Rift valley fever

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 30
OrphanetNr: 319251
OMIM Id:
ICD-10: A92.4
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: Viral hemorrhagic fever
 -Rare infectious disease

Symptom Information: Sort by abundance 

1
 (HPO:0011037) Decreased urine output Occasional [Orphanet] 47 / 7739
2
 (HPO:0008046) Abnormality of the retinal vasculature Occasional [Orphanet] 41 / 7739
3
 (HPO:0000488) Retinopathy Occasional [Orphanet] 75 / 7739
4
 (HPO:0000613) Photophobia Frequent [Orphanet] 158 / 7739
5
 (HPO:0000572) Visual loss Occasional [Orphanet] 272 / 7739
6
 (HPO:0001123) Visual field defect Occasional [Orphanet] 30 / 7739
7
 (HPO:0012375) Chemosis Frequent [Orphanet] 7 / 7739
8
 (HPO:0002315) Headache Frequent [Orphanet] 175 / 7739
9
 (HPO:0001250) Seizures Occasional [Orphanet] 1245 / 7739
10
 (HPO:0000738) Hallucinations Frequent [Orphanet] 60 / 7739
11
 (HPO:0002141) Gait imbalance Frequent [Orphanet] 55 / 7739
12
 (HPO:0001287) Meningitis Occasional [Orphanet] 46 / 7739
13
 (HPO:0004372) Reduced consciousness/confusion Occasional [Orphanet] 73 / 7739
14
 (HPO:0002383) Encephalitis Occasional [Orphanet] 41 / 7739
15
 (HPO:0005059) Arthralgia/arthritis Frequent [Orphanet] 141 / 7739
16
 (HPO:0001387) Joint stiffness Frequent [Orphanet] 322 / 7739
17
 (HPO:0001399) Hepatic failure Occasional [Orphanet] 80 / 7739
18
 (HPO:0002014) Diarrhea Frequent [Orphanet] 225 / 7739
19
 (HPO:0002239) Gastrointestinal hemorrhage Occasional [Orphanet] 97 / 7739
20
 (HPO:0002017) Nausea and vomiting Frequent [Orphanet] 134 / 7739
21
 (HPO:0002039) Anorexia Occasional [Orphanet] 62 / 7739
22
 (HPO:0001396) Cholestasis Occasional [Orphanet] 136 / 7739
23
 (HPO:0004325) Decreased body weight Occasional [Orphanet] 492 / 7739
24
 (HPO:0000978) Bruising susceptibility Occasional [Orphanet] 123 / 7739
25
 (HPO:0001933) Subcutaneous hemorrhage Occasional [Orphanet] 50 / 7739
26
 (HPO:0001695) Cardiac arrest Occasional [Orphanet] 87 / 7739
27
 (HPO:0001945) Fever Very frequent [Orphanet] 218 / 7739
28
 (HPO:0001324) Muscle weakness Very frequent [Orphanet] 859 / 7739
29
 (HPO:0003326) Myalgia Frequent [Orphanet] 143 / 7739
30
 (HPO:0001522) Death in infancy Occasional [Orphanet] 275 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: