Scrub typhus

General Information (adopted from Orphanet):

Synonyms, Signs: Tsutsugamushi disease
Tsutsugamushi fever
Number of Symptoms 28
OrphanetNr: 83317
OMIM Id:
ICD-10: A75.3
UMLs: C0036472
MeSH: D012612
MedDRA: 10039766
Snomed: 271425001

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset: All ages
[Orphanet]

Disease classification (adopted from Orphanet):

Parent Diseases: Rare bacterial infectious disease
 -Rare infectious disease

Symptom Information: Sort by abundance 

1
 (HPO:0000083) Renal insufficiency Occasional [Orphanet] 232 / 7739
2
 (HPO:0001357) Plagiocephaly Very frequent [Orphanet] 106 / 7739
3
 (HPO:0000613) Photophobia Frequent [Orphanet] 158 / 7739
4
 (HPO:0100533) Inflammatory abnormality of the eye Frequent [Orphanet] 70 / 7739
5
 (HPO:0000708) Behavioral abnormality Occasional [Orphanet] 212 / 7739
6
 (HPO:0002315) Headache Frequent [Orphanet] 175 / 7739
7
 (HPO:0001287) Meningitis Occasional [Orphanet] 46 / 7739
8
 (HPO:0001337) Tremor Occasional [Orphanet] 200 / 7739
9
 (HPO:0004372) Reduced consciousness/confusion Very frequent [Orphanet] 73 / 7739
10
 (HPO:0002383) Encephalitis Occasional [Orphanet] 41 / 7739
11
 (HPO:0001250) Seizures Occasional [Orphanet] 1245 / 7739
12
 (HPO:0002027) Abdominal pain Frequent [Orphanet] 184 / 7739
13
 (HPO:0002017) Nausea and vomiting Frequent [Orphanet] 134 / 7739
14
 (HPO:0001744) Splenomegaly Frequent [Orphanet] 337 / 7739
15
 (HPO:0000988) Skin rash Very frequent [Orphanet] 98 / 7739
16
 (HPO:0200042) Skin ulcer Very frequent [Orphanet] 138 / 7739
17
 (HPO:0002615) Hypotension Frequent [Orphanet] 52 / 7739
18
 (HPO:0001637) Abnormality of the myocardium Occasional [Orphanet] 76 / 7739
19
 (HPO:0003010) Prolonged bleeding time Occasional [Orphanet] 88 / 7739
20
 (HPO:0100758) Gangrene Frequent [Orphanet] 25 / 7739
21
 (HPO:0001945) Fever Very frequent [Orphanet] 218 / 7739
22
 (HPO:0002093) Respiratory insufficiency Occasional [Orphanet] 410 / 7739
23
 (HPO:0002091) Restrictive ventilatory defect Occasional [Orphanet] 46 / 7739
24
 (HPO:0002716) Lymphadenopathy Frequent [Orphanet] 129 / 7739
25
 (HPO:0003326) Myalgia Very frequent [Orphanet] 143 / 7739
26
 (MedDRA:10025421) Macule Frequent [Orphanet] 55 / 7739
27
 ([DEL]MedDRA:10011224) Cough Very frequent [Orphanet] 70 / 7739
28
 (HPO:0001522) Death in infancy Occasional [Orphanet] 275 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: