ORPHA:698260
Carotid web
Synonyms: AFMD · Atypical FMD · Atypical fibromuscular dysplasia · CaW · Carotid diaphragm
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Carotid web | AFMD · Atypical FMD · Atypical fibromuscular dysplasia · CaW · Carotid diaphragm |
| fr | Web carotidien | CaW · Carotid web · Diaphragme carotidien · Dysplasie fibromusculaire atypique |
| de | Carotid Web | AFMD · Atypische FMD · Atypische FMD der Carotis · Atypische fibromuskuläre Dysplasie · CaW |
| es | Membrana carotídea | CaW · DFM atípica · Diafragma carotídeo · Displasia fibromuscular atípica · Web carotídeo |
| it | Rete carotidea | AFMD · AFMD atipica · Displasia fibromuscolare atipica · CaW · Diaframma carotideo |
| nl | Carotisweb | AFMD · Atypische FMD · Atypische fibromusculaire dysplasie · CaW · Carotisdiafragma |
| pt | Carotid web | |
| pl | Carotid web | = en |
| cs | Carotid web | = en |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | I77.3 | NTBT | attributed | not yet validated |
| ICD-11 | BD41.0 | NTBT | attributed | not yet 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:458844Rare vascular malformation of major vessels
rare developmental anomalies during embryogenesis; rare circulatory system diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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/698260
- This record as JSON: /data/d/698260.json