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Terminology chevron_right Concepts chevron_right 722034006

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Component

722034006

The component that hold information about this concept.

Fully Specified Name (FSN)

Median nodule of upper lip (disorder)

Shortest Term

Median nodule of upper lip

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

Median nodule of upper lip (disorder)

SCTID: 722034006, Primitive, Active

722034006|Median nodule of upper lip (disorder)|

en Median nodule of upper lip
en Median nodule of upper lip (disorder)

Expression

722034006 |Median nodule of upper lip (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
66091009 |Congenital disease (disorder)| + 
301350008 |Lesion of lip (disorder)| + 
363080007 |Digestive system hereditary disorder (disorder)| + 
1179041001 |Mass of lip (finding)| + 
42357009 |Disorder of digestive system specific to fetus or newborn (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 27925004 |Nodule (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 11681001 |Upper lip 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
3330256019 - Median nodule of upper lip (en) View
3330256019	en	Synonym (core metadata concept)	Median nodule of upper lip	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3325373014 - Median nodule of upper lip (disorder) (en) View
3325373014	en	Fully specified name (core metadata concept)	Median nodule of upper lip (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15880909020) - 722034006 -> 42357009 (116680003) View
116680003 \|Is a (attribute)\|	42357009 \|Disorder of digestive system specific to fetus or newborn (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6772325022) - 722034006 -> 90678009 (116680003) View
116680003 \|Is a (attribute)\|	90678009 \|Disorder of lip (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6772326023) - 722034006 -> 239953001 (116680003) View
116680003 \|Is a (attribute)\|	239953001 \|Lesion of soft tissue (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6772328024) - 722034006 -> 301350008 (116680003) View
116680003 \|Is a (attribute)\|	301350008 \|Lesion of lip (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6772327025) - 722034006 -> 300855001 (116680003) View
116680003 \|Is a (attribute)\|	300855001 \|Mass of digestive structure (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6772330021) - 722034006 -> 432525007 (116680003) View
116680003 \|Is a (attribute)\|	432525007 \|Mass of head (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6772331020) - 722034006 -> 444905003 (116680003) View
116680003 \|Is a (attribute)\|	444905003 \|Mass of soft tissue (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14909594027) - 722034006 -> 1179041001 (116680003) View
116680003 \|Is a (attribute)\|	1179041001 \|Mass of lip (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6772323026) - 722034006 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6772324021) - 722034006 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6772329027) - 722034006 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6772332029) - 722034006 -> 27925004 (116676008) View
116676008 \|Associated morphology (attribute)\|	27925004 \|Nodule (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6772333023) - 722034006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6772334028) - 722034006 -> 11681001 (363698007) View
363698007 \|Finding site (attribute)\|	11681001 \|Upper lip structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1179041001 View
1179041001	Mass of lip (finding)	Mass of lip	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
42357009 View
42357009	Disorder of digestive system specific to fetus or newborn (disorder)	Perinatal digestive system disorders	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
301350008 View
301350008	Lesion of lip (disorder)	Lesion of lip	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
11164009 View
11164009	Autosomal dominant hereditary disorder (disorder)	Ad - autosomal dominant	900000000000074008 \|Necessary but not sufficient concept 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

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 (8d794c3b-7697-5028-9502-8a6789da89b7) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q18.8	TRUE	ALWAYS Q18.8 \| 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)\|
ExtendedMap object (c9d595ec-6162-5e4d-b888-5358ed51808d) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	K13.0	TRUE	ALWAYS K13.0	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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