ORPHA:167762
Rare disease with dentinogenesis imperfecta
- 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 disease with dentinogenesis imperfecta | |
| fr | Maladie rare avec dentinogenèse imparfaite | |
| de | Seltene Krankheit mit Dentinogenesis imperfecta | |
| es | Enfermedad rara con dentinogénesis imperfecta | |
| it | Dentinogenesi imperfetta sindromica | |
| nl | Zeldzame ziekte met dentinogenesis imperfecta | |
| pt | Dentinogénese imperfeita sindrómica | |
| pl | Rzadka choroba z dentinogenesis imperfecta | |
| cs | Vzácná nemoc s dentinogenesis imperfecta | |
| uk | Рідкісне захворювання з недосконалим дентиногенезом | |
| zh | 罕见疾病伴牙本质发育不全 | |
| tr | Dentinogenesis imperfekta ile seyreden nadir hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15669 | E | validated | |
| UMLS | C5680464 | 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 (2):
- ORPHA:98027Rare disease with odontological manifestation
rare odontological diseases - ORPHA:77830Rare genetic odontologic disease
rare genetic diseases
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/167762
- This record as JSON: /data/d/167762.json