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Mondo Disease Ontology
| Preferred Name | bifid nose | |
| Synonyms | ||
| Definitions |
Bifid nose is a rare congenital malformation of presumed autosomal dominant or recessive inheritance 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 while other malformations such as hypertelorbitism and midline clefts of the lip may also be associated. |
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| ID |
http://purl.obolibrary.org/obo/MONDO_0000110 |
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| database_cross_reference |
MEDGEN:66379 UMLS:C0221363 MESH:C535441 icd11.foundation:1824850646 GARD:884 Orphanet:2695
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| definition |
Bifid nose is a rare congenital malformation of presumed autosomal dominant or recessive inheritance 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 while other malformations such as hypertelorbitism and midline clefts of the lip may also be associated.
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| IAO_0000233 | ||
| id |
MONDO:0000110
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| in_subset |
http://purl.obolibrary.org/obo/mondo/mondo-simple#otar http://purl.obolibrary.org/obo/mondo/mondo-simple#orphanet_rare http://purl.obolibrary.org/obo/mondo/mondo-simple#rare http://purl.obolibrary.org/obo/mondo/mondo-simple#ordo_disorder http://purl.obolibrary.org/obo/mondo/mondo-simple#gard_rare http://purl.obolibrary.org/obo/mondo/mondo-simple#ordo_malformation_syndrome |
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| label |
bifid nose
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| notation |
MONDO:0000110
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| prefLabel |
bifid nose
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| skos_exactMatch |
http://purl.obolibrary.org/obo/Orphanet_2695 http://identifiers.org/mesh/C535441 http://identifiers.org/medgen/66379 http://linkedlifedata.com/resource/umls/id/C0221363 http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1824850646 |
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