ORPHA:139042
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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Malformation syndrome with odontal and/or periodontal component | |
| fr | Syndrome malformatif avec composante odontique et/ou péri-odontique | |
| de | Dysmorphie-Syndrom mit odontaler und/oder periodontaler Komponente | |
| es | Síndrome malformativo con componente odontal y/o peridontal | |
| it | Sindrome dismorfica con componente dentale e/o periodontica | |
| nl | Malformatiesyndroom met odontale en/of periodontale component | |
| pt | Síndrome dismórfico com componente dentário e/ou peridodontal | |
| pl | Zespół malformacji z udziałem zębów i/lub przyzębia | |
| cs | Syndromy malformace s odontální a periodontální komponentou | |
| uk | Синдром вад розвитку з одонтальним та/або пародонтальним компонентом | |
| zh | 牙和/或牙周组织发育不良综合征 | |
| tr | Odontal ve / veya periodontal bileşen ile seyreden malformasyon sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15336 | E | validated | |
| UMLS | C5680617 | E | validated | |
| GARD | 19909 | 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:93890Rare developmental defect during embryogenesis
rare developmental anomalies during embryogenesis - ORPHA:98026Rare odontologic disease
rare odontological diseases
Children (68):
- ORPHA:978ADULT syndrome
- ORPHA:401911AXIN2-related polyposis
- ORPHA:1946Amelocerebrohypohidrotic syndrome
- ORPHA:562559Anterior maxillary protrusion-strabismus-intellectual disability syndrome
- ORPHA:1997Blepharo-cheilo-odontic syndrome
- ORPHA:2899Brachyolmia-amelogenesis imperfecta syndrome
- ORPHA:2010Cleft palate-stapes fixation-oligodontia syndrome
- ORPHA:1452Cleidocranial dysplasia
- ORPHA:697356Congenital scalp aplasia cutis-enamel hypoplasia-developmental delay-intellectual disability syndrome
- ORPHA:284149Craniosynostosis-dental anomalies
- ORPHA:307766Curly hair-acral keratoderma-caries syndrome
- ORPHA:3220Deafness-enamel hypoplasia-nail defects syndrome
- ORPHA:3230Deafness-oligodontia 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:314555Facial dysmorphism-ocular anomalies-osteopenia-intellectual disability-dental anomalies 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:2228Hypodontia-dysplasia of nails syndrome
- ORPHA:307936Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome
- ORPHA:684232Intellectual disability-epilepsy-dental anomalies-facial dysmorphism syndrome
- ORPHA:1873Jalili syndrome
- ORPHA:2028Juvenile hyaline fibromatosis
- ORPHA:2332KBG syndrome
- ORPHA:2363Lacrimoauriculodentodigital syndrome
- ORPHA:589608Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies
- ORPHA:180766Malformative syndrome with dentinogenesis imperfecta
- 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:2724Odontomatosis-aortae esophagus stenosis syndrome
- ORPHA:1811Odontomicronychial dysplasia
- ORPHA:2723Odontotrichomelic syndrome
- ORPHA:2791Otodental syndrome
- ORPHA:90650Otopalatodigital syndrome type 1
- ORPHA:90652Otopalatodigital syndrome type 2
- 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:576278SATB2-associated syndrome
- ORPHA:50944Schöpf-Schulz-Passarge syndrome
- ORPHA:3184Steatocystoma multiplex-natal teeth syndrome
- ORPHA:3196Steroid dehydrogenase deficiency-dental anomalies syndrome
- ORPHA:363417Temtamy preaxial brachydactyly syndrome
- ORPHA:3352Tricho-dento-osseous syndrome
- ORPHA:3351Trichodental syndrome
- ORPHA:3353Trichodermodysplasia-dental alterations syndrome
- ORPHA:79129Trichodysplasia-amelogenesis imperfecta syndrome
- ORPHA:3355Trichoodontoonychial dysplasia
- ORPHA:659873Wormian bones-micrognathia-abnormal dentition-progeroid syndrome
- ORPHA:3473Zimmermann-Laband 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/139042
- This record as JSON: /data/d/139042.json