ORPHA:476123
Intermediate Charcot-Marie-Tooth disease
Synonyms: Intermediate CMT · Intermediate hereditary motor and sensory neuropathy
- Type
- Clinical group
- Group
- Group of disorders
- Status
- active
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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Intermediate Charcot-Marie-Tooth disease | Intermediate CMT · Intermediate hereditary motor and sensory neuropathy |
| fr | Maladie de Charcot-Marie-Tooth intermédiare | Neuropathie sensitivo-motrice héréditaire intermédiare |
| de | Charcot-Marie-Tooth-Krankheit, intermediäre | Neuropathie, hereditäre motorisch-sensorische, intermediäre Form |
| es | Enfermedad de Charcot-Marie-Tooth intermedia | Neuropatía hereditaria sensitivo-motora intermedia |
| it | Malattia intermedia di Charcot-Marie-Tooth | |
| nl | Intermediaire ziekte van Charcot-Marie-Tooth | Intermediaire erfelijke motorische en sensorische neuropathie |
| pt | Doença de Charcot-Marie-Tooth intermédia | |
| pl | Pośrednia choroba Charcota, Mariego i Tootha | Pośrednia dziedziczna neuropatia ruchowa i czuciowa |
| cs | Středně pokročilá Charcot-Marie-Toothova nemoc | Intermediate hereditary motor and sensory neuropathy · Středně těžká dědičná motorická a senzorická neuropatie |
| uk | Помірно виражена хвороба Шарко-Марі-Тута | Проміжний CMT · Проміжна спадкова моторна та сенсорна нейропатія |
| zh | 中间亚型夏洛克-玛丽齿病 | 中间亚型遗传性运动和感觉神经病 |
| tr | Orta dereceli Charcot-Marie-Tooth hastalığı | Orta düzey kalıtsal motor ve duyusal nöropati |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 8C20.2 | E | specific | validated |
| MONDO | 0018778 | E | validated | |
| MONDO | 18778 | E | validated | |
| UMLS | C5680108 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:166Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy
rare genetic diseases; rare neurological diseases
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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/476123
- This record as JSON: /data/d/476123.json