Mycoplasma encephalitis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
Mycoplasma encephalitis is a rare infectious encephalitis characterized by an acute onset of neurological signs and symptoms (e.g. altered consciousness, seizures, headaches, meningeal signs, behavioral changes) due to bacterial infection by <i>Mycoplasma pneumoniae</i>. Patients typically present unspecific signs and symptoms, such as fever, nausea, vomiting, fatigue, prior to onset of neurological manifestations and frequently have a history of a respiratory tract infection (e.g. pneumonia, bronchiolitis, pharyngitis).
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Mycoplasma encephalitis | |
| fr | Encéphalite à mycoplasmes | |
| de | Mykoplasmen-Enzephalitis | |
| es | Encefalitis causada por Mycoplasma | |
| it | Encefalite da micoplasma | |
| nl | Mycoplasma-encefalitis | |
| pt | Encefalite por micoplasma | |
| pl | Mykoplazmowe zapalenie mózgu | |
| cs | Mykoplazmová encefalitida | |
| uk | Мікоплазмовий енцефаліт | |
| zh | 支原体脑炎 | |
| tr | Mikoplazma ensefaliti |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | B96.0 | NTBT | attributed | validated |
| ICD-11 | 1D00.0 | NTBT | attributed | validated |
| MONDO | 0019377 | E | validated | |
| UMLS | C4707240 | 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 (2):
- ORPHA:166490Infectious disease with epilepsy
rare neurological diseases - ORPHA:98252Infectious encephalitis
rare neurological diseases; rare infectious diseases
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 | Not yet 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/83482
- This record as JSON: /data/d/83482.json