Unspecified juvenile idiopathic arthritis
Synonyms: Unspecified JIA
- Type
- Disease
- Group
- Disorder
- Age of onset
- Childhood, Infancy
- Status
- active
Unspecified juvenile idiopathic arthritis is a rare, pediatric, rheumatologic disease, a subtype of juvenile idiopathic arthritis (JIA) characterized by arthritis of an unknown cause that persists for at least 6 weeks, and does not fulfill the criteria for any of the other JIA subtypes, or fulfills criteria for more than one of the other subtypes.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Unspecified juvenile idiopathic arthritis | Unspecified JIA |
| fr | Arthrite juvénile idiopathique indéterminée | AJI indéterminée |
| de | Arthritis, idiopathische juvenile, unklassifizierte | Undifferenzierte JIA |
| es | Artritis idiopática juvenil no específica | AIJ no específica |
| it | Artrite idiopatica giovanile aspecifica | |
| nl | Niet-gespecificeerde juveniele idiopathische artritis | Niet-gespecificeerde JIA |
| pt | Artrite idiopática juvenil, não-classificada | |
| pl | Niespecyficzne młodzieńcze idiopatyczne zapalenie stawów | Niespecyficzne JIA |
| cs | Neklasifikovaná juvenilní idiopatická artritida | = en |
| uk | Неуточнений ювенільний ідіопатичний артрит | Невизначений JIA |
| zh | 不明青少年特发性关节炎 | 不明青少年特发性关节炎 |
| tr | Tanımlanmamış juvenil idiyopatik artrit | Tanımlanmamış JIA |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | M08.8 | NTBT | attributed | validated |
| ICD-11 | FA24.Y | NTBT | attributed | validated |
| MONDO | 0019607 | E | validated | |
| UMLS | C5680196 | 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:92Juvenile idiopathic arthritis
rare respiratory diseases; rare systemic and rheumatological diseases; rare systemic or rheumatologic diseases of childhood; rare transplant-related 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/91140
- This record as JSON: /data/d/91140.json