ORPHA:2286
OBSOLETE: Solitary median maxillary central incisor syndrome
inactive · referred to ORPHA:280200Microform holoprosencephaly
Synonyms: OBSOLETE: SMMCI · OBSOLETE: Single upper central incisor
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Microform holoprosencephaly
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Solitary median maxillary central incisor syndrome | OBSOLETE: SMMCI · OBSOLETE: Single upper central incisor |
| fr | OBSOLETE : Incisive centrale maxillaire médiane unique | OBSOLETE : ICMMU · OBSOLETE : Incisive centrale supérieure unique |
| de | OBSOLET: Syndrom des einzelnen maxillären mittleren Schneidezahnes | OBSOLET: SMMCI |
| es | OBSOLETO: Síndrome de incisivo central maxilar medio único | OBSOLETO: Incisivo central superior único · OBSOLETO: SMMCI |
| it | OBSOLETO: Sindrome dell'incisivo centrale mascellare mediano solitario | OBSOLETO: Incisivo superiore centrale unico · OBSOLETO: SMMCI |
| nl | OBSOLEET: Solitaire mediane maxillaire centrale incisief-syndroom | OBSOLEET: Enkele bovenste centrale snijtand · OBSOLEET: SMMCI |
| pt | OBSOLETO: Síndrome de incisivo central maxilar mediano único | OBSOLETO: Incisivo central superior único |
| pl | NIEAKTUALNE: Zespól pojedynczego srodkowego siekacza szczeki | NIEAKTUALNE: Pojedyńczy środkowy siekacz szczęki · NIEAKTUALNE: SMMCI |
| cs | NEAKTUÁLNÍ: Syndrom samostatného centrálního řezáku maxilly | NEAKTUÁLNÍ: SMMCI · NEAKTUÁLNÍ: Jediný horní přední řezák |
| uk | ЗАСТАРІЛО: Синдром поодинокого центрального різця середньої верхньої щелепи | ЗАСТАРІЛО: Одиночний верхній центральний різець · ЗАСТАРІЛО: SMMCI |
| zh | 弃用：上颌正中孤立中切牙综合征 | 单上颌中切牙 |
| tr | Eski adı: Soliter medyan maksiller santral kesici sendrom | SMMCI · Tek üst santral kesici |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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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/2286
- This record as JSON: /data/d/2286.json