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Terminology chevron_right Concepts chevron_right 717003001

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Component

717003001

The component that hold information about this concept.

Fully Specified Name (FSN)

Hereditary cavernous hemangioma of brain (disorder)

Shortest Term

Familial cerebral cavernous malformation

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

Hereditary cavernous hemangioma of brain (disorder)

SCTID: 717003001, Defined, Active

717003001|Hereditary cavernous hemangioma of brain (disorder)|

en Familial cerebral cavernous malformation
en Hereditary cavernous haemangioma of brain
en Hereditary cavernous hemangioma of brain
en Hereditary cavernous hemangioma of brain (disorder)

Expression

717003001 |Hereditary cavernous hemangioma of brain (disorder)|
 === 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
363235000 |Hereditary disorder of nervous system (disorder)| + 
444869007 |Cavernous hemangioma of brain (disorder)| + 
363005004 |Cardiovascular system hereditary disorder (disorder)| + 
92030004 |Benign neoplasm of brain (disorder)| + 
302909007 |Diffuse cerebrovascular disease (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 33377007 |Cavernous hemangioma (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 12738006 |Brain structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 33377007 |Cavernous hemangioma (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 281138005 |Intracranial vascular 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
3308155013 - Familial cerebral cavernous malformation (en) View
3308155013	en	Synonym (core metadata concept)	Familial cerebral cavernous malformation	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3308154012 - Hereditary cavernous haemangioma of brain (en) View
3308154012	en	Synonym (core metadata concept)	Hereditary cavernous haemangioma of brain	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3308153018 - Hereditary cavernous hemangioma of brain (en) View
3308153018	en	Synonym (core metadata concept)	Hereditary cavernous hemangioma of brain	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3308152011 - Hereditary cavernous hemangioma of brain (disorder) (en) View
3308152011	en	Fully specified name (core metadata concept)	Hereditary cavernous hemangioma of brain (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (11104925026) - 717003001 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12092629023) - 717003001 -> 57148006 (116680003) View
116680003 \|Is a (attribute)\|	57148006 \|Congenital anomaly of brain (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12092635023) - 717003001 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13069655025) - 717003001 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12824509027) - 717003001 -> 302909007 (116680003) View
116680003 \|Is a (attribute)\|	302909007 \|Diffuse cerebrovascular disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12092630029) - 717003001 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12092631025) - 717003001 -> 33377007 (116676008) View
116676008 \|Associated morphology (attribute)\|	33377007 \|Cavernous hemangioma (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12092632021) - 717003001 -> 363005004 (116680003) View
116680003 \|Is a (attribute)\|	363005004 \|Cardiovascular system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12092633027) - 717003001 -> 281138005 (363698007) View
363698007 \|Finding site (attribute)\|	281138005 \|Intracranial vascular structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12092634022) - 717003001 -> 92030004 (116680003) View
116680003 \|Is a (attribute)\|	92030004 \|Benign neoplasm of brain (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11104926025) - 717003001 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594826022) - 717003001 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594827029) - 717003001 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594828023) - 717003001 -> 444869007 (116680003) View
116680003 \|Is a (attribute)\|	444869007 \|Cavernous hemangioma of brain (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594829026) - 717003001 -> 33377007 (116676008) View
116676008 \|Associated morphology (attribute)\|	33377007 \|Cavernous hemangioma (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594830020) - 717003001 -> 12738006 (363698007) View
363698007 \|Finding site (attribute)\|	12738006 \|Brain structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
444869007 View
444869007	Cavernous hemangioma of brain (disorder)	Cavernous hemangioma of brain	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
11164009 View
11164009	Autosomal dominant hereditary disorder (disorder)	Ad - autosomal dominant	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
92030004 View
92030004	Benign neoplasm of brain (disorder)	U não lành tính	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
302909007 View
302909007	Diffuse cerebrovascular disease (disorder)	Diffuse cerebrovascular disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363005004 View
363005004	Cardiovascular system hereditary disorder (disorder)	Cardiovascular system hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363235000 View
363235000	Hereditary disorder of nervous system (disorder)	Hereditary disorder of nervous system	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 (31b3dc11-b4f8-59b4-8899-d8126d7bb3ab) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	TRUE	SOURCE SNOMED CONCEPT IS AMBIGUOUS	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447640006 \|Source snomed concept is ambiguous (foundation metadata concept)\|
ExtendedMap object (ea1a7c73-8a21-5e53-a90b-8b683bdf9d61) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q28.3	TRUE	ALWAYS Q28.3	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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