Paracoccidioidomycosis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
A rare mycosis characterized by an acute form mostly occurring in children and young adults presenting with fever, weight loss, lymph node enlargement, hepatosplenomegaly, and bone marrow dysfunction, versus a chronic form which usually involves the lungs and mucosae of the upper respiratory tract, skin, lymph nodes, and adrenal glands, but may affect any part of the body. The most common sequelae are chronic respiratory insufficiency and Addison's disease. The infectious agent, <i>Paracoccidioides brasiliensis</i>, is a fungus limited to Latin America.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Paracoccidioidomycosis | |
| fr | Paracoccidioïdomycose | |
| de | Parakokzidioidomykose | |
| es | Paracoccidiomicosis | |
| it | Paracoccidioidomicosi | |
| nl | Paracoccidioïdomycose | |
| pt | Paracoccidioidomicose | |
| pl | Parakokcydioidomikoza | |
| cs | Paracokcidioidomykóza | |
| uk | Паракокцидіоїдомікоз | |
| zh | 副球孢子菌病 | |
| tr | Parakoksidioidomikoz |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | B41.0 | BTNT | specific | validated |
| ICD-10 | B41.7 | BTNT | specific | validated |
| ICD-10 | B41.8 | BTNT | specific | validated |
| ICD-10 | B41.9 | BTNT | specific | validated |
| ICD-11 | 1F2E | E | specific | validated |
| ICD-11 | 1F2E.0 | BTNT | specific | validated |
| ICD-11 | 1F2E.1 | BTNT | specific | validated |
| ICD-11 | 1F2E.Y | BTNT | attributed | validated |
| MONDO | 0005894 | E | validated | |
| MeSH | D010229 | E | validated | |
| UMLS | C0030409 | E | validated | |
| GARD | 7323 | E | validated | |
| MedDRA | 10061906 | 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:163591Rare mycosis
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 | 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/73260
- This record as JSON: /data/d/73260.json