PLEK

pleckstrin
OMIM: 173570, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red PLEK in Monogenic hearing loss

Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 4.38
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Literature
    Phenotypes
    • Deafness, autosomal dominant 58 MIM#615654