ORPHA:93425
Filamin-related bone disorder
Synonyms: Bone filaminopathy
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Filamin-related bone disorder | Bone filaminopathy |
| fr | Maladie osseuse liée à la filamine | Filaminopathie osseuse |
| de | Filamin-abhängige Knochenkrankheit | Knochen-Filaminopathie |
| es | Trastorno óseo asociado a la filamina | Filaminopatía del hueso |
| it | Difetto osseo legato alla filamina | Filaminopatia scheletrica |
| nl | Filaminegerelateerde botaandoening | Botfilaminopathie |
| pt | Doença óssea filamina-relacionada | |
| pl | Filaminopatia kości | = en |
| cs | Onemocnění kostí asociovaná s defektem filaminu | Kostní filaminopatie |
| uk | Розлад кісток, повязаний з філаміном | Кісткова філамінопатія |
| zh | 细丝蛋白相关骨病 | 骨纤维病 |
| tr | Filamin-ilişkili kemik bozukluğu | Kemik filaminopatisi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019690 | E | validated | |
| UMLS | C5680280 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:364803Rare bone disease related to a common gene or pathway defect
rare genetic diseases
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/93425
- This record as JSON: /data/d/93425.json