ORPHA:2583
Mycetoma
Synonyms: Madura foot
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
A neglected tropical infection, rare in Europe, characterized by subcutaneous tumorous lesions in which mycetoma grains containing the causative agent can be observed. Mycetoma is a broad term encompassing both actinomycetoma (bacterial) and eumycetoma (fungal).
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Mycetoma | Madura foot |
| fr | Mycétome | Pied de Madura |
| de | Myzetom | Madurafuß · Maduramykose |
| es | Micetoma | Pie de madura |
| it | Micetoma | Piede di Madura |
| nl | Mycetoom | Madoera-voet · Madura-voet |
| pt | Micetoma | |
| pl | Grzybica madurska | Stopa madurska |
| cs | Mycetom | Madurská noha |
| uk | Міцетома | Мадурська нога |
| zh | 马杜拉分枝菌病 | 马杜拉足 |
| tr | Misetom | Madura ayak |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | B47.0 | BTNT | specific | validated |
| ICD-10 | B47.1 | BTNT | specific | validated |
| ICD-10 | B47.9 | BTNT | specific | validated |
| ICD-11 | 1C43 | BTNT | specific | validated |
| ICD-11 | 1F29 | BTNT | specific | validated |
| ICD-11 | 1G60.0 | BTNT | specific | validated |
| MONDO | 0016823 | E | validated | |
| MeSH | D008271 | E | validated | |
| UMLS | C0024449 | E | validated | |
| GARD | 3862 | E | validated | |
| MedDRA | 10028427 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:163582Rare bacterial infectious disease
rare infectious diseases - ORPHA:163591Rare mycosis
rare infectious diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
3 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
| Point prevalence | 1-9 / 100 000 | 0.09 / 100 000 | Sudan | Value and class | Validated | 24244780[PMID]_ORPHANET |
| Point prevalence | 1-9 / 100 000 | 0.2 / 100 000 | Mauritania | Value and class | Validated | 24244780[PMID]_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.
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HPO phenotypes
29 annotations · validated 2019-10-10| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Frequent (79-30%) | ||
| HP:0003330 | Abnormal bone structure | |
| HP:0031288 | Cobblestone-like hyperkeratosis | |
| HP:0001015 | Prominent superficial veins | |
| HP:0005406 | Recurrent bacterial skin infections | |
| HP:0002841 | Recurrent fungal infections | |
| HP:0030053 | Stiff skin | |
| HP:0010219 | Structural foot deformity | |
| HP:0001482 | Subcutaneous nodule | |
| Occasional (29-5%) | ||
| HP:0011844 | Abnormal appendicular skeleton morphology | |
| HP:0040072 | Abnormal forearm bone morphology | |
| HP:0001155 | Abnormality of the hand | |
| HP:0002815 | Abnormality of the knee | |
| HP:0100763 | Abnormality of the lymphatic system | |
| HP:0025245 | Cutaneous cyst | |
| HP:0002754 | Osteomyelitis | |
| HP:0000939 | Osteoporosis | |
| Very rare (<4-1%) | ||
| HP:0031500 | Abdominal mass | |
| HP:0003312 | Abnormal form of the vertebral bodies | |
| HP:0000765 | Abnormal thorax morphology | |
| HP:0000152 | Abnormality of head or neck | |
| HP:0000707 | Abnormality of the nervous system | |
| HP:0003418 | Back pain | |
| HP:0012062 | Bone cyst | |
| HP:0002661 | Painless fractures due to injury | |
| HP:0010550 | Paraplegia | |
| HP:0002756 | Pathologic fracture | |
| HP:0031501 | Pelvic mass | |
| HP:0100809 | Scalp tenderness | |
| HP:0002953 | Vertebral compression fracture | |
Annotation source: 29808607[PMID]_26738840[PMID]_28837657[PMID]
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/2583
- This record as JSON: /data/d/2583.json