold information about this concept.

Fully Specified Name (FSN)

X-linked retinitis pigmentosa (disorder)

Shortest Term

X-linked retinitis pigmentosa

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

X-linked retinitis pigmentosa (disorder)

SCTID: 232054005, Defined, Active

232054005|X-linked retinitis pigmentosa (disorder)|

en X-linked retinitis pigmentosa (disorder)
en X-linked retinitis pigmentosa

Expression

232054005 |X-linked retinitis pigmentosa (disorder)|
 === 28835009 |Retinitis pigmentosa (disorder)| + 
128430005 |X-linked hereditary disease (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
620069017 - X-linked retinitis pigmentosa (disorder) (en) View
620069017	en	Fully specified name (core metadata concept)	X-linked retinitis pigmentosa (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
347705019 - X-linked retinitis pigmentosa (en) View
347705019	en	Synonym (core metadata concept)	X-linked retinitis pigmentosa	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (14026347023) - 232054005 -> 128430005 (116680003) View
116680003 \|Is a (attribute)\|	128430005 \|X-linked hereditary disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (502178022) - 232054005 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5049162022) - 232054005 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5049163028) - 232054005 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (43627027) - 232054005 -> 28835009 (116680003) View
116680003 \|Is a (attribute)\|	28835009 \|Retinitis pigmentosa (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
28835009 View
28835009	Retinitis pigmentosa (disorder)	Viêm võng mạc sắc tố	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
128430005 View
128430005	X-linked hereditary disease (disorder)	X-linked hereditary disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
719282008 View
719282008	Primary ciliary dyskinesia and retinitis pigmentosa syndrome (disorder)	Primary ciliary dyskinesia and retinitis pigmentosa syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
719808002 View
719808002	Chromosome xp11.3 microdeletion syndrome (disorder)	Aldred syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
232055006 View
232055006	X-linked retinitis pigmentosa heterozygote (disorder)	X-linked retinitis pigmentosa heterozygote	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 (a240a3ed-1779-5a41-828e-25414abbe520) 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)\|

Terminology chevron_right Concepts chevron_right 232054005

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches