ORPHA:2650
OBSOLETE: Dwarfism-intellectual disability-eye abnormality syndrome
inactive · referred to ORPHA:102283Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
Synonyms: OBSOLETE: Mollica-Pavone-Antener syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Dwarfism-intellectual disability-eye abnormality syndrome | OBSOLETE: Mollica-Pavone-Antener syndrome |
| fr | OBSOLETE : Syndrome de nanisme-déficience intellectuelle-anomalies de l'oeil | OBSOLETE : Syndrome de Mollica-Pavone-Antener |
| de | OBSOLET: Kleinwuchs-Intelligenzminderung-Augenanomalie-Syndrom | OBSOLET: Mollica-Pavone-Antener-Syndrom |
| es | OBSOLETO: Síndrome de talla baja significativa-discapacidad intelectual-anomalías oculares | OBSOLETO: Síndrome de Mollica-Pavone-Antener |
| it | OBSOLETO: Sindrome nanismo-disabilità intellettiva-anomalie oculari | OBSOLETE: Sindrome Mollica-Pavone-Antener |
| nl | OBSOLEET: Dwerggroei - intellectuele achterstand - oogabnormaliteit-syndroom | OBSOLEET: Mollica-Pavone-Antenersyndroom |
| pt | OBSOLETO: Síndrome de nanismo-perturbação do desenvolvimento intelectual-anomalias oculares | OBSOLETO: Síndrome Mollica-Pavone-Antener |
| pl | NIEAKTUALNE: Zespól niskoroslosci, niepelnosprawnosci intelektualnej i wad oka | NIEAKTUALNE: Zespół Mollica, Pavone i Antenera |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující trpaslictví, mentální postižení a abnormality očí | = en |
| uk | ЗАСТАРІЛО: Синдром карликовості-інтелектуальної недостатності-аномалії зору | ЗАСТАРІЛО: Синдром Моліки-Павоне-Антенера |
| zh | 弃用：侏儒症-智力障碍-眼畸形综合征 | Mollica-Pavone-Antener综合征 |
| tr | Eski adı: Cücelik-zihinsel yetersizlik-göz anormalliği sendromu | Mollica-Pavone-Antener sendromu |
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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.
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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/2650
- This record as JSON: /data/d/2650.json