ORPHA:139423
Idiopathic acute transverse myelitis
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
A rare immune-mediated inflammatory demyelinating disorder of the spinal cord with motor, sensory and autonomic involvement.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Idiopathic acute transverse myelitis | |
| fr | Myélite transverse aiguë idiopathique | |
| de | Myelitis, akute transverse, idiopathische | |
| es | Mielitis transversa aguda idiopática | |
| it | Mielite trasversa acuta idiopatica | |
| nl | Idiopathische acute transversale myelitis | |
| pt | Mielite transversa aguda idiopática | |
| pl | Idiopatyczne ostre poprzeczne zapalenie rdzenia | ATM/TM |
| cs | Idiopatická akutní transverzální myelitida | ATM/TM |
| uk | Ідіопатичний гострий поперечний мієліт | |
| zh | 特发性急性横贯性脊髓炎 | 急性横贯性脊髓炎/横贯性脊髓炎 |
| tr | İdiyopatik akut transvers miyelit | ATM/TM |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G37.3 | NTBT | attributed | validated |
| ICD-11 | 8A41.0 | NTBT | attributed | validated |
| MONDO | 0015344 | E | validated | |
| UMLS | C1719404 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:139417Acute transverse myelitis
rare neurological diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | 1-9 / 1 000 000 | 0.25 / 100 000 | Europe | Value and class | Validated | [EXPERT] |
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | [EXPERT] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/139423
- This record as JSON: /data/d/139423.json