ORPHA:140462
OBSOLETE: X-linked recessive hereditary axonal motor and sensory neuropathy
inactive · referred to ORPHA:64747X-linked Charcot-Marie-Tooth disease
- 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 X-linked Charcot-Marie-Tooth disease
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: X-linked recessive hereditary axonal motor and sensory neuropathy | |
| fr | OBSOLETE : Neuropathie sensitivo-motrice axonale héréditaire liée à l'X | |
| de | OBSOLET: Neuropathie, motorische und sensorische, axonale, hereditäre, X-chromosomal-rezessive | |
| es | OBSOLETO: Neuropatía axonal hereditaria sensitivo-motora recesiva ligada a X | |
| it | OBSOLETO: Neuropathy, motor and sensory, axonal, hereditary, X-linked recessive | |
| nl | OBSOLEET: X-gebonden recessieve erfelijke axonale motorische and sensorische neuropathie | |
| pt | OBSOLETO: Neuropatia sensitiva e motora axonal hereditária recessiva ligada ao X | |
| pl | NIEAKTUALNE: Dziedziczna aksonalna neuropatia ruchowa i czuciowa sprzezona z chromosomem X | |
| cs | NEAKTUÁLNÍ: X-vázaná recesivní hereditární axonální motorická a senzorická neuropatie | |
| uk | ЗАСТАРІЛО: Х-зчеплена рецесивна спадкова аксональна моторна та сенсорна нейропатія | |
| zh | 弃用：X连锁隐性遗传轴索运动和感觉神经病 | |
| tr | Eski adı: X'e bağlı resesif kalıtsal aksonal motor ve duyusal 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/140462
- This record as JSON: /data/d/140462.json