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Terminology chevron_right Concepts chevron_right 232074003

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Component

232074003

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital hypertrophy of retinal pigment epithelium (disorder)

Shortest Term

Phì đại biểu mô sắc tố võng mạc bẩm sinh

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

Congenital hypertrophy of retinal pigment epithelium (disorder)

SCTID: 232074003, Defined, Active

232074003|Congenital hypertrophy of retinal pigment epithelium (disorder)|

vi Phì đại biểu mô sắc tố võng mạc bẩm sinh
en Congenital hyperplasia of retinal pigment epithelium
en Congenital hypertrophy of retinal pigment epithelium
en Congenital hypertrophy of retinal pigment epithelium (disorder)
en Chrpe - congenital hypertrophy of retinal pigment epithelium

Expression

232074003 |Congenital hypertrophy of retinal pigment epithelium (disorder)|
 === 49381001 |Congenital anomaly of retina (disorder)| + 
425217005 |Retinal pigment epithelial hypertrophy (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 56246009 |Hypertrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 41275009 |Structure of retinal pigment epithelium (body 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
573091000003110 - phì đại biểu mô sắc tố võng mạc bẩm sinh (vi) View
573091000003110	vi	Synonym (core metadata concept)	phì đại biểu mô sắc tố võng mạc bẩm sinh	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
347734013 - Congenital hyperplasia of retinal pigment epithelium (en) View
347734013	en	Synonym (core metadata concept)	Congenital hyperplasia of retinal pigment epithelium	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
347736010 - Congenital hypertrophy of retinal pigment epithelium (en) View
347736010	en	Synonym (core metadata concept)	Congenital hypertrophy of retinal pigment epithelium	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
620092017 - Congenital hypertrophy of retinal pigment epithelium (disorder) (en) View
620092017	en	Fully specified name (core metadata concept)	Congenital hypertrophy of retinal pigment epithelium (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2646489019 - CHRPE - Congenital hypertrophy of retinal pigment epithelium (en) View
2646489019	en	Synonym (core metadata concept)	CHRPE - Congenital hypertrophy of retinal pigment epithelium	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
347735014 - CHRPE - Congenital hypertophy of retinal pigment epithelium (en) View
347735014	en	Synonym (core metadata concept)	CHRPE - Congenital hypertophy of retinal pigment epithelium	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (3388452028) - 232074003 -> 41275009 (363698007) View
363698007 \|Finding site (attribute)\|	41275009 \|Structure of retinal pigment epithelium (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4980176026) - 232074003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5024778021) - 232074003 -> 90141005 (116676008) View
116676008 \|Associated morphology (attribute)\|	90141005 \|Congenital hypertrophy (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5024779029) - 232074003 -> 41275009 (363698007) View
363698007 \|Finding site (attribute)\|	41275009 \|Structure of retinal pigment epithelium (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6115372021) - 232074003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10533363020) - 232074003 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11104829022) - 232074003 -> 56246009 (116676008) View
116676008 \|Associated morphology (attribute)\|	56246009 \|Hypertrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2572813020) - 232074003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2991693029) - 232074003 -> 424956000 (116680003) View
116680003 \|Is a (attribute)\|	424956000 \|Retinal pigment epithelial hyperplasia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3388453022) - 232074003 -> 50493007 (116676008) View
116676008 \|Associated morphology (attribute)\|	50493007 \|Congenital hyperplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5024777027) - 232074003 -> 425217005 (116680003) View
116680003 \|Is a (attribute)\|	425217005 \|Retinal pigment epithelial hypertrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2572811022) - 232074003 -> 41275009 (363698007) View
363698007 \|Finding site (attribute)\|	41275009 \|Structure of retinal pigment epithelium (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2572812026) - 232074003 -> 50493007 (116676008) View
116676008 \|Associated morphology (attribute)\|	50493007 \|Congenital hyperplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (43658026) - 232074003 -> 92321003 (116680003) View
116680003 \|Is a (attribute)\|	92321003 \|Benign neoplasm of retina (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (502223021) - 232074003 -> 3898006 (116676008) View
116676008 \|Associated morphology (attribute)\|	3898006 \|Neoplasm, benign (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2442990022) - 232074003 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (502222027) - 232074003 -> 31390008 (116676008) View
116676008 \|Associated morphology (attribute)\|	31390008 \|Epithelial hyperplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (502225025) - 232074003 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2532312027) - 232074003 -> 49381001 (116680003) View
116680003 \|Is a (attribute)\|	49381001 \|Congenital anomaly of retina (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2211582024) - 232074003 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2202265025) - 232074003 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1711660027) - 232074003 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (502224026) - 232074003 -> 367634005 (308489006) View
308489006 \|Pathological process (qualifier value)\|	367634005 \|Benign neoplastic process (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (502226029) - 232074003 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
425217005 View
425217005	Retinal pigment epithelial hypertrophy (disorder)	Rpe hypertrophy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
49381001 View
49381001	Congenital anomaly of retina (disorder)	Congenital anomaly of retina	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1142277007 View
1142277007	Solitary congenital hypertrophy of retinal pigment epithelium (disorder)	Solitary congenital hypertrophy of retinal pigment epithelium	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
15986511000119108 View
15986511000119108	Congenital hypertrophy of retinal pigment epithelium of right eye (disorder)	Congenital bear track retinal pigment hypertrophy of right eye	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
15986591000119104 View
15986591000119104	Congenital hypertrophy of retinal pigment epithelium of left eye (disorder)	Congenital bear track retinal pigment hypertrophy of left eye	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 (955b0a42-91d9-52b0-a5ee-5ea46b206db8) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q14.1	TRUE	ALWAYS Q14.1	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)\|

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