ORPHA:71859
Rare genetic neurological disorder
- 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 genetic neurological disorder | |
| fr | Maladie neurologique génétique rare | |
| de | Neurologische Krankheit, genetisch bedingte | |
| es | Enfermedades neurológicas genéticas raras | |
| it | Malattia neurologica genetica | |
| nl | Zeldzame genetische neurologische ziekte | |
| pt | Doença neurológica genética | |
| pl | Rzadka neurologiczna choroba genetyczna | |
| cs | Vzácné genetické neurologické poruchy | |
| uk | Рідкісне генетично обумовлене неврологічне захворювання | |
| zh | 罕见基因神经系统疾病 | |
| tr | Nadir genetik nörolojik bozukluk |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 19117 | E | validated | |
| UMLS | C5681307 | 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:98053Rare genetic disease
rare genetic diseases
Children (27):
- ORPHA:209978Alternating hemiplegia
- ORPHA:164736Familial advanced sleep-phase syndrome
- ORPHA:2047Flynn-Aird syndrome
- ORPHA:183503Genetic central nervous system and retinal vascular disease
- ORPHA:183506Genetic central nervous system malformation
- ORPHA:158124Genetic dementia
- ORPHA:183500Genetic neurodegenerative disease
- ORPHA:98743Genetic neurological channelopathy of the central nervous system
- ORPHA:183497Genetic neuromuscular disease
- ORPHA:98497Genetic peripheral neuropathy
- ORPHA:521232Genetic primary orthostatic disorder
- ORPHA:183518Hereditary ataxia
- ORPHA:210141Inherited congenital spastic tetraplegia
- ORPHA:178506Interstitial lung disease-brain calcification syndrome
- ORPHA:209908Isolated childhood apraxia of speech
- ORPHA:68356Leukodystrophy
- ORPHA:68385Neurometabolic disease
- ORPHA:46348Paroxysmal extreme pain disorder
- ORPHA:730693Rare complex neurodevelopmental disorder without intellectual disability or autism spectrum disorder
- ORPHA:434786Rare genetic autonomic nervous system disorder
- ORPHA:183512Rare genetic epilepsy
- ORPHA:183509Rare genetic headache
- ORPHA:183757Rare genetic intellectual disability
- ORPHA:183515Rare genetic medullar disease
- ORPHA:183521Rare genetic movement disorder
- ORPHA:168778Rare pervasive developmental disorder
- ORPHA:603699Recessive KLHL7-related disorder
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/71859
- This record as JSON: /data/d/71859.json