ORPHA:140474
Autosomal dominant hereditary sensory and autonomic 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 sensory and autonomic neuropathy | |
| fr | Neuropathie sensitive et autonomique héréditaire autosomique dominante | |
| de | Neuropathie, autonome hereditäre sensorische, autosomal-dominant | |
| es | Neuropatía sensitiva autonómica hereditaria autosómica dominante | |
| it | Neuropatia sensoriale e autonomica ereditaria autosomica dominante | |
| nl | Autosomaal dominante erfelijke sensorische en autonome neuropathie | |
| pt | Neuropatia sensitiva e autonómica hereditária autossómica dominante | |
| pl | Autosomalna dominująca dziedziczna neuropatia czuciowa i autonomiczna | |
| cs | Autozomálně dominantní hereditární senzorická a autonomní neuropatie | |
| uk | Аутосомно-домінантна спадкова сенсорна та вегетативна нейропатія | |
| zh | 常染色体显性遗传感觉和自主神经病变 | |
| tr | Otozomal dominant kalıtsal duyusal ve otonom nöropati |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15365 | E | validated | |
| UMLS | C5680674 | E | validated | |
| GARD | 19928 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:140471Hereditary sensory and autonomic neuropathy
rare genetic diseases; rare neurological diseases
Children (7):
- ORPHA:653728Congenital insensitivity to pain syndrome, Marsili type
- ORPHA:36386Hereditary sensory and autonomic neuropathy type 1
- ORPHA:139564Hereditary sensory and autonomic neuropathy type 1B
- ORPHA:391397Hereditary sensory and autonomic neuropathy type 7
- ORPHA:456318Hereditary sensory neuropathy-deafness-dementia syndrome
- ORPHA:397606PrP systemic amyloidosis
- ORPHA:90026Primary erythromelalgia
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/140474
- This record as JSON: /data/d/140474.json