ORPHA:139491
OBSOLETE: Hemochromatosis type 4
inactive · referred to ORPHA:647834SLC40A1-related hemochromatosis
Synonyms: OBSOLETE: Autosomal dominant hereditary hemochromatosis · OBSOLETE: Ferroportin disease · OBSOLETE: Hemochromatosis due to defect in ferroportin
- 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 SLC40A1-related hemochromatosis
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Hemochromatosis type 4 | OBSOLETE: Autosomal dominant hereditary hemochromatosis · OBSOLETE: Ferroportin disease · OBSOLETE: Hemochromatosis due to defect in ferroportin |
| fr | OBSOLETE : Hémochromatose type 4 | OBSOLETE : Hémochromatose héréditaire autosomique dominante · OBSOLETE : Hémochromatose par défaut en ferroportine · OBSOLETE : Maladie ferroportine |
| de | OBSOLET: Hämochromatose Typ 4 | OBSOLET: Hämochromatose durch Ferroportin-Defekt · OBSOLET: Hämochromatose, autosomal-dominante · OBSOLET: Ferroportin-Krankheit |
| es | OBSOLETO: Hemocromatosis tipo 4 | OBSOLETO: Enfermedad de la ferroportina · OBSOLETO: Hemocromatosis hereditaria autosómica dominante · OBSOLETO: Hemocromatosis por un defecto de la ferroportina |
| it | OBSOLETO: Emocromatosi, tipo 4 | OBSOLETO: Emocromatosi da deficit di ferroportina · OBSOLETO: Emocromatosi ereditaria autosomica dominante · OBSOLETO: Malattia da ferroportina |
| nl | OBSOLEET: Hemochromatose type 4 | OBSOLEET: Autosomaal dominante erfelijke hemochromatose · OBSOLEET: Ferroportine-ziekte · OBSOLEET: Hemochromatose door defect van ferroportine |
| pt | OBSOLETO: Doença da ferroportina | |
| pl | NIEAKTUALNE: Hemochromatoza typu 4 | NIEAKTUALNE: Autosomalna dominująca hemochromatoza dziedziczna · NIEAKTUALNE: Choroba ferroportyny · NIEAKTUALNE: Hemochromatoza z powodu defektu ferroportyny |
| cs | NEAKTUÁLNÍ: Hemochromatóza, typ 4 | NEAKTUÁLNÍ: Autozomálně dominantní dědičná hemochromatóza · NEAKTUÁLNÍ: Onemocnění ferroportinu · NEAKTUÁLNÍ: Hemochromatóza způsobená poruchou ve ferroportinu |
| uk | ЗАСТАРІЛО: Гемохроматоз, тип 4 | ЗАСТАРІЛО: Аутосомно-домінантний спадковий гемохроматоз · ЗАСТАРІЛО: Ферропортиновий синдром · ЗАСТАРІЛО: Гемохроматоз внаслідок дефекту феропортину |
| zh | 血色病4型 | 常染色体显性遗传血色素沉着症 |
| tr | Hemokromatoz tip 4 | Ferroportin hastalığı · Ferroportin defektine bağlı hemokromatoz · Otozomal dominant kalıtsal hemokromatoz |
Definition in:
2
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/139491
- This record as JSON: /data/d/139491.json