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Terminology chevron_right Concepts chevron_right 763829004

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Component

763829004

The component that hold information about this concept.

Fully Specified Name (FSN)

Oculopharyngodistal myopathy (disorder)

Shortest Term

Bệnh cơ nhãn hầu

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

Oculopharyngodistal myopathy (disorder)

SCTID: 763829004, Primitive, Active

763829004|Oculopharyngodistal myopathy (disorder)|

vi Bệnh cơ nhãn hầu
en Oculopharyngeal distal myopathy
en Oculopharyngodistal myopathy
en Oculopharyngodistal myopathy (disorder)
en Opdm - oculopharyngodistal myopathy

Expression

763829004 |Oculopharyngodistal myopathy (disorder)|
 <<< 58795000 |Distal muscular dystrophy (disorder)| + 
75860007 |Disorder of pharynx (disorder)| + 
129567005 |Pharyngeal paresis (finding)| + 
363080007 |Digestive system hereditary disorder (disorder)| + 
363343008 |Hereditary disorder of the visual system (disorder)| + 
17097001 |Chronic disease of respiratory system (disorder)| + 
128284006 |Chronic digestive system disorder (disorder)| + 
111235007 |Musculoskeletal disorder of the neck (disorder)| + 
1137511009 |Progressive weakness of muscle (finding)| + 
1119512002 |Progressive ptosis of upper eyelid (disorder)| : 
        { 263502005 |Clinical course (attribute)| = 255314001 |Progressive (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 29696001 |Prolapse (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 38934000 |Upper eyelid structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 60494004 |Muscle structure of pharynx (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 127954009 |Skeletal muscle structure (body structure)|,
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
536021000003115 - bệnh cơ nhãn hầu (vi) View
536021000003115	vi	Synonym (core metadata concept)	bệnh cơ nhãn hầu	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
3644148011 - Oculopharyngeal distal myopathy (en) View
3644148011	en	Synonym (core metadata concept)	Oculopharyngeal distal myopathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3644149015 - Oculopharyngodistal myopathy (en) View
3644149015	en	Synonym (core metadata concept)	Oculopharyngodistal myopathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3644147018 - Oculopharyngodistal myopathy (disorder) (en) View
3644147018	en	Fully specified name (core metadata concept)	Oculopharyngodistal myopathy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3644150015 - OPDM - oculopharyngodistal myopathy (en) View
3644150015	en	Synonym (core metadata concept)	OPDM - oculopharyngodistal myopathy	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9635619028) - 763829004 -> 11934000 (116680003) View
116680003 \|Is a (attribute)\|	11934000 \|Ptosis of eyelid (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9635623020) - 763829004 -> 128296004 (116680003) View
116680003 \|Is a (attribute)\|	128296004 \|Chronic disease of ocular adnexa (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16408155022) - 763829004 -> 1119512002 (116680003) View
116680003 \|Is a (attribute)\|	1119512002 \|Progressive ptosis of upper eyelid (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16286734020) - 763829004 -> 1137511009 (116680003) View
116680003 \|Is a (attribute)\|	1137511009 \|Progressive weakness of muscle (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9159704026) - 763829004 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9159705025) - 763829004 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9238140024) - 763829004 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9238142027) - 763829004 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9635617026) - 763829004 -> 255314001 (263502005) View
263502005 \|Clinical course (attribute)\|	255314001 \|Progressive (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9635620023) - 763829004 -> 60494004 (363698007) View
363698007 \|Finding site (attribute)\|	60494004 \|Muscle structure of pharynx (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9635624025) - 763829004 -> 128237006 (116680003) View
116680003 \|Is a (attribute)\|	128237006 \|Chronic disease of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11538892023) - 763829004 -> 111235007 (116680003) View
116680003 \|Is a (attribute)\|	111235007 \|Musculoskeletal disorder of the neck (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11570278026) - 763829004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9147863025) - 763829004 -> 268163008 (116680003) View
116680003 \|Is a (attribute)\|	268163008 \|Congenital ptosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9147867029) - 763829004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9164210028) - 763829004 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9223874027) - 763829004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9223875026) - 763829004 -> 61989004 (116676008) View
116676008 \|Associated morphology (attribute)\|	61989004 \|Congenital prolapse (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9223876025) - 763829004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9223877023) - 763829004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9238141023) - 763829004 -> 60494004 (363698007) View
363698007 \|Finding site (attribute)\|	60494004 \|Muscle structure of pharynx (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9635621022) - 763829004 -> 17097001 (116680003) View
116680003 \|Is a (attribute)\|	17097001 \|Chronic disease of respiratory system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9635622026) - 763829004 -> 128284006 (116680003) View
116680003 \|Is a (attribute)\|	128284006 \|Chronic digestive system disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9640980022) - 763829004 -> 29696001 (116676008) View
116676008 \|Associated morphology (attribute)\|	29696001 \|Prolapse (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9147860027) - 763829004 -> 58795000 (116680003) View
116680003 \|Is a (attribute)\|	58795000 \|Distal muscular dystrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9147861028) - 763829004 -> 75860007 (116680003) View
116680003 \|Is a (attribute)\|	75860007 \|Disorder of pharynx (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9147862024) - 763829004 -> 129567005 (116680003) View
116680003 \|Is a (attribute)\|	129567005 \|Pharyngeal paresis (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9147864020) - 763829004 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9147865021) - 763829004 -> 363343008 (116680003) View
116680003 \|Is a (attribute)\|	363343008 \|Hereditary disorder of the visual system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9223872028) - 763829004 -> 38934000 (363698007) View
363698007 \|Finding site (attribute)\|	38934000 \|Upper eyelid structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1119512002 View
1119512002	Progressive ptosis of upper eyelid (disorder)	Progressive blepharoptosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1137511009 View
1137511009	Progressive weakness of muscle (finding)	Yếu tiến triển cơ (phát hiện)	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
129567005 View
129567005	Pharyngeal paresis (finding)	Pharyngeal paresis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
75860007 View
75860007	Disorder of pharynx (disorder)	Bệnh hầu họng	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
111235007 View
111235007	Musculoskeletal disorder of the neck (disorder)	Musculoskeletal disorder of the neck	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
17097001 View
17097001	Chronic disease of respiratory system (disorder)	Bệnh hệ hô hấp mạn tính	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
58795000 View
58795000	Distal muscular dystrophy (disorder)	Distal myopathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
128284006 View
128284006	Chronic digestive system disorder (disorder)	Chronic digestive system 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
363343008 View
363343008	Hereditary disorder of the visual system (disorder)	Hereditary disorder of the visual 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 (52f9c73f-7a21-51b0-8322-aa299c59d276) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G71.0	TRUE	ALWAYS G71.0 \| 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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