ORPHA:770
Rabies
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
Rabies is a viral zoonosis leading to a fatal encephalopathy if not treated.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rabies | |
| fr | Rage | |
| de | Tollwut | Rabies |
| es | Rabia | |
| it | Rabbia | |
| nl | Rabiës | Hondsdolheid |
| pt | Raiva | |
| pl | Wścieklizna | |
| cs | Vzteklina | Rabies · Lyssa |
| uk | Сказ | |
| zh | 狂犬病 | |
| tr | Kuduz |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | A82.0 | BTNT | specific | validated |
| ICD-10 | A82.1 | BTNT | specific | validated |
| ICD-10 | A82.9 | BTNT | specific | validated |
| ICD-11 | 1C82 | E | specific | validated |
| MONDO | 0019173 | E | validated | |
| MeSH | D011818 | E | validated | |
| UMLS | C0034494 | E | validated | |
| GARD | 7516 | E | validated | |
| MedDRA | 10037742 | 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:98010Infectious disease of the nervous system
rare neurological diseases - ORPHA:163585Rare viral disease
rare infectious diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
3 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | 1-9 / 1 000 000 | — | Europe | Class only | Validated | [EXPERT] |
| Point prevalence | <1 / 1 000 000 | — | United States | Class only | Not yet validated | 22699971[PMID] |
| Annual incidence | <1 / 1 000 000 | — | Europe | Class only | Validated | European Centre for Disease prevention and Control 2017[OTHER] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
6
HPO phenotypes
19 annotations · validated 2016-06-01| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0002039 | Anorexia | |
| HP:0000739 | Anxiety | |
| HP:0007018 | Attention deficit hyperactivity disorder | |
| HP:0000708 | Atypical behavior | |
| HP:0000716 | Depression | |
| HP:0002014 | Diarrhea | |
| HP:0003781 | Excessive salivation | |
| HP:0001945 | Fever | |
| HP:0000738 | Hallucinations | |
| HP:0100785 | Insomnia | |
| HP:0002076 | Migraine | |
| HP:0002017 | Nausea and vomiting | |
| HP:0003401 | Paresthesia | |
| HP:0100776 | Recurrent pharyngitis | |
| HP:0001604 | Vocal cord paresis | |
| Frequent (79-30%) | ||
| HP:0100021 | Cerebral palsy | |
| Occasional (29-5%) | ||
| HP:0004372 | Reduced consciousness | |
| HP:0001250 | Seizure | |
| HP:0001645 | Sudden cardiac death | |
Run the differential on the 12 obligate / very frequent terms
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/770
- This record as JSON: /data/d/770.json