Skip to main content
Home
Hereditary Hearing Loss Homepage

CHARGE Syndrome

Gene (OMIM) Genomic Location Inheritance Key Reference (PubMed)
SEMA3E 7q21.11 Autosomal Dominant Lalani et al., 2004
CHD7 8q12.2 Autosomal Dominant Vissers et al., 2004

 

Main navigation

Show — Main navigation Hide — Main navigation
  • Home
  • Contact
  • About the HHL Homepage
  • Citing the HHL Homepage
  • Dominant Nonsyndromic Hearing Loss
    • Genes: Dominant NSHL
    • Loci: Dominant NSHL
  • Recessive Nonsyndromic Hearing Loss
    • Genes: Recessive NSHL
    • Loci: Recessive NSHL
  • X-Linked Nonsyndromic Hearing Loss
    • Genes: X-linked NSHL
    • Loci: X-linked NSHL
  • Other Loci
  • Syndromic Hearing Loss
    • Alport Syndrome
    • Branchio-Oto-Renal Syndrome
    • CHARGE Syndrome
    • Jervell & Lange-Nielsen Syndrome
    • Norrie Disease
    • Pendred Syndrome
    • Perrault Syndrome
    • Stickler Syndrome
    • Treacher Collins Syndrome
    • Usher Syndrome
    • Waardenburg Syndrome
  • HHL Updates Log
  • Useful Links

Search The Hereditary Hearing Loss Homepage

User login

  • Reset your password