SPP2

secreted phosphoprotein 2
OMIM: 602637, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red SPP2 in Retinitis pigmentosa_Autosomal Dominant


Level 2: Ophthalmological disorders
Version 0.57

Component of the following Super Panels:

  • Retinal Disorders Superpanel
  • Retinitis Pigmentosa Superpanel
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Red
    • Royal Melbourne Hospital
    Phenotypes
    • Autosomal dominant retinitis pigmentosa