raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:67

Amoebiasis due to Entamoeba histolytica

Type
Disease
Group
Disorder
Inheritance
Not applicable
Age of onset
All ages
Status
active

A parasitic disease caused by the protozoa, <i>Entamoeba histolytica</i>, mainly occurring in tropical regions after the ingestion of an amoebic cyst, and resulting in clinical manifestations that may range from an asymptomatic state to amoebic colitis (violent abdominal pain, a painful contracted feeling around the anal sphincter, blood and mucus in the stools but without the presence of fever), or amoebic liver abscesses (fever, chills, abdominal pain, weight loss, hepatomegaly) that can be fatal if not immediately treated. Extraintestinal involvement elsewhere (i.e. thoracic, hepatic) is extremely rare.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enAmoebiasis due to Entamoeba histolytica
frAmibiase à Entamoeba histolytica
deAmöbiasis durch Entamoeba histolytica
esAmebiasis por Entamoeba histolytica
itAmebiasi da Entamoeba histolytica
nlAmoebiase door Entamoeba histolyticaAmoebiasis door Entamoeba histolytica
ptAmebiose por Entamoeba histolytica
plPełzakowica wywołana Entamoeba histolytica
csAmébiáza způsobená Entamoeba histolytica
ukАмебіаз, спричинений Entamoeba histolytica
zh溶组织内阿米巴所致阿米巴病
trEntamoeba histolytica -ilişkili amipiyaz

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10A06.0BTNTspecificvalidated
ICD-10A06.1BTNTspecificvalidated
ICD-10A06.2BTNTspecificvalidated
ICD-10A06.3BTNTspecificvalidated
ICD-10A06.4BTNTspecificvalidated
ICD-10A06.5BTNTspecificvalidated
ICD-10A06.6BTNTspecificvalidated
ICD-10A06.7BTNTspecificvalidated
ICD-10A06.8BTNTspecificvalidated
ICD-10A06.9BTNTspecificvalidated
ICD-111A36Especificvalidated
ICD-111A36.0BTNTspecificvalidated
ICD-111A36.00BTNTspecificvalidated
ICD-111A36.01BTNTspecificvalidated
ICD-111A36.10BTNTspecificvalidated
MONDO0019028Evalidated
MeSHC531613Evalidated
UMLSC2930799Evalidated

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

1 record
TypeClassValueAreaQualificationValidationSource
Point prevalenceUnknown—WorldwideClass onlyNot yet validatedORPHANET

Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.

6

HPO phenotypes

27 annotations · validated 2020-04-09
HPOTerm (as annotated by Orphanet)Diagnostic
Occasional (29-5%)
HP:0002027Abdominal pain
HP:0025085Bloody diarrhea
HP:0100749Chest pain
HP:0002014Diarrhea
HP:0002579Gastrointestinal dysmotility
HP:0004385Protracted diarrhea
HP:0001824Weight loss
Very rare (<4-1%)
HP:0001697Abnormal pericardium morphology
HP:0032016Abnormal sputum
HP:0100282Acute colitis
HP:0001903Anemia
HP:0001635Congestive heart failure
HP:0002563Constrictive pericarditis
HP:0012735Cough
HP:0002625Deep venous thrombosis
HP:0002094Dyspnea
HP:0003155Elevated circulating alkaline phosphatase concentration
HP:0002910Elevated circulating hepatic transaminase concentration
HP:0001945Fever
HP:0002105Hemoptysis
HP:0003073Hypoalbuminemia
HP:0001974Increased total leukocyte count
HP:0005214Intestinal obstruction
HP:0100523Liver abscess
HP:0025044Lung abscess
HP:0002202Pleural effusion
HP:0011919Pleural empyema

Annotation source: 30631758[PMID]_30255429[PMID]_25101557[PMID]_9504344[PMID]

7

Sources for this card