ORPHA:98006
Rare neurologic disease
Synonyms: Rare nervous system 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 neurologic disease | Rare nervous system disease |
| fr | Maladie neurologique rare | Maladie rare du système nerveux |
| de | Neurologische Krankheit, seltene | |
| es | Enfermedad neurológica rara | |
| it | Malattia neurologica rara | |
| nl | Zeldzame neurologische ziekte | Zeldzame zenuwstelselziekte |
| pt | Doença neurológica rara | |
| pl | Rzadkie choroby neurologiczne | Rzadkie choroby układu nerwowego |
| cs | Vzácná neurologická onemocnění | Vzácná onemocnění nervového systému |
| uk | Рідкісне неврологічне захворювання | Рідкісне захворювання нервової системи |
| zh | 罕见神经系统疾病 | 罕见神经系统疾病 |
| tr | Nadir nörolojik hastalık | Nadir sinir sistemi hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680252 | 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 (47):
- ORPHA:209978Alternating hemiplegia
- ORPHA:137817Arachnoiditis
- ORPHA:69739Athabaskan brainstem dysgenesis syndrome
- ORPHA:363746Balint syndrome
- ORPHA:98044Central nervous system malformation
- ORPHA:83452Complex regional pain syndrome
- ORPHA:2047Flynn-Aird syndrome
- ORPHA:221117Gerstmann syndrome
- ORPHA:238624Idiopathic intracranial hypertension
- ORPHA:276174Idiopathic recurrent stupor
- ORPHA:98010Infectious disease of the nervous system
- ORPHA:210141Inherited congenital spastic tetraplegia
- ORPHA:252190Inherited nervous system cancer-predisposing syndrome
- ORPHA:178506Interstitial lung disease-brain calcification syndrome
- ORPHA:68356Leukodystrophy
- ORPHA:2406Locked-in syndrome
- ORPHA:102000Medullar disease
- ORPHA:90056Moderate and severe traumatic brain injury
- ORPHA:137929Neonatal brainstem dysfunction
- ORPHA:68385Neurometabolic disease
- ORPHA:68381Neuromuscular disease
- ORPHA:36388Paraneoplastic neurologic syndrome
- ORPHA:46348Paroxysmal extreme pain disorder
- ORPHA:398147Persistent idiopathic facial pain
- ORPHA:686468Post 5-alpha-reductase inhibitors treatment syndrome
- ORPHA:686475Post-selective serotonin reuptake inhibitor sexual dysfunction
- ORPHA:521236Primary orthostatic disorder
- ORPHA:102002Rare ataxia
- ORPHA:423662Rare autonomic nervous system disorder
- ORPHA:71281Rare central nervous system and retinal vascular disease
- ORPHA:730693Rare complex neurodevelopmental disorder without intellectual disability or autism spectrum disorder
- ORPHA:466658Rare disease with malignant hyperthermia
- ORPHA:101998Rare epilepsy
- ORPHA:98022Rare headache
- ORPHA:87277Rare intellectual disability
- ORPHA:102003Rare movement disorder
- ORPHA:98062Rare nervous system tumor
- ORPHA:182070Rare neurodegenerative disease
- ORPHA:182064Rare neuroinflammatory or neuroimmunological disease
- ORPHA:98033Rare neurologic disease with psychiatric involvement
- ORPHA:98496Rare peripheral neuropathy
- ORPHA:68354Rare sleep disorder
- ORPHA:603699Recessive KLHL7-related disorder
- ORPHA:211047Specific learning disability
- ORPHA:29822Spontaneous periodic hypothermia
- ORPHA:1314Symmetrical thalamic calcifications
- ORPHA:3465Worster-Drought syndrome
Codes that Orphanet moved or referred to this one:
- ORPHA:2033OBSOLETE: Multifocal muscular fibrosis-obstructed vessels syndrome referred to · inactive
- ORPHA:95426OBSOLETE: Chronic pain requiring intraspinal analgesia referred to · inactive
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/98006
- This record as JSON: /data/d/98006.json