ORPHA:723156
Fetal acetylcholine receptor antibody-related disorder
Synonyms: FARAD
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Antenatal
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Fetal acetylcholine receptor antibody-related disorder | FARAD |
| fr | Trouble lié aux anticorps anti-récepteurs de l'acétylcholine foetaux | = en |
| de | Fetale Acetylcholinrezeptor-Antikörper-Störung | FARAD · Fetales AChR-Inaktivierungs-Syndrom · FARIS |
| es | Trastorno fetal asociado a anticuerpos receptores de acetilcolina | = en |
| it | Malattia correlata agli anticorpi fetali diretti contro il recettore dell'acetilcolina | = en |
| nl | Foetale aandoening gerelateerd aan acetylcholinereceptor-antilichaam | = en |
| pt | Fetal acetylcholine receptor antibody-related disorder | |
| pl | Fetal acetylcholine receptor antibody-related disorder | = en |
| cs | Fetal acetylcholine receptor antibody-related disorder | = en |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:109007Arthrogryposis syndrome
rare developmental anomalies during embryogenesis - ORPHA:251535Maternal disease-related embryofetopathy
rare developmental anomalies during embryogenesis; rare teratologic disorders
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 46 cases | Worldwide | Case(s) | Validated | ORPHANET | |
| Point prevalence | <1 / 1 000 000 | — | 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/723156
- This record as JSON: /data/d/723156.json