ORPHA:2787
OBSOLETE: Osteoporosis-macrocephaly-blindness-joint hyperlaxity syndrome
inactive · referred to ORPHA:93446Primary bone dysplasia with decreased bone density
Synonyms: OBSOLETE: Heide 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 Primary bone dysplasia with decreased bone density
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Osteoporosis-macrocephaly-blindness-joint hyperlaxity syndrome | OBSOLETE: Heide syndrome |
| fr | OBSOLETE : Syndrome d'ostéoporose-macrocéphalie-cécité-hyperlaxité articulaire | OBSOLETE : Syndrome de Heide |
| de | OBSOLET: Osteoporose-Makrozephalie-Blindheit-Gelenkinstabilität-Syndrom | OBSOLET: Heide-Syndrom |
| es | OBSOLETO: Síndrome de osteoporosis-macrocefalia-ceguera-hiperlaxitud articular | OBSOLETO: Síndrome de Heide |
| it | OBSOLETO: Sindrome osteoporosi-macrocefalia-cecità-iperlassità articolare | OBSOLETO: Sindrome di Heide |
| nl | OBSOLEET: Osteoporose - macrocefalie - blindheid - gewrichtshyperlaxiteit-syndroom | OBSOLEET: Syndroom van Heide |
| pt | OBSOLETO: Síndrome de osteoporose-macrocefalia-cegueira-hipermobilidade articular | OBSOLETO: Síndrome Heide |
| pl | NIEAKTUALNE: Zespół osteoporozy, makrocefalii, ślepoty i nadmiernej ruchomości stawów | NIEAKTUALNE: Zespół Heidego |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující osteoporózu, makrocefalii, slepotu a kloubní hyperlaxitu | NEAKTUÁLNÍ: Heideho syndrome |
| uk | Синдром остеопорозу-макроцефалії-сліпоти- гіперлабільності суглобів | Синдром Гейде |
| zh | 骨质疏松症-大头畸形-失明-关节过度松弛综合征 | Heide综合征 |
| tr | Osteoporoz-makrosefali-körlük-eklem hiperlaksite sendromu | Heide sendromu |
Definition in:
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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/2787
- This record as JSON: /data/d/2787.json