Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Central cleft lip |
Is a |
True |
Cleft lip |
Inferred relationship |
Some |
|
Unilateral cleft lip |
Is a |
False |
Cleft lip |
Inferred relationship |
Some |
|
Bilateral cleft lip |
Is a |
False |
Cleft lip |
Inferred relationship |
Some |
|
Cleft palate with cleft lip |
Is a |
True |
Cleft lip |
Inferred relationship |
Some |
|
Cleft lip sequence |
Is a |
True |
Cleft lip |
Inferred relationship |
Some |
|
Cheilognathoschisis |
Is a |
True |
Cleft lip |
Inferred relationship |
Some |
|
Van der Woude syndrome |
Is a |
False |
Cleft lip |
Inferred relationship |
Some |
|
Cleft lip, unspecified |
Is a |
False |
Cleft lip |
Inferred relationship |
Some |
|
Cleft lip NOS |
Is a |
False |
Cleft lip |
Inferred relationship |
Some |
|
H/O: cleft lip |
Associated finding |
False |
Cleft lip |
Inferred relationship |
Some |
1 |
H/O: cleft lip |
Associated finding |
True |
Cleft lip |
Inferred relationship |
Some |
1 |
Family history of cleft lip (situation) |
Associated finding |
False |
Cleft lip |
Inferred relationship |
Some |
1 |
Family history of cleft lip (situation) |
Associated finding |
True |
Cleft lip |
Inferred relationship |
Some |
1 |
Unilateral complete cleft lip and/or alveolus |
Associated finding |
False |
Cleft lip |
Inferred relationship |
Some |
1 |
Unilateral cleft lip |
Associated finding |
False |
Cleft lip |
Inferred relationship |
Some |
1 |
Unilateral incomplete cleft lip |
Associated finding |
False |
Cleft lip |
Inferred relationship |
Some |
1 |
Unilateral complete cleft lip |
Associated finding |
False |
Cleft lip |
Inferred relationship |
Some |
1 |
Unilateral complete cleft lip and/or alveolus |
Associated finding |
False |
Cleft lip |
Inferred relationship |
Some |
1 |
Unilateral complete cleft lip |
Associated finding |
False |
Cleft lip |
Inferred relationship |
Some |
1 |
Unilateral incomplete cleft lip |
Associated finding |
False |
Cleft lip |
Inferred relationship |
Some |
1 |
Family history of cleft lip (situation) |
Associated finding |
False |
Cleft lip |
Inferred relationship |
Some |
1 |
Unilateral cleft lip |
Associated finding |
False |
Cleft lip |
Inferred relationship |
Some |
1 |
A rare developmental defect during embryogenesis characterized by incomplete median clefts of both the lower lip (limited to the vermilion, with no muscle involvement) and upper lip (with muscle involvement), double labial frenulum and fusion of the upper gingival and upper labial mucosa (resulting in a shallow upper vestibular fold), in addition to poor dental alignment, and increased interdental distance between the lower and upper median incisors. |
Is a |
False |
Cleft lip |
Inferred relationship |
Some |
|
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. |
Is a |
False |
Cleft lip |
Inferred relationship |
Some |
|
Cleft of hard palate and cleft lip (disorder) |
Is a |
False |
Cleft lip |
Inferred relationship |
Some |
|
Auriculoocular anomaly and cleft lip syndrome |
Is a |
False |
Cleft lip |
Inferred relationship |
Some |
|
A rare frontonasal dysplasia characterized by median cleft of the upper lip (MCL), midline polyps of the facial skin, nasal mucosa, and pericallosal lipomas. Hypertelorism with ocular anomalies are also observed, generally with normal neuropsychological development. |
Is a |
False |
Cleft lip |
Inferred relationship |
Some |
|
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. |
Is a |
True |
Cleft lip |
Inferred relationship |
Some |
|
A rare median facial cleft characterized by median cleft of the lower lip (ranging in extent from a notch in the vermilion to a complete cleft involving the tongue, lower lip, and chin, and extending to the cervical region), median cleft of the mandible (ranging from notching to a complete cleft), and anomaly of the tongue including bifid tongue and tongue tie. Associated features in severe cases may include absent hyoid, thyroid cartilage, and manubrium sterni, as well as atrophic neck muscles. |
Is a |
False |
Cleft lip |
Inferred relationship |
Some |
|
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. |
Is a |
True |
Cleft lip |
Inferred relationship |
Some |
|
An exceedingly rare association characterized by cleft lip and progressive retinopathy. |
Is a |
True |
Cleft lip |
Inferred relationship |
Some |
|
Cleft lip and cleft of alveolar process of maxilla (disorder) |
Is a |
False |
Cleft lip |
Inferred relationship |
Some |
|
Right cleft lip (disorder) |
Is a |
True |
Cleft lip |
Inferred relationship |
Some |
|
Left cleft lip |
Is a |
True |
Cleft lip |
Inferred relationship |
Some |
|
Millard operation, cleft lip repair |
Has focus |
True |
Cleft lip |
Inferred relationship |
Some |
2 |
Lemesurier operation, cleft lip repair |
Has focus |
True |
Cleft lip |
Inferred relationship |
Some |
1 |
Repair of cleft lip |
Has focus |
True |
Cleft lip |
Inferred relationship |
Some |
1 |
Thompson operation, cleft lip repair |
Has focus |
True |
Cleft lip |
Inferred relationship |
Some |
2 |
Repair of partial cleft lip |
Has focus |
False |
Cleft lip |
Inferred relationship |
Some |
2 |
Rhinocheiloplasty repair for cleft lip |
Has focus |
True |
Cleft lip |
Inferred relationship |
Some |
3 |
Congenital macrostomia of right side of mouth (disorder) |
Is a |
True |
Cleft lip |
Inferred relationship |
Some |
|
Congenital macrostomia of left side of mouth (disorder) |
Is a |
True |
Cleft lip |
Inferred relationship |
Some |
|
Incomplete cleft lip (disorder) |
Is a |
True |
Cleft lip |
Inferred relationship |
Some |
|
Repair of cleft lip with triangular flap (procedure) |
Has focus |
True |
Cleft lip |
Inferred relationship |
Some |
2 |
Repair of cleft lip using straight line technique (procedure) |
Has focus |
True |
Cleft lip |
Inferred relationship |
Some |
2 |
Complete cleft lip (disorder) |
Is a |
True |
Cleft lip |
Inferred relationship |
Some |
|
Cleft lip nasal deformity |
Is a |
True |
Cleft lip |
Inferred relationship |
Some |
|
An isolated non syndromic fissure type embryopathy extending from the upper lip to the nasal base. The cleft is paramedian and located at the level of the philtrum. It presents as a cutaneous, muscular, and mucosal interruption from the lip to the nasal base, associated with nostril and nasal septum deformations. Clinical forms range from a simple notch in the upper lip to a complete cleft lip with an opening at the base of the nostril without reaching as far as the gum (alveolar ridge). This embryopathy appears between the 5th and 12th week of pregnancy due to a failure in the fusion of the frontal processes (fronto-nasal process, medial and lateral nasal processes, maxillary process). |
Is a |
True |
Cleft lip |
Inferred relationship |
Some |
|