CEP162

centrosomal protein 162
OMIM: 610201, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber CEP162 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Retinitis pigmentosa MONDO:0019200, CEP162-related

Amber CEP162 in Retinitis pigmentosa_Autosomal Recessive/X-linked


Level 2: Ophthalmological disorders
Version 0.147

Component of the following Super Panels:

  • Retinal Disorders Superpanel
  • Retinitis Pigmentosa Superpanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Retinitis pigmentosa MONDO:0019200, CEP162-related