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Terminology chevron_right Concepts chevron_right 787413007

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Component

787413007

The component that hold information about this concept.

Fully Specified Name (FSN)

Bifid nose (disorder)

Shortest Term

Bifid nose

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

Bifid nose (disorder)

SCTID: 787413007, Primitive, Active

787413007|Bifid nose (disorder)|

en Bifid nose
en Bifid nose (disorder)

Expression

787413007 |Bifid nose (disorder)|
 <<< 764517009 |Craniofacial cleft (disorder)| + 
1899006 |Autosomal hereditary disorder (disorder)| + 
204521002 |Congenital cleft nose (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 371520008 |Developmental failure of fusion (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 45206002 |Nasal structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
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
3775349012 - Bifid nose (en) View
3775349012	en	Synonym (core metadata concept)	Bifid nose	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3775348016 - Bifid nose (disorder) (en) View
3775348016	en	Fully specified name (core metadata concept)	Bifid nose (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (11544584029) - 787413007 -> 764517009 (116680003) View
116680003 \|Is a (attribute)\|	764517009 \|Craniofacial cleft (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13673365029) - 787413007 -> 449790007 (116680003) View
116680003 \|Is a (attribute)\|	449790007 \|Orofacial cleft (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13054418021) - 787413007 -> 363212003 (116680003) View
116680003 \|Is a (attribute)\|	363212003 \|Hereditary disorder of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13054419029) - 787413007 -> 272679001 (363698007) View
363698007 \|Finding site (attribute)\|	272679001 \|Bone structure of head (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13054420024) - 787413007 -> 371520008 (116676008) View
116676008 \|Associated morphology (attribute)\|	371520008 \|Developmental failure of fusion (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13054421023) - 787413007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13054422027) - 787413007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13069776028) - 787413007 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11544582025) - 787413007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11544583024) - 787413007 -> 204521002 (116680003) View
116680003 \|Is a (attribute)\|	204521002 \|Congenital cleft nose (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11544585028) - 787413007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11544586027) - 787413007 -> 371520008 (116676008) View
116676008 \|Associated morphology (attribute)\|	371520008 \|Developmental failure of fusion (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11544587020) - 787413007 -> 1899006 (116680003) View
116680003 \|Is a (attribute)\|	1899006 \|Autosomal hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11544588026) - 787413007 -> 45206002 (363698007) View
363698007 \|Finding site (attribute)\|	45206002 \|Nasal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
764517009 View
764517009	Craniofacial cleft (disorder)	Prosoposchisis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363070008 View
363070008	Developmental hereditary disorder (disorder)	Developmental hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
204521002 View
204521002	Congenital cleft nose (disorder)	Cleft nose	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1899006 View
1899006	Autosomal hereditary disorder (disorder)	Autosomal hereditary disorder	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
717940006 View
717940006	Bifid nose, anorectal anomaly, renal anomaly syndrome (disorder)	Bnar syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
719948009 View
719948009	Trigonocephaly with bifid nose and acral anomaly syndrome (disorder)	Trigonocephaly with bifid nose and acral anomaly syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (3f02c023-f8da-52c1-8036-74c9bd59ce25) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q30.2	TRUE	ALWAYS Q30.2 \| 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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