ORPHA:2765
OBSOLETE: Hypertrichotic osteochondrodysplasia
inactive · referred to ORPHA:1517Cantú syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Cantú syndrome
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Hypertrichotic osteochondrodysplasia | |
| fr | OBSOLETE : Syndrome d'ostéochondrodysplasie-hypertrichose | |
| de | OBSOLET: Osteochondrodysplasie - Hypertrichose | |
| es | OBSOLETO: Osteocondrodisplasia hipertricosis | |
| it | OBSOLETO: Osteocondrodisplasia ipertricotica | |
| nl | OBSOLEET: Hypertrichotische osteochondrodysplasie | |
| pt | OBSOLETO: Osteo-condrodisplasia hipertricótica | |
| pl | NIEAKTUALNE: Osteochondrodysplazja hipertrichotyczna | |
| cs | NEAKTUÁLNÍ: Hypertrichotická osteochondrodysplázie | |
| uk | ЗАСТАРІЛО: Гіпертрихотична остеохондродисплазія | |
| zh | 弃用：多毛性骨软骨发育不良 | |
| tr | Eski adı: Hipertrikotik osteokondrodisplazi |
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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/2765
- This record as JSON: /data/d/2765.json