Ameloblastoma
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
A rare, benign, slow-growing odontologic tumor located in the mandible, and on occasion the maxilla, characterized by painless, variable-sized jaw swelling, which if left untreated may lead to a grotesque facial appearance. Occasionally, paresthesias, tooth displacement and adjacent root resorption may be associated. Local invasion is frequently observed, but malignant transformation and metastasis are not common.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Ameloblastoma | |
| fr | Améloblastome | |
| de | Ameloblastom | |
| es | Ameloblastoma | Ameloblastoma de la mandíbula |
| it | Ameloblastoma | |
| nl | Ameloblastoom | Ameloblastoom van de kaak |
| pt | Ameloblastoma | |
| pl | Ameloblastoma | |
| cs | Ameloblastom | |
| uk | Амелобластома | |
| zh | 成釉细胞瘤 | |
| tr | Ameloblastom |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D16.4 | NTBT | index | validated |
| ICD-10 | D16.5 | NTBT | index | validated |
| ICD-11 | 2B5J | NTBT | index | validated |
| ICD-11 | 2E83.1 | NTBT | index | validated |
| ICD-11 | XH1SV4 | BTNT | specific | validated |
| ICD-11 | XH96J9 | BTNT | specific | validated |
| MONDO | 0017795 | E | validated | |
| MeSH | D000564 | E | validated | |
| UMLS | C0002448 | E | validated | |
| GARD | 5747 | E | validated | |
| MedDRA | 10066796 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:314425Rare odontogenic tumor
rare odontological diseases; rare neoplastic diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/314419
- This record as JSON: /data/d/314419.json