Rabies
General Information (adopted from Orphanet):
Synonyms, Signs: |
|
Number of Symptoms | 19 |
OrphanetNr: | 770 |
OMIM Id: |
|
ICD-10: |
A82 |
UMLs: |
C0034494 |
MeSH: |
D011818 |
MedDRA: |
10037742 |
Snomed: |
14168008 |
Prevalence, inheritance and age of onset:
Prevalence: | No data available. |
Inheritance: |
Not applicable [Orphanet] |
Age of onset: |
All ages [Orphanet] |
Disease classification (adopted from Orphanet):
Parent Diseases: |
Infectious disease of the nervous system
-Rare neurologic disease Rare viral disease -Rare infectious disease |
Symptom Information:
|
(HPO:0003781) | Excessive salivation | Very frequent [Orphanet] | 15 / 7739 | |||
|
(HPO:0100776) | Recurrent pharyngitis | Very frequent [Orphanet] | 18 / 7739 | |||
|
(HPO:0000738) | Hallucinations | Very frequent [Orphanet] | 60 / 7739 | |||
|
(HPO:0000708) | Behavioral abnormality | Very frequent [Orphanet] | 212 / 7739 | |||
|
(HPO:0100851) | Abnormal emotion/affect behavior | Very frequent [Orphanet] | 85 / 7739 | |||
|
(HPO:0000763) | Sensory neuropathy | Very frequent [Orphanet] | 78 / 7739 | |||
|
(HPO:0002315) | Headache | Very frequent [Orphanet] | 175 / 7739 | |||
|
(HPO:0001250) | Seizures | Occasional [Orphanet] | 1245 / 7739 | |||
|
(HPO:0100785) | Insomnia | Very frequent [Orphanet] | 18 / 7739 | |||
|
(HPO:0011442) | Abnormality of central motor function | Frequent [Orphanet] | 76 / 7739 | |||
|
(HPO:0100021) | Cerebral palsy | Frequent [Orphanet] | 36 / 7739 | |||
|
(HPO:0000752) | Hyperactivity | Very frequent [Orphanet] | 140 / 7739 | |||
|
(HPO:0004372) | Reduced consciousness/confusion | Occasional [Orphanet] | 73 / 7739 | |||
|
(HPO:0002039) | Anorexia | Very frequent [Orphanet] | 62 / 7739 | |||
|
(HPO:0002014) | Diarrhea | Very frequent [Orphanet] | 225 / 7739 | |||
|
(HPO:0002017) | Nausea and vomiting | Very frequent [Orphanet] | 134 / 7739 | |||
|
(HPO:0001695) | Cardiac arrest | Occasional [Orphanet] | 87 / 7739 | |||
|
(HPO:0001945) | Fever | Very frequent [Orphanet] | 218 / 7739 | |||
|
(HPO:0001600) | Abnormality of the larynx | Very frequent [Orphanet] | 15 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
---|