ORPHA:2287
Fused mandibular incisors
- Type
- Morphological anomaly
- Group
- Disorder
- Age of onset
- Adolescent, Adult, Childhood
- Status
- active
Fused manidbular incisors is an extremely rare dental anomaly that is characterized by the union of two, normally separated, incisor tooth germs of the primary dentition. It is frequently associated with hypodontia and an increased risk of pulp exposure.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Fused mandibular incisors | |
| fr | Fusion des incisives mandibulaires | |
| de | Fusionierte mandibuläre Inzisoren | Verschmelzung der Schneidezähne im Unterkiefer |
| es | Fusión de incisivos mandibulares | |
| it | Fusione degli incisivi mandibolari | |
| nl | Gefuseerde mandibulaire snijtanden | |
| pt | Fusão dos incisivos mandibulares | |
| pl | Zlane siekacze żuchwy | |
| cs | Spojené řezáky dolní čelisti | |
| uk | Зрощені різці нижньої щелепи | |
| zh | 下颌切牙融合 | |
| tr | Kaynaşmış mandibular kesici dişler |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 147251 | E | validated | |
| ICD-10 | K00.2 | NTBT | attributed | validated |
| ICD-11 | LA30.4 | NTBT | index | validated |
| MONDO | 0007820 | E | validated | |
| UMLS | C3494175 | E | validated | |
| GARD | 2419 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:420755Rare genetic odontal or periodontal disorder
rare genetic diseases - ORPHA:164001Rare odontal or periodontal disorder
rare odontological diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | 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.
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HPO phenotypes
2 annotations · validated 2016-06-01| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0000164 | Abnormality of the dentition | |
| HP:0006288 | Advanced eruption of teeth | |
Run the differential on the 2 obligate / very frequent terms
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/2287
- This record as JSON: /data/d/2287.json