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References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 29-03-2023
Symbol DFNB114
Location 17p11.2
Name deafness, autosomal recessive 114
Corresponding gene GRAP
Main clinical features
  • congenital profound sensorineural hearing loss
  • nonsyndromic
  • Genetic determination autosomal recessive
    Function/system disorder ear
    Type disease
    Remark(s)