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 |