ORPHA:102003
Rare movement 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 movement disorder | |
| fr | Anomalie rare du mouvement | |
| de | Bewegungsstörung, seltene | |
| es | Enfermedad motora rara | |
| it | Malattia motoria rara | |
| nl | Zeldzame bewegingsstoornis | |
| pt | Doença do movimento, rara | |
| pl | Rzadkie zaburzenie ruchu | |
| cs | Vzácné poruchy pohybu | |
| uk | Рідкісний руховий розлад | |
| zh | 罕见运动障碍 | |
| tr | Nadir hareket bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15143 | E | validated | |
| UMLS | C5681772 | E | validated | |
| GARD | 19817 | 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 (9):
- ORPHA:238722Familial congenital mirror movements
- ORPHA:306773Hyperekplexia
- ORPHA:306695Miscellaneous movement disorder due to neurodegenerative disease
- ORPHA:617440Painful legs and moving toes syndrome
- ORPHA:71519Psychogenic movement disorders
- ORPHA:494457Rare hyperkinetic movement disorder
- ORPHA:68402Rare parkinsonian disorder
- ORPHA:306768Rare paroxysmal movement disorder
- ORPHA:3198Stiff person spectrum disorder
Codes that Orphanet moved or referred to this one:
- ORPHA:1680OBSOLETE: Spastic diplegia, infantile type referred to · inactive
- ORPHA:98204OBSOLETE: Heredodegenerative disease with dystonia as a major feature 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/102003
- This record as JSON: /data/d/102003.json