raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:658909

Fasciolopsiasis

Type
Disease
Group
Disorder
Inheritance
Not applicable
Status
active

A rare parasitic disease characterized by infection with the intestinal parasitic flatworm <i>Fasciolopsis buski</i> by ingestion of metacercariae via undercooked contaminated aquatic plants or contaminated water. Adult worms are the largest flukes infecting humans and attach to and ulcerate the mucosa of the proximal small bowel. Patients may be asymptomatic or present abdominal pain, vomiting, diarrhea, and signs of malabsorption, potentially also intestinal obstruction, 30 to 60&nbsp;days after exposure. Peripheral eosinophilia may be observed. Severe malabsorption may lead to edema and ascites due to protein loss.

1

Names in Orphadata languages

10 of 12 languages
LangNameSynonyms
enFasciolopsiasis
frFasciolopsiose
deFasciolopsiasisDarmegelkrankheit · Fasziolopsiasis
esFasciolopsiasis
itFasciolopsiasi
nlFasciolopsiasisInfectie door Fasciolopsis buski
ptFasciolopsíase
plFasciolopsoza
csFasciolopsióza
ukФасціолопсис

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10B66.5Especificvalidated
ICD-111F83Especificvalidated
MONDO0004672Evalidated
MONDO4672Evalidated
UMLSC0015656Evalidated
MedDRA10016235Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card