loading...| Preferred Name |
Bifid nose |
|
| Synonyms |
Bifid nose (disorder) |
|
| Definitions |
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. |
|
| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/787413007 |
|
| Active |
1 |
|
| altLabel |
Bifid nose (disorder) |
|
| CASE SIGNIFICANCE ID |
900000000000448009 |
|
| CTV3ID |
XVAwx |
|
| cui |
C0221363 |
|
| definition |
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. |
|
| DEFINITION STATUS ID |
900000000000074008 |
|
| Effective time |
20190731 |
|
| Has associated morphology | ||
| Has finding site | ||
| Has pathological process | ||
| notation |
787413007 |
|
| Occurs in | ||
| prefLabel |
Bifid nose |
|
| 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 |
|
| tui |
T019 |
|
| Type ID |
900000000000003001 900000000000013009 |
|
| subClassOf |
http://purl.bioontology.org/ontology/SNOMEDCT/764517009 http://purl.bioontology.org/ontology/SNOMEDCT/363070008 |