ORPHA:164001
Rare odontal or periodontal disorder
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare odontal or periodontal disorder | |
| fr | Affection dentaire ou parodontaire rare | |
| de | Seltene odontale oder periodontale Krankheit | |
| es | Trastornos dentales y periodontales raros | |
| it | Malattia odontale o periodontale rara | |
| nl | Zeldzame odontale of periodontale stoornis | |
| pt | Doença rara odontológica ou periodontal | |
| pl | Rzadkie zaburzenie zębów lub przyzębia | |
| cs | Vzácné odontální a periodontální poruchy | |
| uk | Рідкісні одонтологічні або періодонтальні розлади | |
| zh | 罕见牙齿或牙周疾病 | |
| tr | Nadir odontal veya periodontal bozukluk |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15603 | E | validated | |
| UMLS | C5680435 | 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 (1):
- ORPHA:98026Rare odontologic disease
rare odontological diseases
Children (12):
- ORPHA:88661Amelogenesis imperfecta
- ORPHA:99797Anodontia
- ORPHA:444072Cerebellar-facial-dental syndrome
- ORPHA:1077Dental ankylosis
- ORPHA:83451Florid cemento-osseous dysplasia
- ORPHA:2287Fused mandibular incisors
- ORPHA:167759Hereditary dentin defect
- ORPHA:2024Hereditary gingival fibromatosis
- ORPHA:99798Oligodontia
- ORPHA:412206Primary failure of tooth eruption
- ORPHA:83450Regional odontodysplasia
- ORPHA:67039Segmental odontomaxillary dysplasia
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/164001
- This record as JSON: /data/d/164001.json