Home Page
References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 23/06/2006
Symbol DFNA39
Location 4q22.1
HGNC id 13833
Name neurosensory deafness 39
Other name(s)
  • dentin sialophosphoprotein
  • DFNA39/DGI1 syndrome
  • Corresponding gene DSPP
    Main clinical features with dentinogenesis imperfecta 1
    Genetic determination autosomal dominant
    Function/system disorder ear
    Type disease
    Remark(s)