Variants
Sign InSign Up

Autosomal recessive nonsyndromic hearing loss 63

Your Results

Sign In

Description

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the LRTOMT gene.

MONDO

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

80

SEE THE VARIANTS →

Genes

External Links

  • OMIM

    611451

  • Orphanet
  • HPO
  • Medgen

    C1969621

© 2024 Biocodify. All rights reserved.

TwitterTwitter

Product

HomePricingDashboard

Stay up to date

The latest news and updates from Biocodify, sent to your inbox.