ORPHA:1077
Dental ankylosis
Synonyms: Ankylosis of teeth
- Type
- Malformation syndrome
- Group
- Disorder
- Age of onset
- Adolescent, Adult, Childhood, Elderly
- Status
- active
A rare odontologic disorder characterized by the loss of the periodontal ligament space and orthodontic mobility.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Dental ankylosis | Ankylosis of teeth |
| fr | Ankylose dentaire | Ankylose des dents |
| de | Dentale Ankylose | Ankylose der Zähne |
| es | Anquilosis dental | Anquilosis de los dientes |
| it | Anchilosi dentale | Anchilosi dei denti |
| nl | Dentale ankylose | Ankylose van de tanden |
| pt | Anquilose dentária | Anquilose dos dentes |
| pl | Ankyloza zębów | = en |
| cs | Zubní ankylóza | Ankylóza zubů |
| uk | Зубний анкілоз | Анкілоз зубів |
| zh | 牙-牙槽骨骨性黏连 | 牙-牙槽骨骨性黏连 |
| tr | Dental ankiloz | Dişlerin ankilozu |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | K03.5 | E | specific | validated |
| ICD-11 | DA07.61 | E | specific | validated |
| MONDO | 0008007 | E | validated | |
| MeSH | D020254 | E | validated | |
| UMLS | C0155930 | E | validated | |
| GARD | 701 | E | validated | |
| MedDRA | 10044019 | 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.
4
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 | 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.
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HPO phenotypes
4 annotations · validated 2016-06-01| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0009804 | Tooth agenesis | |
| Frequent (79-30%) | ||
| HP:0000682 | Abnormality of dental enamel | |
| Occasional (29-5%) | ||
| HP:0004209 | Clinodactyly of the 5th finger | |
| HP:0000303 | Mandibular prognathia | |
Run the differential on the 1 obligate / very frequent terms
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/1077
- This record as JSON: /data/d/1077.json