ORPHA:156246
Nose and cavum anomaly
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Nose and cavum anomaly | |
| fr | Anomalie du nez et du cavum | |
| de | Nasen- und Nasenrachenraumanomalie | |
| es | Anomalía de nariz y nasofaringe | |
| it | Anomalia del naso e del cavo | |
| nl | Neus- en cavumanomalie | |
| pt | Anomalia do nariz e cavidade nasal | |
| pl | Wada nosa i jamy nosowej | |
| cs | Anomálie nosu a nosní dutiny | |
| uk | Аномалія носа та порожнини рота | |
| zh | 鼻腔异常 | |
| tr | Burun ve kavum anomalisi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | LA70 | E | specific | validated |
| MONDO | 15503 | E | validated | |
| UMLS | C5680661 | E | 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:96333Rare otorhinolaryngological malformation
rare developmental anomalies during embryogenesis; rare otorhinolaryngological diseases
Children (23):
- ORPHA:217266BNAR syndrome
- ORPHA:2695Bifid nose
- ORPHA:1252Blepharonasofacial malformation syndrome
- ORPHA:1200Burn-McKeown syndrome
- ORPHA:137914Choanal atresia
- ORPHA:589856Choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome
- ORPHA:717646Congenital midnasal stenosis
- ORPHA:157832Craniorhiny
- ORPHA:451612Familial congenital nasolacrimal duct obstruction
- ORPHA:2250Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome
- ORPHA:137622Intractable diarrhea-choanal atresia-eye anomalies syndrome
- ORPHA:1134Isolated arrhinia
- ORPHA:162516Isolated congenital nasal pyriform aperture stenosis
- ORPHA:2363Lacrimoauriculodentodigital syndrome
- ORPHA:99141Lymphedema-posterior choanal atresia syndrome
- ORPHA:141118Nasal encephalocele
- ORPHA:141112Nasal glial heterotopia
- ORPHA:141083Nasolacrimal duct cyst
- ORPHA:141091Polyrrhinia
- ORPHA:141099Proboscis lateralis
- ORPHA:3026Radial ray hypoplasia-choanal atresia syndrome
- ORPHA:141096Supernumerary nostril
- ORPHA:466695Supratip dysplasia
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/156246
- This record as JSON: /data/d/156246.json