NOL10

nucleolar protein 10
OMIM: 616197, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red NOL10 in Mendeliome


Version 1.3664

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • NOL10-related neurological disorder MONDO:0100545

Red NOL10 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.286

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    • Literature
    Phenotypes
    • NOL10-related neurological disorder MONDO:0100545