Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Congenital retrognathism (disorder) |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
Structure of bone marrow of jaw |
Is a |
False |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
|
Periapical abscess |
Finding site |
False |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
2 |
Chronic apical abscess |
Finding site |
False |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
2 |
Periapical abscess with sinus tract |
Finding site |
False |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
2 |
Abscess of jaw |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
2 |
Periapical abscess with facial involvement |
Finding site |
False |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
2 |
Periapical abscess without a sinus |
Finding site |
False |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
2 |
Chronic abscess of jaw (disorder) |
Finding site |
False |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
2 |
Inflammatory disorder of bone of jaw (disorder) |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
Florid cemento-osseous dysplasia (FCOD) is a rare fibro-osseous lesion in the jaw that predominantly affects middle-aged women of African descent. It is generally asymptomatic or may manifest with pain and gingival swelling. Radiologically, it is characterized by multiple dense lobulated bone lesions, often symmetrically located in various regions of the jaw. |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
Acute nonsuppurative osteitis of jaw |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
3 |
Periostitis of jaw |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
Suppurative periostitis of jaw |
Finding site |
False |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
|
Acute periostitis of jaw |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
3 |
Chronic periostitis of jaw |
Finding site |
False |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
|
Normal oral mucous membrane and osseointegrated bone tissue surrounding dental implant (finding) |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
3 |
Neonatal osteomyelitis of jaw |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
Noneruption of teeth - maxillary hypoplasia - genu valgum is an extremely rare syndrome that is characterized by multiple unerupted permanent teeth, hypoplasia of the alveolar process and of the maxillo-zygomatic region, severe genu valgum and deformed ears. |
Finding site |
False |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
5 |
Primary osteosarcoma of bone of jaw (disorder) |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
Exostosis of jaw |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
2 |
Chronic nonsuppurative osteitis of jaw |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
2 |
Chronic abscess of jaw (disorder) |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
Aneurysmal cyst of jaw |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
Traumatic bone cyst of jaw (disorder) |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
PARC syndrome is a rare genetic developmental defect during embryogenesis syndrome characterized by the association of congenital poikiloderma (P), generalized alopecia (A), retrognathism (R) and cleft palate (C). There have been no further descriptions in the literature since 1990. |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
2 |
An ectopic tooth that has erupted on the lingual aspect of the maxilla or mandible. |
Finding site |
False |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
PARC syndrome is a rare genetic developmental defect during embryogenesis syndrome characterized by the association of congenital poikiloderma (P), generalized alopecia (A), retrognathism (R) and cleft palate (C). There have been no further descriptions in the literature since 1990. |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
5 |
The MMEP syndrome is a congenital syndromic form of split-hand/foot malformation. It is characterized by microcephaly, microphthalmia, ectrodactyly of the lower limbs and prognathism. Intellectual deficit has been reported. MMEP syndrome is considered to be a very rare condition, although the exact prevalence remains unknown. The etiology is not completely understood. Disruption of the sorting nexin 3 gene (SNX3; 6q21) has been shown to play a causative role in MMEP, although this was not confirmed in recent studies. |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
3 |
Congenital prognathism |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
Noneruption of teeth - maxillary hypoplasia - genu valgum is an extremely rare syndrome that is characterized by multiple unerupted permanent teeth, hypoplasia of the alveolar process and of the maxillo-zygomatic region, severe genu valgum and deformed ears. |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
3 |
A rare multiple congenital defects/dysmorphic syndrome characterized by variable degrees of bony syngnathia associated with variable additional abnormalities, including growth retardation, intellectual disability, microcephaly, iris coloboma, nystagmus, deafness, and vertebral segmentation defects, as well as genital, limb and additional facial malformations, among others. |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
Dental subperiosteal implant |
Procedure site - Indirect (attribute) |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
Odontogenic ghost cell carcinoma |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
Partially impacted tooth in bone |
Finding site |
False |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
3 |
Completely impacted tooth in bone (disorder) |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
2 |
Odontogenic tumour of jaw |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
Fibrous dysplasia of jaw |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
Congenital asymmetry of jaw (disorder) |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
Osteonecrosis of jaw caused by drug |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
Partially impacted tooth in bone |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
2 |
Implantation of dental endosseous implant (procedure) |
Procedure site - Indirect (attribute) |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
Excessive tuberosity of jaw (disorder) |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome is a rare syndromic intellectual disability characterized by hypotonia, microcephaly, severe developmental delay, seizures, intellectual disability, growth retardation, cardiac septal defects, cryptorchidism, hypospadias, and dysmorphic features - prominent ears, prognathism, thin upper lip, dental crowding. |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
A rare osteonecrosis characterized by an exposed necrotic lesion in the mandible or maxilla present for more than eight weeks, arising as a complication of antiresorptive medication, dental interventions, or trauma and infections. Patients may present with pain, altered neurosensory functions, secondary infections, and (in advanced stages) pathological fractures, or fistulae. |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
Implantation of osseointegrated implant into bone of jaw (procedure) |
Procedure site - Indirect (attribute) |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
Primary odontogenic ghost cell carcinoma (disorder) |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
A rare genetic bone disease characterized by multifocal, painless, benign fibrocemento-osseous lesions of the jaws which expand progressively and can cause severe facial deformity. It usually manifests at an early age and is often associated with abnormalities of the long bones and pathologic fractures. Radiologically, the lesions are of mixed radiopaque/radiolucent appearance. Incomplete surgical removal may lead to more rapid growth of the residual lesion. |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by developmental delay, moderate to severe intellectual disability, dysmorphic features including craniosynostosis, micro-/retrognathia, cleft palate, and brachydactyly, and short stature. Seizures, skeletal anomalies (such as arthrogryposis, gracile bones, and pathological fractures), and renal abnormalities have also been described. Cerebral MRI may show periventricular white matter changes and ventriculomegaly. |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
2 |
Alveolectomy, including sequestrectomy |
Procedure site - Direct (attribute) |
False |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
2 |
Chronic periostitis of jaw |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
2 |
Fracture of bone of jaw (disorder) |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
1 |
Placement of implant material which extends from a pulpal space into bone beyond the end of the root. |
Procedure site - Indirect (attribute) |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
2 |
Periapical osteoperiostitis (disorder) |
Finding site |
True |
Bone structure of jaw (body structure) |
Inferred relationship |
Some |
2 |