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48477009: Lip 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
80770013 Lip en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
495110012 Lip structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
786049011 Lip structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
881711000172117 lèvre de la bouche fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
894771000172113 structure de la lèvre de la bouche fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
956691000172114 labium oris fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
979881000172115 lèvre fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6997821000241112 structure d'une lèvre de la bouche fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


105 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lip structure Is a Structure of oral region of face true Inferred relationship Some
Lip structure Is a Lip and/or palatal structures false Inferred relationship Some
Lip structure Is a Oral soft tissue structure true Inferred relationship Some
Lip structure partie de Entire oral region of face false Additional relationship Some
Lip structure Is a Structure of soft tissue of face (body structure) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Cheilitis due to lupus erythematosus Finding site True Lip structure Inferred relationship Some 2
Congenital double lip Finding site False Lip structure Inferred relationship Some 2
Congenital ectropion of lip Finding site True Lip structure Inferred relationship Some 1
Congenital macrocheilia Finding site True Lip structure Inferred relationship Some 1
Thompson operation, cleft lip repair Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 3
Cheilognathoschisis Finding site False Lip structure Inferred relationship Some 8
Lip adhesion of bilateral cleft lips (procedure) Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 2
Repair of bilateral cleft lip using rotation advancement flap (procedure) Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 3
Repair of bilateral cleft lip with quadrilateral flap Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 3
Primary repair of cleft lip Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 3
Caliber persistent labial artery (disorder) Finding site True Lip structure Inferred relationship Some 1
Cleft hard palate with cleft lip, bilateral Finding site False Lip structure Inferred relationship Some 5
Cleft palate and bilateral cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 6
Bilateral complete cleft palate with cleft lip Finding site False Lip structure Inferred relationship Some 7
Cleft of hard palate and cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 5
Cleft hard and soft palate with cleft lip Finding site False Lip structure Inferred relationship Some 5
Cleft of soft palate and cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 3
Cleft of soft palate and bilateral cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 4
à l'examen : herpès labial, feu sauvage Finding site False Lip structure Inferred relationship Some 2
Infective dermatosis of lip (disorder) Finding site False Lip structure Inferred relationship Some 1
Recurrent herpes simplex labialis (disorder) Finding site False Lip structure Inferred relationship Some 3
Oral mucosal herpes Finding site False Lip structure Inferred relationship Some 3
Herpes labialis Finding site False Lip structure Inferred relationship Some 3
Primary herpes simplex infection of lips (disorder) Finding site False Lip structure Inferred relationship Some 3
Specimen from lip obtained by wedge resection Specimen source topography True Lip structure Inferred relationship Some 1
Zlotogora-Ogur syndrome is an ectodermal dysplasia syndrome characterized by hair, skin and teeth anomalies, facial dysmorphism with cleft lip and palate, cutaneous syndactyly and, in some cases, intellectual disability. Finding site False Lip structure Inferred relationship Some 6
Zlotogora-Ogur syndrome is an ectodermal dysplasia syndrome characterized by hair, skin and teeth anomalies, facial dysmorphism with cleft lip and palate, cutaneous syndactyly and, in some cases, intellectual disability. Finding site True Lip structure Inferred relationship Some 4
Cleft lip/palate-deafness-sacral lipoma syndrome is characterized by cleft lip/palate, profound sensorineural deafness, and a sacral lipoma. It has been described in two brothers of Chinese origin born to non-consanguineous parents. Additional findings included appendages on the heel and thigh, or anterior sacral meningocele and dislocated hip. The mode of inheritance is probably autosomal or X-linked recessive. Finding site False Lip structure Inferred relationship Some 9
A rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by uveal coloboma (typically bilateral) variably associated with cleft lip, palate and/or uvula, hearing impairment, and intellectual disability. The spectrum of eye involvement is also variable and includes iris coloboma extending to the choroid, disc, and/or macula, microphthalmia, cataract, and extraocular movement impairment. Finding site False Lip structure Inferred relationship Some 5
A rare multiple congenital anomaly syndrome characterized by flat face, hypertelorism, flat occiput, upward slanting palpebral fissures, cleft palate, micrognathia, short neck, and severe congenital heart defects. Malrotation of the intestine, bilateral clinodactyly, bilobed tongue, short fourth metatarsals and bifid thumbs may be additionally observed. Finding site False Lip structure Inferred relationship Some 4
Pigmentation disorder of lip (disorder) Finding site True Lip structure Inferred relationship Some 1
A rare multiple congenital malformation syndrome, characterized by an association of cleft lip and palate, patchy pigmentary retinopathy (cat's paw), obstructive liver disease (cholestasis, portal hypertension etc.) and obstructive renal disease (ectopic ureteric insertion, obstruction, vesicoureteral reflux and hydronephrosis). Gastrointestinal tract involvement (malrotation, gastroesophageal reflux etc.) and cardiac involvement (coarctation of aorta, pulmonary artery stenosis, etc.) have also been reported. An overlap with Kabuki syndrome is debated. Finding site False Lip structure Inferred relationship Some 6
Herpes labialis Finding site True Lip structure Inferred relationship Some 1
à l'examen : herpès labial, feu sauvage Finding site False Lip structure Inferred relationship Some 1
Primary herpes simplex infection of lips (disorder) Finding site True Lip structure Inferred relationship Some 1
Recurrent herpes simplex labialis (disorder) Finding site True Lip structure Inferred relationship Some 4
Viral wart on lip (disorder) Finding site True Lip structure Inferred relationship Some 3
Hypertelorism-microtia-facial clefting syndrome, or HMC syndrome, is a very rare syndrome characterized by the combination of hypertelorism, cleft lip and palate and microtia. Finding site False Lip structure Inferred relationship Some 4
Auriculoocular anomaly and cleft lip syndrome Finding site False Lip structure Inferred relationship Some 3
Microbrachycephaly-ptosis-cleft lip syndrome is characterized by the association of intellectual deficit, microbrachycephaly, hypotelorism, palpebral ptosis, a thin/long face, cleft lip, and anomalies of the lumbar vertebra, sacrum and pelvis. It has been described in two Brazilian sisters. Transmission appears to be autosomal recessive. Finding site False Lip structure Inferred relationship Some 7
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by the association of auricular abnormalities (such as external ear abnormalities and postauricular pits) and cleft lip with or without cleft palate. Additional manifestations include myopia, nystagmus, and retinal pigment abnormalities. Finding site False Lip structure Inferred relationship Some 4
Van der Woude syndrome Finding site False Lip structure Inferred relationship Some 1
Lemesurier operation, cleft lip repair Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 2
Synchronous bilateral cleft lip repair Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 2
Asynchronous bilateral cleft lip repair Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 2
Repair of cleft lip Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 2
Repair of bilateral cleft lip Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 2
Repair of bilateral cleft lip using triangular repair Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 2
Pharyngorrhaphy for cleft palate Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 2
Repair of bilateral cleft lip using straight line technique Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 2
Cleft lip/palate-deafness-sacral lipoma syndrome is characterized by cleft lip/palate, profound sensorineural deafness, and a sacral lipoma. It has been described in two brothers of Chinese origin born to non-consanguineous parents. Additional findings included appendages on the heel and thigh, or anterior sacral meningocele and dislocated hip. The mode of inheritance is probably autosomal or X-linked recessive. Finding site True Lip structure Inferred relationship Some 2
A rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by uveal coloboma (typically bilateral) variably associated with cleft lip, palate and/or uvula, hearing impairment, and intellectual disability. The spectrum of eye involvement is also variable and includes iris coloboma extending to the choroid, disc, and/or macula, microphthalmia, cataract, and extraocular movement impairment. Finding site True Lip structure Inferred relationship Some 1
Auriculoocular anomaly and cleft lip syndrome Finding site False Lip structure Inferred relationship Some 1
Cleft hard and soft palate with cleft lip Finding site False Lip structure Inferred relationship Some 2
Cleft of hard palate and cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 2
Cleft palate and bilateral cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 2
Cleft palate with cleft lip Finding site True Lip structure Inferred relationship Some 2
Zlotogora-Ogur syndrome is an ectodermal dysplasia syndrome characterized by hair, skin and teeth anomalies, facial dysmorphism with cleft lip and palate, cutaneous syndactyly and, in some cases, intellectual disability. Finding site False Lip structure Inferred relationship Some 1
Hypertelorism-microtia-facial clefting syndrome, or HMC syndrome, is a very rare syndrome characterized by the combination of hypertelorism, cleft lip and palate and microtia. Finding site False Lip structure Inferred relationship Some 2
Cleft of soft palate and bilateral cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 2
Cleft of soft palate and cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 2
Cheilognathoprosoposchisis Finding site False Lip structure Inferred relationship Some 5
Cleft lip/palate-deafness-sacral lipoma syndrome is characterized by cleft lip/palate, profound sensorineural deafness, and a sacral lipoma. It has been described in two brothers of Chinese origin born to non-consanguineous parents. Additional findings included appendages on the heel and thigh, or anterior sacral meningocele and dislocated hip. The mode of inheritance is probably autosomal or X-linked recessive. Finding site False Lip structure Inferred relationship Some 1
A rare multiple congenital malformation syndrome, characterized by an association of cleft lip and palate, patchy pigmentary retinopathy (cat's paw), obstructive liver disease (cholestasis, portal hypertension etc.) and obstructive renal disease (ectopic ureteric insertion, obstruction, vesicoureteral reflux and hydronephrosis). Gastrointestinal tract involvement (malrotation, gastroesophageal reflux etc.) and cardiac involvement (coarctation of aorta, pulmonary artery stenosis, etc.) have also been reported. An overlap with Kabuki syndrome is debated. Finding site False Lip structure Inferred relationship Some 1
A rare multiple congenital anomaly syndrome characterized by flat face, hypertelorism, flat occiput, upward slanting palpebral fissures, cleft palate, micrognathia, short neck, and severe congenital heart defects. Malrotation of the intestine, bilateral clinodactyly, bilobed tongue, short fourth metatarsals and bifid thumbs may be additionally observed. Finding site True Lip structure Inferred relationship Some 1
Cleft palate and bilateral cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 1
An exceedingly rare association characterized by cleft lip and progressive retinopathy. Finding site False Lip structure Inferred relationship Some 5
Cleft of hard palate and cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 1
A rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by uveal coloboma (typically bilateral) variably associated with cleft lip, palate and/or uvula, hearing impairment, and intellectual disability. The spectrum of eye involvement is also variable and includes iris coloboma extending to the choroid, disc, and/or macula, microphthalmia, cataract, and extraocular movement impairment. Finding site False Lip structure Inferred relationship Some 6
Primary squamous cell carcinoma of lip (disorder) Finding site True Lip structure Inferred relationship Some 1
A rare syndrome with 46,XY disorder of sex development characterized by mild developmental delay and streak gonads associated with short stature, cardiac, renal, musculoskeletal, and ectodermal abnormalities (the latter including scalp defects and unusual hair whorls), and dysmorphic facial features (such as preauricular pits, short columella, and small nares). There have been no further descriptions in the literature since 1980. Finding site True Lip structure Inferred relationship Some 3
Infection of lip Finding site True Lip structure Inferred relationship Some 1
Cleft soft palate with left cleft lip Finding site False Lip structure Inferred relationship Some 2
Cleft soft palate with right cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 2
Cleft palate with left cleft lip Finding site False Lip structure Inferred relationship Some 3
Cleft palate with right cleft lip Finding site False Lip structure Inferred relationship Some 3
Cleft palate with right cleft lip Finding site False Lip structure Inferred relationship Some 2
Cleft hard and soft palate with left cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 3
Cleft hard and soft palate with right cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 3
Cleft hard and soft palate with bilateral cleft lip and bilateral cleft of alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 8
Cleft hard and soft palate with left cleft lip and left alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 8
Cleft hard and soft palate with right cleft lip and cleft of right alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 8
Traumatic amputation of lip (disorder) Finding site True Lip structure Inferred relationship Some 1
Cleft hard palate with bilateral cleft lip and bilateral cleft of alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 7
Cleft hard palate with left cleft lip and cleft of left alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 7
Cleft hard palate with right cleft lip and cleft of right alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 7
Cleft palate with bilateral cleft lip and bilateral cleft of alveolar process of maxilla Finding site False Lip structure Inferred relationship Some 7
Cleft soft palate with bilateral cleft lip and bilateral cleft of alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 5
Cleft soft palate with left cleft lip and cleft of left alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 5
Cleft soft palate with right cleft lip and cleft of right alveolar process of maxilla Finding site False Lip structure Inferred relationship Some 5
Cleft hard palate with left cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 2
Cleft hard palate with right cleft lip (disorder) Finding site False Lip structure Inferred relationship Some 2
Repair of left cleft lip using straight line technique (procedure) Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 1
Repair of right cleft lip using straight line technique Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 1
Application of lubricant to lips Procedure site - Direct (attribute) True Lip structure Inferred relationship Some 1
Repair of left cleft lip with triangular flap Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 1
Repair of right cleft lip with triangular flap (procedure) Procedure site - Direct (attribute) False Lip structure Inferred relationship Some 1
Median cleft lip and cleft of alveolar process of maxilla Finding site False Lip structure Inferred relationship Some 2
Incomplete left cleft lip and incomplete cleft of left alveolar process of maxilla Finding site False Lip structure Inferred relationship Some 2
Incomplete right cleft lip and incomplete cleft of right alveolar process of maxilla Finding site False Lip structure Inferred relationship Some 2
Complete left cleft lip and complete cleft of left alveolar process of maxilla (disorder) Finding site False Lip structure Inferred relationship Some 2

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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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