Hydatidosis

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 43
OrphanetNr: 400
OMIM Id:
ICD-10: B67
UMLs: C0013502
MeSH: D004443
MedDRA: 10014096
Snomed: 74942003

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Not applicable
[Orphanet]
Age of onset: Adult
[Orphanet]

Disease classification (adopted from Orphanet):

Parent Diseases: Rare parasitic disease
 -Rare infectious disease

Symptom Information: Sort by abundance 

1
 (HPO:0000520) Proptosis Occasional [Orphanet] 192 / 7739
2
 (HPO:0000572) Visual loss Occasional [Orphanet] 272 / 7739
3
 (HPO:0002141) Gait imbalance Occasional [Orphanet] 55 / 7739
4
 (HPO:0006824) Cranial nerve paralysis Occasional [Orphanet] 81 / 7739
5
 (HPO:0001250) Seizures Occasional [Orphanet] 1245 / 7739
6
 (HPO:0004374) Hemiplegia/hemiparesis Occasional [Orphanet] 158 / 7739
7
 (HPO:0002516) Increased intracranial pressure Occasional [Orphanet] 47 / 7739
8
 (HPO:0002315) Headache Occasional [Orphanet] 175 / 7739
9
 (HPO:0003468) Abnormality of the vertebrae Occasional [Orphanet] 77 / 7739
10
 (HPO:0012062) Bone cyst Occasional [Orphanet] 19 / 7739
11
 (HPO:0002797) Osteolysis Occasional [Orphanet] 68 / 7739
12
 (HPO:0002017) Nausea and vomiting Very frequent [Orphanet] 134 / 7739
13
 (HPO:0001409) Portal hypertension Occasional [Orphanet] 39 / 7739
14
 (HPO:0012437) Abnormal gallbladder morphology Occasional [Orphanet] 17 / 7739
15
 (HPO:0001394) Cirrhosis Occasional [Orphanet] 102 / 7739
16
 (HPO:0001396) Cholestasis Very frequent [Orphanet] 136 / 7739
17
 (HPO:0001541) Ascites Occasional [Orphanet] 94 / 7739
18
 (HPO:0002240) Hepatomegaly Frequent [Orphanet] 467 / 7739
19
 (HPO:0002239) Gastrointestinal hemorrhage Occasional [Orphanet] 97 / 7739
20
 (HPO:0100575) Neoplasm of the gallbladder Frequent [Orphanet] 6 / 7739
21
 (HPO:0100626) Chronic hepatic failure Occasional [Orphanet] 7 / 7739
22
 (HPO:0006706) Cystic liver disease Very frequent [Orphanet] 8 / 7739
23
 (HPO:0100523) Liver abscess Occasional [Orphanet] 4 / 7739
24
 (HPO:0006554) Acute hepatic failure Occasional [Orphanet] 20 / 7739
25
 (HPO:0001744) Splenomegaly Occasional [Orphanet] 337 / 7739
26
 (HPO:0002027) Abdominal pain Very frequent [Orphanet] 184 / 7739
27
 (HPO:0002040) Esophageal varix Occasional [Orphanet] 23 / 7739
28
 (HPO:0001025) Urticaria Frequent [Orphanet] 73 / 7739
29
 (HPO:0000989) Pruritus Very frequent [Orphanet] 111 / 7739
30
 (HPO:0010783) Erythema Occasional [Orphanet] 138 / 7739
31
 (HPO:0000951) Abnormality of the skin Occasional [Orphanet] 147 / 7739
32
 (HPO:0002615) Hypotension Occasional [Orphanet] 52 / 7739
33
 (HPO:0001879) Abnormality of eosinophils Occasional [Orphanet] 20 / 7739
34
 (HPO:0001945) Fever Frequent [Orphanet] 218 / 7739
35
 (HPO:0002103) Abnormality of the pleura Occasional [Orphanet] 58 / 7739
36
 (HPO:0002105) Hemoptysis Occasional [Orphanet] 30 / 7739
37
 (HPO:0002093) Respiratory insufficiency Occasional [Orphanet] 410 / 7739
38
 (HPO:0100806) Sepsis Occasional [Orphanet] 48 / 7739
39
 (HPO:0100326) Immunologic hypersensitivity Occasional [Orphanet] 28 / 7739
40
 (HPO:0003011) Abnormality of the musculature Occasional [Orphanet] 47 / 7739
41
 ([DEL]MedDRA:10011224) Cough Occasional [Orphanet] 70 / 7739
42
 (HPO:0000238) Hydrocephalus Occasional [Orphanet] 278 / 7739
43
 (HPO:0001522) Death in infancy Occasional [Orphanet] 275 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: