Babesiosis

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 31
OrphanetNr: 108
OMIM Id:
ICD-10: B60.0
UMLs: C0004576
MeSH: D001404
MedDRA: 10003965
Snomed: 21061004

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: Rare parasitic disease
 -Rare infectious disease

Symptom Information: Sort by abundance 

1
 (HPO:0000083) Renal insufficiency Occasional [Orphanet] 232 / 7739
2
 (HPO:0100776) Recurrent pharyngitis Occasional [Orphanet] 18 / 7739
3
 (HPO:0001357) Plagiocephaly Frequent [Orphanet] 106 / 7739
4
 (HPO:0000613) Photophobia Occasional [Orphanet] 158 / 7739
5
 (HPO:0100851) Abnormal emotion/affect behavior Occasional [Orphanet] 85 / 7739
6
 (HPO:0002315) Headache Very frequent [Orphanet] 175 / 7739
7
 (HPO:0004372) Reduced consciousness/confusion Occasional [Orphanet] 73 / 7739
8
 (HPO:0005059) Arthralgia/arthritis Frequent [Orphanet] 141 / 7739
9
 (HPO:0001387) Joint stiffness Occasional [Orphanet] 322 / 7739
10
 (HPO:0001396) Cholestasis Frequent [Orphanet] 136 / 7739
11
 (HPO:0002017) Nausea and vomiting Occasional [Orphanet] 134 / 7739
12
 (HPO:0001744) Splenomegaly Frequent [Orphanet] 337 / 7739
13
 (HPO:0001399) Hepatic failure Occasional [Orphanet] 80 / 7739
14
 (HPO:0002240) Hepatomegaly Frequent [Orphanet] 467 / 7739
15
 (HPO:0002039) Anorexia Occasional [Orphanet] 62 / 7739
16
 (HPO:0004325) Decreased body weight Occasional [Orphanet] 492 / 7739
17
 (HPO:0001677) Coronary artery disease Occasional [Orphanet] 58 / 7739
18
 (HPO:0001635) Congestive heart failure Occasional [Orphanet] 232 / 7739
19
 (HPO:0004936) Venous thrombosis Occasional [Orphanet] 41 / 7739
20
 (HPO:0003010) Prolonged bleeding time Occasional [Orphanet] 88 / 7739
21
 (HPO:0001873) Thrombocytopenia Frequent [Orphanet] 224 / 7739
22
 (HPO:0100724) Hypercoagulability Occasional [Orphanet] 15 / 7739
23
 (HPO:0001878) Hemolytic anemia Very frequent [Orphanet] 83 / 7739
24
 (HPO:0001882) Leukopenia Frequent [Orphanet] 51 / 7739
25
 (HPO:0001945) Fever Very frequent [Orphanet] 218 / 7739
26
 (HPO:0002093) Respiratory insufficiency Occasional [Orphanet] 410 / 7739
27
 (HPO:0010978) Abnormality of immune system physiology Frequent [Orphanet] 148 / 7739
28
 (HPO:0001324) Muscle weakness Frequent [Orphanet] 859 / 7739
29
 (HPO:0003326) Myalgia Frequent [Orphanet] 143 / 7739
30
 (HPO:0001522) Death in infancy Occasional [Orphanet] 275 / 7739
31
 ([DEL]MedDRA:10011224) Cough Frequent [Orphanet] 70 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: