ORPHA:221150
OBSOLETE: Pitt-Hopkins-like syndrome
inactive · referred to ORPHA:163681CNTNAP2-related developmental and epileptic encephalopathy
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using CNTNAP2-related developmental and epileptic encephalopathy
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Pitt-Hopkins-like syndrome | |
| fr | OBSOLETE : Syndrome Pitt-Hopkins-like | |
| de | OBSOLET: Pitt-Hopkins-ähnliches Syndrom | |
| es | OBSOLETO: Síndrome similar a Pitt-Hopkins | OBSOLETO: Síndrome de Pitt-Hopkins-like |
| it | OBSOLETO: Sindrome Pitt-Hopkins-simile | |
| nl | OBSOLEET: Pitt-Hopkins-achtig syndroom | |
| pt | OBSOLETO: Síndrome Pitt-Hopkins-like | |
| pl | NIEAKTUALNE: Zespół podobny do zespołu Pitta i Hopkinsa | |
| cs | NEAKTUÁLNÍ: Pitt-Hopkins-like syndrom | |
| uk | ЗАСТАРІЛО: Синдром Пітта-Хопкінса | |
| zh | 皮特-霍普金斯样综合征 | |
| tr | Pitt-Hopkins benzeri sendrom |
Definition in:
2
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/221150
- This record as JSON: /data/d/221150.json