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Kidney Tissue Atlas Ontology
Preferred Name | bifid nose | |
Synonyms |
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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 |
GARD:0000884 DC:0000479 MESH:C535441 ICD10:Q30.2 Orphanet:2695 UMLS:CN227089
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exactMatch |
http://identifiers.org/mesh/C535441 http://linkedlifedata.com/resource/umls/id/C0221363 |
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id |
MONDO:0000110
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imported from | ||
in_subset |
http://purl.oboInOwllibrary.org/oboInOwl/mondo#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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textual 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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subClassOf |
http://purl.obolibrary.org/obo/MONDO_0015503 http://purl.obolibrary.org/obo/MONDO_0023603 |
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