ORPHA:420755
Rare genetic 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare genetic odontal or periodontal disorder | |
| fr | Affection dentaire ou parodontaire rare d'origine génétique | |
| de | Seltene odontale oder periodontale Krankheit, genetisch bedingt | |
| es | Trastorno dental o periodontal genético raro | |
| it | Disturbo dentale o periodontale genetico raro | |
| nl | Zeldzame genetische odontale of periodontale aandoening | |
| pt | Doença odontal ou periodontal genética rara | |
| pl | Rzadkie zaburzenia zębów i przyzębia uwarunkowane genetycznie | |
| cs | Vzácná genetická odontální nebo periodontální nemoc | |
| uk | Рідкісні генетично обумовлені одонтологічні або пародонтальні розлади | |
| zh | 罕见遗传性牙或牙周病 | |
| tr | Nadir genetik odontal veya periodontal bozukluk |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18488 | E | validated | |
| UMLS | C5681204 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:77830Rare genetic odontologic disease
rare genetic diseases
Children (10):
- ORPHA:88661Amelogenesis imperfecta
- ORPHA:99797Anodontia
- ORPHA:444072Cerebellar-facial-dental syndrome
- ORPHA:1077Dental ankylosis
- ORPHA:314555Facial dysmorphism-ocular anomalies-osteopenia-intellectual disability-dental anomalies syndrome
- ORPHA:2287Fused mandibular incisors
- ORPHA:167759Hereditary dentin defect
- ORPHA:2024Hereditary gingival fibromatosis
- ORPHA:99798Oligodontia
- ORPHA:412206Primary failure of tooth eruption
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/420755
- This record as JSON: /data/d/420755.json