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392081006: Bone structure of jaw (body structure)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1466261017 Bone structure of jaw (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1486067018 Bone structure of jaw en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
896601000172117 os de la mâchoire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
937141000172110 structure osseuse de la mâchoire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


202 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Bone structure of jaw (body structure) Is a Jaw region structure false Inferred relationship Some
Bone structure of jaw (body structure) Is a Bone structure of face true Inferred relationship Some
Bone structure of jaw (body structure) partie de Entire facial bone false Additional relationship Some
Bone structure of jaw (body structure) partie de Entire jaw region (body structure) false Additional relationship Some
Bone structure of jaw (body structure) Is a Bone structure of head false Inferred relationship Some
Bone structure of jaw (body structure) Is a Structure of jaw region of face true Inferred relationship Some

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

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Anatomy structure and entire association reference set (foundation metadata concept)

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