OTX1

orthodenticle homeobox 1
OMIM: 600036, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red OTX1 in Autism


Version 0.36

review Not set
Sources
  • Expert Review Red
  • SFARI
Red OTX1 in Monogenic hearing loss

Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 4.36
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

  • Paediatric disorders
  • review Not set
    Sources
    • Expert