dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 417395001

Production

add

Component

417395001

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital hereditary endothelial dystrophy, 2 (disorder)

Shortest Term

Congenital hereditary endothelial dystrophy, 2

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

Congenital hereditary endothelial dystrophy, 2 (disorder)

SCTID: 417395001, Primitive, Active

417395001|Congenital hereditary endothelial dystrophy, 2 (disorder)|

en Ched ii - congenital hereditary endothelial dystrophy ii
en Congenital hereditary endothelial dystrophy type 2
en Congenital hereditary endothelial dystrophy type 2 (disorder)
en Congenital hereditary endothelial dystrophy, autosomal recessive form

Expression

417395001 |Congenital hereditary endothelial dystrophy, 2 (disorder)|
 <<< 85995004 |Autosomal recessive hereditary disorder (disorder)| + 
417651000 |Congenital hereditary endothelial dystrophy (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 65431007 |Structure of corneal endothelium (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 107673000 |Cellular and/or subcellular abnormality (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 25610001 |Chromosome pair 20 (cell structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3776018018 - CHED II - Congenital hereditary endothelial dystrophy II (en) View
3776018018	en	Synonym (core metadata concept)	CHED II - Congenital hereditary endothelial dystrophy II	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
2913936013 - Congenital hereditary endothelial dystrophy, 2 (en) View
2913936013	en	Synonym (core metadata concept)	Congenital hereditary endothelial dystrophy, 2	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	False
2915201016 - Congenital hereditary endothelial dystrophy, 2 (disorder) (en) View
2915201016	en	Fully specified name (core metadata concept)	Congenital hereditary endothelial dystrophy, 2 (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	False
2548354014 - Congenital hereditary endothelial dystrophy,CHED 2 (en) View
2548354014	en	Synonym (core metadata concept)	Congenital hereditary endothelial dystrophy,CHED 2	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False
3776019014 - Congenital hereditary endothelial dystrophy type 2 (en) View
3776019014	en	Synonym (core metadata concept)	Congenital hereditary endothelial dystrophy type 2	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3776017011 - Congenital hereditary endothelial dystrophy type 2 (disorder) (en) View
3776017011	en	Fully specified name (core metadata concept)	Congenital hereditary endothelial dystrophy type 2 (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2553628017 - Congenital hereditary endothelial dystrophy, autosomal recessive form (en) View
2553628017	en	Synonym (core metadata concept)	Congenital hereditary endothelial dystrophy, autosomal recessive form	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
2546082019 - Congenital hereditary endothelial dystrophy,CHED 2 (disorder) (en) View
2546082019	en	Fully specified name (core metadata concept)	Congenital hereditary endothelial dystrophy,CHED 2 (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13763576026) - 417395001 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13763577024) - 417395001 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2798636025) - 417395001 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3522878024) - 417395001 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4992918027) - 417395001 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4992920029) - 417395001 -> 25610001 (363698007) View
363698007 \|Finding site (attribute)\|	25610001 \|Chromosome pair 20 (cell structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5011381026) - 417395001 -> 107673000 (116676008) View
116676008 \|Associated morphology (attribute)\|	107673000 \|Cellular and/or subcellular abnormality (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2798637023) - 417395001 -> 25610001 (363698007) View
363698007 \|Finding site (attribute)\|	25610001 \|Chromosome pair 20 (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2798639021) - 417395001 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3360453025) - 417395001 -> 65431007 (363698007) View
363698007 \|Finding site (attribute)\|	65431007 \|Structure of corneal endothelium (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3467467021) - 417395001 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3522879027) - 417395001 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3549162027) - 417395001 -> 65431007 (363698007) View
363698007 \|Finding site (attribute)\|	65431007 \|Structure of corneal endothelium (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2798635026) - 417395001 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2798638029) - 417395001 -> 28726007 (363698007) View
363698007 \|Finding site (attribute)\|	28726007 \|Corneal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2777017028) - 417395001 -> 417651000 (116680003) View
116680003 \|Is a (attribute)\|	417651000 \|Congenital hereditary endothelial dystrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
417651000 View
417651000	Congenital hereditary endothelial dystrophy (disorder)	Congenital hereditary endothelial dystrophy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
85995004 View
85995004	Autosomal recessive hereditary disorder (disorder)	Hereditary disorder trait, nos	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 (75edad35-2a45-5627-9084-f77a328396ed) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	H18.5	TRUE	ALWAYS H18.5	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 417395001

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches