| ID |
http://id.who.int/icd/entity/304883627 |
| Preferred Name |
Syndrome de Waardenburg |
| Definitions |
Autosomal dominant inherited syndrome consisting in congenital sensorineural hearing loss and hypomelanosis of skin, hair and irides. |
| Type |
http://www.w3.org/2002/07/owl#Class |
| comment | autosomal dominant vererbtes Syndrom, bestehend aus angeborenem sensorineuralem Hörverlust und Hypomelanose von Haut, Haaren und Iriden. autosomalny dominujący zespół dziedziczny, składający się z wrodzonego niedosłuchu sensorycznie niedosłuchowego i hypomelanosis skóry, włosów i irides. autosomal κυρίαρχο σύνδρομο που αποτελείται από εκ γενετής αισθητηριακή απώλεια ακοής και hypomelanosis του δέρματος, τα μαλλιά και τα ιριδίζοντα. Autosomal dominant inherited syndrome consisting in congenital sensorineural hearing loss and hypomelanosis of skin, hair and irides. syndrome héréditaire autosomique dominant consistant en une perte auditive sensorinéale congénitale et une hypomélanose de la peau, des cheveux et des irides. |
| broaderTransitive | http://id.who.int/icd/entity/2051636429 |
| prefLabel | Syndrome de Waardenburg |
| browserUrl | NA |
| narrowerTransitive | http://id.who.int/icd/entity/847608197 |
| label | σύνδρομο waardenburg zespół waardenburg Waardenburg-Syndrom Syndrome de Waardenburg Waardenburg syndrome |
| subClassOf | http://id.who.int/icd/entity/1106405864 |
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