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Terminology chevron_right Concepts chevron_right 718551002

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Component

718551002

The component that hold information about this concept.

Fully Specified Name (FSN)

Moyamoya disease with early onset achalasia (disorder)

Shortest Term

Moyamoya disease with early onset achalasia

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

Moyamoya disease with early onset achalasia (disorder)

SCTID: 718551002, Primitive, Active

718551002|Moyamoya disease with early onset achalasia (disorder)|

en Moyamoya disease with early onset achalasia
en Moyamoya disease with early onset achalasia (disorder)

Expression

718551002 |Moyamoya disease with early onset achalasia (disorder)|
 <<< 45564002 |Achalasia of esophagus (disorder)| + 
69116000 |Moyamoya disease (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
363005004 |Cardiovascular system hereditary disorder (disorder)| + 
363080007 |Digestive system hereditary disorder (disorder)| + 
363235000 |Hereditary disorder of nervous system (disorder)| : 
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
363714003 |Interprets (attribute)| = 398598008 |Motility (observable entity)| }
        { 246454002 |Occurrence (attribute)| = 3658006 |Infancy (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 25271004 |Cardioesophageal junction structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 28661005 |Cerebrovascular system structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 12738006 |Brain structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3312728012 - Moyamoya disease with early onset achalasia (en) View
3312728012	en	Synonym (core metadata concept)	Moyamoya disease with early onset achalasia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
3312727019 - Moyamoya disease with early onset achalasia (disorder) (en) View
3312727019	en	Fully specified name (core metadata concept)	Moyamoya disease with early onset achalasia (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (7117406021) - 718551002 -> 32849002 (363698007) View
363698007 \|Finding site (attribute)\|	32849002 \|Esophageal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6611135020) - 718551002 -> 3658006 (246454002) View
246454002 \|Occurrence (attribute)\|	3658006 \|Infancy (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6611136021) - 718551002 -> 12738006 (363698007) View
363698007 \|Finding site (attribute)\|	12738006 \|Brain structure (body structure)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6611137028) - 718551002 -> 25271004 (363698007) View
363698007 \|Finding site (attribute)\|	25271004 \|Cardioesophageal junction structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6611138022) - 718551002 -> 28661005 (363698007) View
363698007 \|Finding site (attribute)\|	28661005 \|Cerebrovascular system structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7117407028) - 718551002 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7117408022) - 718551002 -> 398598008 (363714003) View
363714003 \|Interprets (attribute)\|	398598008 \|Motility (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6611129020) - 718551002 -> 45564002 (116680003) View
116680003 \|Is a (attribute)\|	45564002 \|Achalasia of esophagus (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6611130026) - 718551002 -> 69116000 (116680003) View
116680003 \|Is a (attribute)\|	69116000 \|Moyamoya disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6611131027) - 718551002 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6611132023) - 718551002 -> 363005004 (116680003) View
116680003 \|Is a (attribute)\|	363005004 \|Cardiovascular system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6611133029) - 718551002 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6611134024) - 718551002 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
45564002 View
45564002	Achalasia of esophagus (disorder)	Cardiospasm	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
69116000 View
69116000	Moyamoya disease (disorder)	Moyamoya disease	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
363005004 View
363005004	Cardiovascular system hereditary disorder (disorder)	Cardiovascular system hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363080007 View
363080007	Digestive system hereditary disorder (disorder)	Digestive 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 (74f507be-1d49-5bee-9114-d76348aac41f) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	I67.5	TRUE	ALWAYS I67.5 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	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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