ORPHA:168999
Malignant melanoma of the mucosa
- Type
- Disease
- Group
- Disorder
- Age of onset
- Adult, Elderly
- Status
- active
A rare, aggressive, neoplastic disease characterized by the presence of a melanocyte tumor that develops in any mucosal membrane. Clinical manifestations vary depending on the site of occurrence.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Malignant melanoma of the mucosa | |
| fr | Mélanome malin muqueux | |
| de | Malignes Melanom der Mukosa | |
| es | Melanoma maligno mucoso | Melanoma maligno de mucosa |
| it | Melanoma maligno della mucosa | |
| nl | Maligne melanoom van mucosa | Kwaadaardig melanoom van slijmvlies |
| pt | Melanoma maligno da mucosa | |
| pl | Złośliwy czerniak błony śluzowej | |
| cs | Maligní melanom sliznice | |
| uk | Злоякісна меланома слизової оболонки | |
| zh | 恶性粘膜黑色素瘤 | |
| tr | Mukozanın habis melanomu |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | C43.9 | NTBT | attributed | validated |
| ICD-11 | 2E63.Y | NTBT | attributed | validated |
| MONDO | 0015694 | E | validated | |
| UMLS | C5191057 | 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 (1):
- ORPHA:79386Rare skin tumor or hamartoma
rare skin diseases; rare neoplastic diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
5 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | 1-9 / 1 000 000 | 0.26 / 100 000 | Europe | Value and class | Validated | 22119735[PMID]_RARECARE surveillance of rare cancers in Europe[OTHER] |
| Point prevalence | Unknown | — | Europe | Class only | Validated | ORPHANET |
| Lifetime Prevalence | 1-9 / 100 000 | 1.5 / 100 000 | Europe | Value and class | Validated | 22119735[PMID]_RARECARE surveillance of rare cancers in Europe[OTHER] |
| Annual incidence | 1-9 / 1 000 000 | 0.32 / 100 000 | Belgium | Value and class | Validated | Belgium Cancer OTHERistry[OTHER] |
| Annual incidence | 1-9 / 1 000 000 | 0.23 / 100 000 | United States | Value and class | Validated | National Cancer OTHERitute[OTHER]_24272143[PMID] |
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
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/168999
- This record as JSON: /data/d/168999.json