Deafness, autosomal dominant 82

Preferred Label : Deafness, autosomal dominant 82;

Symbol : DFNA82;

Type : Phenotype, molecular basis known;

Prefixed ID : #619804;

Details

Origin ID

619804;

UMLS CUI

C5676948;

Genes related to phenotype
- Atpase, ca(2+)-transporting, plasma membrane, 2 [OMIM gene]
ORDO concept(s)
- Autosomal recessive non-syndromic sensorineural deafness type DFNB [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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