Echinococcosis

disease
On this page

Also known as echinococcal diseaseechinococcosis, unspecified, of liverEchinococcus caused disease or disorderEchinococcus disease or disorderEchinococcus infectious diseasehepatic echinococcosishydatid diseasehydatidosispulmonary echinococcosis

Summary

Echinococcosis (MONDO:0005738) is a disease and 7 clinical trials. A subtype of Cestode infectious disease — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 7

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameechinococcosis
Mondo IDMONDO:0005738
EFOEFO:0007245
MeSHD004443
DOIDDOID:1496
ICD-10-CMB67
ICD-111456802165
NCITC84682
SNOMED CT74942003
UMLSC0013502
MedGen4438
Is cancer (heuristic)no

Also known as: echinococcal disease · echinococcosis · echinococcosis, unspecified, of liver · Echinococcus caused disease or disorder · Echinococcus disease or disorder · Echinococcus infectious disease · hepatic echinococcosis · hydatid disease · hydatidosis · pulmonary echinococcosis

Disease family

An umbrella term covering 3 Mondo subtypes.

Classification path: disease › human disease › disease by etiologic mechanism › disease of primarily extrinsic mechanism › infectious diseaseparasitic infectious diseasehelminthiasis › Cestode infectious disease › echinococcosis

Related subtypes (4): mesocestoidiasis, taeniasis, sparganosis, diphyllobothriasis

Subtypes (3): polycystic echinococcosis, alveolar echinococcosis, echinococcus granulosus infectious disease

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 7.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified6
EARLY_PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT07551063EARLY_PHASE1NOT_YET_RECRUITING5G Remote Robotic Surgery for Hepatic Echinococcosis in High-Altitude Region
NCT05824442Not specifiedRECRUITINGEvaluation of a New Multiplex Quantitative PCR Technique for the Diagnosis of Echinococcosis
NCT03289884Not specifiedUNKNOWNMR Assessment of Hepatic Hydatid Disease
NCT04271176Not specifiedUNKNOWNJaundice as Initial Presentation of Liver Hydatidosis (ICTEHIDA)
NCT05986383Not specifiedUNKNOWNMulti-center Clinical Study on the Decision Tree of Precision Hepatectomy in China Precision Hepatectomy Decision Tree
NCT06289816Not specifiedCOMPLETEDSpleen Preserving Surgery for Splenic Hydatidosis: A Cohort Study on Short and Long-Term Outcomes
NCT06540742Not specifiedCOMPLETEDMultimodal Imaging Diagnosis and Decision Aid System for Hepatic Echinococcosis Based on Image Omics and Vision Macromodel

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.