Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
This syndrome has characteristics of congenital absence of the teeth and sparse or absent hair. Taurodontia is also present in the majority of cases. The syndrome has been described in less than 15 patients from different families. |
Is a |
True |
Malformation of teeth (disorder) |
Inferred relationship |
Some |
|
Crowding of teeth |
Is a |
True |
Malformation of teeth (disorder) |
Inferred relationship |
Some |
|
Horner's teeth (disorder) |
Is a |
True |
Malformation of teeth (disorder) |
Inferred relationship |
Some |
|
Embedded teeth |
Is a |
True |
Malformation of teeth (disorder) |
Inferred relationship |
Some |
|
Anodontia |
Is a |
True |
Malformation of teeth (disorder) |
Inferred relationship |
Some |
|
Tapered teeth (disorder) |
Is a |
True |
Malformation of teeth (disorder) |
Inferred relationship |
Some |
|
Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. |
Is a |
True |
Malformation of teeth (disorder) |
Inferred relationship |
Some |
|
Regional odontodysplasia |
Is a |
True |
Malformation of teeth (disorder) |
Inferred relationship |
Some |
|
Supernumerary teeth |
Is a |
True |
Malformation of teeth (disorder) |
Inferred relationship |
Some |
|
Peg-shaped teeth |
Is a |
True |
Malformation of teeth (disorder) |
Inferred relationship |
Some |
|
Generalized macrodontia |
Is a |
True |
Malformation of teeth (disorder) |
Inferred relationship |
Some |
|
Fusion of teeth |
Is a |
True |
Malformation of teeth (disorder) |
Inferred relationship |
Some |
|
Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome is a rare, genetic multiple congenital anomalies/dysmorphic syndrome characterized by global developmental delay, axial hypotonia, palate abnormalities (including cleft palate and/or high and narrow palate), dysmorphic facial features (including prominent forehead, hypertelorism, downslanting palpebral fissures, wide nasal bridge, thin lips and widely spaced teeth), and short stature. Additional manifestations may include digital anomalies (such as brachydactyly, clinodactyly, and hypoplastic toenails), a single palmar crease, lower limb hypertonia, joint hypermobility, as well as ocular and urogenital anomalies. |
Is a |
True |
Malformation of teeth (disorder) |
Inferred relationship |
Some |
|
Paired teeth microdontia (disorder) |
Is a |
True |
Malformation of teeth (disorder) |
Inferred relationship |
Some |
|
Reverse position of adjacent teeth (disorder) |
Is a |
True |
Malformation of teeth (disorder) |
Inferred relationship |
Some |
|
A rare, genetic, multiple congenital anomalies syndrome characterized by growth retardation, alopecia, pseudoanodontia and ocular manifestations. |
Is a |
True |
Malformation of teeth (disorder) |
Inferred relationship |
Some |
|
Conductive deafness-ptosis-skeletal anomalies syndrome is a rare, genetic ectodermal dysplasia syndrome characterized by conductive hearing loss due to atresia of the external auditory canal and the middle ear complicated by chronic infection, ptosis and skeletal anomalies (internal rotation of hips, dislocation of the radial heads and fifth finger clinodactyly). In addition, a thin, pinched nose, delayed hair growth and dysplastic teeth are associated. There have been no further descriptions in the literature since 1978. |
Is a |
True |
Malformation of teeth (disorder) |
Inferred relationship |
Some |
|