ORPHA:2691
Nevo syndrome
inactive · moved to ORPHA:1900Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency
Synonyms: Cerebral gigantism, Nevo type
- 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 Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Nevo syndrome | Cerebral gigantism, Nevo type |
| fr | Syndrome de Nevo | Gigantisme cérébral type Nevo |
| de | Nevo-Syndrom | Zerebraler Gigantismus Typ Nevo |
| es | Síndrome de Nevo | |
| it | Sindrome di Nevo | Gigantismo cerebrale, tipo Nevo |
| nl | Syndroom van Nevo | Cerebrale reuzengroei, Nevo-type |
| pt | Síndrome Nevo | Gigantismo cerebral, tipo Nevo |
| pl | Zespół Nevo | Gigantyzm mózgu, typu Nevo |
| cs | Nevové syndrom | Cerebrální gigantismus, typ Nevové |
| uk | Синдром Нево | Церебральний гігантизм, тип Нево |
| zh | Nevo综合征 | 脑性巨人症，Nevo型 |
| tr | Nevo sendromu | Serebral jigantizm, Nevo tipi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MeSH | C536113 | E | validated | |
| UMLS | C2936777 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/2691
- This record as JSON: /data/d/2691.json