ORPHA:435
OBSOLETE: Ito hypomelanosis
inactive · referred to ORPHA:79376Hypopigmentation of the skin
Synonyms: OBSOLETE: HI syndrome · OBSOLETE: Hypomelanosis of Ito · OBSOLETE: Pigmentary mosaicism, Ito type
- 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 Hypopigmentation of the skin
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Ito hypomelanosis | OBSOLETE: HI syndrome · OBSOLETE: Hypomelanosis of Ito · OBSOLETE: Pigmentary mosaicism, Ito type |
| fr | OBSOLETE : Hypomélanose d'Ito | OBSOLETE : Incontinentia pigmenti achromians · OBSOLETE : Mosaïcisme pigmentaire de type Ito |
| de | OBSOLET: Hypomelanose Typ Ito | OBSOLET: HI-Syndrom · OBSOLET: Incontinentia pigmenti Typ 1 · OBSOLET: Pigmentmosaik vom Typ Ito |
| es | OBSOLETO: Hipomelanosis de Ito | OBSOLETO: Mosaicismo pigmentario tipo Ito · OBSOLETO: Síndrome HI |
| it | OBSOLETO: Ipomelanosi di Ito | OBSOLETO: Mosaicismo pigmentario, tipo Ito · OBSOLETO: Sindrome HI |
| nl | OBSOLEET: Ito-hypomelanosis | OBSOLEET: HI-syndroom · OBSOLEET: Hypomelanosis van Ito · OBSOLEET: Incontinentia pigmenti type 1 · OBSOLEET: Pigmentair mozaïcisme, Ito-type |
| pt | OBSOLETO: Hipomelanose de Ito | |
| pl | NIEAKTUALNE: Hipomelanoza Ito | NIEAKTUALNE: Mozaikowatosć barwnikowy, typ Ito · NIEAKTUALNE: Nietrzymanie barwnika typu 1 · NIEAKTUALNE: Zespół HI |
| cs | NEAKTUÁLNÍ: Ito hypomelanosis | NEAKTUÁLNÍ: HI syndrom · NEAKTUÁLNÍ: Incontinentia pigmenti, typ 1 · NEAKTUÁLNÍ: Pigmentový mosaicismus, Itův typ |
| uk | ЗАСТАРІЛО: Гіпомеланоз Іто | ЗАСТАРІЛО: HI-синдром · ЗАСТАРІЛО: Гіпомеланоз Іто · ЗАСТАРІЛО: Пігментна мозаїчність, тип Іто |
| zh | 弃用：无色性色素失调症 | 色素镶嵌现象Ito型 |
| tr | Eski adı: Ito hipomelanoz | HI sendromu · Ito'nun hipomelanozu · Pigment mozaisizmi, Ito tipi |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/435
- This record as JSON: /data/d/435.json