ORPHA:183580
Genetic malformation syndrome with odontal and/or periodontal component
- 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 | Genetic malformation syndrome with odontal and/or periodontal component | |
| fr | Syndrome malformatif avec composante odontique et/ou périodontique d'origine génétique | |
| de | Dysmorphie-Syndrom mit odontaler und/oder periodontaler Komponente, genetisch bedingt | |
| es | Síndrome genético malformativo con componente dental y/o periodontal | |
| it | Sindrome malformativa genetica con componente dentale e/o parodontale | |
| nl | Genetisch malformatiesyndroom met odontale en/of periodontale component | |
| pt | Síndrome de malformação genética com componente odontológico e/ou periodontológico | |
| pl | Genetyczny zespół wad z udziałem zębów lub komponent okołozębowych | |
| cs | Geneticky podmíněné malformační syndromy s postižením zubů a/nebo periodontu | |
| uk | Синдром генетично обумовленої вади розвитку з одонтальним та/або періодонтальним компонентом | |
| zh | 遗传性畸形综合征伴牙体或牙周成分 | |
| tr | Odontal ve / veya periodontal bileşenli genetik malformasyon sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680547 | 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:183530Rare genetic developmental defect during embryogenesis
rare genetic diseases
Children (58):
- ORPHA:978ADULT syndrome
- ORPHA:1946Amelocerebrohypohidrotic syndrome
- ORPHA:1997Blepharo-cheilo-odontic syndrome
- ORPHA:2899Brachyolmia-amelogenesis imperfecta syndrome
- ORPHA:2010Cleft palate-stapes fixation-oligodontia syndrome
- ORPHA:284149Craniosynostosis-dental anomalies
- ORPHA:3220Deafness-enamel hypoplasia-nail defects syndrome
- ORPHA:3230Deafness-oligodontia syndrome
- ORPHA:71267Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome
- ORPHA:1660Dermoodontodysplasia
- ORPHA:69083Ectodermal dysplasia with natal teeth, Turnpenny type
- ORPHA:1818Ectodermal dysplasia, trichoodontoonychial type
- ORPHA:1031Enamel-renal syndrome
- ORPHA:598603Facial dysmorphism-hypertrichosis-epilepsy-intellectual disability/developmental delay-gingival overgrowth syndrome
- ORPHA:2067GAPO syndrome
- ORPHA:664438Gingival fibromatosis-aortic root dilatation-facial dysmorphism-intellectual disability syndrome
- ORPHA:2025Gingival fibromatosis-facial dysmorphism syndrome
- ORPHA:2026Gingival fibromatosis-hypertrichosis syndrome
- ORPHA:2027Gingival fibromatosis-progressive deafness syndrome
- ORPHA:2342Haim-Munk syndrome
- ORPHA:2024Hereditary gingival fibromatosis
- ORPHA:2228Hypodontia-dysplasia of nails syndrome
- ORPHA:684232Intellectual disability-epilepsy-dental anomalies-facial dysmorphism syndrome
- ORPHA:1873Jalili syndrome
- ORPHA:2028Juvenile hyaline fibromatosis
- ORPHA:2332KBG syndrome
- ORPHA:2363Lacrimoauriculodentodigital syndrome
- ORPHA:627Nance-Horan syndrome
- ORPHA:2972Non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome
- ORPHA:2719Oculocerebral hypopigmentation syndrome, Cross type
- ORPHA:2720Oculocerebral hypopigmentation syndrome, Preus type
- ORPHA:2709Oculodental syndrome, Rutherfurd type
- ORPHA:2710Oculodentodigital dysplasia
- ORPHA:2712Oculofaciocardiodental syndrome
- ORPHA:99806Oculootodental syndrome
- ORPHA:2722Odonto-onycho dysplasia-alopecia syndrome
- ORPHA:2721Odonto-onycho-dermal dysplasia
- ORPHA:69082Odonto-tricho-ungual-digito-palmar syndrome
- ORPHA:166272Odontochondrodysplasia
- ORPHA:2724Odontomatosis-aortae esophagus stenosis syndrome
- ORPHA:2723Odontotrichomelic syndrome
- ORPHA:2791Otodental syndrome
- ORPHA:477993Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome
- ORPHA:678Papillon-Lefèvre syndrome
- ORPHA:2892Pilodental dysplasia-refractive errors syndrome
- ORPHA:2916Postaxial polydactyly-dental and vertebral anomalies syndrome
- ORPHA:2561Pyramidal molars-abnormal upper lip syndrome
- ORPHA:3019Ramon syndrome
- ORPHA:50944Schöpf-Schulz-Passarge syndrome
- ORPHA:3184Steatocystoma multiplex-natal teeth syndrome
- ORPHA:3196Steroid dehydrogenase deficiency-dental anomalies syndrome
- ORPHA:3352Tricho-dento-osseous syndrome
- ORPHA:3351Trichodental syndrome
- ORPHA:3353Trichodermodysplasia-dental alterations syndrome
- ORPHA:79129Trichodysplasia-amelogenesis imperfecta syndrome
- ORPHA:3355Trichoodontoonychial dysplasia
- ORPHA:166277Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia
- ORPHA:3473Zimmermann-Laband syndrome
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Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/183580
- This record as JSON: /data/d/183580.json