ORPHA:140456
Autosomal dominant hereditary axonal motor and sensory neuropathy
- Type
- Category
- Group
- Group of disorders
- Inheritance
- Autosomal dominant
- 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Autosomal dominant hereditary axonal motor and sensory neuropathy | |
| fr | Neuropathie sensitivo-motrice axonale héréditaire autosomique dominante | |
| de | Autosomal-dominante axonale hereditäre motorisch-sensorische Neuropathie | |
| es | Neuropatía axonal sensitivo-motora hereditaria autosómica dominante | |
| it | Neuropatia motoria e sensoriale assonale ereditaria autosomica dominante | |
| nl | Autosomaal dominante erfelijke axonale motorische en sensorische neuropathie | |
| pt | Neuropatia sensitiva e motora axonal hereditária autossómica dominante | |
| pl | Autosomalna dominująca dziedziczna aksonalna neuropatia ruchowa i czuciowa | |
| cs | Autozomálně dominantní hereditární axonální motorická a senzorická neuropatie | |
| uk | Автосомно-домінантна спадкова аксональна моторна та сенсорна нейропатія | |
| zh | 常染色体显性遗传轴索运动和感觉神经病 | |
| tr | Otozomal dominant kalıtsal aksonal motor ve duyusal nöropati |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15360 | E | validated | |
| UMLS | C5680676 | E | validated | |
| GARD | 19924 | 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:476109Axonal hereditary motor and sensory neuropathy
rare genetic diseases; rare neurological diseases
Children (6):
- ORPHA:64746Autosomal dominant Charcot-Marie-Tooth disease type 2
- ORPHA:1215Autosomal dominant optic atrophy plus syndrome
- ORPHA:64751Hereditary motor and sensory neuropathy type 5
- ORPHA:90120Hereditary motor and sensory neuropathy type 6
- ORPHA:90117Hereditary motor and sensory neuropathy, Okinawa type
- ORPHA:538574Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/140456
- This record as JSON: /data/d/140456.json