SNOMED CT, US Edition

Last uploaded: March 22, 2026
Id http://purl.bioontology.org/ontology/SNOMEDCT/787413007
http://purl.bioontology.org/ontology/SNOMEDCT/787413007
Preferred Name

Bifid nose
Definitions
A rare congenital nose and cavum anomaly characterized by clefting of the nose ranging from a minimally noticeable groove in the columella to complete clefting of the underlying bones and cartilage (resulting in two half noses) with a usually adequate airway. Bifid nose may be seen in frontonasal dysplasia; other malformations such as hypertelorbitism and midline clefts of the lip may also be associated. A rare congenital nose and cavum anomaly characterised by clefting of the nose ranging from a minimally noticeable groove in the columella to complete clefting of the underlying bones and cartilage (resulting in two half noses) with a usually adequate airway. Bifid nose may be seen in frontonasal dysplasia; other malformations such as hypertelorbitism and midline clefts of the lip may also be associated. Bifid nose is a rare congenital malformation of presumed autosomal dominant or recessive inheritance with characteristics of clefting of the nose ranging from a minimally noticeable groove in the columella to complete clefting of the underlying bones and cartilage (resulting in two half noses) with a usually adequate airway. Bifid nose may be seen in frontonasal dysplasia while other malformations such as hypertelorbitism and midline clefts of the lip may also be associated.
Synonyms
Bifid nose (disorder)
Type http://www.w3.org/2002/07/owl#Class

All Properties

definition

A rare congenital nose and cavum anomaly characterized by clefting of the nose ranging from a minimally noticeable groove in the columella to complete clefting of the underlying bones and cartilage (resulting in two half noses) with a usually adequate airway. Bifid nose may be seen in frontonasal dysplasia; other malformations such as hypertelorbitism and midline clefts of the lip may also be associated.

A rare congenital nose and cavum anomaly characterised by clefting of the nose ranging from a minimally noticeable groove in the columella to complete clefting of the underlying bones and cartilage (resulting in two half noses) with a usually adequate airway. Bifid nose may be seen in frontonasal dysplasia; other malformations such as hypertelorbitism and midline clefts of the lip may also be associated.

Bifid nose is a rare congenital malformation of presumed autosomal dominant or recessive inheritance with characteristics of clefting of the nose ranging from a minimally noticeable groove in the columella to complete clefting of the underlying bones and cartilage (resulting in two half noses) with a usually adequate airway. Bifid nose may be seen in frontonasal dysplasia while other malformations such as hypertelorbitism and midline clefts of the lip may also be associated.
prefLabel
Bifid nose
altLabel
Bifid nose (disorder)
Type ID
900000000000003001
900000000000013009
Semantic type UMLS property
Has finding site
Effective time
20190731
cui
C0221363
Has pathological process
CTV3ID
XVAwx
DEFINITION STATUS ID
900000000000074008
CASE SIGNIFICANCE ID
900000000000448009
Occurs in
tui
T019
Active
1
Has associated morphology
notation
787413007
type
subClassOf
Subset member
447562003~MAPRULE~TRUE
6011000124106~MAPTARGET~Q75.03
6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
6011000124106~MAPTARGET~Q87.0
6011000124106~MAPRULE~IFA 717940006 | BNAR syndrome |
6011000124106~MAPADVICE~IF TRIGONOCEPHALY WITH BIFID NOSE AND ACRAL ANOMALY SYNDROME CHOOSE Q74.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~
6011000124106~MAPCATEGORYID~447638001
6011000124106~MAPGROUP~1
6011000124106~MAPGROUP~2
6011000124106~MAPTARGET~Q30.2
6011000124106~MAPADVICE~IF TRIGONOCEPHALY WITH BIFID NOSE AND ACRAL ANOMALY SYNDROME CHOOSE Q75.03 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~ALWAYS Q30.2
6011000124106~MAPTARGET~Q75.0
447562003~MAPGROUP~1
447562003~CORRELATIONID~447561005
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
6011000124106~MAPADVICE~IF BNAR SYNDROME CHOOSE Q87.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF TRIGONOCEPHALY WITH BIFID NOSE AND ACRAL ANOMALY SYNDROME CHOOSE Q30.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~Q74.9
900000000000508004~ACCEPTABILITYID~900000000000548007
447562003~MAPPRIORITY~1
447562003~MAPCATEGORYID~447637006
6011000124106~MAPRULE~OTHERWISE TRUE
6011000124106~MAPCATEGORYID~447639009
6011000124106~MAPADVICE~IF TRIGONOCEPHALY WITH BIFID NOSE AND ACRAL ANOMALY SYNDROME CHOOSE Q75.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~1
6011000124106~CORRELATIONID~447561005
900000000000497000~MAPTARGET~XVAwx
447562003~MAPADVICE~ALWAYS Q30.2 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
6011000124106~MAPRULE~TRUE
6011000124106~MAPGROUP~3
6011000124106~MAPPRIORITY~3
6011000124106~MAPPRIORITY~2
6011000124106~MAPRULE~IFA 719948009 | Trigonocephaly with bifid nose and acral anomaly syndrome |
447562003~MAPTARGET~Q30.2
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