ORPHA:3050
OBSOLETE: Intellectual disability-hypotonia-skin hyperpigmentation syndrome
inactive · referred to ORPHA:102369Rare syndromic intellectual disability
Synonyms: OBSOLETE: Medrano-Roldan syndrome
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Rare syndromic intellectual disability
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Intellectual disability-hypotonia-skin hyperpigmentation syndrome | OBSOLETE: Medrano-Roldan syndrome |
| fr | OBSOLETE : Syndrome de déficience intellectuelle-hypotonie-hyperpigmentation | OBSOLETE : Syndrome de Medrano-Roldan |
| de | OBSOLET: Intelligenzminderung-Hypotonie-Hyperpigmentierung-Syndrom | OBSOLET: Medrano-Roldan-Syndrom |
| es | OBSOLETO: Síndrome de discapacidad intelectual-hipotonía-hiperpigmentación de la piel | OBSOLETO: Síndrome de Medrano-Roldan |
| it | OBSOLETO: Sindrome disabilità intellettiva-ipotonia-iperpigmentazione | OBSOLETO: Sindrome di Medrano-Roldan |
| nl | OBSOLEET: Intellectuele achterstand - hypotonie - hyperpigmentatie van huid-syndroom | OBSOLEET: Syndroom van Medrano-Roldan |
| pt | OBSOLETO: Síndrome de perturbação do desenvolvimento intelectual-hipotonia-hiperpigmentação cutânea | OBSOLETO: Síndrome Medrano-Roldan |
| pl | NIEAKTUALNE: Niepelnosprawnosc intelektualna - hipotonia - hiperpigmentacja skóry | NIEAKTUALNE: Zespół Medrano i Roldana |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující mentální retardaci, hypotonii a hyperpigmentaci kůže | NEAKTUÁLNÍ: Medranův-Roldanův syndrom · NEAKTUÁLNÍ: Medrano-Roldanův syndrom |
| uk | ЗАСТАРІЛО: Синдром розумової відсталості-гіпотонії-гіперпігментації шкіри | ЗАСТАРІЛО: Синдром Медрано-Ролдана |
| zh | 弃用：智力障碍-肌张力低下-皮肤色素沉着过度综合征 | Medrano-Roldan综合征 |
| tr | Eski adı: Zihinsel yetersizlik-hipotoni-cilt hiperpigmentasyon sendromu | Medrano-Roldan 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/3050
- This record as JSON: /data/d/3050.json