ORPHA:182064
Rare neuroinflammatory or neuroimmunological disease
- Type
- Category
- 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare neuroinflammatory or neuroimmunological disease | |
| fr | Maladie neuro-inflammatoire ou neuro-immunologique rare | |
| de | Seltene neuroinflammatorische oder neuroimmunologische Krankheit | |
| es | Enfermedad neuroinmunológica o neuroinflamatoria rara | |
| it | Malattia neuroinfiammatoria o neuroimmunologica rara | |
| nl | Zeldzame neuro-inflammatoire of neuro-immunologische ziekte | |
| pt | Doença neuroinflamatória ou neuroimunológica rara | |
| pl | Rzadka choroba neurozapalna lub neuroimmunologiczna | |
| cs | Vzácná zánětlivá nebo imunologická onemocnění nervového systému | |
| uk | Рідкісне нейрозапальне або нейроімунологічне захворювання | |
| zh | 罕见神经炎症或神经免疫性疾病 | |
| tr | Nadir nöroinflamatuar veya nöroimmünolojik hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15916 | E | validated | |
| UMLS | C5680598 | 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:98006Rare neurologic disease
rare neurological diseases
Children (13):
- ORPHA:139417Acute transverse myelitis
- ORPHA:730230Autoimmune nodopathy
- ORPHA:102005Brain inflammatory disease
- ORPHA:71279CANOMAD syndrome
- ORPHA:284448CLIPPERS
- ORPHA:2932Chronic inflammatory demyelinating polyneuropathy
- ORPHA:2103Guillain-Barré syndrome
- ORPHA:728866Immune effector cell-associated neurotoxicity syndrome
- ORPHA:499096Isolated optic neuritis
- ORPHA:228145Multiple sclerosis variant
- ORPHA:71211Neuromyelitis optica spectrum disorder
- ORPHA:3198Stiff person spectrum disorder
- ORPHA:3437Vogt-Koyanagi-Harada disease
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/182064
- This record as JSON: /data/d/182064.json