Alveolar echinococcosis
General Information (adopted from Orphanet):
Synonyms, Signs: |
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Number of Symptoms | 44 |
OrphanetNr: | 284 |
OMIM Id: |
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ICD-10: |
B67.5 B67.6 B67.7 |
UMLs: |
C0948954 |
MeSH: |
C536591 |
MedDRA: |
10053042 |
Snomed: |
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Prevalence, inheritance and age of onset:
Prevalence: | < 1,000 cases [Orphanet] |
Inheritance: |
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Age of onset: |
Adult Elderly [Orphanet] |
Disease classification (adopted from Orphanet):
Parent Diseases: |
Rare parasitic disease
-Rare infectious disease |
Symptom Information:
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(HPO:0000137) | Abnormality of the ovary | Occasional [Orphanet] | 41 / 7739 | |||
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(HPO:0000572) | Visual loss | Occasional [Orphanet] | 272 / 7739 | |||
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(HPO:0002066) | Gait ataxia | Occasional [Orphanet] | 327 / 7739 | |||
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(HPO:0006824) | Cranial nerve paralysis | Occasional [Orphanet] | 81 / 7739 | |||
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(HPO:0000763) | Sensory neuropathy | Occasional [Orphanet] | 78 / 7739 | |||
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(HPO:0001250) | Seizures | Occasional [Orphanet] | 1245 / 7739 | |||
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(HPO:0004374) | Hemiplegia/hemiparesis | Occasional [Orphanet] | 158 / 7739 | |||
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(HPO:0002315) | Headache | Occasional [Orphanet] | 175 / 7739 | |||
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(HPO:0002167) | Neurological speech impairment | Occasional [Orphanet] | 308 / 7739 | |||
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(HPO:0100835) | Benign neoplasm of the central nervous system | Occasional [Orphanet] | 12 / 7739 | |||
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(HPO:0002516) | Increased intracranial pressure | Occasional [Orphanet] | 47 / 7739 | |||
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(HPO:0100749) | Chest pain | Occasional [Orphanet] | 92 / 7739 | |||
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(HPO:0002797) | Osteolysis | Occasional [Orphanet] | 68 / 7739 | |||
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(HPO:0003468) | Abnormality of the vertebrae | Occasional [Orphanet] | 77 / 7739 | |||
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(HPO:0012062) | Bone cyst | Occasional [Orphanet] | 19 / 7739 | |||
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(HPO:0002040) | Esophageal varix | Occasional [Orphanet] | 23 / 7739 | |||
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(HPO:0001396) | Cholestasis | Very frequent [Orphanet] | 136 / 7739 | |||
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(HPO:0002027) | Abdominal pain | Very frequent [Orphanet] | 184 / 7739 | |||
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(HPO:0001409) | Portal hypertension | Occasional [Orphanet] | 39 / 7739 | |||
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(HPO:0002240) | Hepatomegaly | Frequent [Orphanet] | 467 / 7739 | |||
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(HPO:0006706) | Cystic liver disease | Very frequent [Orphanet] | 8 / 7739 | |||
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(HPO:0012437) | Abnormal gallbladder morphology | Occasional [Orphanet] | 17 / 7739 | |||
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(HPO:0100592) | Peritoneal abscess | Occasional [Orphanet] | 10 / 7739 | |||
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(HPO:0001744) | Splenomegaly | Occasional [Orphanet] | 337 / 7739 | |||
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(HPO:0001541) | Ascites | Occasional [Orphanet] | 94 / 7739 | |||
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(HPO:0002239) | Gastrointestinal hemorrhage | Occasional [Orphanet] | 97 / 7739 | |||
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(HPO:0002017) | Nausea and vomiting | Very frequent [Orphanet] | 134 / 7739 | |||
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(HPO:0100626) | Chronic hepatic failure | Occasional [Orphanet] | 7 / 7739 | |||
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(HPO:0001394) | Cirrhosis | Occasional [Orphanet] | 102 / 7739 | |||
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(HPO:0005242) | Extrahepatic biliary duct atresia | Frequent [Orphanet] | 9 / 7739 | |||
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(HPO:0004325) | Decreased body weight | Frequent [Orphanet] | 492 / 7739 | |||
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(HPO:0000989) | Pruritus | Very frequent [Orphanet] | 111 / 7739 | |||
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(HPO:0000951) | Abnormality of the skin | Occasional [Orphanet] | 147 / 7739 | |||
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(HPO:0002140) | Ischemic stroke | Occasional [Orphanet] | 70 / 7739 | |||
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(HPO:0001903) | Anemia | Frequent [Orphanet] | 289 / 7739 | |||
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(HPO:0001945) | Fever | Frequent [Orphanet] | 218 / 7739 | |||
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(HPO:0002093) | Respiratory insufficiency | Occasional [Orphanet] | 410 / 7739 | |||
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(HPO:0002113) | Pulmonary infiltrates | Occasional [Orphanet] | 36 / 7739 | |||
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(HPO:0002105) | Hemoptysis | Occasional [Orphanet] | 30 / 7739 | |||
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(HPO:0100326) | Immunologic hypersensitivity | Occasional [Orphanet] | 28 / 7739 | |||
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(HPO:0100806) | Sepsis | Occasional [Orphanet] | 48 / 7739 | |||
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(HPO:0003011) | Abnormality of the musculature | Occasional [Orphanet] | 47 / 7739 | |||
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([DEL]MedDRA:10011224) | Cough | Occasional [Orphanet] | 70 / 7739 | |||
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(HPO:0001522) | Death in infancy | Occasional [Orphanet] | 275 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
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