ORPHA:476116
Demyelinating hereditary motor and sensory neuropathy
Synonyms: Demyelinating HMSN
- 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 | Demyelinating hereditary motor and sensory neuropathy | Demyelinating HMSN |
| fr | Neuropathie sensitivo-motrice héréditaire démyélinisante | HMSN démyélinisante · NSMH démyélinisante |
| de | Neuropathie, hereditäre motorisch-sensorische, demyelinisierende From | HMSN, demyelinisierende |
| es | Neuropatía desmielinizante sensitivo-motora hereditaria | HMSN desmielinizante |
| it | Malattia demielinizzante di Charcot-Marie-Tooth | |
| nl | Demyeliniserende erfelijke motorische en sensorische neuropathie | Demyeliniserende HMSN |
| pt | Neuropatia sensitiva e motora hereditária desmielinizante | Doença de Charcot-Marie-Tooth desmielinizante |
| pl | Demielinizująca dziedziczna neuropatia ruchowa i czuciowa | Demielinizująca HMSN |
| cs | Demyelinizační hereditární senzomotorická neuropatie | Demyelinating HMSN · Demyelinizační HMSN |
| uk | Демієлінізуюча спадкова моторна та сенсорна нейропатія | Демієлінізуючий HMSN |
| zh | 遗传性运动和感觉神经脱髓鞘病 | HMSN脱髓鞘 |
| tr | Demiyelinizan kalıtsal motor ve duyusal nöropati | Demiyelinizan HMSN |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0018776 | E | validated | |
| MONDO | 18776 | E | validated | |
| UMLS | C5680106 | 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/476116
- This record as JSON: /data/d/476116.json