Diphyllobothriasis
Synonyms: Bothriocephalosis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
Bothriocephalosis is a mammalian cosmopolitan intestinal parasitosis. In addition to non-specific digestive problems (nausea, abdominal pain, lack of appetite), bothriocephalosis provokes an anaemia caused by vitamin B12 deficiency that resembles Biermer anaemia (anaemia characterised by abnormally large red blood cells).
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Diphyllobothriasis | Bothriocephalosis |
| fr | Diphyllobothriose | Bothriocéphalose |
| de | Diphyllobothriasis | Bothriozephalosis |
| es | Difilobotriasis | Botriocefalosis |
| it | Difillobotriasi | Botriocefalosi |
| nl | Diphyllobothriasis | = en |
| pt | Botriocefalose | |
| pl | Difylobotrioza | = en |
| cs | Difylobotriáza | Botriocefalóza |
| uk | Дифілоботріоз | Ботріоцефальоз |
| zh | 裂头绦虫病 | 裂头绦虫病 |
| tr | Difilobotrtyaz | Bothriosefaloz |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | B70.0 | E | specific | validated |
| ICD-11 | 1F71 | E | specific | validated |
| MONDO | 0015260 | E | validated | |
| MeSH | D004169 | E | validated | |
| UMLS | C0012561 | E | validated | |
| GARD | 942 | E | validated | |
| MedDRA | 10013029 | 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
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | 1-9 / 1 000 000 | 0.88 / 100 000 | France | Value and class | Not yet validated | ORPHANET |
| Point prevalence | <1 / 1 000 000 | — | Europe | Class only | Not yet 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/128
- This record as JSON: /data/d/128.json