ORPHA:99078
Neuhauser anomaly
- Type
- Morphological anomaly
- Group
- Disorder
- Status
- active
Neuhauser anomaly is a rare cardiovascular morphological anomaly due to maldevelopment of embryonal aorta resulting in right aortic arch and left ligamentum arteriosum characterized by tracheoesophageal compression symptoms (stridor, dyspnea, dysphagia, apnoeic episodes, recurrent respiratory infections).
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Neuhauser anomaly | |
| fr | Anomalie de Neuhauser | |
| de | Neuhauser-Anomalie | |
| es | Anomalía de Neuhauser | |
| it | Anomalia di Neuhauser | |
| nl | Anomalie van Neuhauser | |
| pt | Anomalia de Neuhauser | |
| pl | Anomalia Neuhausera | |
| cs | Neuhauserova anomálie | |
| uk | Аномалія Нойхаузера | |
| zh | Neuhauser异常 | |
| tr | Neuhauser anomalisi |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q25.4 | NTBT | attributed | validated |
| ICD-11 | LA8B.2Y | NTBT | attributed | validated |
| MONDO | 0020416 | E | validated | |
| UMLS | C4707820 | 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:1132Aortic arch defects
rare developmental anomalies during embryogenesis; rare cardiac malformations; rare circulatory system diseases
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/99078
- This record as JSON: /data/d/99078.json