ORPHA:228357
OBSOLETE: CLN9 disease
inactive · referred to ORPHA:216Neuronal ceroid lipofuscinosis
- Type
- Etiological 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 Neuronal ceroid lipofuscinosis
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: CLN9 disease | |
| fr | OBSOLETE : Maladie CLN9 | |
| de | OBSOLET: CLN9-Krankheit | |
| es | OBSOLETO: Enfermedad CLN9 | |
| it | OBSOLETO: Malattia CLN9 | |
| nl | OBSOLEET: CLN9-ziekte | |
| pt | OBSOLETO: Doença CLN9 | |
| pl | NIEAKTUALNE: Choroba CLN9 | |
| cs | NEAKTUÁLNÍ: Neuronální ceroidlipofuscinosa, typ 9 | |
| uk | ЗАСТАРІЛО: хвороба CLN9 | |
| zh | 神经元蜡样脂褐质沉积症9型 | |
| tr | CLN9 hastalığı |
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.
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/228357
- This record as JSON: /data/d/228357.json