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Autosomal dominant nonsyndromic hearing loss 18(DFNA18)

MedGen UID:
340051
Concept ID:
C1853760
Disease or Syndrome
Synonym: Deafness, autosomal dominant 18
 
Monarch Initiative: MONDO:0011625
OMIM®: 606012

Definition

An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 3q22. [from MONDO]

Clinical features

From HPO
Progressive hearing impairment
MedGen UID:
331224
Concept ID:
C1842138
Finding
A progressive form of hearing impairment.

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  

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