Deafness, Autosomal Dominant 10

Preferred Label : Deafness, Autosomal Dominant 10;

NCIt synonyms : DFNA10;

NCIt definition : An autosomal dominant condition caused by mutation(s) in the EYA4 gene, encoding eyes absent homolog 4. It is a type of nonsyndromic hearing loss characterized by progressive sensorineural hearing loss.;

Détails

Origin ID

C212887;

Has associated anatomic sites
- Ear [NCIt concept]
- Head and Neck [NCIt concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
disease_has_finding
- Rare Lesion [NCIt concept]
disease_has_primary_anatomic_site
- Ear [NCIt concept]
- Head and Neck [NCIt concept]
disease_mapped_to_gene
- EYA4 Gene [NCIt concept]

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