ORPHA:2679
OBSOLETE: Infantile axonal neuropathy
inactive · referred to ORPHA:98497Genetic peripheral neuropathy
- 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 Genetic peripheral neuropathy
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Infantile axonal neuropathy | |
| fr | OBSOLETE : Neuropathie axonale infantile | |
| de | OBSOLET: Neuropathie, axonale infantile | |
| es | OBSOLETO: Neuropatía axonal infantil | |
| it | OBSOLETO: Neuropatia assonale infantile | |
| nl | OBSOLEET: Infantiele axonale neuropathie | |
| pt | OBSOLETO: Neuropatia axonal do lactente | |
| pl | NIEAKTUALNE: Dziecieca neuropatia aksonalna | |
| cs | NEAKTUÁLNÍ: Dětská axonální neuropatie | |
| uk | ЗАСТАРІЛО: Інфантильна аксональна нейропатія | |
| zh | 弃用：小儿轴突性神经病 | |
| tr | Eski adı: İnfantil aksonal nöropati |
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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/2679
- This record as JSON: /data/d/2679.json