ORPHA:199257
Superficial fibromatosis
- Type
- Clinical group
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Superficial fibromatosis | |
| fr | Fibromatose superficielle | |
| de | Fibromatose, superfizielle | |
| es | Fibromatosis superficial | |
| it | Fibromatosi superficiale | |
| nl | Oppervlakkige fibromatose | |
| pt | Fibromatose superficial | |
| pl | Włokniakowatość powierzchowna | Choroba Ledderhose |
| cs | Povrchová fibromatóza | |
| uk | Поверхневий фіброматоз | |
| zh | 浅表纤维瘤病 | |
| tr | Yüzeyel fibromatoz |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0016037 | E | validated | |
| MONDO | 16037 | E | validated | |
| UMLS | C0406571 | 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
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
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/199257
- This record as JSON: /data/d/199257.json