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45206002: Nasal structure (body structure)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
75377016 Nose en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
494121010 Nasal structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
782420013 Nasal structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
279471000077112 structure nasale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
879871000172111 nez fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
894441000172114 structure du nez fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
913441000172118 nasus fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

270 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Nasal structure Is a Face structure true Inferred relationship Some
Nasal structure partie de Entire head false Additional relationship Some
Nasal structure partie de Entire respiratory system false Additional relationship Some
Nasal structure Is a Upper respiratory tract structure false Inferred relationship Some
Nasal structure partie de Entire upper aerodigestive tract false Inferred relationship Some
Nasal structure Is a Respiratory organ false Inferred relationship Some
Nasal structure Is a Structure of ear, nose, and/or throat true Inferred relationship Some
Nasal structure Is a Nose and nasopharynx structure (body structure) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Control of posterior nasal bleeding (procedure) Procedure site - Direct (attribute) False Nasal structure Inferred relationship Some 1
Control of hemorrhage of nose Procedure site - Direct (attribute) False Nasal structure Inferred relationship Some 1
Tamponade of anterior nasal bleeding using nasal tampon (procedure) Procedure site - Direct (attribute) False Nasal structure Inferred relationship Some 2
contrôle d'une épistaxis Procedure site - Direct (attribute) False Nasal structure Inferred relationship Some 1
Control of epistaxis by excision of nasal mucosa with grafting Procedure site - Direct (attribute) False Nasal structure Inferred relationship Some 3
Control of epistaxis by cautery (procedure) Procedure site - Direct (attribute) False Nasal structure Inferred relationship Some 2
Epistaxis control by cryosurgery Procedure site - Direct (attribute) False Nasal structure Inferred relationship Some 2
Ligation of external carotid artery for nasal hemorrhage Procedure site - Direct (attribute) False Nasal structure Inferred relationship Some 3
Control of anterior nasal bleeding (procedure) Procedure site - Direct (attribute) False Nasal structure Inferred relationship Some 1
Congenital squashed or bent nose Finding site False Nasal structure Inferred relationship Some 2
Congenital anomaly of nose Finding site False Nasal structure Inferred relationship Some 2
Congenital malposition of nares Finding site False Nasal structure Inferred relationship Some 3
Congenital malposition of nasal septum (disorder) Finding site False Nasal structure Inferred relationship Some 3
Congenital notching of tip of nose Finding site False Nasal structure Inferred relationship Some 4
Congenital deformity of nose (disorder) Finding site False Nasal structure Inferred relationship Some 2
Midline fissured, notched and cleft nose Finding site False Nasal structure Inferred relationship Some 2
Congenital absence of nose Finding site False Nasal structure Inferred relationship Some 2
Congenital fissure of nose Finding site False Nasal structure Inferred relationship Some 2
Congenital malposition of nose Finding site False Nasal structure Inferred relationship Some 3
Congenital cleft nose Finding site False Nasal structure Inferred relationship Some 2
Single naris Finding site False Nasal structure Inferred relationship Some 3
Congenital bent nose (disorder) Finding site False Nasal structure Inferred relationship Some 4
Underdevelopment of nose Finding site False Nasal structure Inferred relationship Some 2
Rhinocephaly Finding site False Nasal structure Inferred relationship Some 4
Median nasal dermoid fistula Finding site False Nasal structure Inferred relationship Some 4
Median nasal dermoid fistula Finding site False Nasal structure Inferred relationship Some 5
Congenital anosmia Finding site False Nasal structure Inferred relationship Some 2
Congenital bent nose (disorder) Finding site False Nasal structure Inferred relationship Some 5
Control of hemorrhage of nose Procedure site - Direct (attribute) False Nasal structure Inferred relationship Some 2
Closed rhinoplasty (procedure) Procedure site - Direct (attribute) True Nasal structure Inferred relationship Some 1
Closed rhinoseptoplasty (procedure) Procedure site - Direct (attribute) True Nasal structure Inferred relationship Some 2
Open rhinoseptoplasty (procedure) Procedure site - Direct (attribute) True Nasal structure Inferred relationship Some 2
Sinusitis co-occurrent with nasal polyps Finding site False Nasal structure Inferred relationship Some 3
Congenital bent nose (disorder) Finding site False Nasal structure Inferred relationship Some 2
Secondary rhinoplasty, major revision Procedure site - Direct (attribute) True Nasal structure Inferred relationship Some 3
Secondary rhinoplasty, minor revision Procedure site - Direct (attribute) True Nasal structure Inferred relationship Some 3
Revision rhinoplasty Procedure site - Direct (attribute) True Nasal structure Inferred relationship Some 3
Secondary rhinoplasty, intermediate revision with osteotomies Procedure site - Direct (attribute) True Nasal structure Inferred relationship Some 4
Naso-maxillary dysostosis Finding site False Nasal structure Inferred relationship Some 2
First stage attachment of fixture for nasal prosthesis Procedure site - Indirect (attribute) True Nasal structure Inferred relationship Some 1
Second stage attachment of fixture for nasal prosthesis Procedure site - Indirect (attribute) True Nasal structure Inferred relationship Some 1
Nasotracheal aspirate (specimen) Specimen source topography True Nasal structure Inferred relationship Some 2
Nasal infection Finding site True Nasal structure Inferred relationship Some 2
Rigid rhinoscopy (procedure) Procedure site - Direct (attribute) True Nasal structure Inferred relationship Some 1
Flexible fiberoptic rhinoscopy (procedure) Procedure site - Direct (attribute) True Nasal structure Inferred relationship Some 1
A rare, major congenital malformation characterized by complete duplication of the nose resulting in two fully developed noses often associated with choanal atresia, causing respiratory distress and necessitating surgical repair. Finding site True Nasal structure Inferred relationship Some 1
Proboscis lateralis (PL) is a rare congenital facial abnormality characterized by failed development of the external nose on one side that is replaced by a tubular structure composed of skin and soft tissue usually attached at the inner canthus of the eye and therefore often associated with maldevelopment of the nasal cavity or paranasal sinuses of the affected side. PL is also associated with other craniofacial abnormalities such as orbital anomalies, cleft lip/palate, frontal encephalocele and holoprosencephaly. Finding site True Nasal structure Inferred relationship Some 1
Granulomatosis with polyangiitis of nose Finding site True Nasal structure Inferred relationship Some 1
A rare multiple congenital anomalies/dysmorphic syndrome characterized by trigonobrachycephaly, facial dysmorphism (including narrow forehead, upward-slanting palpebral fissures, bulbous nose with slightly bifid tip, macrostomia with thin upper lip, micrognathia), and various acral anomalies, such as broad thumbs, large toes, bulbous fingertips with short nails, joint laxity of the hands and fifth finger clinodactyly. Short stature, hypotonia and severe psychomotor delay are also associated. There have been no further descriptions in the literature since 1991. Finding site True Nasal structure Inferred relationship Some 4
Trigonocephaly-broad thumbs syndrome is characterized by neonatal trigonocephaly and multiple anomalies including craniosynostosis, shallow orbits, unusual nose, deviation of the terminal phalanges of fingers 1, 2, and 5, and broad toes with duplication of the terminal phalanx. It has been described in a mother and her son. It is transmitted as an autosomal dominant trait. Finding site False Nasal structure Inferred relationship Some 7
A rare multiple congenital anomalies/dysmorphic syndrome characterized by trigonobrachycephaly, facial dysmorphism (including narrow forehead, upward-slanting palpebral fissures, bulbous nose with slightly bifid tip, macrostomia with thin upper lip, micrognathia), and various acral anomalies, such as broad thumbs, large toes, bulbous fingertips with short nails, joint laxity of the hands and fifth finger clinodactyly. Short stature, hypotonia and severe psychomotor delay are also associated. There have been no further descriptions in the literature since 1991. Finding site False Nasal structure Inferred relationship Some 5
A malformation disorder characterized by complete or incomplete absence of nose (arrhinia), choanal atresia, microphthalmia, anophthalmia and cleft or high palate. Finding site True Nasal structure Inferred relationship Some 3
BNAR syndrome is a very rare multiple congenital anomaly syndrome characterized by a bifid nose (with bulbous nasal tip but not associated with hypertelorism) with or without the presence of anal defects (i.e. anteriorly placed anus, rectal stenosis or atresia) and renal dysplasia and without intellectual disability. BNAR syndrome is phenotypically related to Fraser syndrome and oculotrichoanal syndrome. Finding site True Nasal structure Inferred relationship Some 1
Blepharonasofacial syndrome is a rare otorhinolaryngological malformation syndrome characterized by a distinctive mask-like facial dysmorphism, lacrimal duct obstruction, extrapyramidal features, digital malformations and intellectual disability. Finding site True Nasal structure Inferred relationship Some 1
Complete traumatic amputation of nose (disorder) Finding site False Nasal structure Inferred relationship Some 1
Traumatic partial amputation of nose (disorder) Finding site False Nasal structure Inferred relationship Some 1
Burning sensation of nose (finding) Finding site True Nasal structure Inferred relationship Some 1
Repair of laceration of nose (procedure) Procedure site - Direct (attribute) True Nasal structure Inferred relationship Some 1
Aspirin exacerbated respiratory disease Finding site True Nasal structure Inferred relationship Some 1
Intermediate revision rhinoplasty (procedure) Procedure site - Direct (attribute) True Nasal structure Inferred relationship Some 1
Tamponade of anterior nasal bleeding using nasal tampon (procedure) Procedure site - Direct (attribute) False Nasal structure Inferred relationship Some 3
Tamponade of anterior nasal bleeding using urinary catheter (procedure) Procedure site - Direct (attribute) False Nasal structure Inferred relationship Some 3
Endoscopy of nasal sinus with control of nasal hemorrhage (procedure) Procedure site - Direct (attribute) True Nasal structure Inferred relationship Some 2
Control of epistaxis by packing of posterior and anterior nose Procedure site - Direct (attribute) False Nasal structure Inferred relationship Some 5
Rhinocheiloplasty repair for cleft lip Procedure site - Direct (attribute) True Nasal structure Inferred relationship Some 2
Rhinocheiloplasty Procedure site - Direct (attribute) True Nasal structure Inferred relationship Some 1
Postoperative supratip depression of nose Finding site False Nasal structure Inferred relationship Some 2
Overdevelopment of nasal bones Finding site False Nasal structure Inferred relationship Some 2
Kallmann syndrome with cardiopathy is characterized by hypogonadotropic hypogonadism associated with gonadotropin-releasing hormone (GnRH) deficiency, anosmia or hyposmia (with hypoplasia or aplasia of the olfactory bulbs) and complex congenital cardiac malformations (double-outlet right ventricle, dilated cardiomyopathy, right aortic arch). It represents a distinct clinical entity from Kallmann syndrome. Finding site False Nasal structure Inferred relationship Some 6
Hypogonadism with anosmia Finding site False Nasal structure Inferred relationship Some 6
Nasal encephalocele Finding site False Nasal structure Inferred relationship Some 2
Trigonocephaly-broad thumbs syndrome is characterized by neonatal trigonocephaly and multiple anomalies including craniosynostosis, shallow orbits, unusual nose, deviation of the terminal phalanges of fingers 1, 2, and 5, and broad toes with duplication of the terminal phalanx. It has been described in a mother and her son. It is transmitted as an autosomal dominant trait. Finding site True Nasal structure Inferred relationship Some 1
Nasofrontal encephalocele Finding site False Nasal structure Inferred relationship Some 3
Nasopharyngeal encephalocele Finding site False Nasal structure Inferred relationship Some 3
Isolated arhinencephaly is a rare non-syndromic central nervous system malformation defined by the agenesis of the olfactory bulbs and tracts and characterized by complete congenital anosmia. Finding site False Nasal structure Inferred relationship Some 4
Rhinofacial conidiobolomycosis Finding site True Nasal structure Inferred relationship Some 1
Rhinophycomycosis caused by Entomophthora coronata Finding site True Nasal structure Inferred relationship Some 1
A rare frontonasal dysplasia malformation syndrome characterised by an oxycephalic skull with craniosynostosis, wide nose with anteverted nostrils, hirsutism at base of nose, agenesis of the nasolacrimal ducts, and bilateral, symmetrical nasolabial cysts on upper lip. Additional features may include hypertelorism. There have been no further descriptions in the literature since 1991. Finding site True Nasal structure Inferred relationship Some 2
Fishing hook in nose Finding site True Nasal structure Inferred relationship Some 1
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. Finding site True Nasal structure Inferred relationship Some 1
Nasofrontal encephalocele Finding site False Nasal structure Inferred relationship Some 1
Nasopharyngeal encephalocele Finding site False Nasal structure Inferred relationship Some 1
Crusting on nose (finding) Finding site True Nasal structure Inferred relationship Some 1
Foul smelling discharge from nose (finding) Finding site True Nasal structure Inferred relationship Some 1
On examination - nasal discharge-foul smell Finding site False Nasal structure Inferred relationship Some 1
Mucopurulent discharge from nose (finding) Finding site True Nasal structure Inferred relationship Some 1
Purulent nasal discharge Finding site True Nasal structure Inferred relationship Some 1
On examination - nose crusting Finding site False Nasal structure Inferred relationship Some 1
Catarrhal nasal discharge Finding site True Nasal structure Inferred relationship Some 1
Cerebrospinal fluid rhinorrhea Finding site True Nasal structure Inferred relationship Some 1
Cerebrospinal fluid leak from nose and mouth (disorder) Finding site True Nasal structure Inferred relationship Some 3
Administration of intranasal sedation Procedure site - Indirect (attribute) True Nasal structure Inferred relationship Some 1
Fetal nose palpable vaginally Finding site True Nasal structure Inferred relationship Some 1
Foreign body in skin of nose with infection Finding site False Nasal structure Inferred relationship Some 1
Laurin-Sandrow syndrome (LSS) is characterized by complete polysyndactyly of the hands, mirror feet and nose anomalies (hypoplasia of the nasal alae and short columella), often associated with ulnar and/or fibular duplication (and sometimes tibial agenesis). It has been described in less than 20 cases. Some cases with the same clinical signs but without nasal defects have also been reported and may represent the same entity. The etiology of LSS is unknown. Different modes of inheritance have been suggested. Finding site True Nasal structure Inferred relationship Some 3
Lengthening of left side of nasal columella Procedure site - Direct (attribute) True Nasal structure Inferred relationship Some 2
Lengthening of right side of nasal columella Procedure site - Direct (attribute) True Nasal structure Inferred relationship Some 2
Histologic type of primary malignant neoplasm of nasal structure This attribute specifies the location of the entity specified by the attribute "Inheres in". False Nasal structure Inferred relationship Some 5
Acquired absence of nose (disorder) Finding site True Nasal structure Inferred relationship Some 1
Ganglioglioma of nose (disorder) Finding site True Nasal structure Inferred relationship Some 1
Histologic grade of primary malignant neoplasm of nasal structure (observable entity) This attribute specifies the location of the entity specified by the attribute "Inheres in". False Nasal structure Inferred relationship Some 5

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Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

Anatomy structure and part association reference set (foundation metadata concept)

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