ORPHA:137653
Microcephaly-digital anomalies-intellectual disability syndrome
inactive · moved to ORPHA:313795Jawad syndrome
Synonyms: Kelly-Kirson-Wyatt syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Jawad syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Microcephaly-digital anomalies-intellectual disability syndrome | Kelly-Kirson-Wyatt syndrome |
| fr | Syndrome de microcéphalie-anomalies digitales-déficience intellectuelle | Syndrome de Kelly-Kirson-Wyatt |
| de | Mikrozephalie-digitale Anomalien-Intelligenzminderung-Syndrom | Kelly-Kirson-Wyatt-Syndrom |
| es | Síndrome de microcefalia-anomalías digitales-discapacidad intelectual | Síndrome de Kelly-Kirson-Wyatt |
| it | Sindrome microcefalia-anomalie digitali-deficit cognitivo | Sindrome di Kelly-Kirson-Wyatt |
| nl | Microcefalie - vingeranomalieën - intellectuele achterstand-syndroom | Syndroom van Kelly-Kirson-Wyatt |
| pt | Síndrome de microcefalia-anomalias digitais-perturbação do desenvolvimento intelectual | Síndrome Kelly-Kirson-Wyatt |
| pl | Małogłowie - wady palców - niepełnosprawność intelektualna | Zespół Kelly'ego, Kirsona i Wyatta |
| cs | Syndrom zahrnující mikrocefalii, anomálie prstů a mentální retardaci | Kellyho-Kirsonův-Wyattův syndrom · Kelly-Kirson-Wyattův syndrom |
| uk | Синдром мікроцефалії-аномалії пальців-інтелектуальної недостатності | Синдром Келлі-Кірсона-Вайєтта |
| zh | 小头畸形-指异常-智力障碍综合征 | Kelly-Kirson-Wyatt综合征 |
| tr | Mikrosefali-dijital anomaliler-zihinsel yetersizlik sendromu | Kelly-Kirson-Wyatt 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/137653
- This record as JSON: /data/d/137653.json