ORPHA:140471
Hereditary sensory and autonomic neuropathy
Synonyms: HSAN
- 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 | Hereditary sensory and autonomic neuropathy | HSAN |
| fr | Neuropathie héréditaire sensitive et autonomique | HSAN · NHSA |
| de | Hereditäre sensorische und autonome Neuropathie | = en |
| es | Neuropatía sensitiva y autonómica hereditaria | NSAH |
| it | Neuropatia autonomica e sensoriale ereditaria | |
| nl | Hereditaire sensorische en autonome neuropathie | = en |
| pt | Neuropatia sensitiva e autonómica hereditária | |
| pl | Dziedziczna neuropatia czuciowa i autonomiczna | = en |
| cs | Hereditární senzorická a autonomní neuropatie | = en |
| uk | Спадкова сенсорна та вегетативна нейропатія | = en |
| zh | 遗传性感觉和自主神经病变 | = en |
| tr | Kalıtsal duyusal ve otonom nöropati | = en |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 8C21 | E | specific | validated |
| MONDO | 0015364 | E | validated | |
| MONDO | 15364 | E | validated | |
| MeSH | D009477 | E | validated | |
| UMLS | C0027889 | E | validated | |
| GARD | 12688 | 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:98497Genetic peripheral neuropathy
rare genetic diseases; rare neurological diseases
Children (4):
- ORPHA:140474Autosomal dominant hereditary sensory and autonomic neuropathy
- ORPHA:140477Autosomal recessive hereditary sensory and autonomic neuropathy
- ORPHA:217399Congenital insensitivity to pain-hyperhidrosis-absence of cutaneous sensory innervation
- ORPHA:139583X-linked hereditary sensory and autonomic neuropathy with deafness
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/140471
- This record as JSON: /data/d/140471.json