Deafness, Autosomal Dominant 58

Preferred Label : Deafness, Autosomal Dominant 58;

NCIt synonyms : DFNA58;

NCIt definition : A genetic condition inherited in an autosomal dominant fashion linked to chromosome 2p21-p12, characterized by bilateral hearing loss.;

Details

Origin ID

C201585;

UMLS CUI

C3888210;

Has associated anatomic sites
- Ear [NCIt concept]
- Head and Neck [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness, autosomal dominant 58 [OMIM Phenotype]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]

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