Hymenolepiasis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
Hymenolepiasis is a cosmopolitan parasitosis caused by a hymenolepidid tapeworm infection, most commonly <i>Hymenolepis nana</i>, that is reported worldwide but particularly in tropical and subtropical countries and which is usually asymptomatic but in severe cases can also manifest with nausea, abdominal pain, anorexia, diarrhea and overall weakness.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Hymenolepiasis | |
| fr | Hyménolépiose | |
| de | Hymenolepiasis | |
| es | Himenolepiasis | |
| it | Imenolepiasi | |
| nl | Hymenolepiasis | Hymenolepiase |
| pt | Himenolepiose | |
| pl | Hymenolepioza | |
| cs | Hymenolepióza | |
| uk | Гіменолепіаз | |
| zh | 膜壳绦虫病 | |
| tr | Himenolepiyaz |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | B71.0 | E | specific | validated |
| ICD-11 | 1F74 | E | specific | validated |
| MONDO | 0005802 | E | validated | |
| MeSH | D006925 | E | validated | |
| UMLS | C0020413 | E | validated | |
| GARD | 2787 | E | validated | |
| MedDRA | 10020546 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:163588Rare parasitic disease
rare infectious diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/401
- This record as JSON: /data/d/401.json