ORPHA:207031
OBSOLETE: Rare disease with corpus callosum agenesis associated with peripheral neuropathy
inactive · referred to ORPHA:1496Corpus callosum agenesis-neuronopathy syndrome
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Corpus callosum agenesis-neuronopathy syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Rare disease with corpus callosum agenesis associated with peripheral neuropathy | |
| fr | OBSOLETE : Maladie rare avec agénésie du corps calleux associé à une neuropathie périphérique | |
| de | OBSOLET: Corpus callosum-Agenesie mit assoziierter peripherer Neuropathie | |
| es | OBSOLETO: Enfermedad rara con agenesia del cuerpo calloso asociado con una neuropatía periférica | |
| it | OBSOLETO: Malattia rara con agenesia del corpo calloso associata a neuropatia periferica | |
| nl | OBSOLEET: Zeldzame ziekte met agenesie van corpus callosum geassocieerd met perifere neuropathie | |
| pt | OBSOLETO: Doença rara com agenesia do corpo caloso associada com neuropatia periférica | |
| pl | NIEAKTUALNE: Rzadka choroba z agenezja ciala modzelowatyego z towarzyszaca neuropatia obwodowa | |
| cs | NEAKTUÁLNÍ: Vzácná onemocnění s agenezí corpus callosum asociovaná s periferní neuropatií | |
| uk | ЗАСТАРІЛО: Рідкісне захворювання з агенезією мозолистого тіла, повязане з периферичною нейропатією | |
| zh | 弃用：周围神经病相关的胼胝体发育不全罕见病 | |
| tr | Eski adı: Periferik nöropati ilişkili korpus kallozum agenezi ile seyrek görülen hastalık |
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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/207031
- This record as JSON: /data/d/207031.json