ORPHA:77830
Rare genetic odontologic disease
- 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 odontologic disease | |
| fr | Maladie odontologique génétique rare | |
| de | Odontologische Krankheit, genetisch bedingte, seltene | |
| es | Enfermedades odontológicas genéticas raras | |
| it | Malattia odontoiatrica genetica rara | |
| nl | Zeldzame genetische odontologische ziekte | |
| pt | Doença odontológica, genética, rara | |
| pl | Rzadka genetyczna choroba odontologiczna | |
| cs | Vzácná geneticky podmíněná odontologická onemocnění | |
| uk | Рідкісне генетично обумовлене одонтологічне захворювання | |
| zh | 罕见遗传性牙齿疾病 | |
| tr | Nadir genetik odontolojik hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 19183 | E | validated | |
| UMLS | C5681298 | 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:98053Rare genetic disease
rare genetic diseases
Children (9):
- ORPHA:562559Anterior maxillary protrusion-strabismus-intellectual disability syndrome
- ORPHA:99792Dentin dysplasia-sclerotic bones syndrome
- ORPHA:476096Erythrokeratodermia-cardiomyopathy syndrome
- ORPHA:180766Malformative syndrome with dentinogenesis imperfecta
- ORPHA:557003Oculoskeletodental syndrome
- ORPHA:447961Pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome
- ORPHA:167762Rare disease with dentinogenesis imperfecta
- ORPHA:420755Rare genetic odontal or periodontal disorder
- ORPHA:576278SATB2-associated syndrome
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/77830
- This record as JSON: /data/d/77830.json