ORPHA:97349
Postencephalitic parkinsonism
- Type
- Disease
- Group
- Disorder
- Age of onset
- Adult, Elderly
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Postencephalitic parkinsonism | |
| fr | Parkinsonisme postencéphalitique | |
| de | Postenzephalitisches Parkinson-Syndrom | |
| es | Parkinsonismo postencefálico | |
| it | Parkinsonismo post-encefalitico | |
| nl | Postencefalitisch parkinsonisme | |
| pt | Parkinsonismo pós-encefalite | |
| pl | Parkinsonizm pozapalny | |
| cs | Postencefalitický parkinsonismus | |
| uk | Постенцефалічний паркінсонізм | |
| zh | 脑炎后帕金森症 | |
| tr | Postensefalitik parkinsonizm |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G21.3 | E | specific | validated |
| ICD-11 | 8A00.22 | NTBT | index | validated |
| MONDO | 0001945 | E | validated | |
| MeSH | D010301 | E | validated | |
| UMLS | C0030568 | E | validated | |
| GARD | 19370 | 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 (2):
- ORPHA:98542Infectious disease with dementia
rare neurological diseases - ORPHA:306666Rare parkinsonian syndrome due to neurodegenerative disease
rare neurological diseases
No children.
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
41 annotations · validated 2018-03-23| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0002322 | Resting tremor | |
| Frequent (79-30%) | ||
| HP:0007256 | Abnormal pyramidal sign | |
| HP:0003487 | Babinski sign | |
| HP:0002067 | Bradykinesia | |
| HP:0002396 | Cogwheel rigidity | |
| HP:0002329 | Drowsiness | |
| HP:0001945 | Fever | |
| HP:0003324 | Generalized muscle weakness | |
| HP:0004305 | Involuntary movements | |
| HP:0010553 | Oculogyric crisis | |
| HP:0002465 | Poor speech | |
| Occasional (29-5%) | ||
| HP:0025456 | Abnormal CSF protein level | |
| HP:0002795 | Abnormal respiratory system physiology | |
| HP:0000496 | Abnormality of eye movement | |
| HP:0011446 | Abnormality of higher mental function | |
| HP:0045007 | Abnormality of the substantia nigra | |
| HP:0000718 | Aggressive behavior | |
| HP:0002304 | Akinesia | |
| HP:0002381 | Aphasia | |
| HP:0008765 | Auditory hallucinations | |
| HP:0001488 | Bilateral ptosis | |
| HP:0200149 | CSF lymphocytic pleiocytosis | |
| HP:0100595 | Camptocormia | |
| HP:0012735 | Cough | |
| HP:0000716 | Depression | |
| HP:0002374 | Diminished movement | |
| HP:0001260 | Dysarthria | |
| HP:0002015 | Dysphagia | |
| HP:0005329 | Fixed facial expression | |
| HP:0040082 | Happy demeanor | |
| HP:0002315 | Headache | |
| HP:0006801 | Hyperactive deep tendon reflexes | |
| HP:0002808 | Kyphosis | |
| HP:0000194 | Open mouth | |
| HP:0003401 | Paresthesia | |
| HP:0002063 | Rigidity | |
| HP:0001250 | Seizure | |
| HP:0000514 | Slow saccadic eye movements | |
| HP:0030188 | Tremor by anatomical site | |
| HP:0025331 | Upgaze palsy | |
| HP:0002013 | Vomiting | |
Run the differential on the 1 obligate / very frequent terms
Annotation source: 7299406[PMID]
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/97349
- This record as JSON: /data/d/97349.json