ORPHA:2060
Fukuda-Miyanomae-Nakata syndrome
inactive · moved to ORPHA:85199Craniosynostosis-anal anomalies-porokeratosis syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Craniosynostosis-anal anomalies-porokeratosis syndrome
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Fukuda-Miyanomae-Nakata syndrome | |
| fr | Syndrome de Fukuda-Miyanomae-Nakata | |
| de | Fukuda-Miyanomae-Nakata-Syndrom | |
| es | Síndrome de Fukuda-Miyanomae-Nakata | |
| it | Sindrome di Fukuda-Miyanomae-Nakata | |
| nl | Syndroom van Fukuda-Miyanomae-Nakata | |
| pt | Síndrome Fukuda-Miyanomae-Nakata | |
| pl | Zespół Fukuda, Miyanomae i Nakata | |
| cs | Fukudaův-Miyanomaeův-Nakataův syndrom | Fukuda-Miyanomae-Nakataův syndrom |
| uk | Синдром Фукуди-Міяномае-Наката | |
| zh | Fukuda-Miyanomae-Nakata综合征 | |
| tr | Fukuda-Miyanomae-Nakata sendromu |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Not placed in any Orphanet classification in this release.
No children.
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/2060
- This record as JSON: /data/d/2060.json