ORPHA:698012
Fibromuscular dysplasia
Synonyms: FMD
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Fibromuscular dysplasia | FMD |
| fr | Dysplasie fibromusculaire | DFM |
| de | Fibromuskuläre Dysplasie | = en |
| es | Displasia fibromuscular | DFM |
| it | Displasia fibromuscolare | = en |
| nl | Fibromusculaire dysplasie | = en |
| pt | Fibromuscular dysplasia | |
| pl | Fibromuscular dysplasia | = en |
| cs | Fibromuscular dysplasia | = en |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | I77.3 | E | specific | validated |
| ICD-11 | BD41.0 | E | specific | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:496924Non-inflammatory vasculopathy
rare circulatory system diseases
Children (5):
- ORPHA:698069Fibromuscular dysplasia of the arteries of the extremities
- ORPHA:698036Fibromuscular dysplasia of the cervical and intracranial arteries
- ORPHA:698059Fibromuscular dysplasia of the coronary arteries
- ORPHA:698043Fibromuscular dysplasia of the renal arteries
- ORPHA:698063Fibromuscular dysplasia of the visceral arteries
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/698012
- This record as JSON: /data/d/698012.json