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Terminology chevron_right Concepts chevron_right 2167004

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Component

2167004

The component that hold information about this concept.

Fully Specified Name (FSN)

Retinal hemangioblastomatosis (disorder)

Shortest Term

Retinal hemangioblastomatosis

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

Retinal hemangioblastomatosis (disorder)

SCTID: 2167004, Defined, Active

2167004|Retinal hemangioblastomatosis (disorder)|

en Retinal haemangioblastomatosis
en Retinal hemangioblastomatosis
en Retinal hemangioblastomatosis (disorder)

Expression

2167004 |Retinal hemangioblastomatosis (disorder)|
 === 232073009 |Angiomatosis of retina (disorder)| + 
66091009 |Congenital disease (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 32837003 |Hemangioblastomatosis (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 5665001 |Retinal structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
4749015 - Retinal haemangioblastomatosis (en) View
4749015	en	Synonym (core metadata concept)	Retinal haemangioblastomatosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
4748011 - Retinal hemangioblastomatosis (en) View
4748011	en	Synonym (core metadata concept)	Retinal hemangioblastomatosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
750991012 - Retinal hemangioblastomatosis (disorder) (en) View
750991012	en	Fully specified name (core metadata concept)	Retinal hemangioblastomatosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (3492375029) - 2167004 -> 49381001 (116680003) View
116680003 \|Is a (attribute)\|	49381001 \|Congenital anomaly of retina (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10517444028) - 2167004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13645967022) - 2167004 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (726421026) - 2167004 -> 32837003 (116676008) View
116676008 \|Associated morphology (attribute)\|	32837003 \|Hemangioblastomatosis (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (726422022) - 2167004 -> 85026007 (116676008) View
116676008 \|Associated morphology (attribute)\|	85026007 \|Congenital hemangioblastomatosis (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2998987028) - 2167004 -> 300849006 (116680003) View
116680003 \|Is a (attribute)\|	300849006 \|Mass of eye structure (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4980445027) - 2167004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4980446026) - 2167004 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4980447024) - 2167004 -> 81745001 (363698007) View
363698007 \|Finding site (attribute)\|	81745001 \|Structure of eye proper (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4990099027) - 2167004 -> 29555009 (116680003) View
116680003 \|Is a (attribute)\|	29555009 \|Retinal disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4996442021) - 2167004 -> 19416009 (116680003) View
116680003 \|Is a (attribute)\|	19416009 \|Congenital anomaly of eye (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10747776029) - 2167004 -> 232073009 (116680003) View
116680003 \|Is a (attribute)\|	232073009 \|Angiomatosis of retina (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10747777022) - 2167004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (726426020) - 2167004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2225972023) - 2167004 -> 276654001 (116680003) View
116680003 \|Is a (attribute)\|	276654001 \|Congenital malformation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3305082028) - 2167004 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3547398024) - 2167004 -> 85026007 (116676008) View
116676008 \|Associated morphology (attribute)\|	85026007 \|Congenital hemangioblastomatosis (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3553150028) - 2167004 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (183408025) - 2167004 -> 19416009 (116680003) View
116680003 \|Is a (attribute)\|	19416009 \|Congenital anomaly of eye (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2225973029) - 2167004 -> 29555009 (116680003) View
116680003 \|Is a (attribute)\|	29555009 \|Retinal disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2769964020) - 2167004 -> 399981008 (116680003) View
116680003 \|Is a (attribute)\|	399981008 \|Neoplasm and/or hamartoma (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3305081024) - 2167004 -> 81745001 (363698007) View
363698007 \|Finding site (attribute)\|	81745001 \|Structure of eye proper (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3305083022) - 2167004 -> 32837003 (116676008) View
116676008 \|Associated morphology (attribute)\|	32837003 \|Hemangioblastomatosis (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3441721023) - 2167004 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (726424023) - 2167004 -> 5665001 (363698007) View
363698007 \|Finding site (attribute)\|	5665001 \|Retinal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2729817023) - 2167004 -> 81745001 (363698007) View
363698007 \|Finding site (attribute)\|	81745001 \|Structure of eye proper (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2729818029) - 2167004 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2841393024) - 2167004 -> 274751001 (116680003) View
116680003 \|Is a (attribute)\|	274751001 \|Mass in head or neck (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2769965021) - 2167004 -> 300849006 (116680003) View
116680003 \|Is a (attribute)\|	300849006 \|Mass of eye structure (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (183409022) - 2167004 -> 128536001 (116680003) View
116680003 \|Is a (attribute)\|	128536001 \|Disorder of posterior segment of eye (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (726423028) - 2167004 -> 25087005 (363698007) View
363698007 \|Finding site (attribute)\|	25087005 \|Structure of nervous system (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (726425024) - 2167004 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
232073009 View
232073009	Angiomatosis of retina (disorder)	Angiomatosis of retina	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
66091009 View
66091009	Congenital disease (disorder)	Congenital disease	900000000000073002 \|Sufficiently defined by necessary conditions 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 (54b79be1-d5d4-5236-b228-7875978691cc) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D48.7	TRUE	ALWAYS D48.7 \| POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE	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 (6b61c5c5-597a-5446-b0f8-c5415ba9052d) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q14.8	TRUE	ALWAYS Q14.8	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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