ORPHA:700286
Congenital high airway obstruction syndrome
Synonyms: CHAOS
- Type
- Clinical syndrome
- Group
- Disorder
- Age of onset
- Antenatal
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital high airway obstruction syndrome | CHAOS |
| fr | Syndrome congénital d'obstruction des voies aériennes supérieures | |
| de | Syndrom des kongenitalen Verschlusses der oberen Atemwege | CHAO-Syndrom · CHAOS |
| es | Síndrome de obstrucción congénita de las vías aéreas superiores | = en |
| it | Sindrome da ostruzione congenita delle vie aeree superiori | = en |
| nl | Syndroom van congenitale obstructie van bovenste luchtwegen | = en |
| pt | Congenital high airway obstruction syndrome | |
| pl | Congenital high airway obstruction syndrome | = en |
| cs | Congenital high airway obstruction syndrome | = en |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | J98.8 | NTBT | attributed | not yet validated |
| ICD-11 | KB2J.Y | NTBT | attributed | not yet validated |
| MONDO | 1060125 | 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 (2):
- ORPHA:108993Non-syndromic respiratory or mediastinal malformation
rare developmental anomalies during embryogenesis; rare genetic diseases; rare surgical thoracic diseases - ORPHA:182111Respiratory malformation
rare respiratory diseases
No children.
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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.
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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/700286
- This record as JSON: /data/d/700286.json