Juvenile myasthenia gravis
Synonyms: Childhood myasthenia gravis · Juvenile acquired myasthenia · Juvenile autoimmune myasthenia gravis
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Age of onset
- Adolescent, Childhood, Infancy, Neonatal
- Status
- active
Juvenile myasthenia gravis (MG) is a rare form of MG, an autoimmune disorder of the neuromuscular junction resulting in ocular manifestations or generalized weakness, with onset before 18 years of age.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Juvenile myasthenia gravis | Childhood myasthenia gravis · Juvenile acquired myasthenia · Juvenile autoimmune myasthenia gravis |
| fr | Myasthénie auto-immune juvénile | Myasthenia gravis juvénile · Myasthénie acquise juvénile |
| de | Juvenile Myasthenia gravis | Juvenile autoimmune Myasthenia gravis · Myasthenia gravis der Kindheit · Myasthenie, erworbene, juvenile Form |
| es | Miastenia grave juvenil | Miastenia grave autoinmune juvenil · Miastenia grave infantil · Miastenia juvenil adquirida |
| it | Miastenia gravis giovanile | Miastenia acquisita giovanile · Miastenia grave autoimmune giovanile · Miastenia gravis dell'infanzia |
| nl | Juveniele myasthenia gravis | Myasthenia gravis van de kindertijd · Juveniele auto-immune myasthenia gravis · Juveniele verworven myasthenie |
| pt | Miastenia gravis juvenil | |
| pl | Miastenia młodzieńcza | Autoimmunologiczna miastenia młodzieńcza · Miastenia dziecięca · Nabyta miastenia młodzieńcza |
| cs | Juvenilní myasthenia gravis | Juvenilní získaná myastenie · Juvenilní autoimunitní myasthenia gravis · Myastenia gravis dětského věku |
| uk | Ювенільна miastenia gravis | Дитяча міастенія · Ювенільна набута міастенія · Ювенільна аутоімунна міастенія |
| zh | 青少年起病重症肌无力 | 青少年起病自身免疫性重症肌无力 |
| tr | Jüvenil myastenia gravis | Çocukluk çağı myastenia gravis · Jüvenil edinsel myastenia · Jüvenil otoimmün myastenia gravis |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G70.0 | NTBT | attributed | validated |
| ICD-11 | 8C60 | NTBT | attributed | validated |
| MONDO | 0018325 | E | validated | |
| UMLS | C5680023 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:589Myasthenia gravis
rare neurological diseases; rare ophthalmic disorders
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/391497
- This record as JSON: /data/d/391497.json