ORPHA:98036
Rare otorhinolaryngologic disease
- Type
- Category
- Group
- Group of disorders
- Status
- active
- Flag
- Head of classification
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 | Rare otorhinolaryngologic disease | |
| fr | Maladie otorhinolaryngologique rare | |
| de | Otorhinolaryngologische Krankheit, seltene | |
| es | Enfermedad otorrinolaringológica rara | |
| it | Malattia d'interesse otorinolaringoiatrico rara | |
| nl | Zeldzame otorinolaryngologische ziekte | |
| pt | Doença otorrinolaringológica, rara | |
| pl | Rzadkie choroby otorynolaryngologiczne | |
| cs | Vzácná otorinolaryngologická onemocnění | |
| uk | Рідкісне оториноларингологічне захворювання | |
| zh | 罕见耳鼻咽喉疾病 | |
| tr | Nadir kulak burun boğaz hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681545 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Not placed in any Orphanet classification in this release.
Children (17):
- ORPHA:504476Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome
- ORPHA:1467Cogan syndrome
- ORPHA:449566Eosinophilic angiocentric fibrosis
- ORPHA:922Familial nasal acilia
- ORPHA:171684Idiopathic bilateral vestibulopathy
- ORPHA:652681Idiopathic subglottic stenosis
- ORPHA:79078IgG4-related dacryoadenitis and sialadenitis
- ORPHA:449432IgG4-related submandibular gland disease
- ORPHA:88620Isolated congenital anosmia
- ORPHA:210272Mal de débarquement
- ORPHA:68361Rare deafness
- ORPHA:98061Rare otorhinolaryngologic tumor
- ORPHA:96333Rare otorhinolaryngological malformation
- ORPHA:60032Recurrent respiratory papillomatosis
- ORPHA:420402Semicircular canal dehiscence syndrome
- ORPHA:71276Silent sinus syndrome
- ORPHA:156237Syndrome or malformation associated with head and neck malformations
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/98036
- This record as JSON: /data/d/98036.json